- Home
- Publications
- Publication Search
- Publication Details
Title
Treatment implications of C9ORF72
Authors
Keywords
-
Journal
Alzheimers Research & Therapy
Volume 4, Issue 6, Pages 46
Publisher
Springer Nature
Online
2012-11-27
DOI
10.1186/alzrt149
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Pattern of ubiquilin pathology in ALS and FTLD indicates presence of C9ORF72 hexanucleotide expansion
- (2012) Johannes Brettschneider et al. ACTA NEUROPATHOLOGICA
- Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p
- (2012) Heather Stewart et al. ACTA NEUROPATHOLOGICA
- Methylthioninium chloride (methylene blue) induces autophagy and attenuates tauopathy in vitro and in vivo
- (2012) Erin E. Congdon et al. Autophagy
- Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p
- (2012) G.-Y. R. Hsiung et al. BRAIN
- Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations
- (2012) J. S. Snowden et al. BRAIN
- The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions
- (2012) Javier Simón-Sánchez et al. BRAIN
- Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
- (2012) Bradley F. Boeve et al. BRAIN
- Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features
- (2012) C. J. Mahoney et al. BRAIN
- Atypical, slowly progressive behavioural variant frontotemporal dementia associated withC9ORF72hexanucleotide expansion
- (2012) Baber K Khan et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Frontotemporal dementia due to C9ORF72 mutations: Clinical and imaging features
- (2012) S. J. Sha et al. NEUROLOGY
- Characterization of a Large Group of Individuals with Huntington Disease and Their Relatives Enrolled in the COHORT Study
- (2012) E. Ray Dorsey et al. PLoS One
- A Human Stem Cell Model of Early Alzheimer's Disease Pathology in Down Syndrome
- (2012) Y. Shi et al. Science Translational Medicine
- p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
- (2011) Safa Al-Sarraj et al. ACTA NEUROPATHOLOGICA
- Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
- (2011) Melissa E. Murray et al. ACTA NEUROPATHOLOGICA
- A harmonized classification system for FTLD-TDP pathology
- (2011) Ian R. A. Mackenzie et al. ACTA NEUROPATHOLOGICA
- Potential Mechanisms of Progranulin-deficient FTLD
- (2011) Michael Emmerson Ward et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Amyotrophic lateral sclerosis
- (2011) Matthew C Kiernan et al. LANCET
- Emerging targets and treatments in amyotrophic lateral sclerosis
- (2011) Lorne Zinman et al. LANCET NEUROLOGY
- Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia
- (2011) Han-Xiang Deng et al. NATURE
- An algorithm for genetic testing of frontotemporal lobar degeneration
- (2011) J. S. Goldman et al. NEUROLOGY
- Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
- (2011) Mariely DeJesus-Hernandez et al. NEURON
- A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
- (2011) Alan E. Renton et al. NEURON
- Triplet repeat RNA structure and its role as pathogenic agent and therapeutic target
- (2011) W. J. Krzyzosiak et al. NUCLEIC ACIDS RESEARCH
- Identification of 2 Loci at Chromosomes 9 and 14 in a Multiplex Family With Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis
- (2010) Ilse Gijselinck et al. ARCHIVES OF NEUROLOGY
- Primary Central Nervous System Lymphoma
- (2010) Elizabeth R. Gerstner et al. ARCHIVES OF NEUROLOGY
- Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p
- (2010) Justin P. Pearson et al. JOURNAL OF NEUROLOGY
- Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
- (2010) A. L. Boxer et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Safety and efficacy of lithium in combination with riluzole for treatment of amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial
- (2010) Swati P Aggarwal et al. LANCET NEUROLOGY
- TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
- (2010) N. Finch et al. NEUROLOGY
- Methylene blue and dimebon inhibit aggregation of TDP-43 in cellular models
- (2009) Makiko Yamashita et al. FEBS LETTERS
- Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
- (2009) I. Le Ber et al. NEUROLOGY
- Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy
- (2009) S. A. M. Mulders et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Reversal of RNA Dominance by Displacement of Protein Sequestered on Triplet Repeat RNA
- (2009) T. M. Wheeler et al. SCIENCE
- Pedigree with frontotemporal lobar degeneration – motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
- (2008) Agnes A Luty et al. BMC Neurology
- Myotonic dystrophy: Therapeutic strategies for the future
- (2008) Thurman M. Wheeler Neurotherapeutics
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now