98 results on '"Kurlemann G."'
Search Results
2. Unilateral Atrophy of the Tongue: Hypoglossal Palsy Due to Neurovascular Contact?
3. Forceful Monitoring after Acute Pediatric Stroke Can Help Identify the Etiology
4. When It Is Not MS…—Differential Diagnosis of Optic Neuritis and Multifocal Inflammatory Cerebral Lesions in an Adolescent
5. The Enemy Within: Deleterious Consequences of an Inappropriate Antiviral Response for the Central Nervous System
6. Emery-Dreifuss Muscular Dystrophy Type 1 in a 15-Year-Old Patient Due to a Novel Putative Splice-Site Mutation
7. Are Reemergence of Sleep Spindles and Cessation of Hypsarrhythmia Prognostic Factors for Neurodevelopmental Outcome in Adults with a History of West Syndrome in Infancy?
8. Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis
9. Ciliopathies with Hepatic Involvement the Broad Phenotypical Spectrum of TMEM67 Mutations
10. Predictive Value of Cerebrospinal Fluid Flow Cytometry in Pediatric Multiple Sclerosis
11. Unraveling the Genotype-Specific Response to Antiepileptic Medication in LIS1 Associated Classic Lissencephaly
12. Therapy and Clinical Course in 52 Patients with PCDH19 Mutations
13. Acute Onset of a Movement Disorder in Early Childhood: A Family with Rapid Onset Dystonia-Parkinsonism Syndrome
14. Visual Diagnosis: Costello Syndrome
15. Effects of Rapamycin on Monocytes from Pediatric Patients with Tuberous Sclerosis
16. Intrauterine Epileptic Seizures: Possible?
17. A Good View at Proper Diagnosis: Onodi Cell As Rare Cause of Optic Neuritis
18. Long-Term Follow-Up of Patients with BNS Epilepsy for More Than 30 to 40 Years: First Results
19. De Novo SCN2A Mutations Cause Variable Phenotypes in Children with Epilepsy
20. Undine-Syndrome: Really Only a Disease of Infants?
21. Does the mTOR inhibitor everolimus influence the course of epilepsy in children with tuberous sclerosis complex?
22. Ocular myositis
23. Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations
24. Fibroadenoma under therapy with interferons in multiple sclerosis
25. Kleine-Levin syndrome in a 10-year-old boy as the rare cause of hypersomnia
26. Lacosamide in childhood-results of a retrospective analysis
27. Rare cause of oculomotor palsy
28. Vitamin B in paediatric neurology
29. Evolution of a channelopathy, CACNA1 mutation in a young man
30. Ketogenic diet in children with pharmacoresistant epilepsy
31. Listening is all important!
32. Nephronophthisis Registry
33. Neuroborreliosis as a chameleon - mimicking tuberculous meningitis
34. Charcot-Marie-Tooth type 2A2 and idiopathic intracranial hypertension coinciding in a 15-year old boy
35. Is neuritis nervi optici in children a predictor of multiple sclerosis in adulthood?
36. Editorial
37. Rare course of an intraspinal dermoid
38. Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl
39. Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene
40. Potocki-Shaffer Syndrome: A case study
41. First experiences with Lacosamid for treatment of therapy-resistant epilepsy in early childhood
42. Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis
43. CK elevation and progressive toe walking in a 14-year old girl
44. Globoid cell leukodystrophy (Morbus Krabbe) – Case report with characteristic clinical and imaging features
45. Narcolepsy in early childhood – a case study with video
46. Seizure and Cognitive Outcomes in Children and Adolescents with Epilepsy Treated with Topiramate
47. Isolated inflammation of the optic nerve in childhood as a predictor for multiple sclerosis in future?
48. Epilepsy in vitamin B12 deficiency and its treatment in infancy
49. A novel ACTA- 1 mutation in a child with Nemaline Myopathy and reduced acid alpha-glucosidase activity
50. Autosomal dominant chin myoclonus
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