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Browsing publications by Mohamed Al-Hamed.

Newcastle AuthorsTitleYearFull text
Mohamed Al-Hamed
Professor John Sayer
Novel loss of function variants in FRAS1 AND FREM2 underlie renal agenesis in consanguineous families2021
Mohamed Al-Hamed
Professor John Sayer
Fetal anomalies associated with novel pathogenic variants in TMEM942020
Mohamed Al-Hamed
Dr Sarah Rice
Dr Noel Edwards
Professor John Sayer
Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families2019
Mohamed Al-Hamed
Professor John Sayer
Renal tubular dysgenesis: antenatal ultrasound scanning and molecular investigations in a Saudi Arabian family2016
Dr Noel Edwards
Dr Sarah Rice
Dr Ann Marie Hynes
Dr Shalabh Srivastava
Dr Iain Moore
et al.
A novel LMX1B mutation in a family with end-stage renal disease of ‘unknown cause’2015
Mohamed Al-Hamed
Dr Charles van Lennep
Dr Ann Marie Hynes
Paul Chrystal
Dr Lorraine Eley
et al.
Functional modelling of a novel mutation in BBS52014
Mohamed Al-Hamed
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption2013
Dr Shalabh Srivastava
Dr Noel Edwards
Dr Ann Marie Hynes
Dr Katrina Wood
Mohamed Al-Hamed
et al.
Identification of compound heterozygous KCNJ1 mutations (Encoding ROMK) in a kindred with bartter’s syndrome and a functional analysis of their pathogenicity2013
Mohamed Al-Hamed
Dr Roslyn Simms
Professor John Sayer
Investigating Bardet Biedl syndrome: identification and modelling of a novel mutation in BBS52012
Mohamed Al-Hamed
Professor John Sayer
A novel mutation in NPHS2 causing nephrotic syndrome in a Saudi Arabian family2010
Mohamed Al-Hamed
Professor John Sayer
A Novel Mutation in NPHS2 Causing Steroid Resistant Nephrotic Syndrome in a Saudi Arabian Family2009