Page last updated: 2024-10-16

adenine and Symptom Cluster

adenine has been researched along with Symptom Cluster in 33 studies

Research Excerpts

ExcerptRelevanceReference
" He was diagnosed as having fibrinoid syndrome and started on topical prednisolone, brimonidine, timolol-dorzolamide, and orally administered acetazolamide."4.98Anterior chamber fibrinoid syndrome after cataract extraction in a patient on ibrutinib for B-cell chronic lymphocytic leukemia: a case report and review of the literature. ( Hwang, CK; Kim, BJ; Kolomeyer, AM, 2018)
"NOTCH1 mutations in chronic lymphocytic leukemia (CLL) lead to accumulation of NOTCH1 intracellular domain (NICD) and prolong signaling."1.56Bidirectional linkage between the B-cell receptor and NOTCH1 in chronic lymphocytic leukemia and in Richter's syndrome: therapeutic implications. ( Allan, JN; Arruga, F; Bracciamà, V; Coscia, M; D'Arena, G; Deaglio, S; Forconi, F; Furman, RR; Gaidano, G; Gizzi, K; Packham, G; Vaisitti, T; Vitale, N; Yeomans, A, 2020)
"We included patients with Waldenström macroglobulinemia (WM) and a radiologic and/or cytologic diagnosis of BNS treated with ibrutinib monotherapy."1.51Ibrutinib for the treatment of Bing-Neel syndrome: a multicenter study. ( Ansell, SM; Buske, C; Castillo, JJ; Chavez, JC; Eyre, TA; Issa, S; Itchaki, G; Nayak, L; Palomba, ML; Paludo, J; Pasvolsky, O; Shain, KH; Simpson, D; Talaulikar, D; Tam, CS; Tedeschi, A; Treon, SP; Varettoni, M, 2019)
" Additionally, debate exists regarding the recommended dosing strategy for ibrutinib for this indication with disease remission demonstrated at 560 mg and 420 mg."1.51Ibrutinib for the treatment of Bing-Neel syndrome, a complication of Waldenström macroglobulinemia: Patient case report. ( Arnall, JR; Hartsell, L; Janes, A; Larck, C; Park, S, 2019)
"Richter syndrome (RS) is a rare event in chronic lymphocytic leukemia (CLL) that is influenced by biological factors and prior CLL treatments."1.46Ibrutinib treatment of a patient with relapsing chronic lymphocytic leukemia and sustained remission of Richter syndrome. ( Albi, E; Ascani, S; Aureli, P; Baldoni, S; Del Papa, B; Di Ianni, M; Dorillo, E; Falzetti, F; Sportoletti, P, 2017)
"Familial macrothrombocytopenias are a group of rare autosomal dominant platelet disorders including many syndromes in particular the May-Hegglin anomaly."1.33[The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene]. ( Bardet, V; Berda-Haddad, Y; Bernit, E; Camoin, L; Difeo, A; Ebbo, M; Favier, R; Harle, JR; Heudier, P; Kaplanski, G; Mazodier, K; Schleinitz, N; Veit, V, 2006)
"All patients had convulsions or loss of consciousness resulting from hypoglycemia at less than 1 year of age."1.31Novel missense mutations in the glutamate dehydrogenase gene in the congenital hyperinsulinism-hyperammonemia syndrome. ( Hayashi, Y; Kato, H; Miki, Y; Ohura, T; Taki, T; Yanagisawa, M, 2000)

Research

Studies (33)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (6.06)18.2507
2000's10 (30.30)29.6817
2010's16 (48.48)24.3611
2020's5 (15.15)2.80

Authors

AuthorsStudies
Arruga, F1
Bracciamà, V1
Vitale, N1
Vaisitti, T1
Gizzi, K1
Yeomans, A1
Coscia, M1
D'Arena, G1
Gaidano, G1
Allan, JN1
Furman, RR1
Packham, G1
Forconi, F1
Deaglio, S1
Los-Arcos, I1
Aguilar-Company, J1
Ruiz-Camps, I1
Grainger, BT1
Issa, S2
Pabon, CM1
Neff, JL1
Forns, TE1
Wang, J1
Carella, M1
Stefoni, V1
Broccoli, A1
Argnani, L1
Zinzani, PL1
Wasserstrum, Y1
Raanani, P1
Kornowski, R1
Iakobishvili, Z1
Fischer, A1
Bastian, S1
Cogliatti, S1
Mey, U1
Saub, J1
Schanz, U1
Padberg, B1
Hohloch, K1
Albi, E1
Baldoni, S1
Aureli, P1
Dorillo, E1
Del Papa, B1
Ascani, S1
Di Ianni, M1
Falzetti, F1
Sportoletti, P1
Writzl, K1
Maver, A1
Kovačič, L1
Martinez-Valero, P1
Contreras, L1
Satrustegui, J1
Castori, M1
Faivre, L1
Lapunzina, P1
van Kuilenburg, ABP1
Radović, S1
Thauvin-Robinet, C1
Peterlin, B1
Del Arco, A1
Hennekam, RC1
Boudin, L1
Patient, M1
Roméo, E1
Bladé, JS1
de Jauréguiberry, JP1
Kolomeyer, AM1
Hwang, CK1
Kim, BJ1
Castillo, JJ1
Itchaki, G1
Paludo, J1
Varettoni, M1
Buske, C1
Eyre, TA1
Chavez, JC1
Shain, KH1
Palomba, ML1
Pasvolsky, O1
Simpson, D1
Talaulikar, D1
Tam, CS1
Tedeschi, A1
Ansell, SM1
Nayak, L1
Treon, SP1
Hartsell, L1
Janes, A1
Larck, C1
Park, S1
Arnall, JR1
Sutherland, N1
Li Wai Suen, CFD1
Mills, C1
Lokan, J1
Sinclair, M1
Hashmi, H1
Dhanoa, JS1
Emmons, R1
Bayonne Kombo, ES1
Gathse, A1
Loos, D1
Hadeler, J1
Feucht, N1
Spinner, CD1
Schwerdtfeger, C1
Schmid, RM1
Lanzl, I1
Tsang, M1
Shanafelt, TD1
Call, TG1
Ding, W1
Chanan-Khan, A1
Leis, JF1
Nowakowski, GS1
Bowen, D1
Conte, M1
Schwager, SM1
Slager, SL1
Kay, NE1
Hanson, CA1
Parikh, SA1
Cabannes-Hamy, A1
Lemal, R1
Goldwirt, L1
Poulain, S1
Amorim, S1
Pérignon, R1
Berger, J1
Brice, P1
De Kerviler, E1
Bay, JO1
Sauvageon, H1
Beldjord, K1
Mourah, S1
Tournilhac, O1
Thieblemont, C1
Ruella, M1
Kenderian, SS1
Shestova, O1
Klichinsky, M1
Melenhorst, JJ1
Wasik, MA1
Lacey, SF1
June, CH1
Gill, S1
Ali, A1
Singh, SK1
Raman, R1
Nishijima, T1
Tsukada, K1
Nagata, N1
Watanabe, K1
Teruya, K1
Gatanaga, H1
Kikuchi, Y1
Oka, S1
Traboulsi, EI1
Anderson, PJ1
Netherway, DJ1
Cox, TC1
Roscioli, T1
David, DJ1
Vanita, V1
Hejtmancik, JF1
Hennies, HC1
Guleria, K1
Nürnberg, P1
Singh, D1
Sperling, K1
Singh, JR1
Kloeckener-Gruissem, B1
Bartholdi, D1
Abdou, MT1
Zimmermann, DR1
Berger, W1
Schleinitz, N1
Favier, R1
Mazodier, K1
Difeo, A1
Ebbo, M1
Veit, V1
Berda-Haddad, Y1
Bernit, E1
Heudier, P1
Kaplanski, G1
Camoin, L1
Bardet, V1
Harle, JR1
Matsuzawa, N1
Shimozato, K1
Natsume, N1
Niikawa, N1
Yoshiura, K1
Tsigos, C1
Arai, K1
Latronico, AC1
DiGeorge, AM1
Rapaport, R1
Chrousos, GP1
Smith, PR1
Bain, SC1
Good, PA1
Hattersley, AT1
Barnett, AH1
Gibson, JM1
Dodson, PM1
Miki, Y1
Taki, T1
Ohura, T1
Kato, H1
Yanagisawa, M1
Hayashi, Y1
Zoref-Shani, E1
Feinstein, S1
Frishberg, Y1
Bromberg, Y1
Sperling, O1
Sacconi, S1
Salviati, L1
Gooch, C1
Bonilla, E1
Shanske, S1
DiMauro, S1

Reviews

3 reviews available for adenine and Symptom Cluster

ArticleYear
Risk of infection associated with new therapies for lymphoproliferative syndromes.
    Medicina clinica, 2020, 02-14, Volume: 154, Issue:3

    Topics: Adenine; Alemtuzumab; Antibodies, Monoclonal, Humanized; Antineoplastic Agents; Antineoplastic Agent

2020
Bing-Neel syndrome presenting as isolated CNS lymphoplasmacytic lymphoma: A case report and review of the literature.
    Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2020, Volume: 71

    Topics: Adenine; Female; Humans; Lymphoma; Meningeal Carcinomatosis; Middle Aged; Piperidines; Pyrazoles; Py

2020
Anterior chamber fibrinoid syndrome after cataract extraction in a patient on ibrutinib for B-cell chronic lymphocytic leukemia: a case report and review of the literature.
    Journal of medical case reports, 2018, Nov-16, Volume: 12, Issue:1

    Topics: Adenine; Administration, Topical; Aged; Anterior Chamber; Antihypertensive Agents; Antineoplastic Ag

2018

Other Studies

30 other studies available for adenine and Symptom Cluster

ArticleYear
Bidirectional linkage between the B-cell receptor and NOTCH1 in chronic lymphocytic leukemia and in Richter's syndrome: therapeutic implications.
    Leukemia, 2020, Volume: 34, Issue:2

    Topics: Adenine; Adult; Aged; Aged, 80 and over; Amyloid Precursor Protein Secretases; Animals; Calcium; Dia

2020
Complete Response of a Young Woman With MYD88
    Clinical lymphoma, myeloma & leukemia, 2020, Volume: 20, Issue:11

    Topics: Adenine; Adolescent; Agammaglobulinaemia Tyrosine Kinase; Female; Humans; Myeloid Differentiation Fa

2020
A Case of Bing-Neel Syndrome Treated Successfully With Ibrutinib Monotherapy Following Intensive Chemoimmunotherapy.
    Clinical lymphoma, myeloma & leukemia, 2021, Volume: 21, Issue:11

    Topics: Adenine; Aged; Brain Diseases; Central Nervous System Neoplasms; Female; Humans; Immunotherapy; Pipe

2021
Concomitant Treatment with Ibrutinib and Amiodarone Causing Reversible Heart Failure Syndrome.
    The Israel Medical Association journal : IMAJ, 2016, Volume: 18, Issue:7

    Topics: Adenine; Aged; Amiodarone; Atrial Fibrillation; Cytochrome P-450 CYP3A Inhibitors; Drug Interactions

2016
Ibrutinib-induced rapid response in chemotherapy-refractory Richter's syndrome.
    Hematological oncology, 2018, Volume: 36, Issue:1

    Topics: Adenine; Drug Resistance, Neoplasm; Female; Humans; Leukemia, Lymphocytic, Chronic, B-Cell; Lymphoma

2018
Ibrutinib treatment of a patient with relapsing chronic lymphocytic leukemia and sustained remission of Richter syndrome.
    Tumori, 2017, Nov-15, Volume: 103, Issue:Suppl. 1

    Topics: Adenine; Aged; Cell Transformation, Neoplastic; Disease Progression; Humans; Leukemia, Lymphocytic,

2017
De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.
    American journal of human genetics, 2017, Nov-02, Volume: 101, Issue:5

    Topics: Adenine; Adenosine Triphosphate; Aging; Antiporters; Bone Diseases, Developmental; Calcium-Binding P

2017
Efficacy of ibrutinib as first-line treatment of tumoral Bing-Neel syndrome.
    Leukemia & lymphoma, 2018, Volume: 59, Issue:11

    Topics: Adenine; Aged; Brain; Brain Diseases; Humans; Magnetic Resonance Imaging; Male; Piperidines; Pyrazol

2018
Ibrutinib for the treatment of Bing-Neel syndrome: a multicenter study.
    Blood, 2019, 01-24, Volume: 133, Issue:4

    Topics: Adenine; Adult; Aged; Female; Humans; Kaplan-Meier Estimate; Male; Middle Aged; Piperidines; Pyrazol

2019
Ibrutinib for the treatment of Bing-Neel syndrome, a complication of Waldenström macroglobulinemia: Patient case report.
    Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners, 2019, Volume: 25, Issue:6

    Topics: Adenine; Brain Diseases; Humans; Male; Middle Aged; Piperidines; Protein Kinase Inhibitors; Pyrazole

2019
Fibrosing Cholestatic Hepatitis-Like Syndrome in an Immunocompetent Patient With an Acute Flare of Chronic Hepatitis B.
    Hepatology (Baltimore, Md.), 2019, Volume: 70, Issue:4

    Topics: Adenine; Biopsy, Needle; Cholestasis; Disease Progression; Follow-Up Studies; Hepatitis B, Chronic;

2019
Rare case of Bing-Neel syndrome treated successfully with ibrutinib.
    BMJ case reports, 2019, Jun-25, Volume: 12, Issue:6

    Topics: Adenine; Brain; Female; Humans; Magnetic Resonance Imaging; Middle Aged; Mutation; Myeloid Different

2019
[Tenofovir hypersensitivity to tenofovir (DRESS) syndrome in a female patient infected by HIV].
    Medecine et maladies infectieuses, 2013, Volume: 43, Issue:3

    Topics: Adenine; Adult; Alkynes; Anti-HIV Agents; Antiretroviral Therapy, Highly Active; Asthenia; Benzoxazi

2013
[Ophthalmological alterations at the initial diagnosis of HIV infection].
    Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft, 2014, Volume: 111, Issue:7

    Topics: Adenine; Adult; Antiretroviral Therapy, Highly Active; Cyclohexanes; Deoxycytidine; Drug Therapy, Co

2014
The efficacy of ibrutinib in the treatment of Richter syndrome.
    Blood, 2015, Mar-05, Volume: 125, Issue:10

    Topics: Adenine; Agammaglobulinaemia Tyrosine Kinase; Aged; Antibodies, Monoclonal, Murine-Derived; Antineop

2015
Efficacy of ibrutinib in the treatment of Bing-Neel syndrome.
    American journal of hematology, 2016, Volume: 91, Issue:3

    Topics: Adenine; Aged; Central Nervous System Diseases; Female; Humans; Immunoglobulin M; Leukocyte Count; M

2016
Kinase inhibitor ibrutinib to prevent cytokine-release syndrome after anti-CD19 chimeric antigen receptor T cells for B-cell neoplasms.
    Leukemia, 2017, Volume: 31, Issue:1

    Topics: Adenine; Animals; Antibodies; Antigens, CD19; Cytokines; Heterografts; Humans; Lymphoma, B-Cell; Mic

2017
Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.
    The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2009, Volume: 46, Issue:5

    Topics: 3' Untranslated Regions; Abnormalities, Multiple; Adenine; Arginine; Cleft Lip; Cleft Palate; Cohort

2009
Antiretroviral therapy alone resulted in successful resolution of large idiopathic esophageal ulcers in a patient with acute retroviral syndrome.
    AIDS (London, England), 2011, Aug-24, Volume: 25, Issue:13

    Topics: Adenine; Adult; Anti-HIV Agents; Antiviral Agents; Deoxycytidine; Drug Therapy, Combination; Emtrici

2011
Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements.
    Transactions of the American Ophthalmological Society, 2004, Volume: 102

    Topics: Adenine; Adolescent; Adult; Amino Acid Substitution; Arginine; Child; Child, Preschool; Chromosome M

2004
Do Craniosynostosis syndrome phenotypes with both FGFR2 and TWIST mutations have a worse clinical outcome?
    The Journal of craniofacial surgery, 2006, Volume: 17, Issue:1

    Topics: Acrocephalosyndactylia; Adenine; Adolescent; Arginine; Child, Preschool; Craniofacial Dysostosis; Cr

2006
Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.
    Molecular vision, 2006, Feb-21, Volume: 12

    Topics: 5' Untranslated Regions; Adenine; Apoferritins; Cataract; Child, Preschool; Chromosomes, Human, Pair

2006
Identification of the genetic defect in the original Wagner syndrome family.
    Molecular vision, 2006, Apr-17, Volume: 12

    Topics: Adenine; Case-Control Studies; Chondroitin Sulfate Proteoglycans; Chromosome Segregation; DNA, Recom

2006
[The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene].
    La Revue de medecine interne, 2006, Volume: 27, Issue:10

    Topics: Adenine; Adolescent; Exons; Female; Humans; Molecular Motor Proteins; Myosin Heavy Chains; Point Mut

2006
A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis.
    Journal of dental research, 2006, Volume: 85, Issue:12

    Topics: Adenine; Chromosomes, Human, Pair 1; Cleft Lip; Cleft Palate; DNA; Exons; Female; Genetic Linkage; H

2006
A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndrome.
    The Journal of clinical endocrinology and metabolism, 1995, Volume: 80, Issue:7

    Topics: Adenine; Adolescent; Adult; Amino Acid Sequence; Base Sequence; Cell Membrane; Cysteine; DNA; DNA Pr

1995
Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Ophthalmology, 1999, Volume: 106, Issue:6

    Topics: Adenine; Adult; Aged; Aged, 80 and over; Deafness; Diabetes Mellitus, Type 2; DNA, Mitochondrial; El

1999
Novel missense mutations in the glutamate dehydrogenase gene in the congenital hyperinsulinism-hyperammonemia syndrome.
    The Journal of pediatrics, 2000, Volume: 136, Issue:1

    Topics: Adenine; Ammonia; Codon; Cytosine; Female; Glutamate Dehydrogenase; Guanine; Heterozygote; Humans; H

2000
Kelley-Seegmiller syndrome due to a unique variant of hypoxanthine-guanine phosphoribosyltransferase: reduced affinity for 5-phosphoribosyl-1-pyrophosphate manifested only at low, physiological substrate concentrations.
    Biochimica et biophysica acta, 2000, Feb-21, Volume: 1500, Issue:2

    Topics: Acute Kidney Injury; Adenine; Cells, Cultured; Child, Preschool; Culture Media, Conditioned; DNA Mut

2000
Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNA.
    Archives of neurology, 2002, Volume: 59, Issue:6

    Topics: Adenine; Adult; Brain; DNA, Mitochondrial; Guanine; Humans; Male; Muscle, Skeletal; Mutation; Nervou

2002