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Massimo Carella

Showing results (41-50 of 207) with videos related to

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Biochemical and Biophysical Research Communications|October 18, 2005
Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing lossSalvatore Melchionda, Massimiliano Bicego, Elio Marciano, et al.
Journal of Translational Medicine|November 20, 2014
Combined microRNA and ER expression: a new classifier for familial and sporadic breast cancer patientsKatia Danza, Simona De Summa, Brunella Pilato, et al.
Journal of Medical Genetics|December 18, 2012
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restrictionAgostina De Crescenzo, Angela Sparago, Flavia Cerrato, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2004
The common -866G/A polymorphism in the promoter region of the UCP-2 gene is associated with reduced risk of type 2 diabetes in Caucasians from ItalyAngela Bulotta, Ornella Ludovico, Angelo Coco, et al.
International Journal of Pediatric Otorhinolaryngology|November 8, 2008
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian familyMaria Stella Alemanno, Elona Cama, Rosamaria Santarelli, et al.
Seizure|November 21, 2017
The epilepsy phenotype in adult patients with intellectual disability and pathogenic copy number variantsGiuseppe d'Orsi, Tommaso Martino, Orazio Palumbo, et al.
Nucleic Acids Research|December 10, 2020
MitImpact 3: modeling the residue interaction network of the Respiratory Chain subunitsStefano Castellana, Tommaso Biagini, Francesco Petrizzelli, et al.
Frontiers in Oncology|March 3, 2020
Clinical Significance of Circulating miR-1273g-3p and miR-122-5p in Pancreatic CancerTommaso Mazza, Domenica Gioffreda, Andrea Fontana, et al.
Genes|October 28, 2023
Identification of a Novel <i>FOXP1</i> Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech ImpairmentMario Benvenuto, Pietro Palumbo, Ester Di Muro, et al.
BMC Medical Genetics|August 23, 2015
A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature reviewStefano Stagi, Elisabetta Lapi, Marilena Pantaleo, et al.
Pageof 21

Showing results (41-50 of 207) with videos related to

Sort By:
Pageof 21
Biochemical and Biophysical Research Communications|October 18, 2005
Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing lossSalvatore Melchionda, Massimiliano Bicego, Elio Marciano, et al.
Journal of Translational Medicine|November 20, 2014
Combined microRNA and ER expression: a new classifier for familial and sporadic breast cancer patientsKatia Danza, Simona De Summa, Brunella Pilato, et al.
Journal of Medical Genetics|December 18, 2012
Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restrictionAgostina De Crescenzo, Angela Sparago, Flavia Cerrato, et al.
The Journal of Clinical Endocrinology and Metabolism|November 25, 2004
The common -866G/A polymorphism in the promoter region of the UCP-2 gene is associated with reduced risk of type 2 diabetes in Caucasians from ItalyAngela Bulotta, Ornella Ludovico, Angelo Coco, et al.
International Journal of Pediatric Otorhinolaryngology|November 8, 2008
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian familyMaria Stella Alemanno, Elona Cama, Rosamaria Santarelli, et al.
Seizure|November 21, 2017
The epilepsy phenotype in adult patients with intellectual disability and pathogenic copy number variantsGiuseppe d'Orsi, Tommaso Martino, Orazio Palumbo, et al.
Nucleic Acids Research|December 10, 2020
MitImpact 3: modeling the residue interaction network of the Respiratory Chain subunitsStefano Castellana, Tommaso Biagini, Francesco Petrizzelli, et al.
Frontiers in Oncology|March 3, 2020
Clinical Significance of Circulating miR-1273g-3p and miR-122-5p in Pancreatic CancerTommaso Mazza, Domenica Gioffreda, Andrea Fontana, et al.
Genes|October 28, 2023
Identification of a Novel <i>FOXP1</i> Variant in a Patient with Hypotonia, Intellectual Disability, and Severe Speech ImpairmentMario Benvenuto, Pietro Palumbo, Ester Di Muro, et al.
BMC Medical Genetics|August 23, 2015
A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature reviewStefano Stagi, Elisabetta Lapi, Marilena Pantaleo, et al.
Pageof 21