-
1
-
-
84885531986
-
Cardiac involvement in the MPS disorders. In: Moller JH, Hoffman JIE (eds) Pediatric cardiovascular medicine
-
Braunlin EA (2012) Cardiac involvement in the MPS disorders. In: Moller JH, Hoffman JIE (eds) Pediatric cardiovascular medicine. Blackwell, Hoboken, pp 982–991
-
(2012)
Blackwell, Hoboken
, pp. 982-991
-
-
Braunlin, E.A.1
-
2
-
-
0141459294
-
Usefulness of bone marrow transplantation in the Hurler syndrome
-
Braunlin EA, Stauffer NR, Peters CH et al (2003) Usefulness of bone marrow transplantation in the Hurler syndrome. Am J Cardiol 92:882–886
-
(2003)
Am J Cardiol
, vol.92
, pp. 882-886
-
-
Braunlin, E.A.1
Stauffer, N.R.2
Peters, C.H.3
-
3
-
-
33745943855
-
Cardiac findings after enzyme replacement therapy for mucopolysaccharidosis type I
-
Braunlin EA, Berry JM, Whitley CB (2006) Cardiac findings after enzyme replacement therapy for mucopolysaccharidosis type I. Am J Cardiol 98:416–418
-
(2006)
Am J Cardiol
, vol.98
, pp. 416-418
-
-
Braunlin, E.A.1
Berry, J.M.2
Whitley, C.B.3
-
4
-
-
80052455387
-
Clear cells in the atrioventricular valves of infants with severe human mucopolysaccharidosis (Hurler syndrome) are activated valvular interstitial cells
-
Braunlin EA, Tolar J, Mackey-Bojack S, Masinde T, Krivit W, Schoen FJ (2011) Clear cells in the atrioventricular valves of infants with severe human mucopolysaccharidosis (Hurler syndrome) are activated valvular interstitial cells. Cardiovasc Pathol 20:315–321
-
(2011)
Cardiovasc Pathol
, vol.20
, pp. 315-321
-
-
Braunlin, E.A.1
Tolar, J.2
Mackey-Bojack, S.3
Masinde, T.4
Krivit, W.5
Schoen, F.J.6
-
5
-
-
0019471151
-
Coronary artery disease in the hurler syndrome: Qualitative and quantitative analysis of the extent of coronary artery narrowing at necropsy in six children
-
Brosius FC, Roberts WC (1981) Coronary artery disease in the hurler syndrome: qualitative and quantitative analysis of the extent of coronary artery narrowing at necropsy in six children. Am J Cardiol 47:649–653
-
(1981)
Am J Cardiol
, vol.47
, pp. 649-653
-
-
Brosius, F.C.1
Roberts, W.C.2
-
6
-
-
0031834476
-
Cardiovascular changes in children with mucopolysaccharide storage diseases and related disorders – clinical and echocardiographic findings in 64 patients
-
Dangel JH (1998) Cardiovascular changes in children with mucopolysaccharide storage diseases and related disorders – clinical and echocardiographic findings in 64 patients. Eur J Pediatr 57:534–538
-
(1998)
Eur J Pediatr
, vol.57
, pp. 534-538
-
-
Dangel, J.H.1
-
7
-
-
66149099295
-
The natural course and the impact of therapies of cardiac involvement in the mucopolysaccharidoses
-
Fesslova V, Corti P, Sersale G et al (2009) The natural course and the impact of therapies of cardiac involvement in the mucopolysaccharidoses. Cardiol Young 19:170–178
-
(2009)
Cardiol Young
, vol.19
, pp. 170-178
-
-
Fesslova, V.1
Corti, P.2
Sersale, G.3
-
8
-
-
74049159044
-
Enzyme-replacement therapy in a 5-month-old boy with attenuated presymptomatic MPS I: 5 year follow-up
-
Gabrielli O, Clarke LA, Bruni S, Coppa GV (2010) Enzyme-replacement therapy in a 5-month-old boy with attenuated presymptomatic MPS I: 5 year follow-up. Pediatrics 125:e183–187
-
(2010)
Pediatrics
, vol.125
, pp. e183-e187
-
-
Gabrielli, O.1
Clarke, L.A.2
Bruni, S.3
Coppa, G.V.4
-
9
-
-
0031834971
-
Ocular abnormalities in the mucopolysaccharidoses after bone marrow transplantation. Longer follow-up
-
Gillingsrud EO, Krivit W, Summers CG (1998) Ocular abnormalities in the mucopolysaccharidoses after bone marrow transplantation. Longer follow-up. Ophthalmology 105:1099–1105
-
(1998)
Ophthalmology
, vol.105
, pp. 1099-1105
-
-
Gillingsrud, E.O.1
Krivit, W.2
Summers, C.G.3
-
10
-
-
0023760034
-
Echocardiographic abnormalities in the mucopolysaccharide storage diseases
-
Gross DM, Williams JC, Caprioli C, Dominquez B, Howell RR (1988) Echocardiographic abnormalities in the mucopolysaccharide storage diseases. Am J Cardiol 61:170–176
-
(1988)
Am J Cardiol
, vol.61
, pp. 170-176
-
-
Gross, D.M.1
Williams, J.C.2
Caprioli, C.3
Dominquez, B.4
Howell, R.R.5
-
12
-
-
85060306216
-
-
http://graphpad.com
-
-
-
-
13
-
-
0023760034
-
Echocardiographic abnormalities in the mucopolysaccharide storage diseases
-
Gross DM, Williams JC, Caprioli C, Dominquez B, Howell RR (1988) Echocardiographic abnormalities in the mucopolysaccharide storage diseases. Am J Cardiol 61:170–176
-
(1988)
Am J Cardiol
, vol.61
, pp. 170-176
-
-
Gross, D.M.1
Williams, J.C.2
Caprioli, C.3
Dominquez, B.4
Howell, R.R.5
-
14
-
-
33751416578
-
Guidelines and standards for performance of a pediatric echocardiogram: A report from the Task Force of the Pediatric Council of the American Society of Echocardiography
-
Lai WW, Geva T, Shirali GS (2006) Guidelines and standards for performance of a pediatric echocardiogram: a report from the Task Force of the Pediatric Council of the American Society of Echocardiography. J Am Soc Echocardiogr 19:1413–1430
-
(2006)
J am Soc Echocardiogr
, vol.19
, pp. 1413-1430
-
-
Lai, W.W.1
Geva, T.2
Shirali, G.S.3
-
15
-
-
77953550230
-
Echocardiographic study of paediatric patients with mucopolysaccharidosis
-
Leal GN, de Paula AC, Leone C, Kim CA (2010) Echocardiographic study of paediatric patients with mucopolysaccharidosis. Cardiol Young 20:254–261
-
(2010)
Cardiol Young
, vol.20
, pp. 254-261
-
-
Leal, G.N.1
de Paula, A.C.2
Leone, C.3
Kim, C.A.4
-
16
-
-
77951732397
-
Recommendations for quantification methods during the performance of a pediatric echocardiogram: A report from the Pediatric Measurements Writing Group of the American Society of Echocardiography Pediatric and Congenital Heart Disease Council
-
Lopez L, Colan SD, Frommelt PC et al (2010) Recommendations for quantification methods during the performance of a pediatric echocardiogram: a report from the Pediatric Measurements Writing Group of the American Society of Echocardiography Pediatric and Congenital Heart Disease Council. J Am Soc Echocardiogr 23:465–495
-
(2010)
J am Soc Echocardiogr
, vol.23
, pp. 465-495
-
-
Lopez, L.1
Colan, S.D.2
Frommelt, P.C.3
-
17
-
-
77953049350
-
Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age – a sibling control study
-
McGill JJ, Inwood AC, Corman DJ et al (2010) Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age – a sibling control study. Clin Genet 77:492–498
-
(2010)
Clin Genet
, vol.77
, pp. 492-498
-
-
McGill, J.J.1
Inwood, A.C.2
Corman, D.J.3
-
18
-
-
0036345045
-
Cardiovascular changes in children with mucopolysaccharide disorders
-
Mohan UR, Hay AA, Cleary MA, Wraith JE, Patel RG (2002) Cardiovascular changes in children with mucopolysaccharide disorders. Acta Paediatr 91:799–804
-
(2002)
Acta Paediatr
, vol.91
, pp. 799-804
-
-
Mohan, U.R.1
Hay, A.A.2
Cleary, M.A.3
Wraith, J.E.4
Patel, R.G.5
-
19
-
-
0000869162
-
The mucopolysaccharidoses
-
Scriver CR, Beaudet AL, Valle D, Sly WS (eds), McGraw-Hill, New York
-
Neufeld EF, Muenzer J (2001) The mucopolysaccharidoses. In: Scriver CR, Beaudet AL, Valle D, Sly WS (eds) The metabolic basis of inherited diseases, 8th edn. McGraw-Hill, New York, pp 3421–3452
-
(2001)
The Metabolic Basis of Inherited Diseases, 8Th Edn
, pp. 3421-3452
-
-
Neufeld, E.F.1
Muenzer, J.2
-
21
-
-
33846198829
-
A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years
-
Sifuentes M, Doroshow R, Hoft R et al (2007) A follow-up study of MPS I patients treated with laronidase enzyme replacement therapy for 6 years. Mol Genet Metab 90:171–180
-
(2007)
Mol Genet Metab
, vol.90
, pp. 171-180
-
-
Sifuentes, M.1
Doroshow, R.2
Hoft, R.3
-
22
-
-
82955163121
-
Enzyme replacement therapy for mucopolysaccharidosis II from 3 months of age: A 3-year follow-up
-
Tylki-Szymanska A, Jurecka A, Zuber Z, Rozdzynska A, Marucha J, Czartorynska B (2012) Enzyme replacement therapy for mucopolysaccharidosis II from 3 months of age: a 3-year follow-up. Acta Paediatr 101:e42–47
-
(2012)
Acta Paediatr
, vol.101
, pp. e42-e47
-
-
Tylki-Szymanska, A.1
Jurecka, A.2
Zuber, Z.3
Rozdzynska, A.4
Marucha, J.5
Czartorynska, B.6
-
23
-
-
79955501783
-
Fatal coronary artery disease in an infant with severe mucopolysaccharidosis type I
-
Van den Broek L, Backx PC, Coolen H et al (2011) Fatal coronary artery disease in an infant with severe mucopolysaccharidosis type I. Pediatrics 127:e1343–1346
-
(2011)
Pediatrics
, vol.127
, pp. e1343-e1346
-
-
van den Broek, L.1
Backx, P.C.2
Coolen, H.3
-
24
-
-
0347419495
-
Musculoskeletal manifestations of Hurler syndrome: Long-term follow-up after bone marrow transplantation
-
Weisstein JS, Delgado E, Steinbach LS, Hart K, Packman S (2004) Musculoskeletal manifestations of Hurler syndrome: long-term follow-up after bone marrow transplantation. J Pediatr Orthop 24:97–101
-
(2004)
J Pediatr Orthop
, vol.24
, pp. 97-101
-
-
Weisstein, J.S.1
Delgado, E.2
Steinbach, L.S.3
Hart, K.4
Packman, S.5
-
25
-
-
0028889847
-
Mitral and aortic regurgitation in 84 patients with mucopolysaccharidoses
-
Wippermann CF, Beck M, Schranz D, Huth R, Michel-Behnke I, Jungst B-K (1995) Mitral and aortic regurgitation in 84 patients with mucopolysaccharidoses. Eur J Pediatr 154:98–101
-
(1995)
Eur J Pediatr
, vol.154
, pp. 98-101
-
-
Wippermann, C.F.1
Beck, M.2
Schranz, D.3
Huth, R.4
Michel-Behnke, I.5
Jungst, B.-K.6
-
26
-
-
84879688298
-
Management of mucopolysaccharidosis type IH (Hurler’s Syndrome) presenting in infancy with severe dilated cardiomyopathy: A single institution’s experience
-
Wiseman DH, Mercer J, Tylee K et al (2012) Management of mucopolysaccharidosis type IH (Hurler’s Syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution’s experience. J Inherit Metab Dis. doi:10.1007/s10545-012-9500-3
-
(2012)
J Inherit Metab Dis
-
-
Wiseman, D.H.1
Mercer, J.2
Tylee, K.3
|