-
1
-
-
0032860224
-
Glycoprotein lysosomal storage disorders: α- and β-mannosidosis, fucosidosis and α-N-acetylgalactosaminidase deficiency
-
1455
-
Michalski JC, Klein A. Glycoprotein lysosomal storage disorders: α- and β-mannosidosis, fucosidosis and α-N-acetylgalactosaminidase deficiency. Biochim Biophys Acta 1999; 1455: 69-84.
-
(1999)
Biochim. Biophys. Acta
, pp. 69-84
-
-
Michalski, J.C.1
Klein, A.2
-
2
-
-
0031928891
-
Bone marrow transplantation for the treatment of α-mannosidosis
-
Wall DA, Grange DK, Goulding P et al. Bone marrow transplantation for the treatment of α-mannosidosis. J Pediatr 1998; 133: 282-285.
-
(1998)
J. Pediatr.
, vol.133
, pp. 282-285
-
-
Wall, D.A.1
Grange, D.K.2
Goulding, P.3
-
3
-
-
0035977948
-
Recent progress in lysosomal alpha-mannosidase and its deficiency
-
Sun H, Wolfe JH. Recent progress in lysosomal alpha-mannosidase and its deficiency. Exp Mol Med 2001; 33: 1-7.
-
(2001)
Exp. Mol. Med.
, vol.33
, pp. 1-7
-
-
Sun, H.1
Wolfe, J.H.2
-
5
-
-
0033840811
-
Immunodeficiency in alpha-mannosidosis: A matched case-control study on immunoglobulins, complement factors, receptor density, phagocytosis and intracellular killing in leucocytes
-
Malm D, Halvorsen DS, Tranebjaerg L, Sjursen H. Immunodeficiency in alpha-mannosidosis: a matched case-control study on immunoglobulins, complement factors, receptor density, phagocytosis and intracellular killing in leucocytes. Eur J Pediatr 2000; 159: 699-703.
-
(2000)
Eur. J. Pediatr.
, vol.159
, pp. 699-703
-
-
Malm, D.1
Halvorsen, D.S.2
Tranebjaerg, L.3
Sjursen, H.4
-
6
-
-
0034846296
-
Advances in the treatment of lysosomal storage disease
-
Wraith JE. Advances in the treatment of lysosomal storage disease. Dev Med Child Neurol 2001; 43: 639-646.
-
(2001)
Dev. Med. Child. Neurol.
, vol.43
, pp. 639-646
-
-
Wraith, J.E.1
-
7
-
-
0035811624
-
Safety and efficacy of recombinant human α-galactosidase a replacement therapy in Fabry's disease
-
Eng CM, Guffon N, Wilcox WR et al. Safety and efficacy of recombinant human α-galactosidase a replacement therapy in Fabry's disease. N Engl J Med 2001; 345: 9-16.
-
(2001)
N. Engl. J. Med.
, vol.345
, pp. 9-16
-
-
Eng, C.M.1
Guffon, N.2
Wilcox, W.R.3
-
8
-
-
0032941197
-
Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartyl-glucosaminuria, Hurler, Maroteaux-Lamy, and Sly syndromes, and Gaucher disease type III
-
Krivit W, Peters C, Shapiro EG. Bone marrow transplantation as effective treatment of central nervous system disease in globoid cell leukodystrophy, metachromatic leukodystrophy, adrenoleukodystrophy, mannosidosis, fucosidosis, aspartyl-glucosaminuria, Hurler, Maroteaux-Lamy, and Sly syndromes, and Gaucher disease type III. Curr Opin Neurol 1999; 12: 167-176.
-
(1999)
Curr. Opin. Neurol.
, vol.12
, pp. 167-176
-
-
Krivit, W.1
Peters, C.2
Shapiro, E.G.3
-
9
-
-
0028324026
-
Bone marrow transplantation corrects the enzyme defect in neurons of the central nervous system in a lysosomal storage disease
-
Walkley SU, Thrall MA, Dobrenis K et al. Bone marrow transplantation corrects the enzyme defect in neurons of the central nervous system in a lysosomal storage disease. Proc Natl Acad Sci USA 1994; 91: 2970-2974.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 2970-2974
-
-
Walkley, S.U.1
Thrall, M.A.2
Dobrenis, K.3
-
10
-
-
0023949553
-
Perivascular microglial cells of the CNS are bone marrow-derived and present antigen in vivo
-
Hickey WF, Kimura H. Perivascular microglial cells of the CNS are bone marrow-derived and present antigen in vivo. Science 1988; 239: 290-292.
-
(1988)
Science
, vol.239
, pp. 290-292
-
-
Hickey, W.F.1
Kimura, H.2
-
11
-
-
0023638741
-
Bone marrow transplantation in the treatment of α-mannosidosis
-
Will A, Cooper A, Hatton C et al. Bone marrow transplantation in the treatment of α-mannosidosis. Arch Dis Child 1987; 62: 1044-1049.
-
(1987)
Arch. Dis. Child
, vol.62
, pp. 1044-1049
-
-
Will, A.1
Cooper, A.2
Hatton, C.3
-
12
-
-
0018372573
-
An improved thin-layer chromatography method for urinary oligosaccharide screening
-
Sewell AC. An improved thin-layer chromatography method for urinary oligosaccharide screening. Clin Chim Acta 1979; 92: 411-414.
-
(1979)
Clin. Chim. Acta
, vol.92
, pp. 411-414
-
-
Sewell, A.C.1
-
13
-
-
0005583036
-
The construction and validation of a nonverbal test of intelligence: The revision of the Snijders-Oomen tests
-
Tellegen PJ, Laros JA. The construction and validation of a nonverbal test of intelligence: the revision of the Snijders-Oomen tests. Eur J Psychol Assess 1993; 9: 147-157.
-
(1993)
Eur. J. Psychol. Assess.
, vol.9
, pp. 147-157
-
-
Tellegen, P.J.1
Laros, J.A.2
-
14
-
-
0029634358
-
Bone marrow transplantation for lysosomal diseases
-
Wallkley SU, Dobrenis K. Bone marrow transplantation for lysosomal diseases. Lancet 1995; 345: 1382-1383.
-
(1995)
Lancet
, vol.345
, pp. 1382-1383
-
-
Wallkley, S.U.1
Dobrenis, K.2
-
15
-
-
0042062382
-
Low dose donor lymphocyte infusions (DLI) promote donor chimerism after T-cell depleted PBSCT but do not prevent leukemia relapse
-
Albert M, Schuster F, Schulze S et al. Low dose donor lymphocyte infusions (DLI) promote donor chimerism after T-cell depleted PBSCT but do not prevent leukemia relapse. Bone Marrow Transplant 2002; 30 (Suppl. 3): 108.
-
(2002)
Bone Marrow Transplant.
, vol.30
, Issue.SUPPL. 3
, pp. 108
-
-
Albert, M.1
Schuster, F.2
Schulze, S.3
-
16
-
-
85047698432
-
+-selected peripheral stem cell transplantation from parental donors in children with non-malignant diseases
-
+-selected peripheral stem cell transplantation from parental donors in children with non-malignant diseases. Bone Marrow Transplant 2001; 29: 9-13.
-
(2001)
Bone Marrow Transplant.
, vol.29
, pp. 9-13
-
-
Kremens, B.1
Basu, O.2
Peceny, R.3
-
17
-
-
0032055564
-
Hurler syndrome: II, Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty four children
-
Peters C, Shapiro EG, Anderson J et al. Hurler syndrome: II, Outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty four children. Blood 1998; 91: 2601-2608.
-
(1998)
Blood
, vol.91
, pp. 2601-2608
-
-
Peters, C.1
Shapiro, E.G.2
Anderson, J.3
-
18
-
-
2442758015
-
Retrovirus vector-mediated correction and cross-correction of lysosomal alpha-mannosidase deficiency in human and feline fibroblasts
-
Sun H, Yang M, Haskins ME. Retrovirus vector-mediated correction and cross-correction of lysosomal alpha-mannosidase deficiency in human and feline fibroblasts. Hum Gene Ther 1999; 10: 1311-1319.
-
(1999)
Hum. Gene. Ther.
, vol.10
, pp. 1311-1319
-
-
Sun, H.1
Yang, M.2
Haskins, M.E.3
|