A. Máté

发表

The Role of Probabilistic Tractography in the Surgical Treatment of Thalamic Gliomas

Pál Barzó, Dávid Kis, Zsigmond Tamás Kincses, 2014, Neurosurgery.

A “one size fits all” approach to language fMRI: increasing specificity and applicability by adding a self-paced component

M. Wilke, M. Staudt, K. Lidzba, 2015, Experimental Brain Research.

Connectivity-based segmentation of the brainstem by probabilistic tractography

P. Barzó, D. Kis, A. Máté, 2018, Brain Research.

Microvascular reactivity in lean, overweight, and obese hypertensive adolescents

I. Varga, A. Máté, C. Bereczki, 2010, European Journal of Pediatrics.

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

T. Mazza, S. Castellana, E. Valente, 2014, Orphanet Journal of Rare Diseases.

Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III

J. Yates, A. Vanderver, D. Timmann, 2015, Nature Communications.

Predicting the true extent of glioblastoma based on probabilistic tractography

P. Barzó, D. Kis, A. Máté, 2022, Frontiers in Neuroscience.

A “one size fits all” approach to language fMRI: increasing specificity and applicability by adding a self-paced component

M. Wilke, M. Staudt, K. Lidzba, 2016, Experimental Brain Research.

Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability

T. Kalmár, L. Sztriha, A. Máté, 2018, Journal of Human Genetics.

Spectrum of Neurodevelopmental Disabilities

L. Sztriha, A. Máté, Alíz Zimmermann, 2015, Journal of child neurology.

EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations

T. Hortobágyi, F. Baas, E. Aronica, 2014, Orphanet Journal of Rare Diseases.

Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability

T. Kalmár, L. Sztriha, A. Máté, 2018, Journal of Human Genetics.

A Novel Homozygous Frameshift WDR81 Mutation associated with Microlissencephaly, Corpus Callosum Agenesis, and Pontocerebellar Hypoplasia

T. Kalmár, L. Sztriha, A. Máté, 2020, Journal of Pediatric Genetics.