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Volumn 23, Issue 5, 2006, Pages 387-397

Incidence of hereditary spherocytosis in a population of jaundiced neonates

Author keywords

Acquired immune spherocytocis; Hereditary spherocytosis; Neonatal jaundice

Indexed keywords

ARTICLE; CASE REPORT; CONTROLLED STUDY; HEREDITARY SPHEROCYTOSIS; HUMAN; HYPERBILIRUBINEMIA; INCIDENCE; MALE; NEWBORN; NEWBORN JAUNDICE; PHOTOTHERAPY;

EID: 33746812592     PISSN: 08880018     EISSN: 15210669     Source Type: Journal    
DOI: 10.1080/08880010600646662     Document Type: Article
Times cited : (27)

References (32)
  • 2
    • 0034651021 scopus 로고    scopus 로고
    • Natural history of hereditary spherocytosis during the first year of life
    • Delhommeau F, Cynober T, Schischmanoff PO, et al. Natural history of hereditary spherocytosis during the first year of life. Blood. 2000;95:393-397.
    • (2000) Blood , vol.95 , pp. 393-397
    • Delhommeau, F.1    Cynober, T.2    Schischmanoff, P.O.3
  • 3
    • 0014051346 scopus 로고
    • Neonatal manifestations of hereditary spherocytosis
    • Trucco JI, Brown AK. Neonatal manifestations of hereditary spherocytosis. Am J Dis Child. 1967;113:263-270.
    • (1967) Am J Dis Child , vol.113 , pp. 263-270
    • Trucco, J.I.1    Brown, A.K.2
  • 4
    • 0020551069 scopus 로고
    • Diagnosis of hereditary spherocytosis in newborn infants
    • Schr̈oter W, Kahsnitz E. Diagnosis of hereditary spherocytosis in newborn infants. J Pediatr. 1983;103:460-463.
    • (1983) J Pediatr , vol.103 , pp. 460-463
    • Schr̈oter, W.1    Kahsnitz, E.2
  • 7
    • 0003147477 scopus 로고
    • Disorders of the red cell membrane
    • Handin RI, Lux SE, Stossel TP, eds. New York: Lippincott
    • Lux SE, Palek J. Disorders of the red cell membrane. In: Handin RI, Lux SE, Stossel TP, eds. Blood: Principles & Practice of Hematology. New York: Lippincott; 1995:1701-1818.
    • (1995) Blood: Principles & Practice of Hematology , pp. 1701-1818
    • Lux, S.E.1    Palek, J.2
  • 8
    • 0030231133 scopus 로고    scopus 로고
    • Red cell abnormalities in hereditary spherocytosis: Relevance to diagnosis and understanding of the variable expression of clinical severity
    • Cynober T, Mohandas N, Tchernia G. Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity. J Lab Clin Med. 1996;128:259-269.
    • (1996) J Lab Clin Med , vol.128 , pp. 259-269
    • Cynober, T.1    Mohandas, N.2    Tchernia, G.3
  • 9
    • 0024536792 scopus 로고
    • The use of the Technicon H1 in the diagnosis of hereditary spherocytosis
    • Pati AR, Patton WN, Harris RI. The use of the Technicon H1 in the diagnosis of hereditary spherocytosis. Clin Lab Haematol. 1989; 11:27-30.
    • (1989) Clin Lab Haematol , vol.11 , pp. 27-30
    • Pati, A.R.1    Patton, W.N.2    Harris, R.I.3
  • 10
    • 0027180216 scopus 로고
    • Diagnosis of hereditary spherocytosis with dual-angle differential light scattering
    • Gilsanz F, Ricard MP, Millan I. Diagnosis of hereditary spherocytosis with dual-angle differential light scattering. Am J Clin Pathol. 1993;100:119-122.
    • (1993) Am J Clin Pathol , vol.100 , pp. 119-122
    • Gilsanz, F.1    Ricard, M.P.2    Millan, I.3
  • 11
    • 0014214358 scopus 로고
    • Red cells coated with immunoglobulin G: Binding and sphering by mononuclear cells in man
    • Lobuglio AF, Cotran RS, Jandl JH. Red cells coated with immunoglobulin G: binding and sphering by mononuclear cells in man. Science. 1967;158:1582-1585.
    • (1967) Science , vol.158 , pp. 1582-1585
    • Lobuglio, A.F.1    Cotran, R.S.2    Jandl, J.H.3
  • 12
    • 0029850939 scopus 로고    scopus 로고
    • Abnormalities of membrane protein composition in patients with autoimmune haemolytic anemia
    • De Angelis V, De Matteis MC, Cozzi MR, et al. Abnormalities of membrane protein composition in patients with autoimmune haemolytic anemia. Br J Haematol. 1996;95:273-277.
    • (1996) Br J Haematol , vol.95 , pp. 273-277
    • De Angelis, V.1    De Matteis, M.C.2    Cozzi, M.R.3
  • 13
    • 0035892116 scopus 로고    scopus 로고
    • Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia
    • Da Costa L, Mohandas N, Sorette M, Grange MJ, Tchernia G, Cynober T. Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia. Blood. 2001;98:2894-2899.
    • (2001) Blood , vol.98 , pp. 2894-2899
    • Da Costa, L.1    Mohandas, N.2    Sorette, M.3    Grange, M.J.4    Tchernia, G.5    Cynober, T.6
  • 14
    • 0022543618 scopus 로고
    • Accurate and independent measurement of volume and hemoglobin concentration of individual red cells by laser light scattering
    • Mohandas N, Kim YR, Tycko DH, Orlik J, Wyatt J, Groner W. Accurate and independent measurement of volume and hemoglobin concentration of individual red cells by laser light scattering. Blood. 1986;68:506-513.
    • (1986) Blood , vol.68 , pp. 506-513
    • Mohandas, N.1    Kim, Y.R.2    Tycko, D.H.3    Orlik, J.4    Wyatt, J.5    Groner, W.6
  • 15
    • 0020530019 scopus 로고
    • Osmotic gradient ektacytometry: Comprehensive characterisation of red cell volume and surface maintenance
    • Clark MR, Mohandas N, Shohet SB. Osmotic gradient ektacytometry: comprehensive characterisation of red cell volume and surface maintenance. Blood. 1983;61:899-910.
    • (1983) Blood , vol.61 , pp. 899-910
    • Clark, M.R.1    Mohandas, N.2    Shohet, S.B.3
  • 16
    • 0030802681 scopus 로고    scopus 로고
    • Red blood cell abnormalities in hereditary elliptocytosis and their relevance to variable clinical expression
    • Silveira P, Cynober T, Dhermy D, Mohandas N, Tchernia G. Red blood cell abnormalities in hereditary elliptocytosis and their relevance to variable clinical expression. Am J Clin Pathol. 1997;108:391-399.
    • (1997) Am J Clin Pathol , vol.108 , pp. 391-399
    • Silveira, P.1    Cynober, T.2    Dhermy, D.3    Mohandas, N.4    Tchernia, G.5
  • 17
    • 0035705685 scopus 로고    scopus 로고
    • Dehydrated hereditary stomatocytosis: A cause of prenatal ascites
    • Grootenboer S, Barro C, Cynober T, et al. Dehydrated hereditary stomatocytosis: a cause of prenatal ascites. Prenat Diagn. 2001;21:1114-1118.
    • (2001) Prenat Diagn , vol.21 , pp. 1114-1118
    • Grootenboer, S.1    Barro, C.2    Cynober, T.3
  • 18
    • 0025187110 scopus 로고
    • Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: Two genetically distinct forms of the Sp alpha I/74 variant
    • Lecomte MC, Gautero H, Garbarz M, Boivin P, Dhermy D. Abnormal tryptic peptide from the spectrin alpha-chain resulting from alpha- or beta-chain mutations: two genetically distinct forms of the Sp alpha I/74 variant. Br J Haematol. 1990;76:406-413.
    • (1990) Br J Haematol , vol.76 , pp. 406-413
    • Lecomte, M.C.1    Gautero, H.2    Garbarz, M.3    Boivin, P.4    Dhermy, D.5
  • 19
    • 0015236352 scopus 로고
    • Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane
    • Fairbanks G, Steck TL, Wallach DFH. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane. Biochemistry. 1971;10:2606-2617.
    • (1971) Biochemistry , vol.10 , pp. 2606-2617
    • Fairbanks, G.1    Steck, T.L.2    Wallach, D.F.H.3
  • 20
    • 0034584616 scopus 로고    scopus 로고
    • Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis
    • Tchernia G, Delhommeau F, Perrotta S, et al. Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis. Hematol J. 2000;1:146-152.
    • (2000) Hematol J , vol.1 , pp. 146-152
    • Tchernia, G.1    Delhommeau, F.2    Perrotta, S.3
  • 21
    • 0035130741 scopus 로고    scopus 로고
    • Clinical and molecular evaluation of non-dominant hereditary spherocytosis
    • Miraglia del Giudice E, Nobili B, Francese M, et al. Clinical and molecular evaluation of non-dominant hereditary spherocytosis. Br J Haematol. 2001;112:42-47.
    • (2001) Br J Haematol , vol.112 , pp. 42-47
    • Miraglia Del Giudice, E.1    Nobili, B.2    Francese, M.3
  • 22
    • 0031893531 scopus 로고    scopus 로고
    • High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis
    • Miraglia del Giudice E, Francese M, Nobili B, et al. High frequency of de novo mutations in ankyrin gene (ANK1) in children with hereditary spherocytosis. J Pediatr. 1998;132:117-120.
    • (1998) J Pediatr , vol.132 , pp. 117-120
    • Miraglia Del Giudice, E.1    Francese, M.2    Nobili, B.3
  • 23
    • 0022525189 scopus 로고
    • The aging process of human neonatal erythrocytes
    • Matovcik LM, Chiu D, Lubin B, et al. The aging process of human neonatal erythrocytes. Pediatr Res. 1986;20:1091-1096.
    • (1986) Pediatr Res , vol.20 , pp. 1091-1096
    • Matovcik, L.M.1    Chiu, D.2    Lubin, B.3
  • 24
    • 0037404111 scopus 로고    scopus 로고
    • Cord blood red cell osmotic fragility: A comparison between preterm and full-term newborn infants
    • Bautista ML, AltafW, Lall R,Wapnir RA. Cord blood red cell osmotic fragility: a comparison between preterm and full-term newborn infants. Early Hum Dev. 2003;72:37-46.
    • (2003) Early Hum Dev , vol.72 , pp. 37-46
    • Bautista, M.L.1    Altaf, W.2    Lall, R.3    Wapnir, R.A.4
  • 25
    • 0027527892 scopus 로고
    • Mechanical and geometrical properties of density-separated neonatal and adult erythrocytes
    • Linderkamp O, Friederichs E, Meiselman HJ. Mechanical and geometrical properties of density-separated neonatal and adult erythrocytes. Pediatr Res. 1993;34:688-693.
    • (1993) Pediatr Res , vol.34 , pp. 688-693
    • Linderkamp, O.1    Friederichs, E.2    Meiselman, H.J.3
  • 26
    • 0032904041 scopus 로고    scopus 로고
    • Deformability and geometry of neonatal erythrocytes with irregular shapes
    • Ruef P, Linderkamp O. Deformability and geometry of neonatal erythrocytes with irregular shapes. Pediatr Res. 1999;45:114-119.
    • (1999) Pediatr Res , vol.45 , pp. 114-119
    • Ruef, P.1    Linderkamp, O.2
  • 27
    • 0018043471 scopus 로고
    • Erythrocytes of the human neonate
    • Stockman JA, Oski FA. Erythrocytes of the human neonate. Curr Top Hematol. 1978;1:193-232.
    • (1978) Curr Top Hematol , vol.1 , pp. 193-232
    • Stockman, J.A.1    Oski, F.A.2
  • 28
    • 0025719950 scopus 로고
    • Deficiency of α-spectrin synthesis in burst-forming units - Erythroid in lethal hereditary spherocytosis
    • Whitfield CF, Follweiler JB, Lopresti-Morrow L, Miller BA. Deficiency of α-spectrin synthesis in burst-forming units - erythroid in lethal hereditary spherocytosis. Blood. 1991;78:3043-3051.
    • (1991) Blood , vol.78 , pp. 3043-3051
    • Whitfield, C.F.1    Follweiler, J.B.2    Lopresti-Morrow, L.3    Miller, B.A.4
  • 29
    • 0008224001 scopus 로고    scopus 로고
    • Hereditary spherocytosis with total absence of band 3 in a baby with mutation Coimbra (V488M) in the homozygous state
    • Ribeiro ML, Alloisio N, Almeida H, et al. Hereditary spherocytosis with total absence of band 3 in a baby with mutation Coimbra (V488M) in the homozygous state [abstract]. Blood. 1997;90:265a.
    • (1997) Blood , vol.90
    • Ribeiro, M.L.1    Alloisio, N.2    Almeida, H.3
  • 30
    • 0023726325 scopus 로고
    • Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis
    • Chasis JA, Agre P, Mohandas N. Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis. J Clin Invest. 1988;82:617-623.
    • (1988) J Clin Invest , vol.82 , pp. 617-623
    • Chasis, J.A.1    Agre, P.2    Mohandas, N.3
  • 31
    • 0028235386 scopus 로고
    • Prevalence and lack of clinical significance of blood group incompatibility in mothers with blood type A or B
    • Ozolek JA, Watchko JF, Mimouni F. Prevalence and lack of clinical significance of blood group incompatibility in mothers with blood type A or B. J Pediatr. 1994;125:87-91.
    • (1994) J Pediatr , vol.125 , pp. 87-91
    • Ozolek, J.A.1    Watchko, J.F.2    Mimouni, F.3
  • 32
    • 4143053494 scopus 로고    scopus 로고
    • Guidelines for the diagnosis and management of hereditary spherocytosis
    • Bolton-Maggs PHB, Stevens RF, Dodd NJ, Lamont G, Tittensor P, King MJ, on behalf of the General Hematology Task Force of the British Committee for Standards in Haematology. Guidelines for the diagnosis and management of hereditary spherocytosis. Br J Haematol. 2004;126:455-474.
    • (2004) Br J Haematol , vol.126 , pp. 455-474
    • Bolton-Maggs, P.H.B.1    Stevens, R.F.2    Dodd, N.J.3    Lamont, G.4    Tittensor, P.5    King, M.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.