Published in Anal Biochem on August 01, 1984
A report--chronic fatigue syndrome: guidelines for research. J R Soc Med (1991) 7.70
Drug-induced myopathies in man. Lancet (1978) 2.25
Acute cerebral oedema induced by methotrexate. BMJ (1989) 1.79
Screening for mitochondrial cytopathies: the sub-anaerobic threshold exercise test (SATET). J Neurol Neurosurg Psychiatry (1989) 1.56
Glycine and neurodegenerative disease. Lancet (1991) 1.51
Neurological presentations of hypothyroidism: the importance of slow relaxing reflexes. J R Soc Med (1995) 1.51
Gold-induced neuroencephalopathy responding to dimercaprol. Lancet (1991) 1.42
Histological surprise: callosal tuberculoma presenting as malignant glioma. J Neurol Neurosurg Psychiatry (1997) 1.40
Purification and magneto-optical spectroscopic characterization of cytoplasmic membrane and outer membrane multiheme c-type cytochromes from Shewanella frigidimarina NCIMB400. J Biol Chem (2000) 1.34
Persistence of enteroviral RNA in chronic fatigue syndrome is associated with the abnormal production of equal amounts of positive and negative strands of enteroviral RNA. J Gen Virol (1990) 1.33
The genetic status of mothers of isolated cases of Duchenne muscular dystrophy. J Med Genet (1983) 1.32
Letter: Standardization of the E.S.R. Br Med J (1974) 1.28
Inorganic nitrogen metabolism in bacteria. Curr Opin Chem Biol (1999) 1.23
Two conserved glutamates in the bacterial nitric oxide reductase are essential for activity but not assembly of the enzyme. J Bacteriol (2001) 1.15
Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. Am J Hum Genet (1998) 1.11
Fatal lactic acidosis in infancy with a defect of complex III of the respiratory chain. Pediatr Res (1989) 1.08
Lactate responses to exercise in chronic fatigue syndrome. J Neurol Neurosurg Psychiatry (1994) 1.05
Methods for study of normal and abnormal skeletal muscle mitochondria. Methods Biochem Anal (1988) 1.05
Cytochrome cbb(3) oxidase and bacterial microaerobic metabolism. Biochem Soc Trans (2002) 1.04
No direct correlation between serum antiacetylcholine receptor antibody levels and clinical state of individual patients with myasthenia gravis. Neurology (1981) 1.01
A low-redox potential heme in the dinuclear center of bacterial nitric oxide reductase: implications for the evolution of energy-conserving heme-copper oxidases. Biochemistry (1999) 1.01
'Cardiogenic dementia' revisited. J R Soc Med (1991) 1.00
Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation. J Biol Chem (1991) 0.99
Familial cramp due to potassium-aggravated myotonia. J Neurol Neurosurg Psychiatry (1998) 0.98
Intermediates of peroxisomal beta-oxidation. A study of the fatty acyl-CoA esters which accumulate during peroxisomal beta-oxidation of [U-14C]hexadecanoate. Biochem J (1990) 0.97
A new simple screening method for the diagnosis of medium chain acyl-CoA dehydrogenase deficiency. Clin Chim Acta (1987) 0.95
Cytochrome bo from Escherichia coli: identification of haem ligands and reaction of the reduced enzyme with carbon monoxide. Biochem J (1993) 0.93
Intra-operative B-mode ultrasound scanning of the extra-hepatic biliary system and pancreas. Lancet (1980) 0.93
Thalamic hemorrhages in Wernicke-Korsakoff syndrome demonstrated by computed tomography. Ann Neurol (1988) 0.92
Operative ultrasonic features of insulinomas. Am J Surg (1982) 0.92
Hyperammonaemia--an important cause of encephalopathy: three case reports. Ann Clin Biochem (1993) 0.91
Electron transfer between cytochrome c and the isolated CuA domain: identification of substrate-binding residues in cytochrome c oxidase. Biochemistry (1995) 0.91
Persistence of enterovirus RNA in muscle biopsy samples suggests that some cases of chronic fatigue syndrome result from a previous, inflammatory viral myopathy. J Med (1993) 0.90
Familial amyotrophic lateral sclerosis with a point mutation of SOD-1: intrafamilial heterogeneity of disease duration associated with neurofibrillary tangles. J Neurol Neurosurg Psychiatry (1995) 0.90
Oculomotor function in amyotrophic lateral sclerosis: evidence for frontal impairment. Ann Neurol (1995) 0.90
Epsilon aminocaproic acid (EACA) myopathy. Postgrad Med J (1979) 0.88
Polyneuropathy in occult hypothyroidism. Postgrad Med J (1983) 0.87
Magnetic-circular-dichroism studies of Escherichia coli cytochrome bo. Identification of high-spin ferric, low-spin ferric and ferryl [Fe(IV)] forms of heme o. Eur J Biochem (1994) 0.87
Pseudoaxonal Guillain-Barré syndrome: severe demyelination mimicking axonopathy. A case with pupillary involvement. J Neurol Neurosurg Psychiatry (1992) 0.86
Repair of incompetent venous valves: a new technique. J Vasc Surg (1988) 0.86
Intermediates of beta-oxidation. Biochem Soc Trans (1988) 0.86
Limitations of intra-arterial thrombolysis. Cardiovasc Surg (1997) 0.86
Reaction of variant sperm-whale myoglobins with hydrogen peroxide: the effects of mutating a histidine residue in the haem distal pocket. Biochem J (1997) 0.86
Ultraviolet-laser ablation of skin. Arch Dermatol (1985) 0.86
Dermatomyositis in association with transitional cell carcinoma of the bladder. Clin Exp Dermatol (1999) 0.85
The relationship of spinal muscular atrophy to motor neuron disease: investigation of SMN and NAIP gene deletions in sporadic and familial ALS. J Neurol Sci (1997) 0.85
A double-blind, placebo-controlled, crossover study of verapamil in exertional muscle pain. Muscle Nerve (1986) 0.85
Reaction of carbon monoxide with the reduced active site of bacterial nitric oxide reductase. Biochemistry (2001) 0.85
Thymectomy in late-onset myasthenia gravis. Arch Neurol (1982) 0.85
A two-state analysis of co-operative oxygen binding in the three human embryonic haemoglobins. Biochem J (1997) 0.84
An evaluation of some carrier detection techniques in Duchenne muscular dystrophy. J Neurol Sci (1979) 0.84
Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy. Dev Med Child Neurol (1988) 0.84
Bifrontal glioma presenting as a gross movement disorder. Mov Disord (1993) 0.83
Wildervanck or cervico-oculo-acoustic syndrome and MRI findings. J Neurol Neurosurg Psychiatry (1991) 0.83
Electrocardiographic abnormalities in carriers of Duchenne muscular dystrophy. Neurology (1980) 0.83
A switch in heme axial ligation prepares Paracoccus pantotrophus cytochrome cd1 for catalysis. Nat Struct Biol (2000) 0.82
Nonfunctional paraganglioma of the larynx: clinical and pathological considerations. Cancer (1981) 0.82
Cytochrome bo from Escherichia coli: binding of azide to CuB. Biochemistry (1996) 0.81
Testosterone deficiency myopathy. J R Soc Med (1995) 0.80
Pediatric infectious cervical lymphadenitis. Otolaryngol Head Neck Surg (1985) 0.80
The reaction of Escherichia coli cytochrome bo with H2O2: evidence for the formation of an oxyferryl species by two distinct routes. FEBS Lett (1996) 0.80
Intramolecular electron transfer from c heme to d1 heme in bacterial cytochrome cd1 nitrite reductase occurs over the same distances at very different rates depending on the source of the enzyme. Biochemistry (2001) 0.79
The role of beta chains in the control of the hemoglobin oxygen binding function: chimeric human/mouse proteins, structure, and function. Biochemistry (2001) 0.79
Drug-induced neurological disorders. Drugs (1983) 0.79
Ultrasonic indications to explore the common bile duct. Surgery (1982) 0.79
Aneurysm of the internal carotid artery at the base of the skull: an unusual cause of cranial neuropathies. Otolaryngol Head Neck Surg (1979) (1980) 0.79
Oxidase reaction of cytochrome cd(1) from Paracoccus pantotrophus. Biochemistry (2000) 0.78
Defects of fatty acid oxidation in skeletal muscle. J Inherit Metab Dis (1987) 0.78
Operative ultrasonic bile duct scanning. Aust N Z J Surg (1979) 0.78
Neonatal myasthenia gravis in the infant of an asymptomatic thymectomized mother. Can J Neurol Sci (1982) 0.78
Ultraviolet laser ablation of skin: healing studies and a thermal model. Lasers Surg Med (1987) 0.78
Intraoperative B-mode scanning. J Clin Ultrasound (1980) 0.78
Clinical features and management of two cases of encephalitis lethargica. Mov Disord (1997) 0.78
Lymphocyte capping in myotonic dystrophy. J Neurol Neurosurg Psychiatry (1983) 0.78
The role of amino acid alpha38 in the control of oxygen binding to human adult and embryonic haemoglobin Portland. Biochem J (1999) 0.78
Carrier testing in families of isolated cases of duchenne muscular dystrophy. Creatine kinase activities in female relatives of mothers with normal CK activity. J Neurol Sci (1981) 0.78
A novel conformer of oxidized Paracoccus pantotrophus cytochrome cd(1) observed by freeze-quench NIR-MCD spectroscopy. Biochem Biophys Res Commun (2000) 0.77
Variation of serum creatine kinase levels with age in normal females: implications for genetic counselling in Duchenne muscular dystrophy. Clin Chim Acta (1981) 0.77
Trials of verapamil and dantrolene sodium in McArdle disease. Muscle Nerve (1984) 0.77
Investigation of a null mutation of the CNTF gene in familial amyotrophic lateral sclerosis. J Neurol Sci (1995) 0.77
Recent developments in the drug treatment of motor neurone disease. BMJ (1994) 0.76
Bilateral aneuralgic amyotrophy. Br Med J (1978) 0.76
Clinical characteristics of SOD1 gene mutations in UK families with ALS. J Neurol Sci (1999) 0.76
Opiate-induced rhabdomyolysis. Hum Toxicol (1985) 0.76
The reaction of halides with pulsed cytochrome bo from Escherichia coli. Biochem J (1998) 0.76
Real-time intraoperative angiosonography after carotid endarterectomy. Surgery (1982) 0.76
Difficulties in distinguishing sporadic from familial amyotrophic lateral sclerosis. Ann Neurol (1996) 0.76
Oxyphenbutazone-induced goitre. Postgrad Med J (1977) 0.75
Reversal of cognitive deficit by cardiac pacing in a young man with dystrophia myotonica. J R Soc Med (1991) 0.75
Cranial polyneuropathy and brainstem disorder at the time of seroconversion in HIV infection. Int J STD AIDS (1992) 0.75
Inclusion body myositis: a case with associated collagen vascular disease responding to treatment. J Neurol Neurosurg Psychiatry (1985) 0.75
Recurrent epistaxes in hereditary haemorrhagic telangiectasia. J R Soc Med (1997) 0.75
Antibodies to glutamic acid decarboxylase as predictors of insulin-dependent diabetes mellitus. Lancet (1994) 0.75
Asymptomatic carotid stenosis: how should it be managed. Med J Aust (1996) 0.75
Electron transfer kinetics of caa3 oxidase from Bacillus stearothermophilus: a hypothesis for thermophilicity. Biophys J (1999) 0.75
Development of Wolff-Parkinson-White syndrome in a patient with Friedreich's ataxia. J Neurol Neurosurg Psychiatry (1987) 0.75
Disposables: a time for reappraisal. Nurs Times (1974) 0.75
New mutations in Duchenne muscular dystrophy. Lancet (1988) 0.75
Percutaneous control of a portacaval H-graft: description of a new device and its initial clinical application. World J Surg (1990) 0.75