Catherine E. Armstrong
Bristol, ENG, United Kingdom
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 19 publications
The future of hospital at home: a qualitative interview study of healthcare staff.
Journal: European geriatric medicine
Published: January 25, 2024
Biallelic PKP2 loss of function variants are associated with a lethal perinatal-onset biventricular dilated cardiomyopathy with excessive trabeculations and ventricular septal defects.
Journal: Journal of medical genetics
Published: July 01, 2023
Left ventricular noncompaction cardiomyopathy and short QT syndrome due to primary carnitine deficiency.
Journal: Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc
Published: March 29, 2023
Ireland DXA-FRAX may differ significantly and substantially to Web-FRAX.
Journal: Archives of osteoporosis
Published: December 08, 2022
Expanding ACTA2 genotypes with corresponding phenotypes overlapping with smooth muscle dysfunction syndrome.
Journal: American journal of medical genetics. Part A
Published: January 05, 2022
Initial results from an enhanced recovery program for pediatric cardiac surgical patients.
Journal: Paediatric anaesthesia
Published: July 05, 2021
Vertebral Fractures in Ireland: A Sub-analysis of the DXA HIP Project.
Journal: Calcified tissue international
Published: January 27, 2021
Severe refractory Kawasaki disease in seven infants in the COVID-19 era.
Journal: The Lancet. Rheumatology
Published: August 25, 2020
Osteoporotic Vertebral Fractures are Common in Hip Fracture Patients and are Under-recognized.
Journal: Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry
Published: March 30, 2020
A systematic review of the Irish osteoporotic vertebral fracture literature.
Journal: Archives of osteoporosis
Published: November 11, 2019
Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism.
Journal: American journal of human genetics
Published: September 02, 2019
Last Updated: 09/26/2026