Pages that link to "Q39123310"
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The following pages link to Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7. (Q39123310):
Displaying 24 items.
- Clinical and neuroimaging features as diagnostic guides in neonatal neurology diseases with cerebellar involvement (Q26771797) (← links)
- Infantile onset spinocerebellar ataxia 2 (SCA2): a clinical report with review of previous cases (Q30706825) (← links)
- Consensus and controversies in best practices for molecular genetic testing of spinocerebellar ataxias. (Q34329735) (← links)
- Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report (Q35017496) (← links)
- Genetic testing in inherited ataxias (Q35599446) (← links)
- Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles (Q35603679) (← links)
- EST-SSRs as a resource for population genetic analyses. (Q36829463) (← links)
- Germ-line CAG repeat instability causes extreme CAG repeat expansion with infantile-onset spinocerebellar ataxia type 2. (Q36856462) (← links)
- In vivo analysis of cerebellar Purkinje cell activity in SCA2 transgenic mouse model (Q37042016) (← links)
- De novo mutations in ataxin-2 gene and ALS risk (Q37075624) (← links)
- Spinocerebellar ataxia 2 (SCA2). (Q37140787) (← links)
- Spinocerebellar ataxia type 2 presenting with cognitive regression in childhood (Q37216544) (← links)
- Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectives (Q38045212) (← links)
- EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. (Q39213724) (← links)
- The Multiple Faces of Spinocerebellar Ataxia type 2. (Q41510206) (← links)
- Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay (Q41859299) (← links)
- Spinocerebellar ataxia type 2 (SCA2) in an Egyptian family presenting with polyphagia and marked CAG expansion in infancy (Q42525064) (← links)
- Infantile childhood onset of spinocerebellar ataxia type 2. (Q48859574) (← links)
- Spinocerebellar ataxia type 2 in a Turkish family. (Q53532767) (← links)
- Neonatal SCA2 Presenting With Choreic Movements and Dystonia With Dystonic Jerks, Retinitis, Seizures, and Hypotonia (Q57675662) (← links)
- Neurodegenerative Disorders (Q59326701) (← links)
- Diagnosis of Spinocerebellar Ataxias Caused by Trinucleotide Repeat Expansions (Q89508009) (← links)
- Spinocerebellar ataxia (Q93041355) (← links)
- Expanding the genotype-phenotype correlation of childhood sensory polyneuropathy of genetic origin (Q100395210) (← links)