Results 211 to 220 of about 80,683 (293)
Lingual Thyroid in Chronic Hypothyroidism. [PDF]
Onwudiwe O, Oputa-Onwusa O, Rajamani K.
europepmc +1 more source
Fetal growth restriction is associated with placental metabolic adaptations. In small‐for‐gestational‐age placenta (SGA), cholesterol receptors and steroidogenic enzymes are upregulated, enhancing steroidogenesis. NAD salvage pathway is also increased to support NADP+/NADPH requirements.
Serena Xodo +4 more
wiley +1 more source
Investigated mutations in transthyretin (TTR) disrupt the F87‐centered hydrophobic core that stabilizes its tetrameric structure. The mild I107V mutation weakens inter‐chain packing, while H88R fully abolishes tetramer formation, yielding a monomeric, aggregation‐prone form. Structural, biophysical, and computational analyses reveal that both mutations
István L. Bódy +7 more
wiley +1 more source
A case of inappropriate thyroid-stimulating hormone secretion syndrome after thalidomide treatment. [PDF]
Zhu Y, Chen J.
europepmc +1 more source
In 1,468 patients with type 2 diabetes, central obesity (WHtR >0.5) neutralizes the protective effects of higher BMI on muscle strength. Concurrently, visceral adiposity and CKD impose an additive threat, maximizing low handgrip strength risk (aOR = 1.74). Combining WHtR and renal tracking optimizes clinical sarcopenia screening.
Shing‐Hua Chen +4 more
wiley +1 more source
Primary hyperparathyroidism due to dual parathyroid adenomas: one orthotopic, one intrathymic in ectopic cervical thymus. [PDF]
Iglesias M +4 more
europepmc +1 more source
Requesting Diagnostic Imaging in Nurse Practitioner Practice: Results of a National Survey
ABSTRACT Aim To examine how nurse practitioners in Australia request diagnostic imaging and identify educational and system‐level barriers that influence this practice. Design Cross‐sectional national survey. Methods An online survey of nurse practitioners in Australia.
Mary Kearns +3 more
wiley +1 more source
Primary thyroid lymphoma with Hashimoto's thyroiditis: A case report and literature review. [PDF]
Liu F +5 more
europepmc +1 more source
CHARGE Syndrome: A Narrative Review and Update on Diagnosis, Assessment and Management
ABSTRACT Background CHARGE syndrome (CS) is a rare multisystemic genetic condition caused by a pathogenic variant in the DNA‐binding protein‐7 CHD7 gene. The condition affects the development of neural crest cells, which give rise to craniofacial structures, cranial nerves, ears, eyes and the heart, resulting in diverse and complex clinical features ...
Eleni M. van Gelder +7 more
wiley +1 more source

