Pheochromocytoma in Congenital Cyanotic Heart Disease

Studies on genome-wide transcription patterns have shown that many genetic alterations implicated in pheochromocytoma-paraganglioma (P-PGL) syndromes cluster in a common cellular pathway leading to aberrant activation of molecular response to hypoxia in normoxic conditions (the pseudohypoxia hypothe...

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Dades bibliogràfiques
Publicat a:Case Rep Endocrinol
Autors principals: Aresta, Carmen, Butera, Gianfranco, Tufano, Antonietta, Grassi, Giorgia, Luzi, Livio, Benedini, Stefano
Format: Artigo
Idioma:Inglês
Publicat: Hindawi 2018
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6176301/
https://ncbi.nlm.nih.gov/pubmed/30356369
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/2091257
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