Statin-associated myopathy in pediatric settings: Myth or fact?

Buonuomo, Paola Sabrina; Macchiaiolo, Marina; Mastrogiorgio, Gerarda; Rana, Ippolita; Gonfiantini, Michaela Veronika; Bartuli, Andrea

Buonuomo, Paola Sabrina; Macchiaiolo, Marina; Mastrogiorgio, Gerarda; Rana, Ippolita; Gonfiantini, Michaela Veronika; Bartuli, Andrea.

Afiliación

Buonuomo PS; Rare Diseases and Medical Genetics Unit Bambino Gesù Children's Hospital Rome, Italy.
Macchiaiolo M; Rare Diseases and Medical Genetics Unit Bambino Gesù Children's Hospital Rome, Italy.
Mastrogiorgio G; Rare Diseases and Medical Genetics Unit Bambino Gesù Children's Hospital Rome, Italy.
Rana I; Rare Diseases and Medical Genetics Unit Bambino Gesù Children's Hospital Rome, Italy.
Gonfiantini MV; Rare Diseases and Medical Genetics Unit Bambino Gesù Children's Hospital Rome, Italy.
Bartuli A; Rare Diseases and Medical Genetics Unit Bambino Gesù Children's Hospital Rome, Italy.

J Pediatr ; 191: 279, 2017 12.

Article en En | MEDLINE | ID: mdl-28964429

Asunto(s)

Inhibidores de Hidroximetilglutaril-CoA Reductasas; Enfermedades Musculares; Niño; Humanos; Hipercolesterolemia

Palabras clave

creatine kinase; heterozygous familial hypercholesterolemia; myopathy; statin

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Inhibidores de Hidroximetilglutaril-CoA Reductasas / Enfermedades Musculares Tipo de estudio: Risk_factors_studies Límite: Child / Humans Idioma: En Revista: J Pediatr Año: 2017 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Estados Unidos

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