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ABOUT JoVE

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Daria Riva

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Journal of Neuro-Oncology|February 22, 2012

Long-term results of combined preradiation chemotherapy and age-tailored radiotherapy doses for childhood medulloblastomaMaura Massimino, Graziella Cefalo, Daria Riva, et al.

Plos One|October 30, 2014

PDCD10 gene mutations in multiple cerebral cavernous malformationsMaria Sole Cigoli, Francesca Avemaria, Stefano De Benedetti, et al.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 4, 2019

GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary resultsAnna Bersano, Gloria Bedini, Sara Nava, et al.

Plos Genetics|July 23, 2011

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndromeMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2024

CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disordersClara D M van Karnebeek, Maja Tarailo-Graovac, René Leen, et al.

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Search research articles

Showing results (71-80 of 75) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 75 results.

Journal of Neuro-Oncology|February 22, 2012

Long-term results of combined preradiation chemotherapy and age-tailored radiotherapy doses for childhood medulloblastomaMaura Massimino, Graziella Cefalo, Daria Riva, et al.

Plos One|October 30, 2014

PDCD10 gene mutations in multiple cerebral cavernous malformationsMaria Sole Cigoli, Francesca Avemaria, Stefano De Benedetti, et al.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 4, 2019

GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary resultsAnna Bersano, Gloria Bedini, Sara Nava, et al.

Plos Genetics|July 23, 2011

Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndromeMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2024

CIAO1 and MMS19 deficiency: A lethal neurodegenerative phenotype caused by cytosolic Fe-S cluster protein assembly disordersClara D M van Karnebeek, Maja Tarailo-Graovac, René Leen, et al.

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