Drac H - Search Results

1

[Cryptococcosis in patients with transplanted kidney treated with steroids and azathioprine].

Juskowa J, Halweg H, Drac H, Smogorzewski M, Górski A, Rancewicz Z, Małdyk-Durlik M, Stryjecka-Rowińska D, Podsiadło B, Kubicka-Pertkiewicz M. Juskowa J, et al. Among authors: drac h. Pol Arch Med Wewn. 1988 Aug-Sep;80(2-3):113-23. Pol Arch Med Wewn. 1988. PMID: 3271312 Polish. No abstract available.

2

[Changes in the peripheral nerves in chronic renal failure].

Rowińska K, Juskowa J, Drac H, Emeryk B, Hausmanowa-Petrusewicz I, Kopec A, Rowińska D, Karwańska A. Rowińska K, et al. Among authors: drac h. Pol Arch Med Wewn. 1986 Feb;75(2):116-26. Pol Arch Med Wewn. 1986. PMID: 3748829 Polish. No abstract available.

3

Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene.

Kabzińska D, Kochański A, Drac H, Ryniewicz B, Rowińska-Marcińska K, Hausmanowa-Petrusewicz I. Kabzińska D, et al. Among authors: drac h. Neuropediatrics. 2005 Jun;36(3):206-9. doi: 10.1055/s-2005-865606. Neuropediatrics. 2005. PMID: 15944907

4

[Diagnostic yield of electrophysiological and immunological studies in inflammatory myopathies].

Rowińska-Marcińska K, Szmidt-Sałkowska E, Kowalska E, Błaszczyk M, Drac H, Zakrzewska-Pniewska B, Karwańska A, Jabłońska S, Hausmanowa-Petrusewicz I. Rowińska-Marcińska K, et al. Among authors: drac h. Neurol Neurochir Pol. 1994;28(1 Suppl 1):103-13. Neurol Neurochir Pol. 1994. PMID: 8065537 Polish.

5

Dysmyelinating and demyelinating Charcot-Marie-Tooth disease associated with two myelin protein zero gene mutations.

Drac H, Kabzińska D, Moszyńska I, Strugalska-Cynowska H, Hausmanowa-Petrusewicz I, Kochański A. Drac H, et al. J Appl Genet. 2011 May;52(2):177-83. doi: 10.1007/s13353-010-0003-3. Epub 2010 Nov 3. J Appl Genet. 2011. PMID: 21107784

6

Focally folded myelin in Charcot-Marie-Tooth type 1B disease is associated with Asn131Lys mutation in myelin protein zero gene: short report.

Kochański A, Drac H, Jedrzejowska H, Hausmanowa-Petrusewicz I. Kochański A, et al. Among authors: drac h. Eur J Neurol. 2003 Sep;10(5):547-9. doi: 10.1046/j.1468-1331.2003.00640.x. Eur J Neurol. 2003. PMID: 12940837

7

A novel mutation, Thr65Ala, in the MPZ gene in a patient with Charcot-Marie-Tooth type 1B disease with focally folded myelin.

Kochanski A, Drac H, Kabzińska D, Hausmanowa-Petrusewicz I. Kochanski A, et al. Among authors: drac h. Neuromuscul Disord. 2004 Mar;14(3):229-32. doi: 10.1016/j.nmd.2003.12.001. Neuromuscul Disord. 2004. PMID: 15036333

8

A novel MPZ gene mutation in congenital neuropathy with hypomyelination.

Kochanski A, Drac H, Kabzińska D, Ryniewicz B, Rowińska-Marcińska K, Nowakowski A, Hausmanowa-Petrusewicz I. Kochanski A, et al. Among authors: drac h. Neurology. 2004 Jun 8;62(11):2122-3. doi: 10.1212/01.wnl.0000127606.93772.3a. Neurology. 2004. PMID: 15184631

9

Charcot-Marie-Tooth type 4F disease caused by S399fsx410 mutation in the PRX gene.

Kabzinska D, Drac H, Sherman DL, Kostera-Pruszczyk A, Brophy PJ, Kochanski A, Hausmanowa-Petrusewicz I. Kabzinska D, et al. Among authors: drac h. Neurology. 2006 Mar 14;66(5):745-7. doi: 10.1212/01.wnl.0000201269.46071.35. Neurology. 2006. PMID: 16534116

10

Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene.

Kabzinska D, Drac H, Rowinska-Marcinska K, Fidzianska A, Kochanski A, Hausmanowa-Petrusewicz I. Kabzinska D, et al. Among authors: drac h. Acta Myol. 2006 Jun;25(1):34-7. Acta Myol. 2006. PMID: 17039978

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