Beneficial effect of a treatment with Xylitol in a patient with myoadenylate deaminase deficiency von BRUYLAND, M, EBINGER, G

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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis von Van der Zee, J, Gijselinck, I, Van Mossevelde, S, Perrone, F, Dillen, L, Heeman, B, Baumer, V, Engelborghs, S, De Bleecker, J, Baets, J, Gelpi, E, Rojas-Garcia, R, Clarimon, J, Lleo, A, Diehl-Schmid, J, Alexopoulos, P, Perneczky, R, Synofzik, M, Just, J, Schoels, L, Graff, C, Thonberg, H, Borroni, B, Padovani, A, Jordanova, A, Sarafov, S, Tournev, I, De Mendonca, A, Miltenberger-Miltenyi, G, Simoes do Couto, F, Ramirez, A, Jessen, F, Heneka, MT, Gomez-Tortosa, E, Danek, A, Cras, P, Vandenberghe, R, De Jonghe, P, De Deyn, PP, Sleegers, K, Cruts, M, Van Broeckhoven, C, Goeman, J, Nuytten, D, Smets, K, Robberecht, W, Van Damme, P, Santens, P, Dermaut, B, Versijpt, J, Michotte, A, Ivanoiu, A, Deryck, O, Bergmans, B, Delbeck, B, Bruyland, M, Willems, C, Salmon, E, Pastor, P, Ortega-Cubero, S, Benussi, L, Ghidoni, R, Binetti, G, Hernandez, I, Boada, M, Ruiz, A, Sorbi, S, Nacmias, B, Bagnoli, S, Sanchez-Valle, R, Llado, A, Santana, I, Almeida, MR, Frisoni, GB, Maetzler, W, Matej, R, Fraidakis, MJ, Kovacs, GG, Fabrizi, GM, Testi, S

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Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families von Broeckhoven, C. Van, Genthe, A. M, Vandenberghe, A, Horsthemke, B, Backhovens, H, Raeymaekers, P, Hul, W. Van, Wehnert, A, Gheuens, J, Cras, P, Bruyland, M, Martin, J. J, Salbaum, M, Multhaup, G, Masters, C. L, Beyreuther, K, Gurling, H. M. D, Mullan, M. J, Holland, A, Barton, A, Irving, N, Williamson, R, Richards, S. J, Hardy, J. A

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Molecular genetic analysis of familial early-onset Alzheimer's disease linked to chromosome 14q24.3 von Cruts, Marc, Backhovens, Hubert, Wang, Sheng-Yue, Van Gassen, Geert, Theuns, Jessie, De Jonghe, Chris, Wehnert, Anita, De Voecht, Joke, De Winter, Goedele, Cras, Patrick, Bruyland, Marc, Datson, Nicole, Weissenbach, Jean, Dunnen, Johan T.den, Martin, Jean-Jaques, Hendriks, Lydia, Van Broeckhoven, Christine

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Mapping of a gene predisposing to early-onset Alzheimer's disease to chromosome 14q24.3 von Van Broeckhoven, Christine, Backhovens, Hubert, Cruts, Marc, De Winter, Goedele, Bruyland, Marc, Cras, Patrick, Martin, Jean-Jacques

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Hypo-IgG in myotonic dystrophy is due to a selective reduction of the IgG1-subclass serum level von Bruyland, M, Lissens, W, De Waele, M, Demanet, C

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Dynamic training of skeletal muscle ventricles : a method to increase muscular power for cardiac assistance von GULDNER, N. W, EICHSTAEDT, H. C, MESSMER, B. J, BARDOS, P, KLAPPROTH, P, TILMANS, M. H. I, THUAUDET, S, UMBRAIN, V, RUCK, K, WYFFELS, E, BRUYLAND, M, SIGMUND, M

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Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder von St George-Hyslop, P. H, Haines, J. L, Farrer, L. A, Polinsky, R, Broeckhoven, C. Van, Goate, A, McLachlan, D. R. Crapper, Orr, H, Bruni, A. C, Sorbi, S, Rainero, I, Foncin, J.-F, Pollen, D, Cantu, J-M, Tupler, R, Voskresenskaya, N, Mayeux, R, Growdon, J, Fried, V. A, Myers, R. H, Nee, L, Backhovens, H, Martin, J-J, Rossor, M, Owen, M. J, Mullan, M, Percy, M. E, Karlinsky, H, Rich, S, Heston, L, Montesi, M, Mortilla, M, Nacmias, N, Gusella, J. F, Hardy, J. A

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Idiopathic hemiparetic parkinsonism, a syndrome distinct from idiopathic parkinsonism von de Keyser, J., Herroelen, L., Vervaeck, M., Bruyland, M., Ebinger, G.

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Distribution of biogenic amines and their catabolites in brains from patients with Alzheimer's disease von Ebinger, G., Bruyland, M., Martin, J.J., Herregodts, P., Cras, P., Michotte, Y., Gommé, L.

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Sudden hearing loss and facial palsy at the contralateral side following acoustic tumour removal von de Keyser, J, Bruyland, M, Demol, P, Klaes, R, Ebinger, G

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Neonatal myotubular myopathy with a probable X-linked inheritance: observations on a new family with a review of the literature von BRUYLAND, M, LIEBAERS, I, SACRE, L, VANDEPLAS, Y, DE MEIRLEIR, L, MARTIN, J. J

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Recurrent forms of sporadic brachial plexus neuropathy. A report of two cases von MICHOTTE, A, DIERCKX, R, DELEU, R, HERREGODTS, P, SCHMEDDING, E, BRUYLAND, M, EBINGER, G

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Enophthalmos as a rare manifestation of metastatic orbital involvement von de Keyser, J., Bruyland, M., de Greve, J., Bernheim, J., Ebinger, G.

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Pleocore disease: multi-minicore disease and focal loss of cross striations von MARTIN, J. J, BRUYLAND, M, BUSCH, H. F. M, FARRIAUX, J. P, KRIVOSIC, I, CEUTERICK, C

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Osteopathia striata with cranial sclerosis: Report of a case and review of the literature von De Keyser, J., Bruyland, M., De Greve, J., Leemans, J., Potvliege, R., Six, R., Ebinger, G.

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Lower motor neuron disease in a patient with hodgkin's disease treated with radiotherapy von De Greve, Jacques L.P., Bruyland, Marc, De Keyser, Jacques, Storme, Guy, Ebinger, Guy

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An unusual cause of attacks of focal cerebral symptoms: Multiple endocrine neoplasia type IIa von Bruyland, M., Verbruggen, L., Maes, E., Six, R., Somers, G., Ebinger, G.

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Two novel mutations of the porphobilinogen deaminase gene in acute intermittent porphyria von Gu, Xue-Fan, de Rooij, Felix, de Baar, Ellen, Bruyland, Marc, Lissens, Willy, Nordmann, Yves, Grandchamp, Bernard

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Monoaminergic neurotransmitters in Alzheimer's disease: An HPLC study comparing presenile familial and sporadic senile cases von Herregodts, Patrick, Bruyland, Marc, De Keyser, Jacques, Solheid, Claude, Michotte, Yvette, Ebinger, Guy

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