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ARMC5 mutation in a Portuguese family with primary bilateral macronodular adrenal hyperplasia (PBMAH).
Rego, Teresa; Fonseca, Fernando; Espiard, Stéphanie; Perlemoine, Karine; Bertherat, Jérôme; Agapito, Ana.
Affiliation
  • Rego T; Endocrinology Department, Hospital Curry Cabral, Centro Hospitalar de Lisboa Central, LisbonPortugal.
  • Fonseca F; Endocrinology Department, Hospital Curry Cabral, Centro Hospitalar de Lisboa Central, LisbonPortugal.
  • Espiard S; Endocrinology Department, INSERM U1016, Institut Cochin, Paris Descartes University, & Center for Rare Adrenal Diseases, Hôpital Cochin, APHP-Paris, France.
  • Perlemoine K; Endocrinology Department, INSERM U1016, Institut Cochin, Paris Descartes University, & Center for Rare Adrenal Diseases, Hôpital Cochin, APHP-Paris, France.
  • Bertherat J; Endocrinology Department, INSERM U1016, Institut Cochin, Paris Descartes University, & Center for Rare Adrenal Diseases, Hôpital Cochin, APHP-Paris, France.
  • Agapito A; Endocrinology Department, Hospital Curry Cabral, Centro Hospitalar de Lisboa Central, LisbonPortugal.
Endocrinol Diabetes Metab Case Rep ; 20172017.
Article in En | MEDLINE | ID: mdl-28458897
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Health_technology_assessment / Prognostic_studies Language: En Journal: Endocrinol Diabetes Metab Case Rep Year: 2017 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Health_technology_assessment / Prognostic_studies Language: En Journal: Endocrinol Diabetes Metab Case Rep Year: 2017 Document type: Article