Page last updated: 2024-10-20

thiamine and Syndrome

thiamine has been researched along with Syndrome in 71 studies

thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.

Syndrome: A characteristic symptom complex.

Research Excerpts

ExcerptRelevanceReference
" Thiamine-responsive megaloblastic anaemia (TRMA), due to mutations in the thiamine transporter SLC19A2, is associated with the classical clinical triad of diabetes, deafness, and megaloblastic anaemia."8.88Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia. ( Abdullah, M; Ellard, S; Flanagan, SE; Grulich-Henn, J; Habeb, AM; Hattersley, AT; Hussain, K; Matyka, K; Patch, AM; Pomahacova, R; Shaw-Smith, C, 2012)
" The diabetic states that associate with these genetic variants are MODY 2, thiamine responsive anaemia syndrome (TRAS) and mitochondrial diabetes."8.81Mitochondrial diabetes, diabetes and the thiamine-responsive megaloblastic anaemia syndrome and MODY-2. Diseases with common pathophysiology? ( Maassen, JA, 2002)
"5 years, because of the presence of diabetes and sensorineural deafness, she was diagnosed with TRMA syndrome and started treatment with thiamine-HCl, followed very early by benzoyloxymethyl-thiamine (BOM-T)."8.80Long-term follow-up of diabetes in two patients with thiamine-responsive megaloblastic anemia syndrome. ( Franzese, A; Poggi, V; Tenore, A; Valerio, G, 1998)
"Thiamine responsive megaloblastic anemia syndrome (TRMA) is a clinical triad characterized by thiamine-responsive anemia, diabetes mellitus and sensorineural deafness."7.75Thiamine responsive megaloblastic anemia syndrome. ( Ezhilarasi, S; Ganesh, R; Gowrishankar, K; Rajajee, S; Vasanthi, T, 2009)
"Diabetes in this syndrome is due to an insulin insufficiency that initially responds to thiamine supplements; however, most patients become fully insulin dependent after puberty."7.73Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. ( Ariyawansa, I; Barrett, TG; Lo, IF; Minton, JA; Ricketts, CJ; Samuel, J; Wales, JK, 2006)
"Thiamine-responsive megaloblastic anemia (TRMA) syndrome is an autosomal recessive disorder characterized by diabetes mellitus (DM), progressive sensorineural deafness, and thiamine-responsive anemia."7.72Novel mutation in the SLC19A2 gene in an African-American female with thiamine-responsive megaloblastic anemia syndrome. ( Calikoglu, AS; Lagarde, WH; Moats-Staats, BM; Underwood, LE, 2004)
"Thiamine-responsive megaloblastic anaemia (TRMA) syndrome with diabetes and deafness was found in two patients from a Tunisian kindred."7.71A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome. ( Belhani, A; Berul, CI; Fleming, JC; Gritli, S; Guannouni, S; Hafsia, R; Hamdi, M; Jilani, SB; Neufeld, EJ; Omar, S; Steinkamp, MP; Tartaglini, E, 2001)
"Two practical methods are reported for treating feral Baltic salmon with thiamine hydrochloride against M74 syndrome (abnormally high yolk-sac fry mortality of the Baltic salmon)."7.70Treatment with thiamine hydrochloride and astaxanthine for the prevention of yolk-sac mortality in Baltic salmon fry (M74 syndrome). ( Hartikainen, K; Koski, P; Nakari, T; Pakarinen, M; Soivio, A, 1999)
"Thiamine-responsive megaloblastic anaemia syndrome (TRMA; MIM 249270) is an autosomal recessive disorder with features that include megaloblastic anaemia, mild thrombocytopenia and leucopenia, sensorineural deafness and diabetes mellitus."7.70Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. ( Banikazemi, M; Desnick, RJ; Diaz, GA; Gelb, BD; Oishi, K, 1999)
"Thiamine-responsive megaloblastic anemia (TRMA, also known as Rogers syndrome, OMIM 249270) is a rare autosomal recessive disorder characterized by a triad of megaloblastic anemia, diabetes mellitus, and sensorineural deafness."7.70Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity. ( Barrett, T; Cohen, N; Mandel, H; Neufeld, EJ; Nosaka, K; Raz, T; Szargel, R; Viana, MB, 1998)
"We have investigated the cellular pathology of the syndrome called thiamine-responsive megaloblastic anemia (TRMA) with diabetes and deafness."7.70Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts. ( Baker, MA; Cohen, N; Fleming, JC; Neufeld, EJ; Sakamoto, M; Stagg, AR, 1999)
"Thiamine-responsive megaloblastic anaemia with diabetes and deafness (TRMA; MIM 249270) is an autosomal recessive disease thought to be due to a defect in thiamine (vitamin B1) transport."7.70The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. ( Cohen, N; Fleming, JC; Neufeld, EJ; Schorderet, DF; Steinkamp, MP; Tartaglini, E, 1999)
"Thiamine-responsive megaloblastic anaemia (TRMA), also known as Rogers syndrome, is an early onset, autosomal recessive disorder defined by the occurrence of megaloblastic anaemia, diabetes mellitus and sensorineural deafness, responding in varying degrees to thiamine treatment (MIM 249270)."7.70Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. ( Baron, D; Barrett, T; Cohen, N; Gregory, S; Labay, V; Mandel, H; McDonald, L; Nosaka, K; Raz, T; Shalata, A; Szargel, R; Williams, H, 1999)
"Thiamine-responsive megaloblastic anemia, also known as "TRMA" or "Rogers syndrome," is an early-onset autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and sensorineural deafness, responding in varying degrees to thiamine treatment."7.69Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping. ( Barrett, T; Buist, N; Cohen, N; Fauré, S; Mandel, H; Neufeld, EJ; Raz, T; Stagg, A; Szargel, R; Yandava, CN, 1997)
"Three brothers with diabetes mellitus, thiamine-responsive megaloblastic anemia, and sensorineural deafness are reported."7.67Diabetes mellitus, thiamine-dependent megaloblastic anemia, and sensorineural deafness associated with deficient alpha-ketoglutarate dehydrogenase activity. ( Abboud, MR; Alexander, D; Najjar, SS, 1985)
"Rogers syndrome is an autosomal recessive disorder resulting in megaloblastic anemia, diabetes mellitus, and sensorineural deafness."5.32Disruption of transport activity in a D93H mutant thiamine transporter 1, from a Rogers Syndrome family. ( Aronheim, A; Assaraf, YG; Baron, D; Drori, S, 2003)
" Thiamine-responsive megaloblastic anaemia (TRMA), due to mutations in the thiamine transporter SLC19A2, is associated with the classical clinical triad of diabetes, deafness, and megaloblastic anaemia."4.88Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia. ( Abdullah, M; Ellard, S; Flanagan, SE; Grulich-Henn, J; Habeb, AM; Hattersley, AT; Hussain, K; Matyka, K; Patch, AM; Pomahacova, R; Shaw-Smith, C, 2012)
" The diabetic states that associate with these genetic variants are MODY 2, thiamine responsive anaemia syndrome (TRAS) and mitochondrial diabetes."4.81Mitochondrial diabetes, diabetes and the thiamine-responsive megaloblastic anaemia syndrome and MODY-2. Diseases with common pathophysiology? ( Maassen, JA, 2002)
"5 years, because of the presence of diabetes and sensorineural deafness, she was diagnosed with TRMA syndrome and started treatment with thiamine-HCl, followed very early by benzoyloxymethyl-thiamine (BOM-T)."4.80Long-term follow-up of diabetes in two patients with thiamine-responsive megaloblastic anemia syndrome. ( Franzese, A; Poggi, V; Tenore, A; Valerio, G, 1998)
"Thiamine responsive megaloblastic anemia syndrome (TRMA) is a clinical triad characterized by thiamine-responsive anemia, diabetes mellitus and sensorineural deafness."3.75Thiamine responsive megaloblastic anemia syndrome. ( Ezhilarasi, S; Ganesh, R; Gowrishankar, K; Rajajee, S; Vasanthi, T, 2009)
"Thiamine-responsive megaloblastic anemia syndrome is a rare autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and neurosensoriel deafness, responding in varying degrees to thiamine treatment."3.75Unusual case of thiamine responsive megaloblastic anemia. ( Ben Amor, S; Ben Lasouad, M; Bousnina, S; Boussetta, K; Kaabachi, N; Tinsa, F, 2009)
"Diabetes in this syndrome is due to an insulin insufficiency that initially responds to thiamine supplements; however, most patients become fully insulin dependent after puberty."3.73Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families. ( Ariyawansa, I; Barrett, TG; Lo, IF; Minton, JA; Ricketts, CJ; Samuel, J; Wales, JK, 2006)
"Thiamine-responsive megaloblastic anemia (TRMA) syndrome is an autosomal recessive disorder characterized by diabetes mellitus (DM), progressive sensorineural deafness, and thiamine-responsive anemia."3.72Novel mutation in the SLC19A2 gene in an African-American female with thiamine-responsive megaloblastic anemia syndrome. ( Calikoglu, AS; Lagarde, WH; Moats-Staats, BM; Underwood, LE, 2004)
"Thiamine-responsive megaloblastic anaemia (TRMA) syndrome with diabetes and deafness was found in two patients from a Tunisian kindred."3.71A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome. ( Belhani, A; Berul, CI; Fleming, JC; Gritli, S; Guannouni, S; Hafsia, R; Hamdi, M; Jilani, SB; Neufeld, EJ; Omar, S; Steinkamp, MP; Tartaglini, E, 2001)
"Thiamine-responsive megaloblastic anemia (TRMA, also known as Rogers syndrome, OMIM 249270) is a rare autosomal recessive disorder characterized by a triad of megaloblastic anemia, diabetes mellitus, and sensorineural deafness."3.70Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity. ( Barrett, T; Cohen, N; Mandel, H; Neufeld, EJ; Nosaka, K; Raz, T; Szargel, R; Viana, MB, 1998)
"We have investigated the cellular pathology of the syndrome called thiamine-responsive megaloblastic anemia (TRMA) with diabetes and deafness."3.70Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts. ( Baker, MA; Cohen, N; Fleming, JC; Neufeld, EJ; Sakamoto, M; Stagg, AR, 1999)
"Thiamine-responsive megaloblastic anaemia syndrome (TRMA; MIM 249270) is an autosomal recessive disorder with features that include megaloblastic anaemia, mild thrombocytopenia and leucopenia, sensorineural deafness and diabetes mellitus."3.70Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. ( Banikazemi, M; Desnick, RJ; Diaz, GA; Gelb, BD; Oishi, K, 1999)
"Thiamine-responsive megaloblastic anaemia with diabetes and deafness (TRMA; MIM 249270) is an autosomal recessive disease thought to be due to a defect in thiamine (vitamin B1) transport."3.70The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter. ( Cohen, N; Fleming, JC; Neufeld, EJ; Schorderet, DF; Steinkamp, MP; Tartaglini, E, 1999)
"Two practical methods are reported for treating feral Baltic salmon with thiamine hydrochloride against M74 syndrome (abnormally high yolk-sac fry mortality of the Baltic salmon)."3.70Treatment with thiamine hydrochloride and astaxanthine for the prevention of yolk-sac mortality in Baltic salmon fry (M74 syndrome). ( Hartikainen, K; Koski, P; Nakari, T; Pakarinen, M; Soivio, A, 1999)
"Thiamine-responsive megaloblastic anaemia (TRMA), also known as Rogers syndrome, is an early onset, autosomal recessive disorder defined by the occurrence of megaloblastic anaemia, diabetes mellitus and sensorineural deafness, responding in varying degrees to thiamine treatment (MIM 249270)."3.70Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. ( Baron, D; Barrett, T; Cohen, N; Gregory, S; Labay, V; Mandel, H; McDonald, L; Nosaka, K; Raz, T; Shalata, A; Szargel, R; Williams, H, 1999)
"Thiamine-responsive megaloblastic anemia, also known as "TRMA" or "Rogers syndrome," is an early-onset autosomal recessive disorder defined by the occurrence of megaloblastic anemia, diabetes mellitus, and sensorineural deafness, responding in varying degrees to thiamine treatment."3.69Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping. ( Barrett, T; Buist, N; Cohen, N; Fauré, S; Mandel, H; Neufeld, EJ; Raz, T; Stagg, A; Szargel, R; Yandava, CN, 1997)
"Three brothers with diabetes mellitus, thiamine-responsive megaloblastic anemia, and sensorineural deafness are reported."3.67Diabetes mellitus, thiamine-dependent megaloblastic anemia, and sensorineural deafness associated with deficient alpha-ketoglutarate dehydrogenase activity. ( Abboud, MR; Alexander, D; Najjar, SS, 1985)
"The Wernicke-Korsakoff syndrome, commonplace in Australia, might be prevented by the enrichment of alcoholic beverages with thiamine."3.66The attempted enrichment of beer with thiamine alkyl disulphides. ( Crane, S; Price, J, 1983)
"Alcohol abuse is one of the most serious problems in public health and the Wernicke-Korsakoff syndrome is one of the gravest consequences of alcoholism."2.40Wernicke-Korsakoff syndrome. ( Fernandes, JG; Rodnight, R; Zubaran, C, 1997)
"Non-alcoholic Wernicke Encephalopathy (WE) is an overlooked complication of malnourishment in all its forms including undernutrition, inadequate vitamine intake and endocrinological diseases."1.62Apathetic encephalopathy in thyreotoxicosis: an unsual cause of wernicke encephalopathy and osmotic demyelinating syndrome. ( Ciliento, R; Florindo, I; Mutti, C; Parrino, L; Pavesi, G; Zinno, L, 2021)
"Worsening WE may lead to Korsakoff syndrome(KS), in which cognitive impairments such as confabulation and memory deficits and also psychiatric symptoms may occur."1.56From psychosis to Wernicke encephalopathy: a case of hunger strike in prison. ( Akkişi Kumsar, N; Aktaş, S; Durmaz, O, 2020)
"Medications used to treat neuropathic pain may provide relief."1.38Supraclavicular nerve entrapment syndrome. ( Bruyère, PJ; Courtois, AC; Crielaard, JM; Douchamps, F, 2012)
"Rogers syndrome is an autosomal recessive disorder resulting in megaloblastic anemia, diabetes mellitus, and sensorineural deafness."1.32Disruption of transport activity in a D93H mutant thiamine transporter 1, from a Rogers Syndrome family. ( Aronheim, A; Assaraf, YG; Baron, D; Drori, S, 2003)
" The treatment was conducted as monotherapy during 28 days with enerion dosage 400 mg/day."1.32[Use of enerion in psychovegetative syndrome with pronounced asthenia]. ( Fedotova, AV; Gordeev, SA; Veĭn, AM, 2003)
"Cardiac beriberi is classically thought to represent a high-output state with oliguria and lactic acidosis."1.30Shoshin syndrome: two case reports representing opposite ends of the same disease spectrum. ( Carp, L; Daelemans, R; De Raedt, H; Engelmann, I; Shivalkar, B, 1998)
"The triad of Wernicke's encephalopathy--global confusional state, ophthalmoplegia and nystagmus, and ataxia--is occasionally seen in chronic alcoholics and is often attenuated by immediate thiamine treatment."1.26The Wernicke-Korsakoff syndrome. ( Feinberg, JF, 1980)
"Thiamine treatment was followed by a decrease of serum alanine and blood pyruvate and lactate, but there was no clinical improvement during a period of 17 months."1.25Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant. ( Bassewitz, DB; Dominick, HC; Gröbe, H; Pfeiffer, RA, 1975)

Research

Studies (71)

TimeframeStudies, this research(%)All Research%
pre-199031 (43.66)18.7374
1990's13 (18.31)18.2507
2000's18 (25.35)29.6817
2010's5 (7.04)24.3611
2020's4 (5.63)2.80

Authors

AuthorsStudies
Bykov, YV1
Bekker, RA1
Durmaz, O1
Aktaş, S1
Akkişi Kumsar, N1
Mutti, C1
Ciliento, R1
Parrino, L1
Florindo, I1
Pavesi, G1
Zinno, L1
Caldwell, J1
Molehin, A1
Nugent, K1
Karkowski, G1
Kielczewski, S1
Lelakowski, J1
Kuniewicz, M1
Karapanayiotides, T1
Anastasiou, A1
Barmpas, N1
Grigoriadis, N1
Karacostas, D1
Yeşilkaya, E1
Bideci, A1
Temizkan, M1
Kaya, Z1
Camurdan, O1
Koç, A1
Bozkaya, D1
Koçak, U1
Cinaz, P1
PUPO, PP1
GIORGI, D1
Ganesh, R1
Ezhilarasi, S1
Vasanthi, T1
Gowrishankar, K1
Rajajee, S1
Kono, S1
Miyajima, H1
Yoshida, K1
Togawa, A1
Shirakawa, K1
Suzuki, H1
Tinsa, F1
Ben Amor, S1
Kaabachi, N1
Ben Lasouad, M1
Boussetta, K1
Bousnina, S1
Jaroszewska, M1
Lee, BJ2
Dabrowski, K2
Czesny, S1
Rinchard, J2
Trzeciak, P1
Wilczyńska, B1
SUBBARAYA SASTRI, C1
Douchamps, F1
Courtois, AC1
Bruyère, PJ1
Crielaard, JM1
Shaw-Smith, C1
Flanagan, SE1
Patch, AM1
Grulich-Henn, J1
Habeb, AM1
Hussain, K1
Pomahacova, R1
Matyka, K1
Abdullah, M1
Hattersley, AT1
Ellard, S1
Czesny, SJ1
Dettmers, JM1
Cao, Y1
Koski, P2
Maassen, JA1
BERTHIER, C1
BARNAUD, J1
NEVEU, P1
L'HERMIT, M1
RUYER, M1
COLLI, JC1
PERSICO, JJ1
MONEKOSSO, GL1
ASHBY, PH1
Baron, D2
Assaraf, YG1
Drori, S1
Aronheim, A1
Kosaka, K1
Veĭn, AM1
Fedotova, AV1
Gordeev, SA1
MOURIQUAND, G1
EDEL, V1
CHIGHIZOLA, R1
Lagarde, WH1
Underwood, LE1
Moats-Staats, BM1
Calikoglu, AS1
Ricketts, CJ1
Minton, JA1
Samuel, J1
Ariyawansa, I1
Wales, JK1
Lo, IF1
Barrett, TG1
Gréco, M1
Dupré-Goetghebeur, D1
Leroy, JP1
Karam, A1
Jantzem, H1
Sassolas, B1
Misery, L1
Szüts, P1
Katona, Z1
Ilyés, M1
Szabó, I1
Csató, M1
Cox-Klazinga, M1
Endtz, LJ1
Kodama, S1
Yagi, R1
Ninomiya, M1
Goji, K1
Takahashi, T1
Morishita, Y1
Matsuo, T1
Mandel, H4
Berant, M1
Hazani, A1
Naveh, Y1
Crane, S1
Price, J1
Feinberg, JF1
Zubaran, C2
Fernandes, JG1
Rodnight, R1
Fernandes, J1
Martins, F1
Souza, J1
Machado, R1
Cadore, M1
Neufeld, EJ5
Raz, T3
Szargel, R3
Yandava, CN1
Stagg, A1
Fauré, S1
Barrett, T3
Buist, N1
Cohen, N5
Valerio, G1
Franzese, A1
Poggi, V1
Tenore, A1
Shivalkar, B1
Engelmann, I1
Carp, L1
De Raedt, H1
Daelemans, R1
Nosaka, K2
Viana, MB2
Stagg, AR1
Fleming, JC3
Baker, MA1
Sakamoto, M1
Diaz, GA1
Banikazemi, M1
Oishi, K1
Desnick, RJ1
Gelb, BD1
Labay, V1
Williams, H1
McDonald, L1
Shalata, A1
Gregory, S1
Tartaglini, E2
Steinkamp, MP2
Schorderet, DF1
Pakarinen, M1
Nakari, T1
Soivio, A1
Hartikainen, K1
Kuroda, Y1
Naito, E1
Ito, M1
Meire, FM1
Lemmens, K1
Ens-Dokkum, MH1
Pomero, F1
Allione, A1
Molinar Min, A1
La Selva, M1
Porta, M1
Gritli, S1
Omar, S1
Guannouni, S1
Berul, CI1
Hafsia, R1
Jilani, SB1
Belhani, A1
Hamdi, M1
Bappal, B1
Nair, R1
Shaikh, H1
AI Khusaiby, SM1
de Silva, V1
Cooper, JR3
Pincus, JH3
Schreier, K1
Porath, U1
Moran, JR1
Greene, HL1
Flecchia, G1
Carvalho, RI1
Vernant, P1
Gaudeau, S1
Tillement, JP1
Derrida, JP1
Boriskov, VP1
Solitare, GB1
Gröbe, H1
Bassewitz, DB1
Dominick, HC1
Pfeiffer, RA1
Mysliaeva, AV1
Grill, J1
Leblanc, T1
Baruchel, A1
Daniel, MT1
Dresch, C1
Schaison, G1
Ristola, M1
Savilahti, E1
Leirisalo-Repo, M1
Repo, H1
Destito, D1
Canonico, N1
Tentori-Montalto, T1
Abboud, MR1
Alexander, D1
Najjar, SS1
Murphy, JV2
Perper, JA1
Seftel, HC1
Metz, J1
Lakier, JB1
Rabe, EF1
Lonsdale, D1
Dunn, HG1
de Groot, CJ1
Hommes, FA2
Berger, R1
Luit-de-Haan, G1
Leiber, B1
Hövels, O1

Reviews

8 reviews available for thiamine and Syndrome

ArticleYear
[On the specific treatment of asthenic states: focus on sulbutiamine].
    Terapevticheskii arkhiv, 2022, Jun-17, Volume: 94, Issue:5

    Topics: Asthenia; Humans; Syndrome; Thiamine

2022
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
    Pediatric diabetes, 2012, Volume: 13, Issue:4

    Topics: Anemia, Megaloblastic; Consanguinity; Deafness; Diabetes Mellitus; Genes, Recessive; Homozygote; Hum

2012
Mitochondrial diabetes, diabetes and the thiamine-responsive megaloblastic anaemia syndrome and MODY-2. Diseases with common pathophysiology?
    Panminerva medica, 2002, Volume: 44, Issue:4

    Topics: Anemia, Megaloblastic; Diabetes Mellitus; Diabetes Mellitus, Type 2; Humans; Mitochondrial Diseases;

2002
[Amnestic syndrome].
    Ryoikibetsu shokogun shirizu, 2003, Issue:40

    Topics: Amnesia; Cholinesterase Inhibitors; Diagnostic and Statistical Manual of Mental Disorders; Donepezil

2003
Wernicke-Korsakoff syndrome.
    Postgraduate medical journal, 1997, Volume: 73, Issue:855

    Topics: Alcohol Amnestic Disorder; Alcoholism; History, 19th Century; Humans; Metabolic Diseases; Prognosis;

1997
Long-term follow-up of diabetes in two patients with thiamine-responsive megaloblastic anemia syndrome.
    Diabetes care, 1998, Volume: 21, Issue:1

    Topics: Adolescent; Anemia, Megaloblastic; Blood Glucose; Child, Preschool; Deafness; Diabetes Mellitus, Typ

1998
[Vitamin dependency syndrome].
    Ryoikibetsu shokogun shirizu, 2000, Issue:29 Pt 4

    Topics: Biotin; Diagnosis, Differential; Folic Acid; Humans; Metabolism, Inborn Errors; Nervous System Disea

2000
[Congenital metabolic acidosis in the postnatal period].
    Deutsche medizinische Wochenschrift (1946), 1978, Jun-02, Volume: 103, Issue:22

    Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Fructose-1,6-Diphosphatase Deficiency; Glutarates; G

1978

Trials

2 trials available for thiamine and Syndrome

ArticleYear
Increased whole blood chemiluminescence in patients with Shwachman syndrome: therapy trial with thiamine and alpha-tocopherol.
    European journal of pediatrics, 1991, Volume: 150, Issue:3

    Topics: alpha-Tocopherol; Antioxidants; Chemotaxis, Leukocyte; Cystic Fibrosis; Drug Therapy, Combination; E

1991
[Analgesic activity of Benexol-B12 in the painful vertebral syndrome].
    Acta vitaminologica et enzymologica, 1985, Volume: 7, Issue:1-2

    Topics: Adult; Aged; Analgesics; Clinical Trials as Topic; Drug Combinations; Humans; Middle Aged; Pain, Int

1985

Other Studies

61 other studies available for thiamine and Syndrome

ArticleYear
From psychosis to Wernicke encephalopathy: a case of hunger strike in prison.
    Neurocase, 2020, Volume: 26, Issue:4

    Topics: Adult; Antipsychotic Agents; Fasting; Humans; Korsakoff Syndrome; Male; Prisoners; Prisons; Psychoti

2020
Apathetic encephalopathy in thyreotoxicosis: an unsual cause of wernicke encephalopathy and osmotic demyelinating syndrome.
    Acta bio-medica : Atenei Parmensis, 2021, 02-05, Volume: 92, Issue:1

    Topics: Aged; Humans; Male; Malnutrition; Syndrome; Thiamine; Thiamine Deficiency; Wernicke Encephalopathy

2021
Vitamin C and Thiamine Levels in Patients Presenting with Acute Neurologic Syndromes.
    The American journal of the medical sciences, 2021, Volume: 362, Issue:6

    Topics: Ascorbic Acid; Humans; Syndrome; Thiamine; Thiamine Deficiency; Vitamins

2021
Ortner's syndrome after cryoballoon ablation.
    Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing, 2019, Volume: 54, Issue:3

    Topics: Adjuvants, Immunologic; Atrial Fibrillation; Catheter Ablation; Cryosurgery; Humans; Middle Aged; Pu

2019
A 'posterior circulation stroke' that benefits from vitamins.
    The American journal of medicine, 2014, Volume: 127, Issue:2

    Topics: Activities of Daily Living; Aged; Amnesia; Brain; Diagnosis, Differential; Diagnostic Errors; Female

2014
A novel mutation in the SLC19A2 gene in a Turkish female with thiamine-responsive megaloblastic anemia syndrome.
    Journal of tropical pediatrics, 2009, Volume: 55, Issue:4

    Topics: Anemia, Megaloblastic; Child, Preschool; Diabetes Mellitus; Diagnosis, Differential; Female; Genotyp

2009
[Vitaminoterapia in intra-spinal neurogenic syndromes].
    Arquivos de neuro-psiquiatria, 1948, Volume: 6, Issue:3

    Topics: Humans; Syndrome; Thiamine

1948
Thiamine responsive megaloblastic anemia syndrome.
    Indian journal of pediatrics, 2009, Volume: 76, Issue:3

    Topics: Anemia, Megaloblastic; Blood Glucose; Child, Preschool; Diabetes Mellitus, Type 1; Female; Follow-Up

2009
Mutations in a thiamine-transporter gene and Wernicke's-like encephalopathy.
    The New England journal of medicine, 2009, Apr-23, Volume: 360, Issue:17

    Topics: Adult; Blepharoptosis; Diplopia; Epilepsy, Complex Partial; Gene Expression; Heterozygote; Humans; M

2009
Unusual case of thiamine responsive megaloblastic anemia.
    La Tunisie medicale, 2009, Volume: 87, Issue:2

    Topics: Anemia, Megaloblastic; Blood Glucose; Child, Preschool; Consanguinity; Hemoglobins; Humans; Lactates

2009
Effects of vitamin B1 (thiamine) deficiency in lake trout (Salvelinus namaycush) alevins at hatching stage.
    Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 2009, Volume: 154, Issue:2

    Topics: Animals; Brain; Eye; Female; Fish Diseases; Great Lakes Region; Liver; Liver Glycogen; Nutritional S

2009
Thiamin syndrome in children.
    The Antiseptic, 1947, Volume: 44, Issue:3

    Topics: Child; Humans; Syndrome; Thiamine; Thiamine Deficiency

1947
Supraclavicular nerve entrapment syndrome.
    Joint bone spine, 2012, Volume: 79, Issue:1

    Topics: Analgesics; Antirheumatic Agents; Brachial Plexus; Clavicle; Humans; Lidocaine; Male; Middle Aged; N

2012
Does spatial variation in egg thiamine and fatty-acid concentration of Lake Michigan lake trout Salvelinus namaycush lead to differential early mortality syndrome and yolk oedema mortality in offspring?
    Journal of fish biology, 2012, Volume: 80, Issue:7

    Topics: Animals; Egg Proteins; Fatty Acids; Fish Diseases; Lakes; Lipids; Ovum; Survival Analysis; Syndrome;

2012
Parental background predisposes Baltic salmon fry to M74 syndrome.
    Acta veterinaria Scandinavica, 2002, Volume: 43, Issue:2

    Topics: Animals; Animals, Wild; Aquaculture; Female; Fish Diseases; Male; Salmo salar; Syndrome; Thiamine

2002
[Importance of large doses of vitamin B1 in the treatment of alcoholic encephalopathies; 3 case reports].
    Journal de medecine de Lyon, 1957, May-05, Volume: 38, Issue:896

    Topics: Alcohol-Related Disorders; Alcoholism; Humans; Psychotic Disorders; Syndrome; Thiamine; Vitamin B De

1957
[Preventive effect of massive doses of thiamine in the chlorpromazine-induced neuroleptic syndrome].
    Annales medico-psychologiques, 1958, Volume: 116 Vol 2, Issue:2

    Topics: Antipsychotic Agents; Chlorpromazine; Humans; Syndrome; Thiamine

1958
[Experimental synergism of proenzymes with vitamins B-1 and B12 in facial painful syndromes].
    La Semana medica, 1962, Jul-23, Volume: 121

    Topics: Corrinoids; Enzyme Precursors; Facial Neuralgia; Hematinics; Humans; Peptide Hydrolases; Syndrome; T

1962
THE NATURAL HISTORY OF AN AMBLYOPIA SYNDROME IN WESTERN NIGERIA.
    The West African medical journal, 1963, Volume: 12

    Topics: Adolescent; Amblyopia; Child; Humans; Nigeria; Ophthalmoscopy; Riboflavin; Statistics as Topic; Stom

1963
Disruption of transport activity in a D93H mutant thiamine transporter 1, from a Rogers Syndrome family.
    European journal of biochemistry, 2003, Volume: 270, Issue:22

    Topics: Amino Acid Sequence; Anemia, Megaloblastic; Animals; Aspartic Acid; Biological Transport; Cell Line;

2003
[Use of enerion in psychovegetative syndrome with pronounced asthenia].
    Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2003, Volume: 103, Issue:10

    Topics: Adolescent; Adult; Asthenia; Butyrates; Disulfides; Female; Humans; Male; Middle Aged; Psychophysiol

2003
[Compared effect of aerated aneurin on vestibular chronaxia and on the beriberi syndrome].
    Comptes rendus des seances de la Societe de biologie et de ses filiales, 1950, Volume: 144, Issue:15-16

    Topics: Beriberi; Ear, Inner; Humans; Syndrome; Thiamine; Vestibule, Labyrinth

1950
Novel mutation in the SLC19A2 gene in an African-American female with thiamine-responsive megaloblastic anemia syndrome.
    American journal of medical genetics. Part A, 2004, Mar-15, Volume: 125A, Issue:3

    Topics: Anemia, Megaloblastic; Black or African American; Diabetes Mellitus; DNA Mutational Analysis; Female

2004
Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.
    Acta paediatrica (Oslo, Norway : 1992), 2006, Volume: 95, Issue:1

    Topics: Adolescent; Adult; Anemia, Megaloblastic; Child; Child, Preschool; Deafness; Diabetes Mellitus; DNA

2006
[DRESS syndrome related to Hexaquine (quinine and thiamine)].
    Annales de dermatologie et de venereologie, 2006, Volume: 133, Issue:4

    Topics: Adult; Analgesics, Non-Narcotic; Drug Combinations; Drug Eruptions; Eosinophilia; Female; Humans; Qu

2006
Correction of defective chemotaxis with thiamine in Shwachman-Diamond syndrome.
    Lancet (London, England), 1984, May-12, Volume: 1, Issue:8385

    Topics: Agranulocytosis; Chemotaxis, Leukocyte; Humans; Neutropenia; Neutrophils; Pancreatic Diseases; Syndr

1984
Peripheral nerve involvement in pernicious anaemia.
    Journal of the neurological sciences, 1980, Volume: 45, Issue:2-3

    Topics: Aged; Anemia, Pernicious; Female; Humans; Male; Middle Aged; Peripheral Nervous System Diseases; Pyr

1980
The effect of a high fat diet on pyruvate decarboxylase deficiency without central nervous system involvement.
    Brain & development, 1983, Volume: 5, Issue:4

    Topics: Carboxy-Lyases; Child; Dietary Fats; Electroencephalography; Fatigue; Fibroblasts; Humans; Male; Phy

1983
Thiamine-dependent beriberi in the "thiamine-responsive anemia syndrome".
    The New England journal of medicine, 1984, Sep-27, Volume: 311, Issue:13

    Topics: Anemia; Beriberi; Female; Humans; Infant; Syndrome; Thiamine; Thiamine Deficiency

1984
The attempted enrichment of beer with thiamine alkyl disulphides.
    Journal of nutritional science and vitaminology, 1983, Volume: 29, Issue:3

    Topics: Alcohol Amnestic Disorder; Australia; Beer; Drug Stability; Food, Fortified; Fursultiamin; Humans; O

1983
The Wernicke-Korsakoff syndrome.
    American family physician, 1980, Volume: 22, Issue:5

    Topics: Alcohol Amnestic Disorder; Female; Humans; Male; Syndrome; Thiamine; Thiamine Deficiency; Wernicke E

1980
[Clinical and neuropathological aspects of Wernicke-Korsakoff syndrome].
    Revista de saude publica, 1996, Volume: 30, Issue:6

    Topics: Alcohol Amnestic Disorder; Animals; Cognition Disorders; Humans; Prognosis; Rats; Syndrome; Thiamine

1996
Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mapping.
    American journal of human genetics, 1997, Volume: 61, Issue:6

    Topics: Alaska; Anemia, Megaloblastic; Arabs; Chromosome Mapping; Chromosomes, Human, Pair 1; Consanguinity;

1997
Shoshin syndrome: two case reports representing opposite ends of the same disease spectrum.
    Acta cardiologica, 1998, Volume: 53, Issue:4

    Topics: Adult; Beriberi; Cardiac Output; Heart Diseases; Hemodynamics; Humans; Male; Middle Aged; Syndrome;

1998
Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneity.
    Human genetics, 1998, Volume: 103, Issue:4

    Topics: Anemia, Megaloblastic; Child; Child, Preschool; Chromosome Mapping; Chromosomes, Human, Pair 1; Deaf

1998
Defective high-affinity thiamine transporter leads to cell death in thiamine-responsive megaloblastic anemia syndrome fibroblasts.
    The Journal of clinical investigation, 1999, Volume: 103, Issue:5

    Topics: Anemia, Megaloblastic; Apoptosis; Carrier Proteins; Cells, Cultured; Deafness; Diabetes Mellitus; Fi

1999
Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.
    Nature genetics, 1999, Volume: 22, Issue:3

    Topics: Amino Acid Sequence; Anemia, Megaloblastic; Base Sequence; Carrier Proteins; Cloning, Molecular; Dea

1999
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.
    Nature genetics, 1999, Volume: 22, Issue:3

    Topics: Amino Acid Sequence; Anemia, Megaloblastic; Animals; Base Sequence; Carrier Proteins; Cricetinae; De

1999
The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.
    Nature genetics, 1999, Volume: 22, Issue:3

    Topics: Amino Acid Sequence; Anemia, Megaloblastic; Animals; Base Sequence; Carrier Proteins; Cell Line; Dea

1999
Treatment with thiamine hydrochloride and astaxanthine for the prevention of yolk-sac mortality in Baltic salmon fry (M74 syndrome).
    Diseases of aquatic organisms, 1999, Sep-14, Volume: 37, Issue:3

    Topics: Adjuvants, Immunologic; Administration, Topical; Animals; beta Carotene; Chromatography, High Pressu

1999
Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy.
    Ophthalmic genetics, 2000, Volume: 21, Issue:4

    Topics: Adolescent; Anemia, Megaloblastic; Diagnosis, Differential; Electroretinography; Female; Humans; Pho

2000
Thiamine, beta-cell function and peripheral glucose utilization in thiamine-responsive megaloblastic anemia (TRMA) syndrome.
    Acta diabetologica, 2000, Volume: 37, Issue:2

    Topics: Anemia, Megaloblastic; Glucose; Humans; Islets of Langerhans; Syndrome; Thiamine

2000
A novel mutation in the SLC19A2 gene in a Tunisian family with thiamine-responsive megaloblastic anaemia, diabetes and deafness syndrome.
    British journal of haematology, 2001, Volume: 113, Issue:2

    Topics: Anemia, Megaloblastic; Bone Marrow Cells; Cardiomyopathy, Dilated; Carrier Proteins; Child, Preschoo

2001
Five years followup of diabetes mellitus in two siblings with thiamine responsive megaloblastic anemia.
    Indian pediatrics, 2001, Volume: 38, Issue:11

    Topics: Abnormalities, Multiple; Anemia, Megaloblastic; Blood Glucose; Diabetes Mellitus; Female; Follow-Up

2001
The role of thiamine in nervous tissue.
    Neurochemical research, 1979, Volume: 4, Issue:2

    Topics: Animals; Brain; Brain Diseases; Cattle; Coenzymes; Fishes; Ketoglutarate Dehydrogenase Complex; Nerv

1979
The B vitamins and vitamin C in human nutrition. I. General considerations and 'obligatory' B vitamins.
    American journal of diseases of children (1960), 1979, Volume: 133, Issue:2

    Topics: Amino Acids; Anemia, Hypochromic; Ascorbic Acid; Diet; Humans; Nutritional Physiological Phenomena;

1979
[Isolated viral syndrome of the ambiguous nucleus].
    Minerva medica, 1979, Nov-10, Volume: 70, Issue:49

    Topics: Adult; Aged; Amino Acids; Betamethasone; Deglutition Disorders; Galantamine; Glossopharyngeal Nerve;

1979
Thiamine-responsive megaloblastic anemia, sensorineural deafness, and diabetes mellitus: A new syndrome?
    The Journal of pediatrics, 1978, Volume: 93, Issue:2

    Topics: Adult; Anemia, Macrocytic; Anemia, Megaloblastic; Child; Deafness; Diabetes Mellitus; Diabetes Melli

1978
[Hyperkinetic syndromes associated with hypothiaminemia and corrected by administration of vitamin B 1].
    Archives des maladies du coeur et des vaisseaux, 1976, Volume: 69, Issue:10

    Topics: Adolescent; Adult; Cardiac Output; Cardiomyopathies; Diagnosis, Differential; Female; Humans; Hypert

1976
[Nosologic independence and features of the treatment of alcoholic paraphrenia].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1977, Volume: 77, Issue:5

    Topics: Automatism; Bismuth; Defense Mechanisms; Depressive Disorder, Major; Diagnosis, Differential; Electr

1977
Thiamine triphosphate levels and histopathology. Correlation in Leigh disease.
    Archives of neurology, 1976, Volume: 33, Issue:11

    Topics: Adult; Basal Ganglia; Brain Chemistry; Brain Injuries; Brain Neoplasms; Brain Stem; Central Nervous

1976
Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant.
    Acta paediatrica Scandinavica, 1975, Volume: 64, Issue:5

    Topics: Alanine; Brain Stem; Encephalomalacia; Female; Glycogen; Humans; Infant; Intellectual Disability; La

1975
[Lupoid syndrome].
    Terapevticheskii arkhiv, 1975, Volume: 47, Issue:12

    Topics: Adult; Antitubercular Agents; Butadienes; Drug Hypersensitivity; Female; Humans; Lupus Erythematosus

1975
Thiamine responsive anemia: report of a new case associated with a thiamine pyrophosphokinase deficiency.
    Nouvelle revue francaise d'hematologie, 1991, Volume: 33, Issue:6

    Topics: Abnormalities, Multiple; Anemia, Megaloblastic; Cells, Cultured; Diabetes Complications; Hearing Los

1991
Diabetes mellitus, thiamine-dependent megaloblastic anemia, and sensorineural deafness associated with deficient alpha-ketoglutarate dehydrogenase activity.
    The Journal of pediatrics, 1985, Volume: 107, Issue:4

    Topics: Adolescent; Anemia, Macrocytic; Anemia, Megaloblastic; Child; Child, Preschool; Deafness; Diabetes M

1985
Crib-death syndrome.
    Lancet (London, England), 1973, Mar-17, Volume: 1, Issue:7803

    Topics: Brain Chemistry; Brain Stem; Death, Sudden; Encephalomalacia; Humans; Infant; Infant, Newborn; Intel

1973
Cardiomyopathies in Johannesburg Bantu. I. Aetiology and characteristics of beriberi heart disease.
    South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1972, Nov-11, Volume: 46, Issue:45

    Topics: Adult; Alcohol Drinking; Beriberi; Black or African American; Black People; Cardiomegaly; Erythrocyt

1972
Thiamine derivatives in subacute necrotizing encephalomyelopathy. A preliminary report.
    Pediatrics, 1973, Volume: 51, Issue:4

    Topics: Autopsy; Brain Stem; Child; Encephalomalacia; Humans; Intellectual Disability; Medical Records; Psyc

1973
Further speculation on the pathogenesis of Leigh's encephalomyelopathy.
    The Journal of pediatrics, 1973, Volume: 82, Issue:3

    Topics: Aspartic Acid; Brain Stem; Citric Acid Cycle; Encephalomalacia; Humans; Intellectual Disability; Lig

1973
The effect of thiamine treatment on the activity of pyruvate dehydrogenase: relation of the treatment of Leigh's encephalomyelopathy.
    Pediatric research, 1973, Volume: 7, Issue:7

    Topics: Adenosine Diphosphate; Adenosine Triphosphate; Animals; Brain Stem; Encephalomalacia; Female; Humans

1973
[Leigh's syndrome].
    Monatsschrift fur Kinderheilkunde, 1974, Volume: 122, Issue:1

    Topics: Brain Stem; Encephalomalacia; Female; Humans; Infant; Intellectual Disability; Male; Psychomotor Dis

1974