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Serum neurofilament light in professional soccer players: goal on safety.
- Published in:
- Neurological Sciences, 2022, v. 43, n. 8, p. 5087, doi. 10.1007/s10072-022-06109-5
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- Article
Prevalence of frontotemporal lobar degeneration in an isolated population: the Vallecamonica study.
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- Neurological Sciences, 2012, v. 33, n. 4, p. 899, doi. 10.1007/s10072-011-0865-0
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- Article
Atypical presentation of a novel Presenilin 1 R377W mutation: sporadic, late-onset Alzheimer disease with epilepsy and frontotemporal atrophy.
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- Neurological Sciences, 2012, v. 33, n. 2, p. 375, doi. 10.1007/s10072-011-0714-1
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- Article
Seizures Can Precede Cognitive Symptoms in Late-Onset Alzheimer's Disease.
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- Journal of Alzheimer's Disease, 2011, v. 27, n. 4, p. 737, doi. 10.3233/JAD-2011-110896
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- Article
Cerebrospinal Fluid Tau in Frontotemporal Lobar Degeneration: Clinical, Neuroimaging, and Prognostic Correlates.
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- Journal of Alzheimer's Disease, 2011, v. 23, n. 3, p. 505, doi. 10.3233/JAD-2010-101407
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- Publication type:
- Article
The Speech and Language FOXP2 Gene Modulates the Phenotype of Frontotemporal Lobar Degeneration.
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- Journal of Alzheimer's Disease, 2010, v. 22, n. 3, p. 923, doi. 10.3233/JAD-2010-101206
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- Article
VEGF Haplotypes are Associated with Increased Risk to Progressive Supranuclear Palsy and Corticobasal Syndrome.
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- Journal of Alzheimer's Disease, 2010, v. 21, n. 1, p. 87, doi. 10.3233/JAD-2010-091615
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- Publication type:
- Article
Cognitive reserve and TMEM106B genotype modulate brain damage in presymptomatic frontotemporal dementia: a GENFI study.
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- 2017
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- Publication type:
- journal article
Analytical and clinical validation of a progranulin ELISA in the FTD disease spectrum.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.076093
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- Article
IC‐P‐040: FUNCTIONAL NETWORK CONNECTIVITY CHANGES IN EARLY AND LATE ONSET ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 14, p. P41, doi. 10.1016/j.jalz.2018.06.2104
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- Article
P1‐395: FUNCTIONAL NETWORK CONNECTIVITY CHANGES IN EARLY AND LATE ONSET ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P453, doi. 10.1016/j.jalz.2018.06.403
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- Publication type:
- Article
IC‐P‐040: FUNCTIONAL NETWORK CONNECTIVITY CHANGES IN EARLY AND LATE ONSET ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P41, doi. 10.1016/j.jalz.2018.06.2104
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- Publication type:
- Article
Frontotemporal dementia and language networks: cortical thickness reduction is driven by dyslexia susceptibility genes.
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- Scientific Reports, 2016, p. 30848, doi. 10.1038/srep30848
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- Article
Multimodal fMRI Resting-State Functional Connectivity in Granulin Mutations: The Case of Fronto-Parietal Dementia.
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- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106500
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- Article
Cognitive Reserve in <i>Granulin</i>-Related Frontotemporal Dementia: from Preclinical to Clinical Stages.
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- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0074762
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- Article
The role of clonal hematopoiesis as driver of therapy-related myeloid neoplasms after autologous stem cell transplantation.
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- Annals of Hematology, 2022, v. 101, n. 6, p. 1227, doi. 10.1007/s00277-022-04806-x
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- Article
Iron in Frontotemporal Lobar Degeneration: A New Subcortical Pathological Pathway?
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- Neurodegenerative Diseases, 2016, v. 16, n. 3/4, p. 172, doi. 10.1159/000440843
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- Publication type:
- Article
Cerebrospinal Fluid Tau Levels Predict Prognosis in Non-Inherited Frontotemporal Dementia.
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- Neurodegenerative Diseases, 2014, v. 13, n. 4, p. 224, doi. 10.1159/000353280
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- Article
Functional correlates of Apolipoprotein E genotype in Frontotemporal Lobar Degeneration.
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- BMC Neurology, 2006, v. 6, p. 31, doi. 10.1186/1471-2377-6-31
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- Article
Prognostic Relevance of NPM1 and FLT3 Mutations in Acute Myeloid Leukaemia, Longterm Follow-Up—A Single Center Experience.
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- Cancers, 2022, v. 14, n. 19, p. 4716, doi. 10.3390/cancers14194716
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- Article
Neuroanatomical Correlates of Transcranial Magnetic Stimulation in Presymptomatic <italic>Granulin</italic> Mutation Carriers.
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- Brain Topography, 2018, v. 31, n. 3, p. 488, doi. 10.1007/s10548-017-0612-9
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- Publication type:
- Article
Loss of function mutations in the progranulin gene are related to pro-inflammatory cytokine dysregulation in frontotemporal lobar degeneration patients.
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- 2011
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- Publication type:
- journal article
Effect of TMEM106B Polymorphism on Functional Network Connectivity in Asymptomatic GRN Mutation Carriers.
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- JAMA Neurology, 2014, v. 71, n. 2, p. 216, doi. 10.1001/jamaneurol.2013.4835
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- Article
Functional serotonin 5–HTTLPR polymorphism is a risk factor for migraine with aura.
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- Journal of Headache & Pain, 2005, v. 6, n. 4, p. 182, doi. 10.1007/s10194-005-0179-9
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- Publication type:
- Article
Increasing Brain Gamma Activity Improves Episodic Memory and Restores Cholinergic Dysfunction in Alzheimer's Disease.
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- Annals of Neurology, 2022, v. 92, n. 2, p. 322, doi. 10.1002/ana.26411
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- Publication type:
- Article
Impaired long-term potentiation-like cortical plasticity in presymptomatic genetic frontotemporal dementia.
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- 2016
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- Publication type:
- journal article
The Neuroimaging Signature of Frontotemporal Lobar Degeneration Associated with Granulin Mutations: An Effective Connectivity Study.
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- Journal of Nuclear Medicine, 2013, v. 54, n. 7, p. 1066, doi. 10.2967/jnumed.112.111773
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- Publication type:
- Article
Thalamic Infarcts in Young Adults: Relationship between Clinical-Topographic Features and Pathogenesis.
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- European Neurology, 2002, v. 47, n. 1, p. 30, doi. 10.1159/000047944
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- Publication type:
- Article
Postremission therapy with repeated courses of high‐dose cytarabine, idarubicin, and limited autologous stem cell support achieves a very good long‐term outcome in European leukemia net favorable and intermediate‐risk acute myeloid leukemia
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- Hematological Oncology, 2020, v. 38, n. 5, p. 754, doi. 10.1002/hon.2806
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- Article
Subcortical and Deep Cortical Atrophy in Frontotemporal Dementia due to Granulin Mutations.
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- Dementia & Geriatric Cognitive Disorders Extra, 2014, v. 4, n. 1, p. 95, doi. 10.1159/000355428
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- Article
Diagnostic accuracy of research criteria for prodromal frontotemporal dementia.
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- Alzheimer's Research & Therapy, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13195-024-01383-1
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- Article
A Pan- European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats.
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- Human Mutation, 2013, v. 34, n. 2, p. 363, doi. 10.1002/humu.22244
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- Article
A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease.
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- Human Molecular Genetics, 2006, v. 15, n. 16, p. 2446, doi. 10.1093/hmg/ddl167
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- Article
Serum total TDP-43 levels are decreased in frontotemporal dementia patients with C9orf72 repeat expansion or concomitant motoneuron disease phenotype.
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- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-01091-8
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- Publication type:
- Article
Classification accuracy of blood-based and neurophysiological markers in the differential diagnosis of Alzheimer's disease and frontotemporal lobar degeneration.
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- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-01094-5
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- Article
Antibodies Against Calcitonins as a Source of Analytical Errors.
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- Clinical Chemistry & Laboratory Medicine, 1991, v. 29, n. 10, p. 689
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- Article
Age at onset reveals different functional connectivity abnormalities in prodromal Alzheimer's disease.
- Published in:
- 2020
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- Publication type:
- journal article
Progranulin genetic variations in frontotemporal lobar degeneration: evidence for low mutation frequency in an Italian clinical series.
- Published in:
- Neurogenetics, 2008, v. 9, n. 3, p. 197, doi. 10.1007/s10048-008-0127-3
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- Article
Iron and Neurodegeneration: Is Ferritinophagy the Link?
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- Molecular Neurobiology, 2016, v. 53, n. 8, p. 5542, doi. 10.1007/s12035-015-9473-y
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- Article
Functional Connectivity Networks in Asymptomatic and Symptomatic DYT1 Carriers.
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- 2016
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- Publication type:
- journal article
Evidence of Major Genes Effects on Serum Homocysteine and Fibrinogen Levels, and Premature Ischemic Heart Disease in Italian Extended Families.
- Published in:
- Human Heredity, 2008, v. 66, n. 1, p. 50, doi. 10.1159/000114165
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- Article
Analytical and clinical validation of a blood progranulin ELISA in frontotemporal dementias.
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- Clinical Chemistry & Laboratory Medicine, 2023, v. 61, n. 12, p. 2195, doi. 10.1515/cclm-2023-0562
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- Publication type:
- Article
Endothelial Nitric Oxide Synthase (Glu298Asp) Polymorphism is an Independent Risk Factor for Migraine with Aura.
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- Headache: The Journal of Head & Face Pain, 2006, v. 46, n. 10, p. 1575, doi. 10.1111/j.1526-4610.2006.00614.x
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- Article
Investigating the Association Between Notch3 Polymorphism and Migraine.
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- Headache: The Journal of Head & Face Pain, 2006, v. 46, n. 2, p. 317, doi. 10.1111/j.1526-4610.2006.00344.x
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- Publication type:
- Article