Gathof BS - Search Results

1

The restriction enzyme Mse I applied for the detection of a possibly common mutation of the APRT locus.

Gathof BS, Zöllner N. Gathof BS, et al. Clin Investig. 1992 Jun;70(6):535. doi: 10.1007/BF00210238. Clin Investig. 1992. PMID: 1392421 No abstract available.

2

A splice mutation at the adenine phosphoribosyltransferase locus detected in a German family.

Gathof BS, Sahota A, Gresser U, Chen J, Stambrook PS, Tischfield JA, Zöllner N. Gathof BS, et al. Adv Exp Med Biol. 1991;309B:83-6. doi: 10.1007/978-1-4615-7703-4_18. Adv Exp Med Biol. 1991. PMID: 1685862 No abstract available.

3

Identification of a splice mutation at the adenine phosphoribosyltransferase locus in a German family.

Gathof BS, Sahota A, Gresser U, Chen J, Stambrook PJ, Tischfield JA, Zöllner N. Gathof BS, et al. Klin Wochenschr. 1990 Dec 30;69(24):1152-5. doi: 10.1007/BF01815434. Klin Wochenschr. 1990. PMID: 2135300

4

Uric acid levels in southern Germany in 1989. A comparison with studies from 1962, 1971, and 1984.

Gresser U, Gathof B, Zöllner N. Gresser U, et al. Klin Wochenschr. 1990 Dec 17;68(24):1222-8. doi: 10.1007/BF01796514. Klin Wochenschr. 1990. PMID: 2290309

5

Importance of the confounding factors age and sex in the correlation of serum uric acid, cholesterol and triglyceride levels.

Gathof BS, Schreiber MA, Gresser U, Kamilli I, Zöllner N. Gathof BS, et al. Adv Exp Med Biol. 1991;309A:231-4. doi: 10.1007/978-1-4899-2638-8_52. Adv Exp Med Biol. 1991. PMID: 1789214 No abstract available.

6

Pleural effusions in acute mononucleosis.

Gathof BS, Kamilli I, Keller C, Zöllner N. Gathof BS, et al. Bildgebung. 1991;58(4):218-20. Bildgebung. 1991. PMID: 1797252 Review.

7

[Abdominal aortic aneurysm as incidental finding in echographic study of the abdomen].

Zoller WG, Gathof BS, Zöllner N. Zoller WG, et al. Among authors: gathof bs. Ned Tijdschr Geneeskd. 1993 Jan 9;137(2):98-9. Ned Tijdschr Geneeskd. 1993. PMID: 8421536 Dutch. No abstract available.

8

Novel initiation codon mutation Met1Thr identified in a patient with partial hypoxanthine-guanine phosphoribosyltransferase (HPRT) deficiency.

Gathof BS, Geissler J, Wingen AM, Gresser U. Gathof BS, et al. Hum Mutat. 1996;7(2):184. doi: 10.1002/humu.1380070204. Hum Mutat. 1996. PMID: 8829646 No abstract available.

9

HPRT-mutations in Italian Lesch-Nyhan patients.

Gathof BS, Rocchigiani M, Micheli V, Gaigl Z, Gresser U. Gathof BS, et al. Adv Exp Med Biol. 1998;431:151-3. doi: 10.1007/978-1-4615-5381-6_29. Adv Exp Med Biol. 1998. PMID: 9598049 No abstract available.

10

Partial HGPRT-deficiency, pheochromocytoma and erythrocytosis.

Kamilli I, Gresser U, Gathof BS, Gröbner W. Kamilli I, et al. Among authors: gathof bs. J Inherit Metab Dis. 1993;16(2):484-5. doi: 10.1007/BF00710301. J Inherit Metab Dis. 1993. PMID: 8412009 No abstract available.

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