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Birth Defects Research
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May 3, 2017
A novel Xp22.13 microdeletion in Nance-Horan syndrome
Andrea Accogli, Monica Traverso, Francesca Madia, et al.
Human Mutation
|
November 3, 2011
FZD6 is a novel gene for human neural tube defects
Patrizia De Marco, Elisa Merello, Andrea Rossi, et al.
Journal of Molecular Neuroscience : MN
|
August 16, 2012
Genetic analysis of disheveled 2 and disheveled 3 in human neural tube defects
Patrizia De Marco, Elisa Merello, Alessandro Consales, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
May 26, 2018
When and why is surgical revascularization indicated for the treatment of moyamoya syndrome in patients with RASopathies? A systematic review of the literature and a single institute experience
Marcello Scala, Pietro Fiaschi, Valeria Capra, et al.
World Neurosurgery
|
September 10, 2017
Moyamoya Vasculopathy in PHACE Syndrome: Six New Cases and Review of the Literature
Domenico Tortora, Mariasavina Severino, Andrea Accogli, et al.
Journal of Human Genetics
|
November 30, 2005
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk
Patrizia De Marco, Elisa Merello, Maria Grazia Calevo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 10, 2019
Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy
Marcello Scala, Elisabetta Amadori, Lucia Fusco, et al.
Journal of Pediatric Hematology/Oncology
|
August 14, 2024
Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences
Alessio Conte, Damiana De Padova, Serena Giglio, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 12, 2018
Familial ROBO1 deletion associated with ectopic posterior pituitary, duplication of the pituitary stalk and anterior pituitary hypoplasia
Marcello Scala, Andrea Accogli, Anna Maria Elsa Allegri, et al.
Pediatric Neurosurgery
|
January 31, 2023
Practical Algorithm for the Management of Multisutural Craniosynostosis with Associated Chiari Malformation and/or Hydrocephalus
Gelsomina Aruta, Pietro Fiaschi, Marco Ceraudo, et al.
Page
of 18
Search research articles
Search
Showing results (21-30 of 176) with videos related to
Sort By:
Page
of 18
Birth Defects Research
|
May 3, 2017
A novel Xp22.13 microdeletion in Nance-Horan syndrome
Andrea Accogli, Monica Traverso, Francesca Madia, et al.
Human Mutation
|
November 3, 2011
FZD6 is a novel gene for human neural tube defects
Patrizia De Marco, Elisa Merello, Andrea Rossi, et al.
Journal of Molecular Neuroscience : MN
|
August 16, 2012
Genetic analysis of disheveled 2 and disheveled 3 in human neural tube defects
Patrizia De Marco, Elisa Merello, Alessandro Consales, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
May 26, 2018
When and why is surgical revascularization indicated for the treatment of moyamoya syndrome in patients with RASopathies? A systematic review of the literature and a single institute experience
Marcello Scala, Pietro Fiaschi, Valeria Capra, et al.
World Neurosurgery
|
September 10, 2017
Moyamoya Vasculopathy in PHACE Syndrome: Six New Cases and Review of the Literature
Domenico Tortora, Mariasavina Severino, Andrea Accogli, et al.
Journal of Human Genetics
|
November 30, 2005
Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk
Patrizia De Marco, Elisa Merello, Maria Grazia Calevo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 10, 2019
Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy
Marcello Scala, Elisabetta Amadori, Lucia Fusco, et al.
Journal of Pediatric Hematology/Oncology
|
August 14, 2024
Late Relapse in Genetically Determined Infantile Myofibromatosis. A Case Report and Brief Focus on Recurrences
Alessio Conte, Damiana De Padova, Serena Giglio, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
December 12, 2018
Familial ROBO1 deletion associated with ectopic posterior pituitary, duplication of the pituitary stalk and anterior pituitary hypoplasia
Marcello Scala, Andrea Accogli, Anna Maria Elsa Allegri, et al.
Pediatric Neurosurgery
|
January 31, 2023
Practical Algorithm for the Management of Multisutural Craniosynostosis with Associated Chiari Malformation and/or Hydrocephalus
Gelsomina Aruta, Pietro Fiaschi, Marco Ceraudo, et al.
Page
of 18