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Results of search for 'au:"Mercelis, R"', page 1 of 2
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Authors
Akagi, R
Amrom, D
Bracke, P
Bruyninckx, F
Buyssens, N
Ceuterick, C
Chiorazzi, N
Claes, A
Colebunders, R
Cras, P
De Clerck, L S
Garbaczewski, L
Hassoun, A
Horie, Y
Martin, J J
Mercelis, R
Sassa, S
Van den Berghe, G
Verstraeten, L
de Barsy, T
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Topics
Adolescent
Adult
Aged
Biopsy
Electromyography
Female
Humans
Male
Microscopy, Electron
Middle Aged
Motor Neurons
Muscles
Muscular Atrophy
Porphobilinogen Synthase
complications
deficiency
diagnosis
enzymology
pathology
physiology
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English
Your search returned 23 results.
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1.
Electromyography.
[electronic resource]
by
Mercelis, R
Producer:
19860821
In:
Acta oto-rhino-laryngologica Belgica
vol. 40
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2.
Neurophysiological studies in adrenomyeloneuropathy. A report on five cases.
[electronic resource]
by
Vercruyssen, A
Martin, J J
Mercelis, R
Producer:
19830225
In:
Journal of the neurological sciences
vol. 56
Online resources:
Available from publisher's website
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3.
alpha-D-mannosidases in I-cells [proceedings].
[electronic resource]
by
Van Elsen, A
Claes, A
Mercelis, R
Producer:
19800215
In:
Archives internationales de physiologie et de biochimie
vol. 87
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4.
Neurogenic scapuloperoneal syndrome in childhood.
[electronic resource]
by
Mercelis, R
Demeester, J
Martin, J J
Producer:
19810219
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 43
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5.
Arylsulphatases A and B in human diploid fibroblasts: differential assay with 4-methylumbelliferylsulphate and AgNO3.
[electronic resource]
by
Mercelis, R
Van Elsen, A F
Leroy, J G
Producer:
19790716
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 93
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6.
Bulbo-spinal lower motor neuron disease. Accumulation of neurofilaments in perikarya and axons.
[electronic resource]
by
Martin, J J
Mercelis, R
Dua, G
Moens, E
Producer:
19830127
In:
Acta neurologica Belgica
vol. 82
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7.
Centronuclear myopathy: follow-up study of a case reported as an early onset myopathy (1966): muscle biopsies in parents and sibs.
[electronic resource]
by
Mercelis, R
Martin, J J
Martin, L
Ceuterick, C
Producer:
19810421
In:
Acta neurologica Belgica
vol. 80
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8.
Biochemical diagnosis of an hereditary aminolaevulinate dehydratase deficiency in a 63-year-old man.
[electronic resource]
by
Hassoun, A
Verstraeten, L
Mercelis, R
Martin, J J
Producer:
19900130
In:
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie
vol. 27
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9.
Familial periodic paralysis with hypokalaemia. Study of a muscle biopsy in the myopathic stage of the disorder.
[electronic resource]
by
Martin, J J
Ceuterick, C
Mercelis, R
Amrom, D
Producer:
19850228
In:
Acta neurologica Belgica
vol. 84
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10.
Symptomatic sarcoid myopathy with minimal involvement of the peripheral nerves.
[electronic resource]
by
Colebunders, R
Mercelis, R
Buyssens, N
Martin, J J
Producer:
19840614
In:
Acta clinica Belgica
vol. 39
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11.
Pathology of peripheral nerves in metachromatic leucodystrophy. A comparative study of ten cases.
[electronic resource]
by
Martin, J J
Ceuterick, C
Mercelis, R
Joris, C
Producer:
19820412
In:
Journal of the neurological sciences
vol. 53
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12.
Cardiac manifestations of Becker-type muscular dystrophy.
[electronic resource]
by
Vrints, C
Mercelis, R
Vanagt, E
Snoeck, J
Martin, J J
Producer:
19840214
In:
Acta cardiologica
vol. 38
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13.
Dysphagia in a patient with giant osteophytes: case presentation and review of the literature.
[electronic resource]
by
Ebo, D
Goethals, L
Bracke, P
Mercelis, R
De Clerck, L S
Producer:
20000525
In:
Clinical rheumatology
vol. 19
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14.
Porphyric neuropathy and hereditary delta-aminolevulinic acid dehydratase deficiency in an adult.
[electronic resource]
by
Mercelis, R
Hassoun, A
Verstraeten, L
De Bock, R
Martin, J J
Producer:
19900620
In:
Journal of the neurological sciences
vol. 95
Online resources:
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15.
Myoadenylate deaminase deficiency: absence of correlation with exercise intolerance in 452 muscle biopsies.
[electronic resource]
by
Mercelis, R
Martin, J J
de Barsy, T
Van den Berghe, G
Producer:
19871117
In:
Journal of neurology
vol. 234
Online resources:
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16.
Value of somatosensory and motor evoked potentials in predicting arm recovery after a stroke.
[electronic resource]
by
Feys, H
Van Hees, J
Bruyninckx, F
Mercelis, R
De Weerdt, W
Producer:
20000421
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 68
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17.
Hereditary hepatic porphyria due to homozygous delta-aminolevulinic acid dehydratase deficiency: studies in lymphocytes and erythrocytes.
[electronic resource]
by
Sassa, S
Fujita, H
Doss, M
Hassoun, A
Verstraeten, L
Mercelis, R
Kappas, A
Producer:
19910808
In:
European journal of clinical investigation
vol. 21
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18.
Myoadenylate deaminase deficiency in a patient with facial and limb girdle myopathy.
[electronic resource]
by
Mercelis, R
Martin, J J
Dehaene, I
de Barsy, T
Van den Berghe, G
Producer:
19811025
In:
Journal of neurology
vol. 225
Online resources:
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19.
Patient homozygous for a recessive POLG mutation presents with features of MERRF.
[electronic resource]
by
Van Goethem, G
Mercelis, R
Löfgren, A
Seneca, S
Ceuterick, C
Martin, J J
Van Broeckhoven, C
Producer:
20040203
In:
Neurology
vol. 61
Online resources:
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20.
Postural control and the relation with cervical sensorimotor control in patients with idiopathic adult-onset cervical dystonia.
[electronic resource]
by
De Pauw, J
Mercelis, R
Hallemans, A
Van Gils, G
Truijen, S
Cras, P
De Hertogh, W
Producer:
20190129
In:
Experimental brain research
vol. 236
Online resources:
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