Bähring S - Search Results

1

The BK channel beta1 subunit gene is associated with human baroreflex and blood pressure regulation.

Gollasch M, Tank J, Luft FC, Jordan J, Maass P, Krasko C, Sharma AM, Busjahn A, Bähring S. Gollasch M, et al. Among authors: bahring s. J Hypertens. 2002 May;20(5):927-33. doi: 10.1097/00004872-200205000-00028. J Hypertens. 2002. PMID: 12011654

2

Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12.

Schuster H, Wienker TE, Bähring S, Bilginturan N, Toka HR, Neitzel H, Jeschke E, Toka O, Gilbert D, Lowe A, Ott J, Haller H, Luft FC. Schuster H, et al. Among authors: bahring s. Nat Genet. 1996 May;13(1):98-100. doi: 10.1038/ng0596-98. Nat Genet. 1996. PMID: 8673114

3

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: bahring s. Hypertension. 1996 Dec;28(6):1085-92. doi: 10.1161/01.hyp.28.6.1085. Hypertension. 1996. PMID: 8952601

4

Twin zygosity. Automated determination with microsatellites.

Becker A, Busjahn A, Faulhaber HD, Bähring S, Robertson J, Schuster H, Luft FC. Becker A, et al. Among authors: bahring s. J Reprod Med. 1997 May;42(5):260-6. J Reprod Med. 1997. PMID: 9172114

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: bahring s. Stroke. 1997 Sep;28(9):1749-54. doi: 10.1161/01.str.28.9.1749. Stroke. 1997. PMID: 9303020

6

Oligonucleotide ligation assay for detection of apolipoprotein E polymorphisms.

Baron H, Fung S, Aydin A, Bähring S, Jeschke E, Luft FC, Schuster H. Baron H, et al. Among authors: bahring s. Clin Chem. 1997 Oct;43(10):1984-6. Clin Chem. 1997. PMID: 9342023 No abstract available.

7

A xanthomatosis-susceptibility gene may exist in a Syrian family with familial hypercholesterolemia.

Vergopoulos A, Bajari T, Jouma M, Knoblauch H, Aydin A, Bähring S, Mueller-Myhsok B, Dresel A, Joubran R, Luft FC, Schuster H. Vergopoulos A, et al. Among authors: bahring s. Eur J Hum Genet. 1997 Sep-Oct;5(5):315-23. Eur J Hum Genet. 1997. PMID: 9412789

8

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: bahring s. 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.

9

Oligonucleotide ligation assay (OLA) for the diagnosis of familial hypercholesterolemia.

Baron H, Fung S, Aydin A, Bähring S, Luft FC, Schuster H. Baron H, et al. Among authors: bahring s. Nat Biotechnol. 1996 Oct;14(10):1279-82. doi: 10.1038/nbt1096-1279. Nat Biotechnol. 1996. PMID: 9631093

10

A new mutation in the elastin gene causing supravalvular aortic stenosis.

Boeckel T, Dierks A, Vergopoulos A, Bähring S, Knoblauch H, Müller-Myhsok B, Baron H, Aydin A, Bein G, Luft FC, Schuster H. Boeckel T, et al. Among authors: bahring s. Am J Cardiol. 1999 Apr 1;83(7):1141-3, A9-10. doi: 10.1016/s0002-9149(99)00032-6. Am J Cardiol. 1999. PMID: 10190538

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