Results 231 to 240 of about 11,036,926 (400)
Thyroid Function in Human Obesity: Underlying Mechanisms
L. C. Fontenelle+7 more
semanticscholar +1 more source
ABSTRACT KDM1A‐related neurodevelopmental disorder (CPRF, OMIM #616728) is characterized by cleft palate, global developmental delay, and distinct facial gestalt, but phenotypic knowledge of this ultra‐rare autosomal dominant disorder is limited. Here, we report on a 13‐year‐old boy with a novel heterozygous, likely pathogenic germline missense variant
Sebastian Burkart+6 more
wiley +1 more source
Performance validation of Abbott Alinity i chemiluminescence analyzer for five thyroid function tests. [PDF]
Zhang H, Wu B, Ke L, Peng Z.
europepmc +1 more source
ABSTRACT Gastrointestinal defects and immunodeficiency syndrome 1 (GIDID1) is a rare autosomal recessive disorder caused by biallelic variants in TTC7A. GIDID1 is characterized by a broad clinical spectrum ranging from very early‐onset inflammatory bowel disease (VEOIBD) to multiple intestinal atresia (MIA) with or without immunological manifestations.
Julia Imhoff+8 more
wiley +1 more source
Association between the newly proposed dietary index for gut microbiota and thyroid function: NHANES 2007-2012. [PDF]
Peng K, Guo H, Zhang Z, Xiao W.
europepmc +1 more source
ABSTRACT Women with the FMR1 premutation (FXpm) are at heightened genetic vulnerability for depression, with risk compounded by the stressors of parenting a disabled child. Although risk factors persist as FXpm women age, depression in FXpm mothers during midlife and old age is poorly characterized. This study used an accelerated longitudinal design to
Jessica Klusek+8 more
wiley +1 more source
Genetic evidence suggests a causal relationship linking thyroid function to prospective memory and dementia and Parkinson's disease. [PDF]
Wang Y+5 more
europepmc +1 more source