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Rim Amouri

Showing results (21-30 of 42) with videos related to

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Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 1, 2012
Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian familiesMonia Benhamed Hammer, Ghada El Euch-Fayache, Houda Nehdi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser ParkinsonismTheresa Lüth, Carolin Gabbert, Sebastian Koch, et al.
Annals of Neurology|February 24, 2026
The Age at Onset of LRRK2 p.Gly2019Ser Parkinson's Disease Across Ancestries and Countries of OriginTheresa Lüth, Björn-Hergen Laabs, Sebastian Sendel, et al.
International Journal of Molecular Sciences|April 17, 2025
Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin ReductaseFeda E Mohamed, Lara Alzyoud, Mohammad A Ghattas, et al.
Neurobiology of Aging|December 21, 2013
Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonismJoanne Trinh, Rim Amouri, John E Duda, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseKenya Nishioka, Mounir Kefi, Barbara Jasinska-Myga, et al.
Cell Reports|June 21, 2016
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and HumansYubin Wang, Joshua Hersheson, Dulce Lopez, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Archives of Neurology|September 13, 2006
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutationsLianna Ishihara, Liling Warren, Rachel Gibson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North AfricaBarbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, et al.
Pageof 5

Showing results (21-30 of 42) with videos related to

Sort By:
Pageof 5
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|November 1, 2012
Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian familiesMonia Benhamed Hammer, Ghada El Euch-Fayache, Houda Nehdi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 24, 2023
Interaction of Mitochondrial Polygenic Score and Lifestyle Factors in LRRK2 p.Gly2019Ser ParkinsonismTheresa Lüth, Carolin Gabbert, Sebastian Koch, et al.
Annals of Neurology|February 24, 2026
The Age at Onset of LRRK2 p.Gly2019Ser Parkinson's Disease Across Ancestries and Countries of OriginTheresa Lüth, Björn-Hergen Laabs, Sebastian Sendel, et al.
International Journal of Molecular Sciences|April 17, 2025
Clinical Features of Families with a Novel Pathogenic Mutation in Sepiapterin ReductaseFeda E Mohamed, Lara Alzyoud, Mohammad A Ghattas, et al.
Neurobiology of Aging|December 21, 2013
Comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonismJoanne Trinh, Rim Amouri, John E Duda, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 4, 2009
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseKenya Nishioka, Mounir Kefi, Barbara Jasinska-Myga, et al.
Cell Reports|June 21, 2016
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and HumansYubin Wang, Joshua Hersheson, Dulce Lopez, et al.
Neuro-Degenerative Diseases|May 31, 2017
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesMonia B Hammer, Jinhui Ding, Fanny Mochel, et al.
Archives of Neurology|September 13, 2006
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutationsLianna Ishihara, Liling Warren, Rachel Gibson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North AfricaBarbara Jasinska-Myga, Jennifer Kachergus, Carles Vilariño-Güell, et al.
Pageof 5