139 related articles for article (PubMed ID: 35804376)
1. Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation.
Gong X; He Y; Lu G; Zhang Y; Qiu Y; Qiao L; Li Y
BMC Med Genomics; 2022 Jul; 15(1):153. PubMed ID: 35804376
[TBL] [Abstract][Full Text] [Related]
2. Respiratory infections in X-linked hyper-IgM syndrome with CD40LG mutation: a case series of seven children in China.
Fan H; Huang L; Yang D; Zhang C; Zeng Q; Yin G; Lu G; Shen K
BMC Pediatr; 2022 Nov; 22(1):675. PubMed ID: 36419145
[TBL] [Abstract][Full Text] [Related]
3. Complex preimplantation genetic tests for Robertsonian translocation, HLA, and X-linked hyper IgM syndrome caused by a novel mutation of CD40LG gene.
Huang S; Niu Y; Li J; Gao M; Zhang Y; Yan J; Ma S; Gao X; Gao Y
J Assist Reprod Genet; 2020 Aug; 37(8):2025-2031. PubMed ID: 32500460
[TBL] [Abstract][Full Text] [Related]
4. CD40LG mutations in Vietnamese patients with X-linked hyper-IgM syndrome; catastrophic anti-phospholipid syndrome as a new complication.
Phan ANL; Pham TTT; Phan XT; Huynh N; Nguyen TM; Cao CTT; Nguyen DT; Luong KTX; Nguyen TTM; Tran ANK; Pham LTT; Nguyen VVT; Swagemakers S; Bui CB; Van Hagen PM
Mol Genet Genomic Med; 2021 Aug; 9(8):e1732. PubMed ID: 34114358
[TBL] [Abstract][Full Text] [Related]
5. CD40LG-associated X-linked Hyper-IgM Syndrome (XHIGM) with pulmonary alveolar proteinosis: a case report.
Xu HB; Tian MQ; Bai YH; Ran X; Li L; Chen Y
BMC Pediatr; 2023 May; 23(1):239. PubMed ID: 37173671
[TBL] [Abstract][Full Text] [Related]
6. X-linked hyper-IgM syndrome with CD40LG mutation: two case reports and literature review in Taiwanese patients.
Tsai HY; Yu HH; Chien YH; Chu KH; Lau YL; Lee JH; Wang LC; Chiang BL; Yang YH
J Microbiol Immunol Infect; 2015 Feb; 48(1):113-8. PubMed ID: 23010537
[TBL] [Abstract][Full Text] [Related]
7. A Novel
Li L; Ji J; Han M; Xu Y; Zhang X; Liu W; Liu S
Immunol Invest; 2020 Apr; 49(3):307-316. PubMed ID: 31401902
[No Abstract] [Full Text] [Related]
8. Variants Disrupting CD40L Transmembrane Domain and Atypical X-Linked Hyper-IgM Syndrome: A Case Report With Leishmaniasis and Review of the Literature.
Palterer B; Salvati L; Capone M; Mecheri V; Maggi L; Mazzoni A; Cosmi L; Volpi N; Tiberi L; Provenzano A; Giglio S; Parronchi P; Maggiore G; Gallo O; Bartoloni A; Annunziato F; Zammarchi L; Liotta F
Front Immunol; 2022; 13():840767. PubMed ID: 35572607
[TBL] [Abstract][Full Text] [Related]
9. Interstitial pneumonia as the initial presentation in an infant with a novel mutation of CD40 ligand-associated X-linked hyper-IgM syndrome: A case report.
Li J; Miao H; Wu L; Fang Y
Medicine (Baltimore); 2020 Jun; 99(24):e20505. PubMed ID: 32541472
[TBL] [Abstract][Full Text] [Related]
10. An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation.
Kutukculer N; Karaca NE; Aksu G; Aykut A; Pariltay E; Cogulu O
Case Reports Immunol; 2018; 2018():6897935. PubMed ID: 30405923
[TBL] [Abstract][Full Text] [Related]
11. X-linked hyper-immunoglobulin M syndrome: molecular genetic study and long-time follow-up of three generations of a Chinese family.
Lin SC; Shyur SD; Lee WI; Ma YC; Huang LH
Int Arch Allergy Immunol; 2006; 140(1):1-8. PubMed ID: 16508335
[TBL] [Abstract][Full Text] [Related]
12. X-linked Hyper IgM Syndrome Presenting as Pulmonary Alveolar Proteinosis.
Gallagher J; Adams J; Hintermeyer M; Torgerson TR; Lopez-Guisa J; Ochs HD; Szabo S; Salib M; Verbsky J; Routes J
J Clin Immunol; 2016 Aug; 36(6):564-70. PubMed ID: 27324886
[TBL] [Abstract][Full Text] [Related]
13. X-linked hyper-IgM syndrome associated with pulmonary manifestations: A very rare case of functional mutation in CD40L gene in Iran.
Torabizadeh M; Nabavi M; Zadkarami M; Shahrooei M
Curr Res Transl Med; 2019 Feb; 67(1):28-30. PubMed ID: 29525420
[TBL] [Abstract][Full Text] [Related]
14. [Unrelated umbilical cord blood stem cell transplantation in the treatment of hyper-IgM syndrome caused by CD40 ligand gene mutation: a report of three cases and literature review].
Wang P; Qian XW; Wang HS; Jiang WJ; Sun JQ; Wang XC; Zhai XW
Zhonghua Er Ke Za Zhi; 2021 Oct; 59(10):830-835. PubMed ID: 34587678
[No Abstract] [Full Text] [Related]
15. Two novel CD40LG gene mutations causing X-linked hyper IgM syndrome in Vietnamese patients.
Lien NTK; Van Anh NT; Chi LQ; Le NNQ; Huyen TT; Mai NTP; Van Tung N; Hoang NH
Clin Exp Med; 2023 Feb; 23(1):157-161. PubMed ID: 34842998
[TBL] [Abstract][Full Text] [Related]
16. De novo mutation causing X-linked hyper-IgM syndrome: a family study in Taiwan.
Ma YC; Lee WI; Shyur SD; Lin SC; Huang LH; Wu JY
Asian Pac J Allergy Immunol; 2005 Mar; 23(1):53-9. PubMed ID: 15997875
[TBL] [Abstract][Full Text] [Related]
17. A novel CD40LG deletion causes the hyper-IgM syndrome with normal CD40L expression in a 6-month-old child.
López-Herrera G; Maravillas-Montero JL; Vargas-Hernández A; Berrón-Ruíz L; Ramírez-Sánchez E; Yamazaki-Nakashimada MA; Espinosa-Rosales FJ; Santos-Argumedo L
Immunol Res; 2015 May; 62(1):89-94. PubMed ID: 25752457
[TBL] [Abstract][Full Text] [Related]
18. Progressive choreodystonia in X-linked hyper-IgM immunodeficiency: a rare but recurrent presentation.
Škorvánek M; Jech R; Winkelmann J; Zech M
Ann Clin Transl Neurol; 2022 Apr; 9(4):577-581. PubMed ID: 35267244
[TBL] [Abstract][Full Text] [Related]
19. The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients.
Winkelstein JA; Marino MC; Ochs H; Fuleihan R; Scholl PR; Geha R; Stiehm ER; Conley ME
Medicine (Baltimore); 2003 Nov; 82(6):373-84. PubMed ID: 14663287
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial DNA insert into CD40 ligand gene-associated X-linked hyper-IgM syndrome.
Li X; Xu D; Cheng B; Zhou Y; Chen Z; Wang Y
Mol Genet Genomic Med; 2021 May; 9(5):e1646. PubMed ID: 33764006
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
