Browsing by Author/Editor/Contributor De Jonghe, P.

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Issue DateTitleAuthor(s)TypeCat.
2003A deletion in SCN1B is associated with febrile seizures and early-onset absence epilepsyAudenaert, D.; CLAES, Luc ; Ceulemans, B.; Löfgren, A.; Van Broeckhoven, C.; De Jonghe, P.Journal ContributionA1
2002Search for mutations in the EGR2 corepressor proteins, NAB1 and NAB2, in human peripheral neuropathiesVENKEN, Koen ; Di Maria, E.; Bellone, E.; Balestra, P.; Cassandrini, D.; Mandich, P.; De Jonghe, P.; Timmerman, V.; Svaren, J.Journal ContributionA1
2001De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancyCLAES, Luc ; Del-Favero, J.; Ceulemans, B.; Lagae, L.; Van Broeckhoven, C.; De Jonghe, P.Journal ContributionA1
2001Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3IROBI, Joy ; Nelis, E.; Meuleman, J.; VENKEN, Koen ; De Jonghe, P.; Van Broeckhoven, C.; Timmerman, V.Journal ContributionA1
2001Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathiesVENKEN, Koen ; Meuleman, J.; IROBI, Joy ; Ceuterick, C.; Martini, Roberto; De Jonghe, P.; Timmerman, V.Journal ContributionA1
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