Archives of neurology

Label

• Archives of neurology (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• Identification of new presenilin gene mutations in early-onset familial Alzheimer disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Evidence of white matter changes on diffusion tensor imaging in frontotemporal dementia. (Articolo in rivista) (Prodotto della ricerca)
• Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Hemidystonia in Uncontrolled Type 2 Diabetes Mellitus (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease. (Articolo in rivista) (Prodotto della ricerca)
• Orthostatic hypotension in de novo parkinson disease (Articolo in rivista) (Prodotto della ricerca)
• White matter changes in corticobasal degeneration syndrome and correlation with limb apraxia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A Novel Loss-of-Function LGI1 Mutation Linked to Autosomal Dominant Lateral Temporal Epilepsy (Articolo in rivista) (Prodotto della ricerca)
• Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study. (Articolo in rivista) (Prodotto della ricerca)

Alternative label

• Archives of neurology. (literal)
• Arch. neurol. (literal)

Language

• eng (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#issn

• 0003-9942 (literal)

Preferred label

• Archives of neurology (literal)

Publisher

• American Medical Association] [Chicago, USA (literal)

Incoming links:

Rivista

• Heterogeneity of brain glucose metabolism in mild cognitive impairment and clinical progression to Alzheimer disease. (Articolo in rivista) (Prodotto della ricerca)
• Evidence of white matter changes on diffusion tensor imaging in frontotemporal dementia. (Articolo in rivista) (Prodotto della ricerca)
• White matter changes in corticobasal degeneration syndrome and correlation with limb apraxia. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Hemidystonia in Uncontrolled Type 2 Diabetes Mellitus (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Identification of new presenilin gene mutations in early-onset familial Alzheimer disease. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• A Novel Loss-of-Function LGI1 Mutation Linked to Autosomal Dominant Lateral Temporal Epilepsy (Articolo in rivista) (Prodotto della ricerca)
• Orthostatic hypotension in de novo parkinson disease (Articolo in rivista) (Prodotto della ricerca)
• A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
• Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study. (Articolo in rivista) (Prodotto della ricerca)