Sulek A - Search Results

1

Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients.

Elert-Dobkowska E, Stepniak I, Krysa W, Rajkiewicz M, Rakowicz M, Sobanska A, Rudzinska M, Wasielewska A, Pilch J, Kubalska J, Lipczynska-Lojkowska W, Kulczycki J, Kurdziel K, Sikorska A, Beetz C, Zaremba J, Sulek A. Elert-Dobkowska E, et al. Among authors: sulek a. J Neurol Sci. 2015 Dec 15;359(1-2):35-9. doi: 10.1016/j.jns.2015.10.030. Epub 2015 Oct 17. J Neurol Sci. 2015. PMID: 26671083

2

[Clinical and genetic study of juvenile form of Huntington's disease].

Zdzienicka E, Rakowicz M, Mierzewska H, Hoffman-Zacharska D, Jakubowska T, Poniatowska R, Sułek A, Waliniowska E, Zalewska U, Kulczycki J, Zaremba J. Zdzienicka E, et al. Among authors: sulek a. Neurol Neurochir Pol. 2002 Mar-Apr;36(2):245-58. Neurol Neurochir Pol. 2002. PMID: 12046502 Polish.

3

Polymorphism of trinucleotide repeats in non-translated regions of SCA8 and SCA12 genes: allele distribution in a Polish control group.

Sułek A, Hoffman-Zacharska D, Bednarska-Makaruk M, Szirkowiec W, Zaremba J. Sułek A, et al. J Appl Genet. 2004;45(1):101-5. J Appl Genet. 2004. PMID: 14960773

4

CAG repeat polymorphism in the androgen receptor (AR) gene of SBMA patients and a control group.

Sułek A, Hoffman-Zacharska D, Krysa W, Szirkowiec W, Fidziańska E, Zaremba J. Sułek A, et al. J Appl Genet. 2005;46(2):237-9. J Appl Genet. 2005. PMID: 15876692

5

[Spinocerebellar ataxias type 1 and 2: comparison of clinical, electrophysiological and magnetic resonance evaluation].

Rakowicz M, Zdzienicka E, Poniatowska R, Waliniowska E, Sułek A, Jakubowska T, Niedzielska K, Rola R, Wierzbicka A, Hoffman-Zacharska D, Głazowski C, Jakubczyk T, Niewiadomska M, Zaremba J. Rakowicz M, et al. Among authors: sulek a. Neurol Neurochir Pol. 2005 Jul-Aug;39(4):263-275. Neurol Neurochir Pol. 2005. PMID: 16096942 Polish.

6

A phenotypic-genetic study of a group of Polish patients with spinal and bulbar muscular atrophy.

Tomik B, Partyka D, Sułek A, Kurek-Gryz EA, Banach M, Ostrowska M, Zaremba J, Figlewicz DA, Szczudlik A. Tomik B, et al. Among authors: sulek a. Amyotroph Lateral Scler. 2006 Jun;7(2):72-9. doi: 10.1080/17482960600664839. Amyotroph Lateral Scler. 2006. PMID: 16753970

7

A molecular and cytogenetic investigation of FMR1 gene premutations in Polish patients with primary ovarian insufficiency.

Rajkiewicz M, Szlendak-Sauer K, Sulek A, Gawlik-Zawislak S, Krysa W, Radowicki S, Zaremba J. Rajkiewicz M, et al. Among authors: sulek a. Eur J Obstet Gynecol Reprod Biol. 2011 Apr;155(2):176-9. doi: 10.1016/j.ejogrb.2010.12.031. Epub 2011 Jan 26. Eur J Obstet Gynecol Reprod Biol. 2011. PMID: 21276648

8

Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals.

Sulek A, Elert E, Rajkiewicz M, Zdzienicka E, Stepniak I, Krysa W, Zaremba J. Sulek A, et al. Neurol Sci. 2013 Feb;34(2):239-42. doi: 10.1007/s10072-011-0899-3. Epub 2011 Dec 28. Neurol Sci. 2013. PMID: 22203332

9

Rapid detection of large expansions in progressive myoclonus epilepsy type 1, myotonic dystrophy type 2 and spinocerebellar ataxia type 8.

Krysa W, Rajkiewicz M, Sułek A. Krysa W, et al. Among authors: sulek a. Neurol Neurochir Pol. 2012 Mar-Apr;46(2):113-20. doi: 10.5114/ninp.2012.28253. Neurol Neurochir Pol. 2012. PMID: 22581592

10

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.

Jacobi H, Reetz K, du Montcel ST, Bauer P, Mariotti C, Nanetti L, Rakowicz M, Sulek A, Durr A, Charles P, Filla A, Antenora A, Schöls L, Schicks J, Infante J, Kang JS, Timmann D, Di Fabio R, Masciullo M, Baliko L, Melegh B, Boesch S, Bürk K, Peltz A, Schulz JB, Dufaure-Garé I, Klockgether T. Jacobi H, et al. Among authors: sulek a. Lancet Neurol. 2013 Jul;12(7):650-8. doi: 10.1016/S1474-4422(13)70104-2. Epub 2013 May 22. Lancet Neurol. 2013. PMID: 23707147

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