Results 131 to 140 of about 5,617 (179)

Digenic Inheritance of Hereditary Spherocytosis Type III and X-linked Agammaglobulinemia: Coexistence of Two Distinct Recessive Disorders in a Male Child. [PDF]

Cureus
Almutairy KA, Alasmari BG, Rayees S.
europepmc   +1 more source

Abnormal T Cells Function Associated With Intraspinal Cold Abscess Caused by Macrolide-resistant Mycoplasma pneumoniae in a Patient With X-linked Agammaglobulinemia. [PDF]

Pediatr Infect Dis J
Jin YY, Wu J, Ding F, Huang H, Xu XM, Chen QM, Yin MZ, Zhong YM, Jin YL.   +8 more
europepmc   +1 more source

Non-Helicobacter pylori Helicobacter Species as a Cause of Refractory Chronic Cellulitis in X-Linked Agammaglobulinemia. [PDF]

J Clin Immunol
Zhao Q, Ma J, Wu J, Matruzi A, Li C.
europepmc   +1 more source

Hematopoietic stem cell gene editing rescues B-cell development in X-linked agammaglobulinemia. [PDF]

J Allergy Clin Immunol
Bahal S, Zinicola M, Moula SE, Whittaker TE, Schejtman A, Naseem A, Blanco E, Vetharoy W, Hu YT, Rai R, Gomez-Castaneda E, Cunha-Santos C, Burns SO, Morris EC, Booth C, Turchiano G, Cavazza A, Thrasher AJ, Santilli G.   +18 more
europepmc   +1 more source

Dysregulation of Toll-Like Receptor Signaling-Associated Gene Expression in X-Linked Agammaglobulinemia: Implications for Correlations Genotype-Phenotype and Disease Expression. [PDF]

J Innate Immun
Teocchi M, de Andrade Eugênio T, Furlaneto Marega L, Quinti I, Dos Santos Vilela MM.   +4 more
europepmc   +1 more source

Cell-penetrating peptide-conjugated, splice-switching oligonucleotides mitigate the phenotype in <i>BTK</i>/<i>Tec</i> double deficient X-linked agammaglobulinemia model. [PDF]

RSC Chem Biol
Bestas B, Estupiñán HY, Wang Q, Kharazi S, He C, K Mohammad D, Gupta D, Wiklander OPB, Lehto T, Lundin KE, Berglöf A, Karlsson MCI, Abendroth F, El Andaloussi S, Gait MJ, Wood MJA, Leumann CJ, Stetsenko DA, Månsson R, Wengel J, Zain R, Smith CIE.   +21 more
europepmc   +1 more source

Severe Tick-Borne Encephalitis (TBE) in a Patient with X-Linked Agammaglobulinemia; Treatment with TBE Virus IgG Positive Plasma, Clinical Outcome and T Cell Responses. [PDF]

J Clin Immunol
Hedin W, Bergman P, Akhirunessa M, Söderholm S, Buggert M, Granberg T, Gredmark-Russ S, Smith CIE, Pettke A, Wahren Borgström E.   +9 more
europepmc   +1 more source

Multiple Colorectal Neoplasms in X-Linked Agammaglobulinemia [PDF]

Clinical Gastroenterology and Hepatology, 2008
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency disorder caused by germline mutation of the Bruton tyrosine kinase (BTK) gene. It is characterized by disturbed B-cell development, decreased immunoglobulin levels, and increased patient susceptibility to infection.
Brosens, Lodewijk A. A., Tytgat, Kristien M. A. J., Morsink, Folkert H. M., Sinke, Richard J., ten Berge, Ineke J. M., Giardiello, Francis M., Offerhaus, G. Johan A., Keller, Josbert J.   +7 more
openaire   +4 more sources

Some of the next articles are maybe not open access.

Related searches:

Expression of the Gene Defect in X-Linked Agammaglobulinemia

New England Journal of Medicine, 1986
Although X-linked agammaglobulinemia was one of the first immunodeficiencies described,1 the genetic defect responsible for this disorder has not yet been identified.
Jack Singer, W H Raskind, M E Conley
exaly   +3 more sources