Related Experiment Videos
Molecular basis of hereditary neuropathies
Giles D J Watts1, Phillip F Chance
1Neurogenetics Laboratory, Division of Genetics and Development, Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington 98195, USA.
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290.
American journal of human genetics·2008
Charcot-Marie-Tooth disease.
Current treatment options in neurology·2008
Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia.
American journal of medical genetics. Part A·2008
Joubert syndrome (and related disorders) (OMIM 213300).
European journal of human genetics : EJHG·2007
Behavior therapy: other interventions for tic disorders.
Advances in neurology·2006
Treatment of aggression in Tourette syndrome.
Advances in neurology·2006
Treatment of co-morbid obsessive compulsive disorder, mood, and anxiety disorders.
Advances in neurology·2006
Neurobiology of basal ganglia and Tourette syndrome: basal ganglia circuits and thalamocortical outputs.
Advances in neurology·2006
Preclinical models relevant to Tourette syndrome.
Advances in neurology·2006
Regenerative medicine for neurodegenerative diseases:History, Strategies, and Clinical Advances.
Translational research : the journal of laboratory and clinical medicine·2026
Emerging molecular mechanism of neuroinflammation in Parkinson's disease: A JAK/STAT and TGFβ/SMAD signaling crosstalk.
Biochimica et biophysica acta. General subjects·2026
Safety and adverse event profiles in neuromodulation therapies for drug-resistant epilepsy.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics·2026