COVID-19 Stroke Apical Lung Examination Study: A Diagnostic and Prognostic Imaging Biomarker in Suspected Acute Stroke
Siddiqui, J, Bala, F, Sciacca, S, Falzon, A M, Benger, M, Matloob, S A, Miller, F N A C, Simister, R J, Chatterjee, I, Sztriha, L K, Davagnanam, I, Booth, T C
Published in American journal of neuroradiology : AJNR (01.01.2021)
Published in American journal of neuroradiology : AJNR (01.01.2021)
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Journal Article
P244 The effect of transcranial direct current stimulation on motor sequence learning and upper limb function after stroke
Fleming, M, Rothwell, J, Sztriha, L, Teo, J, Newham, D
Published in Clinical neurophysiology (01.03.2017)
Published in Clinical neurophysiology (01.03.2017)
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Journal Article
A Comparison of Chest Radiograph and CTA Apical Pulmonary Findings in Patients Presenting with Suspected Acute Stroke during the COVID-19 Pandemic
Siddiqui, J, Bala, F, Sciacca, S, Falzon, A M, Benger, M, Matloob, S A, Miller, F N A C, Simister, R J, Chatterjee, I, Sztriha, L K, Davagnanam, I, Booth, T C
Published in American journal of neuroradiology : AJNR (01.03.2021)
Published in American journal of neuroradiology : AJNR (01.03.2021)
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Journal Article
Refining the phenotype of α-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly
Morris-Rosendahl, DJ, Najm, J, Lachmeijer, AMA, Sztriha, L, Martins, M, Kuechler, A, Haug, V, Zeschnigk, C, Martin, P, Santos, M, Vasconcelos, C, Omran, H, Kraus, U, Van der Knaap, MS, Schuierer, G, Kutsche, K, Uyanik, G
Published in Clinical genetics (01.11.2008)
Published in Clinical genetics (01.11.2008)
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Journal Article
Genetic polymorphisms of human β-defensins in patients with ischemic stroke
Tiszlavicz, Z., Somogyvári, F., Szolnoki, Z., Sztriha, L. K., Németh, B., Vécsei, L., Mándi, Y.
Published in Acta neurologica Scandinavica (01.08.2012)
Published in Acta neurologica Scandinavica (01.08.2012)
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Journal Article
Refining the phenotype of alpha-1a Tubulin (TUBA1A) mutation in patients with classical lissencephaly
Morris-Rosendahl, D J, Najm, J, Lachmeijer, A M A, Sztriha, L, Martins, M, Kuechler, A, Haug, V, Zeschnigk, C, Martin, P, Santos, M, Vasconcelos, C, Omran, H, Kraus, U, Van der Knaap, M S, Schuierer, G, Kutsche, K, Uyanik, G
Published in Clinical genetics (01.11.2008)
Published in Clinical genetics (01.11.2008)
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Journal Article
P105 – 2378: Microcephaly, pontocerebellar hypoplasia and epilepsy in patients with CASK mutations
Máté, A, Szakszon, K, Nagy, A.J, Zombor, M, Rudas, G, Zimmermann, A, van Ruissen, F, Baas, F, Sztriha, L
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Journal Article
The European association of young neurologists and trainees: advocating young neurologists in Europe
Struhal, W., Falup-Pecurariu, C., Sztriha, L., Sellner, J.
Published in European journal of neurology (01.08.2009)
Published in European journal of neurology (01.08.2009)
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Journal Article
Successful workshop on evidence-based neurology organized by the EAYNT and the Cochrane Neurological Network
Sztriha, L., Struhal, W., Falup-Pecurariu, C., Sellner, J.
Published in European journal of neurology (01.07.2010)
Published in European journal of neurology (01.07.2010)
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Journal Article
Conference Proceeding
Vascular depression and vascular cognitive impairment share some common pathological aspects
Sas, K, Sztriha, L, Vecsei, L, Papp, J.Gy
Published in Journal of the neurological sciences (01.08.2009)
Published in Journal of the neurological sciences (01.08.2009)
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Journal Article
An exciting mix of education, science, and European culture: the activities of the EAYNT in 2011
Varga, E. T., Róna-Vörös, K., Holler, N., Sztriha, L. K., Sellner, J.
Published in European journal of neurology (01.10.2011)
Published in European journal of neurology (01.10.2011)
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Journal Article
L-2-Hydroxyglutaric aciduria: Identification of ten novel mutations in the L2HGDH gene
Sass, J. O., Jobard, F., Topçu, M., Mahfoud, A., Werlé, E., Cure, S., Al-Sannaa, N., Alshahwan, S. A., Bataillard, M., Cimbalistiene, L., Grolik, C., Kemmerich, V., Omran, H., Sztriha, L., Tabache, M., Fischer, J.
Published in Journal of inherited metabolic disease (01.12.2008)
Published in Journal of inherited metabolic disease (01.12.2008)
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Journal Article
A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy
Al-Yahyaee, S, Al-Gazali, L I, De Jonghe, P, Al-Barwany, H, Al-Kindi, M, De Vriendt, E, Chand, P, Koul, R, Jacob, P C, Gururaj, A, Sztriha, L, Parrado, A, Van Broeckhoven, C, Bayoumi, R A
Published in Neurology (25.04.2006)
Published in Neurology (25.04.2006)
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Journal Article
Emerging scientific opportunities for junior neurologists in the European Federation of Neurological Societies
Sztriha, L. K., Struhal, W., Varga, E. T., Brainin, M., Gilhus, N. E., Waldemar, G., Sipido, E., Müller, E., Sellner, J.
Published in European journal of neurology (01.10.2011)
Published in European journal of neurology (01.10.2011)
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Journal Article
Optical platelet aggregometry does not appear useful as a means of assessing the risk of recurrent vascular events in aspirin-treated patients
Sztriha, L. K., Sas, K., Seres, E., Boda, K., Lenti, L., Csifcsak, G., Kovacs, N., Vecsei, L.
Published in Acta neurologica Scandinavica (01.04.2008)
Published in Acta neurologica Scandinavica (01.04.2008)
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Journal Article
Relevance of the genetic polymorphism of NOD1 in Chlamydia pneumoniae seropositive stroke patients
Tiszlavicz, Z., Somogyvári, F., Kocsis, Á. K., Szolnoki, Z., Sztriha, L. K., Kis, Z., Vécsei, L., Mándi, Y.
Published in European journal of neurology (01.11.2009)
Published in European journal of neurology (01.11.2009)
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Journal Article
Epilepsy in children with cerebral palsy
GURURAJ, A.K., SZTRIHA, L., BENER, A., DAWODU, A., EAPEN, V.
Published in Seizure (London, England) (01.03.2003)
Published in Seizure (London, England) (01.03.2003)
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Journal Article
First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvement
Sztriha, L, Panzeri, C, Kálmánchey, R, Szabó, N, Endreffy, E, Túri, S, Baschirotto, C, Bresolin, N, Vekerdy, Z, Bassi, MT
Published in Clinical genetics (01.06.2008)
Published in Clinical genetics (01.06.2008)
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