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Novel paracellin-1 mutations in 25 families with familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
Weber S, Schneider L, Peters M, Misselwitz J, Rönnefarth G, Böswald M, Bonzel KE, Seeman T, Suláková T, Kuwertz-Bröking E, Gregoric A, Palcoux JB, Tasic V, Manz F, Schärer K, Seyberth HW, Konrad M. Weber S, et al. Among authors: sulakova t. J Am Soc Nephrol. 2001 Sep;12(9):1872-1881. doi: 10.1681/ASN.V1291872. J Am Soc Nephrol. 2001. PMID: 11518780
Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene.
Weber S, Hoffmann K, Jeck N, Saar K, Boeswald M, Kuwertz-Broeking E, Meij II, Knoers NV, Cochat P, Suláková T, Bonzel KE, Soergel M, Manz F, Schaerer K, Seyberth HW, Reis A, Konrad M. Weber S, et al. Among authors: sulakova t. Eur J Hum Genet. 2000 Jun;8(6):414-22. doi: 10.1038/sj.ejhg.5200475. Eur J Hum Genet. 2000. PMID: 10878661
[Hereditary form of thrombotic thrombocytopenic purpura].
Hrachovinová I, Rittich S, Salaj P, Suttnar J, Dyr JE, Suláková T, Pták J, Dulícek P, Seeman T. Hrachovinová I, et al. Among authors: sulakova t. Cas Lek Cesk. 2006;145(5):390-2. Cas Lek Cesk. 2006. PMID: 16755777 Czech.
Kidney volume normative values in Central European children aged 0-19 years: a multicenter study.
Obrycki Ł, Sarnecki J, Pac M, Lichosik M, Sopińska M, Placzyńska M, Milart J, Stańczyk M, Mirecka J, Wasilewska A, Michalski M, Lewandowska W, Dereziński T, Šuláková T, Šupík D, Čekuolis A, Vitkevič R, Wierzbicka A, Koziej J, Skoczyński K, Horubała J, Jankauskiene A, Kalicki B, Jobs K, Tkaczyk M, Feber J, Litwin M. Obrycki Ł, et al. Among authors: sulakova t. Pediatr Nephrol. 2024 Jul;39(7):2147-2159. doi: 10.1007/s00467-024-06278-9. Epub 2024 Mar 1. Pediatr Nephrol. 2024. PMID: 38427072
19 results