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BMC Medical Genetics|July 6, 2019
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegiaSalma M Wakil, Safa Alhissi, Haya Al Dossari, et al.Seizure|July 17, 2012
Do pets reduce the likelihood of sudden unexplained death in epilepsy?Vera C Terra, Américo C Sakamoto, Hélio R Machado, et al.Journal of Molecular Neuroscience : MN|January 9, 2016
Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular AtrophyDavide Pareyson, Pietro Fratta, Pierre-François Pradat, et al.Gene|December 10, 2013
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>TSalma M Wakil, Khushnooda Ramzan, Rula Abuthuraya, et al.Pediatric Cardiology|April 2, 2016
Postnatal Outcome of Fetal Left Ventricular Hypertrabeculation/NoncompactionClaudia Stöllberger, Christian Wegner, Abraham Benatar, et al.International Journal of Molecular Sciences|August 12, 2023
Parkinson's Disease and the Heart: Studying Cardiac Metabolism in the 6-Hydroxydopamine ModelVictor Silva da Fonsêca, Valeria de Cassia Goncalves, Mario Augusto Izidoro, et al.Clinics (Sao Paulo, Brazil)|February 12, 2023
The amygdala lesioning due to status epilepticus - Changes in mechanisms controlling chloride homeostasisLuiz E C Santos, Antônio-Carlos G Almeida, Sílvia C B Silva, et al.Case Reports in Genetics|January 16, 2019
Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B GeneSalma M Wakil, Dorota Monies, Samya Hagos, et al.Clinics (Sao Paulo, Brazil)|July 17, 2023
Role of cardiac β1-adrenergic and A1-adenosine receptors in severe arrhythmias related to Parkinson's diseaseFrancisco Sandro Menezes-Rodrigues, Marcelo Pires de Oliveira, Erisvaldo Amarante Araújo, et al.Scientific Reports|August 19, 2021
Amazon rainforest rodents (Proechimys) are resistant to post-stroke epilepsyNancy N Ortiz-Villatoro, Selvin Z Reyes-Garcia, Leandro Freitas, et al.Pageof 70