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Volumn 41, Issue 10, 2002, Pages 899-900

A patient with acute-onset HAM/TSP after blood transfusion complicated with pseudopseudohypoparathyroidism

Author keywords

Gs ; HTLV I; PTH; Short stature

Indexed keywords

MESSENGER RNA; STIMULATORY GUANINE NUCLEOTIDE BINDING PROTEIN;

EID: 0036807294     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.41.899     Document Type: Article
Times cited : (5)

References (5)
  • 1
    • 0027182342 scopus 로고
    • Three cases of juvenile onset HTLV-I-associated myelopathy with pseudohypoparathyroidism
    • Yoshida Y, Sakamoto Y, Yoshimine A, et al. Three cases of juvenile onset HTLV-I-associated myelopathy with pseudohypoparathyroidism. J Neurol Sci 118: 145-149, 1993.
    • (1993) J. Neurol. Sci , vol.118 , pp. 145-149
    • Yoshida, Y.1    Sakamoto, Y.2    Yoshimine, A.3
  • 2
    • 0035830407 scopus 로고    scopus 로고
    • HTLV-I-associated myelopathy/tropical spastic paraparesis with pseudohypoparathyroidism
    • Machigashira N, Yoshida Y, Wang S, Osame M. HTLV-I-associated myelopathy/tropical spastic paraparesis with pseudohypoparathyroidism. Neurolgy 56: 104-106, 2001.
    • (2001) Neurolgy , vol.56 , pp. 104-106
    • Machigashira, N.1    Yoshida, Y.2    Wang, S.3    Osame, M.4
  • 3
    • 0025311515 scopus 로고
    • Nationwide survey of HTLV-I-associated myelopathy in Japan: Association with blood transfusion
    • Osame M, Janssen R, Kuboata H, Nishitani H, et al. Nationwide survey of HTLV-I-associated myelopathy in Japan: association with blood transfusion. Ann Neurol 28: 50-56, 1990.
    • (1990) Ann. Neurol , vol.28 , pp. 50-56
    • Osame, M.1    Janssen, R.2    Kuboata, H.3    Nishitani, H.4
  • 5
    • 0007406646 scopus 로고
    • Genetic deficiency of the α subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy
    • Levine AM, Ahn TG, Klupt SF, et al. Genetic deficiency of the α subunit of the guanine nucleotide-binding protein Gs as the molecular basis for Albright hereditary osteodystrophy. Proc Natl Acad Sci USA 85: 617-621, 1988.
    • (1988) Proc. Natl. Acad. Sci. USA , vol.85 , pp. 617-621
    • Levine, A.M.1    Ahn, T.G.2    Klupt, S.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.