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Cerebral Cortex (New York, N.Y. : 1991)|April 19, 2021
The Prenatal Morphomechanic Impact of Agenesis of the Corpus Callosum on Human Brain Structure and AsymmetryErnst Schwartz, Mariana Cardoso Diogo, Sarah Glatter, et al.
Developmental Medicine and Child Neurology|February 18, 2014
Prevalence, clinical investigation, and management of gallbladder disease in Rett syndromeMichael Freilinger, Michael Böhm, Ines Lanator, et al.
Epilepsy Research|September 16, 2014
Epilepsy surgery in children and adolescents with malformations of cortical development--outcome and impact of the new ILAE classification on focal cortical dysplasiaAngelika Mühlebner, Gudrun Gröppel, Anastasia Dressler, et al.
Research in Developmental Disabilities|April 27, 2023
Learning about neurodiversity from parents - Auditory gestalt perception of prelinguistic vocalisationsDajie Zhang, Sigrun Lang, Bernd Wilken, et al.
Brain and Language|June 19, 2018
When two are better than one: Bilateral mesial temporal lobe contributions associated with better vocabulary skills in children and adolescentsLisa Bartha-Doering, Astrid Novak, Kathrin Kollndorfer, et al.
Brain and Behavior|October 10, 2018
Weaker semantic language lateralization associated with better semantic language performance in healthy right-handed childrenLisa Bartha-Doering, Kathrin Kollndorfer, Gregor Kasprian, et al.
Cerebral Cortex (New York, N.Y. : 1991)|March 27, 2021
The Prenatal Origins of Human Brain Asymmetry: Lessons Learned from a Cohort of Fetuses with Body Lateralization DefectsPatric Kienast, Ernst Schwartz, Mariana C Diogo, et al.
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.
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