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Journal of Child Neurology|May 29, 2014
Spectrum of neurodevelopmental disabilities: a cohort study in hungaryGyurgyinka Gergev, Adrienn Máté, Alíz Zimmermann, et al.Experimental Brain Research|October 31, 2015
A "one size fits all" approach to language fMRI: increasing specificity and applicability by adding a self-paced componentAdrienn Máté, Karen Lidzba, Till-Karsten Hauser, et al.Case Reports in Genetics|March 9, 2016
De Novo Interstitial Microdeletion at 1q32.1 in a 10-Year-Old Boy with Developmental Delay and DysmorphismJennifer Carter, Melinda Zombor, Adrienn Máté, et al.Neurosurgery|March 6, 2014
The role of probabilistic tractography in the surgical treatment of thalamic gliomasDávid Kis, Adrienn Máté, Zsigmond Tamás Kincses, et al.Brain Research|March 21, 2018
Connectivity-based segmentation of the brainstem by probabilistic tractographyAdrienn Máté, Dávid Kis, Andrea Czigner, et al.Journal of Human Genetics|September 6, 2018
Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disabilityMelinda Zombor, Tibor Kalmár, Zoltán Maróti, et al.Journal of Pediatric Genetics|May 17, 2021
A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar HypoplasiaTibor Kalmár, Katalin Szakszon, Zoltán Maróti, et al.European Journal of Pediatrics|June 17, 2010
Microvascular reactivity in lean, overweight, and obese hypertensive adolescentsPéter Monostori, Akos Baráth, Ildikó Fazekas, et al.Orphanet Journal of Rare Diseases|June 3, 2014
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndromeMarta Romani, Alessia Micalizzi, Ichraf Kraoua, et al.Nature Communications|July 8, 2015
Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase IIIIsabelle Thiffault, Nicole I Wolf, Diane Forget, et al.Pageof 2