32 results on '"Sue, Carolyn M."'
Search Results
2. Charcot-Marie-Tooth Disease Type 1
3. Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia
4. Neurofibromatosis Type 1
5. Myoclonus Epilepsy and Ragged Red Fiber (MERRF)
6. Mitochondrial Neurogastrointestinal Encephalopathy (MNGIE) Syndrome
7. Incidental Findings in Genetic Testing
8. Huntington Disease
9. Hereditary Neuropathy with Liability to Pressure Palsies
10. Inherited Prion Diseases
11. Dopa-Responsive Dystonia
12. Coincidental Occurrence of Two Monogenic Disorders
13. The Myotonic Dystrophies
14. Leber Hereditary Optic Neuropathy
15. Sialidosis
16. Spinocerebellar Ataxia Type 2
17. Recessive Parkinson Disease
18. Dominant Parkinson Disease
19. Frontotemporal Dementia—Amyotrophic Lateral Sclerosis Syndrome
20. POLG-Related Mitochondrial Disease
21. Gaucher Disease and Parkinson Disease
22. Paroxysmal Dyskinesia
23. Direct-to-Consumer Genetic Testing
24. Friedreich Ataxia
25. Myoclonus-Dystonia
26. Spinocerebellar Ataxia Type 17
27. Neurodegeneration with Brain Iron Accumulation
28. The Dystrophinopathies
29. Facioscapulohumeral Dystrophy
30. Early-Onset Dystonia
31. Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Syndrome
32. Hereditary Spastic Paraplegia
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