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Results: 1-12 |
Results: 12
Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G -> A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family
Authors: Comabella, M Waye, JS Raguer, N Eng, B Dominguez, C Navarro, C Borras, C Krivit, W Montalban, X
Citation: M. Comabella et al., Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: Compound heterozygosity for the IVS2+1G -> A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family, ANN NEUROL, 50(1), 2001, pp. 108-112
Oral busulfan pharmacokinetics and engraftment in children with Hurler syndrome and other inherited metabolic storage diseases undergoing hematopoietic cell transplantation
Authors: Jacobson, P Park, JJ DeFor, TE Thrall, M Abel, S Krivit, W Peters, C
Citation: P. Jacobson et al., Oral busulfan pharmacokinetics and engraftment in children with Hurler syndrome and other inherited metabolic storage diseases undergoing hematopoietic cell transplantation, BONE MAR TR, 27(8), 2001, pp. 855-861
Coronary artery patency following long-term successful engraftment 14 years after bone marrow transplantation in the Hurler syndrome
Authors: Braunlin, EA Rose, AG Hopwood, JJ Candel, RD Krivit, W
Citation: Ea. Braunlin et al., Coronary artery patency following long-term successful engraftment 14 years after bone marrow transplantation in the Hurler syndrome, AM J CARD, 88(9), 2001, pp. 1075
Correction of odontoid dysplasia following bone-marrow transplantation andengraftment (in Hurler syndrome MPS 1H)
Authors: Hite, SH Peters, C Krivit, W
Citation: Sh. Hite et al., Correction of odontoid dysplasia following bone-marrow transplantation andengraftment (in Hurler syndrome MPS 1H), PEDIAT RAD, 30(7), 2000, pp. 464-470
Wolman disease successfully treated by bone marrow transplantation
Authors: Krivit, W Peters, C Dusenbery, K Ben-Yoseph, Y Ramsay, NKC Wagner, JE Anderson, R
Citation: W. Krivit et al., Wolman disease successfully treated by bone marrow transplantation, BONE MAR TR, 26(5), 2000, pp. 567-570
Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: alpha-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy)
Authors: deCasperi, R Raghavan, SS Sosa, MAG Kolodny, EH Carrier, C Rubenstein, P Peters, C Wagner, J Kurtzberg, J Krivit, W
Citation: R. Decasperi et al., Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: alpha-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy), BONE MAR TR, 25(5), 2000, pp. 541-544
Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome) - Commentary
Authors: Peters, C Krivit, W
Citation: C. Peters et W. Krivit, Hematopoietic cell transplantation for mucopolysaccharidosis IIB (Hunter syndrome) - Commentary, BONE MAR TR, 25(10), 2000, pp. 1097-1099
Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy
Authors: Shapiro, E Krivit, W Lockman, L Jambaque, I Peters, C Cowan, M Harris, R Blanche, S Bordigoni, P Loes, D Ziegler, R Crittenden, M Ris, D Berg, B Cox, C Moser, H Fischer, A Aubourg, P
Citation: E. Shapiro et al., Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy, LANCET, 356(9231), 2000, pp. 713-718
Bone marrow-derived mesenchymal stem cells remain host-derived despite successful hematopoietic engraftment after allogeneic transplantation in patients with lysosomal and peroxisomal storage diseases
Authors: Koc, ON Peters, C Aubourg, P Raghavan, S Dyhouse, S DeGasperi, R Kolodny, EH BenYoseph, Y Gerson, SL Lazarus, HM Caplan, AI Watkins, PA Krivit, W
Citation: On. Koc et al., Bone marrow-derived mesenchymal stem cells remain host-derived despite successful hematopoietic engraftment after allogeneic transplantation in patients with lysosomal and peroxisomal storage diseases, EXP HEMATOL, 27(11), 1999, pp. 1675-1681
Genu valgum deformity in Hurler syndrome after hematopoietic stem cell transplantation: Correction by surgical intervention
Authors: Odunusi, E Peters, C Krivit, W Ogilvie, J
Citation: E. Odunusi et al., Genu valgum deformity in Hurler syndrome after hematopoietic stem cell transplantation: Correction by surgical intervention, J PED ORTH, 19(2), 1999, pp. 270-274
Globoid cell leukodystrophy: Distinguishing early-onset from late-onset disease using a brain MR imaging scoring method
Authors: Loes, DJ Peters, C Krivit, W
Citation: Dj. Loes et al., Globoid cell leukodystrophy: Distinguishing early-onset from late-onset disease using a brain MR imaging scoring method, AM J NEUROR, 20(2), 1999, pp. 316-323
Pediatric neurology on the threshold of a new millenium
Authors: Voit, T Abe, T Antunes, NL Aso, K Beck, M Becker, LE Berthet, F Bourgeois, B Braddick, O Cioni, G Cowan, F DiFazio, MP DiMauro, S Dodge, N Enders, G Forsting, N Frahm, J Futagi, Y Gabreels-Festen, A Gartner, J Gillessen-Kaesbach, G Golden, J Greisen, G Guichenai, P Hagberg, B Heinen, F Hohlfeld, R Holmes, GL Inoue, Y Iwamoto, H Jaeken, J Kaufmann, W Kimura, H Kohyama, J Korinthenberg, R Kramer, H Kreth, W Krivit, W Logan, W Lorenz, B Lou, H Martin, JJ Matshushima, Y Munnich, A Naidu, S Neubauer, W Oguni, H Oka, E Osawa, M Panayiotopoulos, CP Partridge, T Raemaekers, V Rapin, I Reis, A Rivkin, M Roll, C Rosenbaum, T Ross, E Rotteveel, J Schroder, JM Seitz, R Soul, J Steinlein, O Stephani, U Tanaka, J Taylor, G Tome, F Topcu, N Tuxhorn, I Urlesberger, B Wahn, V Wenk, G Wilichowski, E Wraith, JE Wynshaw-Boris, A
Citation: T. Voit et al., Pediatric neurology on the threshold of a new millenium, NEUROPEDIAT, 30(6), 1999, pp. 277-277
Risultati: 1-12 |