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Journal of Endocrinological Investigation|July 19, 2022
MKRN3 circulating levels in Prader-Willi syndrome: a pilot studyM Mariani, D Fintini, G Cirillo, et al.Pediatric Obesity|April 21, 2015
TM6SF2 Glu167Lys polymorphism is associated with low levels of LDL-cholesterol and increased liver injury in obese childrenA Grandone, D Cozzolino, P Marzuillo, et al.Scandinavian Journal of Rheumatology|May 15, 2015
Association between cannabinoid receptor type 2 Q63R variant and oligo/polyarticular juvenile idiopathic arthritisG Bellini, A N Olivieri, A Grandone, et al.Journal of Endocrinological Investigation|March 3, 2022
Role of Wnt-signaling inhibitors DKK-1 and sclerostin in bone fragility associated with Turner syndromeM Chiarito, L Piacente, N Chaoul, et al.Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|July 4, 2012
Subclinical hypothyroidism and myocardial function in obese childrenC Brienza, A Grandone, G Di Salvo, et al.Journal of Endocrinological Investigation|December 19, 2023
MKRN3 circulating levels in girls with central precocious puberty caused by MKRN3 gene mutationsF Aiello, S Palumbo, G Cirillo, et al.Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|January 26, 2016
Impact of PNPLA3 variants on liver histology of 168 patients with HIV infection and chronic hepatitis CC Sagnelli, M Merli, C Uberti-Foppa, et al.Clinical Genetics|March 5, 2016
Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitisA Grandone, A Torella, C Santoro, et al.Journal of Endocrinological Investigation|December 28, 2022
A new DLK1 defect in a family with idiopathic central precocious puberty: elucidation of the male phenotypeS Palumbo, G Cirillo, G Sanchez, et al.Pageof 2