Robert Cramb
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View article: Defining renal phenotype in Alström syndrome
Defining renal phenotype in Alström syndrome Open
Background Alström syndrome (AS) is a rare autosomal recessive ciliopathy with a wide spectrum of clinical features, including cone–rod retinal dystrophy, neuronal deafness, severe insulin resistance and major organ failure. The characteri…
View article: Toward Systematic Screening for Persistent Hepatitis E Virus Infections in Transplant Patients
Toward Systematic Screening for Persistent Hepatitis E Virus Infections in Transplant Patients Open
Transplant recipients in the United Kingdom are at a low but significant risk of HEV infection. HEV-Ag detection could be an alternative to RNA detection where the goal is to identify established persistent HEV infection, particularly wher…
View article: Food intake and appetite following school-based high-intensity interval training in 9–11-year-old children
Food intake and appetite following school-based high-intensity interval training in 9–11-year-old children Open
Using a randomised cross-over design, free-living lunch intake and subjective appetite were examined in 10 children (9.8 ± 0.6 years) following high-intensity interval training (HIIT) versus a control sedentary (SED) period, within a schoo…
View article: Advanced non‐alcoholic fatty liver disease and adipose tissue fibrosis in patients with Alström syndrome
Advanced non‐alcoholic fatty liver disease and adipose tissue fibrosis in patients with Alström syndrome Open
Background and Aims Alström syndrome ( AS ) is a recessive monogenic syndrome characterized by obesity, extreme insulin resistance and multi‐organ fibrosis. Despite phenotypically being high risk of non‐alcoholic fatty liver disease ( NAFL…