Clinical practice: Swallowing problems in cerebral palsy

Tekijä Erasmus, Corrie E., van Hulst, Karen, Rotteveel, Jan J., Willemsen, Michel A. A. P., Jongerius, Peter H.
Julkaistu 2011

Phenytoin as a last‐resort treatment in SCN8A encephalopathy

Tekijä Braakman, Hilde M., Verhoeven, Judith S., Erasmus, Corrie E., Haaxma, Charlotte A., Willemsen, Marjolein H., Schelhaas, H. Jurgen
Julkaisussa Epilepsia Open (2017)

Changes in severity and impact of drooling after submandibular gland botulinum neurotoxin A injections in children with neurodevelopmental disabilities

Tekijä Van Hulst, Karen, Van Der Burg, Jan JW, Jongerius, Peter H, Geurts, Alexander CH, Erasmus, Corrie E
Julkaisussa Dev Med Child Neurol (2019)

Feeding and Swallowing Disorders in Pediatric Neuromuscular Diseases: An Overview

Tekijä van den Engel-Hoek, Lenie, de Groot, Imelda J.M., de Swart, Bert J.M., Erasmus, Corrie E.
Julkaisussa J Neuromuscul Dis (2015)

An evaluation of predictors for success of two-duct ligation for drooling in neurodisabilities

Tekijä Bekkers, Stijn, van Hulst, Karen, Erasmus, Corrie E., Delsing, Corinne P., Scheffer, Arthur R. T., van den Hoogen, Frank J. A.
Julkaisussa J Neurol (2020)

Submandibular duct ligation after botulinum neurotoxin A treatment of drooling in children with cerebral palsy

Tekijä Bekkers, Stijn, Pruijn, Ineke M J, Van Hulst, Karen, Delsing, Corinne P, Erasmus, Corrie E, Scheffer, Arthur R T, Van Den Hoogen, Frank J A
Julkaisussa Dev Med Child Neurol (2020)

Ophthalmological findings in facioscapulohumeral dystrophy

Tekijä Goselink, Rianne J M, Schreur, Vivian, van Kernebeek, Caroline R, Padberg, George W, van der Maarel, Silvère M, van Engelen, Baziel G M, Erasmus, Corrie E, Theelen, Thomas
Julkaisussa Brain Commun (2019)

Dysphagia and Dysarthria in Children with Neuromuscular Diseases, a Prevalence Study

Tekijä Kooi-van Es, Mieke, Erasmus, Corrie E., de Swart, Bert J.M., Voet, Nicoline B.M., van der Wees, Philip J., de Groot, Imelda J.M., van den Engel-Hoek, Lenie
Julkaisussa J Neuromuscul Dis (2020)

Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy

Tekijä Goselink, Rianne J.M., Mul, Karlien, van Kernebeek, Caroline R., Lemmers, Richard J.L.F., van der Maarel, Silvère M., Schreuder, Tim H.A., Erasmus, Corrie E., Padberg, George W., Statland, Jeffrey M., Voermans, Nicol C., van Engelen, Baziel G.M.
Julkaisussa Neurology (2019)

Facioscapulohumeral dystrophy in children: design of a prospective, observational study on natural history, predictors and clinical impact (iFocus FSHD)

Tekijä Goselink, Rianne J. M., Schreuder, Tim H. A., Mul, Karlien, Voermans, Nicol C., Pelsma, Maaike, de Groot, Imelda J. M., van Alfen, Nens, Franck, Bas, Theelen, Thomas, Lemmers, Richard J., Mah, Jean K., van der Maarel, Silvère M., van Engelen, Baziel G., Erasmus, Corrie E.
Julkaisussa BMC Neurol (2016)

Facioscapulohumeral Dystrophy in Childhood: A Nationwide Natural History Study

Tekijä Goselink, Rianne J.M., Schreuder, Tim H.A., van Alfen, Nens, de Groot, Imelda J.M., Jansen, Merel, Lemmers, Richard J.L.F., van der Vliet, Patrick J., van der Stoep, Nienke, Theelen, Thomas, Voermans, Nicol C., van der Maarel, Silvère M., van Engelen, Baziel G.M., Erasmus, Corrie E.
Julkaisussa Ann Neurol (2018)

LBSL: Case Series and DARS2 Variant Analysis in Early Severe Forms With Unexpected Presentations

Tekijä Stellingwerff, Menno D., Figuccia, Sonia, Bellacchio, Emanuele, Alvarez, Karin, Castiglioni, Claudia, Topaloglu, Pinar, Stutterd, Chloe A., Erasmus, Corrie E., Sanchez‐Valle, Amarilis, Lebon, Sebastien, Hughes, Sarah, Schmitt-Mechelke, Thomas, Vasco, Gessica, Chow, Gabriel, Rahikkala, Elisa, Dallabona, Cristina, Okuma, Cecilia, Aiello, Chiara, Goffrini, Paola, Abbink, Truus E.M., Bertini, Enrico S., Van der Knaap, Marjo S.
Julkaisussa Neurol Genet (2021)

Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

Tekijä McMillan, Hugh J., Telegrafi, Aida, Singleton, Amanda, Cho, Megan T., Lelli, Daniel, Lynn, Francis C., Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E., Koolen, David A., Haaxma, Charlotte A., Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J., Henderson, Lindsay B., McLaughlin, Heather, Molday, Laurie L., Molday, Robert S., Yoon, Grace
Julkaisussa Orphanet J Rare Dis (2018)

Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients

Tekijä Molenaar, Joery P, Verhoeven, Jamie I, Rodenburg, Richard J, Kamsteeg, Erik J, Erasmus, Corrie E, Vicart, Savine, Behin, Anthony, Bassez, Guillaume, Magot, Armelle, Péréon, Yann, Brandom, Barbara W, Guglielmi, Valeria, Vattemi, Gaetano, Chevessier, Frédéric, Mathieu, Jean, Franques, Jérôme, Suetterlin, Karen, Hanna, Michael G, Guyant-Marechal, Lucie, Snoeck, Marc M, Roberts, Mark E, Kuntzer, Thierry, Fernandez-Torron, Roberto, Martínez-Arroyo, Amaia, Seeger, Juergen, Kusters, Benno, Treves, Susan, van Engelen, Baziel G, Eymard, Bruno, Voermans, Nicol C, Sternberg, Damien
Julkaisussa Brain (2020)

Mutations in DDHD2, Encoding an Intracellular Phospholipase A(1), Cause a Recessive Form of Complex Hereditary Spastic Paraplegia

Tekijä Schuurs-Hoeijmakers, Janneke H.M., Geraghty, Michael T., Kamsteeg, Erik-Jan, Ben-Salem, Salma, de Bot, Susanne T., Nijhof, Bonnie, van de Vondervoort, Ilse I.G.M., van der Graaf, Marinette, Nobau, Anna Castells, Otte-Höller, Irene, Vermeer, Sascha, Smith, Amanda C., Humphreys, Peter, Schwartzentruber, Jeremy, Ali, Bassam R., Al-Yahyaee, Saeed A., Tariq, Said, Pramathan, Thachillath, Bayoumi, Riad, Kremer, Hubertus P.H., van de Warrenburg, Bart P., van den Akker, Willem M.R., Gilissen, Christian, Veltman, Joris A., Janssen, Irene M., Vulto-van Silfhout, Anneke T., van der Velde-Visser, Saskia, Lefeber, Dirk J., Diekstra, Adinda, Erasmus, Corrie E., Willemsen, Michèl A., Vissers, Lisenka E.L.M., Lammens, Martin, van Bokhoven, Hans, Brunner, Han G., Wevers, Ron A., Schenck, Annette, Al-Gazali, Lihadh, de Vries, Bert B.A., de Brouwer, Arjan P.M.
Julkaistu 2012