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Stroke
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March 1, 2008
Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32
Ynte M Ruigrok, Cisca Wijmenga, Gabriel J E Rinkel, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
October 12, 2022
Tackling Neuroinflammation After Traumatic Brain Injury: Complement Inhibition as a Therapy for Secondary Injury
Inge A M van Erp, Iliana Michailidou, Thomas A van Essen, et al.
Genomics
|
July 3, 2003
Transcriptional profile of the human peripheral nervous system by serial analysis of gene expression
Rosalein R de Jonge, Jeroen P Vreijling, Asker Meintjes, et al.
Experimental Gerontology
|
March 28, 2006
The unfolded protein response affects neuronal cell cycle protein expression: implications for Alzheimer's disease pathogenesis
Jeroen J M Hoozemans, Jens Stieler, Elise S van Haastert, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
April 27, 2010
Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states
Mirjam A G Sprangers, Meike Bartels, Ruut Veenhoven, et al.
Acta Neuropathologica
|
November 20, 2013
Plasminogen activator inhibitor-1 influences cerebrovascular complications and death in pneumococcal meningitis
Matthijs C Brouwer, Joost C M Meijers, Frank Baas, et al.
Stem Cell Research
|
June 3, 2020
Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2
Marga J Bouma, Valeria Orlova, Francijna E van den Hil, et al.
JIMD Reports
|
September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?
Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.
The Journal of Pediatrics
|
November 1, 2002
Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts
Fredoen Valianpour, Ronald J A Wanders, Henk Overmars, et al.
Journal of Neuropathology and Experimental Neurology
|
April 14, 2011
Myelin and axon pathology in a long-term study of PMP22-overexpressing mice
Camiel Verhamme, Rosalind H M King, Anneloor L M A ten Asbroek, et al.
Page
of 24
Search research articles
Search
Showing results (91-100 of 231) with videos related to
Sort By:
Page
of 24
Stroke
|
March 1, 2008
Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32
Ynte M Ruigrok, Cisca Wijmenga, Gabriel J E Rinkel, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
October 12, 2022
Tackling Neuroinflammation After Traumatic Brain Injury: Complement Inhibition as a Therapy for Secondary Injury
Inge A M van Erp, Iliana Michailidou, Thomas A van Essen, et al.
Genomics
|
July 3, 2003
Transcriptional profile of the human peripheral nervous system by serial analysis of gene expression
Rosalein R de Jonge, Jeroen P Vreijling, Asker Meintjes, et al.
Experimental Gerontology
|
March 28, 2006
The unfolded protein response affects neuronal cell cycle protein expression: implications for Alzheimer's disease pathogenesis
Jeroen J M Hoozemans, Jens Stieler, Elise S van Haastert, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation
|
April 27, 2010
Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional states
Mirjam A G Sprangers, Meike Bartels, Ruut Veenhoven, et al.
Acta Neuropathologica
|
November 20, 2013
Plasminogen activator inhibitor-1 influences cerebrovascular complications and death in pneumococcal meningitis
Matthijs C Brouwer, Joost C M Meijers, Frank Baas, et al.
Stem Cell Research
|
June 3, 2020
Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2
Marga J Bouma, Valeria Orlova, Francijna E van den Hil, et al.
JIMD Reports
|
September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?
Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.
The Journal of Pediatrics
|
November 1, 2002
Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblasts
Fredoen Valianpour, Ronald J A Wanders, Henk Overmars, et al.
Journal of Neuropathology and Experimental Neurology
|
April 14, 2011
Myelin and axon pathology in a long-term study of PMP22-overexpressing mice
Camiel Verhamme, Rosalind H M King, Anneloor L M A ten Asbroek, et al.
Page
of 24