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Multimorbidity, control and treatment of non-communicable diseases among primary healthcare attenders in the Western Cape, South Africa
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Published in Journal of computer assisted learning (01.04.2014)
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Dominant GDAP1 mutations cause predominantly mild CMT phenotypes
Zimoń, M, Baets, J, Fabrizi, G M, Jaakkola, E, Kabzińska, D, Pilch, J, Schindler, A B, Cornblath, D R, Fischbeck, K H, Auer-Grumbach, M, Guelly, C, Huber, N, De Vriendt, E, Timmerman, V, Suter, U, Hausmanowa-Petrusewicz, I, Niemann, A, Kochański, A, De Jonghe, P, Jordanova, A
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Mutations in the neurofilament light chain gene (NEFL) cause early onset severe Charcot–Marie–Tooth disease
Jordanova, A., De Jonghe, P., Boerkoel, C. F., Takashima, H., De Vriendt, E., Ceuterick, C., Martin, J.‐J., Butler, I. J., Mancias, P., Papasozomenos, S. Ch, Terespolsky, D., Potocki, L., Brown, C. W., Shy, M., Rita, D. A., Tournev, I., Kremensky, I., Lupski, J. R., Timmerman, V.
Published in Brain (London, England : 1878) (01.03.2003)
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Published in Neurology (31.03.2009)
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Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
Claeys, Kristl G., Züchner, Stephan, Kennerson, Marina, Berciano, José, Garcia, Antonio, Verhoeven, Kristien, Storey, Elsdon, Merory, John R., Bienfait, Henriette M. E., Lammens, Martin, Nelis, Eva, Baets, Jonathan, De Vriendt, Els, Berneman, Zwi N., De Veuster, Ilse, Vance, Jefferey M., Nicholson, Garth, Timmerman, Vincent, De Jonghe, Peter
Published in Brain (London, England : 1878) (01.07.2009)
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Socioeconomic and modifiable predictors of blood pressure control for hypertension in primary care attenders in the Western Cape, South Africa
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Next generation sequencing identifies a novel ATP7A mutation in two brothers with distal hereditary motor neuropathy and autonomic dysfunction
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Published in Neuromuscular disorders : NMD (01.10.2015)
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NeurOmics: EU-funded-omics research for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases
Turner, C, Brice, A, Bushby, K, Riess, O, Hanna, M, van Ommen, G, Muntoni, F, Klockgether, T, Wirth, B, Lochmüller, H, Timmerman, V, Schoells, L, Straub, V, Tabrizi, S
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Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy
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Published in Neurology (24.12.2002)
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G.P.237
Peeters, K, Litvinenko, I, Chamova, T, Asselbergh, B, Almeida-Souza, L, Geuens, T, Ydens, E, Zimon, M, Irobi, J, Vriendt, E. De, Winter, V. De, Ooms, T, Timmerman, V, Tournev, I, Jordanova, A
Published in Neuromuscular disorders : NMD (01.10.2014)
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The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot-Marie-Tooth phenotype
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Published in Brain (London, England : 1878) (01.02.1999)
Published in Brain (London, England : 1878) (01.02.1999)
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