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Screening for Anti-HMGCR Antibodies in a Large Single Myositis Center Reveals Infrequent Exposure to Statins and Diversiform Presentation of the Disease.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.866701
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- Publication type:
- Article
Variability in Skeletal Muscle Protein Synthesis Rates in Critically Ill Patients.
- Published in:
- Nutrients, 2022, v. 14, n. 18, p. N.PAG, doi. 10.3390/nu14183733
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- Publication type:
- Article
Marked heterogeneity of human skeletal muscle lipolysis at rest.
- Published in:
- 2002
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- Publication type:
- journal article
<sup>3</sup>H-Deprenyl and <sup>3</sup>H-PIB autoradiography show different laminar distributions of astroglia and fibrillar β-amyloid in Alzheimer brain.
- Published in:
- Journal of Neuroinflammation, 2013, v. 10, n. 1, p. 1, doi. 10.1186/1742-2094-10-90
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- Publication type:
- Article
³H-deprenyl and ³H-PIB autoradiography show different laminar distributions of astroglia and fibrillar β-amyloid in Alzheimer brain.
- Published in:
- 2013
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- Publication type:
- journal article
Fatal deterioration of neurological disease after orthotopic liver transplantation for valproic acid-induced liver damage.
- Published in:
- Pediatric Transplantation, 2000, v. 4, n. 3, p. 211, doi. 10.1034/j.1399-3046.2000.00115.x
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- Publication type:
- Article
Targeted delivery of nerve growth factor to the cholinergic basal forebrain of Alzheimer's disease patients: application of a second-generation encapsulated cell biodelivery device.
- Published in:
- Alzheimer's Research & Therapy, 2016, v. 8, p. 1, doi. 10.1186/s13195-016-0195-9
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- Publication type:
- Article
Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 11, p. 1260, doi. 10.1038/ejhg.2013.37
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- Publication type:
- Article
Neuropathological characterization of two siblings carrying the MAPT S305S mutation demonstrates features resembling argyrophilic grain disease.
- Published in:
- 2014
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- Publication type:
- Letter
Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence?
- Published in:
- Acta Neuropathologica, 2005, v. 110, n. 3, p. 315, doi. 10.1007/s00401-005-1047-z
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- Publication type:
- Article
Visualization of regional tau deposits using <sup>3</sup>H-THK5117 in Alzheimer brain tissue.
- Published in:
- Acta Neuropathologica Communications, 2015, v. 3, n. 1, p. 1, doi. 10.1186/s40478-015-0220-4
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- Publication type:
- Article
Single‐cell profiling of muscle‐infiltrating T cells in idiopathic inflammatory myopathies.
- Published in:
- EMBO Molecular Medicine, 2023, v. 15, n. 10, p. 1, doi. 10.15252/emmm.202217240
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- Publication type:
- Article
Mutations in the mitochondrial tRNA<sup>Ser(AGY)</sup> gene are associated with deafness, retinal degeneration, myopathy and epilepsy.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 8, p. 897, doi. 10.1038/ejhg.2012.44
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- Publication type:
- Article
Mutations in the mitochondrial tRNA<sup>Ser(AGY)</sup> gene are associated with deafness, retinal degeneration, myopathy and epilepsy.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 8, p. 910, doi. 10.1038/ejhg.2012.123
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- Publication type:
- Article
The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of Aβ in different brain regions.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1202, doi. 10.1038/ejhg.2010.107
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- Publication type:
- Article
Sensory Ataxic Neuropathy in Golden Retriever Dogs Is Caused by a Deletion in the Mitochondrial tRNA<sup>Tyr</sup>Gene.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 5, p. 1, doi. 10.1371/journal.pgen.1000499
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- Publication type:
- Article
Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 2, p. 118, doi. 10.1111/cge.13543
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- Publication type:
- Article
P4‐599: ANTE‐MORTEM BINDING OF <sup>18</sup>F‐THK5317 PET IN A CASE OF FTLD AND POST‐MORTEM COMPARISON OF TAU BINDING USING <sup>3</sup>H‐THK5117 AND <sup>3</sup>H‐MK6240.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1554, doi. 10.1016/j.jalz.2019.08.147
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- Publication type:
- Article
Amyloid tracers binding sites in autosomal dominant and sporadic Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, n. 4, p. 419, doi. 10.1016/j.jalz.2016.08.006
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- Publication type:
- Article
IN VITRO CHARACTERIZATION OF FIBRILLAR AMYLOID, TAU DEPOSITION, AND ACTIVATED ASTROCYTES IN ARCTIC AD BRAIN IN COMPARISON WITH SPORADIC AD BRAIN USING 3H-PIB, 3H-THK5117 AND 3H-DEPRENYL.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P124, doi. 10.1016/j.jalz.2016.06.201
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- Publication type:
- Article
IN VITRO CHARACTERIZATION OF FIBRILLAR AMYLOID, TAU DEPOSITION, AND ACTIVATED ASTROCYTES IN ARCTIC ALZHEIMER'S DISEASE BRAIN IN COMPARISON WITH SPORADIC ALZHEIMER'S DISEASE BRAIN USING 3H-PIB, 3H-THK5117 AND 3H-DEPRENYL.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P442, doi. 10.1016/j.jalz.2016.06.853
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- Publication type:
- Article
Characterization of regional binding of clinical amyloid tracers in autosomal dominant and sporadic Alzheimer’s disease brains and their interactions with resveratrol.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P878, doi. 10.1016/j.jalz.2015.08.083
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- Publication type:
- Article
Resolution of inflammation is altered in Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 1, p. 40, doi. 10.1016/j.jalz.2013.12.024
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- Publication type:
- Article
Characterization of thk5117 binding in ad brain tissue: implication for development of pet tau imaging.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P155, doi. 10.1016/j.jalz.2014.04.125
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- Publication type:
- Article
Laminar distributions of fibrillar β-amyloid and activated astrocytes in Alzheimer's disease autopsy brain: A quantitative autoradiography study
- Published in:
- 2011
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- Publication type:
- Abstract
Progranulin mutation causes frontotemporal dementia in the Swedish Karolinska family
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2008, v. 4, n. 6, p. 414, doi. 10.1016/j.jalz.2008.09.001
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- Publication type:
- Article
Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs.
- Published in:
- Journal of Internal Medicine, 2024, v. 296, n. 3, p. 234, doi. 10.1111/joim.13815
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- Publication type:
- Article
TBK1 haploinsufficiency results in changes in the K63-ubiquitination profiles in brain and fibroblasts from affected and presymptomatic mutation carriers.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 6, p. 3037, doi. 10.1007/s00415-021-10887-x
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- Publication type:
- Article
Case report: Intraneural perineurioma of the sciatic nerve in an adolescent - strategies for revealing the diagnosis.
- Published in:
- Clinical Case Reports, 2016, v. 4, n. 8, p. 777, doi. 10.1002/ccr3.630
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- Publication type:
- Article
Neurogenic vs. Myogenic Origin of Acquired Muscle Paralysis in Intensive Care Unit (ICU) Patients: Evaluation of Different Diagnostic Methods.
- Published in:
- Diagnostics (2075-4418), 2020, v. 10, n. 11, p. 966, doi. 10.3390/diagnostics10110966
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- Publication type:
- Article
CYTOFLUOROMETRIC QUANTIFICATION OF SOMATOPETAL AXONAL TRANSPORT: EFFECTS OF A CONDITIONING LESION AND 2,5-HEXANEDIONE.
- Published in:
- Neuropathology & Applied Neurobiology, 1986, v. 12, n. 4, p. 379, doi. 10.1111/j.1365-2990.1986.tb00149.x
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- Publication type:
- Article
Antibody reactivities to skeletal muscle proteins in a patient with λ light chain secreting multiple myeloma, generalised amyloidosis and rhabdomyolysis.
- Published in:
- European Journal of Haematology, 2001, v. 67, n. 3, p. 189, doi. 10.1034/j.1600-0609.2001.5790499.x
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- Publication type:
- Article
Cortical laminar tau deposits and activated astrocytes in Alzheimer's disease visualised by <sup>3</sup>H-THK5117 and <sup>3</sup>H-deprenyl autoradiography.
- Published in:
- Scientific Reports, 2017, p. 45496, doi. 10.1038/srep45496
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- Publication type:
- Article
Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies.
- Published in:
- 2015
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- Publication type:
- journal article
Effects on muscle tissue remodeling and lipid metabolism in muscle tissue from adult patients with polymyositis or dermatomyositis treated with immunosuppressive agents.
- Published in:
- Arthritis Research & Therapy, 2016, v. 18, p. 1, doi. 10.1186/s13075-016-1033-y
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- Publication type:
- Article
Neuropathologic Assessment of Dementia Markers in Identical and Fraternal Twins.
- Published in:
- Brain Pathology, 2014, v. 24, n. 4, p. 317, doi. 10.1111/bpa.12127
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- Publication type:
- Article
Multitracer study with positron emission tomography in Creutzfeldt-Jakob disease.
- Published in:
- European Journal of Nuclear Medicine & Molecular Imaging, 2003, v. 30, n. 1, p. 85, doi. 10.1007/s00259-002-1008-x
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- Publication type:
- Article
Multitracer study with positron emission tomography in Creutzfeldt-Jakob disease.
- Published in:
- European Journal of Nuclear Medicine & Molecular Imaging, 2003, v. 30, n. 1, p. 187, doi. 10.1007/s00259-002-1071-3
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- Publication type:
- Article
Reduced C-afferent fibre density affects perceived pleasantness and empathy for touch.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 4, p. 1116, doi. 10.1093/brain/awr011
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- Publication type:
- Article
Positron emission tomography imaging and clinical progression in relation to molecular pathology in the first Pittsburgh Compound B positron emission tomography patient with Alzheimer's disease.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Positron emission tomography imaging and clinical progression in relation to molecular pathology in the first Pittsburgh Compound B positron emission tomography patient with Alzheimer’s disease.
- Published in:
- Brain: A Journal of Neurology, 2011, v. 134, n. 1, p. 301, doi. 10.1093/brain/awq349
- By:
- Publication type:
- Article
[<sup>11</sup>C]PBB3 binding in Aβ(–) or Aβ(+) corticobasal syndrome.
- Published in:
- Synapse, 2023, v. 77, n. 4, p. 1, doi. 10.1002/syn.22269
- By:
- Publication type:
- Article
A Novel Duplication in ATXN2 as Modifier for Spinocerebellar Ataxia 3 (SCA3) and C9ORF72‐ALS.
- Published in:
- Movement Disorders, 2021, v. 36, n. 2, p. 508, doi. 10.1002/mds.28334
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- Publication type:
- Article
Amyloid in a multiple sclerosis lesion is clearly of Aλ type.
- Published in:
- Acta Neuropathologica, 2000, v. 100, n. 6, p. 709
- By:
- Publication type:
- Article
PARKIN is not required to sustain OXPHOS function in adult mammalian tissues.
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00707-0
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- Publication type:
- Article
Pathological Study of a FMR1 Premutation Carrier With Progressive Supranuclear Palsy.
- Published in:
- Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00317
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- Publication type:
- Article
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 11, p. 1919, doi. 10.1093/hmg/ddz032
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- Publication type:
- Article
A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gamma.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 13, p. 2515, doi. 10.1093/hmg/ddx146
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- Publication type:
- Article
Bedside diagnosis of rippling muscle disease in CAV3 p.A46T mutation carriers.
- Published in:
- Muscle & Nerve, 2010, v. 41, n. 6, p. 751, doi. 10.1002/mus.21589
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- Publication type:
- Article