(Q30320428)

17 June 2017

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title

Multiple endocrine neoplasia 2B syndrome due to codon 918 mutation: clinical manifestation and course in early and late onset disease (English)

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multiple endocrine neoplasia

17 June 2017

main subject

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8

Henning Dralle

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17 June 2017

Michael Brauckhoff

1

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17 June 2017

Oliver Gimm

2

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17 June 2017

Carl-Ludwig Weiss

3

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17 June 2017

Jörg Ukkat

4

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17 June 2017

Carsten Sekulla

5

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17 June 2017

Katrin Brauckhoff

6

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17 June 2017

Phuong Nguyen Thanh

7

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17 June 2017

publication date

4 November 2004

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17 June 2017

published in

World Journal of Surgery

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17 June 2017

volume

28

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17 June 2017

issue

12

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17 June 2017

page(s)

1305-1311

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Germline mutation of RET codon 883 in two cases of de novo MEN 2B.

17 June 2017

cites work

1 reference

12 December 2020

Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918

1 reference

12 December 2020

Multiple endocrine neoplasia, type 2b

1 reference

12 December 2020

Multiple endocrine neoplasia type 2B--genetic basis and clinical expression

1 reference

12 December 2020

Compartment-oriented microdissection of regional lymph nodes in medullary thyroid carcinoma

1 reference

12 December 2020

Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma

1 reference

12 December 2020

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

1 reference

12 December 2020

Two germline missense mutations at codons 804 and 806 of the RET proto-oncogene in the same allele in a patient with multiple endocrine neoplasia type 2B without codon 918 mutation.

1 reference

12 December 2020

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

1 reference

12 December 2020

A RET double mutation in the germline of a kindred with FMTC.

1 reference

12 December 2020

No mutation at codon 918 of the RET gene in a family with multiple endocrine neoplasia type 2B

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12 December 2020

Genotype-phenotype correlations in hereditary medullary thyroid carcinoma: oncological features and biochemical properties

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12 December 2020

Update on the MEN 2A c804 RET mutation: is prophylactic thyroidectomy indicated?

1 reference

12 December 2020

Familial medullary thyroid carcinoma and prominent corneal nerves associated with the germline V804M and V778I mutations on the same allele of RET.

1 reference

12 December 2020

Medullary thyroid carcinoma as part of a multiple endocrine neoplasia type 2B syndrome: influence of the stage on the clinical course

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12 December 2020

Four cases of mucosal neuroma syndrome: multiple endocrine neoplasm 2B or not 2B?

1 reference

12 December 2020

Prophylactic completion thyroidectomy for differentiated thyroid carcinoma: prediction of extrathyroidal soft tissue infiltrates

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12 December 2020

The Natural Course of Multiple Endocrine Neoplasia Type iib

1 reference

12 December 2020

Prominent corneal nerves in patients with multiple endocrine neoplasia type 2A: diagnostic implications

1 reference

12 December 2020

Syndrome of bilateral pheochromocytoma, medullary thyroid carcinoma and multiple neuromas. A possible regulatory defect in the differentiation of chromaffin tissue

1 reference

12 December 2020

Multiple mucosal neuromata with endocrine tumours: a syndrome allied to von Recklinghausen's disease

1 reference

12 December 2020

Multiple endocrine neoplasia type 2B: more than an endocrine disorder

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12 December 2020

Medullary carcinoma of the thyroid gland

1 reference

12 December 2020

Early Malignant Progression of Hereditary Medullary Thyroid Cancer

1 reference

12 December 2020

Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid—a syndrome

1 reference

12 December 2020

10.1007/S00268-004-7637-4

Identifiers

DOI

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Dimensions Publication ID

17 June 2017

1019164025

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Fatcat ID

release_i777f3ixkvgv7cj4oa3yqutyci

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Fatcat

https://api.fatcat.wiki/v0/release/i777f3ixkvgv7cj4oa3yqutyci

24 November 2022

mapped directly with Wikidata item

1 reference