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Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a). [electronic resource] by
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- Gabreëls-Festen, A A
- Hensels, G W
- Joosten, E M
- Gabreëls, F J
- Zorn, I
- Valentijn, L J
- Baas, F
- Ongerboer de Visser, B W
Producer: 19930611
In:
Neurology vol. 43
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222.
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Sjögren-Larsson syndrome: clinical and MRI/MRS findings in FALDH-deficient patients. [electronic resource] by
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- Willemsen, M A
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- de Jong, J G
- Thijssen, H O
- Heerschap, A
- Cruysberg, J R
- Wanders, R J
- Gabreëls, F J
- Steijlen, P M
Producer: 19990517
In:
Neurology vol. 52
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223.
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Peripheral and central myelinopathy in Cockayne's syndrome. Report of 3 siblings. [electronic resource] by
- Smits, M G
- Gabreëls, F J
- Renier, W O
- Joosten, E M
- Gabreëls-Festen, A A
- ter Laak, H J
- Pinckers, A J
- Hombergen, G C
- Notermans, S L
- Thijssen, H O
Producer: 19821218
In:
Neuropediatrics vol. 13
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Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis. [electronic resource] by
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- Nijeholt, G J
- Barkhof, F
- Van Engelen, B G
- Wesseling, P
- Luyten, J A
- Wevers, R A
- Stam, J
- Wokke, J H
- van den Heuvel, L P
- Keyser, A
- Gabreëls, F J
Producer: 19990907
In:
Brain : a journal of neurology vol. 122 ( Pt 8)
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Coxsackie B1 virus-induced murine myositis: a correlative study of muscular lesions and serological changes. [electronic resource] by
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- Heessen, F W
- Bergmann, I
- de Waal, R M
- ter Laak, H J
- Galama, J M
- van Venrooij, W J
- Gabreels, F J
- van de Putte, L B
- Berden, J H
Producer: 19950420
In:
Journal of autoimmunity vol. 7
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Hereditary neuropathy with liability to pressure palsies. Phenotypic differences between patients with the common deletion and a PMP22 frame shift mutation. [electronic resource] by
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- Gabreëls-Festen, A A
- Valentijn, L J
- Jongen, P J
- van Beersum, S E
- van Engelen, B G
- van Wensen, P J
- Bolhuis, P A
- Gabreëls, F J
- Mariman, E C
Producer: 19980911
In:
Brain : a journal of neurology vol. 121 ( Pt 8)
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227.
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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease. [electronic resource] by
- Gabreëls-Festen, A A
- Hoogendijk, J E
- Meijerink, P H
- Gabreëls, F J
- Bolhuis, P A
- van Beersum, S
- Kulkens, T
- Nelis, E
- Jennekens, F G
- de Visser, M
- van Engelen, B G
- Van Broeckhoven, C
- Mariman, E C
Producer: 19961122
In:
Neurology vol. 47
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Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia. [electronic resource] by
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- van Engelen, B G M
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- Broeks, A
- Verrips, A
- ter Laak, H
- Vingerhoets, H M
- van den Heuvel, L P W
- Lammens, M
- Gabreëls, F J M
- Last, J I
- Taylor, A M R
Producer: 20060814
In:
Neurology vol. 67
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The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients. [electronic resource] by
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- Christensen, E
- Jakobs, C
- Fowler, B
- Clarke, M A
- Hammersen, G
- Raab, K
- Kobori, J
- Moosa, A
- Vollmer, B
- Rossier, E
- Iafolla, A K
- Matern, D
- Brouwer, O F
- Finkelstein, J
- Aksu, F
- Weber, H P
- Bakkeren, J A
- Gabreels, F J
- Bluestone, D
- Barron, T F
- Beauvais, P
- Rabier, D
- Santos, C
- Lehnert, W
Producer: 19970425
In:
Pediatrics vol. 99
Availability: No items available.
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