Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Academic Medicine : Journal of the Association of American Medical Colleges|May 16, 2024
SHARP (SHort Answer, Rationale Provision): A New Item Format to Assess Clinical ReasoningChristopher R Runyon, Miguel A Paniagua, Francine A Rosenthal, et al.
Gene|December 23, 1999
A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosomeF Trettel, E Mantuano, V Calabresi, et al.
Brain : a Journal of Neurology|May 1, 1997
Acetazolamide-responsive episodic ataxia in an Italian family refines gene mapping on chromosome 19p13L Calandriello, L Veneziano, A Francia, et al.
European Urology|January 1, 1992
DNA markers in diagnosis of adult dominant polycystic kidney diseaseL Veneziano, A R D'Angelo, L Burrai, et al.
Brain : a Journal of Neurology|April 29, 1998
The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlatesP Giunti, G Sabbadini, M G Sweeney, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 2, 2017
Dose adjustment of biologic therapies for psoriasis in dermatological practice: a retrospective studyM Esposito, P Gisondi, A Conti, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|May 28, 2011
Teriparatide increases the maturation of circulating osteoblast precursorsP D'Amelio, C Tamone, F Sassi, et al.
The British Journal of Dermatology|January 11, 2013
Small-diameter melanocytic lesions: morphological analysis by means of in vivo confocal microscopyG Pupelli, C Longo, L Veneziano, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 1, 2010
Bone and bone marrow pro-osteoclastogenic cytokines are up-regulated in osteoporosis fragility fracturesP D'Amelio, I Roato, L D'Amico, et al.
Human Molecular Genetics|September 25, 1997
Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19pC Jodice, E Mantuano, L Veneziano, et al.
Pageof 3