Mazabraud's syndrome: A case report supported by molecular studies and review of the literature.

Kaspar, Ludvík; Balko, Jan; Strnadová, Martina; Krsková, Lenka; Máska, David; Zámecník, Josef

Kaspar, Ludvík; Balko, Jan; Strnadová, Martina; Krsková, Lenka; Máska, David; Zámecník, Josef.

Afiliación

Kaspar L; Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague, Czech Republic.
Balko J; Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague, Czech Republic.
Strnadová M; Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague, Czech Republic.
Krsková L; Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague, Czech Republic.
Máska D; Department of Adult and Pediatric Orthopaedic Surgery and Traumatology, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague, Czech Republic.
Zámecník J; Department of Pathology and Molecular Medicine, 2nd Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu 84, 150 06 Prague, Czech Republic.

Bone Rep ; 18: 101685, 2023 Jun.

Article en En | MEDLINE | ID: mdl-37250204

Palabras clave

Fibrous dysplasia; GNAS1 gene mutation; Intramuscular myxoma; Mazabraud's syndrome; Mesenchymal neoplasm

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Bone Rep Año: 2023 Tipo del documento: Article País de afiliación: República Checa Pais de publicación: Estados Unidos

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