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Neurogenetics

Showing results (131-140 of 1,080) with videos related to

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Neurogenetics|February 25, 2009
Comment on the article "Heterogeneous dysregulation of microRNAs across the autism spectrum" by Abu-Elneel et alSteven Buyske
Neurogenetics|October 3, 2008
Assessment of Alzheimer's disease case-control associations using family-based methodsBrit-Maren M Schjeide, Matthew B McQueen, Kristina Mullin, et al.
Neurogenetics|January 21, 2009
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindredEster Cuenca-León, Roser Corominas, Magda Montfort, et al.
Neurogenetics|September 21, 2005
Lrrk2 pathogenic substitutions in Parkinson's diseaseIgnacio F Mata, Jennifer M Kachergus, Julie P Taylor, et al.
Neurogenetics|October 24, 2007
Identification and characterization of a new alpha-synuclein isoform and its role in Lewy body diseasesKatrin Beyer, Montserrat Domingo-Sábat, José I Lao, et al.
Neurogenetics|August 19, 2007
Frataxin gene point mutations in Italian Friedreich ataxia patientsCinzia Gellera, Barbara Castellotti, Caterina Mariotti, et al.
Neurogenetics|January 16, 2007
Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesisAnne Grünewald, Guido J Breedveld, Katja Lohmann-Hedrich, et al.
Neurogenetics|November 18, 2006
Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystoniaDaniela Steinberger, Jutta Trübenbach, Birgit Zirn, et al.
Neurogenetics|November 27, 2008
New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP)Channa Hewamadduma, Christopher McDermott, Janine Kirby, et al.
Neurogenetics|July 8, 2009
Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationCostanza Bacci, Roberta Sestini, Aldesia Provenzano, et al.
Pageof 108

Showing results (131-140 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|February 25, 2009
Comment on the article "Heterogeneous dysregulation of microRNAs across the autism spectrum" by Abu-Elneel et alSteven Buyske
Neurogenetics|October 3, 2008
Assessment of Alzheimer's disease case-control associations using family-based methodsBrit-Maren M Schjeide, Matthew B McQueen, Kristina Mullin, et al.
Neurogenetics|January 21, 2009
Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindredEster Cuenca-León, Roser Corominas, Magda Montfort, et al.
Neurogenetics|September 21, 2005
Lrrk2 pathogenic substitutions in Parkinson's diseaseIgnacio F Mata, Jennifer M Kachergus, Julie P Taylor, et al.
Neurogenetics|October 24, 2007
Identification and characterization of a new alpha-synuclein isoform and its role in Lewy body diseasesKatrin Beyer, Montserrat Domingo-Sábat, José I Lao, et al.
Neurogenetics|August 19, 2007
Frataxin gene point mutations in Italian Friedreich ataxia patientsCinzia Gellera, Barbara Castellotti, Caterina Mariotti, et al.
Neurogenetics|January 16, 2007
Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesisAnne Grünewald, Guido J Breedveld, Katja Lohmann-Hedrich, et al.
Neurogenetics|November 18, 2006
Utility of MLPA in deletion analysis of GCH1 in dopa-responsive dystoniaDaniela Steinberger, Jutta Trübenbach, Birgit Zirn, et al.
Neurogenetics|November 27, 2008
New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP)Channa Hewamadduma, Christopher McDermott, Janine Kirby, et al.
Neurogenetics|July 8, 2009
Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutationCostanza Bacci, Roberta Sestini, Aldesia Provenzano, et al.
Pageof 108