Petrides PE - Search Results

1

Mutations in the von Hippel-Lindau (VHL) tumor suppressor gene and VHL-haplotype analysis in patients with presumable congenital erythrocytosis.

Cario H, Schwarz K, Jorch N, Kyank U, Petrides PE, Schneider DT, Uhle R, Debatin KM, Kohne E. Cario H, et al. Among authors: petrides pe. Haematologica. 2005 Jan;90(1):19-24. Haematologica. 2005. PMID: 15642664

2

The high oxygen-affinity Hemoglobin Johnstown [(beta 109(G11) Val-->Leu] in a German kindred with an elevated erythrocyte hemoglobin content: potential interaction with HFE mutations.

Petrides PE, Beykirch MK, Kohne E. Petrides PE, et al. Blood Cells Mol Dis. 2008 Mar-Apr;40(2):180-2. doi: 10.1016/j.bcmd.2007.08.007. Epub 2007 Oct 22. Blood Cells Mol Dis. 2008. PMID: 17950634

3

Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera.

Schnittger S, Bacher U, Haferlach C, Geer T, Müller P, Mittermüller J, Petrides P, Schlag R, Sandner R, Selbach J, Slawik HR, Tessen HW, Wehmeyer J, Kern W, Haferlach T. Schnittger S, et al. Haematologica. 2009 Mar;94(3):414-8. doi: 10.3324/haematol.13223. Haematologica. 2009. PMID: 19252176 Free PMC article.

4

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

Ivaskevicius V, Biswas A, Bevans C, Schroeder V, Kohler HP, Rott H, Halimeh S, Petrides PE, Lenk H, Krause M, Miterski B, Harbrecht U, Oldenburg J. Ivaskevicius V, et al. Among authors: petrides pe. Haematologica. 2010 Jun;95(6):956-62. doi: 10.3324/haematol.2009.017210. Epub 2010 Feb 23. Haematologica. 2010. PMID: 20179087 Free PMC article.

5

Molecular analysis of acute intermittent porphyria: mutation screening in 20 patients in Germany reveals 11 novel mutations.

von Brasch L, Zang C, Haverkamp T, Schlechte H, Heckers H, Petrides PE. von Brasch L, et al. Among authors: petrides pe. Blood Cells Mol Dis. 2004 Mar-Apr;32(2):309-14. doi: 10.1016/j.bcmd.2003.12.003. Blood Cells Mol Dis. 2004. PMID: 15003823

6

Molecular analysis of Gaucher disease: distribution of eight mutations and the complete gene deletion in 27 patients from Germany.

le Coutre P, Demina A, Beutler E, Beck M, Petrides PE. le Coutre P, et al. Among authors: petrides pe. Hum Genet. 1997 Jun;99(6):816-21. doi: 10.1007/s004390050454. Hum Genet. 1997. PMID: 9187679

7

Characterization of 35 new cases with four different MPLW515 mutations and essential thrombocytosis or primary myelofibrosis.

Schnittger S, Bacher U, Haferlach C, Beelen D, Bojko P, Bürkle D, Dengler R, Distelrath A, Eckart M, Eckert R, Fries S, Knoblich J, Köchling G, Laubenstein HP, Petrides P, Planker M, Pihusch R, Weide R, Kern W, Haferlach T. Schnittger S, et al. Haematologica. 2009 Jan;94(1):141-4. doi: 10.3324/haematol.13224. Epub 2008 Nov 23. Haematologica. 2009. PMID: 19029146 Free PMC article. No abstract available.

8

Hydroxyurea induced oscillations in twelve patients with polycythemia vera.

Tauscher J, Siegel F, Petrides PE. Tauscher J, et al. Among authors: petrides pe. Haematologica. 2010 Jul;95(7):1227-9. doi: 10.3324/haematol.2010.022178. Epub 2010 Mar 10. Haematologica. 2010. PMID: 20220068 Free PMC article. No abstract available.

9

Anagrelide for treatment of patients with chronic myelogenous leukemia and a high platelet count.

Trapp OM, Beykirch MK, Petrides PE. Trapp OM, et al. Among authors: petrides pe. Blood Cells Mol Dis. 1998 Mar;24(1):9-13. doi: 10.1006/bcmd.1998.0166. Blood Cells Mol Dis. 1998. PMID: 9516377 Clinical Trial.

10

Acute porphyrias: a German monocentric study of the biochemical, molecular genetic, and clinical data of 62 families.

Bronisch O, Stauch T, Haverkamp T, Beykirch MK, Petrides PE. Bronisch O, et al. Among authors: petrides pe. Ann Hematol. 2019 Dec;98(12):2683-2691. doi: 10.1007/s00277-019-03831-7. Epub 2019 Nov 19. Ann Hematol. 2019. PMID: 31745600 Clinical Trial.

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