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Results of search for 'au:"Gabreĕls, F J"', page 5 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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81.
A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome.
[electronic resource]
by
de Vries, D D
van Engelen, B G
Gabreëls, F J
Ruitenbeek, W
van Oost, B A
Producer:
19930930
In:
Annals of neurology
vol. 34
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82.
Heterogeneity of spina bifida.
[electronic resource]
by
Blatter, B M
Lafeber, A B
Peters, P W
Roeleveld, N
Verbeek, A L
Gabreëls, F J
Producer:
19970930
In:
Teratology
vol. 55
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83.
[Development and developmental disorders of the human brain. III. Neuronal migration disorders of the cerebrum].
[electronic resource]
by
ten Donkelaar, H J
Lammens, M
Wesseling, P
Thijssen, H O
Renier, W O
Gabreëls, F J
Producer:
20010521
In:
Nederlands tijdschrift voor geneeskunde
vol. 145
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84.
[Development and developmental disorders of the human brain. II. Development of the cerebral cortex and major tract systems].
[electronic resource]
by
ten Donkelaar, H J
Wesseling, P
Lammens, M
Thijssen, H O
Renier, W O
Gabreëls, F J
Producer:
20010503
In:
Nederlands tijdschrift voor geneeskunde
vol. 145
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85.
Chronic inflammatory demyelinating polyneuropathy as a complication of cat scratch disease.
[electronic resource]
by
McNeill, P M
Verrips, A
Mullaart, R
Gabreëls, F J
Gabreëls-Festen, A W
Knibbeler, J G
Producer:
20000626
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 68
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86.
Effect of thymectomy on myasthenia gravis and autoimmune thrombocytopenic purpura in a 13-year-old girl.
[electronic resource]
by
Jansen, P H
Renier, W O
de Vaan, G
Reekers, P
Vingerhoets, D M
Gabreëls, F J
Producer:
19880309
In:
European journal of pediatrics
vol. 146
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87.
Abeta fibers mediate cutaneous reflexes during human walking.
[electronic resource]
by
van Wezel, B M
van Engelen, B G
Gabreëls, F J
Gabreëls-Festen, A A
Duysens, J
Producer:
20000614
In:
Journal of neurophysiology
vol. 83
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88.
[Three hypotonic neonates with hypertrophic cardiomyopathy: Pompe's disease].
[electronic resource]
by
Willemsen, M A
Jira, P E
Gabreëls, F J
van der Ploeg, A T
Smeitink, J A
Producer:
19981030
In:
Nederlands tijdschrift voor geneeskunde
vol. 142
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89.
Recessively inherited 'pure' spastic paraplegia: case study.
[electronic resource]
by
de Coo, I F
Gabreëls, F J
Renier, W O
Colon, E J
ter Haar, B G
Producer:
19830617
In:
Clinical neurology and neurosurgery
vol. 84
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90.
Multicore myopathy with restrictive cardiomyopathy.
[electronic resource]
by
Willemsen, M A
van Oort, A M
ter Laak, H J
Sengers, R C
Gabreëls, F J
Producer:
19980113
In:
Acta paediatrica (Oslo, Norway : 1992)
vol. 86
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91.
Molecular genetic analysis of human folate receptors in neural tube defects.
[electronic resource]
by
Heil, S G
van der Put, N M
Trijbels, F J
Gabreëls, F J
Blom, H J
Producer:
19990628
In:
European journal of human genetics : EJHG
vol. 7
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92.
Scheie syndrome presenting as myopathy.
[electronic resource]
by
Verrips, A
van Engelen, B G
ter Laak, H
Wesseling, P
de Jong, J
Gabreëls, F J
Producer:
20011204
In:
Neuropediatrics
vol. 32
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93.
Polyglucosan bodies in sural nerve biopsies.
[electronic resource]
by
Busard, H L
Gabreëls-Festen, A A
van 't Hof, M A
Renier, W O
Gabreëls, F J
Producer:
19910117
In:
Acta neuropathologica
vol. 80
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94.
Pyruvate metabolism in Lafora disease.
[electronic resource]
by
Busard, H L
Renier, W O
Gabreëls, F J
Trijbels, J M
Janssen, A J
Lamers, K J
Producer:
19890707
In:
Epilepsia
vol. 30
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95.
Benign (nonparoxysmal) familial chorea of early onset: an electroneurophysiological examination of two families.
[electronic resource]
by
Stapert, J L
Busard, B L
Gabreëls, F J
Renier, W O
Colon, E J
Verhey, F H
Producer:
19850627
In:
Brain & development
vol. 7
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96.
Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I).
[electronic resource]
by
Gabreëls-Festen, A A
Joosten, E M
Gabreëls, F J
Jennekens, F G
Janssen-van Kempen, T W
Producer:
19920521
In:
Journal of the neurological sciences
vol. 107
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97.
Ileus in mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes.
[electronic resource]
by
Hiel, J A
Verrips, A
Keyser, A
Jansen, T L
Wesseling, P
de Coo, R
Gabreëls, F J
Producer:
19980917
In:
The Netherlands journal of medicine
vol. 53
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98.
Dihydrothymine dehydrogenase deficiency in a family, leading to elevated levels of uracil and thymine.
[electronic resource]
by
De Abreu, R A
Bakkeren, J A
Braakhekke, J
Gabreels, F J
Maas, J M
Sengers, R C
Producer:
19860805
In:
Advances in experimental medicine and biology
vol. 195 Pt A
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99.
Acute transverse myelopathy as the initial manifestation of probable systemic lupus erythematosus in a child.
[electronic resource]
by
Linssen, W H
Fiselier, T J
Gabreëls, F J
Wevers, R A
Cuppen, M P
Rotteveel, J J
Producer:
19890207
In:
Neuropediatrics
vol. 19
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100.
Early infantile form of neuronal ceroid lipofuscinosis. Four Dutch cases and review of the literature.
[electronic resource]
by
Jongen, P J
Gabreëls, F J
Stekhoven, J H
Renier, W O
le Coultre, R
Begeer, J H
Producer:
19871203
In:
Clinical neurology and neurosurgery
vol. 89
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