Association between thyroid dysfunction during pregnancy and neonatal neurodevelopmental outcomes. [PDF]
Kong Y, An X.
europepmc +1 more source
Data‐Independent Acquisition Mass Spectrometry in Tumor Classification and Cancer Biomarker Research
Abstract Cancer treatment is far from optimal also because current classification systems do not reflect the complex molecular status of the tumor and its phenotype in sufficient detail. To construct molecular tumor classifiers, omics tools provide complex molecular data reflecting many aspects from genotype to phenotype.
Jan Simonik +3 more
wiley +1 more source
Endocrine-Taste Crosstalk: A Scoping Review on Thyroid Dysfunction and Its Genetic Links to Taste Receptors With Dysgeusia. [PDF]
Pai P +6 more
europepmc +1 more source
ABSTRACT The use of MALDI mass spectrometry for the analysis of carbohydrates and glycoconjugates is a well‐established technique and this comprehensive review is the twelfth update of the original article published in 1999 and brings coverage of the literature to the end of 2024.
David J. Harvey
wiley +1 more source
Letter to the editor: Association between thyroid dysfunction and cognitive impairment in type 2 diabetes mellitus: A cross-sectional study. [PDF]
Khalid A, Ram M, Khalid R.
europepmc +1 more source
Genetic Etiologies of Dystonia with Anarthria/Aphonia
Abstract Background Dystonia with anarthria and/or aphonia (DAnAp) represents a distinctive phenotype manifesting across lifespan. Frequently associated with genetic disorders, early recognition is critical for diagnosis and management. Objectives To provide practical recommendations for the clinical evaluation of patients with DAnAp, enhancing ...
Anika Ménétrey +7 more
wiley +1 more source
Association between thyroid dysfunction and cognitive impairment in type 2 diabetes mellitus: A cross-sectional study. [PDF]
Zheng M, Zhong X, Zhang P.
europepmc +1 more source
Intrathyroidal Hematoma, Biphasic Thyroid Dysfunction, and Permanent Hypothyroidism After Fine Needle Aspiration Biopsy. [PDF]
Jay M, Wong RBK, Goens C, Goguen J.
europepmc +1 more source
Abstract Background NKX2‐1–related disorders (NKX2‐1‐RDs) classically present with a triad of neurological, endocrine, and pulmonary manifestations, including benign hereditary chorea. However, in a fraction of patients, NKX2‐1 coding variants are not detected, and variants outside the NKX2‐1 locus have been reported.
Robin Wijngaard +33 more
wiley +1 more source

