-
1
-
-
0000997633
-
Genetics of spherocytosis
-
Morton NE, Mackinney AA, Kosower N, Schilling RE, Gray MP. Genetics of spherocytosis. Am J Hum Genet. 1962;14:170-184.
-
(1962)
Am J Hum Genet
, vol.14
, pp. 170-184
-
-
Morton, N.E.1
Mackinney, A.A.2
Kosower, N.3
Schilling, R.E.4
Gray, M.P.5
-
2
-
-
0034651021
-
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
-
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
-
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
-
5
-
-
0141639284
-
Hereditary spherocytosis in newborns
-
Bellanti JA, Braci R, Prindull G, Xanthou M, eds. Amsterdam: Elsevier Science
-
Iolascon A, Perotta S, Tavano R, Miraglia del Giudice E. Hereditary spherocytosis in newborns. In: Bellanti JA, Braci R, Prindull G, Xanthou M, eds. Neonatal Hematology and Immunology, III: Proceedings of the Third Neonatal Hematology and Immunology Symposium, held in Washington, DC, 29 September-1 October, 1996. Amsterdam: Elsevier Science; 1997:197-202.
-
(1997)
Neonatal Hematology and Immunology, III: Proceedings of the Third Neonatal Hematology and Immunology Symposium, Held in Washington, DC, 29 September-1 October, 1996
, pp. 197-202
-
-
Iolascon, A.1
Perotta, S.2
Tavano, R.3
Miraglia Del Giudice, E.4
-
6
-
-
0001959626
-
The Italian pediatric survey on hereditary spherocytosis
-
Pinto L, Iolascon A, Miraglia Del Giudice E, Matarese S, Nobili B, Perrotta S. The Italian pediatric survey on hereditary spherocytosis. Int J Pediatr Hematol Oncol. 1995;2:43-47.
-
(1995)
Int J Pediatr Hematol Oncol
, vol.2
, pp. 43-47
-
-
Pinto, L.1
Iolascon, A.2
Miraglia Del Giudice, E.3
Matarese, S.4
Nobili, B.5
Perrotta, S.6
-
7
-
-
0003147477
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
28
-
-
0025719950
-
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
-
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
-
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
-
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
-
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
|