72 results on '"Morgan-Hughes, J. A."'
Search Results
2. Blood loss following tonsillectomy in children
3. The diagnosis of carnitine palmitoyltransferase II deficiency is now possible in small skeletal muscle biopsies
4. Late-onset cytoplasmic body myopathy resembling myotonic dystrophy
5. Transthyretin Leu12Pro is associated with systemic, neuropathic and leptomeningeal amyloidosis
6. MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity
7. Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A)
8. Similarities between exercise capacity and ventilation in patients with mitochondrial myopathy and chronic heart failure
9. 3-33-02 Mild mitochondrial myopathy due to the A3243G point mutation in the tRNA (LEU(UUR)) gene
10. Exercise Capacity and Ventilation in Patients with Mitochondrial Myopathy
11. Growth hormone therapy may benefit protein metabolism in mitochondrial encephalomyopathy
12. Affinity of antigen-specific IgG distinguishes multiple sclerosis from encephalitis
13. Drug points: Exacerbation of idiopathic Parkinson's disease by naproxen
14. Effect of timing of ketorolac administration on patient-controlled opioid use
15. A new mitochondrial DNA mutation associated with progressive dementia and chorea: A clinical, pathological, and molecular genetic study
16. Acanthocytosis, Retinitis Pigmentosa, and Pallidal Degeneration
17. Becker muscular dystrophy presenting with complete heart block in the sixth decade
18. The mitochondrial DNA transfer RNA Leu(UUR) A→G(3243) mutation: A clinical and genetic study
19. A MOLECULAR GENETIC STUDY OF FOCAL HISTOCHEMICAL DEFECTS IN MITOCHONDRIAL ENCEPHALOMYOPATHIES
20. The mitochondrial DNA transfer RNALysA→G[8344] mutation and the syndrome of myoclonic epilepsy with ragged red fibres [MERRF]
21. An audit of induction of anaesthesia in neonates and small infants using pulse oximetry
22. Late onset Leber's optic neuropathy: a case confused with ischaemic optic neuropathy.
23. The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies
24. A MOLECULAR GENETIC STUDY OF FOCAL HISTOCHEMICAL DEFECTS IN MITOCHONDRIAL ENCEPHALOMYOPATHIES
25. TREATMENT OF EXPERIMENTAL NADH UBIQUINONE REDUCTASE DEFICIENCY WITH MENADIONE
26. TREATMENT OF EXPERIMENTAL NADH UBIQUINONE REDUCTASE DEFICIENCY WITH MENADIONE
27. A case of progressive encephalomyelitis with rigidity and positive antiglutamic acid decarboxylase antibodies [corrected]
28. Behaviour of small children before induction. The effect of parental presence and EMLA and premedication with triclofos or a placebo
29. Mitochondrial myopathies: genetic defects
30. Pre‐induction behaviour of children A review of placebo‐controlled trials of sedatives
31. A MITOCHONDRIAL ENCEPHALOMYOPATHY WITH SPECIFIC DEFICIENCIES OF TWO RESPIRATORY CHAIN POLYPEPTIDES AND A CIRCULATING AUTOANTIBODY TO A MITOCHONDRIAL MATRIX PROTEIN
32. Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies
33. A MITOCHONDRIAL MYOPATHY CHARACTERIZED BY A DEFICIENCY IN REDUCIBLE CYTOCHROME b
34. A NEW MITOCHONDRIAL MYOPATHY
35. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
36. Mitochondrial DNA polymorphism in mitochondrial myopathy
37. KINETIC ANALYSIS OF ACETYLCHOLINE RECEPTORS (ACHR) IN NORMAL AND MYASTHENIC HUMAN MUSCLE*
38. Forum Paediatric anaesthesia in a district general hospital
39. Interaction of di-iodinated 125I-labelled α-bungarotoxin and reversible cholinergic ligands with intact synaptic acetylcholine receptors on isolated skeletal-muscle fibres from the rat
40. Congenital myasthenia: Further evidence of disease heterogeneity
41. Hexosaminidase A deficiency presenting as juvenile progressive dystonia.
42. Experimentally induced defects of mitochondrial metabolism in rat skeletal muscle. Biological effects of the mitochondrial uncoupling agent 2,4-dinitrophenol
43. CHRONIC DEMYELINATING PERIPHERAL NEUROPATHY ASSOCIATED WITH MULTIFOCAL CENTRAL NERVOUS SYSTEM DEMYELINATION
44. ALTERATIONS IN THE NUMBER AND AFFINITY OF JUNCTIONAL ACETYLCHOLINE RECEPTORS IN A MYOPATHY WITH TUBULAR AGGREGATES
45. Adult onset scapuloperoneal myopathy.
46. MITOCHONDRIAL ENCEPHALOMYOPATHIES
47. 31P NMR examination of two patients with NADH-CoQ reductase deficiency
48. THE PATTERN OF PERIPHERAL NERVE REGENERATION INDUCED BY CRUSH IN RATS WITH SEVERE ACRYLAMIDE NEUROPATHY
49. Isozyme patterns and protein profiles in neuromuscular disorders.
50. Iodine and acetone-containing plastic spray dressings.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.