Mazurczak T - Search Results

1

[Monogenic causes of nonspecific X-linked mental retardation molecular aspects].

Nawara M, Bal J, Mazurczak T. Nawara M, et al. Among authors: mazurczak t. Med Wieku Rozwoj. 2002 Oct-Dec;6(4):281-94. Med Wieku Rozwoj. 2002. PMID: 12810981 Review. Polish.

2

The ARX mutations: a frequent cause of X-linked mental retardation.

Nawara M, Szczaluba K, Poirier K, Chrzanowska K, Pilch J, Bal J, Chelly J, Mazurczak T. Nawara M, et al. Among authors: mazurczak t. Am J Med Genet A. 2006 Apr 1;140(7):727-32. doi: 10.1002/ajmg.a.31151. Am J Med Genet A. 2006. PMID: 16523516

3

[Attention deficit hyperactivity disorder (ADHD)--molecular and genetic aspects].

Migdalska A, Nawara M, Bal J, Mazurczak T. Migdalska A, et al. Among authors: mazurczak t. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):343-54. Med Wieku Rozwoj. 2006. PMID: 17028398 Review. Polish.

4

Novel mutation of IL1RAPL1 gene in a nonspecific X-linked mental retardation (MRX) family.

Nawara M, Klapecki J, Borg K, Jurek M, Moreno S, Tryfon J, Bal J, Chelly J, Mazurczak T. Nawara M, et al. Among authors: mazurczak t. Am J Med Genet A. 2008 Dec 15;146A(24):3167-72. doi: 10.1002/ajmg.a.32613. Am J Med Genet A. 2008. PMID: 19012350

5

[Gene mapping in 14 families with X-linked nonspecific mental retardation].

Nawara M, Jurek M, Bal J, Mazurczak T. Nawara M, et al. Among authors: mazurczak t. Med Wieku Rozwoj. 2009 Apr-Jun;13(2):94-113. Med Wieku Rozwoj. 2009. PMID: 19837990 Polish.

6

[Prenatal diagnosis of spinal muscular atrophy (SMA) -- indications, restrictions, interpretation of results].

Jedrzejowska M, Zimowski J, Wiszniewski W, Sielska D, Bal J, Mazurczak T, Hausmanowa-Petrusewicz I, Zaremba J. Jedrzejowska M, et al. Among authors: mazurczak t. Med Wieku Rozwoj. 2004 Jul-Sep;8(3 Pt 2):651-61. Med Wieku Rozwoj. 2004. PMID: 15858238 Polish.

7

[Prenatal diagnosis of cystic fibrosis in risk families in Poland--results of molecular analysis].

Bal J, Sobczyńska-Tomaszewska A, Czerska K, Obersztyn E, Sands D, Mazurczak T. Bal J, et al. Among authors: mazurczak t. Med Wieku Rozwoj. 2004 Oct-Dec;8(4 Pt 1):871-83. Med Wieku Rozwoj. 2004. PMID: 15951608 Polish.

8

Molecular analysis of defects in the CFTR gene and AZF locus of the Y chromosome in male infertility.

Sobczyńska-Tomaszewska A, Bak D, Wolski JK, Bablok L, Nawara M, Mazurczak T, Bal J. Sobczyńska-Tomaszewska A, et al. Among authors: mazurczak t. J Reprod Med. 2006 Feb;51(2):120-7. J Reprod Med. 2006. PMID: 16572913

9

[Characterization of marker chromosomes using molecular cytogenetic methods in patients with mental retardation and congenital malformations].

Bocian E, Nowakowska B, Obersztyn E, Borg K, Chudoba I, Kostyk E, Kruczek A, Pietrzyk J, Mazurczak T. Bocian E, et al. Among authors: mazurczak t. Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):211-25. Med Wieku Rozwoj. 2006. PMID: 17028390 Polish.

10

A family with paroxysmal nonkinesigenic dyskinesia: genetic and treatment issues.

Szczałuba K, Jurek M, Szczepanik E, Friedman A, Milewski M, Bal J, Mazurczak T. Szczałuba K, et al. Among authors: mazurczak t. Pediatr Neurol. 2009 Aug;41(2):135-8. doi: 10.1016/j.pediatrneurol.2009.02.013. Pediatr Neurol. 2009. PMID: 19589464

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