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Massimo Carella

Showing results (91-100 of 207) with videos related to

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European Journal of Human Genetics : EJHG|October 8, 2004
A second locus mapping to 2q35-36 for familial pseudohyperkalaemiaMassimo Carella, Adamo Pio d'Adamo, Sabine Grootenboer-Mignot, et al.
American Journal of Medical Genetics. Part A|November 12, 2013
Giant breast tumors in a patient with Beckwith-Wiedemann syndromeGerarda Cappuccio, Agostina De Crescenzo, Giuseppe Ciancia, et al.
European Journal of Medical Genetics|June 5, 2012
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: central nervous involvement in two Italian patientsGaetano Terrone, Alessandra D'Amico, Floriana Imperati, et al.
Blood Transfusion = Trasfusione Del Sangue|September 21, 2020
Mortality and clinical outcome of Italian patients undergoing orthopaedic surgery: effect of peri-operative blood transfusionElvira Grandone, Mario Mastroianno, Antonio De Laurenzo, et al.
BMC Bioinformatics|April 28, 2012
BEAT: Bioinformatics Exon Array Tool to store, analyze and visualize Affymetrix GeneChip Human Exon Array data from disease experimentsArianna Consiglio, Massimo Carella, Giorgio De Caro, et al.
Experimental Biology and Medicine (Maywood, N.J.)|October 10, 2012
The expression of leucine-rich repeat gene family members in colorectal cancerAda Piepoli, Orazio Palmieri, Rosalia Maglietta, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traitsCarmela Fusco, Lucia Micale, Bartolomeo Augello, et al.
Bone|December 17, 2020
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlationsMaria Luce Genovesi, Daniele Guadagnolo, Enrica Marchionni, et al.
Clinical Epigenetics|June 18, 2016
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypesSusanne Eriksen Boonen, Andrea Freschi, Rikke Christensen, et al.
Frontiers in Oncology|April 21, 2023
miRNA deregulation and relationship with metabolic parameters after Mediterranean dietary intervention in BRCA-mutated womenSimona De Summa, Debora Traversa, Antonella Daniele, et al.
Pageof 21

Showing results (91-100 of 207) with videos related to

Sort By:
Pageof 21
European Journal of Human Genetics : EJHG|October 8, 2004
A second locus mapping to 2q35-36 for familial pseudohyperkalaemiaMassimo Carella, Adamo Pio d'Adamo, Sabine Grootenboer-Mignot, et al.
American Journal of Medical Genetics. Part A|November 12, 2013
Giant breast tumors in a patient with Beckwith-Wiedemann syndromeGerarda Cappuccio, Agostina De Crescenzo, Giuseppe Ciancia, et al.
European Journal of Medical Genetics|June 5, 2012
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: central nervous involvement in two Italian patientsGaetano Terrone, Alessandra D'Amico, Floriana Imperati, et al.
Blood Transfusion = Trasfusione Del Sangue|September 21, 2020
Mortality and clinical outcome of Italian patients undergoing orthopaedic surgery: effect of peri-operative blood transfusionElvira Grandone, Mario Mastroianno, Antonio De Laurenzo, et al.
BMC Bioinformatics|April 28, 2012
BEAT: Bioinformatics Exon Array Tool to store, analyze and visualize Affymetrix GeneChip Human Exon Array data from disease experimentsArianna Consiglio, Massimo Carella, Giorgio De Caro, et al.
Experimental Biology and Medicine (Maywood, N.J.)|October 10, 2012
The expression of leucine-rich repeat gene family members in colorectal cancerAda Piepoli, Orazio Palmieri, Rosalia Maglietta, et al.
European Journal of Human Genetics : EJHG|June 13, 2013
Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traitsCarmela Fusco, Lucia Micale, Bartolomeo Augello, et al.
Bone|December 17, 2020
GDF5 mutation case report and a systematic review of molecular and clinical spectrum: Expanding current knowledge on genotype-phenotype correlationsMaria Luce Genovesi, Daniele Guadagnolo, Enrica Marchionni, et al.
Clinical Epigenetics|June 18, 2016
Two maternal duplications involving the CDKN1C gene are associated with contrasting growth phenotypesSusanne Eriksen Boonen, Andrea Freschi, Rikke Christensen, et al.
Frontiers in Oncology|April 21, 2023
miRNA deregulation and relationship with metabolic parameters after Mediterranean dietary intervention in BRCA-mutated womenSimona De Summa, Debora Traversa, Antonella Daniele, et al.
Pageof 21