17 results on '"Watson, Eloise"'
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2. Low disease risk and penetrance in Leber hereditary optic neuropathy
3. Author Response: Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis
4. 2366 Pathogenic mtDNA variants and potential disease risk in a healthy older population
5. Fundoscopy use in neurology departments and the utility of smartphone photography: a prospective prevalence and crossover diagnostic accuracy study amongst neurology inpatients
6. Decompensation of cardiorespiratory function and emergence of anemia during pregnancy in a case of mitochondrial myopathy, lactic acidosis, and sideroblastic anemia 2 with compound heterozygousYARS2pathogenic variants
7. 080 The diagnostic journey of mitochondrial disease patients
8. Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is Present
9. Dietary nitrate reduces blood pressure and cerebral artery velocity fluctuations and improves cerebral autoregulation in transient ischemic attack patients
10. Safety and acceptability of clozapine and risperidone in progressive multiple sclerosis: a phase I, randomised, blinded, placebo-controlled trial
11. Safety and acceptability of clozapine and risperidone in progressive multiple sclerosis: a phase 1, randomized, blinded, placebo-controlled trial
12. New diagnostic pathways for mitochondrial disease
13. The neuro-ophthalmology of inherited myopathies
14. Gentamicin vestibulotoxicity with modern systemic dosing regimens: a prospective study using video-oculography
15. Gentamicin vestibulotoxicity is uncommon with modern dosing regimens: a prospective study using video head impulse testing (P6.043)
16. Faciobrachial dystonic seizures in an Lgi1 VGKC-complex antibody-mediated encephalitis
17. “Txt”-induced seizures indicating reading epilepsy in the mobile phone age
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