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Basic & Clinical Pharmacology & Toxicology
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December 4, 2020
Ondansetron in pregnancy revisited: Assessment and pregnancy labelling by the European Medicines Agency (EMA) & Pharmacovigilance Risk Assessment Committee (PRAC)
Per Damkier, Yusuf Cem Kaplan, Svetlana Shechtman, et al.
Italian Journal of Pediatrics
|
October 1, 2022
From clinical to molecular diagnosis: relevance of diagnostic strategy in two cases of branchio-oto-renal syndrome - case report
Elena Cacciatori, Sebastiano Aleo, Giulietta Scuvera, et al.
Seizure
|
September 7, 2011
Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A
Marilena Vecchi, Matteo Cassina, Alberto Casarin, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
December 19, 2012
Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies
Luca de Palma, Clementina Boniver, Matteo Cassina, et al.
Neuropediatrics
|
January 8, 2015
Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancy
Chiara Bertossi, Matteo Cassina, Ambra Cappellari, et al.
JIMD Reports
|
July 26, 2014
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus
Alessandra Zanetti, Rosella Tomanin, Angelica Rampazzo, et al.
Audiology Research
|
October 26, 2021
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature
Ugo Sorrentino, Chiara Piccolo, Chiara Rigon, et al.
Clinical Chemistry
|
February 16, 2026
Characterization of STRC Gene Conversions by Nanopore Sequencing
Chiara Rigon, Ugo Sorrentino, Sara Volta, et al.
Journal of Assisted Reproduction and Genetics
|
March 18, 2022
Epigenetics of pregnancy: looking beyond the DNA code
Daniela Zuccarello, Ugo Sorrentino, Valeria Brasson, et al.
Audiology & Neuro-Otology
|
December 22, 2020
Auditory Outcome after Cochlear Implantation in Children with DFNB7/11 Caused by Pathogenic Variants in TMC1 Gene
Samanta Gallo, Patrizia Trevisi, Chiara Rigon, et al.
Page
of 7
Search research articles
Search
Showing results (21-30 of 70) with videos related to
Sort By:
Page
of 7
Basic & Clinical Pharmacology & Toxicology
|
December 4, 2020
Ondansetron in pregnancy revisited: Assessment and pregnancy labelling by the European Medicines Agency (EMA) & Pharmacovigilance Risk Assessment Committee (PRAC)
Per Damkier, Yusuf Cem Kaplan, Svetlana Shechtman, et al.
Italian Journal of Pediatrics
|
October 1, 2022
From clinical to molecular diagnosis: relevance of diagnostic strategy in two cases of branchio-oto-renal syndrome - case report
Elena Cacciatori, Sebastiano Aleo, Giulietta Scuvera, et al.
Seizure
|
September 7, 2011
Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A
Marilena Vecchi, Matteo Cassina, Alberto Casarin, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
December 19, 2012
Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies
Luca de Palma, Clementina Boniver, Matteo Cassina, et al.
Neuropediatrics
|
January 8, 2015
Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancy
Chiara Bertossi, Matteo Cassina, Ambra Cappellari, et al.
JIMD Reports
|
July 26, 2014
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus
Alessandra Zanetti, Rosella Tomanin, Angelica Rampazzo, et al.
Audiology Research
|
October 26, 2021
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the Literature
Ugo Sorrentino, Chiara Piccolo, Chiara Rigon, et al.
Clinical Chemistry
|
February 16, 2026
Characterization of STRC Gene Conversions by Nanopore Sequencing
Chiara Rigon, Ugo Sorrentino, Sara Volta, et al.
Journal of Assisted Reproduction and Genetics
|
March 18, 2022
Epigenetics of pregnancy: looking beyond the DNA code
Daniela Zuccarello, Ugo Sorrentino, Valeria Brasson, et al.
Audiology & Neuro-Otology
|
December 22, 2020
Auditory Outcome after Cochlear Implantation in Children with DFNB7/11 Caused by Pathogenic Variants in TMC1 Gene
Samanta Gallo, Patrizia Trevisi, Chiara Rigon, et al.
Page
of 7