2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: Developed by the task force for the diagnosis and treatment of pulmonary …

M Humbert, G Kovacs, MM Hoeper… - European heart …, 2022 - academic.oup.com
Pulmonary hypertension (PH) is a pathophysiological disorder that may involve multiple
clinical conditions and may be associated with a variety of cardiovascular and respiratory …

[HTML][HTML] 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension

M Humbert, G Kovacs, MM Hoeper… - European …, 2022 - publications.ersnet.org
2022 ESC/ERS pulmonary hypertension guidelines incorporate changes and adaptations
focusing on clinical management https://bit. ly/3QtUvb4

Standardised practices in the networked management of congenital hyperinsulinism: a UK national collaborative consensus

MG Shaikh, AK Lucas-Herald, A Dastamani… - Frontiers in …, 2023 - frontiersin.org
Congenital hyperinsulinism (CHI) is a condition characterised by severe and recurrent
hypoglycaemia in infants and young children caused by inappropriate insulin over …

Hyperinsulinemic hypoglycemia in children and adolescents: recent advances in understanding of pathophysiology and management

M Gϋemes, SA Rahman, RR Kapoor… - Reviews in Endocrine …, 2020 - Springer
Hyperinsulinemic hypoglycemia (HH) is characterized by unregulated insulin release,
leading to persistently low blood glucose concentrations with lack of alternative fuels, which …

Mitochondrial Volume Regulation and Swelling Mechanisms in Cardiomyocytes

XR Chapa-Dubocq, KM Rodríguez-Graciani… - Antioxidants, 2023 - mdpi.com
Mitochondrion, known as the “powerhouse” of the cell, regulates ion homeostasis, redox
state, cell proliferation and differentiation, and lipid synthesis. The inner mitochondrial …

Congenital hyperinsulinism: recent updates on molecular mechanisms, diagnosis and management

D Giri, K Hawton, S Senniappan - Journal of Pediatric Endocrinology …, 2022 - degruyter.com
Congenital hyperinsulinism (CHI) is a rare disease characterized by an unregulated insulin
release, leading to hypoglycaemia. It is the most frequent cause of persistent and severe …

Implication of potassium channels in the pathophysiology of pulmonary arterial hypertension

H Le Ribeuz, V Capuano, B Girerd, M Humbert… - Biomolecules, 2020 - mdpi.com
Pulmonary arterial hypertension (PAH) is a rare and severe cardiopulmonary disease
without curative treatments. PAH is a multifactorial disease that involves genetic …

Erratum: 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: Developed by the task force for the diagnosis and treatment of …

M Humbert, G Kovacs, MM Hoeper… - … : 2022 ESC/ERS …, 2023 - produccioncientifica.ucm.es
Erratum: 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension:
Developed by the task force for the diagnosis and treatment of pulmonary hypertension of the …

The danger of diazoxide in the neonatal intensive care unit

J Desai, L Key, A Swindall, K Gaston… - … advances in drug …, 2021 - journals.sagepub.com
Background: The most common cause of persistent hypoglycemia in infancy is
hyperinsulinemic hypoglycemia. When conservative measures fail, providers often use …

Whole exome sequence analysis provides novel insights into the genetic framework of childhood-onset pulmonary arterial hypertension

SM Gelinas, CE Benson, MA Khan, RMF Berger… - Genes, 2020 - mdpi.com
Pulmonary arterial hypertension (PAH) describes a rare, progressive vascular disease
caused by the obstruction of pulmonary arterioles, typically resulting in right heart failure …