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Molecular Psychiatry
|
August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
C Francks, S Maegawa, J Laurén, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Clinical Manifestations
Celine N Sakran, Juan-Camilo Vargas-González, Nico Paulo Dimal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Juan-Camilo Vargas-González, Hessah A Alotibi, Kasey Cortez, et al.
The Lancet. Neurology
|
September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative
Rosa Rademakers, Matt Baker, Jennifer Gass, et al.
Nature Genetics
|
August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
Annika Keller, Ana Westenberger, Maria J Sobrido, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
March 1, 2011
Research reporting standards for radioembolization of hepatic malignancies
Riad Salem, Robert J Lewandowski, Vanessa L Gates, et al.
Neurology
|
September 13, 2013
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
Marka van Blitterswijk, Matthew C Baker, Mariely DeJesus-Hernandez, et al.
Annals of Clinical and Translational Neurology
|
May 16, 2018
Poly(GP), neurofilament and grey matter deficits in <i>C9orf72</i> expansion carriers
Lieke H H Meeter, Tania F Gendron, Ana C Sias, et al.
Annals of Neurology
|
July 11, 2023
Network Connectivity Alterations across the MAPT Mutation Clinical Spectrum
Liwen Zhang, Taru M Flagan, Suvi Häkkinen, et al.
JAMA Neurology
|
June 14, 2021
DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya Disease
Adam J Kundishora, Samuel T Peters, Amélie Pinard, et al.
Page
of 81
Search research articles
Search
Showing results (751-760 of 809) with videos related to
Sort By:
Page
of 81
Molecular Psychiatry
|
August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
C Francks, S Maegawa, J Laurén, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Clinical Manifestations
Celine N Sakran, Juan-Camilo Vargas-González, Nico Paulo Dimal, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Juan-Camilo Vargas-González, Hessah A Alotibi, Kasey Cortez, et al.
The Lancet. Neurology
|
September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative
Rosa Rademakers, Matt Baker, Jennifer Gass, et al.
Nature Genetics
|
August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
Annika Keller, Ana Westenberger, Maria J Sobrido, et al.
Journal of Vascular and Interventional Radiology : JVIR
|
March 1, 2011
Research reporting standards for radioembolization of hepatic malignancies
Riad Salem, Robert J Lewandowski, Vanessa L Gates, et al.
Neurology
|
September 13, 2013
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
Marka van Blitterswijk, Matthew C Baker, Mariely DeJesus-Hernandez, et al.
Annals of Clinical and Translational Neurology
|
May 16, 2018
Poly(GP), neurofilament and grey matter deficits in <i>C9orf72</i> expansion carriers
Lieke H H Meeter, Tania F Gendron, Ana C Sias, et al.
Annals of Neurology
|
July 11, 2023
Network Connectivity Alterations across the MAPT Mutation Clinical Spectrum
Liwen Zhang, Taru M Flagan, Suvi Häkkinen, et al.
JAMA Neurology
|
June 14, 2021
DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya Disease
Adam J Kundishora, Samuel T Peters, Amélie Pinard, et al.
Page
of 81