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Diana Rodriguez

Showing results (131-140 of 193) with videos related to

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Nature Genetics|June 16, 2009
RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infectionMarco Henneke, Simone Diekmann, Andreas Ohlenbusch, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 9, 2015
TUBB4A-related hypomyelinating leukodystrophy: New insights from a series of 12 patientsDavide Tonduti, Chiara Aiello, Florence Renaldo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2008
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patientsCyril Gitiaux, Emmanuel Roze, Kiyoka Kinugawa, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 22, 2022
Mood and Behaviors of Adolescents With Depression in a Longitudinal Study Before and During the COVID-19 PandemicNeda Sadeghi, Payton Q Fors, Lillian Eisner, et al.
Neuropediatrics|September 23, 2014
Mutations in ADAR1, IFIH1, and RNASEH2B presenting as spastic paraplegiaYanick J Crow, Maha S Zaki, Mohamed S Abdel-Hamid, et al.
Journal of Occupational and Environmental Medicine|August 10, 2020
Parental Occupational Exposure is Associated With Their Children's Psychopathology: A Study of Families of Israeli First RespondersRonit Kishon, Lupo Geronazzo-Alman, Meir Teichman, et al.
Life (Basel, Switzerland)|January 28, 2026
Interaction Between Frailty and Renal Function in Patients with Heart FailureÁngela Rodríguez-Eguren, José Jesús Broseta, Lydia Izquierdo, et al.
American Journal of Human Genetics|August 23, 2011
Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophyGeneviève Bernard, Eliane Chouery, Maria Lisa Putorti, et al.
Neurology|April 5, 2015
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxiaMarie Coutelier, Lydie Burglen, Emeline Mundwiller, et al.
Brain : a Journal of Neurology|July 12, 2014
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Dominique Bonneau, Estelle Colin, Florine Oca, et al.
Pageof 20

Showing results (131-140 of 193) with videos related to

Sort By:
Pageof 20
Nature Genetics|June 16, 2009
RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infectionMarco Henneke, Simone Diekmann, Andreas Ohlenbusch, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 9, 2015
TUBB4A-related hypomyelinating leukodystrophy: New insights from a series of 12 patientsDavide Tonduti, Chiara Aiello, Florence Renaldo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2008
Spectrum of movement disorders associated with glutaric aciduria type 1: a study of 16 patientsCyril Gitiaux, Emmanuel Roze, Kiyoka Kinugawa, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|April 22, 2022
Mood and Behaviors of Adolescents With Depression in a Longitudinal Study Before and During the COVID-19 PandemicNeda Sadeghi, Payton Q Fors, Lillian Eisner, et al.
Neuropediatrics|September 23, 2014
Mutations in ADAR1, IFIH1, and RNASEH2B presenting as spastic paraplegiaYanick J Crow, Maha S Zaki, Mohamed S Abdel-Hamid, et al.
Journal of Occupational and Environmental Medicine|August 10, 2020
Parental Occupational Exposure is Associated With Their Children's Psychopathology: A Study of Families of Israeli First RespondersRonit Kishon, Lupo Geronazzo-Alman, Meir Teichman, et al.
Life (Basel, Switzerland)|January 28, 2026
Interaction Between Frailty and Renal Function in Patients with Heart FailureÁngela Rodríguez-Eguren, José Jesús Broseta, Lydia Izquierdo, et al.
American Journal of Human Genetics|August 23, 2011
Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophyGeneviève Bernard, Eliane Chouery, Maria Lisa Putorti, et al.
Neurology|April 5, 2015
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxiaMarie Coutelier, Lydie Burglen, Emeline Mundwiller, et al.
Brain : a Journal of Neurology|July 12, 2014
Early-onset Behr syndrome due to compound heterozygous mutations in OPA1Dominique Bonneau, Estelle Colin, Florine Oca, et al.
Pageof 20