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Leila Darki

Showing results (1-10 of 6) with videos related to

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Continuum (Minneapolis, Minn.)|October 18, 2023
Paraproteinemic NeuropathiesSaid R Beydoun, Leila Darki
Journal of Clinical Neuromuscular Disease|November 20, 2020
Polyneuropathy Reveals Origins of Decade-long Gastrointestinal Symptoms in a Patient With Undiagnosed Mitochondrial Neurogastrointestinal Encephalopathy Caused by a Novel MutationLeila Darki, Arash Jalali-Sohi, Said R Beydoun
Journal of the American Geriatrics Society|November 14, 2013
In-hospital mortality and coronary procedure use for individuals with dementia with acute myocardial infarction in the United StatesDavid M Tehrani, Leila Darki, Ashwini Erande, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 17, 2026
A novel case of compound heterozygous GFPT1 congenital myasthenic syndrome with a coexisting heterozygous DYSF mutation: clinical and pathological insightsKamran Moradi, Leila Darki, Ryan W Rebbe, et al.
The Laryngoscope|August 23, 2020
Development of In-Office Laryngeal Nerve Conduction Studies: Computed Tomography and Cadaveric StudyNeel K Bhatt, Franklin M Wu, Leila Darki, et al.
Clinical Neurology and Neurosurgery|July 17, 2021
Reducing body myopathy associated with the LIM2 p.(His123Arg) FHL1 variantLeila Darki, Arash Jalali-Sohi, Samuel Guzman, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Continuum (Minneapolis, Minn.)|October 18, 2023
Paraproteinemic NeuropathiesSaid R Beydoun, Leila Darki
Journal of Clinical Neuromuscular Disease|November 20, 2020
Polyneuropathy Reveals Origins of Decade-long Gastrointestinal Symptoms in a Patient With Undiagnosed Mitochondrial Neurogastrointestinal Encephalopathy Caused by a Novel MutationLeila Darki, Arash Jalali-Sohi, Said R Beydoun
Journal of the American Geriatrics Society|November 14, 2013
In-hospital mortality and coronary procedure use for individuals with dementia with acute myocardial infarction in the United StatesDavid M Tehrani, Leila Darki, Ashwini Erande, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 17, 2026
A novel case of compound heterozygous GFPT1 congenital myasthenic syndrome with a coexisting heterozygous DYSF mutation: clinical and pathological insightsKamran Moradi, Leila Darki, Ryan W Rebbe, et al.
The Laryngoscope|August 23, 2020
Development of In-Office Laryngeal Nerve Conduction Studies: Computed Tomography and Cadaveric StudyNeel K Bhatt, Franklin M Wu, Leila Darki, et al.
Clinical Neurology and Neurosurgery|July 17, 2021
Reducing body myopathy associated with the LIM2 p.(His123Arg) FHL1 variantLeila Darki, Arash Jalali-Sohi, Samuel Guzman, et al.
Pageof 1