Clinical study of 10 Brazilian cases of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). | ORKG Ask

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Utagawa, Cláudia Y.
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The mucopolysaccharidoses (MPS) are a heterogeneous group of inborn errors of lysosomal glycosaminog...

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This paper presents data collected by a Brazilian center in a multinational multicenter observationa...

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Schwartz, I. V.
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Brustolin, S.
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Beheregaray, A. P. C.
Leistner, S.
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Barrios, P.
Marinho, D.
Esteves, P.
Valadares, E.
Boy, R.
Horovitz, Dafne Dain Gandelman
Mabe, P.
Silva, L. C. S. da
Souza, I. C. N. de
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Palhares, D.
Kim, C. A.
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This paper presents data collected by a Brazilian center in amultinational multicenter observational...

Estudo clínico e laboratorial de 19 casos de mucopolissacaridoses

Albano, Lilian M. J.
Sugayama, Sofia S. M. M.
Bertola, Débora R.
Andrade, Carlos E. F.
Utagawa, Cláudia Y.
Puppi, Flávia
Nader, Helena B.
Toma, Leny
Coelho, Janice
Leistner, Sandra
Burin, Maira
Giugliani, Roberto
Chong, A. Kim

December 2000

The mucopolysaccharidoses (MPS) are a heterogeneous group of inborn errors of lysosomal glycosaminog...

A clinical study of 77 patients with mucopolysaccharidosis type II

Schwartz, Ida V. D.
Ribeiro, Márcia G.
Mota, João G.
Toralles, Maria Betânia P.
Correia, Patrícia
Horovitz, Dafne
Santos, Emerson S.
Monlleo, Isabella L.
Fett-Conte, Agnes C.
Sobrinho, Ruy P. Oliveira
Norato, Denise Y. J.
Paula, Anna Carolina
Kim, Chong A.
Duarte, Andréa R
Boy, Raquel
Valadares, Eugênia
Michelena, Maria De
Mabe, Paulina
Martinhago, Cyro D.
Pina-Neto, João M.
Kok, Fernando
Leistner-Segal, Sandra
Burin, Maira G.
Giugliani, Roberto

January 2007

Aim: This study aims to assess the clinical features of 77 South American patients (73 Brazilian) wi...

Clinical and laboratorial study of 19 cases of mucopolysaccharidoses

Albano, Lilian M. J.
Sugayama, Sofia S. M. M.
Bertola, Débora R.
Andrade, Carlos E. F.
Utagawa, Cláudia Y.
Puppi, Flávia
Nader, Helena B.
Toma, Leny
Coelho, Janice
Leistner, Sandra
Burin, Maira
Giugliani, Roberto
Chong, A. Kim

December 2000

The mucopolysaccharidoses (MPS) are a heterogeneous group of inborn errors of lysosomal glycosaminog...