Seif FJ - Search Results

1

Ret oncogene signal transduction via a IRS-2/PI 3-kinase/PKB and a SHC/Grb-2 dependent pathway: possible implication for transforming activity in NIH3T3 cells.

Hennige AM, Lammers R, Arlt D, Höppner W, Strack V, Niederfellner G, Seif FJ, Häring HU, Kellerer M. Hennige AM, et al. Among authors: seif fj. Mol Cell Endocrinol. 2000 Sep 25;167(1-2):69-76. doi: 10.1016/s0303-7207(00)00283-5. Mol Cell Endocrinol. 2000. PMID: 11000521

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. 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

Manifestation of thyroid autoimmunity in patients successfully treated for hypercortisolism.

Müssig K, Gallwitz B, Häring HU, Seif FJ. Müssig K, et al. Among authors: seif fj. Clin Endocrinol (Oxf). 2004 Aug;61(2):284. doi: 10.1111/j.1365-2265.2004.02100.x. Clin Endocrinol (Oxf). 2004. PMID: 15272929 No abstract available.

4

17alpha-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27Stop) in the cytochrome CYP17 gene.

Müssig K, Kaltenbach S, Machicao F, Maser-Gluth C, Hartmann MF, Wudy SA, Schnauder G, Häring HU, Seif FJ, Gallwitz B. Müssig K, et al. Among authors: seif fj. J Clin Endocrinol Metab. 2005 Jul;90(7):4362-5. doi: 10.1210/jc.2005-0136. Epub 2005 Apr 5. J Clin Endocrinol Metab. 2005. PMID: 15811924

5

The importance of multiple endocrine neoplasia syndromes in differential diagnosis.

Schaaf L, Greschner M, Geissler W, Eckert B, Seif FJ, Usadel KH. Schaaf L, et al. Among authors: seif fj. Klin Wochenschr. 1990 Jul 5;68(13):669-72. doi: 10.1007/BF01667014. Klin Wochenschr. 1990. PMID: 1974310

6

Analysis of thyroid stimulating hormone-receptor mutations by temperature-gradient gel electrophoresis.

Koch M, Wahl R, Seif FJ. Koch M, et al. Among authors: seif fj. Electrophoresis. 1995 May;16(5):742-3. doi: 10.1002/elps.11501601121. Electrophoresis. 1995. PMID: 7588555

7

Homozygous mutation within the conserved Ala-Phe-Asn-Glu-Thr motif of exon 7 of the LH receptor causes male pseudohermaphroditism.

Gromoll J, Schulz A, Borta H, Gudermann T, Teerds KJ, Greschniok A, Nieschlag E, Seif FJ. Gromoll J, et al. Among authors: seif fj. Eur J Endocrinol. 2002 Nov;147(5):597-608. doi: 10.1530/eje.0.1470597. Eur J Endocrinol. 2002. PMID: 12444891

8

Prognostic factors in medullary thyroid carcinoma: evaluation of 741 patients from the German Medullary Thyroid Carcinoma Register.

Raue F, Kotzerke J, Reinwein D, Schröder S, Röher HD, Deckart H, Höfer R, Ritter M, Seif F, Buhr H, et al. Raue F, et al. Clin Investig. 1993 Jan;71(1):7-12. doi: 10.1007/BF00210956. Clin Investig. 1993. PMID: 8095831

9

The natural course of multiple endocrine neoplasia type IIb. A study of 18 cases.

Vasen HF, van der Feltz M, Raue F, Kruseman AN, Koppeschaar HP, Pieters G, Seif FJ, Blum WF, Lips CJ. Vasen HF, et al. Among authors: seif fj. Arch Intern Med. 1992 Jun;152(6):1250-2. Arch Intern Med. 1992. PMID: 1350898

10

[Diagnosis, therapy and screening of multiple endocrine neoplasia type I (MEN I) in four endocrinologic centers].

Schaaf L, Nies G, Raue F, Tuschy U, Seif FJ, Trojan J, Usadel KU. Schaaf L, et al. Among authors: seif fj. Med Klin (Munich). 1994 Jan 15;89(1):1-6. Med Klin (Munich). 1994. PMID: 7908402 German.

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