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Results of search for 'au:"Gabreĕls, F J"', page 7 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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121.
Dihydropyrimidine dehydrogenase deficiency. Neurological aspects.
[electronic resource]
by
Braakhekke, J P
Renier, W O
Gabreëls, F J
De Abreu, R A
Bakkeren, J A
Sengers, R C
Producer:
19870608
In:
Journal of the neurological sciences
vol. 78
Online resources:
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122.
Defect of NADH dehydrogenase in Leigh syndrome.
[electronic resource]
by
Van Erven, P M
Fischer, J C
Gabreëls, F J
Renier, W O
Trijbels, J M
Janssen, A J
Producer:
19861204
In:
Acta neurologica Scandinavica
vol. 74
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123.
Sural nerve biopsy in the diagnosis of progressive cerebral degenerative disorders of childhood. A retrospective study.
[electronic resource]
by
Vos, A J
Joosten, E M
Gabreëls-Festen, A A
Gabreëls, F J
Krijgsman, J B
Renier, W O
Producer:
19830617
In:
Clinical neurology and neurosurgery
vol. 84
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124.
An X-linked syndrome with microcephaly, severe mental retardation, spasticity, epilepsy and deafness.
[electronic resource]
by
Renier, W O
Gabreëls, F J
Jasper, H H
Hustinx, T W
Geelen, J A
van Haelst, U J
Producer:
19820719
In:
Journal of mental deficiency research
vol. 26
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125.
Treatment of leptomeningeal dissemination of medulloblastoma. Report of a case with a long-term survival.
[electronic resource]
by
Stevering, C J
Gabreëls, F J
Lippens, R J
Renier, W O
Thijssen, H O
ter Laak, H J
Producer:
19860409
In:
Clinical neurology and neurosurgery
vol. 87
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126.
Rhabdomyolysis and acute encephalopathy in late onset medium chain acyl-CoA dehydrogenase deficiency.
[electronic resource]
by
Ruitenbeek, W
Poels, P J
Turnbull, D M
Garavaglia, B
Chalmers, R A
Taylor, R W
Gabreëls, F J
Producer:
19950404
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 58
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127.
Spinal muscular atrophy combined with congenital heart disease: a report of two cases.
[electronic resource]
by
Mulleners, W M
van Ravenswaay, C M
Gabreëls, F J
Hamel, B C
van Oort, A
Sengers, R C
Producer:
19970512
In:
Neuropediatrics
vol. 27
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128.
Cranio-vertebral pathology in Down syndrome.
[electronic resource]
by
Braakhekke, J P
Gabreëls, F J
Renier, W O
van Rens, T J
Thijssen, H O
Begeer, J H
Producer:
19851216
In:
Clinical neurology and neurosurgery
vol. 87
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129.
Lafora's disease. Comparison of inclusion bodies in skin and in brain.
[electronic resource]
by
Busard, B L
Renier, W O
Gabreëls, F J
Jaspar, H H
van Haelst, U J
Slooff, J L
Producer:
19860320
In:
Archives of neurology
vol. 43
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130.
Calcium-phosphate metabolism in autosomal recessive idiopathic strio-pallido-dentate calcinosis and Cockayne's syndrome.
[electronic resource]
by
Smits, M G
Gabreëls, F J
Froeling, P G
de Abreu, R A
Thijssen, H O
Renier, W O
Producer:
19840107
In:
Clinical neurology and neurosurgery
vol. 85
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131.
The diagnostic value of sural nerve biopsy in metachromatic leucodystrophy and other conditions with low leucocyte arylsulphatase A activities.
[electronic resource]
by
Vos, A J
Joosten, E M
Gabreëls-Festen, A A
Gabreëls, F J
Notermans, S L
Lamers, K J
Producer:
19820719
In:
Neuropediatrics
vol. 13
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132.
Association of congenital muscular dystrophy with hypoplasia of the lateral abdominal wall musculature and hypoplasia of the external genitalia.
[electronic resource]
by
Leyten, Q H
Renier, W O
Gabreëls, F J
Brunner, H G
ter Laak, H J
Mullaart, R A
Producer:
19961118
In:
Neuropediatrics
vol. 27
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133.
Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.
[electronic resource]
by
Gabreëls-Festen, A A
Gabreëls, F J
Hoogendijk, J E
Bolhuis, P A
Jongen, P J
Vingerhoets, H M
Producer:
19940317
In:
Acta neuropathologica
vol. 86
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134.
Charcot-Marie-Tooth disease type 1A: morphological phenotype of the 17p duplication versus PMP22 point mutations.
[electronic resource]
by
Gabreëls-Festen, A A
Bolhuis, P A
Hoogendijk, J E
Valentijn, L J
Eshuis, E J
Gabreëls, F J
Producer:
19960605
In:
Acta neuropathologica
vol. 90
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135.
Cerebrospinal fluid levels of amino acids in infants and young children with chronic renal failure.
[electronic resource]
by
Gerrits, G P
Kamphuis, S
Monnens, L A
Trijbels, J M
Schröder, C H
Koster, A
Gabreëls, F J
Producer:
19980714
In:
Neuropediatrics
vol. 29
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136.
Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.
[electronic resource]
by
Gabreëls-Festen, A A
Joosten, E M
Gabreëls, F J
Jennekens, F G
Gooskens, R H
Stegeman, D F
Producer:
19911010
In:
Brain : a journal of neurology
vol. 114 ( Pt 4)
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137.
Psychometric assessment of families with X-linked mental retardation.
[electronic resource]
by
van Roosmalen, T
Smits, A P
Thoonen, G H
Hamel, B C
Assman-Hulmans, C F
Gabreels, F J
Producer:
19990610
In:
American journal of medical genetics
vol. 83
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138.
Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths.
[electronic resource]
by
Gabreëls-Festen, A A
Joosten, E M
Gabreëls, F J
Stegeman, D F
Vos, A J
Busch, H F
Producer:
19910301
In:
Brain : a journal of neurology
vol. 113 ( Pt 6)
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139.
Congenital muscular dystrophy.
[electronic resource]
by
Leyten, Q H
Gabreëls, F J
Renier, W O
Ter Laak, H J
Sengers, R C
Mullaart, R A
Producer:
19890829
In:
The Journal of pediatrics
vol. 115
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140.
A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.
[electronic resource]
by
Van Erven, P M
Gabreëls, F J
Ruitenbeek, W
Renier, W O
Ter Laak, H J
Stadhouders, A M
Producer:
19880915
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 51
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