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27 subtopics

 

  • Alexander Disease
  • Amyloid Neuropathies, Familial
  • Bulbo-Spinal Atrophy, X-Linked
  • Canavan Disease
  • Cockayne Syndrome
  • Dystonia Musculorum Deformans
  • Gerstmann-Straussler-Scheinker Disease
  • Pantothenate Kinase-Associated Neurodegeneration
  • Hepatolenticular Degeneration
  • Hereditary Central Nervous System Demyelinating Diseases
  • Hereditary Motor and Sensory Neuropathies
  • Hereditary Sensory and Autonomic Neuropathies
  • Huntington Disease
  • Lafora Disease
  • Lesch-Nyhan Syndrome
  • Menkes Kinky Hair Syndrome
  • Myotonia Congenita
  • Myotonic Dystrophy
  • Neurofibromatoses
  • Neuronal Ceroid-Lipofuscinoses
  • Optic Atrophies, Hereditary
  • Rett Syndrome
  • Spinal Muscular Atrophies of Childhood
  • Spinocerebellar Degenerations
  • Tourette Syndrome
  • Tuberous Sclerosis
  • Unverricht-Lundborg Syndrome

Heredodegenerative Disorders, Nervous SystemFollow by RSS 

You've reached a pubget topic page. Below are the latest papers on this topic, with subtopics on the left.

keywords > Nervous System Diseases > Neurodegenerative Diseases > Heredodegenerative Disorders, Nervous System

Latest papers

Aceruloplasminemia: a novel mutation in a family with marked phenotypic variability.

Dysfunctional astrocytes as key players in the pathogenesis of central nervous system disorders.

Genetic impairment of autophagy intensifies expanded polyglutamine toxicity in Caenorhabditis elegans.

Gene-targeted therapies for the central nervous system.

Relapsing encephalopathy in a patient with alpha-methylacyl-CoA racemase deficiency.

Hereditary neuropathy with liability to pressure palsies: description of seven patients without known family history.

Thrombin-induced oxidative stress contributes to the death of hippocampal neurons: role of neuronal NADPH oxidase.

A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes.

Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations.

Differential effects of melatonin on hippocampal neurodegeneration in different aged accelerated senescence prone mouse-8.

Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases.

Lysine 63-linked ubiquitination promotes the formation and autophagic clearance of protein inclusions associated with neurodegenerative diseases.

Depletion of mitochondrial DNA in leukocytes of patients with poly-Q diseases.

Cloning of the neurodegeneration gene drop-dead and characterization of additional phenotypes of its mutation.

Differential production of superoxide by neuronal mitochondria.

[Torrent of madmen: the language of degeneration in Portuguese psychiatry at the close of the 19th century].

CAG repeat disorder models and human neuropathology: similarities and differences.

Treatment of fragile X-associated tremor ataxia syndrome (FXTAS) and related neurological problems.

MRI and SPECT of midbrain and striatal degeneration in fragile X-associated tremor/ataxia syndrome.

Cognitive and behavioral assessment in the early stages of neurodegenerative extrapyramidal syndromes

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