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Peter Heutink

Showing results (71-80 of 240) with videos related to

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Annals of Neurology|December 24, 2005
Neonatal porencephaly and adult stroke related to mutations in collagen IV A1Marjo S van der Knaap, Leo M E Smit, Frederik Barkhof, et al.
Neuro-Degenerative Diseases|October 21, 2016
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal DementiaCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Plos One|June 19, 2015
Evidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson's DiseaseAnke A Dijkstra, Angela Ingrassia, Renee X de Menezes, et al.
Acta Neuropathologica|May 7, 2023
Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypesKatherine Fodder, Megha Murthy, Patrizia Rizzu, et al.
Plos One|September 27, 2014
Trehalose improves human fibroblast deficits in a new CHIP-mutation related ataxiaMaria Jose Casarejos, Juan Perucho, Jose Luis López-Sendón, et al.
European Journal of Human Genetics : EJHG|March 2, 2012
Dissecting the genetic make-up of North-East Sardinia using a large set of haploid and autosomal markersLuba M Pardo, Giovanna Piras, Rosanna Asproni, et al.
European Journal of Human Genetics : EJHG|January 18, 2007
Progranulin mutations in Dutch familial frontotemporal lobar degenerationIraad F Bronner, Patrizia Rizzu, Harro Seelaar, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13.1-13.2 in a Chinese kindredHongshan Zhao, Yong Tian, Guido Breedveld, et al.
Acta Neuropathologica Communications|April 16, 2016
C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriersPatrizia Rizzu, Cornelis Blauwendraat, Sasja Heetveld, et al.
Parkinsonism & Related Disorders|March 15, 2016
A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish familyHasmet A Hanagasi, Anamika Giri, Ece Kartal, et al.
Pageof 24

Showing results (71-80 of 240) with videos related to

Sort By:
Pageof 24
Annals of Neurology|December 24, 2005
Neonatal porencephaly and adult stroke related to mutations in collagen IV A1Marjo S van der Knaap, Leo M E Smit, Frederik Barkhof, et al.
Neuro-Degenerative Diseases|October 21, 2016
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal DementiaCarlo Wilke, Frank Gillardon, Christian Deuschle, et al.
Plos One|June 19, 2015
Evidence for Immune Response, Axonal Dysfunction and Reduced Endocytosis in the Substantia Nigra in Early Stage Parkinson's DiseaseAnke A Dijkstra, Angela Ingrassia, Renee X de Menezes, et al.
Acta Neuropathologica|May 7, 2023
Brain DNA methylomic analysis of frontotemporal lobar degeneration reveals OTUD4 in shared dysregulated signatures across pathological subtypesKatherine Fodder, Megha Murthy, Patrizia Rizzu, et al.
Plos One|September 27, 2014
Trehalose improves human fibroblast deficits in a new CHIP-mutation related ataxiaMaria Jose Casarejos, Juan Perucho, Jose Luis López-Sendón, et al.
European Journal of Human Genetics : EJHG|March 2, 2012
Dissecting the genetic make-up of North-East Sardinia using a large set of haploid and autosomal markersLuba M Pardo, Giovanna Piras, Rosanna Asproni, et al.
European Journal of Human Genetics : EJHG|January 18, 2007
Progranulin mutations in Dutch familial frontotemporal lobar degenerationIraad F Bronner, Patrizia Rizzu, Harro Seelaar, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
Postaxial polydactyly type A/B (PAP-A/B) is linked to chromosome 19p13.1-13.2 in a Chinese kindredHongshan Zhao, Yong Tian, Guido Breedveld, et al.
Acta Neuropathologica Communications|April 16, 2016
C9orf72 is differentially expressed in the central nervous system and myeloid cells and consistently reduced in C9orf72, MAPT and GRN mutation carriersPatrizia Rizzu, Cornelis Blauwendraat, Sasja Heetveld, et al.
Parkinsonism & Related Disorders|March 15, 2016
A novel homozygous DJ1 mutation causes parkinsonism and ALS in a Turkish familyHasmet A Hanagasi, Anamika Giri, Ece Kartal, et al.
Pageof 24