메뉴 건너뛰기




Volumn 104, Issue 2, 2011, Pages 150-152

Hereditary spherocytosis with leg ulcers healing after splenectomy

Author keywords

hereditary spherocytosis; leg ulcers; splenectomya

Indexed keywords

ANTIBIOTIC AGENT; ANTIINFECTIVE AGENT;

EID: 79251645449     PISSN: 00384348     EISSN: None     Source Type: Journal    
DOI: 10.1097/SMJ.0b013e318200c6ba     Document Type: Article
Times cited : (11)

References (14)
  • 2
    • 67650724767 scopus 로고    scopus 로고
    • Hereditary spherocytosis
    • Behrman RE, Kliegman RM, Jenson HB eds:, Philadelphia, Saunders, ed 17
    • Segel GB. Hereditary spherocytosis, in Behrman RE, Kliegman RM, Jenson HB (eds): Nelson's Textbook of Pediatrics. Philadelphia, Saunders, ed 17, 2004, pp 1620-1621.
    • (2004) Nelson's Textbook of Pediatrics , pp. 1620-1621
    • Segel, G.B.1
  • 4
    • 0034136236 scopus 로고    scopus 로고
    • Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population
    • Yawata Y, Kanzaki A, Yawata A, et al. Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population. Int J Hematol 2000;71:118-135.
    • (2000) Int. J. Hematol. , vol.71 , pp. 118-135
    • Yawata, Y.1    Kanzaki, A.2    Yawata, A.3
  • 5
    • 0025041070 scopus 로고
    • Variable clinical severity of hereditary spherocytosis: Relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis
    • Eber SW, Armbrust R, Schröter W. Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis. J Pediatr 1990;177:409-416.
    • (1990) J. Pediatr. , vol.177 , pp. 409-416
    • Eber, S.W.1    Armbrust, R.2    Schröter, W.3
  • 6
    • 50849126820 scopus 로고    scopus 로고
    • Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect
    • Marinani M, Barcellini W, Vereellati C, et al. Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect. Haematologica 2008;93:1310-1317.
    • (2008) Haematologica , vol.93 , pp. 1310-1317
    • Marinani, M.1    Barcellini, W.2    Vereellati, C.3
  • 7
    • 0002077443 scopus 로고    scopus 로고
    • Red cell membrane disorders
    • Hoffman R, Benz EJ Jr, Shattil SJ, et al eds:, Philadelphia, WB Saunders, ed 4
    • Gallagher PG, Jarolim P. Red cell membrane disorders, in Hoffman R, Benz EJ Jr, Shattil SJ, et al (eds): Hematology: Basic Principles and Practice. Philadelphia, WB Saunders, ed 4, 2005, pp 669-691.
    • (2005) Hematology: Basic Principles and Practice , pp. 669-691
    • Gallagher, P.G.1    Jarolim, P.2
  • 9
    • 0025345518 scopus 로고
    • Leg ulcers in a patient with spherocytosis: A clinicopathological report
    • Vanscheidt W, Leder O, Vanscheidt E, et al. Leg ulcers in a patient with spherocytosis: a clinicopathological report. Dermatologica 1990;181:56-59.
    • (1990) Dermatologica , vol.181 , pp. 56-59
    • Vanscheidt, W.1    Leder, O.2    Vanscheidt, E.3
  • 10
    • 0022283489 scopus 로고
    • Foot and ankle ulcers associated with hematologic disorders
    • Levy LA. Foot and ankle ulcers associated with hematologic disorders. Clin Podiatry 1985;2:631-637.
    • (1985) Clin. Podiatry , vol.2 , pp. 631-637
    • Levy, L.A.1
  • 11
    • 0030781050 scopus 로고    scopus 로고
    • Hereditary spherocytosis with leg ulcers which healed after splenectomy
    • Peretz E, Hallel-Halevy D, Grunwald M, et al. Hereditary spherocytosis with leg ulcers which healed after splenectomy. Eur J Dermatol 1997;7:527-528.
    • (1997) Eur. J. Dermatol. , vol.7 , pp. 527-528
    • Peretz, E.1    Hallel-Halevy, D.2    Grunwald, M.3
  • 13
    • 0037105613 scopus 로고    scopus 로고
    • Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin-and band 3-deficient hereditary spherocytosis
    • Reliene R, Mariani M, Zanella A, et al. Splenectomy prolongs in vivo survival of erythrocytes differently in spectrin/ankyrin-and band 3-deficient hereditary spherocytosis. Blood 2002;100:2208-2215.
    • (2002) Blood , vol.100 , pp. 2208-2215
    • Reliene, R.1    Mariani, M.2    Zanella, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.