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Rainer Seidl

Showing results (61-70 of 77) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 10, 2018
Clinical and magnetic resonance imaging features of children, adolescents, and adults with a clinically isolated syndromeRuxandra-Iulia Milos, Martin Szimacsek, Fritz Leutmezer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 13, 2016
Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseasesMatthias Baumann, Eva-Maria Hennes, Kathrin Schanda, et al.
European Journal of Medical Genetics|March 5, 2013
Mutations at Ser331 in the HSN type I gene SPTLC1 are associated with a distinct syndromic phenotypeMichaela Auer-Grumbach, Heiko Bode, Thomas R Pieber, et al.
Developmental Science|January 14, 2025
Lateralization of Neural Speech Discrimination at Birth Is a Predictor for Later Language DevelopmentLisa Bartha-Doering, Vito Giordano, Sophie Mandl, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutationsGabriel Miltenberger-Miltenyi, Thomas Schwarzbraun, Wolfgang N Löscher, et al.
Cerebral Cortex (New York, N.Y. : 1991)|February 22, 2023
Fetal MRI based brain atlas analysis detects initial in utero effects of prenatal alcohol exposureMarlene Stuempflen, Ernst Schwartz, Mariana C Diogo, et al.
Plos One|March 3, 2026
Protocol for the establishment of the Pediatric Registry for Stroke as a Multidisciplinary Approach to healthcare research (PRiSMA) studyLucia Gerstl, Victoria Lieftüchter, Eva Jung, et al.
Communications Biology|January 27, 2023
Fetal temporal sulcus depth asymmetry has prognostic value for language developmentLisa Bartha-Doering, Kathrin Kollndorfer, Ernst Schwartz, et al.
Orphanet Journal of Rare Diseases|April 19, 2015
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotypeJohannes Koch, Peter Freisinger, René G Feichtinger, et al.
European Journal of Neurology|February 20, 2024
Rituximab treatment in pediatric-onset multiple sclerosisMarkus Breu, Fredrik Sandesjö, Ruxandra-Iulia Milos, et al.
Pageof 8

Showing results (61-70 of 77) with videos related to

Sort By:
Pageof 8
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 10, 2018
Clinical and magnetic resonance imaging features of children, adolescents, and adults with a clinically isolated syndromeRuxandra-Iulia Milos, Martin Szimacsek, Fritz Leutmezer, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 13, 2016
Children with multiphasic disseminated encephalomyelitis and antibodies to the myelin oligodendrocyte glycoprotein (MOG): Extending the spectrum of MOG antibody positive diseasesMatthias Baumann, Eva-Maria Hennes, Kathrin Schanda, et al.
European Journal of Medical Genetics|March 5, 2013
Mutations at Ser331 in the HSN type I gene SPTLC1 are associated with a distinct syndromic phenotypeMichaela Auer-Grumbach, Heiko Bode, Thomas R Pieber, et al.
Developmental Science|January 14, 2025
Lateralization of Neural Speech Discrimination at Birth Is a Predictor for Later Language DevelopmentLisa Bartha-Doering, Vito Giordano, Sophie Mandl, et al.
European Journal of Human Genetics : EJHG|March 5, 2009
Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutationsGabriel Miltenberger-Miltenyi, Thomas Schwarzbraun, Wolfgang N Löscher, et al.
Cerebral Cortex (New York, N.Y. : 1991)|February 22, 2023
Fetal MRI based brain atlas analysis detects initial in utero effects of prenatal alcohol exposureMarlene Stuempflen, Ernst Schwartz, Mariana C Diogo, et al.
Plos One|March 3, 2026
Protocol for the establishment of the Pediatric Registry for Stroke as a Multidisciplinary Approach to healthcare research (PRiSMA) studyLucia Gerstl, Victoria Lieftüchter, Eva Jung, et al.
Communications Biology|January 27, 2023
Fetal temporal sulcus depth asymmetry has prognostic value for language developmentLisa Bartha-Doering, Kathrin Kollndorfer, Ernst Schwartz, et al.
Orphanet Journal of Rare Diseases|April 19, 2015
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotypeJohannes Koch, Peter Freisinger, René G Feichtinger, et al.
European Journal of Neurology|February 20, 2024
Rituximab treatment in pediatric-onset multiple sclerosisMarkus Breu, Fredrik Sandesjö, Ruxandra-Iulia Milos, et al.
Pageof 8