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No "Technical Knockout": Giap's Artillery at Dien Bien Phu.
- Published in:
- Journal of Military History, 2014, v. 78, n. 4, p. 1349
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- Publication type:
- Article
Learning to Forget: U.S. Army Counterinsurgency Doctrine and Practice from Vietnam to Iraq.
- Published in:
- 2014
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- Publication type:
- Book Review
Goodnight Saigon: American Provincial Advisors' Final Impressions of the Vietnam War.
- Published in:
- Journal of Military History, 2014, v. 78, n. 1, p. 233
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- Publication type:
- Article
The Red Queen's Race: Operation Washington Green and Pacification in Binh Dinh Province, 1969-70.
- Published in:
- Journal of Military History, 2009, v. 73, n. 4, p. 1195, doi. 10.1353/jmh.0.0411
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- Publication type:
- Article
Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin.
- Published in:
- Annals of Neurology, 1995, v. 38, n. 3, p. 367, doi. 10.1002/ana.410380305
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- Publication type:
- Article
Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
- Published in:
- Annals of Neurology, 1992, v. 32, n. 3, p. 404, doi. 10.1002/ana.410320318
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- Publication type:
- Article
Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita.
- Published in:
- Annals of Neurology, 1992, v. 31, n. 3, p. 337, doi. 10.1002/ana.410310318
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- Publication type:
- Article
DNA length polymorphism 5′ to the myelin basic protein gene is associated with multiple sclerosis.
- Published in:
- Annals of Neurology, 1990, v. 27, n. 3, p. 291, doi. 10.1002/ana.410270311
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- Publication type:
- Article
Clinical and neuropathological features of ALS/FTD with TIA1 mutations.
- Published in:
- Acta Neuropathologica Communications, 2017, v. 5, p. 1, doi. 10.1186/s40478-017-0493-x
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- Publication type:
- Article
Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72-associated amyotrophic lateral sclerosis.
- Published in:
- 2017
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- Publication type:
- journal article
Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease.
- Published in:
- Acta Neuropathologica, 2017, v. 134, n. 5, p. 715, doi. 10.1007/s00401-017-1760-4
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- Publication type:
- Article
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bank.
- Published in:
- Acta Neuropathologica, 2015, v. 130, n. 6, p. 877, doi. 10.1007/s00401-015-1502-4
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- Publication type:
- Article
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration.
- Published in:
- 2015
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- Publication type:
- Report
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease.
- Published in:
- Acta Neuropathologica, 2015, v. 130, n. 1, p. 77, doi. 10.1007/s00401-015-1436-x
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- Publication type:
- Article
Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress.
- Published in:
- Acta Neuropathologica, 2014, v. 128, n. 4, p. 505, doi. 10.1007/s00401-014-1336-5
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- Publication type:
- Article
Antisense transcripts of the expanded <i>C9ORF72</i> hexanucleotide repeat form nuclear RNA foci and undergo repeat-associated non-ATG translation in c9FTD/ALS.
- Published in:
- Acta Neuropathologica, 2013, v. 126, n. 6, p. 829, doi. 10.1007/s00401-013-1192-8
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- Publication type:
- Article
Reduced <i>C9orf72</i> gene expression in c9FTD/ALS is caused by histone trimethylation, an epigenetic event detectable in blood.
- Published in:
- Acta Neuropathologica, 2013, v. 126, n. 6, p. 895, doi. 10.1007/s00401-013-1199-1
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- Publication type:
- Article
Tau pathology in frontotemporal lobar degeneration with C9ORF72 hexanucleotide repeat expansion.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 2, p. 289, doi. 10.1007/s00401-012-1048-7
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- Publication type:
- Article
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72.
- Published in:
- Acta Neuropathologica, 2011, v. 122, n. 6, p. 673, doi. 10.1007/s00401-011-0907-y
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- Publication type:
- Article
Nonpharmacologic Management Strategies in ALS #300.
- Published in:
- Journal of Palliative Medicine, 2016, v. 19, n. 3, p. 333, doi. 10.1089/jpm.2015.0361
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- Publication type:
- Article
Old age amyotrophic lateral sclerosis and limbic TDP‐43 pathology.
- Published in:
- Brain Pathology, 2022, v. 32, n. 6, p. 1, doi. 10.1111/bpa.13100
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- Publication type:
- Article
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.
- Published in:
- Nature, 2013, v. 495, n. 7442, p. 467, doi. 10.1038/nature11922
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- Publication type:
- Article
Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 17, p. 3421, doi. 10.1093/hmg/ddx233
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- Publication type:
- Article
Amyotrophic lateral sclerosis-specific quality of life-short form (ALSSQOL-SF): A brief, reliable, and valid version of the ALSSQOL-R.
- Published in:
- 2018
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- Publication type:
- journal article
ALS biomarkers for therapy development: State of the field and future directions.
- Published in:
- 2016
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- Publication type:
- journal article
Wild-Type Human TDP-43 Expression Causes TDP-43 Phosphorylation, Mitochondrial Aggregation, Motor Deficits, and Early Mortality in Transgenic Mice.
- Published in:
- Journal of Neuroscience, 2010, v. 30, n. 32, p. 10851, doi. 10.1523/JNEUROSCI.1630-10.2010
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- Publication type:
- Article
TDP-43 PATHOLOGY DISRUPTS NUCLEAR PORE COMPLEXES AND NUCLEOCYTOPLASMIC TRANSPORT IN ALS/FTD.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P602, doi. 10.1016/j.jalz.2017.07.247
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- Publication type:
- Article
Characterization of frontotemporal dementia +/- amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
- Published in:
- 2012
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- Publication type:
- Abstract
Wild-type human TDP-43 induces mitochondrial abnormalities and axonal degeneration in transgenic mice
- Published in:
- 2010
- By:
- Publication type:
- Abstract
Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72.
- Published in:
- Brain: A Journal of Neurology, 2012, v. 135, n. 3, p. 765, doi. 10.1093/brain/aws004
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- Publication type:
- Article
De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis.
- Published in:
- Human Mutation, 2010, v. 31, n. 5, p. E1377, doi. 10.1002/humu.21241
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- Publication type:
- Article
Nine Days in May: The Battles of the 4th Infantry Division on the Cambodian Border, 1967.
- Published in:
- 2018
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- Publication type:
- Book Review
Howard Jones. My Lai: Vietnam, 1968, and the Descent into Darkness.
- Published in:
- 2018
- By:
- Publication type:
- Book Review
Immunoreactivity of the phosphorylated axonal neurofilament H subunit (pNF-H) in blood of ALS model rodents and ALS patients: evaluation of blood pNF-H as a potential ALS biomarker.
- Published in:
- Journal of Neurochemistry, 2009, v. 111, n. 5, p. 1182, doi. 10.1111/j.1471-4159.2009.06386.x
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- Publication type:
- Article