Scheffer H - Search Results

1

ACE polymorphism does not determine short-term renal response to ACE-inhibition in proteinuric patients.

van der Kleij FG, Navis GJ, Gansevoort RT, Heeg JE, Scheffer H, de Zeeuw D, de Jong PE. van der Kleij FG, et al. Among authors: scheffer h. Nephrol Dial Transplant. 1997;12 Suppl 2:42-6. Nephrol Dial Transplant. 1997. PMID: 9269699

2

Association between angiotensin-converting-enzyme gene polymorphism and failure of renoprotective therapy.

van Essen GG, Rensma PL, de Zeeuw D, Sluiter WJ, Scheffer H, Apperloo AJ, de Jong PE. van Essen GG, et al. Among authors: scheffer h. Lancet. 1996 Jan 13;347(8994):94-5. doi: 10.1016/s0140-6736(96)90213-5. Lancet. 1996. PMID: 8538349 Clinical Trial.

3

Hereditary myokymia and paroxysmal ataxia linked to chromosome 12 is responsive to acetazolamide.

Lubbers WJ, Brunt ER, Scheffer H, Litt M, Stulp R, Browne DL, van Weerden TW. Lubbers WJ, et al. Among authors: scheffer h. J Neurol Neurosurg Psychiatry. 1995 Oct;59(4):400-5. doi: 10.1136/jnnp.59.4.400. J Neurol Neurosurg Psychiatry. 1995. PMID: 7561920 Free PMC article.

4

A highly informative dinucleotide repeat polymorphism at D13S201, between RB1 and WND.

Kooy RF, Verlind E, Wijngaard A, Shapiro DN, Scheffer H, Buys CH. Kooy RF, et al. Among authors: scheffer h. Hum Genet. 1995 May;95(5):589. doi: 10.1007/BF00223877. Hum Genet. 1995. PMID: 7759085 No abstract available.

5

The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol.

van Essen AJ, Kneppers AL, van der Hout AH, Scheffer H, Ginjaar IB, ten Kate LP, van Ommen GJ, Buys CH, Bakker E. van Essen AJ, et al. Among authors: scheffer h. J Med Genet. 1997 Oct;34(10):805-12. doi: 10.1136/jmg.34.10.805. J Med Genet. 1997. PMID: 9350811 Free PMC article.

6

The tumour necrosis factor receptor superfamily member 1b 676T>G polymorphism in relation to response to infliximab and adalimumab treatment and disease severity in rheumatoid arthritis.

Toonen EJ, Coenen MJ, Kievit W, Fransen J, Eijsbouts AM, Scheffer H, Radstake TR, Creemers MC, de Rooij DJ, van Riel PL, Franke B, Barrera P. Toonen EJ, et al. Among authors: scheffer h. Ann Rheum Dis. 2008 Aug;67(8):1174-7. doi: 10.1136/ard.2008.088138. Epub 2008 Apr 2. Ann Rheum Dis. 2008. PMID: 18385279

7

Search for genes predisposing to atopic diseases.

Scheffer H. Scheffer H. Lancet. 1996 Aug 31;348(9027):560-1. doi: 10.1016/S0140-6736(05)64793-9. Lancet. 1996. PMID: 8774564 No abstract available.

8

Number and sex of offspring of delta F508 carriers outside cystic fibrosis families.

de Vries HG, Collée JM, Meeuwsen WP, Scheffer H, Ten Kate LP. de Vries HG, et al. Among authors: scheffer h. Hum Genet. 1995 May;95(5):575-6. doi: 10.1007/BF00223873. Hum Genet. 1995. PMID: 7538971

9

Identification of key recombinants in multiplex SMA families.

van der Steege G, Cobben JM, Brahe C, Osinga J, Zappata S, Scheffer H, Neri G, van Ommen GJ, ten Kate LP, Buys CH. van der Steege G, et al. Among authors: scheffer h. Genomics. 1994 Jul 1;22(1):219-22. doi: 10.1006/geno.1994.1367. Genomics. 1994. PMID: 7959774

10

The EUROGEM map of human chromosome 13.

Kooy RF, Wijngaard A, Verlind E, Vergnaud G, Scheffer H, Buys CH. Kooy RF, et al. Among authors: scheffer h. Eur J Hum Genet. 1994;2(3):228-9. Eur J Hum Genet. 1994. PMID: 7834293 No abstract available.

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