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Volumn 142, Issue 3, 2003, Pages 358-

Growth hormone deficiency caused by pituitary stalk interruption in Diamond-Blackfan anemia [2]

Author keywords

[No Author keywords available]

Indexed keywords

GLUCAGON; GROWTH HORMONE;

EID: 0037340633     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1067/mpd.2003.57     Document Type: Letter
Times cited : (16)

References (6)
  • 1
    • 0032723176 scopus 로고    scopus 로고
    • Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anaemia patients
    • DBA group of Societé d'Hématologie et d'Immunologie Pédiatrique (SHIP-, Gesellshaft fur Padiatrische Onkologie und Hamatologie [GPOH], and the European Society for Pediatric Hematology and Immunology [ESPHI])
    • Willig TN, Niemeyer CM, Leblanc T, Tiemann C, Robert A, Budde J, et al. Identification of new prognosis factors from the clinical and epidemiologic analysis of a registry of 229 Diamond-Blackfan anaemia patients. DBA group of Societé d'Hématologie et d'Immunologie Pédiatrique (SHIP-, Gesellshaft fur Padiatrische Onkologie und Hamatologie [GPOH], and the European Society for Pediatric Hematology and Immunology [ESPHI]). Pediatr Res 1999;46:553-61.
    • (1999) Pediatr Res , vol.46 , pp. 553-561
    • Willig, T.N.1    Niemeyer, C.M.2    Leblanc, T.3    Tiemann, C.4    Robert, A.5    Budde, J.6
  • 3
    • 0035143078 scopus 로고    scopus 로고
    • Growth hormone deficiency caused by pituitary stalk interruption in Fanconi's anaemia
    • Dupuis-Girod S, Gluckman E, Souberbielle JC, Brauner R. Growth hormone deficiency caused by pituitary stalk interruption in Fanconi's anaemia. J Pediatr 2001;138:129-33.
    • (2001) J Pediatr , vol.138 , pp. 129-133
    • Dupuis-Girod, S.1    Gluckman, E.2    Souberbielle, J.C.3    Brauner, R.4
  • 4
    • 0035313157 scopus 로고    scopus 로고
    • Evidence for linkage for familial Blackfan-Diamond anaemia to chromosome 8p23.3-p22 and for non-19q non-8p disease
    • Gazda H, Lipton JM, Willig TN, Ball S, Niemeyer CM, Tchernia G, et al. Evidence for linkage for familial Blackfan-Diamond anaemia to chromosome 8p23.3-p22 and for non-19q non-8p disease. Blood 2001;97:2145-50.
    • (2001) Blood , vol.97 , pp. 2145-2150
    • Gazda, H.1    Lipton, J.M.2    Willig, T.N.3    Ball, S.4    Niemeyer, C.M.5    Tchernia, G.6
  • 5
    • 13044266374 scopus 로고    scopus 로고
    • Mutations in ribosomal protein S19 and Diamond-Blackfan anaemia: Wide variations in phenotypic expression
    • Willig TN, Draptchinskaia I, Dianzani I, Ball S, Niemeyer CM, Ramenghi U, et al. Mutations in ribosomal protein S19 and Diamond-Blackfan anaemia: wide variations in phenotypic expression. Blood 1999;94:4294-306.
    • (1999) Blood , vol.94 , pp. 4294-4306
    • Willig, T.N.1    Draptchinskaia, I.2    Dianzani, I.3    Ball, S.4    Niemeyer, C.M.5    Ramenghi, U.6
  • 6
    • 0001652428 scopus 로고
    • The bone marrow failure syndromes p 216
    • Nathan DG, Oski FA, eds. Philadelphia (PA): WB Saunders
    • Alter BP. The bone marrow failure syndromes p 216. In Nathan DG, Oski FA, eds. Hematology of infancy and childhood, 4th ed. Philadelphia (PA): WB Saunders; 1993.
    • (1993) Hematology of Infancy and Childhood, 4th Ed.
    • Alter, B.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.