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Nutrients|September 27, 2025
Prospective Observational Case Series in Infertile Women with Overweight or Obesity Treated with a Very-Low Calorie Ketogenic Diet (VLCKD) Prior to an In Vitro Fertilization (IVF) TreatmentMaíra Casalechi, Alessandra Piontini, Annaelisa Nicolosi, et al.International Journal of Molecular Sciences|September 28, 2023
The Benefits of Water from Nitrodi's Spring: The In Vitro Studies Leading the Potential Clinical ApplicationsIlaria Mormile, Fabiana Tuccillo, Francesca Della Casa, et al.Orphanet Journal of Rare Diseases|June 27, 2013
Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathyTeresa Esposito, Simone Sampaolo, Giuseppe Limongelli, et al.Radiology Case Reports|December 15, 2018
Late adult-onset adrenomyeloneuropathy evolving with atypical severe frontal lobe syndrome: Importance of neuroimagingClemente Dato, Guglielmo Capaldo, Chiara Terracciano, et al.American Journal of Medical Genetics. Part A|October 15, 2019
Intrafamilial "DOA-plus" phenotype variability related to different OMI/HTRA2 expressionFilomena Napolitano, Chiara Terracciano, Giorgia Bruno, et al.Evidence-Based Complementary and Alternative Medicine : Ecam|May 24, 2019
Hericium erinaceus Improves Mood and Sleep Disorders in Patients Affected by Overweight or Obesity: Could Circulating Pro-BDNF and BDNF Be Potential Biomarkers?Luisella Vigna, Federica Morelli, Gianna M Agnelli, et al.Nephron|February 9, 2017
Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked GlycosylationTeresa Esposito, Giovanni De Stefano, Mafalda Giovanna Reccia, et al.Journal of Clinical Medicine|November 13, 2021
Soluble Urokinase Receptor as a Promising Marker for Early Prediction of Outcome in COVID-19 Hospitalized PatientsFilomena Napolitano, Gaetano Di Spigna, Maria Vargas, et al.Journal of Medical Genetics|July 24, 2017
Identification of the first dominant mutation of LAMA5 gene causing a complex multisystem syndrome due to dysfunction of the extracellular matrixSimone Sampaolo, Filomena Napolitano, Alfonsina Tirozzi, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 4, 2025
Targeting RPSA to modulate endosomal trafficking and amyloidogenesis in genetic Alzheimer's diseaseAdriana Limone, Clelia Di Napoli, Filomena Napolitano, et al.Pageof 8