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Publications by Maeve A. Caldwell
A Defect in the Retromer Accessory Protein, SNX27, Manifests by Infantile Myoclonic Epilepsy and Neurodegeneration
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
Related publications
TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy
American Journal of Human Genetics
Genetics
Juvenile Myoclonic Epilepsy
BMJ
Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy
Headache in Juvenile Myoclonic Epilepsy
Journal of Headache and Pain
Medicine
Neurology
Anesthesiology
Pain Medicine
Photosensitivity in Juvenile Myoclonic Epilepsy
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Juvenile Myoclonic Epilepsy.
BMJ
Juvenile Myoclonic Epilepsy Mimicking Focal Epilepsy
Arquivos de Neuro-Psiquiatria
Biological Psychiatry
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West Syndrome Followed by Juvenile Myoclonic Epilepsy: A Coincidental Occurrence?
BMC Neurology
Medicine
Neurology