Joosten EM - Search Results

1

Pyruvate carboxylase activity is not abnormal in fibroblasts of patients with Friedreich's ataxia.

Dijkstra UJ, Trijbels JM, Ruitenbeek W, Bakkeren JA, Janssen AJ, Gabreëls FJ, Joosten EM. Dijkstra UJ, et al. Among authors: joosten em. Ann Neurol. 1984 Aug;16(2):262. doi: 10.1002/ana.410160220. Ann Neurol. 1984. PMID: 6476800 No abstract available.

2

Friedreich's ataxia: intravenous pyruvate load to demonstrate a defect in pyruvate metabolism.

Dijkstra U, Gabreëls F, Joosten E, Wevers R, Lamers K, Doesburg W, Renier W. Dijkstra U, et al. Neurology. 1984 Nov;34(11):1493-7. doi: 10.1212/wnl.34.11.1493. Neurology. 1984. PMID: 6493499

3

Friedreich ataxia and low pyruvate carboxylase activity in liver and fibroblasts.

Dijkstra UJ, Willems JL, Joosten EM, Gabreëls FJ. Dijkstra UJ, et al. Among authors: joosten em. Ann Neurol. 1983 Mar;13(3):325-7. doi: 10.1002/ana.410130317. Ann Neurol. 1983. PMID: 6847147

4

Autosomal recessive form of hereditary motor and sensory neuropathy type I.

Gabreëls-Festen AA, Gabreëls FJ, Jennekens FG, Joosten EM, Janssen-van Kempen TW. Gabreëls-Festen AA, et al. Among authors: joosten em. Neurology. 1992 Sep;42(9):1755-61. doi: 10.1212/wnl.42.9.1755. Neurology. 1992. PMID: 1513466

5

Adult polyglucosan body disease: the diagnostic value of axilla skin biopsy.

Busard HL, Gabreëls-Festen AA, Renier WO, Gabreëls FJ, Joosten EM, van 't Hof MA, Rensing JB. Busard HL, et al. Among authors: joosten em. Ann Neurol. 1991 Apr;29(4):448-51. doi: 10.1002/ana.410290420. Ann Neurol. 1991. PMID: 1656844

6

Familial adult-onset muscular dystrophy with leukoencephalopathy.

van Engelen BG, Leyten QH, Bernsen PL, Gabreëls FJ, Barkhof F, Joosten EM, Hamel BC, ter Laak HJ, Ruijs MB, Cruysberg JR, et al. van Engelen BG, et al. Among authors: joosten em. Ann Neurol. 1992 Oct;32(4):577-80. doi: 10.1002/ana.410320415. Ann Neurol. 1992. PMID: 1456743

7

Sensory axonopathy in hereditary distal spinal muscular atrophy.

Frequin ST, Gabreëls FJ, Gabreëls-Festen AA, Joosten EM. Frequin ST, et al. Among authors: joosten em. Clin Neurol Neurosurg. 1991;93(4):323-6. doi: 10.1016/0303-8467(91)90099-b. Clin Neurol Neurosurg. 1991. PMID: 1665767

8

Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a).

Hoogendijk JE, Janssen EA, Gabreëls-Festen AA, Hensels GW, Joosten EM, Gabreëls FJ, Zorn I, Valentijn LJ, Baas F, Ongerboer de Visser BW, et al. Hoogendijk JE, et al. Among authors: joosten em. Neurology. 1993 May;43(5):1010-5. doi: 10.1212/wnl.43.5.1010. Neurology. 1993. PMID: 8492918

9

Madopar versus sinemet. A clinical study on their effectiveness.

Korten JJ, Keyser A, Joosten EM, Gabreëls FJ. Korten JJ, et al. Among authors: joosten em. Eur Neurol. 1975;13(2):65-71. doi: 10.1159/000114663. Eur Neurol. 1975. PMID: 1095374 Clinical Trial.

10

Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.

Gabreëls-Festen AA, Joosten EM, Gabreëls FJ, Jennekens FG, Gooskens RH, Stegeman DF. Gabreëls-Festen AA, et al. Among authors: joosten em. Brain. 1991 Aug;114 ( Pt 4):1855-70. doi: 10.1093/brain/114.4.1855. Brain. 1991. PMID: 1884182

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