Your browser doesn't support javascript.
loading
Familial partial lipodystrophy syndromes.
Fernández-Pombo, Antía; Sánchez-Iglesias, Sofía; Cobelo-Gómez, Silvia; Hermida-Ameijeiras, Álvaro; Araújo-Vilar, David.
Afiliación
  • Fernández-Pombo A; UETeM-Molecular Pathology of Rare Diseases Group, Department of Psychiatry, Radiology, Public Health, Nursing and Medicine, IDIS-CiMUS, University of Santiago de Compostela, Santiago de Compostela 15782, Spain; Division of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Comp
  • Sánchez-Iglesias S; UETeM-Molecular Pathology of Rare Diseases Group, Department of Psychiatry, Radiology, Public Health, Nursing and Medicine, IDIS-CiMUS, University of Santiago de Compostela, Santiago de Compostela 15782, Spain.
  • Cobelo-Gómez S; UETeM-Molecular Pathology of Rare Diseases Group, Department of Psychiatry, Radiology, Public Health, Nursing and Medicine, IDIS-CiMUS, University of Santiago de Compostela, Santiago de Compostela 15782, Spain.
  • Hermida-Ameijeiras Á; UETeM-Molecular Pathology of Rare Diseases Group, Department of Psychiatry, Radiology, Public Health, Nursing and Medicine, IDIS-CiMUS, University of Santiago de Compostela, Santiago de Compostela 15782, Spain; Division of Internal Medicine, University Clinical Hospital of Santiago de Compostela, 15
  • Araújo-Vilar D; UETeM-Molecular Pathology of Rare Diseases Group, Department of Psychiatry, Radiology, Public Health, Nursing and Medicine, IDIS-CiMUS, University of Santiago de Compostela, Santiago de Compostela 15782, Spain; Division of Endocrinology and Nutrition, University Clinical Hospital of Santiago de Comp
Presse Med ; 50(3): 104071, 2021 Nov.
Article en En | MEDLINE | ID: mdl-34610417

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lipodistrofia Parcial Familiar Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans Idioma: En Revista: Presse Med Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Lipodistrofia Parcial Familiar Tipo de estudio: Diagnostic_studies / Etiology_studies Límite: Humans Idioma: En Revista: Presse Med Año: 2021 Tipo del documento: Article