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

424 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature.
van der Laan L, Silva A, Kleinendorst L, Rooney K, Haghshenas S, Lauffer P, Alanay Y, Bhai P, Brusco A, de Munnik S, de Vries BBA, Vega AD, Engelen M, Herkert JC, Hochstenbach R, Hopman S, Kant SG, Kira R, Kato M, Keren B, Kroes HY, Levy MA, Lock-Hock N, Maas SM, Mancini GMS, Marcelis C, Matsumoto N, Mizuguchi T, Mussa A, Mignot C, Närhi A, Nordgren A, Pfundt R, Polstra AM, Trajkova S, van Bever Y, José van den Boogaard M, van der Smagt JJ, Barakat TS, Alders M, Mannens MMAM, Sadikovic B, van Haelst MM, Henneman P. van der Laan L, et al. Among authors: engelen m. HGG Adv. 2025 Jan 9;6(1):100380. doi: 10.1016/j.xhgg.2024.100380. Epub 2024 Nov 4. HGG Adv. 2025. PMID: 39501558 Free PMC article.
Reduced MUNC18-1 Levels, Synaptic Proteome Changes, and Altered Network Activity in STXBP1-Related Disorder Patient Neurons.
van Berkel AA, Lammertse HCA, Öttl M, Koopmans F, Misra-Isrie M, Meijer M, Dilena R, van Hasselt PM, Engelen M, van Haelst M, Smit AB, van der Sluis S, Toonen RF, Verhage M. van Berkel AA, et al. Among authors: engelen m. Biol Psychiatry Glob Open Sci. 2023 May 30;4(1):284-298. doi: 10.1016/j.bpsgos.2023.05.004. eCollection 2024 Jan. Biol Psychiatry Glob Open Sci. 2023. PMID: 38298782 Free PMC article.
MRI pattern recognition in white matter disease.
Wolf NI, Engelen M, van der Knaap MS. Wolf NI, et al. Among authors: engelen m. Handb Clin Neurol. 2024;204:37-50. doi: 10.1016/B978-0-323-99209-1.00019-3. Handb Clin Neurol. 2024. PMID: 39322391 Review.
Peroxisomal leukodystrophy.
Engelen M. Engelen M. Handb Clin Neurol. 2024;204:139-145. doi: 10.1016/B978-0-323-99209-1.00021-1. Handb Clin Neurol. 2024. PMID: 39322376 Review.
MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deterioration.
Hammann N, Lenz D, Bianzano A, Husain RA, Forman E, Bernstein JA, Dattner T, Engelen M, Hanson-Kahn AK, Isidor B, Kotzaeridou U, Tietze A, Trollmann R, Weiß C, Wolffenbuttel BHR, Kölker S, Hoffmann GF, Crushell E, Staufner C, Mohr A, Harting I. Hammann N, et al. Among authors: engelen m. J Inherit Metab Dis. 2024 Sep;47(5):1028-1046. doi: 10.1002/jimd.12764. Epub 2024 Jul 1. J Inherit Metab Dis. 2024. PMID: 38951950
Improving paediatric movement disorders care: Insights on rating scales utilization and clinical practice.
Amato ME, Darling A, Stovickova L, Attard S, Eggink H, Engelen M, Freilinger M, Grosso S, Hadzsiev K, Moroni I, Nardocci N, Neubauer D, Nicita F, Pagliano E, Siegert S, Soler D, van de Pol LA, Vasco G, Vidailhet M, Willemsen MA, Zibordi F, Zorzi G, Zumrova A, Reinhard C, Sevin C, Wolf N, Rodriguez-Blazquez C, Sival DA, Ortigoza-Escobar JD; Pediatric issues working group of the European Reference Network for Rare Neurological Diseases (ERN-RND). Amato ME, et al. Among authors: engelen m. Eur J Paediatr Neurol. 2024 Sep;52:10-19. doi: 10.1016/j.ejpn.2024.06.011. Epub 2024 Jun 29. Eur J Paediatr Neurol. 2024. PMID: 38970889
424 results