Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  42 results for ""MESH: Male""

Your Filters

Publication : brain
Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Academic Journal

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Subjects: Male; 0301 basic medicine; amyotrophic lateral sclerosis

  • Source: BrainDipòsit Digital de Documents de la UABUniversitat Autònoma de BarcelonaBRAINr-IIB SANT PAU. Repositorio

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

Subjects: Male; 0301 basic medicine; Malalties cerebrals

  • Source: BrainDipòsit Digital de la UBUniversidad de BarcelonaArticles publicats en revistes (Genètica, Microbiologia i Estadística)instname

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms

Subjects: Male; MESH: Epilepsy / genetics; TDP-43

  • Source: Brain, Vol. 143, No 1 (2020) pp. 303-319Brain, vol. 143, no. 1 (2020) p. 303-319Brain-A Journal

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis

Subjects: MESH: Signal Transduction; Male; 0301 basic medicine

  • Source: Brain 139(4), 1106-1122 (2016). doi:10.1093/brain/aww004Brain-A Journal of Neurology

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Early and protective microglial activation in Alzheimer’s disease: a prospective study using18F-DPA-714 PET imaging

Subjects: Male; 0301 basic medicine; Fluorine Radioisotopes

  • Source: Brain-A Journal of NeurologyBrain-A Journal of Neurology, Oxford University Press (OUP), 2016, 139 (Pt 4), pp.1252-64.

Record details

Read Online Read More Add to Saved list
×
Academic Journal

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

Subjects: Male; Ornithine; [SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases

  • Source: Brain 138(8), 2191-2205 (2015). doi:10.1093/brain/awv143Brain-A Journal of Neurology

Record details

Read Online Read More Add to Saved list
×
Academic Journal

TMEM240 mutations cause spinocerebellar ataxia 21 with mental retardation and severe cognitive impairment

Subjects: Male; MESH: Intellectual Disability / genetics; MESH: Introns

  • Source: Brain-A Journal of NeurologyBrain-A Journal of Neurology, Oxford University Press (OUP), 2014, 137 (10), pp.2657-2663.

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Abnormal recruitment of extracellular matrix proteins by excess Notch3ECD: a new pathomechanism in CADASIL

Subjects: MESH: Extracellular Matrix Proteins; Male; MESH: Protein Transport

  • Source: Brain-A Journal of NeurologyBrain-A Journal of Neurology, Oxford University Press (OUP), 2013, 136 (Pt 6), pp.1830-45.

Record details

Read Online Read More Add to Saved list
×
Academic Journal

Theory of mind impairments in patients with semantic dementia

Subjects: Male; cognitive/affective theory of mind; Theory of Mind

  • Source: Brain-A Journal of NeurologyBrain-A Journal of Neurology, Oxford University Press (OUP), 2012, 135 (Pt 1), pp.228-41.

Record details

Read Online Read More Add to Saved list
×
Academic Journal

A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C

Subjects: Adult; Male; Adolescent

  • Source: Brain-A Journal of NeurologyBrain-A Journal of Neurology, Oxford University Press (OUP), 2012, 135 (2), pp.483-492. ⟨10.1093/

Record details

Read Online Read More Add to Saved list
×
  • 1-10 of  42 results for ""MESH: Male""