-
1
-
-
0000124912
-
Neutropenia and neutrophilia
-
Williams WJ, et al., editors. New York: McGraw-Hill
-
Dale DC. Neutropenia and neutrophilia. In: Williams WJ, et al., editors. Hematology. 6th edition. New York: McGraw-Hill; 2001. p 823-834.
-
(2001)
Hematology. 6th Edition
, pp. 823-834
-
-
Dale, D.C.1
-
2
-
-
0018761439
-
Chronic neutropenia
-
Dale DC, Guerry D, Wewerka JR, Bull JM, Chusid MJ. Chronic neutropenia. Medicine 1979;58:128-144.
-
(1979)
Medicine
, vol.58
, pp. 128-144
-
-
Dale, D.C.1
Guerry, D.2
Wewerka, J.R.3
Bull, J.M.4
Chusid, M.J.5
-
3
-
-
0014942940
-
Defective myelopoiesis in congenital neutropenia
-
Wriedt K, Kauder E, Mauer A. Defective myelopoiesis in congenital neutropenia. N Engl J Med 1970;283:1072-1077.
-
(1970)
N Engl J Med
, vol.283
, pp. 1072-1077
-
-
Wriedt, K.1
Kauder, E.2
Mauer, A.3
-
4
-
-
0017286805
-
Granulopoiesis in severe congenital neutropenia
-
Amato D, Freedman M, Saunders E. Granulopoiesis in severe congenital neutropenia. Blood 1976;47:531-538.
-
(1976)
Blood
, vol.47
, pp. 531-538
-
-
Amato, D.1
Freedman, M.2
Saunders, E.3
-
6
-
-
0030814335
-
Severe chronic neutropenia: Pathophysiology and therapy
-
Welte K, Boxer LA. Severe chronic neutropenia: pathophysiology and therapy. Semin Hematol 1997;34:267-278.
-
(1997)
Semin Hematol
, vol.34
, pp. 267-278
-
-
Welte, K.1
Boxer, L.A.2
-
7
-
-
0023695353
-
Cyclic neutropenia: A clinical review
-
Dale DC, Hammond WP 4th. Cyclic neutropenia: a clinical review. Blood 1988;3:178-185.
-
(1988)
Blood
, vol.3
, pp. 178-185
-
-
Dale, D.C.1
Hammond W.P. IV2
-
9
-
-
0026060733
-
Chronic neutropenia during childhood. A 13-year experience in a single institution
-
Jonsson OG, Buchanan GR. Chronic neutropenia during childhood. A 13-year experience in a single institution . Am J Dis Child 1991;145:232-235.
-
(1991)
Am J Dis Child
, vol.145
, pp. 232-235
-
-
Jonsson, O.G.1
Buchanan, G.R.2
-
10
-
-
0011982978
-
Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy
-
Freedman MH, Bonilla MA, Fier C, Bolyard AA, Scarlata D, Boxer LA, Brown S, Cham B, Kannourakis G, Kinsey SE, Mori PG, Cottle T, Welte K, Dale DC. Myelodysplasia syndrome and acute myeloid leukemia in patients with congenital neutropenia receiving G-CSF therapy. Blood 2000;96:429-436.
-
(2000)
Blood
, vol.96
, pp. 429-436
-
-
Freedman, M.H.1
Bonilla, M.A.2
Fier, C.3
Bolyard, A.A.4
Scarlata, D.5
Boxer, L.A.6
Brown, S.7
Cham, B.8
Kannourakis, G.9
Kinsey, S.E.10
Mori, P.G.11
Cottle, T.12
Welte, K.13
Dale, D.C.14
-
11
-
-
0031452316
-
High incidence of significant bone loss in patients with severe congenital neutropenia
-
Yakisan E, Schirg E, Zeidler C, Bishop NJ, Reiter A, Hirt A, Riehm H, Welte K. High incidence of significant bone loss in patients with severe congenital neutropenia. J Pediatr 1997;131:592-597.
-
(1997)
J Pediatr
, vol.131
, pp. 592-597
-
-
Yakisan, E.1
Schirg, E.2
Zeidler, C.3
Bishop, N.J.4
Reiter, A.5
Hirt, A.6
Riehm, H.7
Welte, K.8
-
12
-
-
77049235105
-
Infantile genetic agranulocytosis
-
Kostmann R. Infantile genetic agranulocytosis. Acta Pediatr Scand 1956;45(Suppl 105):1-78.
-
(1956)
Acta Pediatr Scand
, vol.45
, Issue.SUPPL. 105
, pp. 1-78
-
-
Kostmann, R.1
-
13
-
-
0029792176
-
Dominantly inherited severe congenital neutropenia
-
Briars GL, Parry HF, Ansari BM. Dominantly inherited severe congenital neutropenia. J Infect 1996;33:123-126.
-
(1996)
J Infect
, vol.33
, pp. 123-126
-
-
Briars, G.L.1
Parry, H.F.2
Ansari, B.M.3
-
14
-
-
0035874541
-
Shwachman-Diamond syndrome marrow cells show abnormally increased apoptosis mediated through the Fas pathway
-
Dror Y, Freedman MH. Shwachman-Diamond syndrome marrow cells show abnormally increased apoptosis mediated through the Fas pathway. Blood 2001;97:3011-3016.
-
(2001)
Blood
, vol.97
, pp. 3011-3016
-
-
Dror, Y.1
Freedman, M.H.2
-
15
-
-
0033837865
-
Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type 1b: Results of the European Study on Glycogen Storage Disease type I
-
Visser G, Rake JP, Fernandes J, Labrune P, Leonard JV, Moses S, Ullrich K, Smit GP. Neutropenia, neutrophil dysfunction, and inflammatory bowel disease in glycogen storage disease type 1b: results of the European Study on Glycogen Storage Disease type I. J Pediatr 2000;173:187-191.
-
(2000)
J Pediatr
, vol.173
, pp. 187-191
-
-
Visser, G.1
Rake, J.P.2
Fernandes, J.3
Labrune, P.4
Leonard, J.V.5
Moses, S.6
Ullrich, K.7
Smit, G.P.8
-
16
-
-
0032831035
-
The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type 1 non-a
-
Veiga-da-Cunha M, Gerin I, Chen YT, Lee PJ, Leonard JV, Maire I, Wendel U, Vikkula M, Van Schaftinger E. The putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type 1 non-a. Eur J Hum Genet 1999;7:717-723.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 717-723
-
-
Veiga-da-Cunha, M.1
Gerin, I.2
Chen, Y.T.3
Lee, P.J.4
Leonard, J.V.5
Maire, I.6
Wendel, U.7
Vikkula, M.8
Van Schaftinger, E.9
-
17
-
-
0033972915
-
Myelokathexis, a congenital disorder of severe neutropenia characterized by accelerated apoptosis and defective expression of bcl-x in neutrophil precursors
-
Aprikyan AA, Liles WC, Park JR, Jonas M, Chi EY, Dale DC. Myelokathexis, a congenital disorder of severe neutropenia characterized by accelerated apoptosis and defective expression of bcl-x in neutrophil precursors. Blood 2000;95:320-327.
-
(2000)
Blood
, vol.95
, pp. 320-327
-
-
Aprikyan, A.A.1
Liles, W.C.2
Park, J.R.3
Jonas, M.4
Chi, E.Y.5
Dale, D.C.6
-
18
-
-
0030459532
-
Genetics, phenotype, and natural history of autosomal dominant cyclic hematopoiesis
-
Palmer SE, Stephens K, Dale DC. Genetics, phenotype, and natural history of autosomal dominant cyclic hematopoiesis. Am J Med Genet 1996;66:413-422.
-
(1996)
Am J Med Genet
, vol.66
, pp. 413-422
-
-
Palmer, S.E.1
Stephens, K.2
Dale, D.C.3
-
19
-
-
0031964652
-
Diagnosis and clinical course of autoimmune neutropenia in infancy: Analysis of 240 cases
-
Bux J, Behrens G, Jaeger G, Welte K. Diagnosis and clinical course of autoimmune neutropenia in infancy: analysis of 240 cases. Blood 1998;91:181-186.
-
(1998)
Blood
, vol.91
, pp. 181-186
-
-
Bux, J.1
Behrens, G.2
Jaeger, G.3
Welte, K.4
-
20
-
-
0027408563
-
Autoimmune neutropenia
-
Shastri KA, Logue GL. Autoimmune neutropenia. Blood 1993;81:1984-1995.
-
(1993)
Blood
, vol.81
, pp. 1984-1995
-
-
Shastri, K.A.1
Logue, G.L.2
-
22
-
-
12244286923
-
Chronic neutropenia in siblings. The effect of steroids
-
Rossman PL, Hummer GJ. Chronic neutropenia in siblings. The effect of steroids. Ann Intern Med 1960;52:242-253.
-
(1960)
Ann Intern Med
, vol.52
, pp. 242-253
-
-
Rossman, P.L.1
Hummer, G.J.2
-
23
-
-
0016131994
-
A study of steroid induced granulocytosis in a patient with chronic benign neutropenia of childhood
-
Deinhard AS, Page AR. A study of steroid induced granulocytosis in a patient with chronic benign neutropenia of childhood. Br J Haematol 1974;28:333-345.
-
(1974)
Br J Haematol
, vol.28
, pp. 333-345
-
-
Deinhard, A.S.1
Page, A.R.2
-
25
-
-
0019500322
-
Lithium therapy of children with chronic neutropenia
-
Chan HSL, Freedman MH, Saunders EF. Lithium therapy of children with chronic neutropenia. Am J Med 1981;70:1073-1077.
-
(1981)
Am J Med
, vol.70
, pp. 1073-1077
-
-
Chan, H.S.L.1
Freedman, M.H.2
Saunders, E.F.3
-
26
-
-
0023245804
-
Treatment of idiopathic chronic neutropenia with high-dose intravenous immunoglobulin
-
Lakos A, Timar L. Treatment of idiopathic chronic neutropenia with high-dose intravenous immunoglobulin. Am J Dis Child 1987;141:12-13.
-
(1987)
Am J Dis Child
, vol.141
, pp. 12-13
-
-
Lakos, A.1
Timar, L.2
-
27
-
-
0023911749
-
Intravenous treatment with gammaglobulin of autoimmune neutropenia of infancy
-
Bussel J, Lalezari P, Fikring S. Intravenous treatment with gammaglobulin of autoimmune neutropenia of infancy. J Pediatr 1988;112:298-301.
-
(1988)
J Pediatr
, vol.112
, pp. 298-301
-
-
Bussel, J.1
Lalezari, P.2
Fikring, S.3
-
28
-
-
0025255616
-
Differential effects of granulocyte-macrophage colony-stimulating factor and granulocyte colony-stimulating factor in children with severe congenital neutropenia
-
Welte K, Zeidler C, Reiter A, Muller W, Odenwald E. Souza L, Riehm H. Differential effects of granulocyte-macrophage colony-stimulating factor and granulocyte colony-stimulating factor in children with severe congenital neutropenia. Blood 1990;75:1056-1063.
-
(1990)
Blood
, vol.75
, pp. 1056-1063
-
-
Welte, K.1
Zeidler, C.2
Reiter, A.3
Muller, W.4
Odenwald, E.5
Souza, L.6
Riehm, H.7
-
29
-
-
70449208737
-
Leukemia and agranulocytosis in a family with hereditary leukopenia
-
DeVries A, Peketh L, Joshua H. Leukemia and agranulocytosis in a family with hereditary leukopenia. Acta Med Orient 1958;17:26-32.
-
(1958)
Acta Med Orient
, vol.17
, pp. 26-32
-
-
DeVries, A.1
Peketh, L.2
Joshua, H.3
-
30
-
-
0014882993
-
Congenital agranulocytosis: Prolonged survival and terminal acute leukemia
-
Gilman PA, Jackson DP, Guild HG. Congenital agranulocytosis: prolonged survival and terminal acute leukemia. Blood 1970;36:576-585.
-
(1970)
Blood
, vol.36
, pp. 576-585
-
-
Gilman, P.A.1
Jackson, D.P.2
Guild, H.G.3
-
31
-
-
0027262406
-
Terminal acute myelogenous leukemia in a patient with congenital agranulocytosis
-
Wong W, Williams D, Slovak ML, Charak B, Mazunder A, Snyder D, Powers DR, Byrnes RK. Terminal acute myelogenous leukemia in a patient with congenital agranulocytosis. Am J Hematol 1993;43:133-138.
-
(1993)
Am J Hematol
, vol.43
, pp. 133-138
-
-
Wong, W.1
Williams, D.2
Slovak, M.L.3
Charak, B.4
Mazunder, A.5
Snyder, D.6
Powers, D.R.7
Byrnes, R.K.8
-
32
-
-
0018371661
-
Congenital agranulocytosis terminating in acute myelomonocytic leukemia
-
Rosen RB, Kang SJ. Congenital agranulocytosis terminating in acute myelomonocytic leukemia. J Pediatr 1979;94:406-408.
-
(1979)
J Pediatr
, vol.94
, pp. 406-408
-
-
Rosen, R.B.1
Kang, S.J.2
-
33
-
-
0000535984
-
Kostmann's syndrome
-
Young NS, Alter BP, editors. Philadelphia: Saunders
-
Young NS, Alter BP. Kostmann's syndrome. In: Young NS, Alter BP, editors. Aplastic anemia: acquired and inherited. Philadelphia: Saunders; 1994. p 391-394.
-
(1994)
Aplastic Anemia: Acquired and Inherited
, pp. 391-394
-
-
Young, N.S.1
Alter, B.P.2
-
34
-
-
0028910402
-
Childhood monosomy 7: Epidemiology, biology, and mechanistic implications
-
Apr 15
-
Luna-Fineman S, Shannon KM, Lange BJ. Childhood monosomy 7: epidemiology, biology, and mechanistic implications. Blood 1995(Apr 15);85(8):1985-1999.
-
(1995)
Blood
, vol.85
, Issue.8
, pp. 1985-1999
-
-
Luna-Fineman, S.1
Shannon, K.M.2
Lange, B.J.3
-
35
-
-
0029929155
-
Haematological abnormalities in Shwachman-Diamond syndrome
-
Smith OP, Hann IM, Chessels JM, Reeves BR, Milla P. Haematological abnormalities in Shwachman-Diamond syndrome. Br J Haematol 1996;94:279-284.
-
(1996)
Br J Haematol
, vol.94
, pp. 279-284
-
-
Smith, O.P.1
Hann, I.M.2
Chessels, J.M.3
Reeves, B.R.4
Milla, P.5
-
36
-
-
0029807493
-
Shwachman syndrome: Exocrine pancreatic dysfunction and variable phenotypic expression
-
Mack DR, Forstner GG, Wilschanski M, Freedman MH, Durie PR. Shwachman syndrome: exocrine pancreatic dysfunction and variable phenotypic expression. Gastroenterology 1996;111:1593-1602.
-
(1996)
Gastroenterology
, vol.111
, pp. 1593-1602
-
-
Mack, D.R.1
Forstner, G.G.2
Wilschanski, M.3
Freedman, M.H.4
Durie, P.R.5
-
37
-
-
0028807618
-
Monosomy 7 and activating ras mutations accompany malignant transformation in patients with congenital neutropenia
-
Kalra R, Dale D, Freedman M, Bonilla MA, Weinblatt M, Ganser A, Bowman P, Abish S, Priest J, Oseas RS, et al. Monosomy 7 and activating ras mutations accompany malignant transformation in patients with congenital neutropenia. Blood 1995;86:4579-4586.
-
(1995)
Blood
, vol.86
, pp. 4579-4586
-
-
Kalra, R.1
Dale, D.2
Freedman, M.3
Bonilla, M.A.4
Weinblatt, M.5
Ganser, A.6
Bowman, P.7
Abish, S.8
Priest, J.9
Oseas, R.S.10
-
38
-
-
0029129034
-
Mutations in the gene for the granulocyte colony-stimulating factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia
-
Dong F, Brynes RK, Tidow N, Welte K, Lowenberg B, Touw IP. Mutations in the gene for the granulocyte colony-stimulating factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia. N Engl J Med 1995;333:487-493.
-
(1995)
N Engl J Med
, vol.333
, pp. 487-493
-
-
Dong, F.1
Brynes, R.K.2
Tidow, N.3
Welte, K.4
Lowenberg, B.5
Touw, I.P.6
-
39
-
-
0030945921
-
Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colonystimulating factor (G-CSF) receptor gene in patients with severe congenital neutropenia
-
Tidow N, Pilz C, Teichmann B, Muller-Brechlin A, Germeshausen M, Kasper B, Rauprich P, Sykora KW, Welte K. Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colonystimulating factor (G-CSF) receptor gene in patients with severe congenital neutropenia. Blood 1997;89:2369-2375.
-
(1997)
Blood
, vol.89
, pp. 2369-2375
-
-
Tidow, N.1
Pilz, C.2
Teichmann, B.3
Muller-Brechlin, A.4
Germeshausen, M.5
Kasper, B.6
Rauprich, P.7
Sykora, K.W.8
Welte, K.9
-
40
-
-
16944361974
-
Mutations in the granulocyte-colony stimulating factor receptor gene in patients with severe congenital neutropenia
-
Dong F, Dale DC, Bonilla MA, Freedman M, Fasth A, Neijens HJ, Palmblad J, Briars GL, Carisson G, Veermau AJ, Welte K, Lowenberg B, Touw IP. Mutations in the granulocyte-colony stimulating factor receptor gene in patients with severe congenital neutropenia. Leukemia 1997;11:120-125.
-
(1997)
Leukemia
, vol.11
, pp. 120-125
-
-
Dong, F.1
Dale, D.C.2
Bonilla, M.A.3
Freedman, M.4
Fasth, A.5
Neijens, H.J.6
Palmblad, J.7
Briars, G.L.8
Carisson, G.9
Veermau, A.J.10
Welte, K.11
Lowenberg, B.12
Touw, I.P.13
-
41
-
-
0027942372
-
Long-term safety treatment with recombinant human granulocyte colony-stimulating factor (rmetHuG-CSF) in patients with severe congenital neutropenias
-
Bonilla MA, Dale D, Zeidler C, Last L, Reiter A, Ruggeiro M, Davis M, Koci B, Hammond W, Gillo A, et al. Long-term safety treatment with recombinant human granulocyte colony-stimulating factor (rmetHuG-CSF) in patients with severe congenital neutropenias. Br J Haematol 1994;88:723-730.
-
(1994)
Br J Haematol
, vol.88
, pp. 723-730
-
-
Bonilla, M.A.1
Dale, D.2
Zeidler, C.3
Last, L.4
Reiter, A.5
Ruggeiro, M.6
Davis, M.7
Koci, B.8
Hammond, W.9
Gillo, A.10
-
42
-
-
0003235371
-
Administration of r-metHuG-CSF during pregnancy in patients with severe chronic neutropenia (SCN)
-
Boxer L, Dale DC, Bonilla MA, Cham B, Freedman M, Kannourakis G, Brown S, Fier C, Welte K. Administration of r-metHuG-CSF during pregnancy in patients with severe chronic neutropenia (SCN) [abstract]. Blood 1995;86:508a.
-
(1995)
Blood
, vol.86
-
-
Boxer, L.1
Dale, D.C.2
Bonilla, M.A.3
Cham, B.4
Freedman, M.5
Kannourakis, G.6
Brown, S.7
Fier, C.8
Welte, K.9
-
43
-
-
12244309370
-
Treatment of cyclic neutropenia with G-CSF during pregnancy
-
Dicato M, Ries F, Richard F. Treatment of cyclic neutropenia with G-CSF during pregnancy [abstract]. Blood 1993;82:1972.
-
(1993)
Blood
, vol.82
, pp. 1972
-
-
Dicato, M.1
Ries, F.2
Richard, F.3
-
44
-
-
0027269718
-
A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropenia
-
Dale DC, Bonilla MA, Davis MW, Nakanishi AM, Hammond WP, Kurtzberg J, Wang W, Jakubowski A, Winton E, Lalezari P, et al. A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropenia. Blood 1993;81:2496-2502.
-
(1993)
Blood
, vol.81
, pp. 2496-2502
-
-
Dale, D.C.1
Bonilla, M.A.2
Davis, M.W.3
Nakanishi, A.M.4
Hammond, W.P.5
Kurtzberg, J.6
Wang, W.7
Jakubowski, A.8
Winton, E.9
Lalezari, P.10
-
45
-
-
0032757863
-
Neutrophil elastase mutations define a 21-day biological clock in cyclic hematopoiesis
-
Horwitz M, Benson KF, Person RE, Aprikyan AG, Dale DC. Neutrophil elastase mutations define a 21-day biological clock in cyclic hematopoiesis. Nat Genet 1999;23:433-436.
-
(1999)
Nat Genet
, vol.23
, pp. 433-436
-
-
Horwitz, M.1
Benson, K.F.2
Person, R.E.3
Aprikyan, A.G.4
Dale, D.C.5
-
47
-
-
0035161158
-
Impaired survival of bone marrow hematopoietic progenitor cells in cyclic neutropenia
-
Aprikyan AG, Liles WC, Rodger E, Jonas M, Chi EY, Dale DC. Impaired survival of bone marrow hematopoietic progenitor cells in cyclic neutropenia. Blood 2001;97:147-153.
-
(2001)
Blood
, vol.97
, pp. 147-153
-
-
Aprikyan, A.G.1
Liles, W.C.2
Rodger, E.3
Jonas, M.4
Chi, E.Y.5
Dale, D.C.6
-
48
-
-
0034307655
-
Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia
-
Dale DC. Person RE, Bolyard AA, Aprikvan AG, Bos C, Bonilla MA, Boxer LA, Kannourakis G, Zeidler C, Welte K, Benson KF, Horwitz M. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 2000;96:2317-2322.
-
(2000)
Blood
, vol.96
, pp. 2317-2322
-
-
Dale, D.C.1
Person, R.E.2
Bolyard, A.A.3
Aprikvan, A.G.4
Bos, C.5
Bonilla, M.A.6
Boxer, L.A.7
Kannourakis, G.8
Zeidler, C.9
Welte, K.10
Benson, K.F.11
Horwitz, M.12
-
49
-
-
0001358850
-
Accelerated apoptosis of bone marrow progenitor cells in severe congenital neutropenia
-
Aprikyan AAG, Liles WC, Person RE, Rodger E, Dale DC. Accelerated apoptosis of bone marrow progenitor cells in severe congenital neutropenia [abstract]. Blood 2000;94:482a
-
(2000)
Blood
, vol.94
-
-
Aprikyan, A.A.G.1
Liles, W.C.2
Person, R.E.3
Rodger, E.4
Dale, D.C.5
-
50
-
-
0035017460
-
Clinical implications of mutations of neutrophil elastase in congenital and cyclic neutropenia
-
Dale DC, Liles WC, Garwicz D, Aprikyan AG. Clinical implications of mutations of neutrophil elastase in congenital and cyclic neutropenia. J Pediatr Hematol/Oncol 2001;4:208-210.
-
(2001)
J Pediatr Hematol/Oncol
, vol.4
, pp. 208-210
-
-
Dale, D.C.1
Liles, W.C.2
Garwicz, D.3
Aprikyan, A.G.4
|