Malina M - Search Results

1

Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.

Fencl F, Malina M, Stará V, Zieg J, Mixová D, Seeman T, Bláhová K. Fencl F, et al. Among authors: malina m. Eur J Pediatr. 2012 Jan;171(1):121-4. doi: 10.1007/s00431-011-1497-3. Epub 2011 May 26. Eur J Pediatr. 2012. PMID: 21614510

2

Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation.

Malina M, Cinek O, Janda J, Seeman T. Malina M, et al. Pediatr Nephrol. 2009 Oct;24(10):2051-3. doi: 10.1007/s00467-009-1211-0. Epub 2009 Jun 3. Pediatr Nephrol. 2009. PMID: 19495806

3

Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93.

Bezdíčka M, Štolbová Š, Seeman T, Cinek O, Malina M, Šimánková N, Průhová Š, Zieg J. Bezdíčka M, et al. Among authors: malina m. Pediatr Nephrol. 2018 Aug;33(8):1347-1363. doi: 10.1007/s00467-018-3950-2. Epub 2018 Jun 4. Pediatr Nephrol. 2018. PMID: 29869118

4

Manifestation of atypical hemolytic uremic syndrome caused by novel mutations in MCP.

Provaznikova D, Rittich S, Malina M, Seeman T, Marinov I, Riedl M, Hrachovinova I. Provaznikova D, et al. Among authors: malina m. Pediatr Nephrol. 2012 Jan;27(1):73-81. doi: 10.1007/s00467-011-1943-5. Epub 2011 Jun 27. Pediatr Nephrol. 2012. PMID: 21706448

5

Genetics of hemolytic uremic syndromes.

Malina M, Roumenina LT, Seeman T, Le Quintrec M, Dragon-Durey MA, Schaefer F, Fremeaux-Bacchi V. Malina M, et al. Presse Med. 2012 Mar;41(3 Pt 2):e105-14. doi: 10.1016/j.lpm.2011.10.028. Epub 2012 Jan 20. Presse Med. 2012. PMID: 22265161 Review.

6

Peripheral gangrene in children with atypical hemolytic uremic syndrome.

Malina M, Gulati A, Bagga A, Majid MA, Simkova E, Schaefer F. Malina M, et al. Pediatrics. 2013 Jan;131(1):e331-5. doi: 10.1542/peds.2012-0903. Epub 2012 Dec 10. Pediatrics. 2013. PMID: 23230076

7

Extensive hemispheric diffusion restriction in haemolytic uremic syndrome.

Boppel T, Schaefer F, Gaudino C, Malina M, Radbruch A, Meyburg J, Bendszus M, Seitz A. Boppel T, et al. Among authors: malina m. Clin Radiol. 2012 Mar;67(3):292-4. doi: 10.1016/j.crad.2011.09.007. Epub 2011 Nov 25. Clin Radiol. 2012. PMID: 22119293 No abstract available.

8

Eculizumab Use for Kidney Transplantation in Patients With a Diagnosis of Atypical Hemolytic Uremic Syndrome.

Siedlecki AM, Isbel N, Vande Walle J, James Eggleston J, Cohen DJ; Global aHUS Registry. Siedlecki AM, et al. Kidney Int Rep. 2018 Dec 3;4(3):434-446. doi: 10.1016/j.ekir.2018.11.010. eCollection 2019 Mar. Kidney Int Rep. 2018. PMID: 30899871 Free PMC article.

9

Eculizumab in severe Shiga-toxin-associated HUS.

Lapeyraque AL, Malina M, Fremeaux-Bacchi V, Boppel T, Kirschfink M, Oualha M, Proulx F, Clermont MJ, Le Deist F, Niaudet P, Schaefer F. Lapeyraque AL, et al. Among authors: malina m. N Engl J Med. 2011 Jun 30;364(26):2561-3. doi: 10.1056/NEJMc1100859. Epub 2011 May 25. N Engl J Med. 2011. PMID: 21612462 No abstract available.

10

Late recovery of renal function by rituximab in a patient with Wegener's granulomatosis.

Malina M, Schaefer B, Waldherr R, Wühl E, Schaefer F, Schmitt CP. Malina M, et al. Pediatr Nephrol. 2013 Mar;28(3):511-4. doi: 10.1007/s00467-012-2332-4. Epub 2012 Nov 6. Pediatr Nephrol. 2013. PMID: 23124537

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