17 results on '"Gorman, Mark P."'
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2. Inaugural Patient-Reported Registry of Pediatric Opsoclonus-Myoclonus-Ataxia Syndrome: Presentation, Diagnosis, and Treatment of 194 Patients
3. Assessing Needs and Perceptions of Research Participation in Pediatric-Onset Multiple Sclerosis: A Multistakeholder Survey
4. Functional analysis of a de novo variant in the neurodevelopment and generalized epilepsy disease gene NBEA
5. Central nervous system–restricted familial hemophagocytic lymphohistiocytosis responds to hematopoietic cell transplantation
6. An International Pediatric-Onset Opsoclonus-Myoclonus Ataxia Syndrome Registry and Clinical Research Network: Development, Progress, and Vision
7. Pain and spinal cord imaging measures in children with demyelinating disease
8. Evaluation and Treatment of Autoimmune Neurologic Disorders in the Pediatric Intensive Care Unit
9. Visual Outcomes in Pediatric Optic Neuritis
10. Increased Th17 response to myelin peptides in pediatric MS
11. Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2
12. Posterior-onset Rasmussen's encephalitis with ipsilateral cerebellar atrophy and uveitis resistant to rituximab
13. Postvaricella Acute Transverse Myelitis in a Previously Vaccinated Child
14. Neonatal Hypocalcemic Seizures in Siblings Exposed to Topiramate In Utero
15. Neuromyelitis Optica in an Adolescent After Bone Marrow Transplantation
16. Reply
17. A Human Kidney cDNA Which Induces a Cell Surface Protein Epitope Recognized by a Monoclonal Antibody against Galactosylceramide
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