Höppner W - Search Results

1

Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.

Ritter MM, Frilling A, Crossey PA, Höppner W, Maher ER, Mulligan L, Ponder BA, Engelhardt D. Ritter MM, et al. Among authors: hoppner w. J Clin Endocrinol Metab. 1996 Mar;81(3):1035-7. doi: 10.1210/jcem.81.3.8772572. J Clin Endocrinol Metab. 1996. PMID: 8772572

2

Mutations of the ret protooncogene in German multiple endocrine neoplasia families: relation between genotype and phenotype. German Medullary Thyroid Carcinoma Study Group.

Frank-Raue K, Höppner W, Frilling A, Kotzerke J, Dralle H, Haase R, Mann K, Seif F, Kirchner R, Rendl J, Deckart HF, Ritter MM, Hampel R, Klempa J, Scholz GH, Raue F. Frank-Raue K, et al. Among authors: hoppner w. J Clin Endocrinol Metab. 1996 May;81(5):1780-3. doi: 10.1210/jcem.81.5.8626834. J Clin Endocrinol Metab. 1996. PMID: 8626834

3

A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A.

Berndt I, Reuter M, Saller B, Frank-Raue K, Groth P, Grussendorf M, Raue F, Ritter MM, Höppner W. Berndt I, et al. Among authors: hoppner w. J Clin Endocrinol Metab. 1998 Mar;83(3):770-4. doi: 10.1210/jcem.83.3.4619. J Clin Endocrinol Metab. 1998. PMID: 9506724

4

Presymptomatic genetic screening in families with multiple endocrine neoplasia type 2.

Frilling A, Höppner W, Eng C, Mulligan L, Raue F, Broelsch CE. Frilling A, et al. Among authors: hoppner w. J Mol Med (Berl). 1995 May;73(5):229-33. doi: 10.1007/BF00189922. J Mol Med (Berl). 1995. PMID: 7670926

5

A duplication of 12 bp in the critical cysteine rich domain of the RET proto-oncogene results in a distinct phenotype of multiple endocrine neoplasia type 2A.

Höppner W, Ritter MM. Höppner W, et al. Hum Mol Genet. 1997 Apr;6(4):587-90. doi: 10.1093/hmg/6.4.587. Hum Mol Genet. 1997. PMID: 9097963

6

[Multiple endocrine neoplasia].

Ritter MM, Höppner W. Ritter MM, et al. Among authors: hoppner w. Internist (Berl). 1999 May;40(5):486-92. doi: 10.1007/s001080050362. Internist (Berl). 1999. PMID: 10407758 Review. German. No abstract available.

7

Prophylactic thyroidectomy in 75 children and adolescents with hereditary medullary thyroid carcinoma: German and Austrian experience.

Dralle H, Gimm O, Simon D, Frank-Raue K, Görtz G, Niederle B, Wahl RA, Koch B, Walgenbach S, Hampel R, Ritter MM, Spelsberg F, Heiss A, Hinze R, Höppner W. Dralle H, et al. Among authors: hoppner w. World J Surg. 1998 Jul;22(7):744-50; discussion 750-1. doi: 10.1007/s002689900463. World J Surg. 1998. PMID: 9606292

8

Diagnosis and management of pheochromocytomas in patients with multiple endocrine neoplasia type 2-relevance of specific mutations in the RET proto-oncogene.

Frank-Raue K, Kratt T, Höppner W, Buhr H, Ziegler R, Raue F. Frank-Raue K, et al. Among authors: hoppner w. Eur J Endocrinol. 1996 Aug;135(2):222-5. doi: 10.1530/eje.0.1350222. Eur J Endocrinol. 1996. PMID: 8810737

9

Application of genetic screening in families with hereditary medullary thyroid carcinoma.

Frank-Raue K, Höppner W, Buhr H, Herfarth C, Ziegler R, Raue F. Frank-Raue K, et al. Among authors: hoppner w. Exp Clin Endocrinol Diabetes. 1996;104 Suppl 4:108-10. doi: 10.1055/s-0029-1211715. Exp Clin Endocrinol Diabetes. 1996. PMID: 8981015

10

Developing effective screening strategies in multiple endocrine neoplasia type 1 (MEN 1) on the basis of clinical and sequencing data of German patients with MEN 1.

Schaaf L, Pickel J, Zinner K, Hering U, Höfler M, Goretzki PE, Spelsberg F, Raue F, von zur Mühlen A, Gerl H, Hensen J, Bartsch DK, Rothmund M, Schneyer U, Dralle H, Engelbach M, Karges W, Stalla GK, Höppner W. Schaaf L, et al. Among authors: hoppner w. Exp Clin Endocrinol Diabetes. 2007 Sep;115(8):509-17. doi: 10.1055/s-2007-970160. Exp Clin Endocrinol Diabetes. 2007. PMID: 17853334

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