Repa C - Search Results

1

Severe impairment of regulatory T-cells and Th1-lymphocyte polarization in patients with Gaucher disease.

Sotiropoulos C, Theodorou G, Repa C, Marinakis T, Verigou E, Solomou E, Karakantza M, Symeonidis A. Sotiropoulos C, et al. Among authors: repa c. JIMD Rep. 2015;18:107-15. doi: 10.1007/8904_2014_357. Epub 2014 Oct 12. JIMD Rep. 2015. PMID: 25308560 Free PMC article.

2

Dendritic cells in patients with type I Gaucher disease are decreased in number but functionally normal.

Micheva I, Marinakis T, Repa C, Kouraklis-Symeonidis A, Vlacha V, Anagnostopoulos N, Zoumbos N, Symeonidis A. Micheva I, et al. Among authors: repa c. Blood Cells Mol Dis. 2006 Mar-Apr;36(2):298-307. doi: 10.1016/j.bcmd.2005.12.029. Epub 2006 Mar 13. Blood Cells Mol Dis. 2006. PMID: 16533613

3

Subtelomeric rearrangements as neutral genomic polymorphisms.

Hengstschläger M, Prusa A, Repa C, Deutinger J, Pollak A, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Am J Med Genet A. 2005 Feb 15;133A(1):48-52. doi: 10.1002/ajmg.a.30520. Am J Med Genet A. 2005. PMID: 15637704 Review.

4

Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: a new case and discussion of the literature.

Hengstschläger M, Mittermayer C, Repa C, Drahonsky R, Deutinger J, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Fetal Diagn Ther. 2004 Nov-Dec;19(6):510-2. doi: 10.1159/000080164. Fetal Diagn Ther. 2004. PMID: 15539876 Review.

5

Prenatal diagnosis of tetrasomy 9p with Dandy-Walker malformation.

Hengstschläger M, Bettelheim D, Drahonsky R, Repa C, Deutinger J, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Prenat Diagn. 2004 Aug;24(8):623-6. doi: 10.1002/pd.933. Prenat Diagn. 2004. PMID: 15305350

6

Patient with partial trisomy 9q and learning disability but no pyloric stenosis.

Hengstschläger M, Prusa AR, Repa C, Drahonsky R, Deutinger J, Pollak A, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Dev Med Child Neurol. 2004 Jan;46(1):57-9. doi: 10.1017/s0012162204000106. Dev Med Child Neurol. 2004. PMID: 14974649 Free article.

7

Prenatal diagnosis of a de novo inversion of chromosome (2)(p21q11).

Hengstschläger M, Mittermayer C, Prusa AR, Drahonsky R, Repa C, Deutinger J, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Arch Gynecol Obstet. 2003 Aug;268(3):230-2. doi: 10.1007/s00404-002-0313-8. Epub 2002 May 15. Arch Gynecol Obstet. 2003. PMID: 12942256 Review.

8

Sex chromosome aberrations and transsexualism.

Hengstschläger M, van Trotsenburg M, Repa C, Marton E, Huber JC, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Fertil Steril. 2003 Mar;79(3):639-40. doi: 10.1016/s0015-0282(02)04805-7. Fertil Steril. 2003. PMID: 12620457 Free article. No abstract available.

9

A fetus with trisomy 9p and trisomy 10p originating from unbalanced segregation of a maternal complex chromosome rearrangement t(4;10;9).

Hengstschläger M, Bettelheim D, Repa C, Lang S, Deutinger J, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Fetal Diagn Ther. 2002 Jul-Aug;17(4):243-6. doi: 10.1159/000063401. Fetal Diagn Ther. 2002. PMID: 12065954

10

Extended prenatal survival of a non-mosaic trisomy 22 with aneuploid cytotrophoblasts.

Hengstschläger M, Bettelheim D, Rosner M, Repa C, Deutinger J, Bernaschek G. Hengstschläger M, et al. Among authors: repa c. Prenat Diagn. 2001 Oct;21(10):897-9. doi: 10.1002/pd.154. Prenat Diagn. 2001. PMID: 11746140 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

16 results

Search Page