Komlósi K - Search Results

1

[Identifying rare genomic disorders with array comparative genomic hybridization in Hungary].

Duga B, Czakó M, Hadzsiev K, Komlósi K, Sümegi K, Kisfali P, Kosztolányi G, Melegh B. Duga B, et al. Among authors: komlosi k. Orv Hetil. 2014 Mar 2;155(9):358-61. doi: 10.1556/OH.2014.29825. Orv Hetil. 2014. PMID: 24566700 Hungarian.

2

[Molecular genetic diagnosis of neurofibromatosis type I].

Polgár N, Komlósi K, Hadzsiev K, Illés T, Melegh B. Polgár N, et al. Among authors: komlosi k. Orv Hetil. 2011 Mar 13;152(11):415-9. doi: 10.1556/OH.2011.29059. Orv Hetil. 2011. PMID: 21362601 Hungarian.

3

[Larsen-syndrome: final diagnosis following multiple surgical interventions].

Kisfali P, Komlósi K, Hadzsiev K, Melegh B. Kisfali P, et al. Among authors: komlosi k. Orv Hetil. 2013 Jan 27;154(4):143-6. doi: 10.1556/OH.2013.29534. Orv Hetil. 2013. PMID: 23335724 Hungarian.

4

[Novel TSC1 mutation associated with variable phenotypes in tuberous sclerosis].

Kövesdi E, Hadzsiev K, Komlósi K, Kassay M, Barsi P, Melegh B. Kövesdi E, et al. Among authors: komlosi k. Orv Hetil. 2013 Jun 9;154(23):914-8. doi: 10.1556/OH.2013.29634. Orv Hetil. 2013. PMID: 23728315 Hungarian.

5

[Attention deficit hyperactivity disorder analyzed with array comparative genome hybridization method. Case report].

Duga B, Czakó M, Komlósi K, Hadzsiev K, Sümegi K, Kisfali P, Melegh M, Melegh B. Duga B, et al. Among authors: komlosi k. Orv Hetil. 2014 Oct 5;155(40):1598-601. doi: 10.1556/OH.2014.30006. Orv Hetil. 2014. PMID: 25261991 Hungarian.

6

[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: komlosi k. Orv Hetil. 2015 Jan 18;156(3):113-7. doi: 10.1556/OH.2015.30014. Orv Hetil. 2015. PMID: 25577683 Hungarian.

7

[De novo SCN1A gene deletion in therapy-resistant Dravet syndrome].

Bene J, Hadzsiev K, Komlósi K, Kövesdi E, Mátyás P, Melegh B. Bene J, et al. Among authors: komlosi k. Orv Hetil. 2015 Dec 6;156(49):2009-12. doi: 10.1556/650.2015.30308. Orv Hetil. 2015. PMID: 26614543 Hungarian.

8

[Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].

Komlósi K, Bene J, Havasi V, Tihanyi M, Herczegfalvi A, Móser J, Melegh B. Komlósi K, et al. Orv Hetil. 2004 Aug 29;145(35):1805-9. Orv Hetil. 2004. PMID: 15493224 Hungarian.

9

[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. Orv Hetil. 2011 Dec 4;152(49):1965-70. doi: 10.1556/OH.2011.29241. Orv Hetil. 2011. PMID: 22106164 Hungarian.

10

[Significance of thiopurine s-methyltransferase gene test in a clinical case].

Sipeky C, Maász A, Tarlós G, Komlósi K, Pollák É, Melegh B. Sipeky C, et al. Among authors: komlosi k. Orv Hetil. 2012 Feb 5;153(5):191-4. doi: 10.1556/OH.2012.29289. Orv Hetil. 2012. PMID: 22275734 Hungarian.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

79 results

Search Page

Filters