Krajewska-Walasek M - Search Results

1

Cranial MRI in the Nijmegen breakage syndrome.

Bekiesińska-Figatowska M, Chrzanowska KH, Sikorska J, Walecki J, Krajewska-Walasek M, Jóźwiak S, Kleijer WJ. Bekiesińska-Figatowska M, et al. Neuroradiology. 2000 Jan;42(1):43-7. doi: 10.1007/s002340050011. Neuroradiology. 2000. PMID: 10663471

2

Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome.

Chrzanowska KH, Kleijer WJ, Krajewska-Walasek M, Białecka M, Gutkowska A, Goryluk-Kozakiewicz B, Michałkiewicz J, Stachowski J, Gregorek H, Lysón-Wojciechowska G, et al. Chrzanowska KH, et al. Am J Med Genet. 1995 Jul 3;57(3):462-71. doi: 10.1002/ajmg.1320570321. Am J Med Genet. 1995. PMID: 7545870 Review.

3

High prevalence of primary ovarian insufficiency in girls and young women with Nijmegen breakage syndrome: evidence from a longitudinal study.

Chrzanowska KH, Szarras-Czapnik M, Gajdulewicz M, Kalina MA, Gajtko-Metera M, Walewska-Wolf M, Szufladowicz-Wozniak J, Rysiewski H, Gregorek H, Cukrowska B, Syczewska M, Piekutowska-Abramczuk D, Janas R, Krajewska-Walasek M. Chrzanowska KH, et al. J Clin Endocrinol Metab. 2010 Jul;95(7):3133-40. doi: 10.1210/jc.2009-2628. Epub 2010 May 5. J Clin Endocrinol Metab. 2010. PMID: 20444919

4

The Dubowitz syndrome--one more case.

Chrzanowska KH, Krajewska-Walasek M. Chrzanowska KH, et al. Klin Padiatr. 1987 Sep-Oct;199(5):370-2. doi: 10.1055/s-2008-1026822. Klin Padiatr. 1987. PMID: 3316825 Review.

5

A further report of Brachmann-de Lange syndrome in two sibs with normal parents.

Krajewska-Walasek M, Chrzanowska K, Tylki-Szymańska A, Białecka M. Krajewska-Walasek M, et al. Clin Genet. 1995 Jun;47(6):324-7. doi: 10.1111/j.1399-0004.1995.tb03974.x. Clin Genet. 1995. PMID: 7554368 Review.

6

Kabuki (Niikawa-Kuroki) syndrome associated with immunodeficiency.

Chrzanowska KH, Krajewska-Walasek M, Kuś J, Michałkiewicz J, Maziarka D, Wolski JK, Brecevic L, Madaliński K. Chrzanowska KH, et al. Clin Genet. 1998 Apr;53(4):308-12. doi: 10.1111/j.1399-0004.1998.tb02702.x. Clin Genet. 1998. PMID: 9650771

7

Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients.

Chrzanowska KH, Fryns JP, Krajewska-Walasek M, Wisniewski L, Van den Berghe H. Chrzanowska KH, et al. Clin Genet. 1989 Feb;35(2):157-60. doi: 10.1111/j.1399-0004.1989.tb02922.x. Clin Genet. 1989. PMID: 2721025

8

Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: a variant example of the Lenz-Majewski syndrome.

Chrzanowska KH, Fryns JP, Krajewska-Walasek M, Van den Berghe H, Wisniewski L. Chrzanowska KH, et al. Am J Med Genet. 1989 Apr;32(4):470-4. doi: 10.1002/ajmg.1320320407. Am J Med Genet. 1989. PMID: 2773987

9

Minimal clinical findings in a patient with 15qter microdeletion syndrome: delineation of the associated phenotype.

Jezela-Stanek A, Kucharczyk M, Pelc M, Chrzanowska KH, Krajewska-Walasek M. Jezela-Stanek A, et al. Am J Med Genet A. 2012 Apr;158A(4):922-6. doi: 10.1002/ajmg.a.34440. Epub 2012 Feb 17. Am J Med Genet A. 2012. PMID: 22344789 No abstract available.

10

History and molecular characteristics of a patient with terminal deletion of 14q. Is this another syndrome with a striking phenotype?

Jezela-Stanek A, Kucharczyk M, Gutkowska A, Pelc M, Ciara E, Chrzanowska KH, Krajewska-Walasek M. Jezela-Stanek A, et al. Clin Dysmorphol. 2012 Apr;21(2):97-100. doi: 10.1097/MCD.0b013e32834e92b8. Clin Dysmorphol. 2012. PMID: 22391620 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

151 results

Search Page