Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

255 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[The danger of chickenpox during pregnancy].
Willemsen MA, Loogman MCM, van Buggenum H, Langenveld J, Wassen MMLH. Willemsen MA, et al. Ned Tijdschr Geneeskd. 2020 Aug 5;164:D3830. Ned Tijdschr Geneeskd. 2020. PMID: 32779928 Dutch.
[Dystonia in cerebral palsy; what are the treatment options?].
van de Pol LA, Bonouvrié LA, Vermeulen RJ, de Koning-Tijssen MAJ, van Egmond ME, Willemsen MA, Buizer AI. van de Pol LA, et al. Among authors: willemsen ma. Ned Tijdschr Geneeskd. 2022 Feb 16;166:D5868. Ned Tijdschr Geneeskd. 2022. PMID: 35499589 Review. Dutch.
A post hoc study on gene panel analysis for the diagnosis of dystonia.
van Egmond ME, Lugtenberg CHA, Brouwer OF, Contarino MF, Fung VSC, Heiner-Fokkema MR, van Hilten JJ, van der Hout AH, Peall KJ, Sinke RJ, Roze E, Verschuuren-Bemelmans CC, Willemsen MA, Wolf NI, Tijssen MA, de Koning TJ. van Egmond ME, et al. Among authors: willemsen ma. Mov Disord. 2017 Apr;32(4):569-575. doi: 10.1002/mds.26937. Epub 2017 Feb 10. Mov Disord. 2017. PMID: 28186668 Free article.
De novo SPAST mutations may cause a complex SPG4 phenotype.
Schieving JH, de Bot ST, van de Pol LA, Wolf NI, Brilstra EH, Frints SG, van Gaalen J, Misra-Isrie M, Pennings M, Verschuuren-Bemelmans CC, Kamsteeg EJ, van de Warrenburg BP, Willemsen MA. Schieving JH, et al. Among authors: willemsen ma. Brain. 2019 Jul 1;142(7):e31. doi: 10.1093/brain/awz140. Brain. 2019. PMID: 31157359 No abstract available.
A detailed description of the phenotypic spectrum of North Sea Progressive Myoclonus Epilepsy in a large cohort of seventeen patients.
Polet SS, Anderson DG, Koens LH, van Egmond ME, Drost G, Brusse E, Willemsen MA, Sival DA, Brouwer OF, Kremer HP, de Vries JJ, Tijssen MA, de Koning TJ. Polet SS, et al. Among authors: willemsen ma. Parkinsonism Relat Disord. 2020 Mar;72:44-48. doi: 10.1016/j.parkreldis.2020.02.005. Epub 2020 Feb 18. Parkinsonism Relat Disord. 2020. PMID: 32105965 Free article.
Dystonia in childhood: Rising networks.
Willemsen MA. Willemsen MA. Eur J Paediatr Neurol. 2018 Mar;22(2):219-220. doi: 10.1016/j.ejpn.2018.01.020. Eur J Paediatr Neurol. 2018. PMID: 29447766 No abstract available.
Eyes on MEGDEL: distinctive basal ganglia involvement in dystonia deafness syndrome.
Wortmann SB, van Hasselt PM, Barić I, Burlina A, Darin N, Hörster F, Coker M, Ucar SK, Krumina Z, Naess K, Ngu LH, Pronicka E, Riordan G, Santer R, Wassmer E, Zschocke J, Schiff M, de Meirleir L, Alowain MA, Smeitink JA, Morava E, Kozicz T, Wevers RA, Wolf NI, Willemsen MA. Wortmann SB, et al. Among authors: willemsen ma. Neuropediatrics. 2015 Apr;46(2):98-103. doi: 10.1055/s-0034-1399755. Epub 2015 Feb 2. Neuropediatrics. 2015. PMID: 25642805 Free article.
255 results