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Daniel H Geschwind

Showing results (421-430 of 474) with videos related to

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Neurology|July 5, 2022
Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar DegenerationPhilip Wade Tipton, Angela B Deutschlaender, Rodolfo Savica, et al.
Nature Genetics|May 5, 2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate exportAndrea Legati, Donatella Giovannini, Gaël Nicolas, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autismPatrícia B S Celestino-Soper, Sara Violante, Emily L Crawford, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Nature|January 17, 2025
Brain-wide neuronal circuit connectome of human glioblastomaYusha Sun, Xin Wang, Daniel Y Zhang, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
Clinical ManifestationsCeline 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 ManifestationsJuan-Camilo Vargas-González, Hessah A Alotibi, Kasey Cortez, et al.
Nature Genetics|August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and miceAnnika Keller, Ana Westenberger, Maria J Sobrido, et al.
Annals of Neurology|July 11, 2023
Network Connectivity Alterations across the MAPT Mutation Clinical SpectrumLiwen Zhang, Taru M Flagan, Suvi Häkkinen, et al.
JAMA Neurology|June 14, 2021
DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya DiseaseAdam J Kundishora, Samuel T Peters, Amélie Pinard, et al.
Pageof 48

Showing results (421-430 of 474) with videos related to

Sort By:
Pageof 48
Neurology|July 5, 2022
Differences in Motor Features of <i>C9orf72</i>, <i>MAPT</i>, or <i>GRN</i> Variant Carriers With Familial Frontotemporal Lobar DegenerationPhilip Wade Tipton, Angela B Deutschlaender, Rodolfo Savica, et al.
Nature Genetics|May 5, 2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate exportAndrea Legati, Donatella Giovannini, Gaël Nicolas, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 9, 2012
A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autismPatrícia B S Celestino-Soper, Sara Violante, Emily L Crawford, et al.
Medrxiv : the Preprint Server for Health Sciences|December 3, 2025
Common and rare variant genetic contributions in African Americans with autismMatilde Cirnigliaro, Jennifer K Lowe, Alexander O Flynn-Carroll, et al.
Nature|January 17, 2025
Brain-wide neuronal circuit connectome of human glioblastomaYusha Sun, Xin Wang, Daniel Y Zhang, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 25, 2025
Clinical ManifestationsCeline 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 ManifestationsJuan-Camilo Vargas-González, Hessah A Alotibi, Kasey Cortez, et al.
Nature Genetics|August 6, 2013
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and miceAnnika Keller, Ana Westenberger, Maria J Sobrido, et al.
Annals of Neurology|July 11, 2023
Network Connectivity Alterations across the MAPT Mutation Clinical SpectrumLiwen Zhang, Taru M Flagan, Suvi Häkkinen, et al.
JAMA Neurology|June 14, 2021
DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya DiseaseAdam J Kundishora, Samuel T Peters, Amélie Pinard, et al.
Pageof 48