Leis T - Search Results

1

HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disorders.

Reuter MS, Sass JO, Leis T, Köhler J, Mayr JA, Feichtinger RG, Rauh M, Schanze I, Bähr L, Trollmann R, Uebe S, Ekici AB, Reis A. Reuter MS, et al. Among authors: leis t. Am J Med Genet A. 2014 Dec;164A(12):3162-9. doi: 10.1002/ajmg.a.36766. Epub 2014 Sep 23. Am J Med Genet A. 2014. PMID: 25251209

2

A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells.

Gillert E, Leis T, Repp R, Reichel M, Hösch A, Breitenlohner I, Angermüller S, Borkhardt A, Harbott J, Lampert F, Griesinger F, Greil J, Fey GH, Marschalek R. Gillert E, et al. Among authors: leis t. Oncogene. 1999 Aug 19;18(33):4663-71. doi: 10.1038/sj.onc.1202842. Oncogene. 1999. PMID: 10467413

3

Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: almost identical MLL breakpoints in therapy-related AML after treatment without etoposides.

Langer T, Metzler M, Reinhardt D, Viehmann S, Borkhardt A, Reichel M, Stanulla M, Schrappe M, Creutzig U, Ritter J, Leis T, Jacobs U, Harbott J, Beck JD, Rascher W, Repp R. Langer T, et al. Among authors: leis t. Genes Chromosomes Cancer. 2003 Apr;36(4):393-401. doi: 10.1002/gcc.10167. Genes Chromosomes Cancer. 2003. PMID: 12619163

4

Biased distribution of chromosomal breakpoints involving the MLL gene in infants versus children and adults with t(4;11) ALL.

Reichel M, Gillert E, Angermüller S, Hensel JP, Heidel F, Lode M, Leis T, Biondi A, Haas OA, Strehl S, Panzer-Grümayer ER, Griesinger F, Beck JD, Greil J, Fey GH, Uckun FM, Marschalek R. Reichel M, et al. Among authors: leis t. Oncogene. 2001 May 24;20(23):2900-7. doi: 10.1038/sj.onc.1204401. Oncogene. 2001. PMID: 11420702

5

Cloning and characterization of AFX, the gene that fuses to MLL in acute leukemias with a t(X;11)(q13;q23).

Borkhardt A, Repp R, Haas OA, Leis T, Harbott J, Kreuder J, Hammermann J, Henn T, Lampert F. Borkhardt A, et al. Among authors: leis t. Oncogene. 1997 Jan 16;14(2):195-202. doi: 10.1038/sj.onc.1200814. Oncogene. 1997. PMID: 9010221

6

A new fingerprint method for sequence analysis of chromosomal translocations at the genomic DNA level.

Leis T, Repp R, Borkhardt A, Metzler M, Schläger F, Harbott J, Lampert F. Leis T, et al. Leukemia. 1998 May;12(5):758-63. doi: 10.1038/sj.leu.2401006. Leukemia. 1998. PMID: 9593275

7

Drug utilisation on a preterm and neonatal intensive care unit in Germany: a prospective, cohort-based analysis.

Neubert A, Lukas K, Leis T, Dormann H, Brune K, Rascher W. Neubert A, et al. Among authors: leis t. Eur J Clin Pharmacol. 2010 Jan;66(1):87-95. doi: 10.1007/s00228-009-0722-8. Epub 2009 Sep 16. Eur J Clin Pharmacol. 2010. PMID: 19756556

8

Prospective assessment of complications associated with ultrasound activated resorbable pin osteosynthesis in pediatric craniofacial surgery: preliminary results.

Nkenke E, Vairaktaris E, Schwarz S, Eyüpoglu I, Ganslandt O, Leis T, Knipfer C, Stelzle F. Nkenke E, et al. Among authors: leis t. Neurocirugia (Astur). 2011 Dec;22(6):498-506. doi: 10.1016/s1130-1473(11)70105-1. Neurocirugia (Astur). 2011. PMID: 22167280

9

Intrafamilial neurological phenotypic variability due to either biallelic or monoallelic pathogenic variants in CACNA1A.

Mammadova D, Kraus C, Leis T, Popp B, Zweier C, Reis A, Trollmann R. Mammadova D, et al. Among authors: leis t. Front Neurol. 2024 Oct 2;15:1458109. doi: 10.3389/fneur.2024.1458109. eCollection 2024. Front Neurol. 2024. PMID: 39416668 Free PMC article.

10

Reintegrating seriously violent and personality-disordered offenders from a supermaximum security institution into the general offender population.

Wong SC, Veen SV, Leis TA, Parrish H, Gu D, Liber EU, Middleton HL. Wong SC, et al. Among authors: leis ta. Int J Offender Ther Comp Criminol. 2005 Aug;49(4):362-75. doi: 10.1177/0306624X05274501. Int J Offender Ther Comp Criminol. 2005. PMID: 15983052

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