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Parastoo Momeni

Showing results (1-10 of 47) with videos related to

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Journal of Molecular Neuroscience : MN|September 8, 2011
Frontotemporal dementia: from Mendelian genetics towards genome wide association studiesRaffaele Ferrari, John Hardy, Parastoo Momeni
Expert Opinion on Therapeutic Targets|October 15, 2008
Challenges and new opportunities in the investigation of new drug therapies to treat frontotemporal dementiaEdward D Huey, Nicole Armstrong, Parastoo Momeni, et al.
Alzheimer Disease and Associated Disorders|July 2, 2010
Novel missense mutation in charged multivesicular body protein 2B in a patient with frontotemporal dementiaRaffaele Ferrari, Dimitrios Kapogiannis, Edward D Huey, et al.
Neuroscience Letters|February 14, 2006
A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's diseaseTerri Edwards-Lee, Johnny Wen, Jason Bell, et al.
Neurobiology of Disease|March 1, 2006
A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementiaRoneil Malkani, Ian D'Souza, Katrina Gwinn-Hardy, et al.
Case Reports in Medicine|August 9, 2014
Familial thoracic aortic aneurysm with dissection presenting as flash pulmonary edema in a 26-year-old manSabry Omar, Tyler Moore, Drew Payne, et al.
Neuroscience Letters|November 11, 2006
Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2BParastoo Momeni, Jason Bell, Jaime Duckworth, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2009
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutationsSarah Teixeira Camargos, Leonardo Oliveira Dornas, Parastoo Momeni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2007
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystoniaSarah Teixeira Camargos, Francisco Cardoso, Parastoo Momeni, et al.
Neurobiology of Aging|July 12, 2005
Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID)Parastoo Momeni, Nigel J Cairns, Robert H Perry, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Journal of Molecular Neuroscience : MN|September 8, 2011
Frontotemporal dementia: from Mendelian genetics towards genome wide association studiesRaffaele Ferrari, John Hardy, Parastoo Momeni
Expert Opinion on Therapeutic Targets|October 15, 2008
Challenges and new opportunities in the investigation of new drug therapies to treat frontotemporal dementiaEdward D Huey, Nicole Armstrong, Parastoo Momeni, et al.
Alzheimer Disease and Associated Disorders|July 2, 2010
Novel missense mutation in charged multivesicular body protein 2B in a patient with frontotemporal dementiaRaffaele Ferrari, Dimitrios Kapogiannis, Edward D Huey, et al.
Neuroscience Letters|February 14, 2006
A presenilin-1 mutation (T245P) in transmembrane domain 6 causes early onset Alzheimer's diseaseTerri Edwards-Lee, Johnny Wen, Jason Bell, et al.
Neurobiology of Disease|March 1, 2006
A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementiaRoneil Malkani, Ian D'Souza, Katrina Gwinn-Hardy, et al.
Case Reports in Medicine|August 9, 2014
Familial thoracic aortic aneurysm with dissection presenting as flash pulmonary edema in a 26-year-old manSabry Omar, Tyler Moore, Drew Payne, et al.
Neuroscience Letters|November 11, 2006
Sequence analysis of all identified open reading frames on the frontal temporal dementia haplotype on chromosome 3 fails to identify unique coding variants except in CHMP2BParastoo Momeni, Jason Bell, Jaime Duckworth, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2009
Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutationsSarah Teixeira Camargos, Leonardo Oliveira Dornas, Parastoo Momeni, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2007
Novel GCH1 mutation in a Brazilian family with dopa-responsive dystoniaSarah Teixeira Camargos, Francisco Cardoso, Parastoo Momeni, et al.
Neurobiology of Aging|July 12, 2005
Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID)Parastoo Momeni, Nigel J Cairns, Robert H Perry, et al.
Pageof 5