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International Journal of Environmental Research and Public Health|November 27, 2021
The Quality Evaluation of Rare Disease Registries-An Assessment of the Essential Features of a Disease RegistrySalma Rashid Ali, Jillian Bryce, Yllka Kodra, et al.
Journal of Assisted Reproduction and Genetics|August 19, 2018
Mitochondrial DNA copy number in peripheral blood: a potential non-invasive biomarker for female subfertilityAndrea Busnelli, Debora Lattuada, Raffaella Rossetti, et al.
Frontiers in Endocrinology|August 22, 2022
FSH and bone: Comparison between males with central versus primary hypogonadismLuca Giovanelli, Richard Quinton, Biagio Cangiano, et al.
Clinical Endocrinology|July 17, 2003
Recombinant human TSH testing is a valuable tool for differential diagnosis of congenital hypothyroidism during L-thyroxine replacementLaura Fugazzola, Luca Persani, Deborah Mannavola, et al.
Frontiers in Endocrinology|November 12, 2025
Case Report: Bilateral lens dislocation as an atypical presentation of acromegaly and review of the ocular effects of GH/IGF-1 excessLaura Vitale, Letizia Maria Fatti, Marco Bonomi, et al.
Frontiers in Endocrinology|October 11, 2024
Primary ovarian insufficiency: update on clinical and genetic findingsSilvia Federici, Raffaella Rossetti, Silvia Moleri, et al.
European Journal of Endocrinology|September 20, 2019
Pulsed intravenous methylprednisolone combined with oral steroids as a treatment for poorly responsive type 2 amiodarone-induced thyrotoxicosisIrene Campi, Giovanni B Perego, Antonella Ravogli, et al.
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