Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family. (Q54581150)

1 June 2018

title

Coexistence of multiple endocrine neoplasia type 1 and type 2 in a large Italian family. (English)

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1 June 2018

multiple endocrine neoplasia

main subject

Italy

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multiple endocrine neoplasia type 1

inferred from title

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inferred from title

author

Lucia Anna Muscarella

9

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Vito Guarnieri

10

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author name string

Sandra Mastroianno

1

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Massimo Torlontano

2

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Alfredo Scillitani

3

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Leonardo D'Aloiso

4

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Antonella Verrienti

5

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Nazario Bonfitto

6

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Antonio De Bonis

7

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Leonardo D'Agruma

8

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Franca Dicembrino

11

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Marianna Maranghi

12

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Cosimo Durante

13

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Sebastiano Filetti

14

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publication date

17 June 2011

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1 June 2018

published in

Endocrine

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volume

40

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issue

3

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page(s)

481-485

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Multiple endocrine neoplasia type 1.

cites work

1 reference

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Guidelines for diagnosis and therapy of MEN type 1 and type 2.

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Multiple endocrine neoplasia syndrome: genetic basis for clinical management

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Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene

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RET as a diagnostic and therapeutic target in sporadic and hereditary endocrine tumors

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Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases

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Four novel RET germline variants in exons 8 and 11 display an oncogenic potential in vitro

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Familial Medullary Thyroid Carcinoma: Clinical Variability and Low Aggressiveness Associated with RET Mutation at Codon 804

21 January 2018

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A novel de novo germ-line V292M mutation in the extracellular region of RET in a patient with phaeochromocytoma and medullary thyroid carcinoma: functional characterization

21 January 2018

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12 December 2020

Increasing incidence of thyroid cancer in the United States, 1973-2002

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12 December 2020

Coincidence of multiple endocrine neoplasia types 1 and 2: mutations in the RET protooncogene and MEN1 tumor suppressor gene in a family presenting with recurrent primary hyperparathyroidism

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12 December 2020

Multiple endocrine neoplasia type 1: atypical presentation, clinical course, and genetic analysis of multiple tumors

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Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics

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Familial medullary thyroid carcinoma: clinical variability and low aggressiveness associated with RET mutation at codon 804.

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Identifiers

DOI

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1 June 2018

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1 June 2018