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Journal of Pediatric Surgery
Volumn 42, Issue 6, 2007, Pages 1153-
Very early manifestation of hereditary medullary thyroid cancer in carriers of intracellular-domain RET mutations
Author keywords

[No Author keywords available]
Indexed keywords

AGE; ALLELE; CANCER DIAGNOSIS; CLINICAL ARTICLE; CODON; CONSANGUINITY; CORRELATION ANALYSIS; EARLY DIAGNOSIS; FAMILIAL CANCER; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HETEROZYGOTE DETECTION; HUMAN; LETTER; MALIGNANT TRANSFORMATION; ONCOGENE RET; PRIORITY JOURNAL; PROTO ONCOGENE; RISK FACTOR; THYROID MEDULLARY CARCINOMA;
EID: 34249800946     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpedsurg.2007.03.053     Document Type: Letter
Times cited : (1)
References (8)
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    • Early malignant progression of hereditary medullary thyroid cancer
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  • 3
    • 0141481958 scopus 로고    scopus 로고
    • Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutations
    • Machens A., Holzhausen H.J., Thanh P.N., et al. Malignant progression from C-cell hyperplasia to medullary thyroid carcinoma in 167 carriers of RET germline mutations. Surgery 134 (2003) 425-431
    • (2003) Surgery , vol.134 , pp. 425-431
    • Machens, A.1    Holzhausen, H.J.2    Thanh, P.N.3
  • 4
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    • Lecube A., Hernandez C., Oriola J., et al. V804M RET mutation and familial medullary thyroid carcinoma: report of a large family with expression of the disease only in the homozygous gene carriers. Surgery 131 (2002) 509-514
    • (2002) Surgery , vol.131 , pp. 509-514
    • Lecube, A.1    Hernandez, C.2    Oriola, J.3
  • 5
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    • Germline homozygous mutations at codon 804 in the RET protooncogene in medullary thyroid carcinoma/multiple endocrine neoplasia 2A patients
    • Lesueur F., Cebrian A., Cranston A., et al. Germline homozygous mutations at codon 804 in the RET protooncogene in medullary thyroid carcinoma/multiple endocrine neoplasia 2A patients. J Clin Endocrinol Metab 90 (2005) 3454-3457
    • (2005) J Clin Endocrinol Metab , vol.90 , pp. 3454-3457
    • Lesueur, F.1    Cebrian, A.2    Cranston, A.3
  • 6
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    • Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition
    • Elisei R., Cosci B., Romei C., et al. Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition. J Clin Endocrinol Metab 89 (2004) 5823-5827
    • (2004) J Clin Endocrinol Metab , vol.89 , pp. 5823-5827
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  • 7
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    • Familial medullary thyroid carcinoma: clinical variability and low aggressiveness associated with RET mutation at codon 804
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.