-
1
-
-
0029756483
-
Results of Expedicion Humana. I. Analysis of HLA class II (DRB1-DQA1-DPB1) alleles and DR-DQ haplotypes in nine Amerindian populations from Colombia
-
Trachtenberg EA, Keyeux G, Bernal JE, et al. Results of Expedicion Humana. I. Analysis of HLA class II (DRB1-DQA1-DPB1) alleles and DR-DQ haplotypes in nine Amerindian populations from Colombia. Tissue Antigens 1996;48:174-81.
-
(1996)
Tissue Antigens
, vol.48
, pp. 174-81
-
-
Trachtenberg, E.A.1
Keyeux, G.2
Bernal, J.E.3
-
2
-
-
31644446680
-
Cumulative incidence rates of the mucopolysaccharidoses in Germany
-
Baehner F, Schmiedeskamp C, Krummenauer F, et al. Cumulative incidence rates of the mucopolysaccharidoses in Germany. J Inherit Metab Dis 2005;28:1011-17.
-
(2005)
J Inherit Metab Dis
, vol.28
, pp. 1011-17
-
-
Baehner, F.1
Schmiedeskamp, C.2
Krummenauer, F.3
-
3
-
-
53749104461
-
Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence
-
Malm G, Lund AM, Månsson JE, et al. Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence. Acta Paediatr 2008;97:1577-81.
-
(2008)
Acta Paediatr
, vol.97
, pp. 1577-81
-
-
Malm, G.1
Lund, A.M.2
Månsson, J.E.3
-
4
-
-
34447310543
-
Quantifying emerging drugs for very rare conditions
-
Miles KA, Packer C, Stevens A. Quantifying emerging drugs for very rare conditions. QJM 2007;100:291-5.
-
(2007)
QJM
, vol.100
, pp. 291-5
-
-
Miles, K.A.1
Packer, C.2
Stevens, A.3
-
5
-
-
34547682071
-
Management guidelines for mucopolysaccharidosis VI
-
Giugliani R, Harmatz P, Wraith JE. Management guidelines for mucopolysaccharidosis VI. Pediatrics 2007;120:405-18.
-
(2007)
Pediatrics
, vol.120
, pp. 405-18
-
-
Giugliani, R.1
Harmatz, P.2
Wraith, J.E.3
-
6
-
-
0037343066
-
Replacement therapy in mucopolysaccharidosis type VI: advantages of early onset of therapy
-
Auclair D, Hopwood JJ, Brooks DA, et al. Replacement therapy in mucopolysaccharidosis type VI: advantages of early onset of therapy. Mol Genet Metab 2003;78:163-74.
-
(2003)
Mol Genet Metab
, vol.78
, pp. 163-74
-
-
Auclair, D.1
Hopwood, J.J.2
Brooks, D.A.3
-
7
-
-
33744978567
-
Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study
-
Harmatz P, Giugliani R, Schwartz I, et al. Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study. J Pediatr 2006;148:533-9.
-
(2006)
J Pediatr
, vol.148
, pp. 533-9
-
-
Harmatz, P.1
Giugliani, R.2
Schwartz, I.3
-
8
-
-
77649237484
-
Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
-
Harmatz P. Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase. J Inherit Metab Dis 2010;33:51-60.
-
(2010)
J Inherit Metab Dis
, vol.33
, pp. 51-60
-
-
Harmatz, P.1
-
9
-
-
77954629021
-
Enzyme replacement therapy for mucopolysaccharidosis VI: growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
-
Decker C, Giugliani R, Schwartz IV, et al. Enzyme replacement therapy for mucopolysaccharidosis VI: growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase. J Pediatr Rehabil Med 2010;3:89-100.
-
(2010)
J Pediatr Rehabil Med
, vol.3
, pp. 89-100
-
-
Decker, C.1
Giugliani, R.2
Schwartz, I.V.3
-
10
-
-
67649411650
-
Expensive drugs for rare disorders: to treat or not to treat? The case of enzyme replacement therapy for mucopolysaccharidosis VI
-
Schlander M, Beck M. Expensive drugs for rare disorders: to treat or not to treat? The case of enzyme replacement therapy for mucopolysaccharidosis VI. Curr Med Res Opin 2009;25:1285-93.
-
(2009)
Curr Med Res Opin
, vol.25
, pp. 1285-93
-
-
Schlander, M.1
Beck, M.2
-
11
-
-
84871129733
-
-
Bogotá: Instituto Colombiano de Cultura Hispánica
-
Bernal J, Briceño I, Duncan R. El arte del chamanismo, la salud y la vida, Tumaco-La Tolita. Bogotá: Instituto Colombiano de Cultura Hispánica, 1993.
-
(1993)
El arte del chamanismo, la salud y la vida, Tumaco-La Tolita
-
-
Bernal, J.1
Briceño, I.2
Duncan, R.3
-
13
-
-
33747091220
-
Genetic and other diseases in the pottery of Tumaco-la Tolita culture in Colombia-Ecuador
-
Bernal JE, Briceno I. Genetic and other diseases in the pottery of Tumaco-la Tolita culture in Colombia-Ecuador. Clin Genet 2006;70:188-91.
-
(2006)
Clin Genet
, vol.70
, pp. 188-91
-
-
Bernal, J.E.1
Briceno, I.2
-
14
-
-
84871177900
-
Los pueblos indígenas de Colombia en el umbral del nuevo milenio
-
accessed 4 Mar 2011
-
Sánchez E, Arango R. Los pueblos indígenas de Colombia en el umbral del nuevo milenio. Bogota: Departamento Nacional de Planeación, 2004. http://www.dnp.gov. co (accessed 4 Mar 2011).
-
(2004)
Bogota: Departamento Nacional de Planeación
-
-
Sánchez, E.1
Arango, R.2
-
15
-
-
78649700786
-
Rare diseases, orphan drugs and their regulation: questions and misconceptions
-
Tambuyzer E. Rare diseases, orphan drugs and their regulation: questions and misconceptions. Nat Rev Drug Discov 2010;9:921e9.
-
(2010)
Nat Rev Drug Discov
, vol.9
, pp. 921-929
-
-
Tambuyzer, E.1
-
16
-
-
55249116853
-
Public healthcare resource allocation and the Rule of Rescue
-
Cookson R, McCabe C, Tsuchiya A. Public healthcare resource allocation and the Rule of Rescue. J Med Ethics 2008;34:540e4.
-
(2008)
J Med Ethics
, vol.34
, pp. 540-544
-
-
Cookson, R.1
Mccabe, C.2
Tsuchiya, A.3
-
17
-
-
84871137485
-
Chile mine rescue to cost $20m
-
accessed 31 May 2011, 14 October
-
Lane E. Chile mine rescue to cost $20m. BBC News. 14 October 2010. http://www.bbc.co.uk/news/business-11541634 (accessed 31 May 2011).
-
(2010)
BBC News
-
-
Lane, E.1
-
18
-
-
0027360434
-
Tay-Sachs disease-carrier screening, prenatal diagnosis, and the molecular era: an international perspective, 1970 to 1993
-
Kaback M, Lim-Steele J, Dabholkar D, et al. Tay-Sachs disease-carrier screening, prenatal diagnosis, and the molecular era: an international perspective, 1970 to 1993. JAMA 1993;270:2307-15.
-
(1993)
JAMA
, vol.270
, pp. 2307-2315
-
-
Kaback, M.1
Lim-steele, J.2
Dabholkar, D.3
|