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Massimo Carella

Showing results (1-10 of 207) with videos related to

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Journal of Nephrology|December 31, 2003
Nanotechnologies and microchips in genetic diseasesMassimo Carella, Stefano Volinia, Paolo Gasparini
Frontiers in Psychiatry|November 22, 2018
The Emerging Role of Altered d-Aspartate Metabolism in Schizophrenia: New Insights From Preclinical Models and Human StudiesFrancesco Errico, Tommaso Nuzzo, Massimo Carella, et al.
Frontiers in Neurology|October 24, 2022
Electro-clinical features and management of the late stage of Lafora diseaseGiuseppe d'Orsi, Maria Teresa Di Claudio, Orazio Palumbo, et al.
Gene|November 13, 2012
8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: case report and critical review of the literatureOrazio Palumbo, Pietro Palumbo, Raffaella Stallone, et al.
Nucleic Acids Research|June 25, 2004
GOAL: automated Gene Ontology analysis of expression profilesStefano Volinia, Rita Evangelisti, Francesca Francioso, et al.
Molecular Cytogenetics|January 5, 2012
A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case reportOrazio Palumbo, Pietro Palumbo, Teresa Palladino, et al.
International Journal of Molecular Sciences|March 19, 2020
A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15Alessia Casamassa, Daniela Ferrari, Maurizio Gelati, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|July 9, 2008
Molecular detection of neuron-specific ELAV-like-positive cells in the peripheral blood of patients with small-cell lung cancerVito D'Alessandro, Lucia Anna Muscarella, Massimiliano Copetti, et al.
Molecular Cytogenetics|August 18, 2015
De novo microduplication of CHL1 in a patient with non-syndromic developmental phenotypesOrazio Palumbo, Rita Fischetto, Pietro Palumbo, et al.
International Journal of Pediatric Otorhinolaryngology|May 8, 2014
EYA1-related disorders: two clinical cases and a literature reviewAlessandro Castiglione, Salvatore Melchionda, Massimo Carella, et al.
Pageof 21

Showing results (1-10 of 207) with videos related to

Sort By:
Pageof 21
Journal of Nephrology|December 31, 2003
Nanotechnologies and microchips in genetic diseasesMassimo Carella, Stefano Volinia, Paolo Gasparini
Frontiers in Psychiatry|November 22, 2018
The Emerging Role of Altered d-Aspartate Metabolism in Schizophrenia: New Insights From Preclinical Models and Human StudiesFrancesco Errico, Tommaso Nuzzo, Massimo Carella, et al.
Frontiers in Neurology|October 24, 2022
Electro-clinical features and management of the late stage of Lafora diseaseGiuseppe d'Orsi, Maria Teresa Di Claudio, Orazio Palumbo, et al.
Gene|November 13, 2012
8q12.1q12.3 de novo microdeletion involving the CHD7 gene in a patient without the major features of CHARGE syndrome: case report and critical review of the literatureOrazio Palumbo, Pietro Palumbo, Raffaella Stallone, et al.
Nucleic Acids Research|June 25, 2004
GOAL: automated Gene Ontology analysis of expression profilesStefano Volinia, Rita Evangelisti, Francesca Francioso, et al.
Molecular Cytogenetics|January 5, 2012
A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case reportOrazio Palumbo, Pietro Palumbo, Teresa Palladino, et al.
International Journal of Molecular Sciences|March 19, 2020
A Link between Genetic Disorders and Cellular Impairment, Using Human Induced Pluripotent Stem Cells to Reveal the Functional Consequences of Copy Number Variations in the Central Nervous System-A Close Look at Chromosome 15Alessia Casamassa, Daniela Ferrari, Maurizio Gelati, et al.
Cellular Oncology : the Official Journal of the International Society for Cellular Oncology|July 9, 2008
Molecular detection of neuron-specific ELAV-like-positive cells in the peripheral blood of patients with small-cell lung cancerVito D'Alessandro, Lucia Anna Muscarella, Massimiliano Copetti, et al.
Molecular Cytogenetics|August 18, 2015
De novo microduplication of CHL1 in a patient with non-syndromic developmental phenotypesOrazio Palumbo, Rita Fischetto, Pietro Palumbo, et al.
International Journal of Pediatric Otorhinolaryngology|May 8, 2014
EYA1-related disorders: two clinical cases and a literature reviewAlessandro Castiglione, Salvatore Melchionda, Massimo Carella, et al.
Pageof 21