de Meirleir L - Search Results

1

Phenotypic plasticity and the perception-action-cognition-environment paradigm in neurodevelopmental genetic disorders.

Dan B, Pelc K, de Meirleir L, Cheron G. Dan B, et al. Among authors: de meirleir l. Dev Med Child Neurol. 2015 Apr;57 Suppl 2:52-4. doi: 10.1111/dmcn.12694. Dev Med Child Neurol. 2015. PMID: 25690118 Free article. Review.

2

Effect of ankle-foot orthoses on trunk sway and lower limb intersegmental coordination in children with bilateral cerebral palsy.

Degelean M, De Borre L, Salvia P, Pelc K, Kerckhofs E, De Meirleir L, Cheron G, Dan B. Degelean M, et al. Among authors: de meirleir l, de borre l. J Pediatr Rehabil Med. 2012;5(3):171-9. doi: 10.3233/PRM-2012-0209. J Pediatr Rehabil Med. 2012. PMID: 23023249 Clinical Trial.

3

Effect of ankle-foot orthoses on gait in typically developing children: Developmental trend in segmental coordination.

Degelaen M, Leurs F, De Borre L, Kerckhofs E, De Meirleir L, Cheron G, Dan B. Degelaen M, et al. Among authors: de meirleir l, de borre l. J Pediatr Rehabil Med. 2010;3(3):163-70. doi: 10.3233/PRM-2010-0125. J Pediatr Rehabil Med. 2010. PMID: 21791847

4

Influence of botulinum toxin therapy on postural control and lower limb intersegmental coordination in children with spastic cerebral palsy.

Degelaen M, de Borre L, Kerckhofs E, de Meirleir L, Buyl R, Cheron G, Dan B. Degelaen M, et al. Among authors: de meirleir l, de borre l. Toxins (Basel). 2013 Jan 11;5(1):93-105. doi: 10.3390/toxins5010093. Toxins (Basel). 2013. PMID: 23344454 Free PMC article.

5

Effect of supporting 3D-garment on gait postural stability in children with bilateral spastic cerebral palsy.

Degelaen M, De Borre L, Buyl R, Kerckhofs E, De Meirleir L, Dan B. Degelaen M, et al. Among authors: de meirleir l, de borre l. NeuroRehabilitation. 2016 Jun 23;39(2):175-81. doi: 10.3233/NRE-161349. NeuroRehabilitation. 2016. PMID: 27341370

6

Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy.

Lemke JR, Geider K, Helbig KL, Heyne HO, Schütz H, Hentschel J, Courage C, Depienne C, Nava C, Heron D, Møller RS, Hjalgrim H, Lal D, Neubauer BA, Nürnberg P, Thiele H, Kurlemann G, Arnold GL, Bhambhani V, Bartholdi D, Pedurupillay CR, Misceo D, Frengen E, Strømme P, Dlugos DJ, Doherty ES, Bijlsma EK, Ruivenkamp CA, Hoffer MJ, Goldstein A, Rajan DS, Narayanan V, Ramsey K, Belnap N, Schrauwen I, Richholt R, Koeleman BP, Sá J, Mendonça C, de Kovel CG, Weckhuysen S, Hardies K, De Jonghe P, De Meirleir L, Milh M, Badens C, Lebrun M, Busa T, Francannet C, Piton A, Riesch E, Biskup S, Vogt H, Dorn T, Helbig I, Michaud JL, Laube B, Syrbe S. Lemke JR, et al. Among authors: de kovel cg, de meirleir l, de jonghe p. Neurology. 2016 Jun 7;86(23):2171-8. doi: 10.1212/WNL.0000000000002740. Epub 2016 May 6. Neurology. 2016. PMID: 27164704 Free PMC article.

7

Access to early diagnostics, intervention, and support for children with a neurobiological developmental delay or disorder.

Cloet E, Leys M, De Meirleir L. Cloet E, et al. Among authors: de meirleir l. Dev Med Child Neurol. 2017 Dec;59(12):1215-1216. doi: 10.1111/dmcn.13583. Epub 2017 Sep 25. Dev Med Child Neurol. 2017. PMID: 28944462 Free article. No abstract available.

8

Mutation of a potassium channel-related gene in progressive myoclonic epilepsy.

Van Bogaert P, Azizieh R, Désir J, Aeby A, De Meirleir L, Laes JF, Christiaens F, Abramowicz MJ. Van Bogaert P, et al. Among authors: de meirleir l. Ann Neurol. 2007 Jun;61(6):579-86. doi: 10.1002/ana.21121. Ann Neurol. 2007. PMID: 17455289

9

Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.

Méneret A, Depienne C, Riant F, Trouillard O, Bouteiller D, Cincotta M, Bitoun P, Wickert J, Lagroua I, Westenberger A, Borgheresi A, Doummar D, Romano M, Rossi S, Defebvre L, De Meirleir L, Espay AJ, Fiori S, Klebe S, Quélin C, Rudnik-Schöneborn S, Plessis G, Dale RC, Sklower Brooks S, Dziezyc K, Pollak P, Golmard JL, Vidailhet M, Brice A, Roze E. Méneret A, et al. Among authors: de meirleir l. Neurology. 2014 Jun 3;82(22):1999-2002. doi: 10.1212/WNL.0000000000000477. Epub 2014 May 7. Neurology. 2014. PMID: 24808016 Free PMC article.

10

The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.

Kölker S, Garcia-Cazorla A, Valayannopoulos V, Lund AM, Burlina AB, Sykut-Cegielska J, Wijburg FA, Teles EL, Zeman J, Dionisi-Vici C, Barić I, Karall D, Augoustides-Savvopoulou P, Aksglaede L, Arnoux JB, Avram P, Baumgartner MR, Blasco-Alonso J, Chabrol B, Chakrapani A, Chapman K, I Saladelafont EC, Couce ML, de Meirleir L, Dobbelaere D, Dvorakova V, Furlan F, Gleich F, Gradowska W, Grünewald S, Jalan A, Häberle J, Haege G, Lachmann R, Laemmle A, Langereis E, de Lonlay P, Martinelli D, Matsumoto S, Mühlhausen C, de Baulny HO, Ortez C, Peña-Quintana L, Ramadža DP, Rodrigues E, Scholl-Bürgi S, Sokal E, Staufner C, Summar ML, Thompson N, Vara R, Pinera IV, Walter JH, Williams M, Burgard P. Kölker S, et al. Among authors: de meirleir l, de lonlay p, de baulny ho. J Inherit Metab Dis. 2015 Nov;38(6):1041-57. doi: 10.1007/s10545-015-9839-3. Epub 2015 Apr 15. J Inherit Metab Dis. 2015. PMID: 25875215

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