adenine has been researched along with Symptom Cluster in 33 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| " He was diagnosed as having fibrinoid syndrome and started on topical prednisolone, brimonidine, timolol-dorzolamide, and orally administered acetazolamide." | 4.98 | 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. ( 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." | 1.56 | Bidirectional 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." | 1.51 | Ibrutinib 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." | 1.51 | Ibrutinib 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." | 1.46 | Ibrutinib 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." | 1.31 | Novel 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) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (6.06) | 18.2507 |
| 2000's | 10 (30.30) | 29.6817 |
| 2010's | 16 (48.48) | 24.3611 |
| 2020's | 5 (15.15) | 2.80 |
| Authors | Studies |
|---|---|
| Arruga, F | 1 |
| Bracciamà, V | 1 |
| Vitale, N | 1 |
| Vaisitti, T | 1 |
| Gizzi, K | 1 |
| Yeomans, A | 1 |
| Coscia, M | 1 |
| D'Arena, G | 1 |
| Gaidano, G | 1 |
| Allan, JN | 1 |
| Furman, RR | 1 |
| Packham, G | 1 |
| Forconi, F | 1 |
| Deaglio, S | 1 |
| Los-Arcos, I | 1 |
| Aguilar-Company, J | 1 |
| Ruiz-Camps, I | 1 |
| Grainger, BT | 1 |
| Issa, S | 2 |
| Pabon, CM | 1 |
| Neff, JL | 1 |
| Forns, TE | 1 |
| Wang, J | 1 |
| Carella, M | 1 |
| Stefoni, V | 1 |
| Broccoli, A | 1 |
| Argnani, L | 1 |
| Zinzani, PL | 1 |
| Wasserstrum, Y | 1 |
| Raanani, P | 1 |
| Kornowski, R | 1 |
| Iakobishvili, Z | 1 |
| Fischer, A | 1 |
| Bastian, S | 1 |
| Cogliatti, S | 1 |
| Mey, U | 1 |
| Saub, J | 1 |
| Schanz, U | 1 |
| Padberg, B | 1 |
| Hohloch, K | 1 |
| Albi, E | 1 |
| Baldoni, S | 1 |
| Aureli, P | 1 |
| Dorillo, E | 1 |
| Del Papa, B | 1 |
| Ascani, S | 1 |
| Di Ianni, M | 1 |
| Falzetti, F | 1 |
| Sportoletti, P | 1 |
| Writzl, K | 1 |
| Maver, A | 1 |
| Kovačič, L | 1 |
| Martinez-Valero, P | 1 |
| Contreras, L | 1 |
| Satrustegui, J | 1 |
| Castori, M | 1 |
| Faivre, L | 1 |
| Lapunzina, P | 1 |
| van Kuilenburg, ABP | 1 |
| Radović, S | 1 |
| Thauvin-Robinet, C | 1 |
| Peterlin, B | 1 |
| Del Arco, A | 1 |
| Hennekam, RC | 1 |
| Boudin, L | 1 |
| Patient, M | 1 |
| Roméo, E | 1 |
| Bladé, JS | 1 |
| de Jauréguiberry, JP | 1 |
| Kolomeyer, AM | 1 |
| Hwang, CK | 1 |
| Kim, BJ | 1 |
| Castillo, JJ | 1 |
| Itchaki, G | 1 |
| Paludo, J | 1 |
| Varettoni, M | 1 |
| Buske, C | 1 |
| Eyre, TA | 1 |
| Chavez, JC | 1 |
| Shain, KH | 1 |
| Palomba, ML | 1 |
| Pasvolsky, O | 1 |
| Simpson, D | 1 |
| Talaulikar, D | 1 |
| Tam, CS | 1 |
| Tedeschi, A | 1 |
| Ansell, SM | 1 |
| Nayak, L | 1 |
| Treon, SP | 1 |
| Hartsell, L | 1 |
| Janes, A | 1 |
| Larck, C | 1 |
| Park, S | 1 |
| Arnall, JR | 1 |
| Sutherland, N | 1 |
| Li Wai Suen, CFD | 1 |
| Mills, C | 1 |
| Lokan, J | 1 |
| Sinclair, M | 1 |
| Hashmi, H | 1 |
| Dhanoa, JS | 1 |
| Emmons, R | 1 |
| Bayonne Kombo, ES | 1 |
| Gathse, A | 1 |
| Loos, D | 1 |
| Hadeler, J | 1 |
| Feucht, N | 1 |
| Spinner, CD | 1 |
| Schwerdtfeger, C | 1 |
| Schmid, RM | 1 |
| Lanzl, I | 1 |
| Tsang, M | 1 |
| Shanafelt, TD | 1 |
| Call, TG | 1 |
| Ding, W | 1 |
| Chanan-Khan, A | 1 |
| Leis, JF | 1 |
| Nowakowski, GS | 1 |
| Bowen, D | 1 |
| Conte, M | 1 |
| Schwager, SM | 1 |
| Slager, SL | 1 |
| Kay, NE | 1 |
| Hanson, CA | 1 |
| Parikh, SA | 1 |
| Cabannes-Hamy, A | 1 |
| Lemal, R | 1 |
| Goldwirt, L | 1 |
| Poulain, S | 1 |
| Amorim, S | 1 |
| Pérignon, R | 1 |
| Berger, J | 1 |
| Brice, P | 1 |
| De Kerviler, E | 1 |
| Bay, JO | 1 |
| Sauvageon, H | 1 |
| Beldjord, K | 1 |
| Mourah, S | 1 |
| Tournilhac, O | 1 |
| Thieblemont, C | 1 |
| Ruella, M | 1 |
| Kenderian, SS | 1 |
| Shestova, O | 1 |
| Klichinsky, M | 1 |
| Melenhorst, JJ | 1 |
| Wasik, MA | 1 |
| Lacey, SF | 1 |
| June, CH | 1 |
| Gill, S | 1 |
| Ali, A | 1 |
| Singh, SK | 1 |
| Raman, R | 1 |
| Nishijima, T | 1 |
| Tsukada, K | 1 |
| Nagata, N | 1 |
| Watanabe, K | 1 |
| Teruya, K | 1 |
| Gatanaga, H | 1 |
| Kikuchi, Y | 1 |
| Oka, S | 1 |
| Traboulsi, EI | 1 |
| Anderson, PJ | 1 |
| Netherway, DJ | 1 |
| Cox, TC | 1 |
| Roscioli, T | 1 |
| David, DJ | 1 |
| Vanita, V | 1 |
| Hejtmancik, JF | 1 |
| Hennies, HC | 1 |
| Guleria, K | 1 |
| Nürnberg, P | 1 |
| Singh, D | 1 |
| Sperling, K | 1 |
| Singh, JR | 1 |
| Kloeckener-Gruissem, B | 1 |
| Bartholdi, D | 1 |
| Abdou, MT | 1 |
| Zimmermann, DR | 1 |
| Berger, W | 1 |
| Schleinitz, N | 1 |
| Favier, R | 1 |
| Mazodier, K | 1 |
| Difeo, A | 1 |
| Ebbo, M | 1 |
| Veit, V | 1 |
| Berda-Haddad, Y | 1 |
| Bernit, E | 1 |
| Heudier, P | 1 |
| Kaplanski, G | 1 |
| Camoin, L | 1 |
| Bardet, V | 1 |
| Harle, JR | 1 |
| Matsuzawa, N | 1 |
| Shimozato, K | 1 |
| Natsume, N | 1 |
| Niikawa, N | 1 |
| Yoshiura, K | 1 |
| Tsigos, C | 1 |
| Arai, K | 1 |
| Latronico, AC | 1 |
| DiGeorge, AM | 1 |
| Rapaport, R | 1 |
| Chrousos, GP | 1 |
| Smith, PR | 1 |
| Bain, SC | 1 |
| Good, PA | 1 |
| Hattersley, AT | 1 |
| Barnett, AH | 1 |
| Gibson, JM | 1 |
| Dodson, PM | 1 |
| Miki, Y | 1 |
| Taki, T | 1 |
| Ohura, T | 1 |
| Kato, H | 1 |
| Yanagisawa, M | 1 |
| Hayashi, Y | 1 |
| Zoref-Shani, E | 1 |
| Feinstein, S | 1 |
| Frishberg, Y | 1 |
| Bromberg, Y | 1 |
| Sperling, O | 1 |
| Sacconi, S | 1 |
| Salviati, L | 1 |
| Gooch, C | 1 |
| Bonilla, E | 1 |
| Shanske, S | 1 |
| DiMauro, S | 1 |
3 reviews available for adenine and Symptom Cluster
| Article | Year |
|---|---|
Risk of infection associated with new therapies for lymphoproliferative syndromes.
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.
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.
Topics: Adenine; Administration, Topical; Aged; Anterior Chamber; Antihypertensive Agents; Antineoplastic Ag | 2018 |
30 other studies available for adenine and Symptom Cluster
| Article | Year |
|---|---|
Bidirectional linkage between the B-cell receptor and NOTCH1 in chronic lymphocytic leukemia and in Richter's syndrome: therapeutic implications.
Topics: Adenine; Adult; Aged; Aged, 80 and over; Amyloid Precursor Protein Secretases; Animals; Calcium; Dia | 2020 |
Complete Response of a Young Woman With MYD88
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.
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.
Topics: Adenine; Aged; Amiodarone; Atrial Fibrillation; Cytochrome P-450 CYP3A Inhibitors; Drug Interactions | 2016 |
Ibrutinib-induced rapid response in chemotherapy-refractory Richter's syndrome.
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.
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.
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.
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.
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.
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.
Topics: Adenine; Biopsy, Needle; Cholestasis; Disease Progression; Follow-Up Studies; Hepatitis B, Chronic; | 2019 |
Rare case of Bing-Neel syndrome treated successfully with ibrutinib.
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].
Topics: Adenine; Adult; Alkynes; Anti-HIV Agents; Antiretroviral Therapy, Highly Active; Asthenia; Benzoxazi | 2013 |
[Ophthalmological alterations at the initial diagnosis of HIV infection].
Topics: Adenine; Adult; Antiretroviral Therapy, Highly Active; Cyclohexanes; Deoxycytidine; Drug Therapy, Co | 2014 |
The efficacy of ibrutinib in the treatment of Richter syndrome.
Topics: Adenine; Agammaglobulinaemia Tyrosine Kinase; Aged; Antibodies, Monoclonal, Murine-Derived; Antineop | 2015 |
Efficacy of ibrutinib in the treatment of Bing-Neel syndrome.
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.
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.
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.
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.
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?
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.
Topics: 5' Untranslated Regions; Adenine; Apoferritins; Cataract; Child, Preschool; Chromosomes, Human, Pair | 2006 |
Identification of the genetic defect in the original Wagner syndrome family.
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].
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.
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.
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.
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.
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.
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.
Topics: Adenine; Adult; Brain; DNA, Mitochondrial; Guanine; Humans; Male; Muscle, Skeletal; Mutation; Nervou | 2002 |