Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Scientific Reports|January 13, 2019
A Nervous System-Specific Model of Creatine Transporter Deficiency Recapitulates the Cognitive Endophenotype of the Disease: a Longitudinal StudyAngelo Molinaro, Maria Grazia Alessandrì, Elena Putignano, et al.
Development (Cambridge, England)|May 16, 2023
Mesodermal FGF and BMP govern the sequential stages of zebrafish thyroid specificationBenoit Haerlingen, Robert Opitz, Isabelle Vandernoot, et al.
The Journal of Sexual Medicine|July 10, 2022
Genital Sensitivity and Perceived Orgasmic Intensity in Transgender Women With Gender Dysphoria After Gender-Affirming Surgery: A Pilot Study Comparing Pelvic Floor Evoked Somatosensory Potentials and Patient Subjective ExperienceDomenico Canale, Angelo Molinaro, Claudio Marcocci, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|May 13, 2016
Proteomic analysis of fine-needle aspiration in differential diagnosis of thyroid nodulesFederica Ciregia, Laura Giusti, Angelo Molinaro, et al.
Human Molecular Genetics|July 29, 2016
A mouse model for creatine transporter deficiency reveals early onset cognitive impairment and neuropathology associated with brain agingLaura Baroncelli, Angelo Molinaro, Francesco Cacciante, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 20, 2015
Analysis of Multiple Families With Single Individuals Affected by Pseudohypoparathyroidism Type Ib (PHP1B) Reveals Only One Novel Maternally Inherited GNAS DeletionRieko Takatani, Angelo Molinaro, Giedre Grigelioniene, et al.
Plos One|September 12, 2013
Presence in the pre-surgical fine-needle aspiration of potential thyroid biomarkers previously identified in the post-surgical oneFederica Ciregia, Laura Giusti, Angelo Molinaro, et al.
European Journal of Endocrinology|June 26, 2012
MicroRNA expression profile helps to distinguish benign nodules from papillary thyroid carcinomas starting from cells of fine-needle aspirationPatrizia Agretti, Eleonora Ferrarini, Teresa Rago, et al.
Bone|May 23, 2015
Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B)Rieko Takatani, Masanori Minagawa, Angelo Molinaro, et al.
Neuroscience|April 29, 2019
Brain mitochondrial proteome alteration driven by creatine deficiency suggests novel therapeutic venues for creatine deficiency syndromesLaura Giusti, Angelo Molinaro, Maria Grazia Alessandrì, et al.
Pageof 2