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Best matches for Rothämel T[au]:

Molecular characterization of disseminated pilocytic astrocytomas. Gessi M et al. Neuropathol Appl Neurobiol. (2016)

Candidate gene variants of the immune system and sudden infant death syndrome. Fard D et al. Int J Legal Med. (2016)

Polymorphisms in genes of respiratory control and sudden infant death syndrome. Läer K et al. Int J Legal Med. (2015)

Search results

Items: 26

1.

Evidence for an association of interferon gene variants with sudden infant death syndrome.

Hafke A, Schürmann P, Rothämel T, Dörk T, Klintschar M.

Int J Legal Med. 2019 May;133(3):863-869. doi: 10.1007/s00414-018-1974-6. Epub 2019 Jan 8.

PMID:
30617847
2.

Transcriptomic signatures of neuronal differentiation and their association with risk genes for autism spectrum and related neuropsychiatric disorders.

Chiocchetti AG, Haslinger D, Stein JL, de la Torre-Ubieta L, Cocchi E, Rothämel T, Lindlar S, Waltes R, Fulda S, Geschwind DH, Freitag CM.

Transl Psychiatry. 2016 Aug 2;6(8):e864. doi: 10.1038/tp.2016.119.

3.

Candidate gene variants of the immune system and sudden infant death syndrome.

Fard D, Läer K, Rothämel T, Schürmann P, Arnold M, Cohen M, Vennemann M, Pfeiffer H, Bajanowski T, Pfeufer A, Dörk T, Klintschar M.

Int J Legal Med. 2016 Jul;130(4):1025-1033. doi: 10.1007/s00414-016-1347-y. Epub 2016 Mar 14.

PMID:
26975745
4.

Polymorphisms in genes of respiratory control and sudden infant death syndrome.

Läer K, Dörk T, Vennemann M, Rothämel T, Klintschar M.

Int J Legal Med. 2015 Sep;129(5):977-84. doi: 10.1007/s00414-015-1232-0. Epub 2015 Jul 22.

PMID:
26198620
5.

Molecular characterization of disseminated pilocytic astrocytomas.

Gessi M, Engels AC, Lambert S, Rothämel T, von Hornstein S, Collins VP, Denkhaus D, Gnekow A, Pietsch T.

Neuropathol Appl Neurobiol. 2016 Apr;42(3):273-8. doi: 10.1111/nan.12256. Epub 2015 Jul 20.

PMID:
26084390
6.

Mitochondrial deoxyribonucleic acid may play a role in a subset of sudden infant death syndrome cases.

Läer K, Vennemann M, Rothämel T, Klintschar M.

Acta Paediatr. 2014 Jul;103(7):775-9.

PMID:
25025098
7.

Monoamine oxidase A and sudden infant death syndrome.

Klintschar M, Rothämel T, Läer K.

J Pediatr. 2013 Nov;163(5):1533. doi: 10.1016/j.jpeds.2013.07.009. Epub 2013 Aug 20. No abstract available.

PMID:
23968743
8.

Association between polymorphisms in the P2RY1 and SSTR2 genes and sudden infant death syndrome.

Läer K, Vennemann M, Rothämel T, Klintschar M.

Int J Legal Med. 2013 Nov;127(6):1087-91. doi: 10.1007/s00414-013-0887-7. Epub 2013 Jul 5.

PMID:
23828624
9.

Activation of the B cell antigen receptor triggers reactivation of latent Kaposi's sarcoma-associated herpesvirus in B cells.

Kati S, Tsao EH, Günther T, Weidner-Glunde M, Rothämel T, Grundhoff A, Kellam P, Schulz TF.

J Virol. 2013 Jul;87(14):8004-16. doi: 10.1128/JVI.00506-13. Epub 2013 May 15.

10.

A pyrosequencing-based assay for the rapid detection of IDH1 mutations in clinical samples.

Setty P, Hammes J, Rothämel T, Vladimirova V, Kramm CM, Pietsch T, Waha A.

J Mol Diagn. 2010 Nov;12(6):750-6. doi: 10.2353/jmoldx.2010.090237. Epub 2010 Sep 16.

11.

Sensitive and rapid quantification of the cannabinoid receptor agonist naphthalen-1-yl-(1-pentylindol-3-yl)methanone (JWH-018) in human serum by liquid chromatography-tandem mass spectrometry.

Teske J, Weller JP, Fieguth A, Rothämel T, Schulz Y, Tröger HD.

J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Oct 1;878(27):2659-63. doi: 10.1016/j.jchromb.2010.03.016. Epub 2010 Mar 18.

PMID:
20378423
12.

Losses of chromosome arms 4q, 8p, 13q and gain of 8q are correlated with increasing chromosomal instability in hepatocellular carcinoma.

Hertz S, Rothämel T, Skawran B, Giere C, Steinemann D, Flemming P, Becker T, Flik J, Wiese B, Soudah B, Kreipe H, Schlegelberger B, Wilkens L.

Pathobiology. 2008;75(5):312-22. doi: 10.1159/000151712. Epub 2008 Oct 15.

13.

The German Stain Commission: recommendations for the interpretation of mixed stains.

Schneider PM, Fimmers R, Keil W, Molsberger G, Patzelt D, Pflug W, Rothämel T, Schmitter H, Schneider H, Brinkmann B.

Int J Legal Med. 2009 Jan;123(1):1-5. doi: 10.1007/s00414-008-0244-4. Epub 2008 Jul 5.

PMID:
18604547
14.

Y-chromosomal STR haplotypes in Kalmyk population samples.

Roewer L, Krüger C, Willuweit S, Nagy M, Rodig H, Kokshunova L, Rothämel T, Kravchenko S, Jobling MA, Stoneking M, Nasidze I.

Forensic Sci Int. 2007 Dec 20;173(2-3):204-9. Epub 2007 Feb 20.

PMID:
17314020
15.

Increased chimerism of bronchial and alveolar epithelium in human lung allografts undergoing chronic injury.

Kleeberger W, Versmold A, Rothämel T, Glöckner S, Bredt M, Haverich A, Lehmann U, Kreipe H.

Am J Pathol. 2003 May;162(5):1487-94.

16.

High frequency of epithelial chimerism in liver transplants demonstrated by microdissection and STR-analysis.

Kleeberger W, Rothämel T, Glöckner S, Flemming P, Lehmann U, Kreipe H.

Hepatology. 2002 Jan;35(1):110-6.

PMID:
11786966
17.

Characterization of human myocardial fibroblasts immortalized by HPV16 E6--E7 genes.

Harms W, Rothämel T, Miller K, Harste G, Grassmann M, Heim A.

Exp Cell Res. 2001 Aug 15;268(2):252-61.

PMID:
11478851
18.

Vaginorectal impalement injury in a 2-year-old child--caused by sexual abuse or an accident?

Rothämel T, Bürger D, Debertin AS, Kleemann WJ.

Forensic Sci Int. 2001 Jul 15;119(3):330-3.

PMID:
11390149
19.

Laser-assisted microdissection and short tandem repeat PCR for the investigation of graft chimerism after solid organ transplantation.

Kleeberger W, Rothämel T, Glöckner S, Lehmann U, Kreipe H.

Pathobiology. 2000;68(4-5):196-201.

PMID:
11279346
20.

Reliability of SE33 typing by capillary electrophoresis.

Rothämel T, Kleemann WJ, Tröger HD.

Forensic Sci Int. 2000 Sep 11;113(1-3):33-8.

PMID:
10978598
21.

Evaluation of serological screening of cadaveric sera for donor selection for cornea transplantation.

Heim A, Wagner D, Rothämel T, Hartmann U, Flik J, Verhagen W.

J Med Virol. 1999 Jul;58(3):291-5.

PMID:
10447426
22.

Body and head position, covering of the head by bedding and risk of sudden infant death (SID).

Kleemann WJ, Schlaud M, Fieguth A, Hiller AS, Rothämel T, Tröger HD.

Int J Legal Med. 1998;112(1):22-6.

PMID:
9932737
23.

Menin mutations in patients with multiple endocrine neoplasia type 1.

Mayr B, Apenberg S, Rothämel T, von zur Mühlen A, Brabant G.

Eur J Endocrinol. 1997 Dec;137(6):684-7.

PMID:
9437237
24.

Hyperthermia in sudden infant death.

Kleemann WJ, Schlaud M, Poets CF, Rothämel T, Tröger HD.

Int J Legal Med. 1996;109(3):139-42.

PMID:
8956988
25.

[Subendocardial hemorrhage from the forensic medicine viewpoint].

Keil W, Rothämel T, Tröger HD.

Beitr Gerichtl Med. 1991;49:45-53. German.

PMID:
1811532
26.

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