Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.

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Multiple Endocrine Neoplasia and Hyperparathyroid-Jaw Tumor Syndromes: Clinical Features, Genetics, and Surveillance Recommendations in Childhood.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

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2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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Multiple Endocrine Neoplasia a ...... Recommendations in Childhood.

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Multiple Endocrine Neoplasia a ...... Recommendations in Childhood.

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Multiple Endocrine Neoplasia a ...... Recommendations in Childhood.

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Multiple Endocrine Neoplasia a ...... Recommendations in Childhood.

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Multiple Endocrine Neoplasia a ...... Recommendations in Childhood.

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Multiple Endocrine Neoplasia a ...... Recommendations in Childhood.

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P1476

Multiple Endocrine Neoplasia a ...... Recommendations in Childhood.

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P2093

Andreu Parareda

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Anita Villani

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Christian P Kratz

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Gail E Tomlinson

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Harriet Druker

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Jonathan D Wasserman

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Joshua D Schiffman

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Junne Kamihara

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Kristian W Pajtler

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Kristin Zelley

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P2860

Hereditary hyperparathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome 1q21-q31

Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans

Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine

An update on the genetics of pheochromocytoma

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

Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study.

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.

Gastrointestinal manifestations of multiple endocrine neoplasia type 2.

Prevalence by age and predictors of medullary thyroid cancer in patients with lower risk germline RET proto-oncogene mutations.

Are patients with multiple endocrine neoplasia type I prone to premature death?

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e123-e132

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scholarly article

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10.1158/1078-0432.CCR-17-0548

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English

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P478

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Katherine L Nathanson

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2017-07-01T00:00:00Z

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28674121

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5547889

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