Corrigendum to "Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases" [Mol. Genet. Metab. 118 (2016) 206-213].

Cassiman, David; Packman, Seymour; Bembi, Bruno; Turkia, Hadhami Ben; Al-Sayed, Moeenaldeen; Schiff, Manuel; Imrie, Jackie; Mabe, Paulina; Takahashi, Tsutomu; Mengel, Karl Eugen; Giugliani, Roberto; Cox, Gerald F

Cassiman, David; Packman, Seymour; Bembi, Bruno; Turkia, Hadhami Ben; Al-Sayed, Moeenaldeen; Schiff, Manuel; Imrie, Jackie; Mabe, Paulina; Takahashi, Tsutomu; Mengel, Karl Eugen; Giugliani, Roberto; Cox, Gerald F.

Afiliação

Cassiman D; Metabolic Center, University of Leuven, Leuven, Belgium.
Packman S; University of California San Francisco, San Francisco, CA,United States.
Bembi B; Academic Medical Centre Hospital of Udine, Udine, Italy.
Turkia HB; La Rabta Hospital, Tunis, Tunisia.
Al-Sayed M; King Faisal Specialist Hospital & Research Center, Riyadh, Saudi Arabia.
Schiff M; University of Paris-Diderot, APHP and INSERM U1141, Reference Center for Inborn Errors of Metabolism, Robert-Debré Hospital, Paris, France.
Imrie J; Niemann-Pick Disease Group (UK), Tyne and Wear, UK.
Mabe P; Hospital Dr. Exequiel González Cortés, Santiago, Chile.
Takahashi T; Akita University School of Medicine, Akita, Japan.
Mengel KE; Villa Metabolica, Center of Pediatric and Adolescents Medicine, University Medical Center, Mainz, Germany.
Giugliani R; Medical Genetics Service, HCPA, Dep. Genetics, UFRGS and INAGEMP, Porto Alegre, Brazil.
Cox GF; Clinical Development, Sanofi Genzyme, Cambridge, MA,United States. Electronic address: geraldcox17@yahoo.com.

Mol Genet Metab ; 125(4): 360, 2018 12.

Article em En | MEDLINE | ID: mdl-29129654

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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Mol Genet Metab Assunto da revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Bélgica

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