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Maria J Molnar

Showing results (1-10 of 13) with videos related to

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Nature Reviews. Neurology|July 3, 2023
AI-based tools for the diagnosis and treatment of rare neurological disordersMaria J Molnar, Viktor Molnar
Cellular Immunology|April 24, 2007
Establishing a neurological-psychiatric biobank: banking, informatics, ethicsMaria J Molnar, Peter Bencsik
Handbook of Clinical Neurology|October 9, 2017
Mitochondrial diseasesMaria J Molnar, Gabor G Kovacs
American Journal of Human Genetics|August 12, 2009
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletionsHenna Tyynismaa, Emil Ylikallio, Mehul Patel, et al.
Journal of the Neurological Sciences|January 24, 2025
Awareness and care practices for rare neurologic diseases among senior neurologists: A global surveyDae-Gyu Jang, Antonio Federico, Masha G Savelieff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 18, 2009
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and choreaGabor G Kovacs, Jill R Murrell, Sandor Horvath, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 1, 2004
Factors influencing the efficacy, longevity, and safety of electroporation-assisted plasmid-based gene transfer into mouse musclesMaria J Molnar, Rénald Gilbert, Yifan Lu, et al.
Acta Neuropathologica|December 11, 2007
MAPT S305I mutation: implications for argyrophilic grain diseaseGabor G Kovacs, Alan Pittman, Tamas Revesz, et al.
Neurogenetics|June 19, 2012
Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's diseaseEva C Schulte, Brit Mollenhauer, Alexander Zimprich, et al.
Plos One|November 19, 2013
Rare variants in PLXNA4 and Parkinson's diseaseEva C Schulte, Immanuel Stahl, Darina Czamara, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Nature Reviews. Neurology|July 3, 2023
AI-based tools for the diagnosis and treatment of rare neurological disordersMaria J Molnar, Viktor Molnar
Cellular Immunology|April 24, 2007
Establishing a neurological-psychiatric biobank: banking, informatics, ethicsMaria J Molnar, Peter Bencsik
Handbook of Clinical Neurology|October 9, 2017
Mitochondrial diseasesMaria J Molnar, Gabor G Kovacs
American Journal of Human Genetics|August 12, 2009
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletionsHenna Tyynismaa, Emil Ylikallio, Mehul Patel, et al.
Journal of the Neurological Sciences|January 24, 2025
Awareness and care practices for rare neurologic diseases among senior neurologists: A global surveyDae-Gyu Jang, Antonio Federico, Masha G Savelieff, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 18, 2009
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and choreaGabor G Kovacs, Jill R Murrell, Sandor Horvath, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 1, 2004
Factors influencing the efficacy, longevity, and safety of electroporation-assisted plasmid-based gene transfer into mouse musclesMaria J Molnar, Rénald Gilbert, Yifan Lu, et al.
Acta Neuropathologica|December 11, 2007
MAPT S305I mutation: implications for argyrophilic grain diseaseGabor G Kovacs, Alan Pittman, Tamas Revesz, et al.
Neurogenetics|June 19, 2012
Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's diseaseEva C Schulte, Brit Mollenhauer, Alexander Zimprich, et al.
Plos One|November 19, 2013
Rare variants in PLXNA4 and Parkinson's diseaseEva C Schulte, Immanuel Stahl, Darina Czamara, et al.
Pageof 2