12 results on '"Volk, Alexander E."'
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2. Hot-spot KIF5A mutations cause familial ALS
3. A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction
4. The rapid evolution of molecular genetic diagnostics in neuromuscular diseases
5. Neurofilament as a blood marker for diagnosis and monitoring of primary progressive aphasias
6. NEK1 mutations in familial amyotrophic lateral sclerosis
7. Neurofilaments in the diagnosis of motoneuron diseases: a prospective study on 455 patients
8. Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis
9. Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
10. Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers
11. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories
12. A Novel MYO6 Splice Site Mutation Causes Autosomal Dominant Sensorineural Hearing Loss Type DFNA22 with a Favourable Outcome after Cochlear Implantation
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