P191 – 2505: Two siblings with a CDKL5 mutation: Genotype and phenotype evaluation
Hagebeuk, E.E.O, Marcelis, C.L, Alders, M, Kaspers, A, de Weerd, A.W
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Journal Article
PP05.14 – 3044: The use of acetazolamide for severe central apnea in developmental disorders
Hagebeuk, E.E.O, van den Bossche, R, Gutter, T, de Weerd, A.W
Published in European journal of paediatric neurology (01.05.2015)
Published in European journal of paediatric neurology (01.05.2015)
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Journal Article
A case of neonatal dural sinus malformation: Clinical symptoms, imaging and neuropathological investigations
de Haan, T.R, Padberg, R.D, Hagebeuk, E.E.O, Aronica, E, van Rijn, R.R, Majoie, C.B.L.M, Kok, J.H
Published in European journal of paediatric neurology (01.01.2008)
Published in European journal of paediatric neurology (01.01.2008)
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Journal Article
Molecular and clinical characterization of a Moroccan Cog7 deficient patient
Ng, Bobby G., Kranz, Christian, Hagebeuk, E.E.O., Duran, M., Abeling, N.G.G.M., Wuyts, B., Ungar, Daniel, Lupashin, Vladimir, Hartdorff, C.M., Poll-The, B.T., Freeze, Hudson H.
Published in Molecular genetics and metabolism (01.06.2007)
Published in Molecular genetics and metabolism (01.06.2007)
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