Neurogenetics
- Label
- Neurogenetics (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi
- Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonism (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort. (Articolo in rivista) (Prodotto della ricerca)
- Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus. (Articolo in rivista) (Prodotto della ricerca)
- Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability (Articolo in rivista) (Prodotto della ricerca)
- Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Natural history of neurofibromatosis type 2 with onset before the age of 1 year (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Expanding the spectrum of megalencephalic leukoencephalopathy with subcortical cysts in two patients with GLIALCAM mutations (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. (Articolo in rivista) (Prodotto della ricerca)
- Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification, (Articolo in rivista) (Prodotto della ricerca)
- Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL) (Articolo in rivista) (Prodotto della ricerca)
- Alternative label
- Neurogenetics (literal)
- Neurogenetics (Berlin. Print) (literal)
- Neurogenetics. (literal)
- Language
- eng (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#issn
- 1364-6745 (literal)
- Preferred label
- Neurogenetics (literal)
- Publisher
- Springer Berlin : DEU (literal)
Incoming links:
- Rivista
- Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort. (Articolo in rivista) (Prodotto della ricerca)
- Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. (Articolo in rivista) (Prodotto della ricerca)
- Different spectra of genomic deletions within the CCM genes between Italian and American CCM patient cohorts (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A G301R Na+/K+ -ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification, (Articolo in rivista) (Prodotto della ricerca)
- Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability (Articolo in rivista) (Prodotto della ricerca)
- Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus. (Articolo in rivista) (Prodotto della ricerca)
- Shorter telomeres in patients with cerebral autosomal dominant arteriopathy and leukoencephalopathy (CADASIL) (Articolo in rivista) (Prodotto della ricerca)
- Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonism (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Expanding the spectrum of megalencephalic leukoencephalopathy with subcortical cysts in two patients with GLIALCAM mutations (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Natural history of neurofibromatosis type 2 with onset before the age of 1 year (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)