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[Molecular genetic diagnosis of neurofibromatosis type I].
Polgár N, Komlósi K, Hadzsiev K, Illés T, Melegh B. Polgár N, et al. Among authors: melegh b. Orv Hetil. 2011 Mar 13;152(11):415-9. doi: 10.1556/OH.2011.29059. Orv Hetil. 2011. PMID: 21362601 Hungarian.
[Unusual clinical manifestations of type 1 neurofibromatosis].
Komlósi K, Polgár N, Hadzsiev K, Ottóffy G, Illés T, Dóczi T, Melegh B. Komlósi K, et al. Among authors: melegh b. Orv Hetil. 2011 Dec 4;152(49):1965-70. doi: 10.1556/OH.2011.29241. Orv Hetil. 2011. PMID: 22106164 Hungarian.
[Genetic testing in hereditary spastic paraplegia].
Hadzsiev K, Balikó L, Komlósi K, Lőcsei-Fekete A, Csábi G, Bene J, Kisfali P, Melegh B. Hadzsiev K, et al. Among authors: melegh b. Orv Hetil. 2015 Jan 18;156(3):113-7. doi: 10.1556/OH.2015.30014. Orv Hetil. 2015. PMID: 25577683 Hungarian.
447 results