Results 221 to 230 of about 1,610,988 (356)
ABSTRACT Hypoparathyroidism, sensorineural deafness, and renal dysplasia (HDR) syndrome is caused by pathogenic variants in the GATA3 gene located on chromosome 10p14. Here we present a 10‐year‐old girl with HDR syndrome who also has oligoarticular juvenile idiopathic arthritis (JIA).
Lauren N. Meiss +8 more
wiley +1 more source
Global, regional, and national trends and burden of diabetes mellitus type 2 among youth from 1990 to 2021: an analysis from the global burden of disease study 2021. [PDF]
Deng L, Lu S, Zeng J, Liu H.
europepmc +1 more source
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young +6 more
wiley +1 more source
Serum Antibody Titres Against <i>Porphyromonas gingivalis</i> Fim A in Patients with Periodontitis with and Without Diabetes Mellitus Type 2. [PDF]
Groeger S +3 more
europepmc +1 more source
Surgical ablation for atrial fibrillation: impact of Diabetes Mellitus type 2. [PDF]
Kogan A +11 more
europepmc +1 more source
The experimental type 2 diabetes model in rats induced by streptozotocin and nicotinamide showed that silver nanoparticles synthesized from lemongrass extract modulate blood glucose, water and food intake, and enhance antioxidant enzyme synthesis and weight gains.
Milad Faraji +6 more
wiley +1 more source
The Role of Hypoxia-Sensitive <i>miRNA181a</i>, <i>miRNA199a</i>, <i>SIRT1</i>, and Adiponectin in Diabetes Mellitus Type 2 Development in Obstructive Sleep Apnea Patients. [PDF]
Karuga FF +7 more
europepmc +1 more source

