99 related articles for article (PubMed ID: 22657410)
1. Evaluation of a patient with hyper-IgM syndrome.
Uygungil B; Bonilla F; Lederman H
J Allergy Clin Immunol; 2012 Jun; 129(6):1692-3.e4. PubMed ID: 22657410
[No Abstract] [Full Text] [Related]
2. Ataxia-telangiectasia patients presenting with hyper-IgM syndrome.
Noordzij JG; Wulffraat NM; Haraldsson A; Meyts I; van't Veer LJ; Hogervorst FB; Warris A; Weemaes CM
Arch Dis Child; 2009 Jun; 94(6):448-9. PubMed ID: 19224889
[TBL] [Abstract][Full Text] [Related]
3. Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype.
Lougaris V; Faletra F; Lanzi G; Vozzi D; Marcuzzi A; Valencic E; Piscianz E; Bianco A; Girardelli M; Baronio M; Loganes C; Fasth A; Salvini F; Trizzino A; Moratto D; Facchetti F; Giliani S; Plebani A; Tommasini A
Clin Immunol; 2015 Jul; 159(1):33-6. PubMed ID: 25939554
[No Abstract] [Full Text] [Related]
4. Hyper IgM Syndrome with low IgM and thrombocytosis: an unusual case of immunodeficiency.
Yousef E; Arshad Alvi M
Eur Ann Allergy Clin Immunol; 2016 Sep; 48(5):194-6. PubMed ID: 27608476
[TBL] [Abstract][Full Text] [Related]
5. Ataxia Telangiectasia Masquerading as Hyper IgM Syndrome.
Rawat A; Imai K; Suri D; Gupta A; Bhisikar S; Saikia B; Minz RW; Sehgal S; Singh S
Indian J Pediatr; 2016 Mar; 83(3):270-1. PubMed ID: 26220245
[No Abstract] [Full Text] [Related]
6. Visceral Leishmaniasis May Unmask X-linked Hyper-IgM Syndrome.
Gonzalez-Granado LI; Dominguez-Pinilla N; Gallego-Bustos F; Ruiz-Contreras J; Allende LM
J Clin Immunol; 2016 May; 36(4):363-5. PubMed ID: 26984850
[No Abstract] [Full Text] [Related]
7. Immunodeficiency and autoimmune phenomena in female hyper-IgM syndrome.
Melegari A; Mascia MT; Sandri G; Carbonieri A
Ann N Y Acad Sci; 2007 Aug; 1109():106-8. PubMed ID: 17785295
[TBL] [Abstract][Full Text] [Related]
8. Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.
Mahdaviani SA; Hirbod-Mobarakeh A; Wang N; Aghamohammadi A; Hammarström L; Masjedi MR; Pan-Hammarström Q; Rezaei N
Expert Rev Clin Immunol; 2012 Aug; 8(6):539-46. PubMed ID: 22992148
[TBL] [Abstract][Full Text] [Related]
9. [Clinical and immunological profile of 15 Moroccan patients with Hyper IgM syndrome].
Ouair H; Benhsaien I; Jeddane L; El Bakkouri J; Elhafidi N; Rada N; Najib J; Ailal F; Alj HS; Bousfiha AA
Pan Afr Med J; 2017; 26():212. PubMed ID: 28690727
[TBL] [Abstract][Full Text] [Related]
10. Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL.
Bajin İY; Ayvaz DÇ; Ünal S; Özgür TT; Çetin M; Gümrük F; Tezcan İ; de Villartay JP; Sanal Ö
Mol Immunol; 2013 Dec; 56(4):354-7. PubMed ID: 23911390
[TBL] [Abstract][Full Text] [Related]
11. Coexistence of Two Rare Autosomal Recessive Disorders: Activation-Induced Cytidine Deaminase Deficiency and Sjogren-Larsson Syndrome.
Shamriz O; Molho-Pessach V; Shaag A; Daum H; Stepensky P
Isr Med Assoc J; 2016 Oct; 18(10):636-638. PubMed ID: 28471629
[No Abstract] [Full Text] [Related]
12. Hyper-immunoglobulin M syndrome type 3 with normal CD40 cell surface expression.
Karaca NE; Forveille M; Aksu G; Durandy A; Kutukculer N
Scand J Immunol; 2012 Jul; 76(1):21-5. PubMed ID: 22443339
[TBL] [Abstract][Full Text] [Related]
13. Late-Onset Lymphopenia and ITP in a Patient with Hyper IgM Syndrome Due to a Homozygous Variant in AICDA.
Adatia A; Ritchie B
J Clin Immunol; 2023 Oct; 43(7):1540-1542. PubMed ID: 37402930
[No Abstract] [Full Text] [Related]
14. Hyper IgM syndrome in an infant.
Gunasekera TM; de Silva R; Faizal MA; Karunatilake DH; de Silva S
Ceylon Med J; 2007 Dec; 52(4):139-40. PubMed ID: 18286778
[No Abstract] [Full Text] [Related]
15. Hyper-IgM syndrome--a case report and a clinical perspective.
Silva R; Da Costa JT
Eur Ann Allergy Clin Immunol; 2010 Oct; 42(5):194-6. PubMed ID: 21192628
[TBL] [Abstract][Full Text] [Related]
16. IgM predominance in autoimmune disease: genetics and gender.
Duarte-Rey C; Bogdanos DP; Leung PS; Anaya JM; Gershwin ME
Autoimmun Rev; 2012 May; 11(6-7):A404-12. PubMed ID: 22178509
[TBL] [Abstract][Full Text] [Related]
17. A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome.
Chou J; Hanna-Wakim R; Tirosh I; Kane J; Fraulino D; Lee YN; Ghanem S; Mahfouz I; Mégarbané A; Lefranc G; Inati A; Dbaibo G; Giliani S; Notarangelo LD; Geha RS; Massaad MJ
J Allergy Clin Immunol; 2012 Dec; 130(6):1414-6. PubMed ID: 22841008
[No Abstract] [Full Text] [Related]
18. Successful treatment of autoimmune and lymphoproliferative complications of patients with intrinsic B-cell immunodeficiencies with Rituximab.
Hennig C; Baumann U; Ilginus C; Horneff G; Foell J; Hansen G
Br J Haematol; 2010 Feb; 148(3):445-8. PubMed ID: 19922533
[TBL] [Abstract][Full Text] [Related]
19. Severe congenital neutropenia or hyper-IgM syndrome? A novel mutation of CD40 ligand in a patient with severe neutropenia.
Rezaei N; Aghamohammadi A; Ramyar A; Pan-Hammarstrom Q; Hammarstrom L
Int Arch Allergy Immunol; 2008; 147(3):255-9. PubMed ID: 18594157
[TBL] [Abstract][Full Text] [Related]
20. The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management.
Yazdani R; Fekrvand S; Shahkarami S; Azizi G; Moazzami B; Abolhassani H; Aghamohammadi A
Clin Immunol; 2019 Jan; 198():19-30. PubMed ID: 30439505
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]