Associated Papers
Liver Fibrosis and Steatosis in Alström Syndrome: A Genetic Model for Metabolic Syndrome.
Bettini S et al.
Diagnostics (basel, Switzerland), 2021
Neurocognitive assessment and DNA sequencing expand the phenotype and genotype spectrum of Alström syndrome.
Dassie F et al.
American Journal of Medical Genetics. Part A, 2021
Familial Alström syndrome: a rare cause of bilateral progressive hearing loss.
Bahmad F et al.
Brazilian Journal of Otorhinolaryngology, 2014
Alström syndrome: cardiac magnetic resonance findings.
Corbetti F et al.
International Journal of Cardiology, 2013
ALMS1-deficient fibroblasts over-express extra-cellular matrix components, display cell cycle delay and are resistant to apoptosis.
Zulato E et al.
Plos One, 2011
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