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Volumn 54, Issue SUPPL. 1, 2000, Pages 86s-89s

Clinical aspects of hyperparathyroidism in Japanese multiple endocrine neoplasia type 1

Author keywords

Hyperparathyroidism; Japanese; MEN 1

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DIAGNOSTIC IMAGING; FEMALE; GERM LINE; HETEROZYGOSITY; HUMAN; HUMAN TISSUE; HYPERPARATHYROIDISM; HYPOPHYSIS TUMOR; INCIDENCE; JAPAN; MALE; MULTIPLE ENDOCRINE NEOPLASIA; PANCREAS TUMOR; PARATHYROIDECTOMY; PRIORITY JOURNAL;

EID: 0033933259     PISSN: 07533322     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0753-3322(00)80020-7     Document Type: Article
Times cited : (12)

References (13)
  • 6
    • 0031766295 scopus 로고    scopus 로고
    • Identification of five novel germline mutations of the MEN1 gene in Japanese multiple endocrine neoplasia type 1 (MEN 1) families
    • Sato M, Matsubara S, MiyauchiA, Ohye H, Imachi H, Murao K, et al. Identification of five novel germline mutations of the MEN1 gene in Japanese multiple endocrine neoplasia type 1 (MEN 1) families. J Med Genet 1998 ; 35 : 915-9.
    • (1998) J Med Genet , vol.35 , pp. 915-919
    • Sato, M.1    Matsubara, S.2    Miyauchi, A.3    Ohye, H.4    Imachi, H.5    Murao, K.6
  • 7
    • 0033383042 scopus 로고    scopus 로고
    • No evidence of germline mutation or somatic deletion of the MEN1 gene in a case of familial multiple endocrine neoplasia type 1 (MEN 1)
    • Namihira H, Sato M, Matsubara S, Ohye H, Bhuiyan MMR, Murao K, et al. No evidence of germline mutation or somatic deletion of the MEN1 gene in a case of familial multiple endocrine neoplasia type 1 (MEN 1). Endocr J 1999 ; 46 : 811-6.
    • (1999) Endocr J , vol.46 , pp. 811-816
    • Namihira, H.1    Sato, M.2    Matsubara, S.3    Ohye, H.4    Bhuiyan, M.M.R.5    Murao, K.6
  • 8
    • 0033061737 scopus 로고    scopus 로고
    • A novel germline mutation of multiple endocrine neoplasia type 1 (MEN1 ) gene in a Japanese MEN 1 patient and her daughter
    • Ohye H, Sato M, Matsubara S, Miyauchi A, Kishi-Imai K, Murao K, et al. A novel germline mutation of multiple endocrine neoplasia type 1 (MEN1 ) gene in a Japanese MEN 1 patient and her daughter. Endocr J 1999 ; 46 : 325-9.
    • (1999) Endocr J , vol.46 , pp. 325-329
    • Ohye, H.1    Sato, M.2    Matsubara, S.3    Miyauchi, A.4    Kishi-Imai, K.5    Murao, K.6
  • 10
    • 85085715658 scopus 로고    scopus 로고
    • A newly recognized germline mutation of the MEN1 gene identified in a patient with parathyroid adenoma and carcinoma
    • in press
    • Sato M, Miyauchi A, Namihira H, Bhuiyan MMR, Imachi H, Murao K, et al. A newly recognized germline mutation of the MEN1 gene identified in a patient with parathyroid adenoma and carcinoma. Endocrine (in press).
    • Endocrine
    • Sato, M.1    Miyauchi, A.2    Namihira, H.3    Bhuiyan, M.M.R.4    Imachi, H.5    Murao, K.6
  • 11
    • 0031765567 scopus 로고    scopus 로고
    • Detection of a novel nonsense mutation of the MEN1 gene in a familial multiple endocrine neoplasia type 1 patient and its screening in the family members
    • Matsubara S, Sato M, Ohye H, Iwata Y, Imachi H, Yokote R, et al. Detection of a novel nonsense mutation of the MEN1 gene in a familial multiple endocrine neoplasia type 1 patient and its screening in the family members. Endocr J 1998 ; 45 : 653-7.
    • (1998) Endocr J , vol.45 , pp. 653-657
    • Matsubara, S.1    Sato, M.2    Ohye, H.3    Iwata, Y.4    Imachi, H.5    Yokote, R.6
  • 12
    • 0032441919 scopus 로고    scopus 로고
    • A family of MEN 1 with a novel germline missense mutation and benign polymorphisms
    • Miyauchi A, Sato M, Matsubara S, Ohye H, Kihara M, Matsusaka K, et al. A family of MEN 1 with a novel germline missense mutation and benign polymorphisms. Endocr J 1998 ; 45 : 753-9.
    • (1998) Endocr J , vol.45 , pp. 753-759
    • Miyauchi, A.1    Sato, M.2    Matsubara, S.3    Ohye, H.4    Kihara, M.5    Matsusaka, K.6
  • 13
    • 0034137111 scopus 로고    scopus 로고
    • Different phenotypes of multiple endocrine neoplasia type 1 (MEN 1) in monozygotic twins found in a Japanese MEN 1 family with MEN1 gene mutation
    • Namihira H, Sato M, Miyauchi A, Ohye H, Matsubara S, Bhuiyan MMR, et al. Different phenotypes of multiple endocrine neoplasia type 1 (MEN 1) in monozygotic twins found in a Japanese MEN 1 family with MEN1 gene mutation. Endocr J 2000 ; 47 : 37-73.
    • (2000) Endocr J , vol.47 , pp. 37-73
    • Namihira, H.1    Sato, M.2    Miyauchi, A.3    Ohye, H.4    Matsubara, S.5    Bhuiyan, M.M.R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.