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Shamiram Melhem

Showing results (1-10 of 18) with videos related to

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Neurobiology of Aging|February 25, 2019
Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutationsTsz Hang Wong, Harro Seelaar, Shamiram Melhem, et al.
Brain : a Journal of Neurology|March 6, 2026
Transcriptomic signature of frontotemporal lobar degeneration with TDP-43 type C pathologyAna Rajicic, Merel O Mol, Shamiram Melhem, et al.
Acta Neuropathologica Communications|March 15, 2019
HR23B pathology preferentially co-localizes with p62, pTDP-43 and poly-GA in C9ORF72-linked frontotemporal dementia and amyotrophic lateral sclerosisFrederike W Riemslagh, Hannes Lans, Harro Seelaar, et al.
Nature Communications|March 24, 2023
FTD-tau S320F mutation stabilizes local structure and allosterically promotes amyloid motif-dependent aggregationDailu Chen, Sofia Bali, Ruhar Singh, et al.
Glia|December 20, 2024
WDR49-Positive Astrocytes Mark Severity of Neurodegeneration in Frontotemporal Lobar Degeneration and Alzheimer's DiseaseAna Rajicic, Lucia A A Giannini, Emma Gerrits, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counselingTitis Widowati, Shamiram Melhem, Suryono Y Patria, et al.
Parkinsonism & Related Disorders|June 1, 2019
LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the NetherlandsLeonie J M Vergouw, Annemieke Ruitenberg, Tsz Hang Wong, et al.
Brain Pathology (Zurich, Switzerland)|September 1, 2020
Unfolded protein response activation in C9orf72 frontotemporal dementia is associated with dipeptide pathology and granulovacuolar degeneration in granule cellsPriya Gami-Patel, Irene van Dijken, Lieke H Meeter, et al.
Neurology. Genetics|April 28, 2020
Clinical and pathologic phenotype of a large family with heterozygous <i>STUB1</i> mutationMerel O Mol, Jeroen G J van Rooij, Esther Brusse, et al.
Brain Pathology (Zurich, Switzerland)|March 28, 2023
Cortical iron accumulation in MAPT- and C9orf 72-associated frontotemporal lobar degenerationLucia A A Giannini, Marjolein Bulk, Boyd Kenkhuis, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Neurobiology of Aging|February 25, 2019
Genetic screening in early-onset Alzheimer's disease identified three novel presenilin mutationsTsz Hang Wong, Harro Seelaar, Shamiram Melhem, et al.
Brain : a Journal of Neurology|March 6, 2026
Transcriptomic signature of frontotemporal lobar degeneration with TDP-43 type C pathologyAna Rajicic, Merel O Mol, Shamiram Melhem, et al.
Acta Neuropathologica Communications|March 15, 2019
HR23B pathology preferentially co-localizes with p62, pTDP-43 and poly-GA in C9ORF72-linked frontotemporal dementia and amyotrophic lateral sclerosisFrederike W Riemslagh, Hannes Lans, Harro Seelaar, et al.
Nature Communications|March 24, 2023
FTD-tau S320F mutation stabilizes local structure and allosterically promotes amyloid motif-dependent aggregationDailu Chen, Sofia Bali, Ruhar Singh, et al.
Glia|December 20, 2024
WDR49-Positive Astrocytes Mark Severity of Neurodegeneration in Frontotemporal Lobar Degeneration and Alzheimer's DiseaseAna Rajicic, Lucia A A Giannini, Emma Gerrits, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counselingTitis Widowati, Shamiram Melhem, Suryono Y Patria, et al.
Parkinsonism & Related Disorders|June 1, 2019
LRP10 variants in Parkinson's disease and dementia with Lewy bodies in the South-West of the NetherlandsLeonie J M Vergouw, Annemieke Ruitenberg, Tsz Hang Wong, et al.
Brain Pathology (Zurich, Switzerland)|September 1, 2020
Unfolded protein response activation in C9orf72 frontotemporal dementia is associated with dipeptide pathology and granulovacuolar degeneration in granule cellsPriya Gami-Patel, Irene van Dijken, Lieke H Meeter, et al.
Neurology. Genetics|April 28, 2020
Clinical and pathologic phenotype of a large family with heterozygous <i>STUB1</i> mutationMerel O Mol, Jeroen G J van Rooij, Esther Brusse, et al.
Brain Pathology (Zurich, Switzerland)|March 28, 2023
Cortical iron accumulation in MAPT- and C9orf 72-associated frontotemporal lobar degenerationLucia A A Giannini, Marjolein Bulk, Boyd Kenkhuis, et al.
Pageof 2