Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Wahab A. Khan"'
Autor:
Iman Salem, MD, MS, Emma L. Hodson, MS, Matthew J. Davis, MD, Wahab A. Khan, PhD, Edward G. Hughes, PhD, Leanne J. Cook, MPH, Denise M. Aaron, MD, Aravindhan Sriharan, MD
Publikováno v:
JAAD Case Reports, Vol 36, Iss , Pp 4-7 (2023)
Externí odkaz:
https://doaj.org/article/f9978b5186eb4993861735cf400d2486
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract Background The chromosome 3q29 microdeletion syndrome is characterized by a clinical phenotype that includes behavioral features consistent with autism and attention deficit hyperactivity disorder, mild to moderate developmental delay, langu
Externí odkaz:
https://doaj.org/article/cd2111d3f1e54d35bc9b59683ed7524b
Autor:
Gail H, Vance, Wahab A, Khan
Publikováno v:
Clinics in Laboratory Medicine. 42:573-586
Publikováno v:
JK Practitioner. Oct-Dec2021, Vol. 26 Issue 4, p83-86. 4p.
Publikováno v:
Cureus.
Publikováno v:
Cureus.
Publikováno v:
Cureus.
Publikováno v:
Journal of Community Hospital Internal Medicine Perspectives. 13
Publikováno v:
American Journal of Clinical Pathology.
Objectives The HLA-DQA1*05 variant (rs2097432) is associated with increased risk of immunogenicity to tumor necrosis factor antagonists, with subsequent resistance to therapy in patients with inflammatory bowel disease. Identification of these patien
Publikováno v:
Cureus.