Bähring S - Search Results

1

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.

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

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. Am J Hum Genet. 1997 Mar;60(3):732-5. Am J Hum Genet. 1997. PMID: 9042935 Free PMC article. No abstract available.

5

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

6

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

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

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: bahring s. 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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