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EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders.
Published in:
European Journal of Neurology, 2011, v. 18, n. 2, p. 207, doi. 10.1111/j.1468-1331.2010.03069.x
By:
- Burgunder, J.-M.;
- Schöls, L.;
- Baets, J.;
- Andersen, P.;
- Gasser, T.;
- Szolnoki, Z.;
- Fontaine, B.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- De Jonghe, P.;
- Lynch, T.;
- Mariotti, C.;
- Spinazzola, A.;
- Tabrizi, S. J.;
- Tallaksen, C.;
- Zeviani, M.;
- Harbo, H. F.;
- Finsterer, J.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementias.
Published in:
European Journal of Neurology, 2010, v. 17, n. 5, p. 641, doi. 10.1111/j.1468-1331.2010.02985.x
By:
- Burgunder, J.-M.;
- Finsterer, J.;
- Szolnoki, Z.;
- Fontaine, B.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- De Jonghe, P.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Tabrizi, S. J.;
- Tallaksen, C.;
- Zeviani, M.;
- Harbo, H. F.;
- Gasser, T.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias.
Published in:
European Journal of Neurology, 2010, v. 17, n. 2, p. 179, doi. 10.1111/j.1468-1331.2009.02873.x
By:
- Gasser, T.;
- Finsterer, J.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- Fontaine, B.;
- De Jonghe, P.;
- Lossos, A.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Szolnoki, Z.;
- Tabrizi, S. J.;
- Tallaksen, C. M. E.;
- Zeviani, M.;
- Burgunder, J.-M.;
- Harbo, H. F.
Publication type:
Article
Relevance of the genetic polymorphism of NOD1 in Chlamydia pneumoniae seropositive stroke patients.
Published in:
European Journal of Neurology, 2009, v. 16, n. 11, p. 1224, doi. 10.1111/j.1468-1331.2009.02698.x
By:
- Tiszlavicz, Z.;
- Somogyvári, F.;
- Kocsis, Á. K.;
- Szolnoki, Z.;
- Sztriha, L. K.;
- Kis, Z.;
- Vécsei, L.;
- Mándi, Y.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of mitochondrial disorders.
Published in:
European Journal of Neurology, 2009, v. 16, n. 12, p. 1255, doi. 10.1111/j.1468-1331.2009.02811.x
By:
- Finsterer, J.;
- Harbo, H. F.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- Fontaine, B.;
- De Jonghe, P.;
- Lossos, A.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Szolnoki, Z.;
- Tabrizi, S. J.;
- Tallaksen, C. M. E.;
- Zeviani, M.;
- Burgunder, J.-M.;
- Gasser, T.
Publication type:
Article
EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington’s disease, Parkinson’s disease and dystonias.
Published in:
European Journal of Neurology, 2009, v. 16, n. 7, p. 777, doi. 10.1111/j.1468-1331.2009.02646.x
By:
- Harbo, H. F.;
- Finsterer, J.;
- Baets, J.;
- Van Broeckhoven, C.;
- Di Donato, S.;
- Fontaine, B.;
- De Jonghe, P.;
- Lossos, A.;
- Lynch, T.;
- Mariotti, C.;
- Schöls, L.;
- Spinazzola, A.;
- Szolnoki, Z.;
- Tabrizi, S. J.;
- Tallaksen, C.;
- Zeviani, M.;
- Burgunder, J.-M.;
- Gasser, T.
Publication type:
Article
Evaluation of the roles of common genetic mutations in leukoaraiosis.
Published in:
Acta Neurologica Scandinavica, 2001, v. 104, n. 5, p. 281, doi. 10.1034/j.1600-0404.2001.00355.x
By:
- Szolnoki, Z.;
- Somogyvári, F.;
- Kondacs, A.;
- Szabó, M.;
- Fodor, L.
Publication type:
Article
A clustering of unfavourable common genetic mutations in stroke cases.
Published in:
Acta Neurologica Scandinavica, 2000, v. 102, n. 2, p. 124, doi. 10.1034/j.1600-0404.2000.102002124.x
By:
- Szolnoki, Z.;
- Somogyvári, F.;
- Szabó, M.;
- Fodor, L.
Publication type:
Article
Genetic polymorphisms of human β-defensins in patients with ischemic stroke.
Published in:
Acta Neurologica Scandinavica, 2012, v. 126, n. 2, p. 109, doi. 10.1111/j.1600-0404.2011.01613.x
By:
- Tiszlavicz, Z.;
- Somogyvári, F.;
- Szolnoki, Z.;
- Sztriha, L. K.;
- Németh, B.;
- Vécsei, L.;
- Mándi, Y.
Publication type:
Article
A homozygous genetic variant of mitochondrial uncoupling protein 4 affects the occurrence of leukoaraiosis.
Published in:
Acta Neurologica Scandinavica, 2011, v. 123, n. 5, p. 352, doi. 10.1111/j.1600-0404.2010.01391.x
By:
- Szolnoki, Z.;
- Kondacs, A.;
- Mandi, Y.;
- Bodor, A.;
- Somogyvari, F.
Publication type:
Article
Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke.
Published in:
Acta Neurologica Scandinavica, 2005, v. 111, n. 1, p. 29, doi. 10.1111/j.1600-0404.2004.00345.x
By:
- Szolnoki, Z.;
- Havasi, V.;
- Bene, J.;
- Komlósi, K.;
- Szöke, D.;
- Somogyvári, F.;
- Kondacs, A.;
- Szabó, M.;
- Fodor, L.;
- Bodor, A.;
- Gáti, I.;
- Wittman, I.;
- Melegh, B.
Publication type:
Article
Specific APO E genotypes in combination with the ACE D/D or MTHFR 677TT mutation yield an independent genetic risk of leukoaraiosis.
Published in:
Acta Neurologica Scandinavica, 2004, v. 109, n. 3, p. 222, doi. 10.1046/j.1600-0404.2003.00218.x
By:
- Szolnoki, Z.;
- Somogyvári, F.;
- Kondacs, A.;
- Szabó, M.;
- Fodor, L.;
- Bene, J.;
- Melegh, B.
Publication type:
Article
Search for Factor V Arg[sup 306] Cambridge and Hong Kong Mutations in Mixed Hungarian Population Samples.
Published in:
Acta Haematologica, 2003, v. 110, n. 4, p. 220, doi. 10.1159/000074233
By:
- Kom&loacute;si, K.;
- Havasi, V.;
- Bene, J.;
- Ghosh, M.;
- Szolnoki, Z.;
- Melegh, G.;
- Nagy, Á.;
- Stankovics, J.;
- Császár, A.;
- Papp, E.;
- Gasztonyi, B.;
- Tóth, K.;
- Mózsik, G.;
- Romics, L.;
- Ten Cate, H.;
- Smits, P.;
- Méhes, K.;
- Kosztolányi, G.;
- Melegh, Béla
Publication type:
Article

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