Research

Lenstra, J. J., Pikstra, A. R. A., Fock, J. M., Metting, Z., & van der Naalt, J. (2017). Influence of guidelines on management of paediatric mild traumatic brain injury: CT-assessment and admission policy. European Journal of Paediatric Neurology, 21(6), 816-822. https://doi.org/10.1016/j.ejpn.2017.07.019

Pikstra, A. R. A., Metting, Z., Fock, J. M., & van der Naalt, J. (2017). The juvenile head trauma syndrome Deterioration after mild TBI: Diagnosis and clinical presentation at the Emergency Department. European Journal of Paediatric Neurology, 21(2), 344-349. https://doi.org/10.1016/j.ejpn.2016.09.005

O'Grady, G. L., Verschuuren, C., Yuen, M., Webster, R., Menezes, M., Fock, J. M., ... Cooper, S. T. (2016). Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. Neurology, 87(14), 1442-1448. https://doi.org/10.1212/WNL.0000000000003179

Helfferich, J., Nijmeijer, R., Brouwer, O. F., Boon, M., Fock, A., Hoving, E. W., ... de Bont, E. S. J. M. (2016). Neurofibromatosis type 1 associated low grade gliomas: A comparison with sporadic low grade gliomas. Critical Reviews in Oncology/Hematology, 104, 30-41. https://doi.org/10.1016/j.critrevonc.2016.05.008

Gerkes, E. H., Fock, J. M., den Dunnen, W. F. A., van Belzen, M. J., van der Lans, C. A., Hoving, E. W., ... Olderode-Berends, M. J. W. (2016). A heritable form of SMARCE1-related meningiomas with important implications for follow-up and family screening. Neurogenetics, 17(2), 83-89. https://doi.org/10.1007/s10048-015-0472-y

Kevelam, S. H., Klouwer, F. C. C., Fock, J. M., Salomons, G. S., Bugiani, M., & van der Knaap, M. S. (2016). Absent Thalami Caused by a Homozygous EARS2 Mutation: Expanding Disease Spectrum of LTBL. Neuropediatrics, 47(1), 64-67. https://doi.org/10.1055/s-0035-1568987

Wolf, N. I., Salomons, G. S., Rodenburg, R. J., Pouwels, P. J. W., Schieving, J. H., Derks, T. G. J., ... Waisfisz, Q. (2014). Mutations in RARS cause hypomyelination. Annals of Neurology, 76(1), 134-139. https://doi.org/10.1002/ana.24167

van den Bergen, J. C., Ginjaar, H. B., Van Essen, A. J., Pangalila, R., De Groot, I. J. M., Wijkstra, P. J., ... Verschuuren, J. J. G. M. (2014). Forty-five years of Duchenne muscular dystrophy in The Netherlands. Journal of Neuromuscular Diseases, 1(1), 99-109. https://doi.org/10.3233/JND-140005

Stalpers, X., Verrips, A., Poll-The, B-T., Cobben, J. M., Snoeck, I., De Coo, I., ... Lemmink, H. (2013). Clinical and Mutational Characteristics of SMARD1 Patients in the Netherlands. Neurology, 80.

Ebberink, M. S., Koster, J., Visser, G., van Spronsen, F., Stolte-Dijkstra, I., Smit, G. P. A., ... Waterham, H. R. (2012). A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11 beta gene. JOURNAL OF MEDICAL GENETICS, 49(5), 307-313. https://doi.org/10.1136/jmedgenet-2012-100778

Fokke, C., Fock, J. M., Brouwer, O. F., & Elting, J. W. J. (2011). BENIGN NEONATAL SLEEP MYOCLONUS: A CASE WITH A SPINAL GENERATOR? Neurology, 77(13), 1308-1309. https://doi.org/10.1212/WNL.0b013e31823020ad

Cornips, E. M. J., Razenberg, F. G. E. M., van Rhijn, L. W., Soudant, D. L. H. M., van Raak, E. P. M., Weber, J. W., ... Vles, J. S. H. (2010). The lumbosacral angle does not reflect progressive tethered cord syndrome in children with spinal dysraphism. CHILDS NERVOUS SYSTEM, 26(12), 1757-1764. https://doi.org/10.1007/s00381-010-1281-0

Elting, J. W., van der Naalt, J., & Fock, J. M. (2010). Mild hypothermia for refractory focal status epilepticus in an infant with hemimegalencephaly. European Journal of Paediatric Neurology, 14(5), 452-455. https://doi.org/10.1016/j.ejpn.2009.12.001

Meinesz, A. F., Bladder, G., Goorhuis, J. F., Fock, J. M., Staal-Schreinemachers, A. L., Zijlstra, J., & Wijkstra, P. J. (2007). 18 jaar ervaring met chronische beademing bij patiënten met spierdystrofie van Duchenne. Nederlands Tijdschrift voor Geneeskunde, 151(33), 1830-1833.

Hadders-Algra, M., van der Heide, J. C., Fock, J. M., Stremmelaar, E., van Eykern, L. A., & Otten, B. (2007). Effect of seat surface inclination on postural control during reaching in preterm children with cerebral palsy. Physical Therapy, 87(7), 861-871. https://doi.org/10.2522/ptj.20060330

Sijens, P. E., Fock, J. M., Meiners, L. C., Potze, J. H., Irwan, R., & Oudkerk, M. (2007). MR spectroscopy and diffusion tensor imaging of the brain in congenital muscular dystrophy with merosin deficiency: Metabolite level decreases, fractional anisotropy decreases, and apparent diffusion coefficient increases in the white matter. Brain & Development, 29(5), 317-321. https://doi.org/10.1016/j.braindev.2006.10.004

Rump, P., Lemmink, HH., Verschuuren-Bemelmans, CC., Grootscholten, PM., Fock, JM., Hayflick, SJ., ... van Essen, AJ. (2005). A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect. Neurogenetics, 6(4), 201-207. https://doi.org/10.1007/s10048-005-0018-9

Van Der Heide, JC., Fock, JM., Otten, B., Stremmelaar, E., & Hadders-Algra, M. (2005). Kinematic characteristics of reaching movements in preterm children with cerebral palsy. Pediatric Research, 57(6), 883-889. https://doi.org/10.1203/01.PDR.0000157771.20683.14

Beenakker, EAC., Fock, JM., Van Tol, M., Maurits, NM., Koopman, HM., Brouwer, OF., & Van der Hoeven, JH. (2005). Intermittent prednisone therapy in Duchenne muscular dystrophy: A randomized controlled trial. Archives of Neurology, 62(1), 128-132. https://doi.org/10.1001/archneur.62.1.128

Beenakker, EAC., Maurits, NM., Fock, JM., Brouwer, OF., & van der Hoeven, JH. (2005). Functional ability and muscle force in healthy children and ambulant Duchenne muscular dystrophy patients. European Journal of Paediatric Neurology, 9(6), 387-393. https://doi.org/10.1016/j.ejpn.2005.06.004

Maurits, NM., Beenakker, EAC., Van Schaik, DEC., Fock, JM., & Van der Hoeven, JH. (2004). Muscle ultrasound in children: Normal values and application to neuromuscular disorders. Ultrasound in Medicine and Biology, 30(8), 1017-1027. https://doi.org/10.1016/j.ultrasmedbio.2004.05.013

ter Horst, H., Sommer, C., Fock, JM., van Weerden, TW., & Bos, AF. (2004). Prognostic significance of amplitude-integrated EEG during the first 72 hours after birth in severely asphyxiated neonates. Pediatric Research, 55(6), 1026-1033. https://doi.org/10.1203/01.pdr.0000127019.52562.8c

van der Heide, JC., Begeer, C., Fock, JM., Otten, B., Stremmelaar, E., van Eykern, LA., & Hadders-Algra, M. (2004). Postural control during reaching in preterm children with cerebral palsy. Developmental Medicine and Child Neurology, 46(4), 253-266. https://doi.org/10.1017/S0012162204000416

Beenakker, EAC., de Vries, J., Fock, JM., van Tol, M., Brouwer, OF., Maurits, NM., & van der Hoeven, JH. (2003). Calf circumference in Duchenne muscular dystrophy: Reply. Neuromuscular disorders, 13(5), 426-427. https://doi.org/10.1016/S0960-8966(03)00045-2

Beenakker, EAC., de Vries, J., Fock, JM., van Tol, M., Brouwer, OF., Maurits, NM., & van der Hoeven, JH. (2002). Quantitative assessment of calf circumference in Duchenne muscular dystrophy patients. Neuromuscular disorders, 12(7-8), 639-642. [PII S0960-8966(02)00019-6].

Hew, JM., Fock, JM., & Kamps, WA. (2002). Predictive value of clinical evaluation in the follow-up of children with a brain tumor. Medical and Pediatric Oncology, 38(4), 254-257. https://doi.org/10.1002/mpo.10054

Beenakker, E. A., van der Hoeven, J. H., Fock, J. M., & Maurits, N. M. (2001). Reference values of maximum isometric muscle force obtained in 270 children aged 4-16 years by hand-held dynamometry. Neuromuscular disorders, 11(5), 441-446.

Zeinstra, E., Fock, J. M., Begeer, J. H., van Weerden, T. W., Maurits, N. M., & Zweens, M. J. (2001). The prognostic value of serial EEG recordings following acute neonatal asphyxia in full-term infants. European Journal of Paediatric Neurology, 5(4), 155-160. https://doi.org/10.1053/ejpn.2001.0496

Dam, A., Fock, J. M., Hayes, VM., Molenaar, WM., & van den Berg, E. (2000). Recurrent astrocytoma in a child: A report of cytogenetics and TP53 gene mutation screening. Neuro-Oncology, 2(3), 184-189. https://doi.org/10.1093/neuonc/2.3.184

Reinders-Messelink, H. A., van Weerden, T. W., Fock, J. M., Gidding, C. E. M., Vingerhoets, H. M., Schoemaker, M. M., ... Kamps, W. A. (2000). Mild axonal neuropathy of children during treatment for acute lymphoblastic leukemia. European Journal of Paediatric Neurology, 4, 233-239.

Fock, J. M., Dam, A., & Molenaar, W. M. (1999). DNA-ploidy in medulloblastoma. European Journal of Paediatric Neurology, 3.

Muntinghe, F., Fock, J., van Essen, A., & Molenaar, W. (1999). Duchenne-spierdystrofie; een diagnose met omwegen. Tijdschrift voor Kindergeneeskunde, 67, 174-178.

FOCK, JM., BEGEER, JH., & PRINS, TR. (1995). METACHROMATIC LEUKODYSTROPHY AND COINCIDENTAL FINDING OF PAPILLOMATOSIS OF THE GALLBLADDER - A CASE-REPORT. Neuropediatrics, 26(1), 55-56.