-
1
-
-
0000788042
-
Familiarer, angeborener Morbus Werlhofii?
-
Wiskott A. Familiarer, angeborener Morbus Werlhofii? Monatsschrift Kinderheilkunde. 68:1937;212-216.
-
(1937)
Monatsschrift Kinderheilkunde
, vol.68
, pp. 212-216
-
-
Wiskott, A.1
-
2
-
-
0001102239
-
Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea
-
Aldrich R.A., Steinberg A.G., Campbell D.C. Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. Pediatrics. 13:1954;133-139.
-
(1954)
Pediatrics
, vol.13
, pp. 133-139
-
-
Aldrich, R.A.1
Steinberg, A.G.2
Campbell, D.C.3
-
3
-
-
0018932524
-
The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979)
-
Perry G.S., Spector B.D., Schuman L.M., Mandel J.S., Anderson V.E., McHugh R.B., Hanson M.R., Fahlstrom S.M., Krivit W., Kersey J.H. The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979). J.Pediatr. 97:1980;72-78.
-
(1980)
J.Pediatr.
, vol.97
, pp. 72-78
-
-
Perry, G.S.1
Spector, B.D.2
Schuman, L.M.3
Mandel, J.S.4
Anderson, V.E.5
McHugh, R.B.6
Hanson, M.R.7
Fahlstrom, S.M.8
Krivit, W.9
Kersey, J.H.10
-
4
-
-
0027937223
-
Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
-
Derry J.M.J., Ochs H.D., Francke U. Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell. 78:1994;635-644.
-
(1994)
Cell
, vol.78
, pp. 635-644
-
-
Derry, J.M.J.1
Ochs, H.D.2
Francke, U.3
-
6
-
-
0029075648
-
WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia
-
Derry J.M., Kerns J.A., Weinberg K.I., Ochs H.D., Volpini V., Estivill X., Walker A.P., Francke U. WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Hum. Mol. Genet. 4:1995;1127-1135.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1127-1135
-
-
Derry, J.M.1
Kerns, J.A.2
Weinberg, K.I.3
Ochs, H.D.4
Volpini, V.5
Estivill, X.6
Walker, A.P.7
Francke, U.8
-
7
-
-
0030804315
-
Wiskott-Aldrich syndrome/X-linked thrombocytopenia: WASP gene mutations, protein expression, and phenotype
-
Zhu Q., Watanabe C., Liu T., Hollenbaugh D., Blaese R.M., Kanner S.B., Aruffo A., Ochs H.D. Wiskott-Aldrich syndrome/X-linked thrombocytopenia WASP gene mutations, protein expression, and phenotype . Blood. 90:1997;2680-2689.
-
(1997)
Blood
, vol.90
, pp. 2680-2689
-
-
Zhu, Q.1
Watanabe, C.2
Liu, T.3
Hollenbaugh, D.4
Blaese, R.M.5
Kanner, S.B.6
Aruffo, A.7
Ochs, H.D.8
-
8
-
-
0037085797
-
Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia
-
Notarangelo L.D., Mazza C., Giliani S., D'Aria C., Gandellini F., Ravelli C., Locatelli M.G., Nelson D.L., Ochs H.D., Notarangelo L.D. Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia. Blood. 99:2002;2268-2269.
-
(2002)
Blood
, vol.99
, pp. 2268-2269
-
-
Notarangelo, L.D.1
Mazza, C.2
Giliani, S.3
D'Aria, C.4
Gandellini, F.5
Ravelli, C.6
Locatelli, M.G.7
Nelson, D.L.8
Ochs, H.D.9
Notarangelo, L.D.10
-
9
-
-
0030006284
-
Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
-
Symons M., Derry J.M., Karlak B., Jiang S., Lemahieu V., Mccormick F., Francke U., Abo A. Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization. Cell. 84:1996;723-734.
-
(1996)
Cell
, vol.84
, pp. 723-734
-
-
Symons, M.1
Derry, J.M.2
Karlak, B.3
Jiang, S.4
Lemahieu, V.5
McCormick, F.6
Francke, U.7
Abo, A.8
-
10
-
-
0029680639
-
Two GTPases, Cdc42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott-Aldrich syndrome
-
Aspenstrom P., Lindberg U., Hall A. Two GTPases, Cdc42 and Rac, bind directly to a protein implicated in the immunodeficiency disorder Wiskott-Aldrich syndrome. Curr. Biol. 6:1996;70-75.
-
(1996)
Curr. Biol.
, vol.6
, pp. 70-75
-
-
Aspenstrom, P.1
Lindberg, U.2
Hall, A.3
-
11
-
-
0035093787
-
Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia
-
Devriendt K., Kim A.S., Mathijs G., Frints S.G., Schwartz M., Van Oord Den J.J., Verhoef G.E., Boogaerts M.A., Fryns J.P., You D., Rosen M.K., Vandenberghe P. Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia. Nat. Genet. 27:2001;313-317.
-
(2001)
Nat. Genet.
, vol.27
, pp. 313-317
-
-
Devriendt, K.1
Kim, A.S.2
Mathijs, G.3
Frints, S.G.4
Schwartz, M.5
Van Oord Den, J.J.6
Verhoef, G.E.7
Boogaerts, M.A.8
Fryns, J.P.9
You, D.10
Rosen, M.K.11
Vandenberghe, P.12
-
12
-
-
0018901335
-
Splenectomy in the management of the thrombocytopenia of the Wiskott-Aldrich syndrome
-
Lum L.G., Tubergen D.G., Corash L., Blaese R.M. Splenectomy in the management of the thrombocytopenia of the Wiskott-Aldrich syndrome. N. Engl. J. Med. 302:1980;892-896.
-
(1980)
N. Engl. J. Med.
, vol.302
, pp. 892-896
-
-
Lum, L.G.1
Tubergen, D.G.2
Corash, L.3
Blaese, R.M.4
-
13
-
-
0027437515
-
Splenectomy and/or bone marrow transplantation in the management of the Wiskott-Aldrich syndrome: Long-term follow-up of 62 cases
-
Mullen C.A., Anderson K.D., Blaese R.M. Splenectomy and/or bone marrow transplantation in the management of the Wiskott-Aldrich syndrome long-term follow-up of 62 cases . Blood. 82:1993;2961-2966.
-
(1993)
Blood
, vol.82
, pp. 2961-2966
-
-
Mullen, C.A.1
Anderson, K.D.2
Blaese, R.M.3
-
14
-
-
0029903853
-
Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome
-
Litzman J., Jones A., Hann I., Chapel H., Strobel S., Morgan G. Intravenous immunoglobulin, splenectomy, and antibiotic prophylaxis in Wiskott-Aldrich syndrome. Arch. Dis. Child. 75:1996;436-439.
-
(1996)
Arch. Dis. Child
, vol.75
, pp. 436-439
-
-
Litzman, J.1
Jones, A.2
Hann, I.3
Chapel, H.4
Strobel, S.5
Morgan, G.6
-
15
-
-
0030405001
-
Bone marrow transplantation in 26 patients with Wiskott-Aldrich syndrome from a single center
-
Ozsahin H., Le Deist F., Benkerrou M., Cavazzana-Calvo M., Gomez L., Griscelli C., Blanche S., Fischer A. Bone marrow transplantation in 26 patients with Wiskott-Aldrich syndrome from a single center. J. Pediatr. 129:1996;238-244.
-
(1996)
J. Pediatr.
, vol.129
, pp. 238-244
-
-
Ozsahin, H.1
Le Deist, F.2
Benkerrou, M.3
Cavazzana-Calvo, M.4
Gomez, L.5
Griscelli, C.6
Blanche, S.7
Fischer, A.8
-
16
-
-
0035869537
-
Impact of donor type on outcome of bone marrow transplantation for Wiskott-Aldrich syndrome: Collaborative study of the International Bone Marrow Transplant Registry and the National Marrow Donor Program
-
Filipovich A.H., Stone J.V., Tomany S.C., Ireland M., Kollman C., Pelz C.J., Casper J.T., Cowan M.J., Edwards J.R., Fasth A., Gale R.P., Junker A., Kamani N.R., Loechelt B.J., et al. Impact of donor type on outcome of bone marrow transplantation for Wiskott-Aldrich syndrome collaborative study of the International Bone Marrow Transplant Registry and the National Marrow Donor Program . Blood. 97:2001;1598-1603.
-
(2001)
Blood
, vol.97
, pp. 1598-1603
-
-
Filipovich, A.H.1
Stone, J.V.2
Tomany, S.C.3
Ireland, M.4
Kollman, C.5
Pelz, C.J.6
Casper, J.T.7
Cowan, M.J.8
Edwards, J.R.9
Fasth, A.10
Gale, R.P.11
Junker, A.12
Kamani, N.R.13
Loechelt, B.J.14
-
17
-
-
0029077448
-
Effect of intravenous gammaglobulin (IVIG) on the platelet count in patients with Wiskott-Aldrich syndrome
-
Mathew P., Conley M.E. Effect of intravenous gammaglobulin (IVIG) on the platelet count in patients with Wiskott-Aldrich syndrome. Pediatr. Allergy Immunol. 6:1995;91-94.
-
(1995)
Pediatr. Allergy Immunol.
, vol.6
, pp. 91-94
-
-
Mathew, P.1
Conley, M.E.2
-
18
-
-
0034604048
-
Thymic function after hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency
-
Patel D.D., Gooding M.E., Parrott R.E., Curtis K.M., Haynes B.F., Buckley R.H. Thymic function after hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency. N. Engl. J. Med. 342:2000;1325-1332.
-
(2000)
N. Engl. J. Med.
, vol.342
, pp. 1325-1332
-
-
Patel, D.D.1
Gooding, M.E.2
Parrott, R.E.3
Curtis, K.M.4
Haynes, B.F.5
Buckley, R.H.6
-
19
-
-
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., Cavazzana-Calvo M., Veys P., Vossen J., Fasth A., Heilmann C., Wulffraat N., Seger R., Blanche S., Friedrich W., Abinun M., Davies G., 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
Cavazzana-Calvo, M.4
Veys, P.5
Vossen, J.6
Fasth, A.7
Heilmann, C.8
Wulffraat, N.9
Seger, R.10
Blanche, S.11
Friedrich, W.12
Abinun, M.13
Davies, G.14
-
20
-
-
0000419304
-
Agammaglobulinemia
-
Bruton O.C. Agammaglobulinemia. Pediatrics. 9:1952;722-728.
-
(1952)
Pediatrics
, vol.9
, pp. 722-728
-
-
Bruton, O.C.1
-
21
-
-
0023178863
-
Results of a prospective controlled two-dose crossover study with intravenous immunoglobulin and comparison (retrospective) with plasma treatment
-
Bernatowska E., Madalinski K., Janowicz W., Weremowicz R., Gutkowski P., Wolf H.M., Eibl M.M. Results of a prospective controlled two-dose crossover study with intravenous immunoglobulin and comparison (retrospective) with plasma treatment. Clin. Immunol. Immunopathol. 43:1987;153-162.
-
(1987)
Clin. Immunol. Immunopathol.
, vol.43
, pp. 153-162
-
-
Bernatowska, E.1
Madalinski, K.2
Janowicz, W.3
Weremowicz, R.4
Gutkowski, P.5
Wolf, H.M.6
Eibl, M.M.7
-
22
-
-
0026769737
-
High- vs low-dose immunoglobulin therapy in the long-term treatment of X-linked agammaglobulinemia
-
Liese J.G., Wintergerst U., Tympner K.D., Belohradsky B.H. High- vs low-dose immunoglobulin therapy in the long-term treatment of X-linked agammaglobulinemia. Am. J. Dis. Child. 146:1992;335-339.
-
(1992)
Am. J. Dis. Child
, vol.146
, pp. 335-339
-
-
Liese, J.G.1
Wintergerst, U.2
Tympner, K.D.3
Belohradsky, B.H.4
-
23
-
-
0033511446
-
Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: A retrospective survey of 31 patients
-
Quartier P., Debre M., De Blic J., de Sauverzac R., Sayegh N., Jabado N., Haddad E., Blanche S., Casanova J.L., Smith C.I., Le Deist F., de Saint B.G., Fischer A. Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia a retrospective survey of 31 patients . J. Pediatr. 134:1999;589-596.
-
(1999)
J. Pediatr.
, vol.134
, pp. 589-596
-
-
Quartier, P.1
Debre, M.2
De Blic, J.3
De Sauverzac, R.4
Sayegh, N.5
Jabado, N.6
Haddad, E.7
Blanche, S.8
Casanova, J.L.9
Smith, C.I.10
Le Deist, F.11
De Saint, B.G.12
Fischer, A.13
-
24
-
-
0023551435
-
Immunologic reconstitution after haploidentical bone marrow transplantation for immune deficiency disorders: Treatment of bone marrow cells with monoclonal antibody CT-2 and complement
-
Moen R.C., Horowitz S.D., Sondel P.M., Borcherding W.R., Trigg M.E., Billing R., Hong R. Immunologic reconstitution after haploidentical bone marrow transplantation for immune deficiency disorders treatment of bone marrow cells with monoclonal antibody CT-2 and complement . Blood. 70:1987;664-669.
-
(1987)
Blood
, vol.70
, pp. 664-669
-
-
Moen, R.C.1
Horowitz, S.D.2
Sondel, P.M.3
Borcherding, W.R.4
Trigg, M.E.5
Billing, R.6
Hong, R.7
-
25
-
-
0029742950
-
Successful transplantation of HLA-matched and HLA-mismatched umbilical cord blood from unrelated donors: Analysis of engraftment and acute graft-versus-host disease
-
Wagner J.E., Rosenthal J., Sweetman R., Shu X.O., Davies S.M., Ramsay N.K., McGlave P.B., Sender L., Cairo M.S. Successful transplantation of HLA-matched and HLA-mismatched umbilical cord blood from unrelated donors analysis of engraftment and acute graft-versus-host disease . Blood. 88:1996;795-802.
-
(1996)
Blood
, vol.88
, pp. 795-802
-
-
Wagner, J.E.1
Rosenthal, J.2
Sweetman, R.3
Shu, X.O.4
Davies, S.M.5
Ramsay, N.K.6
McGlave, P.B.7
Sender, L.8
Cairo, M.S.9
-
26
-
-
0035238524
-
Non-myeloablative transplants for malignant disease
-
R. F. Storb, R. Champlin, S. R. Riddell, M. Murata, S. Bryant, E. H. Warren, Non-myeloablative transplants for malignant disease, Hematology (Am. Soc. Hematol. Educ. Program) (2001) 375-391.
-
(2001)
Hematology (Am. Soc. Hematol. Educ. Program)
, pp. 375-391
-
-
Storb, R.F.1
Champlin, R.2
Riddell, S.R.3
Murata, M.4
Bryant, S.5
Warren, E.H.6
-
27
-
-
0036362457
-
Non-myeloablative stem cell transplantation for congenital immunodeficiencies
-
Gaspar H.B., Amrolia P., Hassan A., Webb D., Jones A., Sturt N., Vergani G., Pagliuca A., Mufti G., Hadzic N., Davies G., Veys P. Non-myeloablative stem cell transplantation for congenital immunodeficiencies. Recent Results Cancer Res. 159:2002;134-142.
-
(2002)
Recent Results Cancer Res.
, vol.159
, pp. 134-142
-
-
Gaspar, H.B.1
Amrolia, P.2
Hassan, A.3
Webb, D.4
Jones, A.5
Sturt, N.6
Vergani, G.7
Pagliuca, A.8
Mufti, G.9
Hadzic, N.10
Davies, G.11
Veys, P.12
-
28
-
-
0032982479
-
Retrovirus-mediated WASP gene transfer corrects defective actin polymerization in B cell lines from Wiskott-Aldrich syndrome patients carrying "null" mutations
-
Candotti F., Facchetti F., Blanzuoli L., Stewart D.M., Nelson D.L., Blaese R.M. Retrovirus-mediated WASP gene transfer corrects defective actin polymerization in B cell lines from Wiskott-Aldrich syndrome patients carrying "null" mutations. Gene Ther. 6:1999;1170-1174.
-
(1999)
Gene Ther.
, vol.6
, pp. 1170-1174
-
-
Candotti, F.1
Facchetti, F.2
Blanzuoli, L.3
Stewart, D.M.4
Nelson, D.L.5
Blaese, R.M.6
-
29
-
-
0033994632
-
Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins
-
Huang M.M., Tsuboi S., Wong A., Yu X.J., Oh-Eda M., Derry J.M., Francke U., Fukuda M., Weinberg K.I., Kohn D.B. Expression of human Wiskott-Aldrich syndrome protein in patients' cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins. Gene Ther. 7:2000;314-320.
-
(2000)
Gene Ther.
, vol.7
, pp. 314-320
-
-
Huang, M.M.1
Tsuboi, S.2
Wong, A.3
Yu, X.J.4
Oh-Eda, M.5
Derry, J.M.6
Francke, U.7
Fukuda, M.8
Weinberg, K.I.9
Kohn, D.B.10
-
30
-
-
0037443395
-
Gene therapy for Wiskott-Aldrich syndrome: Rescue of T-cell signaling and amelioration of colitis upon transplantation of retrovirally transduced hematopoietic stem cells in mice
-
Klein C., Nguyen D., Liu C.H., Mizoguchi A., Bhan A.K., Miki H., Takenawa T., Rosen F.S., Alt F.W., Mulligan R.C., Snapper S.B. Gene therapy for Wiskott-Aldrich syndrome rescue of T-cell signaling and amelioration of colitis upon transplantation of retrovirally transduced hematopoietic stem cells in mice . Blood. 101:2003;2159-2166.
-
(2003)
Blood
, vol.101
, pp. 2159-2166
-
-
Klein, C.1
Nguyen, D.2
Liu, C.H.3
Mizoguchi, A.4
Bhan, A.K.5
Miki, H.6
Takenawa, T.7
Rosen, F.S.8
Alt, F.W.9
Mulligan, R.C.10
Snapper, S.B.11
|