| Nome |
# |
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Two families with novel missense mutations in COL4A1: When diagnosis can be missed., file e27ce427-8f63-2581-e053-d805fe0acbaa
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332
|
|
Chronic Helicobacter pylori infection and migraine: a case-control study., file e27ce426-b121-2581-e053-d805fe0acbaa
|
326
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A review of the recent advances in neuroimaging of frontotemporal lobar degeneration, file e27ce42a-c470-2581-e053-d805fe0acbaa
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312
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|
Cognitive and neurophysiological effects of non-invasive brain stimulation in stroke patients after motor rehabilitation, file e27ce42a-c473-2581-e053-d805fe0acbaa
|
247
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Association between Major Mood Disorders and the hypocretin receptor 1 gene, file e27ce42a-44e8-2581-e053-d805fe0acbaa
|
230
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Response to combined radiotherapy and chemotherapy of a leptomeningeal spread from choroid plexus carcinoma: case report., file e27ce427-0c47-2581-e053-d805fe0acbaa
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216
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A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia, file e27ce428-4e5c-2581-e053-d805fe0acbaa
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214
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Novel mutation of SLC20A2 in an Italian patient presenting with migraine., file e27ce428-b481-2581-e053-d805fe0acbaa
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205
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Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia, file e27ce42c-4ad6-2581-e053-d805fe0acbaa
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198
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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia, file e27ce42c-7650-2581-e053-d805fe0acbaa
|
190
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Investigation of C9orf72 in 4 Neurodegenerative Disorders, file e27ce427-a031-2581-e053-d805fe0acbaa
|
189
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SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis, file e27ce426-ec3d-2581-e053-d805fe0acbaa
|
188
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Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies, file e27ce42c-4f3e-2581-e053-d805fe0acbaa
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176
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Double-cone coil TMS stimulation of the medial cortex inhibits central pain habituation, file e27ce428-50f3-2581-e053-d805fe0acbaa
|
173
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Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients., file e27ce427-f0d7-2581-e053-d805fe0acbaa
|
169
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Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38), file e27ce428-ecdd-2581-e053-d805fe0acbaa
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167
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The chemotherapy long-term effect on cognitive functions and brain metabolism in lymphoma patients, file e27ce42a-f22e-2581-e053-d805fe0acbaa
|
164
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Recent advances in the molecular genetics of frontotemporal lobar degeneration, file e27ce42b-daf1-2581-e053-d805fe0acbaa
|
158
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Cerebrospinal fluid levels of orexin-A and corticotropin- releasing factor suggest their involvement in the negative motivational state that driver "drug dependence" in medicational overuse, file e27ce426-d43f-2581-e053-d805fe0acbaa
|
155
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Genetic variants in the NOTCH4 gene influence the clinical features of migraine, file e27ce426-e0bf-2581-e053-d805fe0acbaa
|
154
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The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients., file e27ce42b-4b40-2581-e053-d805fe0acbaa
|
154
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An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2, file e27ce428-4d69-2581-e053-d805fe0acbaa
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146
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Age of Onset of Mood Disorders and Complexity of Personality Traits, file e27ce426-e4d1-2581-e053-d805fe0acbaa
|
143
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Multivariate analysis of brain metabolism reveals chemotherapy effects on prefrontal cerebellar system when related to dorsal attention network, file e27ce427-ebd2-2581-e053-d805fe0acbaa
|
141
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Selective genetic overlap between amyotrophic lateral sclerosis and diseases of the frontotemporal dementia spectrum, file e27ce42d-8334-2581-e053-d805fe0acbaa
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136
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Evidence for an association between migraine and the hypocretin receptor 1 gene, file e27ce42a-46d3-2581-e053-d805fe0acbaa
|
135
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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population, file e27ce42c-958f-2581-e053-d805fe0acbaa
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135
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Neurofunctional Signature of Hyperfamiliarity for Unknown Faces, file e27ce428-e425-2581-e053-d805fe0acbaa
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132
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Prevalence of the placebo and nocebo responses in patients with migraine and tension- type headache, file e27ce426-d333-2581-e053-d805fe0acbaa
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129
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Genes and primary headaches: discovering new potential therapeutic targets, file e27ce426-ff46-2581-e053-d805fe0acbaa
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129
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Efficacy of Frovatriptan vs. Other Triptans in Weekend Migraine: Pooled Analysis of Three Double-Blind, Randomized, Crossover, Multicenter Studies, file e27ce427-0a4e-2581-e053-d805fe0acbaa
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129
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The rehabilitative effects on written language of a combined language and parietal dual-tDCS treatment in a stroke case, file e27ce42a-f23c-2581-e053-d805fe0acbaa
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125
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Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases, file e27ce42c-68b6-2581-e053-d805fe0acbaa
|
119
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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers, file e27ce42d-7dbc-2581-e053-d805fe0acbaa
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108
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Protein network analysis reveals selectively vulnerable regions and biological processes in FTD, file e27ce42d-2e66-2581-e053-d805fe0acbaa
|
106
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CXCR4 involvement in neurodegenerative diseases, file e27ce42d-87c8-2581-e053-d805fe0acbaa
|
102
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Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia, file e27ce42d-84e0-2581-e053-d805fe0acbaa
|
100
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O056. Migraine as presenting symptom of SLC20A2gene mutations, file e27ce42c-19a3-2581-e053-d805fe0acbaa
|
97
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Genetic risk for neurodegenerative disorders, and its overlap with cognitive ability and physical function, file e27ce42d-88f7-2581-e053-d805fe0acbaa
|
93
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|
Atypical hereditary spastic paraplegia mimicking multiple sclerosis associated with a novel SPG11 mutation., file e27ce42a-8f95-2581-e053-d805fe0acbaa
|
92
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Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS, file e27ce42d-7c62-2581-e053-d805fe0acbaa
|
90
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Fattori scatenanti delle crisi nelle cefalee essenziali in età giovanile, file e27ce426-ee31-2581-e053-d805fe0acbaa
|
85
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Opzioni terapeutiche nella cefalea cronica quotidiana, file e27ce426-ee32-2581-e053-d805fe0acbaa
|
77
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Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: A meta-analysis., file e27ce42b-5acc-2581-e053-d805fe0acbaa
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68
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Polimorfismi del gene dell’interleuchina-1α ed emicrania, file e27ce426-ee33-2581-e053-d805fe0acbaa
|
59
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Neural correlates of reduced awareness in instrumental activities of daily living in frontotemporal dementia, file e27ce42a-66f2-2581-e053-d805fe0acbaa
|
51
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O057. Altered plasma adipokines concentrations in chronic migraine, file e27ce42d-87d0-2581-e053-d805fe0acbaa
|
43
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The neurobiological basis of the Distress Thermometer: a PET study in cancer patients., file e27ce42a-3361-2581-e053-d805fe0acbaa
|
41
|
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Chemotherapy-Induced Neurotoxicity: Evidence of a Protective Role of CC Homozygosis in the Interleukin-1β Gene-511 C>T Polymorphism, file e27ce42a-f4cc-2581-e053-d805fe0acbaa
|
38
|
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Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations., file e27ce428-7692-2581-e053-d805fe0acbaa
|
29
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The hemochromatosis (HFE) gene influences the clinical features of migraine, file e27ce426-d334-2581-e053-d805fe0acbaa
|
28
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Focal gray matter decrease in the cerebral pain network of migraine patients, file e27ce426-d441-2581-e053-d805fe0acbaa
|
20
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Neuroendocrine function is altered in patients with chronic migraine and medication-overuse headache, file e27ce426-eb4c-2581-e053-d805fe0acbaa
|
14
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The neurobiological basis of the Distress Thermometer: a PET study in cancer patients., file e27ce427-494c-2581-e053-d805fe0acbaa
|
14
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P055. Prevalence of migraine in subclinical hypothyroidism: a case-control study, file e27ce42d-87d1-2581-e053-d805fe0acbaa
|
14
|
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The rehabilitative effects on written language of a combined language and parietal dual-tDCS treatment in a stroke case, file e27ce428-4627-2581-e053-d805fe0acbaa
|
9
|
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Neural correlates of reduced awareness in instrumental activities of daily living in frontotemporal dementia, file e27ce42a-63f9-2581-e053-d805fe0acbaa
|
7
|
|
Cluster headache is associated with the alcohol dehydrogenase 4 (ADH4) gene., file e27ce426-be3f-2581-e053-d805fe0acbaa
|
6
|
|
Paroxysmal perceptual alteration in a schizophrenic patient treated with paliperidone: A case report, file e27ce428-49d1-2581-e053-d805fe0acbaa
|
6
|
|
Noninvasive Vagal Nerve Stimulation in Chronic Migraine with Medication Overuse Headache, file e27ce42d-2937-2581-e053-d805fe0acbaa
|
6
|
|
Proinflammatory cytokine gene polymorphisms and susceptibility to Paget's disease of bone: An association study., file e27ce426-d75d-2581-e053-d805fe0acbaa
|
5
|
|
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients., file e27ce428-4618-2581-e053-d805fe0acbaa
|
5
|
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The chemotherapy long-term effect on cognitive functions and brain metabolism in lymphoma patients, file e27ce42a-d61f-2581-e053-d805fe0acbaa
|
5
|
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Heterosexual pedophilia in a frontotemporal dementia patient with a mutation in the progranulin gene, file e27ce426-d304-2581-e053-d805fe0acbaa
|
4
|
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Subclinical hypothyroidism is associated with migraine: A case-control study, file e27ce42d-7dba-2581-e053-d805fe0acbaa
|
4
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Migraine: Genetic Variants and Clinical Phenotypes, file e27ce42d-84de-2581-e053-d805fe0acbaa
|
4
|
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Anger and emotional distress in patients with migraine and tension-type headache, file e27ce426-cdf2-2581-e053-d805fe0acbaa
|
3
|
|
Brain Arteriovenous Malformations are associated with Interleukin-1 Cluster Gene Polymorphisms., file e27ce426-d6cb-2581-e053-d805fe0acbaa
|
3
|
|
Apolipoprotein E polymorphisms in frontotemporal lobar degeneration: A meta-analysis., file e27ce426-e0c1-2581-e053-d805fe0acbaa
|
3
|
|
Frontotemporal dementia and its subtypes: a genome-wide association study., file e27ce427-0a49-2581-e053-d805fe0acbaa
|
3
|
|
HLA-DRB1 genotyping in Italian migraine patients, file e27ce426-af9e-2581-e053-d805fe0acbaa
|
2
|
|
Vascular endothelial growth factor gene polymorphisms and intracranial aneurysms., file e27ce426-e3d9-2581-e053-d805fe0acbaa
|
2
|
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Occurrence of ecchymotic angioedema-like cutaneous lesions as a possible side effect of fingolimod., file e27ce426-f764-2581-e053-d805fe0acbaa
|
2
|
|
Is HCRTR2 a Genetic Risk Factor for Alzheimer's Disease?, file e27ce427-0a48-2581-e053-d805fe0acbaa
|
2
|
|
Association between polymorphisms rs1333040 and rs7865618 of chromosome 9p21 and sporadic brain arteriovenous malformations., file e27ce427-0a4d-2581-e053-d805fe0acbaa
|
2
|
|
Italian Frontotemporal Dementia Network (FTD Group-SINDEM): sharing clinical and diagnostic procedures in Frontotemporal Dementia in Italy, file e27ce427-0d58-2581-e053-d805fe0acbaa
|
2
|
|
Association between Major Mood Disorders and the hypocretin receptor 1 gene, file e27ce42a-25f2-2581-e053-d805fe0acbaa
|
2
|
|
Two families with novel missense mutations in COL4A1: When diagnosis can be missed., file e27ce42b-f3a8-2581-e053-d805fe0acbaa
|
2
|
|
Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood, file cb476e2e-86cb-483f-8109-9b637ab08445
|
1
|
|
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia, file d5d6ea78-297b-42fd-a30a-6237688a857e
|
1
|
|
Lack of association between the apolipoprotein E gene and aneurysmal subarachnoid hemorrhage in an Italian population, file e27ce426-9e60-2581-e053-d805fe0acbaa
|
1
|
|
Association between the G1246A polymorphism of the hypocretin receptor 2 gene and cluster headache: a meta-analysis, file e27ce426-9e66-2581-e053-d805fe0acbaa
|
1
|
|
The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease, file e27ce426-a158-2581-e053-d805fe0acbaa
|
1
|
|
Interleukin 6 gene polymorphisms are not associated with aneurysmal subarachnoid haemorrhage in an Italian population, file e27ce426-a743-2581-e053-d805fe0acbaa
|
1
|
|
The 1246G-->A polymorphism of the HCRTR2 gene is not associated with migraine, file e27ce426-aab0-2581-e053-d805fe0acbaa
|
1
|
|
A polymorphism of the hypocretin receptor 2 gene is associated with cluster headache, file e27ce426-aac9-2581-e053-d805fe0acbaa
|
1
|
|
Association between migraine and HLA-DRB1 gene polymorphisms, file e27ce426-ac1a-2581-e053-d805fe0acbaa
|
1
|
|
Haemochromatosis gene (HFE) polymorphisms and migraine: an association study, file e27ce426-ad11-2581-e053-d805fe0acbaa
|
1
|
|
Association between the tumor necrosis factor-alpha -308 G/A gene polymorphism and migraine, file e27ce426-ad85-2581-e053-d805fe0acbaa
|
1
|
|
Quantitative EEG responses to ischaemic arm stress in migraine, file e27ce426-b13a-2581-e053-d805fe0acbaa
|
1
|
|
Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis, file e27ce426-b241-2581-e053-d805fe0acbaa
|
1
|
|
Endocrine function is altered in chronic migraine patients with medication-overuse, file e27ce426-b673-2581-e053-d805fe0acbaa
|
1
|
|
Genetics of cluster headache: an update, file e27ce426-b674-2581-e053-d805fe0acbaa
|
1
|
|
Prevalence of HFE (hemochromatosis) gene mutations in patients with cluster headache, file e27ce426-b80c-2581-e053-d805fe0acbaa
|
1
|
|
Lack of association between the 3092 T→C Clock gene polymorphism and cluster headache, file e27ce426-b811-2581-e053-d805fe0acbaa
|
1
|
|
Tumor necrosis factor-alpha gene and cerebral aneurysms, file e27ce426-bbbc-2581-e053-d805fe0acbaa
|
1
|
|
Resolution of cluster headache after closure of an anterior communicating artery aneurysm: the role of pericarotid sympathetic fibres, file e27ce426-c6ff-2581-e053-d805fe0acbaa
|
1
|
|
Insulin sensitivity is impaired in patients with migraine, file e27ce426-c701-2581-e053-d805fe0acbaa
|
1
|
|
Worldwide distribution of PSEN1 Met146Leu mutation: a large variability for a founder mutation, file e27ce426-cbe3-2581-e053-d805fe0acbaa
|
1
|
|
Investigating the genetic role of aquaporin4 gene in migraine, file e27ce426-cbe6-2581-e053-d805fe0acbaa
|
1
|
| Totale |
7396 |