Wienker T - Search Results

1

A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.

Reif A, Herterich S, Strobel A, Ehlis AC, Saur D, Jacob CP, Wienker T, Töpner T, Fritzen S, Walter U, Schmitt A, Fallgatter AJ, Lesch KP. Reif A, et al. Among authors: wienker t. Mol Psychiatry. 2006 Mar;11(3):286-300. doi: 10.1038/sj.mp.4001779. Mol Psychiatry. 2006. PMID: 16389274

2

Chymase gene locus is not associated with myocardial infarction and is not linked to heart size or blood pressure.

Pfeufer A, Busjahn A, Vergopoulos A, Knoblauch H, Urata H, Osterziel KJ, Menz M, Wienker TF, Faulhaber HD, Steinmetz A, Schuster H, Dietz R, Luft FC. Pfeufer A, et al. Among authors: wienker tf. Am J Cardiol. 1998 Oct 15;82(8):979-81. doi: 10.1016/s0002-9149(98)00518-9. Am J Cardiol. 1998. PMID: 9794357

3

Strauch et al reply.

Strauch K, Fimmers R, Wienker TF, Baur MP, Cichon S, Propping P, Nothen MM. Strauch K, et al. Mol Psychiatry. 2000 Mar;5(2):126-7. doi: 10.1038/sj.mp.4000668. Mol Psychiatry. 2000. PMID: 10822336 No abstract available.

4

An angiotensin-converting enzyme gene variant is associated with acute myocardial infarction in women but not in men.

Schuster H, Wienker TF, Stremmler U, Noll B, Steinmetz A, Luft FC. Schuster H, et al. Among authors: wienker tf. Am J Cardiol. 1995 Sep 15;76(8):601-3. doi: 10.1016/s0002-9149(99)80164-7. Am J Cardiol. 1995. PMID: 7677086

5

Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly.

Naraghi R, Schuster H, Toka HR, Bähring S, Toka O, Oztekin O, Bilginturan N, Knoblauch H, Wienker TF, Busjahn A, Haller H, Fahlbusch R, Luft FC. Naraghi R, et al. Among authors: wienker tf. Stroke. 1997 Sep;28(9):1749-54. doi: 10.1161/01.str.28.9.1749. Stroke. 1997. PMID: 9303020

6

Beta-2 adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension: The Bergen Blood Pressure Study.

Timmermann B, Mo R, Luft FC, Gerdts E, Busjahn A, Omvik P, Li GH, Schuster H, Wienker TF, Hoehe MR, Lund-Johansen P. Timmermann B, et al. Among authors: wienker tf. Kidney Int. 1998 Jun;53(6):1455-60. doi: 10.1046/j.1523-1755.1998.00926.x. Kidney Int. 1998. PMID: 9607174 Free article.

7

A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly.

Schuster H, Toka O, Toka HR, Busjahn A, Oztekin O, Wienker TF, Bilginturan N, Bähring S, Skrabal F, Haller H, Luft FC. Schuster H, et al. Among authors: wienker tf. Kidney Int. 1998 Jan;53(1):167-72. doi: 10.1046/j.1523-1755.1998.00732.x. Kidney Int. 1998. PMID: 9453014 Free article. Clinical Trial.

8

Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension.

Schuster H, Wienker TF, Toka HR, Bähring S, Jeschke E, Toka O, Busjahn A, Hempel A, Tahlhammer C, Oelkers W, Kunze J, Bilginturan N, Haller H, Luft FC. Schuster H, et al. Among authors: wienker tf. Hypertension. 1996 Dec;28(6):1085-92. doi: 10.1161/01.hyp.28.6.1085. Hypertension. 1996. PMID: 8952601

9

Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family.

Bähring S, Nagai T, Toka HR, Nitz I, Toka O, Aydin A, Mühl A, Wienker TF, Schuster H, Luft FC. Bähring S, et al. Among authors: wienker tf. Am J Hum Genet. 1997 Mar;60(3):732-5. Am J Hum Genet. 1997. PMID: 9042935 Free PMC article. No abstract available.

10

Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension.

Toka HR, Bähring S, Chitayat D, Melby JC, Whitehead R, Jeschke E, Wienker TF, Toka O, Schuster H, Luft FC. Toka HR, et al. Among authors: wienker tf. Ann Intern Med. 1998 Aug 1;129(3):204-8. doi: 10.7326/0003-4819-129-3-199808010-00008. Ann Intern Med. 1998. PMID: 9696728

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