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.
| Excerpt | Relevance | Reference |
|---|---|---|
| " 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." | 8.88 | Recessive 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." | 8.81 | Mitochondrial 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)." | 8.80 | Long-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." | 7.75 | Thiamine 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." | 7.73 | Thiamine-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." | 7.72 | Novel 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." | 7.71 | A 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)." | 7.70 | Treatment 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." | 7.70 | Mutations 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." | 7.70 | Refined 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." | 7.70 | Defective 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." | 7.70 | The 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)." | 7.70 | Mutations 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." | 7.69 | Localization 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." | 7.67 | Diabetes 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." | 5.32 | Disruption 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." | 4.88 | Recessive 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." | 4.81 | Mitochondrial 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)." | 4.80 | Long-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." | 3.75 | Thiamine 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." | 3.75 | Unusual 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." | 3.73 | Thiamine-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." | 3.72 | Novel 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." | 3.71 | A 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." | 3.70 | Refined 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." | 3.70 | Defective 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." | 3.70 | Mutations 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." | 3.70 | The 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)." | 3.70 | Treatment 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)." | 3.70 | Mutations 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." | 3.69 | Localization 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." | 3.67 | Diabetes 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." | 3.66 | The 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." | 2.40 | Wernicke-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." | 1.62 | Apathetic 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." | 1.56 | From 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." | 1.38 | Supraclavicular 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." | 1.32 | Disruption 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." | 1.30 | Shoshin 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." | 1.26 | The 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." | 1.25 | Subacute necrotizing encephalomyelopathy. Clinical, ultrastructural, biochemical and therapeutic studies in an infant. ( Bassewitz, DB; Dominick, HC; Gröbe, H; Pfeiffer, RA, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 31 (43.66) | 18.7374 |
| 1990's | 13 (18.31) | 18.2507 |
| 2000's | 18 (25.35) | 29.6817 |
| 2010's | 5 (7.04) | 24.3611 |
| 2020's | 4 (5.63) | 2.80 |
| Authors | Studies |
|---|---|
| Bykov, YV | 1 |
| Bekker, RA | 1 |
| Durmaz, O | 1 |
| Aktaş, S | 1 |
| Akkişi Kumsar, N | 1 |
| Mutti, C | 1 |
| Ciliento, R | 1 |
| Parrino, L | 1 |
| Florindo, I | 1 |
| Pavesi, G | 1 |
| Zinno, L | 1 |
| Caldwell, J | 1 |
| Molehin, A | 1 |
| Nugent, K | 1 |
| Karkowski, G | 1 |
| Kielczewski, S | 1 |
| Lelakowski, J | 1 |
| Kuniewicz, M | 1 |
| Karapanayiotides, T | 1 |
| Anastasiou, A | 1 |
| Barmpas, N | 1 |
| Grigoriadis, N | 1 |
| Karacostas, D | 1 |
| Yeşilkaya, E | 1 |
| Bideci, A | 1 |
| Temizkan, M | 1 |
| Kaya, Z | 1 |
| Camurdan, O | 1 |
| Koç, A | 1 |
| Bozkaya, D | 1 |
| Koçak, U | 1 |
| Cinaz, P | 1 |
| PUPO, PP | 1 |
| GIORGI, D | 1 |
| Ganesh, R | 1 |
| Ezhilarasi, S | 1 |
| Vasanthi, T | 1 |
| Gowrishankar, K | 1 |
| Rajajee, S | 1 |
| Kono, S | 1 |
| Miyajima, H | 1 |
| Yoshida, K | 1 |
| Togawa, A | 1 |
| Shirakawa, K | 1 |
| Suzuki, H | 1 |
| Tinsa, F | 1 |
| Ben Amor, S | 1 |
| Kaabachi, N | 1 |
| Ben Lasouad, M | 1 |
| Boussetta, K | 1 |
| Bousnina, S | 1 |
| Jaroszewska, M | 1 |
| Lee, BJ | 2 |
| Dabrowski, K | 2 |
| Czesny, S | 1 |
| Rinchard, J | 2 |
| Trzeciak, P | 1 |
| Wilczyńska, B | 1 |
| SUBBARAYA SASTRI, C | 1 |
| Douchamps, F | 1 |
| Courtois, AC | 1 |
| Bruyère, PJ | 1 |
| Crielaard, JM | 1 |
| Shaw-Smith, C | 1 |
| Flanagan, SE | 1 |
| Patch, AM | 1 |
| Grulich-Henn, J | 1 |
| Habeb, AM | 1 |
| Hussain, K | 1 |
| Pomahacova, R | 1 |
| Matyka, K | 1 |
| Abdullah, M | 1 |
| Hattersley, AT | 1 |
| Ellard, S | 1 |
| Czesny, SJ | 1 |
| Dettmers, JM | 1 |
| Cao, Y | 1 |
| Koski, P | 2 |
| Maassen, JA | 1 |
| BERTHIER, C | 1 |
| BARNAUD, J | 1 |
| NEVEU, P | 1 |
| L'HERMIT, M | 1 |
| RUYER, M | 1 |
| COLLI, JC | 1 |
| PERSICO, JJ | 1 |
| MONEKOSSO, GL | 1 |
| ASHBY, PH | 1 |
| Baron, D | 2 |
| Assaraf, YG | 1 |
| Drori, S | 1 |
| Aronheim, A | 1 |
| Kosaka, K | 1 |
| Veĭn, AM | 1 |
| Fedotova, AV | 1 |
| Gordeev, SA | 1 |
| MOURIQUAND, G | 1 |
| EDEL, V | 1 |
| CHIGHIZOLA, R | 1 |
| Lagarde, WH | 1 |
| Underwood, LE | 1 |
| Moats-Staats, BM | 1 |
| Calikoglu, AS | 1 |
| Ricketts, CJ | 1 |
| Minton, JA | 1 |
| Samuel, J | 1 |
| Ariyawansa, I | 1 |
| Wales, JK | 1 |
| Lo, IF | 1 |
| Barrett, TG | 1 |
| Gréco, M | 1 |
| Dupré-Goetghebeur, D | 1 |
| Leroy, JP | 1 |
| Karam, A | 1 |
| Jantzem, H | 1 |
| Sassolas, B | 1 |
| Misery, L | 1 |
| Szüts, P | 1 |
| Katona, Z | 1 |
| Ilyés, M | 1 |
| Szabó, I | 1 |
| Csató, M | 1 |
| Cox-Klazinga, M | 1 |
| Endtz, LJ | 1 |
| Kodama, S | 1 |
| Yagi, R | 1 |
| Ninomiya, M | 1 |
| Goji, K | 1 |
| Takahashi, T | 1 |
| Morishita, Y | 1 |
| Matsuo, T | 1 |
| Mandel, H | 4 |
| Berant, M | 1 |
| Hazani, A | 1 |
| Naveh, Y | 1 |
| Crane, S | 1 |
| Price, J | 1 |
| Feinberg, JF | 1 |
| Zubaran, C | 2 |
| Fernandes, JG | 1 |
| Rodnight, R | 1 |
| Fernandes, J | 1 |
| Martins, F | 1 |
| Souza, J | 1 |
| Machado, R | 1 |
| Cadore, M | 1 |
| Neufeld, EJ | 5 |
| Raz, T | 3 |
| Szargel, R | 3 |
| Yandava, CN | 1 |
| Stagg, A | 1 |
| Fauré, S | 1 |
| Barrett, T | 3 |
| Buist, N | 1 |
| Cohen, N | 5 |
| Valerio, G | 1 |
| Franzese, A | 1 |
| Poggi, V | 1 |
| Tenore, A | 1 |
| Shivalkar, B | 1 |
| Engelmann, I | 1 |
| Carp, L | 1 |
| De Raedt, H | 1 |
| Daelemans, R | 1 |
| Nosaka, K | 2 |
| Viana, MB | 2 |
| Stagg, AR | 1 |
| Fleming, JC | 3 |
| Baker, MA | 1 |
| Sakamoto, M | 1 |
| Diaz, GA | 1 |
| Banikazemi, M | 1 |
| Oishi, K | 1 |
| Desnick, RJ | 1 |
| Gelb, BD | 1 |
| Labay, V | 1 |
| Williams, H | 1 |
| McDonald, L | 1 |
| Shalata, A | 1 |
| Gregory, S | 1 |
| Tartaglini, E | 2 |
| Steinkamp, MP | 2 |
| Schorderet, DF | 1 |
| Pakarinen, M | 1 |
| Nakari, T | 1 |
| Soivio, A | 1 |
| Hartikainen, K | 1 |
| Kuroda, Y | 1 |
| Naito, E | 1 |
| Ito, M | 1 |
| Meire, FM | 1 |
| Lemmens, K | 1 |
| Ens-Dokkum, MH | 1 |
| Pomero, F | 1 |
| Allione, A | 1 |
| Molinar Min, A | 1 |
| La Selva, M | 1 |
| Porta, M | 1 |
| Gritli, S | 1 |
| Omar, S | 1 |
| Guannouni, S | 1 |
| Berul, CI | 1 |
| Hafsia, R | 1 |
| Jilani, SB | 1 |
| Belhani, A | 1 |
| Hamdi, M | 1 |
| Bappal, B | 1 |
| Nair, R | 1 |
| Shaikh, H | 1 |
| AI Khusaiby, SM | 1 |
| de Silva, V | 1 |
| Cooper, JR | 3 |
| Pincus, JH | 3 |
| Schreier, K | 1 |
| Porath, U | 1 |
| Moran, JR | 1 |
| Greene, HL | 1 |
| Flecchia, G | 1 |
| Carvalho, RI | 1 |
| Vernant, P | 1 |
| Gaudeau, S | 1 |
| Tillement, JP | 1 |
| Derrida, JP | 1 |
| Boriskov, VP | 1 |
| Solitare, GB | 1 |
| Gröbe, H | 1 |
| Bassewitz, DB | 1 |
| Dominick, HC | 1 |
| Pfeiffer, RA | 1 |
| Mysliaeva, AV | 1 |
| Grill, J | 1 |
| Leblanc, T | 1 |
| Baruchel, A | 1 |
| Daniel, MT | 1 |
| Dresch, C | 1 |
| Schaison, G | 1 |
| Ristola, M | 1 |
| Savilahti, E | 1 |
| Leirisalo-Repo, M | 1 |
| Repo, H | 1 |
| Destito, D | 1 |
| Canonico, N | 1 |
| Tentori-Montalto, T | 1 |
| Abboud, MR | 1 |
| Alexander, D | 1 |
| Najjar, SS | 1 |
| Murphy, JV | 2 |
| Perper, JA | 1 |
| Seftel, HC | 1 |
| Metz, J | 1 |
| Lakier, JB | 1 |
| Rabe, EF | 1 |
| Lonsdale, D | 1 |
| Dunn, HG | 1 |
| de Groot, CJ | 1 |
| Hommes, FA | 2 |
| Berger, R | 1 |
| Luit-de-Haan, G | 1 |
| Leiber, B | 1 |
| Hövels, O | 1 |
8 reviews available for thiamine and Syndrome
| Article | Year |
|---|---|
[On the specific treatment of asthenic states: focus on sulbutiamine].
Topics: Asthenia; Humans; Syndrome; Thiamine | 2022 |
Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
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?
Topics: Anemia, Megaloblastic; Diabetes Mellitus; Diabetes Mellitus, Type 2; Humans; Mitochondrial Diseases; | 2002 |
[Amnestic syndrome].
Topics: Amnesia; Cholinesterase Inhibitors; Diagnostic and Statistical Manual of Mental Disorders; Donepezil | 2003 |
Wernicke-Korsakoff syndrome.
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.
Topics: Adolescent; Anemia, Megaloblastic; Blood Glucose; Child, Preschool; Deafness; Diabetes Mellitus, Typ | 1998 |
[Vitamin dependency syndrome].
Topics: Biotin; Diagnosis, Differential; Folic Acid; Humans; Metabolism, Inborn Errors; Nervous System Disea | 2000 |
[Congenital metabolic acidosis in the postnatal period].
Topics: Acidosis; Amino Acid Metabolism, Inborn Errors; Fructose-1,6-Diphosphatase Deficiency; Glutarates; G | 1978 |
2 trials available for thiamine and Syndrome
| Article | Year |
|---|---|
Increased whole blood chemiluminescence in patients with Shwachman syndrome: therapy trial with thiamine and alpha-tocopherol.
Topics: alpha-Tocopherol; Antioxidants; Chemotaxis, Leukocyte; Cystic Fibrosis; Drug Therapy, Combination; E | 1991 |
[Analgesic activity of Benexol-B12 in the painful vertebral syndrome].
Topics: Adult; Aged; Analgesics; Clinical Trials as Topic; Drug Combinations; Humans; Middle Aged; Pain, Int | 1985 |
61 other studies available for thiamine and Syndrome
| Article | Year |
|---|---|
From psychosis to Wernicke encephalopathy: a case of hunger strike in prison.
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.
Topics: Aged; Humans; Male; Malnutrition; Syndrome; Thiamine; Thiamine Deficiency; Wernicke Encephalopathy | 2021 |
Vitamin C and Thiamine Levels in Patients Presenting with Acute Neurologic Syndromes.
Topics: Ascorbic Acid; Humans; Syndrome; Thiamine; Thiamine Deficiency; Vitamins | 2021 |
Ortner's syndrome after cryoballoon ablation.
Topics: Adjuvants, Immunologic; Atrial Fibrillation; Catheter Ablation; Cryosurgery; Humans; Middle Aged; Pu | 2019 |
A 'posterior circulation stroke' that benefits from vitamins.
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.
Topics: Anemia, Megaloblastic; Child, Preschool; Diabetes Mellitus; Diagnosis, Differential; Female; Genotyp | 2009 |
[Vitaminoterapia in intra-spinal neurogenic syndromes].
Topics: Humans; Syndrome; Thiamine | 1948 |
Thiamine responsive megaloblastic anemia syndrome.
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.
Topics: Adult; Blepharoptosis; Diplopia; Epilepsy, Complex Partial; Gene Expression; Heterozygote; Humans; M | 2009 |
Unusual case of thiamine responsive megaloblastic anemia.
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.
Topics: Animals; Brain; Eye; Female; Fish Diseases; Great Lakes Region; Liver; Liver Glycogen; Nutritional S | 2009 |
Thiamin syndrome in children.
Topics: Child; Humans; Syndrome; Thiamine; Thiamine Deficiency | 1947 |
Supraclavicular nerve entrapment syndrome.
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?
Topics: Animals; Egg Proteins; Fatty Acids; Fish Diseases; Lakes; Lipids; Ovum; Survival Analysis; Syndrome; | 2012 |
Parental background predisposes Baltic salmon fry to M74 syndrome.
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].
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].
Topics: Antipsychotic Agents; Chlorpromazine; Humans; Syndrome; Thiamine | 1958 |
[Experimental synergism of proenzymes with vitamins B-1 and B12 in facial painful syndromes].
Topics: Corrinoids; Enzyme Precursors; Facial Neuralgia; Hematinics; Humans; Peptide Hydrolases; Syndrome; T | 1962 |
THE NATURAL HISTORY OF AN AMBLYOPIA SYNDROME IN WESTERN NIGERIA.
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.
Topics: Amino Acid Sequence; Anemia, Megaloblastic; Animals; Aspartic Acid; Biological Transport; Cell Line; | 2003 |
[Use of enerion in psychovegetative syndrome with pronounced asthenia].
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].
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.
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.
Topics: Adolescent; Adult; Anemia, Megaloblastic; Child; Child, Preschool; Deafness; Diabetes Mellitus; DNA | 2006 |
[DRESS syndrome related to Hexaquine (quinine and thiamine)].
Topics: Adult; Analgesics, Non-Narcotic; Drug Combinations; Drug Eruptions; Eosinophilia; Female; Humans; Qu | 2006 |
Correction of defective chemotaxis with thiamine in Shwachman-Diamond syndrome.
Topics: Agranulocytosis; Chemotaxis, Leukocyte; Humans; Neutropenia; Neutrophils; Pancreatic Diseases; Syndr | 1984 |
Peripheral nerve involvement in pernicious anaemia.
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.
Topics: Carboxy-Lyases; Child; Dietary Fats; Electroencephalography; Fatigue; Fibroblasts; Humans; Male; Phy | 1983 |
Thiamine-dependent beriberi in the "thiamine-responsive anemia syndrome".
Topics: Anemia; Beriberi; Female; Humans; Infant; Syndrome; Thiamine; Thiamine Deficiency | 1984 |
The attempted enrichment of beer with thiamine alkyl disulphides.
Topics: Alcohol Amnestic Disorder; Australia; Beer; Drug Stability; Food, Fortified; Fursultiamin; Humans; O | 1983 |
The Wernicke-Korsakoff syndrome.
Topics: Alcohol Amnestic Disorder; Female; Humans; Male; Syndrome; Thiamine; Thiamine Deficiency; Wernicke E | 1980 |
[Clinical and neuropathological aspects of Wernicke-Korsakoff syndrome].
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.
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.
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.
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.
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.
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.
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.
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).
Topics: Adjuvants, Immunologic; Administration, Topical; Animals; beta Carotene; Chromatography, High Pressu | 1999 |
Thiamine-responsive megaloblastic anemia syndrome (TRMA) with cone-rod dystrophy.
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.
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.
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.
Topics: Abnormalities, Multiple; Anemia, Megaloblastic; Blood Glucose; Diabetes Mellitus; Female; Follow-Up | 2001 |
The role of thiamine in nervous tissue.
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.
Topics: Amino Acids; Anemia, Hypochromic; Ascorbic Acid; Diet; Humans; Nutritional Physiological Phenomena; | 1979 |
[Isolated viral syndrome of the ambiguous nucleus].
Topics: Adult; Aged; Amino Acids; Betamethasone; Deglutition Disorders; Galantamine; Glossopharyngeal Nerve; | 1979 |
Thiamine-responsive megaloblastic anemia, sensorineural deafness, and diabetes mellitus: A new syndrome?
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].
Topics: Adolescent; Adult; Cardiac Output; Cardiomyopathies; Diagnosis, Differential; Female; Humans; Hypert | 1976 |
[Nosologic independence and features of the treatment of alcoholic paraphrenia].
Topics: Automatism; Bismuth; Defense Mechanisms; Depressive Disorder, Major; Diagnosis, Differential; Electr | 1977 |
Thiamine triphosphate levels and histopathology. Correlation in Leigh disease.
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.
Topics: Alanine; Brain Stem; Encephalomalacia; Female; Glycogen; Humans; Infant; Intellectual Disability; La | 1975 |
[Lupoid syndrome].
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.
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.
Topics: Adolescent; Anemia, Macrocytic; Anemia, Megaloblastic; Child; Child, Preschool; Deafness; Diabetes M | 1985 |
Crib-death syndrome.
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.
Topics: Adult; Alcohol Drinking; Beriberi; Black or African American; Black People; Cardiomegaly; Erythrocyt | 1972 |
Thiamine derivatives in subacute necrotizing encephalomyelopathy. A preliminary report.
Topics: Autopsy; Brain Stem; Child; Encephalomalacia; Humans; Intellectual Disability; Medical Records; Psyc | 1973 |
Further speculation on the pathogenesis of Leigh's encephalomyelopathy.
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.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Animals; Brain Stem; Encephalomalacia; Female; Humans | 1973 |
[Leigh's syndrome].
Topics: Brain Stem; Encephalomalacia; Female; Humans; Infant; Intellectual Disability; Male; Psychomotor Dis | 1974 |