Results 161 to 170 of about 161,849 (206)

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

X-Linked Agammaglobulinemia: Report on a United States Registry of 201 Patients

Medicine, 2006
J. Winkelstein, M. Marino, H. Lederman, S. Jones, K. Sullivan, A. Burks, M. Conley, C. Cunningham-Rundles, H. Ochs   +8 more
semanticscholar   +1 more source

Comparison of oral microflora in selective IgA deficiency and x linked agammaglobulinemia cases with control group

, 2013
Ayça Aslan KIYKIM, Nursen TOPÇUOĞLU, Güven KÜLEKÇİ, Haluk Çokuğraş, Necla Akçakaya, Yıldız Çamcıoğlu   +5 more
openalex   +1 more source

Recent Advances in the Diagnosis of X-linked Agammaglobulinemia

Internal Medicine, 1999
openaire   +4 more sources

Helicobacter cinaedi bacteremia mimicking eosinophilic fasciitis in a patient with X-linked agammaglobulinemia

JAAD Case Reports, 2018
Ashley Hill, MD, Adam Byrne, MD, Danielle Bouffard, MD, Me Linh Luong, MD, Melissa Saber, MD, Hugo Chapdelaine, MD   +5 more
doaj  

X-linked Agammaglobulinemia [PDF]

The Indian Journal of Pediatrics, 2016
X-linked agammaglobulinemia (XLA) is one of the commonest primary immune deficiencies encountered in pediatric clinical practice. In adults, common variable immunodeficiency (CVID) is the most common primary immunodeficiency disease (PID). It is an X-linked disorder characterized by increased susceptibility to encapsulated bacteria, severe ...
Amit Rawat, Deepti Suri, Surjit Singh
openaire   +4 more sources

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X-Linked Agammaglobulinemia

Clinical Reviews in Allergy & Immunology, 2000
The identification of the gene responsible for XLA has made it possible to clarify the clinical and laboratory findings in this disorder. It has markedly improved our ability to provide informative genetic counseling for affected families and it has helped unmask disorders that are clinically similar to XLA but genotypically different.
Jurg Rohrer, Mary Ellen Conley, Yoshiyuki Minegishi   +2 more
openaire   +3 more sources