Corrinda M. Black
Aberdeen, SCT, United Kingdom
Last Updated: 09/26/2026
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Found 13 publications
Anaesthesia management of a child with aromatic L-amino acid decarboxylase deficiency.
Journal: Anaesthesia reports
Published: March 02, 2022
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin.
Journal: Journal of the American Society of Nephrology : JASN
Published: April 11, 2021
Prevalence of secondary care multimorbidity in mid-life and its association with premature mortality in a large longitudinal cohort study.
Journal: BMJ open
Published: May 07, 2020
Impact of educational attainment on the association between social class at birth and multimorbidity in middle age in the Aberdeen Children of the 1950s cohort study.
Journal: BMJ open
Published: January 31, 2019
Congenital cataracts in females caused by BCOR mutations; report of six further families demonstrating clinical variability and diverse genetic mechanisms.
Journal: European journal of medical genetics
Published: December 10, 2018
Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach.
Journal: Eye (London, England)
Published: October 20, 2015
Long-term prognosis after acute kidney injury (AKI): what is the role of baseline kidney function and recovery? A systematic review.
Journal: BMJ open
Published: January 08, 2015
A novel mutation in IL36RN underpins childhood pustular dermatosis.
Journal: Journal of the European Academy of Dermatology and Venereology : JEADV
Published: June 24, 2014
3-M syndrome: a growth disorder associated with IGF2 silencing.
Journal: Endocrine connections
Published: October 24, 2013
Last Updated: 09/26/2026