36 results on '"Graf, W. D."'
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2. PRACTICE PARAMETER: EVALUATION OF THE CHILD WITH MICROCEPHALY (AN EVIDENCE-BASED REVIEW): REPORT OF THE QUALITY STANDARDS SUBCOMMITTEE OF THE AMERICAN ACADEMY OF NEUROLOGY AND THE PRACTICE COMMITTEE OF THE CHILD NEUROLOGY SOCIETY
3. Book Reviews
4. Catecholamines in patients with 22q11.2 deletion syndrome and the low-activity COMT polymorphism
5. Can bioinformatics help trace the steps from gene mutation to disease?
6. A placebo-controlled trial of lamotrigine add-on therapy for partial seizures in children
7. Radical reactions from missing ceruloplasmin
8. Clinical features associated with the a → g transition at nucleotide 8344 of mtdna (“merrf mutation”)
9. Ahomocysteinemia in molybdenum cofactor deficiency
10. Video Games May Trigger Seizures in Some People
11. Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA
12. Clinical features associated with the A → G transition at nucleotide 8344 of mtDNA (“MERRF mutation”)
13. Identification of Copy Number Variants on Human Chromosome 22 in Patients with a Variety of Clinical Findings.
14. Telomere Capture as a Frequent Mechanism for Stabilization of the Terminal Chromosomal Deletion Associated with Inverted Duplication.
15. Dopa-responsive dystonia simulating spastic paraplegia due to tyrosine hydroxylase (TH) gene mutations.
16. The Study of Neural Tube Defects After the Human Genome Project and Folic Acid Fortification of Foods.
17. Outcome in severe pediatric Guillain-Barré syndrome after immunotherapy or supportive care.
18. The Pachygyria-Polymicrogyria Spectrum of Cortical Dysplasia in X-Linked Hydrocephalus.
19. Altered Antioxidant Enzyme Activities in Children with a Serious Adverse Experience Related to Valproic Acid Therapy.
20. Comparison of erythrocyte antioxidant enzyme activities and embryologic level of neural tube defects.
21. Erythrocyte antioxidant enzyme activities in children with myelomeningocele.
22. Cell Cycle Properties in Lymphocytes from Children with Myelomeningocele.
23. Plasma Homocysteine and Methionine Concentrations in Children with Neural Tube Defects.
24. Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation.
25. Diffusion-weighted magnetic resonance imaging in boys with neural cell adhesion molecule L1 mutations and congenital hydrocephalus.
26. Brainstem diffusion-weighted MRI in boys with L1CAM mutations.
27. Outcome of children after near drowning.
28. Uterine contraction in the development of Möbius syndrome.
29. Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A.
30. Predicting outcome in pediatric submersion victims.
31. Pharmacologic treatment of recurrent pediatric headache.
32. Video game-related seizures: a report on 10 patients and a review of the literature.
33. Stroke and mixed connective tissue disease.
34. Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation").
35. Diazepam use & intubation.
36. Electrodiagnosis reliability in the diagnosis of infant botulism.
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