Christina Lampe
AuthID: R-00G-CEH
11
TÃTULO: The effect of galsulfase enzyme replacement therapy on the growth of patients with mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) Full Text
AUTORES: Harmatz, P; Hendriksz, CJ; Lampe, C; McGill, JJ; Parini, R; Leao Teles, E; Valayannopoulos, V; Tj. Cole; Matousek, R; Graham, S; Guffon, N; Quartel, A;
PUBLICAÇÃO: 2017, FONTE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 122, NÚMERO: 1-2
AUTORES: Harmatz, P; Hendriksz, CJ; Lampe, C; McGill, JJ; Parini, R; Leao Teles, E; Valayannopoulos, V; Tj. Cole; Matousek, R; Graham, S; Guffon, N; Quartel, A;
PUBLICAÇÃO: 2017, FONTE: MOLECULAR GENETICS AND METABOLISM, VOLUME: 122, NÚMERO: 1-2
INDEXADO EM: 
WOS
WOS12
TÃTULO: Natural History and Galsulfase Treatment in Mucopolysaccharidosis VI (MPS VI, Maroteaux-Lamy Syndrome)-10-Year Follow-Up of Patients who Previously Participated in an MPS VI Survey Study Full Text
AUTORES: Roberto Giugliani; Christina Lampe; Nathalie Guffon; David Ketteridge; Elisa Leao Teles; James E Wraith; Simon A Jones; Cheri Piscia Nichols; Ping Lin; Adrian Quartel; Paul Harmatz;
PUBLICAÇÃO: 2014, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164A, NÚMERO: 8
AUTORES: Roberto Giugliani; Christina Lampe; Nathalie Guffon; David Ketteridge; Elisa Leao Teles; James E Wraith; Simon A Jones; Cheri Piscia Nichols; Ping Lin; Adrian Quartel; Paul Harmatz;
PUBLICAÇÃO: 2014, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART A, VOLUME: 164A, NÚMERO: 8
13
TÃTULO: Design, baseline characteristics, and early findings of the MPS VI (mucopolysaccharidosis VI) Clinical Surveillance Program (CSP) Full Text
AUTORES: Christian J Hendriksz; Roberto Giugliani; Paul Harmatz; Christina Lampe; Ana Maria Martins; Gregory M Pastores; Robert D Steiner; Elisa Leao Teles; Vassili Valayannopoulos;
PUBLICAÇÃO: 2013, FONTE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 36, NÚMERO: 2
AUTORES: Christian J Hendriksz; Roberto Giugliani; Paul Harmatz; Christina Lampe; Ana Maria Martins; Gregory M Pastores; Robert D Steiner; Elisa Leao Teles; Vassili Valayannopoulos;
PUBLICAÇÃO: 2013, FONTE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 36, NÚMERO: 2
14
TÃTULO: Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease Full Text
AUTORES: Maurizio Scarpa; Zsuzsanna Almassy; Michael Beck; Olaf Bodamer; Iain A Bruce; Linda De Meirleir; Nathalie Guffon; Encarna Guillen Navarro; Pauline Hensman; Simon Jones; Wolfgang Kamin; Christoph Kampmann; Christina Lampe; Christine A Lavery; Elisa Leao Teles; Bianca Link; Allan M Lund; Gunilla Malm; Susanne Pitz; Michael Rothera; ...Mais
PUBLICAÇÃO: 2011, FONTE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 6, NÚMERO: 1
AUTORES: Maurizio Scarpa; Zsuzsanna Almassy; Michael Beck; Olaf Bodamer; Iain A Bruce; Linda De Meirleir; Nathalie Guffon; Encarna Guillen Navarro; Pauline Hensman; Simon Jones; Wolfgang Kamin; Christoph Kampmann; Christina Lampe; Christine A Lavery; Elisa Leao Teles; Bianca Link; Allan M Lund; Gunilla Malm; Susanne Pitz; Michael Rothera; ...Mais
PUBLICAÇÃO: 2011, FONTE: ORPHANET JOURNAL OF RARE DISEASES, VOLUME: 6, NÚMERO: 1
