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Volumn 29, Issue 2, 2007, Pages 128-129

Hereditary pyropoikilocytosis: A rare but potentially severe form of congenital hemolytic anemia

Author keywords

Hemolytic anemia; Hereditary elliptocytosis; Hereditary pyropoikilocytosis; Red cell membrane disorder

Indexed keywords

ARTICLE; CASE REPORT; DISEASE SEVERITY; ERYTHROCYTE DISORDER; FEMALE; HEREDITARY HEMOLYTIC ANEMIA; HEREDITARY PYROPOIKILOCYTOSIS; HUMAN; HUMAN CELL; LABORATORY TEST; NEWBORN; PRIORITY JOURNAL;

EID: 33846844821     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0b013e3180320b6f     Document Type: Article
Times cited : (12)

References (6)
  • 1
    • 0029824292 scopus 로고    scopus 로고
    • Pseudopyropoikilocytosis: A striking artefact
    • Bain BJ, Liesner R. Pseudopyropoikilocytosis: a striking artefact. J Clin Pathol. 1996;49:772-773.
    • (1996) J Clin Pathol , vol.49 , pp. 772-773
    • Bain, B.J.1    Liesner, R.2
  • 2
    • 0016491247 scopus 로고
    • A congenital hemolytic anemia with thermal sensitivity of the erythrocyte membrane
    • Zarkowski HS, Mohandas N, Speaker CB, et al. A congenital hemolytic anemia with thermal sensitivity of the erythrocyte membrane. Br J Haematol. 1975;29:537-545.
    • (1975) Br J Haematol , vol.29 , pp. 537-545
    • Zarkowski, H.S.1    Mohandas, N.2    Speaker, C.B.3
  • 3
    • 0027181238 scopus 로고
    • Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis
    • Hanspal M, Hanspal JS, Sahr KE, et al. Molecular basis of spectrin deficiency in hereditary pyropoikilocytosis. Blood. 1993;82:1652-1660.
    • (1993) Blood , vol.82 , pp. 1652-1660
    • Hanspal, M.1    Hanspal, J.S.2    Sahr, K.E.3
  • 4
    • 0028949701 scopus 로고
    • Erythrocytes carrying mutations in spectrin and protein 4.1 show differing sensitivities to invasion by Plasmodium falciparum
    • Facer CA. Erythrocytes carrying mutations in spectrin and protein 4.1 show differing sensitivities to invasion by Plasmodium falciparum. Parasitol Res. 1995;81:52-57.
    • (1995) Parasitol Res , vol.81 , pp. 52-57
    • Facer, C.A.1
  • 5
    • 0023259279 scopus 로고
    • Clinical and laboratory study of two Caucasian families with hereditary pyropoikilocytosis and hereditary elliptocytosis
    • Peterson LC, Dampier C, Coetzer T, et al. Clinical and laboratory study of two Caucasian families with hereditary pyropoikilocytosis and hereditary elliptocytosis. Am J Clin Pathol. 1987;88:58-65.
    • (1987) Am J Clin Pathol , vol.88 , pp. 58-65
    • Peterson, L.C.1    Dampier, C.2    Coetzer, T.3
  • 6
    • 0027391041 scopus 로고
    • Hereditary pyropoikilocytosis: Clinical and laboratory analysis in eight infants and young children
    • DePalma L, Luban NLC. Hereditary pyropoikilocytosis: clinical and laboratory analysis in eight infants and young children. Am J Dis Child. 1993;147:93-95.
    • (1993) Am J Dis Child , vol.147 , pp. 93-95
    • DePalma, L.1    Luban, N.L.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.