237 related articles for article (PubMed ID: 31838659)
21. Recent advances in understanding RAG deficiencies.
Gennery A
F1000Res; 2019; 8():. PubMed ID: 30800289
[TBL] [Abstract][Full Text] [Related]
22. Novel RAG1 mutation and the occurrence of mycobacterial and Chromobacterium violaceum infections in a case of leaky SCID.
Khan TA; Iqbal A; Rahman H; Cabral-Marques O; Ishfaq M; Muhammad N
Microb Pathog; 2017 Aug; 109():114-119. PubMed ID: 28552805
[TBL] [Abstract][Full Text] [Related]
23. [Omenn Syndrome and DNA recombination defects].
Yachie A
Nihon Rinsho Meneki Gakkai Kaishi; 2017; 40(3):179-189. PubMed ID: 28747605
[TBL] [Abstract][Full Text] [Related]
24. A novel homozygous
Melika S; Hossein E; Mona S; Elham R; Samaneh Z; Sepideh S; Raul Jimenez H; Ana K; Kaan B; Nima R
Allergol Immunopathol (Madr); 2021; 49(4):91-97. PubMed ID: 34224223
[TBL] [Abstract][Full Text] [Related]
25. IL7R and RAG1/2 genes mutations/polymorphisms in patients with SCID.
Safaei S; Pourpak Z; Moin M; Houshmand M
Iran J Allergy Asthma Immunol; 2011 Jun; 10(2):129-32. PubMed ID: 21625022
[TBL] [Abstract][Full Text] [Related]
26. Severe combined immunodeficiency in Serbia and Montenegro between years 1986 and 2010: a single-center experience.
Pasic S; Vujic D; Veljković D; Slavkovic B; Mostarica-Stojkovic M; Minic P; Minic A; Ristic G; Giliani S; Villa A; Sobacchi C; Lilić D; Abinun M
J Clin Immunol; 2014 Apr; 34(3):304-8. PubMed ID: 24481607
[TBL] [Abstract][Full Text] [Related]
27. Omenn syndrome with mutation in RAG1 gene.
Jaouad IC; Ouldim K; Ali Ou Alla S; Kriouile Y; Villa A; Sefiani A
Indian J Pediatr; 2008 Sep; 75(9):944-6. PubMed ID: 19011808
[TBL] [Abstract][Full Text] [Related]
28. Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine).
Sharapova SO; Guryanova IE; Pashchenko OE; Kondratenko IV; Kostyuchenko LV; Rodina YA; Varlamova TV; Bondarenko AV; Chernyshova LI; Gyseva MN; Belevtsev MV; Minakovskaya NV; Aleinikova OV
J Clin Immunol; 2016 Jan; 36(1):46-55. PubMed ID: 26596586
[TBL] [Abstract][Full Text] [Related]
29. A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection.
de Villartay JP; Lim A; Al-Mousa H; Dupont S; Déchanet-Merville J; Coumau-Gatbois E; Gougeon ML; Lemainque A; Eidenschenk C; Jouanguy E; Abel L; Casanova JL; Fischer A; Le Deist F
J Clin Invest; 2005 Nov; 115(11):3291-9. PubMed ID: 16276422
[TBL] [Abstract][Full Text] [Related]
30. A Decade Experience on Severe Combined Immunodeficiency Phenotype in Oman, Bridging to Newborn Screening.
Al Sukaiti N; Ahmed K; Alshekaili J; Al Kindi M; Cook MC; Farsi TA
Front Immunol; 2020; 11():623199. PubMed ID: 33519828
[TBL] [Abstract][Full Text] [Related]
31. Evolution of a T-B- SCID into an Omenn syndrome phenotype following parainfluenza 3 virus infection.
Dalal I; Tabori U; Bielorai B; Golan H; Rosenthal E; Amariglio N; Rechavi G; Toren A
Clin Immunol; 2005 Apr; 115(1):70-3. PubMed ID: 15870023
[TBL] [Abstract][Full Text] [Related]
32. [Ichtyosiform erythroderma revealing a severe combined immunodeficiency].
Ghariani Fetoui N; Boussofara L; Hmida D; Mokni S; Mekki N; Ben Mustapha I; Belajouza C; Ghariani N; Picard C; Denguezli M
Ann Dermatol Venereol; 2020 Feb; 147(2):131-134. PubMed ID: 31973905
[TBL] [Abstract][Full Text] [Related]
33. Leaky RAG Deficiency in Adult Patients with Impaired Antibody Production against Bacterial Polysaccharide Antigens.
Geier CB; Piller A; Linder A; Sauerwein KM; Eibl MM; Wolf HM
PLoS One; 2015; 10(7):e0133220. PubMed ID: 26186701
[TBL] [Abstract][Full Text] [Related]
34. The immunophenotypic and immunogenotypic B-cell differentiation arrest in bone marrow of RAG-deficient SCID patients corresponds to residual recombination activities of mutated RAG proteins.
Noordzij JG; de Bruin-Versteeg S; Verkaik NS; Vossen JM; de Groot R; Bernatowska E; Langerak AW; van Gent DC; van Dongen JJ
Blood; 2002 Sep; 100(6):2145-52. PubMed ID: 12200379
[TBL] [Abstract][Full Text] [Related]
35. Novel mutatıons and diverse clinical phenotypes in recombinase-activating gene 1 deficiency.
Kutukculer N; Gulez N; Karaca NE; Aksu G; Berdeli A
Ital J Pediatr; 2012 Mar; 38():8. PubMed ID: 22424479
[TBL] [Abstract][Full Text] [Related]
36. Homozygous deletion of RAG1, RAG2 and 5' region TRAF6 causes severe immune suppression and atypical osteopetrosis.
Weisz Hubshman M; Basel-Vanagaite L; Krauss A; Konen O; Levy Y; Garty BZ; Smirin-Yosef P; Maya I; Lagovsky I; Taub E; Marom D; Gaash D; Shichrur K; Avigad S; Hayman-Manzur L; Villa A; Sobacchi C; Shohat M; Yaniv I; Stein J
Clin Genet; 2017 Jun; 91(6):902-907. PubMed ID: 27808398
[TBL] [Abstract][Full Text] [Related]
37. From variant of uncertain significance to likely pathogenic in two siblings with atypical RAG2 Deficiency: a case report and review of the literature.
Taghizadeh N; Mohammadi S; Abolhassani H; Shokri S; Nabavi M; Fallahpour M; Bemanian MH
BMC Pediatr; 2024 Feb; 24(1):116. PubMed ID: 38350907
[TBL] [Abstract][Full Text] [Related]
38. Three faces of recombination activating gene 1 (RAG1) mutations.
Patiroglu T; Akar HH; Van Der Burg M
Acta Microbiol Immunol Hung; 2015 Dec; 62(4):393-401. PubMed ID: 26689875
[TBL] [Abstract][Full Text] [Related]
39. Clinical characteristics and molecular analysis of three Chinese children with Omenn syndrome.
Zhang ZY; Zhao XD; Jiang LP; Liu EM; Cui YX; Wang M; Wei H; Yu J; An YF; Yang XQ
Pediatr Allergy Immunol; 2011 Aug; 22(5):482-7. PubMed ID: 21771083
[TBL] [Abstract][Full Text] [Related]
40. Omenn syndrome: a disorder of Rag1 and Rag2 genes.
Villa A; Santagata S; Bozzi F; Imberti L; Notarangelo LD
J Clin Immunol; 1999 Mar; 19(2):87-97. PubMed ID: 10226883
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
