Frilling A - Search Results

1

Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation.

Gimm O, Marsh DJ, Andrew SD, Frilling A, Dahia PL, Mulligan LM, Zajac JD, Robinson BG, Eng C. Gimm O, et al. Among authors: frilling a. J Clin Endocrinol Metab. 1997 Nov;82(11):3902-4. doi: 10.1210/jcem.82.11.4508. J Clin Endocrinol Metab. 1997. PMID: 9360560

2

Presymptomatic DNA screening in families with multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma.

Frilling A, Dralle H, Eng C, Raue F, Broelsch CE. Frilling A, et al. Surgery. 1995 Dec;118(6):1099-103; discussion 1103-4. doi: 10.1016/s0039-6060(05)80120-5. Surgery. 1995. PMID: 7491529

3

Mutation of the RET protooncogene in sporadic medullary thyroid carcinoma.

Eng C, Mulligan LM, Smith DP, Healey CS, Frilling A, Raue F, Neumann HP, Pfragner R, Behmel A, Lorenzo MJ, et al. Eng C, et al. Among authors: frilling a. Genes Chromosomes Cancer. 1995 Mar;12(3):209-12. doi: 10.1002/gcc.2870120308. Genes Chromosomes Cancer. 1995. PMID: 7536460

4

Low frequency of germline mutations in the RET proto-oncogene in patients with apparently sporadic medullary thyroid carcinoma.

Eng C, Mulligan LM, Smith DP, Healey CS, Frilling A, Raue F, Neumann HP, Ponder MA, Ponder BA. Eng C, et al. Among authors: frilling a. Clin Endocrinol (Oxf). 1995 Jul;43(1):123-7. doi: 10.1111/j.1365-2265.1995.tb01903.x. Clin Endocrinol (Oxf). 1995. PMID: 7641404

5

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. J Mol Med (Berl). 1995 May;73(5):229-33. doi: 10.1007/BF00189922. J Mol Med (Berl). 1995. PMID: 7670926

6

Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

Mulligan LM, Eng C, Attié T, Lyonnet S, Marsh DJ, Hyland VJ, Robinson BG, Frilling A, Verellen-Dumoulin C, Safar A, et al. Mulligan LM, et al. Among authors: frilling a. Hum Mol Genet. 1994 Dec;3(12):2163-7. doi: 10.1093/hmg/3.12.2163. Hum Mol Genet. 1994. PMID: 7881414

7

Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC.

Mulligan LM, Eng C, Healey CS, Clayton D, Kwok JB, Gardner E, Ponder MA, Frilling A, Jackson CE, Lehnert H, et al. Mulligan LM, et al. Among authors: frilling a. Nat Genet. 1994 Jan;6(1):70-4. doi: 10.1038/ng0194-70. Nat Genet. 1994. PMID: 7907913

8

Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma.

Eng C, Mulligan LM, Healey CS, Houghton C, Frilling A, Raue F, Thomas GA, Ponder BA. Eng C, et al. Among authors: frilling a. Cancer Res. 1996 May 1;56(9):2167-70. Cancer Res. 1996. PMID: 8616867

9

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: frilling a. J Clin Endocrinol Metab. 1996 May;81(5):1780-3. doi: 10.1210/jcem.81.5.8626834. J Clin Endocrinol Metab. 1996. PMID: 8626834

10

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: frilling a. J Clin Endocrinol Metab. 1996 Mar;81(3):1035-7. doi: 10.1210/jcem.81.3.8772572. J Clin Endocrinol Metab. 1996. PMID: 8772572

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