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54. Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy

57. Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia

59. Charcot–Marie–tooth disease causing mutation (p.R158H) in pyruvate dehydrogenase kinase 3 (PDK3) affects synaptic transmission, ATP production and causes neurodegeneration in a CMTX6C. elegansmodel

62. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

63. Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders

64. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

65. Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy

66. FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis

67. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy

69. Replication of association between ELAVL4 and Parkinson disease: the GenePD study

71. Genetic analysis of GLT8D1 and ARPP21 in Australian familial and sporadic amyotrophic lateral sclerosis

73. Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia

74. Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

75. Sodium valproate increases activity of the sirtuin pathway resulting in beneficial effects for spinocerebellar ataxia-3 in vivo

78. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

79. Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease

81. Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4

82. A Simple Differentiation Protocol for Generation of Induced Pluripotent Stem Cell-Derived Basal Forebrain-Like Cholinergic Neurons for Alzheimer's Disease and Frontotemporal Dementia Disease Modeling

83. Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosis

84. Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome

85. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

88. DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

94. Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosis

100. Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics

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