10 results on '"Casali, C"'
Search Results
2. Ataxia with oculomotor apraxia type 2
3. Novel SACSmutations in autosomal recessive spastic ataxia of Charlevoix-Saguenay type
4. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum
5. SPG3A
6. Mitochondrial myopathy, parkinsonism, and multiple mtDNA deletions in a Sephardic Jewish family
7. Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses
8. Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE
9. Mitochondrial G8363A mutation presenting as cerebellar ataxia and lipomas in an Italian family
10. mtDNA A3243G MELAS mutation is not associated with multigenerational female migraine
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