Items where Author is " Gergev Gyurgyinka"

Number of items: 6.

Gajda Anna and Ferdinandyné Horváth Emese and Hortobágyi Tibor and Gergev Gyurgyinka and Szabó Hajnalka and Farkas Katalin and Nagy Nikoletta and Széll Márta and Sztriha László: Nemaline Myopathy Type 2 (NEM2): Two Novel Mutations in the Nebulin (NEB) Gene.
Journal of Child Neurology, 30 (5). pp. 627-630. ISSN 0883-0738 (2015)

Gergev Gyurgyinka and Máté Adrienn and Zimmermann Aliz and Rárosi Ferenc and Sztriha László: Spectrum of neurodevelopmental disabilities: a cohort study in Hungary.
JOURNAL OF CHILD NEUROLOGY, 30 (3). pp. 344-356. ISSN 0883-0738 (2015)

Zádori Dénes and Máté Adrienn and Róna-Vörös Krisztina and Gergev Gyurgyinka and Zimmermann Aliz and Nagy Nikoletta and Széll Márta and Vécsei László and Sztriha László and Klivényi Péter: The clinical manifestations of two novel SPAST mutations.
CLINICAL NEUROLOGY AND NEUROSURGERY, 136. pp. 82-85. ISSN 0303-8467 (2015)

Ferdinandyné Horváth Emese and Horváth Zsuzsanna and Isaszegi Dóra and Gergev Gyurgyinka and Nagy Nikoletta and Szabó János and Sztriha László and Széll Márta and Endreffy Emőke: Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases.
Molecular Cytogenetics, 6 (1). Azonosító: 35-Terjedelem: 5 p.. ISSN 1755-8166 (2013)

Szabó Nóra and Gergev Gyurgyinka and Kóbor Jenő Dezső and Bereg Edit and Túri Sándor and Sztriha László: Corpus Callosum Anomalies: Birth Prevalence and Clinical Spectrum in Hungary.
Pediatric Neurology, 44 (6). pp. 420-426. ISSN 0887-8994 (2011)

Szabó Nóra and Gergev Gyurgyinka and Kóbor Jenő Dezső and Szűcs Péter and Túri Sándor and Sztriha László: Holoprosencephaly in Hungary: Birth Prevalence and Clinical Spectrum.
Journal of Child Neurology, 26 (8). pp. 1029-1032. ISSN 0883-0738 (2011)

This list was generated on 2024. június 15. 00:24:47 CEST.