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Livia Garavelli

Showing results (1-10 of 156) with videos related to

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Italian Journal of Pediatrics|February 23, 2010
Current themes in molecular pediatrics: molecular medicine and its applicationsAndrea Superti-Furga, Livia Garavelli
Orphanet Journal of Rare Diseases|October 26, 2007
Mowat-Wilson syndromeLivia Garavelli, Paola Cerruti Mainardi
European Journal of Human Genetics : EJHG|February 24, 2011
Clinical utility gene card for: Mowat-Wilson syndromeMarcella Zollino, Livia Garavelli, Anita Rauch
World Journal of Gastroenterology|December 7, 2017
Metabolically based liver damage pathophysiology in patients with urea cycle disorders - A new hypothesisIvan Ivanovski, Miloš Ješić, Ana Ivanovski, et al.
Epilepsia|July 3, 2013
Epilepsy in Mowat-Wilson syndrome: is it a matter of GABA?Duccio M Cordelli, Alessandro Pellicciari, Demetrio Kiriazopulos, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|October 3, 2015
Mitotic crossover promotes leukemogenesis in children born with TEL-AML1 via the generation of loss of heterozygosity at 12pIvan Ivanovski, Livia Garavelli, Olivera Djurić, et al.
Genes|February 25, 2022
Smith-Magenis Syndrome-Clinical Review, Biological Background and Related DisordersBerardo Rinaldi, Roberta Villa, Alessandra Sironi, et al.
Pediatric Reports|May 4, 2018
Anesthesia in Mowat-Wilson syndrome: information on 11 Italian patientsMarianna Spunton, Livia Garavelli, Paola Cerutti Mainardi, et al.
Children (Basel, Switzerland)|December 23, 2022
Gait Alterations in Two Young Siblings with Progressive Pseudorheumatoid DysplasiaSilvia Sassi, Silvia Faccioli, Giuseppina Mariagrazia Farella, et al.
Journal of Human Genetics|July 12, 2020
Characterization of a novel loss-of-function variant in TDP2 in two adult patients with spinocerebellar ataxia autosomal recessive 23 (SCAR23)Edoardo Errichiello, Guido Zagnoli-Vieira, Romana Rizzi, et al.
Pageof 16

Showing results (1-10 of 156) with videos related to

Sort By:
Pageof 16
Italian Journal of Pediatrics|February 23, 2010
Current themes in molecular pediatrics: molecular medicine and its applicationsAndrea Superti-Furga, Livia Garavelli
Orphanet Journal of Rare Diseases|October 26, 2007
Mowat-Wilson syndromeLivia Garavelli, Paola Cerruti Mainardi
European Journal of Human Genetics : EJHG|February 24, 2011
Clinical utility gene card for: Mowat-Wilson syndromeMarcella Zollino, Livia Garavelli, Anita Rauch
World Journal of Gastroenterology|December 7, 2017
Metabolically based liver damage pathophysiology in patients with urea cycle disorders - A new hypothesisIvan Ivanovski, Miloš Ješić, Ana Ivanovski, et al.
Epilepsia|July 3, 2013
Epilepsy in Mowat-Wilson syndrome: is it a matter of GABA?Duccio M Cordelli, Alessandro Pellicciari, Demetrio Kiriazopulos, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|October 3, 2015
Mitotic crossover promotes leukemogenesis in children born with TEL-AML1 via the generation of loss of heterozygosity at 12pIvan Ivanovski, Livia Garavelli, Olivera Djurić, et al.
Genes|February 25, 2022
Smith-Magenis Syndrome-Clinical Review, Biological Background and Related DisordersBerardo Rinaldi, Roberta Villa, Alessandra Sironi, et al.
Pediatric Reports|May 4, 2018
Anesthesia in Mowat-Wilson syndrome: information on 11 Italian patientsMarianna Spunton, Livia Garavelli, Paola Cerutti Mainardi, et al.
Children (Basel, Switzerland)|December 23, 2022
Gait Alterations in Two Young Siblings with Progressive Pseudorheumatoid DysplasiaSilvia Sassi, Silvia Faccioli, Giuseppina Mariagrazia Farella, et al.
Journal of Human Genetics|July 12, 2020
Characterization of a novel loss-of-function variant in TDP2 in two adult patients with spinocerebellar ataxia autosomal recessive 23 (SCAR23)Edoardo Errichiello, Guido Zagnoli-Vieira, Romana Rizzi, et al.
Pageof 16