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Results of search for 'au:"Gabreĕls, F J"', page 3 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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41.
[Subdural empyema. The importance of rapid diagnosis].
[electronic resource]
by
Hageman, A T
Gabreëls, F J
De Coo, I F
Merx, J L
Producer:
19920302
In:
Tijdschrift voor kindergeneeskunde
vol. 59
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42.
[Future prospects for children with spina bifida aperta].
[electronic resource]
by
Rotteveel, J J
Mullaart, R A
Gabreels, F J
Van Overbeeke, J J
Producer:
19961202
In:
Nederlands tijdschrift voor geneeskunde
vol. 140
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43.
[Active euthanasia in newborn infants with spina bifida?].
[electronic resource]
by
Rotteveel, J J
Mullaart, R A
Gabreëls, F J
van Overbeeke, J J
Producer:
19961004
In:
Nederlands tijdschrift voor geneeskunde
vol. 140
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44.
Conversion disorders in childhood: a retrospective follow-up study of 84 inpatients.
[electronic resource]
by
Spierings, C
Poels, P J
Sijben, N
Gabreëls, F J
Renier, W O
Producer:
19910128
In:
Developmental medicine and child neurology
vol. 32
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45.
The Moya-Moya syndrome: a report of two children.
[electronic resource]
by
van Erven, P M
Gabreëls, F J
Thijssen, H O
Renier, W O
Producer:
19830317
In:
Clinical neurology and neurosurgery
vol. 84
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46.
Are muscle cramps in Isaacs' syndrome triggered by human immunoglobulin?
[electronic resource]
by
Van Engelen, B G
Benders, A A
Gabreels, F J
Veerkamp, J H
Producer:
19950427
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 58
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47.
Clinical features of Niemann-Pick disease type C. An example of the delayed onset, slowly progressive phenotype and an overview of recent literature.
[electronic resource]
by
van de Vlasakker, C J
Gabreëls, F J
Wijburg, H C
Wevers, R A
Producer:
19941024
In:
Clinical neurology and neurosurgery
vol. 96
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48.
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome.
[electronic resource]
by
Tranebjaerg, L
Hamel, B C
Gabreels, F J
Renier, W O
Van Ghelue, M
Producer:
20001016
In:
European journal of human genetics : EJHG
vol. 8
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49.
Spina bifida and parental occupation.
[electronic resource]
by
Blatter, B M
Roeleveld, N
Zielhuis, G A
Mullaart, R A
Gabreëls, F J
Producer:
19961204
In:
Epidemiology (Cambridge, Mass.)
vol. 7
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50.
Hyperkalemic periodic paralysis in Gordon's syndrome: a possible defect in atrial natriuretic peptide function.
[electronic resource]
by
Pasman, J W
Gabreëls, F J
Semmekrot, B
Renier, W O
Monnens, L A
Producer:
19891108
In:
Annals of neurology
vol. 26
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51.
Hereditary prothrombin deficiency presenting as intracranial haematoma in infancy.
[electronic resource]
by
Strijks, E
Poort, S R
Renier, W O
Gabreëls, F J
Bertina, R M
Producer:
20000316
In:
Neuropediatrics
vol. 30
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52.
Maternal occupational exposure during pregnancy and the risk of spina bifida.
[electronic resource]
by
Blatter, B M
Roeleveld, N
Zielhuis, G A
Gabreëls, F J
Verbeek, A L
Producer:
19960913
In:
Occupational and environmental medicine
vol. 53
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53.
Congenital myotonic dystrophy; a report on thirteen cases and a review of the literature.
[electronic resource]
by
Hageman, A T
Gabreëls, F J
Liem, K D
Renkawek, K
Boon, J M
Producer:
19930511
In:
Journal of the neurological sciences
vol. 115
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54.
Congenital fibre type disproportion a time-locked diagnosis: a clinical and morphological follow-up study.
[electronic resource]
by
Bartholomeus, M G
Gabreëls, F J
ter Laak, H J
van Engelen, B G
Producer:
20000822
In:
Clinical neurology and neurosurgery
vol. 102
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55.
Anomalies of the cerebral cortex in a case of epilepsia partialis continua.
[electronic resource]
by
Verhagen, W I
Renier, W O
ter Laak, H
Jaspar, H H
Gabreels, F J
Producer:
19880310
In:
Epilepsia
vol. 29
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56.
Mannosidosis: a study of two patients, presenting clinical heterogeneity.
[electronic resource]
by
Jansen, P H
Schoonderwaldt, H C
Renier, W O
Wevers, R A
Gabreëls, F J
Producer:
19871203
In:
Clinical neurology and neurosurgery
vol. 89
Online resources:
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57.
The status of HMSN type III.
[electronic resource]
by
Gabreëls-Festen, A A
Gabreëls, F J
Jennekens, F G
Janssen-van Kempen, T W
Producer:
19940608
In:
Neuromuscular disorders : NMD
vol. 4
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58.
Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency.
[electronic resource]
by
van Erven, P M
Gabreëls, F J
Ruitenbeek, W
Renier, W O
Fischer, J C
Producer:
19870723
In:
Archives of neurology
vol. 44
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59.
Neonatal status convulsivus, spongiform encephalopathy, and low activity of Na+/K(+)-ATPase in the brain.
[electronic resource]
by
Renkawek, K
Renier, W O
de Pont, J J
Vogels, O J
Gabreëls, F J
Producer:
19920228
In:
Epilepsia
vol. 33
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60.
Some patients with cerebro-macular degeneration in the cadre of Batten's disease.
[electronic resource]
by
Bolmers, D J
Gabreëls, F J
Joosten, E M
Gabreëls-Festen, A
Pinckers, A J
Producer:
19741226
In:
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde
vol. 169
Online resources:
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