Crystel T. Bonnet
Paris, 75012, France
Last Updated: 09/26/2026
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Found 95 publications
New insights into the complex genetic architecture of age-related hearing loss.
Journal: European journal of medical genetics
Published: February 09, 2026
Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: December 08, 2025
The Reticular formation: An integrative network for postural control.
Journal: Neurophysiologie clinique = Clinical neurophysiology
Published: July 15, 2025
Ambulatory introduction of foslevodopa/foscarbidopa in Parkinson's disease in private practice. Case series of the first 22 patients.
Journal: Revue neurologique
Published: May 29, 2025
Short Communication: True Cost Accounting (TCA) as a transformative approach for livestock agri-food systems.
Journal: Animal : an international journal of animal bioscience
Published: December 18, 2024
Genetic diversity of Usher syndrome in Moroccan patients.
Journal: Human genetics
Published: November 20, 2024
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Journal: Frontiers in genetics
Published: May 23, 2024
Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.
Journal: Molecular biology reports
Published: April 25, 2024
Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment.
Journal: Journal of applied genetics
Published: February 14, 2024
Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia.
Journal: Revue neurologique
Published: January 24, 2024
Last Updated: 09/26/2026