DOI: 10.1055/s-00000041

Neuropediatrics

Issue 01 · Volume 50 · February 2019 DOI: 10.1055/s-009-42318

Editorial Commentary

  • 001
    Willemsen, Michèl A.:

    Failing Transmission

    • Review Article

  • 002
    Brennenstuhl, Heiko; Jung-Klawitter, Sabine; Assmann, Birgit; Opladen, Thomas:

    Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and Treatment

    • Original Article

  • 015
    Akin, Mustafa Ali; Sahin, Ozlem; Cansever, Murat; Sirakaya, Ender; Robertson, Nicola Jayne:

    Early Retinal Findings Following Cooling in Neonatal Encephalopathy

  • 022
    Ben Chehida, Amel; Ben Messaoud, Sana; Ben Abdelaziz, Rim; Ben Ali, Nadia; Boudabous, Hela; Ben Abdelaziz, Ines; Ben Ameur, Zeineb; Sassi, Yosra; Kaabachi, Neziha; Abdelhak, Sonia; Abdelmoula, Mohamed Slim; Fradj, Mohamed; Azzouz, Hatem; Tebib, Neji:

    Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients

    Supplementary Material (PDF)
  • 031
    Baudou, E.; Benevent, J.; Montastruc, J. L.; Touati, G.; Hachon LeCamus, C.:

    Adverse Effects of Treatment with Valproic Acid during the Neonatal Period

  • 041
    Ardıçlı, Didem; Haliloğlu, Goknur; Alikaşifoğlu, Mehmet; Topaloğlu, Haluk:

    Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience

  • 046
    Alhusani, Alhanouf; Obaid, Abdulrahman; Blom, Henk J.; Wedell, Anna; Alfadhel, Majid:

    Adenosine Kinase Deficiency: Report and Review

    • Short Communication

  • 051
    Ünal, Özlem; Ceylaner, Serdar; Akın, Rıdvan:

    A Very Rare Etiology of Hypotonia and Seizures: Congenital Glutamine Synthetase Deficiency

  • 054
    Smolders, Joost; Jacobs, Bart C.; Tio-Gillen, Anne P.; Nijhuis, Frouke; Verrips, Aad:

    Mycoplasma Pneumoniae and Antibodies against Galactocerebroside in a 9-Year-Old Boy with Encephalitis

    Supplementary Material (PDF)
  • 057
    Sedláčková, Lucie; Laššuthová, Petra; Štěrbová, Katalin; Haberlová, Jana; Vyhnálková, Emílie; Neupauerová, Jana; Staněk, David; Šedivá, Marie; Kršek, Pavel; Seeman, Pavel:

    UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in Childhood

  • 061
    Kosma, Konstantina; Mitrakos, Anastasios; Sofokleous, Christalena; Papadimas, George; Fryssira, Helena; Kitsiou-Tzeli, Sofia; Tzetis, Maria:

    A Female Patient with Xq28 Microduplication Presenting with Myotubular Myopathy, Confirmed with a Custom-Designed X-array

    • Letter to Editor

  • 064
    Dhawan, Sumeet R.; Suthar, Renu; Padmanabha, Hansashree; Singh, Paramjeet; Dayal, Devi; Sankhyan, Naveen:

    Bilateral Posterior Circulation Stroke in a Child with Type 1 Diabetes Mellitus

    • Images in Neuropediatrics

  • 066
    Dhawan, Sumeet R.; Goswami, Jyotindra N.; Suthar, Renu; Dayal, Devi; Vyas, Sameer; Singhi, Pratibha D.:

    A Child with Central Variant Posterior Reversible Encephalopathy Syndrome

  • 068
    Dhawan, Sumeet R.; Kesavan, Shivan; Saini, Lokesh; Singh, Paramjeet; Sahu, Jitendra K.; Sankhyan, Naveen:

    Diffuse White Matter Involvement in Subacute Sclerosing Panencephalitis