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...
Saved in:
Main Authors: | Carmen Aresta, Gianfranco Butera, Antonietta Tufano, Giorgia Grassi, Livio Luzi, Stefano Benedini |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2018-01-01
|
Series: | Case Reports in Endocrinology |
Online Access: | http://dx.doi.org/10.1155/2018/2091257 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Adrenal Ganglioneuroblastoma in Adults: A Case Report and Review of the Literature
by: Stefano Benedini, et al.
Published: (2017-01-01) -
COVID-19 in Cyanotic Congenital Heart Disease
by: Lama A Ammar, et al.
Published: (2023-01-01) -
New Horizon of Intervention in Congenital Heart Disease: AFR in a Complex Cyanotic Patient
by: Zahra Khajali, et al.
Published: (2020-01-01) -
Autoimmune Polyendocrine Syndrome 3 Onset with Severe Ketoacidosis in a 74-Year-Old Woman
by: Stefano Benedini, et al.
Published: (2015-01-01) -
Precision fetal cardiology detects cyanotic congenital heart disease using maternal saliva metabolome and artificial intelligence
by: Ray Bahado-Singh, et al.
Published: (2025-01-01)