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Page 1
Iliopsoas hematoma in a young patient with type I Gaucher disease.
Jmoudiak M, Itzchaki M, Hadas-Halpern I, Hrebicek M, Hodanova K, Elstein D, Zimran A. Jmoudiak M, et al. Among authors: hodanova k. Isr Med Assoc J. 2003 Sep;5(9):673-4. Isr Med Assoc J. 2003. PMID: 14509164 Free article. No abstract available.
[Enzyme therapy in children with severe forms of Gaucher's disease].
Zeman J, Hrebícek M, Vepreková L, Kytnarová J, Houstková H, Malinová V, Hodanová K, Poupĕtová H, Ledvinová J, Hoza J. Zeman J, et al. Among authors: hodanova k. Cas Lek Cesk. 1997 Feb 5;136(3):95-7. Cas Lek Cesk. 1997. PMID: 9221177 Czech.
Genetic and clinical features of patients with Gaucher disease in Hungary.
Erdos M, Hodanova K, Taskó S, Palicz A, Stolnaja L, Dvorakova L, Hrebicek M, Maródi L. Erdos M, et al. Among authors: hodanova k. Blood Cells Mol Dis. 2007 Jul-Aug;39(1):119-23. doi: 10.1016/j.bcmd.2007.02.005. Epub 2007 Mar 28. Blood Cells Mol Dis. 2007. PMID: 17395504 Clinical Trial.
Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes.
Stibůrková B, Majewski J, Hodanová K, Ondrová L, Jerábková M, Zikánová M, Vylet'al P, Sebesta I, Marinaki A, Simmonds A, Matthijs G, Fryns JP, Torres R, Puig JG, Ott J, Kmoch S. Stibůrková B, et al. Among authors: hodanova k. Eur J Hum Genet. 2003 Feb;11(2):145-54. doi: 10.1038/sj.ejhg.5200937. Eur J Hum Genet. 2003. PMID: 12634862
Alterations of uromodulin biology: a common denominator of the genetically heterogeneous FJHN/MCKD syndrome.
Vylet'al P, Kublová M, Kalbácová M, Hodanová K, Baresová V, Stibůrková B, Sikora J, Hůlková H, Zivný J, Majewski J, Simmonds A, Fryns JP, Venkat-Raman G, Elleder M, Kmoch S. Vylet'al P, et al. Among authors: hodanova k. Kidney Int. 2006 Sep;70(6):1155-69. doi: 10.1038/sj.ki.5001728. Epub 2006 Aug 2. Kidney Int. 2006. PMID: 16883323 Free article.
54 results