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Clinical and molecular genetic findings in COLQ-mutant congenital myasthenic syndromes.
Brain. 2008 Mar;131(Pt 3):747-59. doi: 10.1093/brain/awm325. Epub 2008 Jan 7.
Brain. 2008.
PMID: 18180250
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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Metabolic cause of Reye-like syndrome.
Bzduch V, Behulova D, Lehnert W, Fabriciova K, Kozak L, Salingova A, Hrabincova E, Benedekova M.
Bzduch V, et al. Among authors: fabriciova k.
Bratisl Lek Listy. 2001;102(9):427-9.
Bratisl Lek Listy. 2001.
PMID: 11763681
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