Praulich I - Search Results

1

Patient-specific analysis of FLT3 internal tandem duplications for the prognostication and monitoring of acute myeloid leukemia.

Schiller J, Praulich I, Krings Rocha C, Kreuzer KA. Schiller J, et al. Among authors: praulich i. Eur J Haematol. 2012 Jul;89(1):53-62. doi: 10.1111/j.1600-0609.2012.01785.x. Epub 2012 May 9. Eur J Haematol. 2012. PMID: 22458420

2

Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient.

Jancuskova T, Plachy R, Zemankova L, Hardekopf DW, Stika J, Zejskova L, Praulich I, Kreuzer KA, Rothe A, Othman MA, Kosyakova N, Pekova S. Jancuskova T, et al. Among authors: praulich i. Mol Cytogenet. 2014 Jul 15;7:47. doi: 10.1186/1755-8166-7-47. eCollection 2014. Mol Cytogenet. 2014. PMID: 25071866 Free PMC article.

3

A rare case of t(11;22) in a mantle cell lymphoma like B-cell neoplasia resulting in a fusion of IGL and CCND1: case report.

Rocha CK, Praulich I, Gehrke I, Hallek M, Kreuzer KA. Rocha CK, et al. Among authors: praulich i. Mol Cytogenet. 2011 Apr 1;4(1):8. doi: 10.1186/1755-8166-4-8. Mol Cytogenet. 2011. PMID: 21457541 Free PMC article.

4

Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.

Ripperger T, Tauscher M, Praulich I, Pabst B, Teigler-Schlegel A, Yeoh A, Göhring G, Schlegelberger B, Flotho C, Niemeyer CM, Steinemann D. Ripperger T, et al. Among authors: praulich i. Br J Haematol. 2011 Oct;155(2):209-17. doi: 10.1111/j.1365-2141.2011.08817.x. Epub 2011 Aug 18. Br J Haematol. 2011. PMID: 21848520 Free article. Review.

5

Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome.

Steinemann D, Praulich I, Otto N, Göhring G, Niemeyer CM, Schlegelberger B. Steinemann D, et al. Among authors: praulich i. Br J Haematol. 2009 May;145(4):533-4. doi: 10.1111/j.1365-2141.2009.07634.x. Br J Haematol. 2009. PMID: 19298594 Free article. No abstract available.

6

Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1.

Steinemann D, Arning L, Praulich I, Stuhrmann M, Hasle H, Stary J, Schlegelberger B, Niemeyer CM, Flotho C. Steinemann D, et al. Among authors: praulich i. Haematologica. 2010 Feb;95(2):320-3. doi: 10.3324/haematol.2009.010355. Epub 2009 Dec 16. Haematologica. 2010. PMID: 20015894 Free PMC article.

7

Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.

Praulich I, Tauscher M, Göhring G, Glaser S, Hofmann W, Feurstein S, Flotho C, Lichter P, Niemeyer CM, Schlegelberger B, Steinemann D. Praulich I, et al. Genes Chromosomes Cancer. 2010 Oct;49(10):885-900. doi: 10.1002/gcc.20797. Genes Chromosomes Cancer. 2010. PMID: 20589934

8

Array-CGH in childhood MDS.

Tauscher M, Praulich I, Steinemann D. Tauscher M, et al. Among authors: praulich i. Methods Mol Biol. 2013;973:267-78. doi: 10.1007/978-1-62703-281-0_17. Methods Mol Biol. 2013. PMID: 23412796

9

Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?

Steinemann D, Tauscher M, Praulich I, Niemeyer CM, Flotho C, Schlegelberger B. Steinemann D, et al. Among authors: praulich i. Haematologica. 2010 Sep;95(9):1616. doi: 10.3324/haematol.2010.024984. Epub 2010 May 11. Haematologica. 2010. PMID: 20460640 Free PMC article. No abstract available.

10

Phenotypic spectrum of BLM- and RMI1-related Bloom syndrome.

Gönenc II, Elcioglu NH, Martinez Grijalva C, Aras S, Großmann N, Praulich I, Altmüller J, Kaulfuß S, Li Y, Nürnberg P, Burfeind P, Yigit G, Wollnik B. Gönenc II, et al. Among authors: praulich i. Clin Genet. 2022 May;101(5-6):559-564. doi: 10.1111/cge.14125. Epub 2022 Mar 11. Clin Genet. 2022. PMID: 35218564

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