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Metabolic cause of Reye-like syndrome.
Bratisl Lek Listy. 2001;102(9):427-9.
Bratisl Lek Listy. 2001.
PMID: 11763681
Serum free carnitine in medium chain acyl-CoA dehydrogenase deficiency.
Bzduch V, Behulova D, Salingova A, Ponec J, Fabriciova K, Kozak L.
Bzduch V, et al. Among authors: fabriciova k.
Bratisl Lek Listy. 2003;104(12):405-7.
Bratisl Lek Listy. 2003.
PMID: 15053333
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[A pediatrician's views on the treatment of extensive hemangiomas in childhood].
Hornová J, Haviar D, Fabriciová K, Tichá L, Horn F, Babala J, Cingel V, Benedeková M.
Hornová J, et al. Among authors: fabriciova k.
Rozhl Chir. 2002 Mar;81(3):138-43.
Rozhl Chir. 2002.
PMID: 11925656
Slovak.
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Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes.
Mihaylova V, Müller JS, Vilchez JJ, Salih MA, Kabiraj MM, D'Amico A, Bertini E, Wölfle J, Schreiner F, Kurlemann G, Rasic VM, Siskova D, Colomer J, Herczegfalvi A, Fabriciova K, Weschke B, Scola R, Hoellen F, Schara U, Abicht A, Lochmüller H.
Mihaylova V, et al. Among authors: fabriciova k.
Brain. 2008 Mar;131(Pt 3):747-59. doi: 10.1093/brain/awm325. Epub 2008 Jan 7.
Brain. 2008.
PMID: 18180250
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