Deutz-Terlouw PP - Search Results

1

Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460.

Bertina RM, Ploos van Amstel HK, van Wijngaarden A, Coenen J, Leemhuis MP, Deutz-Terlouw PP, van der Linden IK, Reitsma PH. Bertina RM, et al. Among authors: deutz terlouw pp. Blood. 1990 Aug 1;76(3):538-48. Blood. 1990. PMID: 2143091 Free article.

2

Two ELISA's for measurement of protein S, and their use in the laboratory diagnosis of protein S deficiency.

Deutz-Terlouw PP, Ballering L, van Wijngaarden A, Bertina RM. Deutz-Terlouw PP, et al. Clin Chim Acta. 1990 Jan 31;186(3):321-34. doi: 10.1016/0009-8981(90)90318-m. Clin Chim Acta. 1990. PMID: 2138066

3

Application of two neutral MspI DNA polymorphisms in the analysis of hereditary protein C deficiency.

Reitsma PH, te Lintel Hekkert W, Koenhen E, van der Velden PA, Allaart CF, Deutz-Terlouw PP, Poort SR, Bertina RM. Reitsma PH, et al. Among authors: deutz terlouw pp. Thromb Haemost. 1990 Oct 22;64(2):239-44. Thromb Haemost. 1990. PMID: 1702905

4

Immunoradiometric assay for the calcium-stabilized conformation of human protein S.

Poort SR, Deutz-Terlouw PP, van Wijngaarden A, Bertina RM. Poort SR, et al. Thromb Haemost. 1987 Dec 18;58(4):998-1004. Thromb Haemost. 1987. PMID: 2965428

5

Immunoradiometric assays for the Ca(II)-dependent and Ca(II)-independent conformation of human protein C.

Poort SR, Deutz-Terlouw PP, van Wijngaarden A, Bertina RM. Poort SR, et al. Thromb Res. 1988 Oct 15;52(2):87-100. doi: 10.1016/0049-3848(88)90087-4. Thromb Res. 1988. PMID: 3194894

6

Screening for mutations in haemophilia A patients by multiplex PCR-SSCP, Southern blotting and RNA analysis: the detection of a genetic abnormality in the factor VIII gene in 30 out of 35 patients.

Pieneman WC, Deutz-Terlouw PP, Reitsma PH, Briët E. Pieneman WC, et al. Among authors: deutz terlouw pp. Br J Haematol. 1995 Jun;90(2):442-9. doi: 10.1111/j.1365-2141.1995.tb05108.x. Br J Haematol. 1995. PMID: 7794769

7

Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients.

Arruda VR, Pieneman WC, Reitsma PH, Deutz-Terlouw PP, Annichino-Bizzacchi JM, Briët E, Costa FF. Arruda VR, et al. Among authors: deutz terlouw pp. Blood. 1995 Oct 15;86(8):3015-20. Blood. 1995. PMID: 7579394 Free article.

8

Point mutation screening for 16 exons of the dystrophin gene by multiplex single-strand conformation polymorphism analysis.

Kneppers AL, Deutz-Terlouw PP, den Dunnen JT, van Ommen GJ, Bakker E. Kneppers AL, et al. Among authors: deutz terlouw pp. Hum Mutat. 1995;5(3):235-42. doi: 10.1002/humu.1380050308. Hum Mutat. 1995. PMID: 7599634

9

Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.

Deutz-Terlouw PP, Losekoot M, Olmer R, Pieneman WC, de Vries-v d Weerd S, Briët E, Bakker E. Deutz-Terlouw PP, et al. J Med Genet. 1995 Apr;32(4):296-300. doi: 10.1136/jmg.32.4.296. J Med Genet. 1995. PMID: 7643361 Free PMC article.

10

Asn540Thr substitution in the fibroblast growth factor receptor 3 tyrosine kinase domain causing hypochondroplasia.

Deutz-Terlouw PP, Losekoot M, Aalfs CM, Hennekam RC, Bakker E. Deutz-Terlouw PP, et al. Hum Mutat. 1998;Suppl 1:S62-5. doi: 10.1002/humu.1380110122. Hum Mutat. 1998. PMID: 9452043 No abstract available.

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