-
1
-
-
33745943855
-
Cardiac Findings after Enzyme Replacement Therapy for Mucopolysaccharidosis Type I
-
DOI 10.1016/j.amjcard.2006.02.047, PII S0002914906007314
-
Braunlin EA, Berry JM, Whitley CB. Cardiac findings after enzyme replacement therapy for mucopolysaccharidosis type 1. Am J Cardiol. 2006;98(3):416-418 (Pubitemid 44062452)
-
(2006)
American Journal of Cardiology
, vol.98
, Issue.3
, pp. 416-418
-
-
Braunlin, E.A.1
Berry, J.M.2
Whitley, C.B.3
-
2
-
-
33747160480
-
Long-term outcomes of adaptive functions for children with mucopolysaccharidosis I (Hurler syndrome) treated with hematopoietic stem cell transplantation
-
DOI 10.1097/00004703-200608000-00002, PII 0000470320060800000002
-
Bjoraker KJ, Delaney K, Peters C, Krivit W, Shapiro EG. Long-term outcomes of adaptive functions for children with mucopolysaccharidosis I (Hurler syndrome) treated with hematopoietic stem cell transplantation. J Dev Behav Pediatr. 2006;27(4): 290-296 (Pubitemid 44231667)
-
(2006)
Journal of Developmental and Behavioral Pediatrics
, vol.27
, Issue.4
, pp. 290-296
-
-
Bjoraker, K.J.1
Delaney, K.2
Peters, C.3
Krivit, W.4
Shapiro, E.G.5
-
3
-
-
0141459294
-
Usefulness of bone marrow transplantation in the Hurler syndrome
-
DOI 10.1016/S0002-9149(03)00909-3
-
Braunlin EA, Stauffer NR, Peters CH, et al. Usefulness of bone marrow transplantation in the Hurler syndrome. Am J Cardiol. 2003; 92(7):882-886 (Pubitemid 37163595)
-
(2003)
American Journal of Cardiology
, vol.92
, Issue.7
, pp. 882-886
-
-
Braunlin, E.A.1
Stauffer, N.R.2
Peters, C.H.3
Bass, J.L.4
Berry, J.M.5
Hopwood, J.J.6
Krivit, W.7
-
4
-
-
33846198829
-
A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years
-
DOI 10.1016/j.ymgme.2006.08.007, PII S1096719206002873
-
Sifuentes M, Doroshow R, Hoft R, et al. A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years. Mol Genet Metab. 2007;90(2): 171-180 (Pubitemid 46108607)
-
(2007)
Molecular Genetics and Metabolism
, vol.90
, Issue.2
, pp. 171-180
-
-
Sifuentes, M.1
Doroshow, R.2
Hoft, R.3
Mason, G.4
Walot, I.5
Diament, M.6
Okazaki, S.7
Huff, K.8
Cox, G.F.9
Swiedler, S.J.10
Kakkis, E.D.11
-
5
-
-
0035499168
-
Coronary artery patency following long-term successful engraftment 14 years after bone marrow transplantation in the hurler syndrome
-
DOI 10.1016/S0002-9149(01)01999-3, PII S0002914901019993
-
Braunlin EA, Rose AG, Hopwood JJ, Candel RD, Krivit W. Coronary artery patency following long-term successful engraftment 14 years after bone marrow transplantation in the Hurler syndrome. Am J Cardiol. 2001;88(9): 1075-1077 (Pubitemid 33042633)
-
(2001)
American Journal of Cardiology
, vol.88
, Issue.9
, pp. 1075-1077
-
-
Braunlin, E.A.1
Rose, A.G.2
Hopwood, J.J.3
Candel, R.D.4
Krivit, W.5
-
6
-
-
0024517211
-
Long-term effects of bone marrow transplantation in dogs with mucopolysaccharidosis I
-
Breider MA, Shull RM, Constantopoulos G. Long-term effects of bone marrow transplantation in dogs with mucopolysaccharidosis I. Am J Pathol. 1989;134(3):677-692 (Pubitemid 19082862)
-
(1989)
American Journal of Pathology
, vol.134
, Issue.3
, pp. 677-692
-
-
Breider, M.A.1
Shull, R.M.2
Constantopoulos, G.3
-
7
-
-
0026721298
-
Evaluation of coronary artery disease in the Hurler syndrome by angiography
-
Braunlin EA, Hunter DW, Krivit W, et al. Evaluation of coronary artery disease in the Hurler syndrome by angiography. Am J Cardiol. 1992;69(17):1487-1489
-
(1992)
Am J Cardiol
, vol.69
, Issue.17
, pp. 1487-1489
-
-
Braunlin, E.A.1
Hunter, D.W.2
Krivit, W.3
-
8
-
-
0028841213
-
Molecular genetics of mucopolysaccharidosis type I: Diagnostic, clinical, and biological implications
-
Scott HS, Bunge S, Gal A, Clarke LA, Morris CP, Hopwood JJ. Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications. Hum Mutat. 1995;6(4):288-302
-
(1995)
Hum Mutat
, vol.6
, Issue.4
, pp. 288-302
-
-
Scott, H.S.1
Bunge, S.2
Gal, A.3
Clarke, L.A.4
Morris, C.P.5
Hopwood, J.J.6
-
9
-
-
66849122069
-
Mucopolysaccharidosis type I in 21 Czech and Slovak patients: Mutation analysis suggests a functional importance of C-terminus of the IDUA protein
-
Vazna A, Beesley C, Berna L, et al. Mucopolysaccharidosis type I in 21 Czech and Slovak patients: mutation analysis suggests a functional importance of C-terminus of the IDUA protein. Am J Med Genet A. 2009;149A(5): 965-974
-
(2009)
Am J Med Genet A
, vol.149 A
, Issue.5
, pp. 965-974
-
-
Vazna, A.1
Beesley, C.2
Berna, L.3
|