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personal data approved: 2015. XII. 08.
Personal data
name László Sztriha
year of birth 1947
name of institution
doctoral school
SzTE Doctoral School of Clinical Medicine (Supervisor)
Contact details
E-mail address sztriha.laszlomed.u-szeged.hu
phone number +36 62 342-076
mobile phone number +36 20 535-1323
Academic title
scientific degree, title Ph.D.
year degree was obtained 1989
discipline to which degree belongs clinical medicine
institution granting the degree HAS
scientific degree, title DSc
year degree was obtained 2002
discipline to which degree belongs clinical medicine
institution granting the degree HAS
Employment
2005 - Szegedi Tudományegyetem Általános Orvostudományi Kar Gyermekgyógyászati Klinika (research institute, not university)
Thesis topic supervisor
number of doctoral students supervised until now 2
number of students who fulfilled course requirements 0
students who obtained their degrees:
Gyurgyinka Gergev PhD 2015  DSCM-SzTE
(50%) Emese Beatrix Horváth PhD 2014  DSCM-SzTE
Nóra Zsuzsanna Szabó PhD 2012  DSCM-SzTE

present PhD students:
Melinda Zombor (PhD) (2017/08)  DSCM-SzTE
  Thesis topic proposals
Research
research area Neurodevelopmental disabilities in infancy and childhood: aetiology, clinical features, management and epidemiology
research field in which current research is conducted clinical medicine
Publications
2015

Zadori D, Mate A, Rona-Voros K, Gergev G, Zimmermann A, Nagy N, Szell M, Vecsei L, Sztriha L, Klivenyi P: The clinical manifestations of two novel SPAST mutations., CLINICAL NEUROLOGY AND NEUROSURGERY 136: pp. 82-85.
type of document: Journal paper/Article
language: English
DOI 
2013

Horvath E, Horvath Z, Isaszegi D, Gergev G, Nagy N, Szabo J, Sztriha L, Szell M, Endreffy E: Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases., MOLECULAR CYTOGENETICS 6: (1) 5 p. Paper 35.
type of document: Journal paper/Article
number of independent citations: 1
language: English
DOI 
2013

Gajda A, Szabó H, Gergev G, Karcagi V, Szabó N, Endreffy E, Túri S, Sztriha L: Congenital myasthenic syndromes and transient myasthenia gravis, IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE 66: (5-6) pp. 200-203.
type of document: Journal paper/Article
language: English
2013

Szabo N, Gergev G, Valek A, Eller J, Kaizer L, Sztriha L: Birth prevalence of neural tube defects: a population-based study in South-Eastern Hungary, CHILDS NERVOUS SYSTEM 29: (4) pp. 621-627.
type of document: Journal paper/Article
language: English
DOI 
2012

Mokánszki Attila, Körhegyi Ivett, Szabó Nóra, Bereg Edit, Gergev Gyurgyinka, Balogh Erzsébet, Bessenyei Beáta, Sümegi Andrea, Sztriha László, Oláh Éva, Morris-Rosendahl DeborahJ: Lissencephaly and Band Heterotopia : LIS1, TUBA1A, and DCX Mutations in Hungary, JOURNAL OF CHILD NEUROLOGY 27: (12) pp. 1534-1540. Paper 10.1177/0883073811436326.
type of document: Journal paper/Article
number of independent citations: 6
language: English
DOI 
2011

Braunitzer G, Rokszin A, Kobor J, Nagy A, Sztriha L, Benedek G: Development of visual contour integration in children with migraine without aura, CEPHALALGIA 31: (9) pp. 1048-1056.
type of document: Journal paper/Article
number of independent citations: 4
language: English
DOI 
2009

Szabó N, Hegyi A, Boda M, Páncsics M, Pap Cs, Zágonyi K, Romhányi E, Túri S, Sztriha L: Bilateral Operculum Syndrome in Childhood, JOURNAL OF CHILD NEUROLOGY 24: (5) pp. 544-550.
type of document: Journal paper/Article
number of independent citations: 1
language: English
DOI 
2004

Dixon-Salazar T, Silhavy JL, Marsh SE, Louie CM, Scott LC, Gururaj A, Al-Gazali L, Al-Tawari AA, Kayserili H, Sztriha L, Gleeson JG: Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria., AMERICAN JOURNAL OF HUMAN GENETICS 75: (6) pp. 979-987.
type of document: Journal paper/Article
language: English
DOI 
1999

Saar K, Al-Gazali L, Sztriha L, Rueschendorf F, Nur-E-Kamal M, Reis A, Bayoumi R: Homozygosity mapping in families with Joubert syndrome identifies a locus on chromosome 9q34.3 and evidence for genetic heterogeneity, AMERICAN JOURNAL OF HUMAN GENETICS 65: (6) pp. 1666-1671.
type of document: Journal paper/Article
language: English
1998

Sztriha L, Al-Gazali L, Dawodu A, Bakir M, Chandran P: Agyria-pachygyria and agenesis of the corpus callosum: autosomal recessive inheritance with neonatal death., NEUROLOGY 50: (5) pp. 1466-1469.
type of document: Journal paper/Article
language: English
Number of independent citations to these publications:12 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
118
number of scientific publications:
146
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
1 
number of independent citations to scientific publications and creative works:
409

 
All rights reserved © 2007, Hungarian Doctoral Council. Doctoral Council registration number at commissioner for data protection: 02003/0001. Program version: 1.2318 ( 2016. XI. 26. )