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Number of items: 5.

Müller, A; Helbig, I; Jansen, C; Bast, T; Guerrini, R; Jähn, J; Muhle, H; Auvin, S; Korenke, G C; Philip, S; Keimer, R; Striano, P; Wolf, N I; Püst, B; Thiels, Ch; Fogarasi, A; Waltz, S; Kurlemann, G; Kovacevic-Preradovic, T; Ceulemans, B; Schmitt, B; Philippi, H; Tarquinio, D; Buerki, S; von Stülpnagel, C; Kluger, G (2016). Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5-related epilepsy. European Journal of Paediatric Neurology, 20(1):147-151.

Poretti, A; Limperopoulos, C; Roulet-Perez, E; Wolf, N I; Rauscher, C; Prayer, D; Müller, A; Weissert, M; Kotzaeridou, U; Du Plessis, A J; Huisman, T A G M; Boltshauser, E (2010). Outcome of severe unilateral cerebellar hypoplasia. Developmental Medicine and Child Neurology, 52(8):718-724.

Wolff, A; Koch, M J; Benzinger, S; van Waes, H; Wolf, N I; Boltshauser, E; Luder, H U (2010). Rare dental peculiarities associated with the hypomyelinating leukoencephalopathy 4H syndrome/ADDH. Pediatric Dentistry, 32(5):386-392.

Wolf, N I; Rahman, S; Schmitt, B; Taanman, J W; Duncan, A J; Harting, I; Wohlrab, G; Ebinger, F; Rating, D; Bast, T (2009). Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features. Epilepsia, 50(6):1596-1607.

Poretti, A; Wolf, N I; Boltshauser, E (2008). Differential diagnosis of cerebellar atrophy in childhood. European Journal of Paediatric Neurology, 12(3):155-167.

This list was generated on Mon Apr 22 16:30:43 2019 CEST.