170 results on '"Leiz, Steffen"'
Search Results
2. Clinical and epilepsy characteristics in Wolf-Hirschhorn syndrome (4p-): A review
3. Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome
4. De novo variants in GABRA4are associated with a neurological phenotype including developmental delay, behavioral abnormalities and epilepsy
5. High association of MOG-IgG antibodies in children with bilateral optic neuritis
6. Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation
7. Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
8. Author Correction: Aberrant activity of mitochondrial NCLX is linked to impaired synaptic transmission and is associated with mental retardation
9. MRI of the first event in pediatric acquired demyelinating syndromes with antibodies to myelin oligodendrocyte glycoprotein
10. Impaired Brain Growth in Myelin Oligodendrocyte Glycoprotein Antibody–Associated Acute Disseminated Encephalomyelitis
11. Effectiveness of antiepileptic therapy in patients with PCDH19 mutations
12. Autoimmune Encephalitis with Autoantibodies to NMDAR1 following Herpes Encephalitis in Children and Adolescents
13. Clinical and epilepsy characteristics in Wolf-Hirschhorn syndrome (4p-): A review
14. MR imaging in children with transverse myelitis and acquired demyelinating syndromes
15. Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
16. CAD mutations and uridine-responsive epileptic encephalopathy
17. De novo GABRG2 mutations associated with epileptic encephalopathies
18. Autoimmune Encephalitis with Autoantibodies to NMDAR1 following Herpes Encephalitis in Children and Adolescents.
19. Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases
20. A de novo missense variant in GABRA4 alters receptor function in an epileptic and neurodevelopmental phenotype
21. Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes
22. Effectiveness and Tolerability of Perampanel in Children and Adolescents with Refractory Epilepsies: First Experiences
23. Human COQ4 deficiency: delineating the clinical, metabolic and neuroimaging phenotypes.
24. Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
25. De novo variants in neurodevelopmental disorders—experiences from a tertiary care center
26. Additional file 4 of Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
27. Additional file 5 of Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
28. Additional file 8 of Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
29. Additional file 2 of Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
30. Additional file 1 of Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
31. Additional file 3 of Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
32. Additional file 7 of Cerebrospinal fluid findings in patients with myelin oligodendrocyte glycoprotein (MOG) antibodies. Part 2: Results from 108 lumbar punctures in 80 pediatric patients
33. Mercury poisoning of a 4-year-old child by indirect contact to a mercury-containing facial cream: A case report
34. CT and MRI in haemolytic uraemic syndrome with central nervous system involvement: distribution of lesions and prognostic value of imaging findings
35. Mercury Poisoning of a 4-Year-old Child by Indirect Contact to a Mercury Containing Facial Cream: Case Report
36. GLRB is the third major gene of effect in hyperekplexia
37. Impaired Brain Growth in Myelin Oligodendrocyte Glycoprotein Antibody–Associated Acute Disseminated Encephalomyelitis.
38. A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome
39. Expanding the phenotypic and molecular spectrum of RNA polymerase III–related leukodystrophy
40. Disturbed bile secretion and cytochrome P-450 function during the acute state of experimental colitis in rats
41. Failure of Expected Brain Growth in Children with ADEM
42. Frequency of Spinal Cord Involvement and Autoantibody Status in a Large Cohort of Children Presenting with a First Acute Demyelinating Syndrome
43. Epilepsy Surgery in the First Months of Life
44. Heart and Brain: Homozygous Mutations of GNB5 Gene in Two Siblings with Early Onset Sinus Node Dysfunction and Severe Neurological Symptoms
45. Epilepsy surgery in the first months of life: a large type IIb focal cortical dysplasia causing neonatal drug‐resistant epilepsy
46. P 857. Unusual Presentation of Three Children with Alexander’s Disease and Therapy with Steroids
47. Impact of Hippotherapy on Gross Motor Function and Quality of Life in Children with Bilateral Cerebral Palsy: A Randomized Open-Label Crossover Study
48. Rituximab, IVIg, and Tetracosactide (ACTH1–24) Combination Immunotherapy (“RITE-CI”) for Pediatric Opsoclonus-Myoclonus Syndrome: Immunomarkers and Clinical Observations
49. Prognostic relevance of MOG antibodies in children with an acquired demyelinating syndrome
50. Reversible epileptic encephalopathy upon uridine treatment in patients with CAD mutations
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.