Lohse P - Search Results

1

Impact of thrombophilic gene mutations and graft-versus-host disease on thromboembolic complications after allogeneic hematopoietic stem-cell transplantation.

Pihusch M, Lohse P, Reitberger J, Hiller E, Andreesen R, Kolb HJ, Holler E, Pihusch R. Pihusch M, et al. Among authors: lohse p. Transplantation. 2004 Sep 27;78(6):911-8. doi: 10.1097/01.tp.0000136988.38919.fb. Transplantation. 2004. PMID: 15385813

2

Impact of thrombophilic gene mutations on thrombosis risk in patients with gastrointestinal carcinoma.

Pihusch R, Danzl G, Scholz M, Harich D, Pihusch M, Lohse P, Hiller E. Pihusch R, et al. Among authors: lohse p. Cancer. 2002 Jun 15;94(12):3120-6. doi: 10.1002/cncr.10590. Cancer. 2002. PMID: 12115343 Free article.

3

Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester.

Pihusch R, Buchholz T, Lohse P, Rübsamen H, Rogenhofer N, Hasbargen U, Hiller E, Thaler CJ. Pihusch R, et al. Among authors: lohse p. Am J Reprod Immunol. 2001 Aug;46(2):124-31. doi: 10.1111/j.8755-8920.2001.460202.x. Am J Reprod Immunol. 2001. PMID: 11506076

4

Polymorphisms in the ACE and PAI-1 genes are associated with recurrent spontaneous miscarriages.

Buchholz T, Lohse P, Rogenhofer N, Kosian E, Pihusch R, Thaler CJ. Buchholz T, et al. Among authors: lohse p. Hum Reprod. 2003 Nov;18(11):2473-7. doi: 10.1093/humrep/deg474. Hum Reprod. 2003. PMID: 14585904

5

[47-year-old patient with resistant pulmonary embolism in congenital hemodynamic disorder].

Tischer J, Forstpointner R, Lohse P, Hiller E. Tischer J, et al. Among authors: lohse p. Internist (Berl). 2000 Jan;41(1):61-5. doi: 10.1007/s001080050009. Internist (Berl). 2000. PMID: 10663080 Review. German. No abstract available.

6

Substitution of cyclophosphamide and busulfan by fludarabine, treosulfan and melphalan in a preparative regimen for children and adolescents with Shwachman-Diamond syndrome.

Sauer M, Zeidler C, Meissner B, Rehe K, Hanke A, Welte K, Lohse P, Sykora KW. Sauer M, et al. Among authors: lohse p. Bone Marrow Transplant. 2007 Feb;39(3):143-7. doi: 10.1038/sj.bmt.1705553. Epub 2007 Jan 8. Bone Marrow Transplant. 2007. PMID: 17211437 Clinical Trial.

7

Paternal thrombophilic gene mutations are not associated with recurrent miscarriage.

Toth B, Vocke F, Rogenhofer N, Friese K, Thaler CJ, Lohse P. Toth B, et al. Among authors: lohse p. Am J Reprod Immunol. 2008 Oct;60(4):325-32. doi: 10.1111/j.1600-0897.2008.00630.x. Am J Reprod Immunol. 2008. PMID: 18754836

8

The number of dichorionic twin pregnancies is reduced by the common MTHFR 677C-->T mutation.

Hasbargen U, Lohse P, Thaler CJ. Hasbargen U, et al. Among authors: lohse p. Hum Reprod. 2000 Dec;15(12):2659-62. doi: 10.1093/humrep/15.12.2659. Hum Reprod. 2000. PMID: 11098041

9

Effects of the common 677C>T mutation of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene on ovarian responsiveness to recombinant follicle-stimulating hormone.

Thaler CJ, Budiman H, Ruebsamen H, Nagel D, Lohse P. Thaler CJ, et al. Among authors: lohse p. Am J Reprod Immunol. 2006 Apr;55(4):251-8. doi: 10.1111/j.1600-0897.2005.00357.x. Am J Reprod Immunol. 2006. PMID: 16533336

PROBLEM: The common 677C>T mutation of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene is less prevalent in mothers of spontaneously conceived dichorionic twins than in those with singleton pregnancies. (Hasbargen U, Lohse P, Thaler CJ: Hum Reprod 2000; …

PROBLEM: The common 677C>T mutation of the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene is less prevalent in mothers of spontane …

10

The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohn's disease.

Brand S, Staudinger T, Schnitzler F, Pfennig S, Hofbauer K, Dambacher J, Seiderer J, Tillack C, Konrad A, Crispin A, Göke B, Lohse P, Ochsenkühn T. Brand S, et al. Among authors: lohse p. Inflamm Bowel Dis. 2005 Jul;11(7):645-52. doi: 10.1097/01.mib.0000168372.94907.d2. Inflamm Bowel Dis. 2005. PMID: 15973118

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