Neuropediatrics

Ausgabe 04 · August 2018

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Ausgabe
Editorial
229
Ebrahimi-Fakhari, Darius; Neubauer, Bernd; Plecko, Barbara; Wolf, Nicole I.: Resident and Fellow Section in Neuropediatrics

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Review Article
231
Finsterer, Josef; Zarrouk-Mahjoub, Sinda: Phenotypic and Genotypic Heterogeneity of RRM2B Variants

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Original Article
238
Cizmeci, Mehmet N.; Thewissen, Liesbeth; Zecic, Alexandra; Woerdeman, Peter A.; Boer, Bart de; Baert, Edward; Govaert, Paul; Dudink, Jeroen; Groenendaal, Floris; Lequin, Maarten; de Vries, Linda S.: Bedside Ultrasound-Guided Percutaneous Needle Aspiration of Intra- and Extra-Axial Intracranial Hemorrhage in Neonates

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246
Blumkin, Lubov; Lerman-Sagie, Tally; Westenberger, Ana; Ben-Pazi, Hilla; Zerem, Ayelet; Yosovich, Keren; Lev, Dorit: Multiple Causes of Pediatric Early Onset Chorea—Clinical and Genetic Approach

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256
Knuutinen, Oula; Kousi, Maria; Suo-Palosaari, Maria; Moilanen, Jukka S.; Tuominen, Hannu; Vainionpää, Leena; Joensuu, Tarja; Anttonen, Anna-Kaisa; Uusimaa, Johanna; Lehesjoki, Anna-Elina; Vieira, Päivi: Neonatal Alexander Disease: Novel GFAP Mutation and Comparison to Previously Published Cases

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262
Toelle, Sandra P.; Avetisyan, Tamara; Kuyumjyan, Nune; Sukhudyan, Biayna; Boltshauser, Eugen; Hackenberg, Annette: Infantile Basal Ganglia Stroke after Mild Head Trauma Associated with Mineralizing Angiopathy of Lenticulostriate Arteries: An Under Recognized Entity

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269
Garbade, Sven F.; Boy, Nikolas; Heringer, Jana; Kölker, Stefan; Harting, Inga: Age-Related Changes and Reference Values of Bicaudate Ratio and Sagittal Brainstem Diameters on MRI

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Zusatzmaterial

Supplementary Material File 1

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Short Communication
276
Lotte, Jan; Grothe, Stefan; Kluger, Gerhard Josef: Seizure Freedom in Patients with Dravet Syndrome with Contraceptives: A Case Report with Two Patients

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279
Krijgh, E. J. C.; Catsman-Berrevoets, C. E.; Neuteboom, R. F.: Early Seizure Freedom Is a Prognostic Factor for Survival in Patients with West Syndrome

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283
Arican, Pinar; Gencpinar, Pinar; Cavusoglu, Dilek; Olgac Dundar, Nihal: Clinical and Genetic Features of Congenital Myasthenic Syndromes due to CHAT Mutations: Case Report and Literature Review

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289
Al Dhaibani, Muna A.; El-Hattab, Ayman W.; Ismayl, Omar; Suleiman, Jehan: B3GALNT2-Related Dystroglycanopathy: Expansion of the Phenotype with Novel Mutation Associated with Muscle-Eye-Brain Disease, Walker–Warburg Syndrome, Epileptic Encephalopathy-West Syndrome, and Sensorineural Hearing Loss

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Videos and Images in Neuropediatrics
296
Flotats-Bastardas, Marina; Hebert, Eva; Raspall-Chaure, Miquel; Munell, Francina; Macaya, Alfons; Lohmann, Katja: Novel GCH1 Compound Heterozygosity Mutation in Infancy-Onset Generalized Dystonia

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Book Review
298
Boltshauser, Eugen: Rhoton's Atlas of Head, Neck, and Brain

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In Memoriam
299
Neubauer, Bernd A.; Schara, Ulrike; On behalf of the Gesellschaft für Neuropädiatrie: In Memoriam: Professor Hermann Doose FREIER ZUGRIFF

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