BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 37207212)

  • 21. ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study.
    Caorsi R; Penco F; Grossi A; Insalaco A; Omenetti A; Alessio M; Conti G; Marchetti F; Picco P; Tommasini A; Martino S; Malattia C; Gallizzi R; Podda RA; Salis A; Falcini F; Schena F; Garbarino F; Morreale A; Pardeo M; Ventrici C; Passarelli C; Zhou Q; Severino M; Gandolfo C; Damonte G; Martini A; Ravelli A; Aksentijevich I; Ceccherini I; Gattorno M
    Ann Rheum Dis; 2017 Oct; 76(10):1648-1656. PubMed ID: 28522451
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Deficiency of Adenosine Deaminase Type 2: A Description of Phenotype and Genotype in Fifteen Cases.
    Nanthapisal S; Murphy C; Omoyinmi E; Hong Y; Standing A; Berg S; Ekelund M; Jolles S; Harper L; Youngstein T; Gilmour K; Klein NJ; Eleftheriou D; Brogan PA
    Arthritis Rheumatol; 2016 Sep; 68(9):2314-22. PubMed ID: 27059682
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Deficiency of ADA2 mimicking autoimmune lymphoproliferative syndrome in the absence of livedo reticularis and vasculitis.
    Alsultan A; Basher E; Alqanatish J; Mohammed R; Alfadhel M
    Pediatr Blood Cancer; 2018 Apr; 65(4):. PubMed ID: 29271561
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Deficiency of Adenosine Deaminase 2: Clinical Manifestations, Diagnosis, and Treatment.
    Grim A; Veiga KR; Saad N
    Rheum Dis Clin North Am; 2023 Nov; 49(4):773-787. PubMed ID: 37821195
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2.
    Özen S; Batu ED; Taşkıran EZ; Özkara HA; Ünal Ş; Güleray N; Erden A; Karadağ Ö; Gümrük F; Çetin M; Sönmez HE; Bilginer Y; Ayvaz DÇ; Tezcan I
    J Rheumatol; 2020 Jan; 47(1):117-125. PubMed ID: 31043544
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variants.
    Parlar K; Tahir Turanli E; Nuhoglu Kantarci E; Hacioglu A; Kirectepe Aydin A; Ayla AY; Voyvoda U; Ozdogan H; Ugurlu S
    Mod Rheumatol Case Rep; 2023 Dec; 8(1):121-124. PubMed ID: 37542433
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A Novel Germline Mutation of
    Vai S; Marin E; Cosso R; Saettini F; Bonanomi S; Cattoni A; Chiodini I; Persani L; Falchetti A
    Int J Mol Sci; 2021 Aug; 22(15):. PubMed ID: 34361096
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cutaneous vasculitis in autoinflammatory diseases.
    Chen KR
    J Dermatol; 2024 Feb; 51(2):150-159. PubMed ID: 37955334
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two cases of ADA2 deficiency presenting as childhood polyarteritis nodosa: novel ADA2 variant, atypical CNS manifestations, and literature review.
    Ganhão S; Loureiro GB; Oliveira DR; Dos-Reis-Maia R; Aguiar F; Quental R; Moura C; Barreira JL; Rodrigues M; Brito I
    Clin Rheumatol; 2020 Dec; 39(12):3853-3860. PubMed ID: 32535845
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Monogenic polyarteritis: the lesson of ADA2 deficiency.
    Caorsi R; Penco F; Schena F; Gattorno M
    Pediatr Rheumatol Online J; 2016 Sep; 14(1):51. PubMed ID: 27609179
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Vasculitis associated with adenosine deaminase 2 deficiency: at the crossroads between Behçet's disease and autoinflammation. A viewpoint.
    Colangelo A; Tromby F; Cafaro G; Gerli R; Bartoloni E; Perricone C
    Reumatismo; 2023 Sep; 75(3):. PubMed ID: 37721348
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Deficiency of adenosine deaminase 2 (DADA2): Review.
    Sharma V; Deo P; Sharma A
    Best Pract Res Clin Rheumatol; 2023 Mar; 37(1):101844. PubMed ID: 37328410
    [TBL] [Abstract][Full Text] [Related]  

  • 33. ADA2 Deficiency: Case Series of Five Patients with Varying Phenotypes.
    Tanatar A; Karadağ ŞG; Sözeri B; Sönmez HE; Çakan M; Kendir Demirkol Y; Aktay Ayaz N
    J Clin Immunol; 2020 Feb; 40(2):253-258. PubMed ID: 31848804
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Importance of the determination of enzymatic activity in the diagnosis of deficiency of adenosine deaminase 2 (DADA2).
    Abbasi A; Batllori M; Gil-Sáez FJ; Rodríguez-Pintó I; Antón López J; Iglesias Jímenez E
    Med Clin (Barc); 2022 Sep; 159(6):283-286. PubMed ID: 35241284
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genotype and Phenotype of Adenosine Deaminase 2 Deficiency: a Report from Saudi Arabia.
    Alabbas F; Alanzi T; Alrasheed A; Essa M; Elyamany G; Asiri A; Almutairi S; Al-Mayouf S; Alenazi A; Alsafadi D; Ballourah W; Albalawi N; Hanafy E; Al-Hebshi A; Alrashidi S; Albatniji F; Alfaraidi H; Ali TB; Al Qwaiee M; AlHilali M; Aldeeb H; Alhaidey A; Aljasem H; Althubaiti S; Alsultan A
    J Clin Immunol; 2023 Feb; 43(2):338-349. PubMed ID: 36239861
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel frameshift variant in the ADA2 gene of a patient with a neurological phenotype: a case report.
    Lucane Z; Davidsone Z; Micule I; Auzenbaha M; Kurjane N
    Pediatr Rheumatol Online J; 2022 Dec; 20(1):118. PubMed ID: 36528591
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A case report on deficiency of adenosine deaminase 2 with relapse-remission course and analysis of genotype-phenotype correlation.
    Cai Q; Feng F; Tian Y; Luo R; Mu D; Yang F; Yang Z; Zhou Z
    Am J Med Genet A; 2024 Jun; 194(6):e63568. PubMed ID: 38353426
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Adenosine Deaminase 2 Deficiency Caused by Biallele Variants Including Splicing Variant: The First Case in Korea.
    Cho S; Park S; Lee JS; Ju YS; Choi YJ; Lee S
    J Rheum Dis; 2022 Oct; 29(4):254-260. PubMed ID: 37476427
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Vasculitic peripheral neuropathy in deficiency of adenosine deaminase 2.
    Carneiro DR; Rebelo O; Matos A; Baldeiras I; Almendra L; Fernandes C; Negrão L; Almeida MR; Matias F; Brás J; Guerreiro R; Santo GC
    Neuromuscul Disord; 2021 Sep; 31(9):891-895. PubMed ID: 34210540
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Early-onset stroke and vasculopathy associated with mutations in ADA2.
    Zhou Q; Yang D; Ombrello AK; Zavialov AV; Toro C; Zavialov AV; Stone DL; Chae JJ; Rosenzweig SD; Bishop K; Barron KS; Kuehn HS; Hoffmann P; Negro A; Tsai WL; Cowen EW; Pei W; Milner JD; Silvin C; Heller T; Chin DT; Patronas NJ; Barber JS; Lee CC; Wood GM; Ling A; Kelly SJ; Kleiner DE; Mullikin JC; Ganson NJ; Kong HH; Hambleton S; Candotti F; Quezado MM; Calvo KR; Alao H; Barham BK; Jones A; Meschia JF; Worrall BB; Kasner SE; Rich SS; Goldbach-Mansky R; Abinun M; Chalom E; Gotte AC; Punaro M; Pascual V; Verbsky JW; Torgerson TR; Singer NG; Gershon TR; Ozen S; Karadag O; Fleisher TA; Remmers EF; Burgess SM; Moir SL; Gadina M; Sood R; Hershfield MS; Boehm M; Kastner DL; Aksentijevich I
    N Engl J Med; 2014 Mar; 370(10):911-20. PubMed ID: 24552284
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.