Frontotemporal lobar degeneration: current knowledge and future challenges. - Wikidata - awgldk - TriplyDB

Frontotemporal lobar degeneration: current knowledge and future challenges.

Frontotemporal lobar degeneration: current knowledge and future challenges.

http://www.wikidata.org/entity/Q38005348

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Mechanisms of granulin deficiency: lessons from cellular and animal models Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype When a Little Knowledge Can Be Dangerous: False-Positive Diagnosis of Behavioral Variant Frontotemporal Dementia among Community Clinicians.The role of the innate immune system in Alzheimer's disease and frontotemporal lobar degeneration: an eye on microglia.The behavioral variant of frontotemporal dementia: linking neuropathology to social cognition.Genetics of Frontotemporal Lobar Degeneration: From the Bench to the Clinic.What we know about TMEM106B in neurodegeneration.Stability of Progranulin Under Pre-Analytical Conditions in Serum and Cerebrospinal Fluid.Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes.Emotional empathy in amyotrophic lateral sclerosis: a behavioural and voxel-based morphometry study.

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P2860

Frontotemporal lobar degeneration: current knowledge and future challenges.

http://www.wikidata.org/entity/Q38005348

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Frontotemporal lobar degeneration: current knowledge and future challenges.

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Frontotemporal lobar degeneration: current knowledge and future challenges.

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Frontotemporal lobar degeneration: current knowledge and future challenges.

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Journal of Neurology

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Frontotemporal lobar degeneration: current knowledge and future challenges

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Chiara Cerami

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ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

UBAP1 is a component of an endosome-specific ESCRT-I complex that is essential for MVB sorting

Classification of primary progressive aphasia and its variants

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

A harmonized classification system for FTLD-TDP pathology

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Cognition and anatomy in three variants of primary progressive aphasia

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s00415-012-6507-5

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2278-2286

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10.1007/S00415-012-6507-5

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11

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Daniela Galimberti

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2012-04-25T00:00:00Z

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224835851

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1048918702

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