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564 results
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Prospective assessment of falls in Parkinson's disease.
Bloem BR, Grimbergen YA, Cramer M, Willemsen M, Zwinderman AH. Bloem BR, et al. Among authors: willemsen m. J Neurol. 2001 Nov;248(11):950-8. doi: 10.1007/s004150170047. J Neurol. 2001. PMID: 11757958
The Multiple Tasks Test: development and normal strategies.
Bloem BR, Valkenburg VV, Slabbekoorn M, Willemsen MD. Bloem BR, et al. Among authors: willemsen md. Gait Posture. 2001 Dec;14(3):191-202. doi: 10.1016/s0966-6362(01)00141-2. Gait Posture. 2001. PMID: 11600322
Roth spots in pyridoxine dependent epilepsy.
Bok LA, Halbertsma F, Kerkhoff F, Jakobs C, Duijsters C, Willemsen M. Bok LA, et al. Among authors: willemsen m. BMJ Case Rep. 2011 Aug 17;2011:bcr0520114209. doi: 10.1136/bcr.05.2011.4209. BMJ Case Rep. 2011. PMID: 22688935 Free PMC article.
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism.
Miceli F, Millevert C, Soldovieri MV, Mosca I, Ambrosino P, Carotenuto L, Schrader D, Lee HK, Riviello J, Hong W, Risen S, Emrick L, Amin H, Ville D, Edery P, de Bellescize J, Michaud V, Van-Gils J, Goizet C, Willemsen MH, Kleefstra T, Møller RS, Bayat A, Devinsky O, Sands T, Korenke GC, Kluger G, Mefford HC, Brilstra E, Lesca G, Milh M, Cooper EC, Taglialatela M, Weckhuysen S. Miceli F, et al. Among authors: willemsen mh. EBioMedicine. 2022 Jun 30;81:104130. doi: 10.1016/j.ebiom.2022.104130. Online ahead of print. EBioMedicine. 2022. PMID: 35780567
Parents' experiences with a home-based upper limb training program using a video coaching approach for infants and toddlers with unilateral cerebral palsy: a qualitative interview study.
Verhaegh AP, Nuijen NB, Aarts PB, Nijhuis-van der Sanden MWG, Willemsen MA, Groen BE, Vriezekolk JE. Verhaegh AP, et al. Among authors: willemsen ma. BMC Pediatr. 2022 Jun 29;22(1):380. doi: 10.1186/s12887-022-03432-w. BMC Pediatr. 2022. PMID: 35768858 Free PMC article.
Reanalysis of exome negative patients with rare disease: a pragmatic workflow for diagnostic applications.
Schobers G, Schieving JH, Yntema HG, Pennings M, Pfundt R, Derks R, Hofste T, de Wijs I, Wieskamp N, van den Heuvel S, Galbany JC, Gilissen C, Nelen M, Brunner HG, Kleefstra T, Kamsteeg EJ, Willemsen MAAP, Vissers LELM. Schobers G, et al. Among authors: willemsen maap. Genome Med. 2022 Jun 17;14(1):66. doi: 10.1186/s13073-022-01069-z. Genome Med. 2022. PMID: 35710456 Free PMC article.
Retinal Capillary Abnormalities in Sjögren-Larsson Syndrome Maculopathy.
Staps P, de Breuk A, Cruysberg JRM, Willemsen M, Theelen T. Staps P, et al. Among authors: willemsen m. Case Rep Ophthalmol. 2022 May 2;13(2):341-349. doi: 10.1159/000524591. eCollection 2022 May-Aug. Case Rep Ophthalmol. 2022. PMID: 35702653 Free PMC article.
A disease-associated missense mutation in CYP4F3 affects the metabolism of leukotriene B4 via disruption of electron transfer.
Smeets E, Huang S, Lee XY, Van Nieuwenhove E, Helsen C, Handle F, Moris L, El Kharraz S, Eerlings R, Devlies W, Willemsen M, Bücken L, Prezzemolo T, Humblet-Baron S, Voet A, Rochtus A, Van Schepdael A, de Zegher F, Claessens F. Smeets E, et al. Among authors: willemsen m. J Cachexia Sarcopenia Muscle. 2022 Jun 9. doi: 10.1002/jcsm.13022. Online ahead of print. J Cachexia Sarcopenia Muscle. 2022. PMID: 35686338 Free article.
564 results