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Garavelli

Showing results (541-550 of 610) with videos related to

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Genes|August 27, 2021
Posterior Lissencephaly Associated with Subcortical Band Heterotopia Due to a Variation in the <i>CEP85L</i> Gene: A Case Report and Refining of the Phenotypic SpectrumGianluca Contrò, Alessia Micalizzi, Sara Giangiobbe, et al.
American Journal of Hypertension|April 1, 1996
Prevalence and clinical correlates of microalbuminuria in stage I hypertension. Results from the Hypertension and Ambulatory Recording Venetia Study (HARVEST Study)P Palatini, G R Graniero, P Mormino, et al.
Genes|July 2, 2021
Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous CouplesFrancesca Peluso, Stefano Giuseppe Caraffi, Roberta Zuntini, et al.
Human Genetics|August 7, 2007
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16Marcella Zollino, Rosetta Lecce, Marina Murdolo, et al.
Journal of Clinical Medicine|June 2, 2021
Risk Factors for Mortality in COVID-19 Hospitalized Patients in Piedmont, Italy: Results from the Multicenter, Regional, CORACLE RegistryFrancesco Giuseppe De Rosa, Annagloria Palazzo, Tiziana Rosso, et al.
Diabetes|October 24, 2020
CD31<sup>+</sup> Extracellular Vesicles From Patients With Type 2 Diabetes Shuttle a miRNA Signature Associated With Cardiovascular ComplicationsFrancesco Prattichizzo, Valeria De Nigris, Jacopo Sabbatinelli, et al.
Italian Journal of Pediatrics|December 24, 2025
3-M syndrome: evolution of the phenotype over timeIsabelle Bacchi, Sara Vandelli, Emanuele Coccia, et al.
European Journal of Human Genetics : EJHG|August 22, 2013
Clinical and biochemical features guiding the diagnostics in neurometabolic cutis laxaThatjana Gardeitchik, Miski Mohamed, Björn Fischer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 10, 2010
A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parentsMonica Marini, Renata Bocciardi, Stefania Gimelli, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Noonan syndrome-like disorder with loose anagen hair: a second case with neuroblastomaLivia Garavelli, Viviana Cordeddu, Stefania Errico, et al.
Pageof 61

Showing results (541-550 of 610) with videos related to

Sort By:
Pageof 61
Genes|August 27, 2021
Posterior Lissencephaly Associated with Subcortical Band Heterotopia Due to a Variation in the <i>CEP85L</i> Gene: A Case Report and Refining of the Phenotypic SpectrumGianluca Contrò, Alessia Micalizzi, Sara Giangiobbe, et al.
American Journal of Hypertension|April 1, 1996
Prevalence and clinical correlates of microalbuminuria in stage I hypertension. Results from the Hypertension and Ambulatory Recording Venetia Study (HARVEST Study)P Palatini, G R Graniero, P Mormino, et al.
Genes|July 2, 2021
Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous CouplesFrancesca Peluso, Stefano Giuseppe Caraffi, Roberta Zuntini, et al.
Human Genetics|August 7, 2007
Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16Marcella Zollino, Rosetta Lecce, Marina Murdolo, et al.
Journal of Clinical Medicine|June 2, 2021
Risk Factors for Mortality in COVID-19 Hospitalized Patients in Piedmont, Italy: Results from the Multicenter, Regional, CORACLE RegistryFrancesco Giuseppe De Rosa, Annagloria Palazzo, Tiziana Rosso, et al.
Diabetes|October 24, 2020
CD31<sup>+</sup> Extracellular Vesicles From Patients With Type 2 Diabetes Shuttle a miRNA Signature Associated With Cardiovascular ComplicationsFrancesco Prattichizzo, Valeria De Nigris, Jacopo Sabbatinelli, et al.
Italian Journal of Pediatrics|December 24, 2025
3-M syndrome: evolution of the phenotype over timeIsabelle Bacchi, Sara Vandelli, Emanuele Coccia, et al.
European Journal of Human Genetics : EJHG|August 22, 2013
Clinical and biochemical features guiding the diagnostics in neurometabolic cutis laxaThatjana Gardeitchik, Miski Mohamed, Björn Fischer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 10, 2010
A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parentsMonica Marini, Renata Bocciardi, Stefania Gimelli, et al.
American Journal of Medical Genetics. Part A|April 8, 2015
Noonan syndrome-like disorder with loose anagen hair: a second case with neuroblastomaLivia Garavelli, Viviana Cordeddu, Stefania Errico, et al.
Pageof 61