Your browser doesn't support javascript.
loading
Case report: Early-onset osteoporosis in a patient carrying a novel heterozygous variant of the WNT1 gene.
Campopiano, Maria Cristina; Fogli, Antonella; Michelucci, Angela; Mazoni, Laura; Longo, Antonella; Borsari, Simona; Pardi, Elena; Benelli, Elena; Sardella, Chiara; Pierotti, Laura; Dinoi, Elisa; Marcocci, Claudio; Cetani, Filomena.
Afiliación
  • Campopiano MC; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Fogli A; Laboratory of Molecular Genetics, University Hospital of Pisa, Pisa, Italy.
  • Michelucci A; Laboratory of Molecular Genetics, University Hospital of Pisa, Pisa, Italy.
  • Mazoni L; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Longo A; Department of Biological Sciences and BioDiscovery Institute, University of North Texas, Denton, TX, United States.
  • Borsari S; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Pardi E; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Benelli E; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Sardella C; Unit of Endocrinology, University Hospital of Pisa, Pisa, Italy.
  • Pierotti L; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Dinoi E; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Marcocci C; Department of Clinical and Experimental Medicine, Unit of Endocrinology, University of Pisa, Pisa, Italy.
  • Cetani F; Unit of Endocrinology, University Hospital of Pisa, Pisa, Italy.
Front Endocrinol (Lausanne) ; 13: 918682, 2022.
Article en En | MEDLINE | ID: mdl-36004351
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Osteoporosis Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Osteoporosis Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2022 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Suiza