Noina Abid
Belfast, NIR, United Kingdom
Last Updated: 09/26/2026
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Found 15 publications
XLH Matters 2024: expert insights and practical tools for enhancing care of people living with X-linked hypophosphataemia.
Journal: Orphanet journal of rare diseases
Published: September 19, 2025
Skeletal abnormalities and a low alkaline phosphatase.
Journal: Archives of disease in childhood. Education and practice edition
Published: October 14, 2024
Toddler with isolated gross motor delay.
Journal: Archives of disease in childhood. Education and practice edition
Published: May 10, 2024
Fourteen-year-old girl with complicated hypothyroidism.
Journal: Archives of disease in childhood. Education and practice edition
Published: October 18, 2023
Congenital hypothyroidism in Northern Ireland: 40 years' experience of national screening programme.
Congenital hypothyroidism in Northern Ireland: 40 years' experience of national screening programme.
Journal: Clinical endocrinology
Published: February 16, 2023
A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome.
Journal: Clinical endocrinology
Published: May 23, 2018
Resolution of Consumptive Hypothyroidism Secondary to Infantile Hepatic Hemangiomatosis with a Combination of Propranolol and Levothyroxine
Journal: Journal of clinical research in pediatric endocrinology
Published: March 15, 2018
Hyperglycaemia-related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetes.
Journal: Diabetic medicine : a journal of the British Diabetic Association
Published: February 03, 2017
Diagnostic value of exome and whole genome sequencing in craniosynostosis.
Journal: Journal of medical genetics
Published: August 24, 2016
Last Updated: 09/26/2026