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Results of search for 'au:"Gabreĕls, F J"', page 6 of 12
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Gabreels, F J
Gabreëls, F J
Gabreëls-Festen, A A
Janssen, A J
Joosten, E M
Keyser, A
Lamers, K J
Leyten, Q H
Mullaart, R A
Renier, W O
Rotteveel, J J
Ruitenbeek, W
Sengers, R C
Slooff, J L
Thijssen, H O
Trijbels, J M
Verrips, A
Wevers, R A
ter Laak, H J
van Engelen, B G
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101.
Phenotypic expression in mucopolysaccharidosis VII.
[electronic resource]
by
Bernsen, P L
Wevers, R A
Gabreëls, F J
Lamers, K J
Sonnen, A E
Stekhoven, J H
Producer:
19870902
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 50
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102.
Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver.
[electronic resource]
by
Prick, M J
Gabreëls, F J
Renier, W O
Trijbels, J M
Sengers, R C
Slooff, J L
Producer:
19820222
In:
Archives of neurology
vol. 38
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103.
Cerebrospinal fluid amino acids, purines and pyrimidines as a tool in the study of metabolic brain diseases.
[electronic resource]
by
Gerrits, G P
Monnens, L A
Gabreëls, F J
De Abreu, R A
Koster, A
Trijbels, J M
Producer:
19931122
In:
Journal of inherited metabolic disease
vol. 16
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104.
Hypokinesia and rigidity as clinical manifestations of mitochondrial encephalomyopathy: report of three cases.
[electronic resource]
by
van Erven, P M
Renier, W O
Gabreëls, F J
Thijssen, H O
Ruitenbeek, W
Horstink, M W
Producer:
19890417
In:
Developmental medicine and child neurology
vol. 31
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105.
Congenital muscular dystrophy with eye and brain malformations in six Dutch patients.
[electronic resource]
by
Leyten, Q H
Gabreëls, F J
Renier, W O
Renkawek, K
ter Laak, H J
Mullaart, R A
Producer:
19930302
In:
Neuropediatrics
vol. 23
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106.
Melanotic rhabdomyomedulloblastoma or teratoid tumour of the cerebellar vermis.
[electronic resource]
by
Duinkerke, S J
Slooff, J L
Gabreëls, F J
Renier, W O
Thijssen, H O
Biesta, J H
Producer:
19820222
In:
Clinical neurology and neurosurgery
vol. 83
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107.
Cerebrospinal fluid examinations in cryptogenic West and Lennox-Gastaut syndrome before and after intravenous immunoglobulin administration.
[electronic resource]
by
van Engelen, B G
Renier, W O
Weemaes, C M
Lamers, K J
Gabreels, F J
Meinardi, H
Producer:
19941207
In:
Epilepsy research
vol. 18
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108.
Congenital muscular dystrophy. A study on the variability of morphological changes and dystrophin distribution in muscle biopsies.
[electronic resource]
by
Leyten, Q H
ter Laak, H J
Gabreëls, F J
Renier, W O
Renkawek, K
Sengers, R C
Producer:
19940113
In:
Acta neuropathologica
vol. 86
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109.
Botulinum toxin A: a new option for treatment of drooling in children with cerebral palsy. Presentation of a case series.
[electronic resource]
by
Jongerius, P H
Rotteveel, J J
van den Hoogen, F
Joosten, F
van Hulst, K
Gabreëls, F J
Producer:
20020103
In:
European journal of pediatrics
vol. 160
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110.
Autosomal dominant paroxysmal kinesigenic choreoathetosis. An electroneurophysiological study.
[electronic resource]
by
Busard, H L
Renier, W O
Gabreëls, F J
Vos, A J
Declerck, A C
Verhey, F H
Producer:
19850206
In:
Clinical neurology and neurosurgery
vol. 86
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111.
Autosomal recessive form of hereditary motor and sensory neuropathy type I.
[electronic resource]
by
Gabreëls-Festen, A A
Gabreëls, F J
Jennekens, F G
Joosten, E M
Janssen-van Kempen, T W
Producer:
19921001
In:
Neurology
vol. 42
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112.
Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome).
[electronic resource]
by
van Erven, P M
Ruitenbeek, W
Gabreëls, F J
Renier, W O
Fischer, J C
Janssen, A J
Producer:
19860501
In:
Neuropediatrics
vol. 17
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113.
Measurement of radioactivity of pyruvate and other 2-oxo-acids labelled at the 1-position.
[electronic resource]
by
van Laack, H L
Janssen, A J
Ruitenbeek, W
Trijbels, J M
Sengers, R C
Gabreëls, F J
Producer:
19860609
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 156
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114.
Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.
[electronic resource]
by
van Erven, P M
Gabreëls, F J
Ruitenbeek, W
Renier, W O
Lamers, K J
Sloof, J L
Producer:
19870828
In:
Journal of neurology
vol. 234
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115.
A mentally retarded child with a translocation involving chromosomes 12 and 19.
[electronic resource]
by
Histinx, T W
Gabreëls, F J
Rutten, F J
Korten, I I
Scheres, J M
Joosten, E M
Producer:
19751011
In:
Journal of medical genetics
vol. 12
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116.
Multiple pterygium syndrome. A report of two unrelated cases.
[electronic resource]
by
Kok, J G
Gabreëls, F J
Renier, W O
ter Laak, H J
Slot, G H
Bouwsma, G
Producer:
19840822
In:
Clinical neurology and neurosurgery
vol. 86
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117.
Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study.
[electronic resource]
by
ter Laak, H J
Leyten, Q H
Gabreëls, F J
Kuppen, H
Renier, W O
Sengers, R C
Producer:
19980814
In:
Clinical neurology and neurosurgery
vol. 100
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118.
Preterm birth in Sjögren-Larsson syndrome.
[electronic resource]
by
Willemsen, M A
Rotteveel, J J
van Domburg, P H
Gabreëls, F J
Mayatepek, E
Sengers, R C
Producer:
20000316
In:
Neuropediatrics
vol. 30
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119.
Cerebrospinal neuron-specific enolase, S-100 and myelin basic protein in neurological disorders.
[electronic resource]
by
Lamers, K J
van Engelen, B G
Gabreëls, F J
Hommes, O R
Borm, G F
Wevers, R A
Producer:
19951222
In:
Acta neurologica Scandinavica
vol. 92
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120.
Disturbances of cerebral purine and pyrimidine metabolism in young children with chronic renal failure.
[electronic resource]
by
Gerrits, G P
Monnens, L A
De Abreu, R A
Schröder, C H
Trijbels, J M
Gabreëls, F J
Producer:
19911024
In:
Nephron
vol. 58
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