Transforming Parkinson's Care in Africa (TraPCAf): protocol for a multimethodology National Institute for Health and Care Research Global Health Research Group project
Walker, R, Fothergill-Misbah, N, Kariuki, S, Ojo, O, Cilia, R, Dekker, M. C. J, Agabi, O, Akpalu, A, Amod, F, Breckons, M, Cham, M, Del Din, S, Dotchin, C, Guggsa, S, Kwasa, J, Mushi, D, Nwaokorie, F. O, Park, T, Rochester, L, Rogathi, J, Sarfo, F. S, Shalash, A, Ternent, L, Urasa, S, Okubadejo, N
Published in BMC neurology (19.10.2023)
Published in BMC neurology (19.10.2023)
Get full text
Journal Article
Parkinson’s disease: piecing together a genetic jigsaw
Dekker, M. C. J., Bonifati, V., van Duijn, C. M.
Published in Brain (London, England : 1878) (01.08.2003)
Published in Brain (London, England : 1878) (01.08.2003)
Get full text
Journal Article
A clinical-genetic study of Parkinson's disease in a genetically isolated community
DEKKER, M. C. J, VAN SWIETEN, J. C, HOUWING-DUISTERMAAT, J. J, SNIJDERS, P. J. L. M, BOEREN, E, HOFMAN, A, BRETELER, M. M. B, HEUTINK, P, OOSTRA, B. A, VAN DUIJN, C. M
Published in Journal of neurology (01.09.2003)
Published in Journal of neurology (01.09.2003)
Get full text
Journal Article
Freeman–Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa
Hamel, Ben C. J., Kamsteeg, E.-J., Kinabo, Grace, Mbwasi, R. M., Ali, A. M., Dekker, Marieke C. J.
Published in Case reports in genetics (01.01.2017)
Published in Case reports in genetics (01.01.2017)
Get full text
Journal Article
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
Di Fonzo, A, Dekker, M C J, Montagna, P, Baruzzi, A, Yonova, E H, Correia Guedes, L, Szczerbinska, A, Zhao, T, Dubbel-Hulsman, L O M, Wouters, C H, de Graaff, E, Oyen, W J G, Simons, E J, Breedveld, G J, Oostra, B A, Horstink, M W, Bonifati, V
Published in Neurology (20.01.2009)
Published in Neurology (20.01.2009)
Get more information
Journal Article
PRKN-related familial Parkinson's disease: First molecular confirmation from East Africa
Dekker, M.C.J., Suleiman, J.M., Bhwana, D., Howlett, W.P., Rashid, S.M., van Minkelen, R., Hamel, B.C.
Published in Parkinsonism & related disorders (01.04.2020)
Published in Parkinsonism & related disorders (01.04.2020)
Get full text
Journal Article
First familial Becker muscular dystrophy in Tanzania: Clinical and genetic features
Dekker, M.C.J., Tieleman, A.A., Igogo, O.J., van Duyvenvoorde, H.A., Howlett, W.P., Hamel, B.C.
Published in Neuromuscular disorders : NMD (01.04.2019)
Published in Neuromuscular disorders : NMD (01.04.2019)
Get full text
Journal Article
Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene
Ebberink, Merel S, Csanyi, Barbara, Chong, Wui K, Denis, Simone, Sharp, Peter, Mooijer, Petra A W, Dekker, Conny J M, Spooner, Claire, Ngu, Lock H, De Sousa, Carlos, Wanders, Ronald J A, Fietz, Michael J, Clayton, Peter T, Waterham, Hans R, Ferdinandusse, Sacha
Published in Journal of medical genetics (01.09.2010)
Published in Journal of medical genetics (01.09.2010)
Get full text
Journal Article
PET neuroimaging and mutations in the DJ-1 gene
Dekker, M C J, Eshuis, S A, Maguire, R P, Veenma-van der Duijn, L, Pruim, J, Snijders, P J L M, Oostra, B A, van Duijn, C M, Leenders, K L
Published in Journal of Neural Transmission (01.12.2004)
Published in Journal of Neural Transmission (01.12.2004)
Get full text
Journal Article
PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36
van Duijn, C.M., Dekker, M.C.J., Bonifati, V., Galjaard, R.J., Houwing-Duistermaat, J.J., Snijders, P.J.L.M., Testers, L., Breedveld, G.J., Horstink, M., Sandkuijl, L.A., van Swieten, J.C., Oostra, B.A., Heutink, P.
Published in American journal of human genetics (01.09.2001)
Published in American journal of human genetics (01.09.2001)
Get full text
Journal Article
Posterior Glenoid Augmentation With Extra-articular Iliac Crest Autograft for Recurrent Posterior Shoulder Instability
Arner, Justin W., Elrick, Bryant P., Nolte, Philip-C., Goldenberg, Brandon, Dekker, Travis J., Millett, Peter J.
Published in Arthroscopy techniques (Amsterdam) (01.09.2020)
Published in Arthroscopy techniques (Amsterdam) (01.09.2020)
Get full text
Journal Article
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7
Bonifati, V, Dekker, M C J, Vanacore, N, Fabbrini, G, Squitieri, F, Marconi, R, Antonini, A, Brustenghi, P, Dalla Libera, A, De Mari, M, Stocchi, F, Montagna, P, Gallai, V, Rizzu, P, van Swieten, J C, Oostra, B, van Duijn, C M, Meco, G, Heutink, P
Published in Neurological sciences (01.09.2002)
Published in Neurological sciences (01.09.2002)
Get full text
Journal Article
PARK7, a novel locus for autosomal recessive early-onset Parkinsonism, on chromosome 1 p36
VAN DUIJN, C. M, DEKKER, M. C. J, VAN SWIETEN, J. C, OOSTRA, B. A, HEUTINK, P, BONIFATI, V, GALJAARD, R. J, HOUWING-DUISTERMAAT, J. J, SNIJDERS, P. J. L. M, TESTERS, L, BREEDVELD, G. J, HORSTINK, M, SANDKUIJL, L. A
Published in American journal of human genetics (2001)
Get full text
Published in American journal of human genetics (2001)
Journal Article
Longitudinal Analysis of Body Weight and Feed Intake in Selection Lines for Residual Feed Intake in Pigs
Cai, W, Wu, H, Dekkers, J.C.M
Published in Asian-australasian journal of animal sciences (01.01.2011)
Published in Asian-australasian journal of animal sciences (01.01.2011)
Get full text
Journal Article
Physiotherapy in hip and knee osteoarthritis: development of a practice guideline concerning initial assessment, treatment and evaluation
Peter, W F, Jansen, M J, Hurkmans, E J, Bloo, H, Dekker, J, Dilling, R G, Hilberdink, W, Kersten-Smit, C, de Rooij, M, Veenhof, C, Vermeulen, H M, de Vos, R J, Schoones, J W, Vliet Vlieland, T P
Published in Acta reumatológica portuguesa (01.07.2011)
Get full text
Published in Acta reumatológica portuguesa (01.07.2011)
Journal Article