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Items: 1 to 50 of 166

1.

Endovascular Therapy for Tandem Occlusion in Acute Ischemic Stroke: Intravenous Thrombolysis Improves Outcomes.

Pikija S, Magdic J, Sztriha LK, Killer-Oberpfalzer M, Bubel N, Lukic A, Sellner J.

J Clin Med. 2019 Feb 10;8(2). pii: E228. doi: 10.3390/jcm8020228.

2.

A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature.

Zombor M, Kalmár T, Nagy N, Berényi M, Telcs B, Maróti Z, Brandau O, Sztriha L.

J Appl Genet. 2019 May;60(2):151-162. doi: 10.1007/s13353-019-00486-y. Epub 2019 Feb 1.

PMID:
30706430
3.

Cerebrovascular manifestations of herpes simplex virus infection of the central nervous system: a systematic review.

Hauer L, Pikija S, Schulte EC, Sztriha LK, Nardone R, Sellner J.

J Neuroinflammation. 2019 Jan 29;16(1):19. doi: 10.1186/s12974-019-1409-4.

4.

Neutrophil to lymphocyte ratio predicts intracranial hemorrhage after endovascular thrombectomy in acute ischemic stroke.

Pikija S, Sztriha LK, Killer-Oberpfalzer M, Weymayr F, Hecker C, Ramesmayer C, Hauer L, Sellner J.

J Neuroinflammation. 2018 Nov 15;15(1):319. doi: 10.1186/s12974-018-1359-2.

5.

Contribution of Serum Lipid Profiles to Outcome After Endovascular Thrombectomy for Anterior Circulation Ischemic Stroke.

Pikija S, Sztriha LK, Killer-Oberpfalzer M, Weymayr F, Hecker C, Ramesmayer C, Hauer L, Sellner J.

Mol Neurobiol. 2019 Jun;56(6):4582-4588. doi: 10.1007/s12035-018-1391-3. Epub 2018 Oct 23.

6.

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

Zombor M, Kalmár T, Maróti Z, Zimmermann A, Máté A, Bereczki C, Sztriha L.

J Hum Genet. 2018 Nov;63(11):1189-1193. doi: 10.1038/s10038-018-0508-x. Epub 2018 Sep 4.

PMID:
30181650
7.

Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.

Smith RS, Kenny CJ, Ganesh V, Jang A, Borges-Monroy R, Partlow JN, Hill RS, Shin T, Chen AY, Doan RN, Anttonen AK, Ignatius J, Medne L, Bönnemann CG, Hecht JL, Salonen O, Barkovich AJ, Poduri A, Wilke M, de Wit MCY, Mancini GMS, Sztriha L, Im K, Amrom D, Andermann E, Paetau R, Lehesjoki AE, Walsh CA, Lehtinen MK.

Neuron. 2018 Sep 5;99(5):905-913.e7. doi: 10.1016/j.neuron.2018.07.052. Epub 2018 Aug 23.

PMID:
30146301
8.

Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephaly.

Alcantara D, Timms AE, Gripp K, Baker L, Park K, Collins S, Cheng C, Stewart F, Mehta SG, Saggar A, Sztriha L, Zombor M, Caluseriu O, Mesterman R, Van Allen MI, Jacquinet A, Ygberg S, Bernstein JA, Wenger AM, Guturu H, Bejerano G, Gomez-Ospina N, Lehman A, Alfei E, Pantaleoni C, Conti V, Guerrini R, Moog U, Graham JM Jr, Hevner R, Dobyns WB, O'Driscoll M, Mirzaa GM.

Brain. 2017 Oct 1;140(10):2610-2622. doi: 10.1093/brain/awx203.

9.

Idarucizumab in Dabigatran-Treated Patients with Acute Ischemic Stroke Receiving Alteplase: A Systematic Review of the Available Evidence.

Pikija S, Sztriha LK, Sebastian Mutzenbach J, Golaszewski SM, Sellner J.

CNS Drugs. 2017 Sep;31(9):747-757. doi: 10.1007/s40263-017-0460-x. Review.

10.

The effect of transcranial direct current stimulation on motor sequence learning and upper limb function after stroke.

Fleming MK, Rothwell JC, Sztriha L, Teo JT, Newham DJ.

Clin Neurophysiol. 2017 Jul;128(7):1389-1398. doi: 10.1016/j.clinph.2017.03.036. Epub 2017 Mar 31.

11.

Non-invasive brain stimulation for the lower limb after stroke: what do we know so far and what should we be doing next?

Fleming MK, Pavlou M, Newham DJ, Sztriha L, Teo JT.

Disabil Rehabil. 2017 Apr;39(7):714-720. doi: 10.3109/09638288.2016.1161835. Epub 2016 Mar 25. Review.

PMID:
27013330
12.

De Novo Interstitial Microdeletion at 1q32.1 in a 10-Year-Old Boy with Developmental Delay and Dysmorphism.

Carter J, Zombor M, Máté A, Sztriha L, Waters JJ.

Case Rep Genet. 2016;2016:2501741. doi: 10.1155/2016/2501741. Epub 2016 Feb 3.

13.

Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication.

Kodani A, Yu TW, Johnson JR, Jayaraman D, Johnson TL, Al-Gazali L, Sztriha L, Partlow JN, Kim H, Krup AL, Dammermann A, Krogan NJ, Walsh CA, Reiter JF.

Elife. 2015 Aug 22;4. doi: 10.7554/eLife.07519.

14.

Mutations in KIAA0586 Cause Lethal Ciliopathies Ranging from a Hydrolethalus Phenotype to Short-Rib Polydactyly Syndrome.

Alby C, Piquand K, Huber C, Megarbané A, Ichkou A, Legendre M, Pelluard F, Encha-Ravazi F, Abi-Tayeh G, Bessières B, El Chehadeh-Djebbar S, Laurent N, Faivre L, Sztriha L, Zombor M, Szabó H, Failler M, Garfa-Traore M, Bole C, Nitschké P, Nizon M, Elkhartoufi N, Clerget-Darpoux F, Munnich A, Lyonnet S, Vekemans M, Saunier S, Cormier-Daire V, Attié-Bitach T, Thomas S.

Am J Hum Genet. 2015 Aug 6;97(2):311-8. doi: 10.1016/j.ajhg.2015.06.003. Epub 2015 Jul 9.

15.

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

Thiffault I, Wolf NI, Forget D, Guerrero K, Tran LT, Choquet K, Lavallée-Adam M, Poitras C, Brais B, Yoon G, Sztriha L, Webster RI, Timmann D, van de Warrenburg BP, Seeger J, Zimmermann A, Máté A, Goizet C, Fung E, van der Knaap MS, Fribourg S, Vanderver A, Simons C, Taft RJ, Yates JR 3rd, Coulombe B, Bernard G.

Nat Commun. 2015 Jul 7;6:7623. doi: 10.1038/ncomms8623.

16.

The clinical manifestations of two novel SPAST mutations.

Zádori D, Máté A, Róna-Vörös K, Gergev G, Zimmermann A, Nagy N, Széll M, Vécsei L, Sztriha L, Klivényi P.

Clin Neurol Neurosurg. 2015 Sep;136:82-5. doi: 10.1016/j.clineuro.2015.05.009. Epub 2015 Jun 6. No abstract available.

PMID:
26086985
17.

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

Romani M, Micalizzi A, Kraoua I, Dotti MT, Cavallin M, Sztriha L, Ruta R, Mancini F, Mazza T, Castellana S, Hanene B, Carluccio MA, Darra F, Máté A, Zimmermann A, Gouider-Khouja N, Valente EM.

Orphanet J Rare Dis. 2014 May 5;9:72. doi: 10.1186/1750-1172-9-72.

18.

Spectrum of neurodevelopmental disabilities: a cohort study in hungary.

Gergev G, Máté A, Zimmermann A, Rárosi F, Sztriha L.

J Child Neurol. 2015 Mar;30(3):344-56. doi: 10.1177/0883073814532543. Epub 2014 May 26.

PMID:
24868008
19.

Clinical presentation and outcome in a series of 88 patients with the cblC defect.

Fischer S, Huemer M, Baumgartner M, Deodato F, Ballhausen D, Boneh A, Burlina AB, Cerone R, Garcia P, Gökçay G, Grünewald S, Häberle J, Jaeken J, Ketteridge D, Lindner M, Mandel H, Martinelli D, Martins EG, Schwab KO, Gruenert SC, Schwahn BC, Sztriha L, Tomaske M, Trefz F, Vilarinho L, Rosenblatt DS, Fowler B, Dionisi-Vici C.

J Inherit Metab Dis. 2014 Sep;37(5):831-40. doi: 10.1007/s10545-014-9687-6. Epub 2014 Mar 6.

PMID:
24599607
20.

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

Eggens VR, Barth PG, Niermeijer JM, Berg JN, Darin N, Dixit A, Fluss J, Foulds N, Fowler D, Hortobágyi T, Jacques T, King MD, Makrythanasis P, Máté A, Nicoll JA, O'Rourke D, Price S, Williams AN, Wilson L, Suri M, Sztriha L, Dijns-de Wissel MB, van Meegen MT, van Ruissen F, Aronica E, Troost D, Majoie CB, Marquering HA, Poll-Thé BT, Baas F.

Orphanet J Rare Dis. 2014 Feb 13;9:23. doi: 10.1186/1750-1172-9-23.

21.

Nemaline myopathy type 2 (NEM2): two novel mutations in the nebulin (NEB) gene.

Gajda A, Horváth E, Hortobágyi T, Gergev G, Szabó H, Farkas K, Nagy N, Széll M, Sztriha L.

J Child Neurol. 2015 Apr;30(5):627-30. doi: 10.1177/0883073813494476. Epub 2013 Sep 20.

PMID:
24056153
22.

Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases.

Horváth E, Horváth Z, Isaszegi D, Gergev G, Nagy N, Szabó J, Sztriha L, Széll M, Endreffy E.

Mol Cytogenet. 2013 Sep 8;6(1):35. doi: 10.1186/1755-8166-6-35.

23.

Determinants of mismatch in acute ischaemic stroke.

Sztriha LK, Cusack U, Kandasamy N, Jarosz J, Kalra L.

J Neurol Sci. 2013 Nov 15;334(1-2):10-3. doi: 10.1016/j.jns.2013.07.002. Epub 2013 Aug 23.

PMID:
23978421
24.

Congenital myasthenic syndromes and transient myasthenia gravis.

Gajda A, Szabó H, Gergev G, Karcagi V, Szabó N, Endreffy E, Túri S, Sztriha L.

Ideggyogy Sz. 2013 May 30;66(5-6):200-3.

PMID:
23909021
25.

Aspirin and clopidogrel resistance: possible mechanisms and clinical relevance. Part II: Potential causes and laboratory tests.

Vadász D, Sztriha LK, Sas K, Vécsei L.

Ideggyogy Sz. 2013 Jan 30;66(1-2):15-22. Review.

PMID:
23607225
26.

E-learning preferences of European junior neurologists-an EAYNT survey.

Sztriha LK, Varga ET, Róna-Vörös K, Holler N, Ilea R, Kobeleva X, Falup-Pecurariu C, Struhal W, Sellner J.

Front Neurol. 2012 Dec 4;3:167. doi: 10.3389/fneur.2012.00167. eCollection 2012. No abstract available.

27.

Aspirin and clopidogrel resistance: possible mechanisms and clinical relevance. Part I: Concept of resistance.

Vadász D, Sztriha LK, Sas K, Vecsei L.

Ideggyogy Sz. 2012 Nov 30;65(11-12):377-85. Review.

PMID:
23289172
28.

Pontocerebellar hypoplasia type 1: clinical spectrum and relevance of EXOSC3 mutations.

Rudnik-Schöneborn S, Senderek J, Jen JC, Houge G, Seeman P, Puchmajerová A, Graul-Neumann L, Seidel U, Korinthenberg R, Kirschner J, Seeger J, Ryan MM, Muntoni F, Steinlin M, Sztriha L, Colomer J, Hübner C, Brockmann K, Van Maldergem L, Schiff M, Holzinger A, Barth P, Reardon W, Yourshaw M, Nelson SF, Eggermann T, Zerres K.

Neurology. 2013 Jan 29;80(5):438-46. doi: 10.1212/WNL.0b013e31827f0f66. Epub 2013 Jan 2.

29.

Birth prevalence of neural tube defects: a population-based study in South-Eastern Hungary.

Szabó N, Gergev G, Valek A, Eller J, Kaizer L, Sztriha L.

Childs Nerv Syst. 2013 Apr;29(4):621-7. doi: 10.1007/s00381-012-1951-1. Epub 2012 Oct 30.

PMID:
23108919
30.

Monitoring brain repair in stroke using advanced magnetic resonance imaging.

Sztriha LK, O'Gorman RL, Modo M, Barker GJ, Williams SC, Kalra L.

Stroke. 2012 Nov;43(11):3124-31. doi: 10.1161/STROKEAHA.111.649244. Epub 2012 Sep 25. Review. No abstract available.

31.

Career mentorship for young neurologists in Europe.

Paterson RW, Waldermar G, Chaudhuri KR, Varga ET, Sztriha LK, Sellner J, Sauerbier A, Kondziella D, Macerollo A, Valkovic P, Oertel WH.

Neurology. 2012 Jul 24;79(4):381-3. doi: 10.1212/WNL.0b013e318260cdd7. No abstract available.

PMID:
22826543
32.

Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.

Mokánszki A, Körhegyi I, Szabó N, Bereg E, Gergev G, Balogh E, Bessenyei B, Sümegi A, Morris-Rosendahl DJ, Sztriha L, Oláh E.

J Child Neurol. 2012 Dec;27(12):1534-40. doi: 10.1177/0883073811436326. Epub 2012 Mar 8.

PMID:
22408144
33.

Evolutionarily assembled cis-regulatory module at a human ciliopathy locus.

Lee JH, Silhavy JL, Lee JE, Al-Gazali L, Thomas S, Davis EE, Bielas SL, Hill KJ, Iannicelli M, Brancati F, Gabriel SB, Russ C, Logan CV, Sharif SM, Bennett CP, Abe M, Hildebrandt F, Diplas BH, Attié-Bitach T, Katsanis N, Rajab A, Koul R, Sztriha L, Waters ER, Ferro-Novick S, Woods CG, Johnson CA, Valente EM, Zaki MS, Gleeson JG.

Science. 2012 Feb 24;335(6071):966-9. doi: 10.1126/science.1213506. Epub 2012 Jan 26.

34.

Genetic polymorphisms of human β-defensins in patients with ischemic stroke.

Tiszlavicz Z, Somogyvári F, Szolnoki Z, Sztriha LK, Németh B, Vécsei L, Mándi Y.

Acta Neurol Scand. 2012 Aug;126(2):109-15. doi: 10.1111/j.1600-0404.2011.01613.x. Epub 2011 Nov 2.

PMID:
22050386
35.

Safety and clinical outcome of thrombolysis in ischaemic stroke using a perfusion CT mismatch between 3 and 6 hours.

Sztriha LK, Manawadu D, Jarosz J, Keep J, Kalra L.

PLoS One. 2011;6(10):e25796. doi: 10.1371/journal.pone.0025796. Epub 2011 Oct 10.

36.

Development of visual contour integration in children with migraine without aura.

Braunitzer G, Rokszin A, Kóbor J, Nagy A, Sztriha L, Benedek G.

Cephalalgia. 2011 Jul;31(9):1048-56. doi: 10.1177/0333102411410611. Epub 2011 May 31.

PMID:
21628436
37.

European Association of Young Neurologists and Trainees: position paper on teaching courses for Generation Y.

Struhal W, Falup-Pecurariu C, Sztriha LK, Grisold W, Sellner J.

Eur Neurol. 2011;65(6):352-4. doi: 10.1159/000327696. Epub 2011 May 27.

PMID:
21625140
38.

Corpus callosum anomalies: birth prevalence and clinical spectrum in Hungary.

Szabó N, Gergev G, Kóbor J, Bereg E, Túri S, Sztriha L.

Pediatr Neurol. 2011 Jun;44(6):420-6. doi: 10.1016/j.pediatrneurol.2011.01.002.

PMID:
21555052
39.

[Role of carotid stents in stroke prevention].

Sztriha L.

Ideggyogy Sz. 2011 Mar 30;64(3-4):133-5. Hungarian. No abstract available.

PMID:
21545011
40.

Holoprosencephaly in hungary: birth prevalence and clinical spectrum.

Szabó N, Gergev G, Kóbor J, Szucs P, Túri S, Sztriha L.

J Child Neurol. 2011 Aug;26(8):1029-32. doi: 10.1177/0883073811399095. Epub 2011 Apr 22.

PMID:
21515784
41.

International Issues: the EAYNT: ten years of unifying European junior neurologists.

Struhal W, Sztriha LK, Rejdak K, Petzold A, Sellner J.

Neurology. 2011 Jan 11;76(2):e4-6. doi: 10.1212/WNL.0b013e318205d4bb. No abstract available.

PMID:
21220714
42.

Clinical, neuroradiological and genetic findings in pontocerebellar hypoplasia.

Namavar Y, Barth PG, Kasher PR, van Ruissen F, Brockmann K, Bernert G, Writzl K, Ventura K, Cheng EY, Ferriero DM, Basel-Vanagaite L, Eggens VR, Krägeloh-Mann I, De Meirleir L, King M, Graham JM Jr, von Moers A, Knoers N, Sztriha L, Korinthenberg R; PCH Consortium, Dobyns WB, Baas F, Poll-The BT.

Brain. 2011 Jan;134(Pt 1):143-56. doi: 10.1093/brain/awq287. Epub 2010 Oct 15.

PMID:
20952379
43.

Successful workshop on evidence-based neurology organized by the EAYNT and the Cochrane Neurological Network.

Sztriha L, Struhal W, Falup-Pecurariu C, Sellner J.

Eur J Neurol. 2010 Jul;17(7):e50-1. doi: 10.1111/j.1468-1331.2010.03013.x. Epub 2010 Apr 8. No abstract available.

PMID:
20402750
44.

Epidemiology and clinical spectrum of schizencephaly in south-eastern Hungary.

Szabó N, Gyurgyinka G, Kóbor J, Bereg E, Túri S, Sztriha L.

J Child Neurol. 2010 Nov;25(11):1335-9. doi: 10.1177/0883073810364854. Epub 2010 Mar 31.

PMID:
20357239
45.

Primary microcephaly in Hungary: epidemiology and clinical features.

Szabó N, Pap C, Kóbor J, Svékus A, Túri S, Sztriha L.

Acta Paediatr. 2010 May;99(5):690-693. doi: 10.1111/j.1651-2227.2009.01666.x. Epub 2010 Jan 7.

PMID:
20064139
46.

The use of covered stents for the endovascular treatment of extracranial internal carotid artery stenosis: a prospective study with a 5-year follow-up.

Szólics A, Sztriha LK, Szikra P, Szólics M, Palkó A, Vörös E.

Eur Radiol. 2010 Jul;20(7):1772-6. doi: 10.1007/s00330-009-1696-8. Epub 2009 Dec 22.

PMID:
20033177
47.

Expanding CEP290 mutational spectrum in ciliopathies.

Travaglini L, Brancati F, Attie-Bitach T, Audollent S, Bertini E, Kaplan J, Perrault I, Iannicelli M, Mancuso B, Rigoli L, Rozet JM, Swistun D, Tolentino J, Dallapiccola B, Gleeson JG, Valente EM; International JSRD Study Group, Zankl A, Leventer R, Grattan-Smith P, Janecke A, D'Hooghe M, Sznajer Y, Van Coster R, Demerleir L, Dias K, Moco C, Moreira A, Kim CA, Maegawa G, Petkovic D, Abdel-Salam GM, Abdel-Aleem A, Zaki MS, Marti I, Quijano-Roy S, Sigaudy S, de Lonlay P, Romano S, Touraine R, Koenig M, Lagier-Tourenne C, Messer J, Collignon P, Wolf N, Philippi H, Kitsiou Tzeli S, Halldorsson S, Johannsdottir J, Ludvigsson P, Phadke SR, Udani V, Stuart B, Magee A, Lev D, Michelson M, Ben-Zeev B, Fischetto R, Benedicenti F, Stanzial F, Borgatti R, Accorsi P, Battaglia S, Fazzi E, Giordano L, Pinelli L, Boccone L, Bigoni S, Ferlini A, Donati MA, Caridi G, Divizia MT, Faravelli F, Ghiggeri G, Pessagno A, Briguglio M, Briuglia S, Salpietro CD, Tortorella G, Adami A, Castorina P, Lalatta F, Marra G, Riva D, Scelsa B, Spaccini L, Uziel G, Del Giudice E, Laverda AM, Ludwig K, Permunian A, Suppiej A, Signorini S, Uggetti C, Battini R, Di Giacomo M, Cilio MR, Di Sabato ML, Leuzzi V, Parisi P, Pollazzon M, Silengo M, De Vescovi R, Greco D, Romano C, Cazzagon M, Simonati A, Al-Tawari AA, Bastaki L, Mégarbané A, Sabolic Avramovska V, de Jong MM, Stromme P, Koul R, Rajab A, Azam M, Barbot C, Martorell Sampol L, Rodriguez B, Pascual-Castroviejo I, Teber S, Anlar B, Comu S, Karaca E, Kayserili H, Yüksel A, Akcakus M, Al Gazali L, Sztriha L, Nicholl D, Woods CG, Bennett C, Hurst J, Sheridan E, Barnicoat A, Hennekam R, Lees M, Blair E, Bernes S, Sanchez H, Clark AE, DeMarco E, Donahue C, Sherr E, Hahn J, Sanger TD, Gallager TE, Dobyns WB, Daugherty C, Krishnamoorthy KS, Sarco D, Walsh CA, McKanna T, Milisa J, Chung WK, De Vivo DC, Raynes H, Schubert R, Seward A, Brooks DG, Goldstein A, Caldwell J, Finsecke E, Maria BL, Holden K, Cruse RP, Swoboda KJ, Viskochil D.

Am J Med Genet A. 2009 Oct;149A(10):2173-80. doi: 10.1002/ajmg.a.33025.

48.

Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies.

Bielas SL, Silhavy JL, Brancati F, Kisseleva MV, Al-Gazali L, Sztriha L, Bayoumi RA, Zaki MS, Abdel-Aleem A, Rosti RO, Kayserili H, Swistun D, Scott LC, Bertini E, Boltshauser E, Fazzi E, Travaglini L, Field SJ, Gayral S, Jacoby M, Schurmans S, Dallapiccola B, Majerus PW, Valente EM, Gleeson JG.

Nat Genet. 2009 Sep;41(9):1032-6. doi: 10.1038/ng.423. Epub 2009 Aug 9.

49.

[Stroke prevention: the role of carotid stenting and antithrombotic therapy].

Sztriha L.

Ideggyogy Sz. 2009 May 30;62(5-6):199-203. Hungarian. No abstract available.

PMID:
19579671
50.

Relevance of the genetic polymorphism of NOD1 in Chlamydia pneumoniae seropositive stroke patients.

Tiszlavicz Z, Somogyvári F, Kocsis AK, Szolnoki Z, Sztriha LK, Kis Z, Vécsei L, Mándi Y.

Eur J Neurol. 2009 Nov;16(11):1224-9. doi: 10.1111/j.1468-1331.2009.02698.x. Epub 2009 Jun 15.

PMID:
19538217

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