-
2
-
-
0031723552
-
Adenosine deaminase deficiency: Clinical expression, molecular basis, and therapy
-
Hershfield M.S. Adenosine deaminase deficiency: Clinical expression, molecular basis, and therapy Seminars in Hematology 35 1998 291-298
-
(1998)
Seminars in Hematology
, vol.35
, pp. 291-298
-
-
Hershfield, M.S.1
-
3
-
-
0000930996
-
Immunodeficiency disease due to deficiency of adenosine deaminase
-
H. Ochs, C. Smith, & J. Puck (Eds.), Oxford: Oxford University Press
-
Hirschorn R. Immunodeficiency disease due to deficiency of adenosine deaminase Ochs H. Smith C. & Puck J. (Eds.) Primary Immunodeficiency Diseases 1999 121-139 Oxford University Press, Oxford
-
(1999)
Primary Immunodeficiency Diseases
, pp. 121-139
-
-
Hirschorn, R.1
-
4
-
-
0034613689
-
The binding site of human adenosine deaminase for CD26/dipeptidyl peptidase IV. The arg142gln mutation impairs binding to cd26 but does not cause immune deficiency
-
Richard E. Arredondo-Vega F.X. Santisteban I. et al. The binding site of human adenosine deaminase for CD26/dipeptidyl peptidase IV. The arg142gln mutation impairs binding to cd26 but does not cause immune deficiency Journal of Experimental Medicine 192 2000 1223-1236
-
(2000)
Journal of Experimental Medicine
, vol.192
, pp. 1223-1236
-
-
Richard, E.1
Arredondo-Vega, F.X.2
Santisteban, I.3
-
5
-
-
0242267944
-
Capillary electrophoresis in diagnosis and monitoring of adenosine deaminase deficiency
-
Carlucci F. Tabucchi A. Aiuti A. et al. Capillary electrophoresis in diagnosis and monitoring of adenosine deaminase deficiency Clinical Chemistry 49 2003 1830-1838
-
(2003)
Clinical Chemistry
, vol.49
, pp. 1830-1838
-
-
Carlucci, F.1
Tabucchi, A.2
Aiuti, A.3
-
6
-
-
0032231355
-
Adenosine deaminase deficiency: Genotype-phenotype correlations based on expressed activity of 29 mutant alleles
-
Arredondo V.F. Santisteban I. Daniels S. et al. Adenosine deaminase deficiency: Genotype-phenotype correlations based on expressed activity of 29 mutant alleles American Journal of Human Genetics 63 1998 1049-1059
-
(1998)
American Journal of Human Genetics
, vol.63
, pp. 1049-1059
-
-
Arredondo, V.F.1
Santisteban, I.2
Daniels, S.3
-
8
-
-
0024849405
-
Pathologic findings in adenosine deaminase deficient-severe combined immunodeficiency. II. Thymus, spleen, lymph node, and gastrointestinal tract lymphoid tissue alterations
-
Ratech H. Hirschhorn R. Greco M.A. Pathologic findings in adenosine deaminase deficient-severe combined immunodeficiency. II. Thymus, spleen, lymph node, and gastrointestinal tract lymphoid tissue alterations American Journal Patholology 135 1989 1145-1156
-
(1989)
American Journal Patholology
, vol.135
, pp. 1145-1156
-
-
Ratech, H.1
Hirschhorn, R.2
Greco, M.A.3
-
9
-
-
0034968336
-
Cognitive and behavioral abnormalities in adenosine deaminase deficient severe combined immunodeficiency
-
Rogers M.H. Lwin R. Fairbanks L. et al. Cognitive and behavioral abnormalities in adenosine deaminase deficient severe combined immunodeficiency Journal of Pediatrics 139 2001 44-50
-
(2001)
Journal of Pediatrics
, vol.139
, pp. 44-50
-
-
Rogers, M.H.1
Lwin, R.2
Fairbanks, L.3
-
10
-
-
0037442176
-
Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: Report of the European experience 1968-99
-
Antoine C. Muller S. Cant A. et al. Long-term survival and transplantation of haemopoietic stem cells for immunodeficiencies: report of the European experience 1968-99 Lancet 361 2003 553-560
-
(2003)
Lancet
, vol.361
, pp. 553-560
-
-
Antoine, C.1
Muller, S.2
Cant, A.3
-
11
-
-
0019857583
-
Bone marrow transplantation only partially restores purine metabolites to normal in adenosine deaminase-deficient patients
-
Hirschhorn R. Roegner M.V. Kuritsky L. et al. Bone marrow transplantation only partially restores purine metabolites to normal in adenosine deaminase-deficient patients The Journal of Clinical Investigation 68 1981 1387-1393
-
(1981)
The Journal of Clinical Investigation
, vol.68
, pp. 1387-1393
-
-
Hirschhorn, R.1
Roegner, M.V.2
Kuritsky, L.3
-
12
-
-
0026782851
-
Antibody responses to bacteriophage phi X174 in patients with adenosine deaminase deficiency
-
Ochs H.D. Buckley R.H. Kobayashi R.H. et al. Antibody responses to bacteriophage phi X174 in patients with adenosine deaminase deficiency Blood 80 1992 1163-1171
-
(1992)
Blood
, vol.80
, pp. 1163-1171
-
-
Ochs, H.D.1
Buckley, R.H.2
Kobayashi, R.H.3
-
13
-
-
0027180016
-
Lymphocyte ontogeny in adenosine deaminase-deficient severe combined immune deficiency after treatment with polyethylene glycol-modified adenosine deaminase
-
Weinberg K. Hershfield M.S. Bastian J. et al. Lymphocyte ontogeny in adenosine deaminase-deficient severe combined immune deficiency after treatment with polyethylene glycol-modified adenosine deaminase The Journal of Clinical Investigation 92 1993 596-602
-
(1993)
The Journal of Clinical Investigation
, vol.92
, pp. 596-602
-
-
Weinberg, K.1
Hershfield, M.S.2
Bastian, J.3
-
14
-
-
0036230462
-
Therapeutic applications for hematopoietic stem cell gene transfer
-
Bordignon C. Roncarolo M.G. Therapeutic applications for hematopoietic stem cell gene transfer Nature Immunology 3 2002 318-321
-
(2002)
Nature Immunology
, vol.3
, pp. 318-321
-
-
Bordignon, C.1
Roncarolo, M.G.2
-
16
-
-
0345940337
-
Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transfer
-
Kantoff P. Kohn D. Mitsuya H. et al. Correction of adenosine deaminase deficiency in cultured human T and B cells by retrovirus-mediated gene transfer Proceedings of National Academy Sciences, USA 83 1986 6563-6567
-
(1986)
Proceedings of National Academy Sciences, USA
, vol.83
, pp. 6563-6567
-
-
Kantoff, P.1
Kohn, D.2
Mitsuya, H.3
-
17
-
-
0025811758
-
An in vivo model of somatic cell gene therapy for human severe combined immunodeficiency
-
Ferrari G. Rossini S. Giavazzi R. et al. An in vivo model of somatic cell gene therapy for human severe combined immunodeficiency Science 251 1991 1363-1366
-
(1991)
Science
, vol.251
, pp. 1363-1366
-
-
Ferrari, G.1
Rossini, S.2
Giavazzi, R.3
-
18
-
-
0026670175
-
Transfer of the ADA gene into human ADA-deficient T lymphocytes reconstitutes specific immune functions
-
Ferrari G. Rossini S. Nobili N. et al. Transfer of the ADA gene into human ADA-deficient T lymphocytes reconstitutes specific immune functions Blood 80 1992 1120-1124
-
(1992)
Blood
, vol.80
, pp. 1120-1124
-
-
Ferrari, G.1
Rossini, S.2
Nobili, N.3
-
19
-
-
0029902033
-
Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency
-
Hirschhorn R. Yang D.R. Puck J.M. et al. Spontaneous in vivo reversion to normal of an inherited mutation in a patient with adenosine deaminase deficiency Nature Genetics 13 1996 290-295
-
(1996)
Nature Genetics
, vol.13
, pp. 290-295
-
-
Hirschhorn, R.1
Yang, D.R.2
Puck, J.M.3
-
20
-
-
0036464720
-
Adenosine deaminase deficiency with mosaicism for a "second-site suppressor" of a splicing mutation: Decline in revertant T lymphocytes during enzyme replacement therapy
-
Arredondo-Vega F.X. Santisteban I. Richard E. et al. Adenosine deaminase deficiency with mosaicism for a "second-site suppressor" of a splicing mutation: Decline in revertant T lymphocytes during enzyme replacement therapy Blood 99 2002 1005-1013
-
(2002)
Blood
, vol.99
, pp. 1005-1013
-
-
Arredondo-Vega, F.X.1
Santisteban, I.2
Richard, E.3
-
22
-
-
0027738402
-
Transfer of the ADA gene into bone marrow cells and peripheral blood lymphocytes for the treatment of patients affected by ADA-deficient SCID
-
Bordignon C. Mavilio F. Ferrari G. et al. Transfer of the ADA gene into bone marrow cells and peripheral blood lymphocytes for the treatment of patients affected by ADA-deficient SCID Human Gene Therapy 4 1993 513-520
-
(1993)
Human Gene Therapy
, vol.4
, pp. 513-520
-
-
Bordignon, C.1
Mavilio, F.2
Ferrari, G.3
-
23
-
-
0028789792
-
Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patients
-
Bordignon C. Notarangelo L.D. Nobili N. et al. Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patients Science 270 1995 470-475
-
(1995)
Science
, vol.270
, pp. 470-475
-
-
Bordignon, C.1
Notarangelo, L.D.2
Nobili, N.3
-
24
-
-
0028807727
-
Lymphocyte-directed gene therapy for ADA-SCID: Initial trial results after 4 years
-
Blaese R.M. Culver K.W. Miller A.D. et al. Lymphocyte-directed gene therapy for ADA-SCID: Initial trial results after 4 years Science 270 1995 475-480
-
(1995)
Science
, vol.270
, pp. 475-480
-
-
Blaese, R.M.1
Culver, K.W.2
Miller, A.D.3
-
25
-
-
0028864561
-
Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency
-
Kohn D.B. Weinberg K.I. Nolta J.A. et al. Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency Nature Medicine 1 1995 1017-1023
-
(1995)
Nature Medicine
, vol.1
, pp. 1017-1023
-
-
Kohn, D.B.1
Weinberg, K.I.2
Nolta, J.A.3
-
26
-
-
0031975088
-
Successful peripheral T-lymphocyte-directed gene transfer for a patient with severe combined immune deficiency caused by adenosine deaminase deficiency
-
Onodera M. Ariga T. Kawamura N. et al. Successful peripheral T-lymphocyte-directed gene transfer for a patient with severe combined immune deficiency caused by adenosine deaminase deficiency Blood 91 1998 30-36
-
(1998)
Blood
, vol.91
, pp. 30-36
-
-
Onodera, M.1
Ariga, T.2
Kawamura, N.3
-
27
-
-
0033567063
-
In vivo kinetics of transduced cells in peripheral T cell-directed gene therapy: Role of CD8+cells in improved immunological function in an adenosine deaminase (ADA)-SCID patient
-
Kawamura N. Ariga T. Ohtsu M. et al. In vivo kinetics of transduced cells in peripheral T cell-directed gene therapy: Role of CD8+cells in improved immunological function in an adenosine deaminase (ADA)-SCID patient The Journal of Immunology 163 1999 2256-2261
-
(1999)
The Journal of Immunology
, vol.163
, pp. 2256-2261
-
-
Kawamura, N.1
Ariga, T.2
Ohtsu, M.3
-
28
-
-
18444376150
-
Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement
-
Aiuti A. Vai S. Mortellaro A. et al. Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement Nature Medicine 8 2002 423-425
-
(2002)
Nature Medicine
, vol.8
, pp. 423-425
-
-
Aiuti, A.1
Vai, S.2
Mortellaro, A.3
-
29
-
-
0038446699
-
Persistence and expression of the adenosine deaminase gene for 12 years and immune reaction to gene transfer components: Long-term results of the first clinical gene therapy trial
-
Muul L.M. Tuschong L.M. Soenen S.L. et al. Persistence and expression of the adenosine deaminase gene for 12 years and immune reaction to gene transfer components: Long-term results of the first clinical gene therapy trial Blood 101 2003 2563-2569
-
(2003)
Blood
, vol.101
, pp. 2563-2569
-
-
Muul, L.M.1
Tuschong, L.M.2
Soenen, S.L.3
-
31
-
-
9244243165
-
Bone marrow gene transfer in three patients with adenosine deaminase deficiency
-
Hoogerbrugge P.M. van Beusechem V. Fischer A. et al. Bone marrow gene transfer in three patients with adenosine deaminase deficiency Gene Therapy 3 1996 179-183
-
(1996)
Gene Therapy
, vol.3
, pp. 179-183
-
-
Hoogerbrugge, P.M.1
van Beusechem, V.2
Fischer, A.3
-
32
-
-
0031593688
-
Lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+cells in ADA-deficient SCID neonates
-
Kohn D.B. Hershfield M.S. Carbonaro D. et al. lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34+cells in ADA-deficient SCID neonates Nature Medicine 4 1998 775-780
-
(1998)
Nature Medicine
, vol.4
, pp. 775-780
-
-
Kohn, D.B.1
Hershfield, M.S.2
Carbonaro, D.3
-
33
-
-
0345144017
-
Clonality analysis after retroviral-mediated gene transfer to CD34+cells from the cord blood of ADA-deficient SCID neonates
-
Schmidt M. Carbonaro D.A. Speckmann C. et al. Clonality analysis after retroviral-mediated gene transfer to CD34+cells from the cord blood of ADA-deficient SCID neonates Nature Medicine 9 2003 463-468
-
(2003)
Nature Medicine
, vol.9
, pp. 463-468
-
-
Schmidt, M.1
Carbonaro, D.A.2
Speckmann, C.3
-
34
-
-
0037189401
-
Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning
-
Aiuti A. Slavin S. Aker M. et al. Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning Science 296 2002 2410-2413
-
(2002)
Science
, vol.296
, pp. 2410-2413
-
-
Aiuti, A.1
Slavin, S.2
Aker, M.3
-
35
-
-
0033587581
-
Optimization of retroviral gene transduction of mobilized primitive hematopoietic progenitors by using thrombopoietin, Flt3, and Kit ligands and RetroNectin culture
-
Murray L. Luens K. Tushinski R. et al. Optimization of retroviral gene transduction of mobilized primitive hematopoietic progenitors by using thrombopoietin, Flt3, and Kit ligands and RetroNectin culture Human Gene Therapy 10 1999 1743-1752
-
(1999)
Human Gene Therapy
, vol.10
, pp. 1743-1752
-
-
Murray, L.1
Luens, K.2
Tushinski, R.3
-
36
-
-
0033215441
-
Direct evidence for multiple self-renewal divisions of human in vivo repopulating hematopoietic cells in short-term culture
-
Glimm H. Eaves C.J. Direct evidence for multiple self-renewal divisions of human in vivo repopulating hematopoietic cells in short-term culture Blood 94 1999 2161-2168
-
(1999)
Blood
, vol.94
, pp. 2161-2168
-
-
Glimm, H.1
Eaves, C.J.2
-
37
-
-
0034131481
-
Efficient retrovirus-mediated transfer of the multidrug resistance 1 gene into autologous human long-term repopulating hematopoietic stem cells
-
Abonour R. Williams D.A. Einhorn L. et al. Efficient retrovirus-mediated transfer of the multidrug resistance 1 gene into autologous human long-term repopulating hematopoietic stem cells Nature Medicine 6 2000 652-658
-
(2000)
Nature Medicine
, vol.6
, pp. 652-658
-
-
Abonour, R.1
Williams, D.A.2
Einhorn, L.3
-
38
-
-
0034943202
-
The impact of ex vivo cytokine stimulation on engraftment of primitive hematopoietic cells in a non-human primate model
-
discussion 244-235
-
Dunbar C.E. Takatoku M. Donahue R.E. The impact of ex vivo cytokine stimulation on engraftment of primitive hematopoietic cells in a non-human primate model Annals of the New York Academy of Sciences 938 2001 236-244 discussion 244-235
-
(2001)
Annals of the New York Academy of Sciences
, vol.938
, pp. 236-244
-
-
Dunbar, C.E.1
Takatoku, M.2
Donahue, R.E.3
-
39
-
-
0035351101
-
Optimisation of retroviral supernatant production conditions for the genetic modification of human CD34+cells
-
Dando J.S. Aiuti A. Deola S. et al. Optimisation of retroviral supernatant production conditions for the genetic modification of human CD34+cells The Journal of Gene Medicine 3 2001 219-227
-
(2001)
The Journal of Gene Medicine
, vol.3
, pp. 219-227
-
-
Dando, J.S.1
Aiuti, A.2
Deola, S.3
-
40
-
-
0033042219
-
Retroviral-fibronectin interactions in transduction of mammalian cells
-
discussion 113-104
-
Williams D.A. Retroviral-fibronectin interactions in transduction of mammalian cells Annals of the New York Academy of Sciences 872 1999 109-113 discussion 113-104
-
(1999)
Annals of the New York Academy of Sciences
, vol.872
, pp. 109-113
-
-
Williams, D.A.1
-
41
-
-
0034016713
-
An evaluation of engraftment, toxicity and busulfan concentration in children receiving bone marrow transplantation for leukemia or genetic disease
-
Bolinger A.M. Zangwill A.B. Slattery J.T. et al. An evaluation of engraftment, toxicity and busulfan concentration in children receiving bone marrow transplantation for leukemia or genetic disease Bone Marrow Transplant 25 2000 925-930
-
(2000)
Bone Marrow Transplant
, vol.25
, pp. 925-930
-
-
Bolinger, A.M.1
Zangwill, A.B.2
Slattery, J.T.3
-
42
-
-
0036344648
-
Non-myeloablative stem cell transplantation for the treatment of cancer and life-threatening non-malignant disorders; past accomplishments and future goals
-
Slavin S. Aker M. Shapira M.Y. et al. Non-myeloablative stem cell transplantation for the treatment of cancer and life-threatening non-malignant disorders; past accomplishments and future goals Transfusion & Apheresis Science 27 2002 159-166
-
(2002)
Transfusion & Apheresis Science
, vol.27
, pp. 159-166
-
-
Slavin, S.1
Aker, M.2
Shapira, M.Y.3
-
43
-
-
0033587487
-
Retroviral marking and transplantation of rhesus hematopoietic cells by nonmyeloablative conditioning
-
Huhn R.D. Tisdale J.F. Agricola B. et al. Retroviral marking and transplantation of rhesus hematopoietic cells by nonmyeloablative conditioning Human Gene Therapy 10 1999 1783-1790
-
(1999)
Human Gene Therapy
, vol.10
, pp. 1783-1790
-
-
Huhn, R.D.1
Tisdale, J.F.2
Agricola, B.3
-
44
-
-
0033214219
-
Efficient and durable gene marking of hematopoietic progenitor cells in nonhuman primates after nonablative conditioning
-
Rosenzweig M. MacVittie T.J. Harper D. et al. Efficient and durable gene marking of hematopoietic progenitor cells in nonhuman primates after nonablative conditioning Blood 94 1999 2271-2286
-
(1999)
Blood
, vol.94
, pp. 2271-2286
-
-
Rosenzweig, M.1
MacVittie, T.J.2
Harper, D.3
-
45
-
-
1942506376
-
Safety and efficacy of stem cell gene therapy combined with nonmyeloablative conditioning for the treatment of ADA-SCID
-
Aiuti A. Cattaneo F. Cassani B. et al. Safety and efficacy of stem cell gene therapy combined with nonmyeloablative conditioning for the treatment of ADA-SCID Blood 102 2003 531
-
(2003)
Blood
, vol.102
, pp. 531
-
-
Aiuti, A.1
Cattaneo, F.2
Cassani, B.3
-
46
-
-
0344511772
-
Safety of retroviral gene marking with a truncated NGF receptor
-
Bonini C. Grez M. Traversari C. et al. Safety of retroviral gene marking with a truncated NGF receptor Nature Medicine 9 2003 367-369
-
(2003)
Nature Medicine
, vol.9
, pp. 367-369
-
-
Bonini, C.1
Grez, M.2
Traversari, C.3
-
47
-
-
10744233858
-
American Society of Gene Therapy (ASGT) Ad Hoc Subcommittee on retroviral-mediated gene transfer to hematopoietic stem cells
-
Kohn D.B. Sadelain M. Dunbar C. et al. American Society of Gene Therapy (ASGT) Ad Hoc Subcommittee on retroviral-mediated gene transfer to hematopoietic stem cells Molecular Therapy 8 2003 180-187
-
(2003)
Molecular Therapy
, vol.8
, pp. 180-187
-
-
Kohn, D.B.1
Sadelain, M.2
Dunbar, C.3
-
48
-
-
0142084745
-
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1
-
Hacein-Bey-Abina S. Von Kalle C. Schmidt M. et al. LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1 Science 302 2003 415-419
-
(2003)
Science
, vol.302
, pp. 415-419
-
-
Hacein-Bey-Abina, S.1
Von Kalle, C.2
Schmidt, M.3
-
49
-
-
0042738935
-
Occurrence of leukaemia following gene therapy of X-linked SCID
-
Kohn D.B. Sadelain M. Glorioso J.C. Occurrence of leukaemia following gene therapy of X-linked SCID Nature Review Cancer 3 2003 477-488
-
(2003)
Nature Review Cancer
, vol.3
, pp. 477-488
-
-
Kohn, D.B.1
Sadelain, M.2
Glorioso, J.C.3
-
51
-
-
0347634456
-
Gene therapy insertional mutagenesis insights
-
Dave U.P. Jenkins N.A. Copeland N.G. Gene therapy insertional mutagenesis insights Science 303 2004 333
-
(2004)
Science
, vol.303
, pp. 333
-
-
Dave, U.P.1
Jenkins, N.A.2
Copeland, N.G.3
-
53
-
-
0142168693
-
Corrective gene transfer into bone marrow CD34+cells for adenosine deaminase (ADA) deficiency: Results in four patients after one year of follow-up
-
Candotti F. Podsakoff G. Schurman S. et al. Corrective gene transfer into bone marrow CD34+cells for adenosine deaminase (ADA) deficiency: results in four patients after one year of follow-up Molecular Therapy 7 2003 S448-S449
-
(2003)
Molecular Therapy
, vol.7
-
-
Candotti, F.1
Podsakoff, G.2
Schurman, S.3
-
54
-
-
0034724857
-
Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease
-
Cavazzana-Calvo M. Hacein B.S. de Saint Basile G. et al. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease Science 288 2000 669-672
-
(2000)
Science
, vol.288
, pp. 669-672
-
-
Cavazzana-Calvo, M.1
Hacein, B.S.2
de Saint Basile, G.3
-
55
-
-
0037129435
-
Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy
-
Hacein-Bey-Abina S. Le Deist F. Carlier F. et al. Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy New England Journal of Medicine 346 2002 1185-1193
-
(2002)
New England Journal of Medicine
, vol.346
, pp. 1185-1193
-
-
Hacein-Bey-Abina, S.1
Le Deist, F.2
Carlier, F.3
-
56
-
-
0025182977
-
European experience of bone-marrow transplantation for severe combined immunodeficiency
-
Fischer A. Landais P. Friedrich W. et al. European experience of bone-marrow transplantation for severe combined immunodeficiency Lancet 336 1990 850-854
-
(1990)
Lancet
, vol.336
, pp. 850-854
-
-
Fischer, A.1
Landais, P.2
Friedrich, W.3
-
57
-
-
18244411938
-
Long-term immune reconstitution and outcome after HLA-nonidentical T-cell-depleted bone marrow transplantation for severe combined immunodeficiency: A European retrospective study of 116 patients
-
Haddad E. Landais P. Friedrich W. et al. Long-term immune reconstitution and outcome after HLA-nonidentical T-cell-depleted bone marrow transplantation for severe combined immunodeficiency: A European retrospective study of 116 patients Blood 91 1998 3646-3653
-
(1998)
Blood
, vol.91
, pp. 3646-3653
-
-
Haddad, E.1
Landais, P.2
Friedrich, W.3
|