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Publications by Bassam Abu-Libdeh

A Defect in the Retromer Accessory Protein, SNX27, Manifests by Infantile Myoclonic Epilepsy and Neurodegeneration

Neurogenetics
Molecular NeuroscienceGeneticsCellular
2015English

Erratum To: PARP10 Deficiency Manifests by Severe Developmental Delay and DNA Repair Defect

Neurogenetics
Molecular NeuroscienceGeneticsCellular
2017English

Related publications

TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy

American Journal of Human Genetics
Genetics
2010English

Juvenile Myoclonic Epilepsy

BMJ
2012English

Juvenile Myoclonic Epilepsy

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Juvenile Myoclonic Epilepsy

2020English

Headache in Juvenile Myoclonic Epilepsy

Journal of Headache and Pain
MedicineNeurologyAnesthesiologyPain Medicine
2011English

Photosensitivity in Juvenile Myoclonic Epilepsy

Seizure : the journal of the British Epilepsy Association
MedicineNeurology
2000English

Juvenile Myoclonic Epilepsy.

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1992English

Juvenile Myoclonic Epilepsy Mimicking Focal Epilepsy

Arquivos de Neuro-Psiquiatria
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2012English

West Syndrome Followed by Juvenile Myoclonic Epilepsy: A Coincidental Occurrence?

BMC Neurology
MedicineNeurology
2013English

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