drs. J.M. Fock
Telephone:
E-mail:
j.m.fock umcg.nl
Research
1 - 32 out of 32Page size: 50
- 2017
- 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
- 2016
- 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
- 2014
- 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
- 2013
- 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.
- 2012
- 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
- 2011
- 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
- 2010
- 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
- 2007
- 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
- 2005
- 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
- 2004
- 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
- 2003
- 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
- 2002
- 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].
- 2001
- 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
- 2000
- 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.
- 1999
- 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.
- 1995
- 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.
ID: 72410