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Neurogenetics

Showing results (81-90 of 1,080) with videos related to

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Neurogenetics|August 29, 2001
Hereditary neuralgic amyotrophyJ Meuleman, V Timmerman, C Van Broeckhoven, et al.
Neurogenetics|November 21, 2001
APOE and APOC1 genetic polymorphisms in age-associated memory impairmentD Bartrés-Faz, I C Clemente, C Junqué, et al.
Neurogenetics|December 17, 2002
De novo MECP2 mutation in a 46,XX male patient with Rett syndromeRobert Maiwald, Anselm Bönte, Helena Jung, et al.
Neurogenetics|December 4, 2016
Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutationsMichelangelo Cao, Marta Donà, Maria Lucia Valentino, et al.
Neurogenetics|November 29, 2016
A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesiaAna L Kolicheski, Gary S Johnson, Tendai Mhlanga-Mutangadura, et al.
Neurogenetics|February 26, 2014
Brain-derived neurotrophic factor: its impact upon neuroplasticity and neuroplasticity inducing transcranial brain stimulation protocolsL Chaieb, A Antal, G G Ambrus, et al.
Neurogenetics|March 25, 2014
Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissueMelanie Vanessa Heck, Mekhman Azizov, Tanja Stehning, et al.
Neurogenetics|January 27, 2017
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrumHuma Tariq, Sadaf Naz
Neurogenetics|March 22, 2019
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian familyEliana Marisa Ramos, Alessandro Roca, Noravit Chumchim, et al.
Neurogenetics|March 29, 2019
Rs10230207 genotype confers changes in HDAC9 and TWIST1, but not FERD3L in lymphoblasts from patients with intracranial aneurysmTheresa A Lansdell, Courtney Fisher, Kent Simmonds, et al.
Pageof 108

Showing results (81-90 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|August 29, 2001
Hereditary neuralgic amyotrophyJ Meuleman, V Timmerman, C Van Broeckhoven, et al.
Neurogenetics|November 21, 2001
APOE and APOC1 genetic polymorphisms in age-associated memory impairmentD Bartrés-Faz, I C Clemente, C Junqué, et al.
Neurogenetics|December 17, 2002
De novo MECP2 mutation in a 46,XX male patient with Rett syndromeRobert Maiwald, Anselm Bönte, Helena Jung, et al.
Neurogenetics|December 4, 2016
Erratum to: Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutationsMichelangelo Cao, Marta Donà, Maria Lucia Valentino, et al.
Neurogenetics|November 29, 2016
A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesiaAna L Kolicheski, Gary S Johnson, Tendai Mhlanga-Mutangadura, et al.
Neurogenetics|February 26, 2014
Brain-derived neurotrophic factor: its impact upon neuroplasticity and neuroplasticity inducing transcranial brain stimulation protocolsL Chaieb, A Antal, G G Ambrus, et al.
Neurogenetics|March 25, 2014
Dysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissueMelanie Vanessa Heck, Mekhman Azizov, Tanja Stehning, et al.
Neurogenetics|January 27, 2017
TFG associated hereditary spastic paraplegia: an addition to the phenotypic spectrumHuma Tariq, Sadaf Naz
Neurogenetics|March 22, 2019
Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian familyEliana Marisa Ramos, Alessandro Roca, Noravit Chumchim, et al.
Neurogenetics|March 29, 2019
Rs10230207 genotype confers changes in HDAC9 and TWIST1, but not FERD3L in lymphoblasts from patients with intracranial aneurysmTheresa A Lansdell, Courtney Fisher, Kent Simmonds, et al.
Pageof 108