278 results on '"Van Hove, J."'
Search Results
2. Prevention of Crosstalk in Dual Chamber Pacemakers
3. Benzoate treatment and the glycine index in nonketotic hyperglycinaemia
4. Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase defiency
5. Plasma damage in p-GaN
6. Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders
7. A founder mutation in the GLRX5 gene is responsible for one form of atypical, late-onset non-ketotic hyperglycinemia: C1–P2
8. Uniformity and Performance Characterization of GaN p-i-n Photodetectors Fabricated from 3-Inch Epitaxy
9. A study of the electrical characteristics of various metals on p-type GaN for ohmic contacts
10. One-methyl group metabolism in non-ketotic hyperglycinaemia: Mildly elevated cerebrospinal fluid homocysteine levels
11. Optimization of III-N Based Devices Grown by RF Atomic Nitrogen Plasma Using In-Situ Cathodoluminescence
12. High Temperature GaN and AlGaN Photovoltaic Detectors for UV Sensing Applications
13. The role of ion characteristics in determining the structural and electrical quality of InN grown by metalorganic molecular beam epitaxy
14. Plasma characteristics and the growth of group III-nitrides by metalorganic molecular beam epitaxy
15. Mitochondrial respiratory states and rate
16. Acute pancreatitis in an infant with lactic acidosis and a mutation at nucleotide 3243 in the mitochondrial DNA tRNALeu[UUR] gene
17. 3-Hydroxyisovalerylcarnitine in 3-methylcrotonyl-CoA carboxylase deficiency
18. Glycine andl-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency
19. Outcome after three years of laronidase enzyme replacement therapy in a patient with Hurler syndrome
20. Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency
21. Acylcarnitines in amniotic fluid: Application to the prenatal diagnosis of propionic acidaemia
22. Photoluminescence characterization of AlGaN-GaN pseudomorphic quantum wells and calculation of strain induced bandgap shifts
23. Optical characterization of AlGaN-GaN-AlGaN quantum wells
24. Neuroleptic malignant syndrome in juvenile neuronal ceroid lipofuscinosis associated with low-dose risperidone therapy
25. p-GaAs Base Regrowth for GaN HBTs and BJTs
26. Device Processing for GaN High Power Electronics
27. Surface Conversion Effects in Plasma-Damaged p-GaN
28. High Density Plasma Damage Induced in n-GaN Schottky Diodes Using Cl2/Ar Discharges
29. Uniformity and Performance Characterization of GaN P-I-N Photodetectors Fabricated From 3-Inch Epitaxy
30. 300°C GaN/AlGaN Heterojunction Bipolar Transistor
31. Atomic layer epitaxy of YBaCuO for optoelectronic applications
32. Electronic states in modulation doped p-AlGaN/GaN superlattices.
33. Ordinary optical dielectric functions of anisotropic hexagonal GaN film determined by variable angle spectroscopic ellipsometry.
34. The clinical spectrum of cytochrome c deficiency in Leigh syndrome patients with and without mutations in the SURF1 gene
35. MG-134 Update on novel treatments for pyridoxine-dependent epilepsy due to antiquitin deficiency
36. 2015 update on triple therapy for pyridoxine-dependent epilepsy
37. Transcriptional profiling of the lectin ArathEULS3 from Arabidopsis thaliana toward abiotic stresses
38. Expansion cranioplasty with jackscrew distracters for craniosynostosis and intracranial hypertension in transplanted osteopetrosis
39. Ophthalmological findings in a patient with mucolipidosis III (pseudo-hurler polydystrophy). A case report
40. Conductivity and hall-effect characterization of highly resistive molecular-beam epitaxial GaN layers
41. Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial
42. An new mutation m.3928G>C p.V208L in ND1 causes Leigh disease
43. ND3 Mutation 10191T>C causes rapidly progressive infantile Leigh disease
44. Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood
45. MRI of the brain and cervical spinal cord in rhizomelic chondrodysplasia punctata
46. 47 MUTATIONAL ANALYSIS OF PATIENTS WITH NONKETOTIC HYPERGLYCINEMIA AND THE IDENTIFICATION OF LARGE DELETIONS IN THE GLDC GENE USING A NOVEL DETECTION SYSTEM.
47. 119 MUTATIONAL ANALYSIS OF PATIENTS WITH NONKETOTIC HYPERGLYCINEMIA AND THE IDENTIFICATION OF LARGE DELETIONS IN THE GLDC GENE USING A NOVEL DETECTION SYSTEM.
48. Natural history of nonketotic hyperglycinemia in 65 patients
49. Idebenone treatment in Friedreich's ataxia: Neurological, cardiac, and biochemical monitoring
50. Characterization of High Dose Mn, Fe, and Ni implantation intop-GaN
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