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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
Polyglucosan bodies in intramuscular motor nerves.
Bernsen RA, Busard HL, Ter Laak HJ, Gabreëls FJ, Renier WO, Joosten EM, Theeuwes AG. Bernsen RA, et al. Among authors: joosten em. Acta Neuropathol. 1989;77(6):629-33. doi: 10.1007/BF00687891. Acta Neuropathol. 1989. PMID: 2546356
The rigid spine syndrome.
van Munster ET, Joosten EM, van Munster-Uijtdehaage MA, Kruls HJ, ter Laak HJ. van Munster ET, et al. Among authors: joosten em. J Neurol Neurosurg Psychiatry. 1986 Nov;49(11):1292-7. doi: 10.1136/jnnp.49.11.1292. J Neurol Neurosurg Psychiatry. 1986. PMID: 3025374 Free PMC article.
Chronic inflammatory demyelinating polyneuropathy in two siblings.
Gabreëls-Festen AA, Hageman AT, Gabreëls FJ, Joosten EM, Renier WO, Weemaes CM, ter Laak HJ. Gabreëls-Festen AA, et al. Among authors: joosten em. J Neurol Neurosurg Psychiatry. 1986 Feb;49(2):152-6. doi: 10.1136/jnnp.49.2.152. J Neurol Neurosurg Psychiatry. 1986. PMID: 3456424 Free PMC article.
An autosomal dominant type of congenital muscular dystrophy.
Leyten QH, Gabreëls FJ, Joosten EM, Renier WO, Ter Laak HJ, Ter Haar BG, Stadhouders AM. Leyten QH, et al. Among authors: joosten em. Brain Dev. 1986;8(5):533-7. doi: 10.1016/s0387-7604(86)80099-7. Brain Dev. 1986. PMID: 3799922
Congenital fibre type disproportion.
ter Laak HJ, Jaspar HH, Gabreëls FJ, Breuer TJ, Sengers RC, Joosten EM, Stadhouders AM, Gabreëls-Festen AA. ter Laak HJ, et al. Among authors: joosten em. Clin Neurol Neurosurg. 1981;83(2):67-79. doi: 10.1016/0303-8467(81)90004-4. Clin Neurol Neurosurg. 1981. PMID: 6271433
88 results