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American Journal of Medical Genetics. Part A
|
December 6, 2011
Medical care of adolescents and women with Rett syndrome: an Italian study
Aglaia Vignoli, Francesca La Briola, Angela Peron, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
March 28, 2013
Neonatal suppression-burst without epileptic seizures: expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathy
Massimo Mastrangelo, Angela Peron, Luigina Spaccini, et al.
European Journal of Human Genetics : EJHG
|
July 2, 2025
The European Certificate in Medical Genetics and Genomics (ECMGG)
Peter D Turnpenny, Laura Pölsler, Ute Moog, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 14, 2016
Long-term outcome of epilepsy with onset in the first three years of life: Findings from a large cohort of patients
Aglaia Vignoli, Angela Peron, Katherine Turner, et al.
Orphanet Journal of Rare Diseases
|
September 7, 2020
The TAND checklist: a useful screening tool in children with tuberous sclerosis and neurofibromatosis type 1
Francesca Cervi, Veronica Saletti, Katherine Turner, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2013
Snyder-Robinson syndrome: a novel nonsense mutation in spermine synthase and expansion of the phenotype
Angela Peron, Luigina Spaccini, Joy Norris, et al.
Orphanet Journal of Rare Diseases
|
December 4, 2015
Autism spectrum disorder in tuberous sclerosis complex: searching for risk markers
Aglaia Vignoli, Francesca La Briola, Angela Peron, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 27, 2018
Current concepts on epilepsy management in tuberous sclerosis complex
Maria Paola Canevini, Katarzyna Kotulska-Jozwiak, Paolo Curatolo, et al.
Prenatal Diagnosis
|
July 5, 2014
Prenatal and postnatal findings in five cases of Fryns syndrome
Angela Peron, Maria Francesca Bedeschi, Isabella Fabietti, et al.
Acta Neurologica Scandinavica
|
March 22, 2021
Epilepsy in adult patients with tuberous sclerosis complex
Aglaia Vignoli, Francesca La Briola, Katherine Turner, et al.
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of 8
Search research articles
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Showing results (21-30 of 79) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics. Part A
|
December 6, 2011
Medical care of adolescents and women with Rett syndrome: an Italian study
Aglaia Vignoli, Francesca La Briola, Angela Peron, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
March 28, 2013
Neonatal suppression-burst without epileptic seizures: expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathy
Massimo Mastrangelo, Angela Peron, Luigina Spaccini, et al.
European Journal of Human Genetics : EJHG
|
July 2, 2025
The European Certificate in Medical Genetics and Genomics (ECMGG)
Peter D Turnpenny, Laura Pölsler, Ute Moog, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 14, 2016
Long-term outcome of epilepsy with onset in the first three years of life: Findings from a large cohort of patients
Aglaia Vignoli, Angela Peron, Katherine Turner, et al.
Orphanet Journal of Rare Diseases
|
September 7, 2020
The TAND checklist: a useful screening tool in children with tuberous sclerosis and neurofibromatosis type 1
Francesca Cervi, Veronica Saletti, Katherine Turner, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2013
Snyder-Robinson syndrome: a novel nonsense mutation in spermine synthase and expansion of the phenotype
Angela Peron, Luigina Spaccini, Joy Norris, et al.
Orphanet Journal of Rare Diseases
|
December 4, 2015
Autism spectrum disorder in tuberous sclerosis complex: searching for risk markers
Aglaia Vignoli, Francesca La Briola, Angela Peron, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
September 27, 2018
Current concepts on epilepsy management in tuberous sclerosis complex
Maria Paola Canevini, Katarzyna Kotulska-Jozwiak, Paolo Curatolo, et al.
Prenatal Diagnosis
|
July 5, 2014
Prenatal and postnatal findings in five cases of Fryns syndrome
Angela Peron, Maria Francesca Bedeschi, Isabella Fabietti, et al.
Acta Neurologica Scandinavica
|
March 22, 2021
Epilepsy in adult patients with tuberous sclerosis complex
Aglaia Vignoli, Francesca La Briola, Katherine Turner, et al.
Page
of 8