Skip to search formSkip to main contentSkip to account menu

Hyper-IgM Immunodeficiency Syndrome, Type 1

Known as: HYPER-IgM SYNDROME, Immunodeficiencies, X-Linked Hyper-IgM, Syndrome, HIGM1 
An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
We investigated the effect of exercise timing on attenuation of postprandial hyper-triglyceridemia (PHTG) in individuals with… 
Highly Cited
1999
Highly Cited
1999
Polarized hyper-Rayleigh scattering (HRS) has been used to interrogate a putative octupolar “super” chromophore Ru(trans-4,4… 
Highly Cited
1998
Highly Cited
1998
Serial measurements, taken around the clock in the laboratory and clinic, can be analyzed by computer-implemented curve-fitting… 
Highly Cited
1996
Highly Cited
1996
CBA/N mice carry an X-linked immunodeficiency (xid) due to a point mutation in the Bruton's tyrosine kinase (btk) gene. xid mice… 
Highly Cited
1994
Highly Cited
1994
Btk is a cytoplasmic protein tyrosine kinase (PTK) that has been directly implicated in the pathogenesis of X-linked… 
Highly Cited
1990
Highly Cited
1990
The hyper-IgE (HIE) syndrome is characterized by high IgE serum levels, chronic dermatitis, and recurrent infections. The… 
Highly Cited
1984
Highly Cited
1984
One hundred and sixteen patients with detrusor instability, detrusor hyper-reflexia or bladder hypersensitivity who had failed to…