DOI: 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 50 · April 2019 DOI: 10.1055/s-009-42660

Original Article

  • 71
    Kluger, Gerhard Josef; Kirsch, Andreas; Hessenauer, Melanie; Aust, Holger; Berweck, Steffen; Sperl, Wolfgang; Betzler, Cornelia; von Stülpnagel-Steinbeis, Celina; Staudt, Martin:

    Unresponsive Wakefulness Syndrome in Children after Near-Drowning: Long-Term Outcome and Impact on the Families

    Supplementary Material (PDF)
  • 080
    Krawiec, Conrad; Ceneviva, Gary D.; Thomas, Neal J.:

    Assessing and Improving Documentation of Pediatric Brain Death Determination within an Electronic Health Record

  • 089
    Staps, Pippa; de Groot, Imelda J.M.; van Gerven, Marjo H.J.C.; Willemsen, Michèl A.A.P.:

    Daily Functioning and Quality of Life in Patients with Sjögren–Larsson Syndrome

  • 096
    Waldrop, Megan A.; Pastore, Matthew; Schrader, Rachel; Sites, Emily; Bartholomew, Dennis; Tsao, Chang-Yong; Flanigan, Kevin M.:

    Diagnostic Utility of Whole Exome Sequencing in the Neuromuscular Clinic

  • 103
    Lampe, Renée; Turova, Varvara; Botkin, Nikolai; Eckardt, Laura; Felderhoff-Müser, Ursula; Rieger-Fackeldey, Esther; Alves-Pinto, Ana; Kovtanyuk, Andrey; Sidorenko, Irina:

    Postnatal Paraclinical Parameters Associated to Occurrence of Intracerebral Hemorrhage in Preterm Infants

    • Short Communication

  • 111
    Tian, Maoqiang; Li, Juan; Lei, Wenting; Shu, Xiaomei:

    Japanese Encephalitis Virus-Induced Anti-N-Methyl-D-Aspartate Receptor Encephalitis: A Case Report and Review of Literature

  • 116
    Ben Younes, Thouraya; Benrhouma, Hanene; Klaa, Hedia; Ben Aoun, Rania; Rouissi, Aida; Ben Ahmed, Melika; Kraoua, Ichraf; Ben Youssef-Turki, Ilhem:

    Muscle-Specific Kinase Autoimmune Myasthenia Gravis: Report of a Pediatric Case and Literature Review

  • 122
    Sen, Kuntal; Hicks, Melissa A.; Huq, A.H.M.; Agarwal, Rajkumar:

    Homozygous TANGO2 Single Nucleotide Variants Presenting with Additional Manifestations Resembling Alternating Hemiplegia of Childhood–Expanding the Phenotype of a Recently Reported Condition

  • 126
    Yoshimura, Ayumi; Kibe, Tetsuya; Hasegawa, Hiroshi; Ichida, Kimiyoshi; Koshimizu, Eriko; Miyatake, Satoko; Matsumoto, Naomichi; Yokochi, Kenji:

    The Persistent Generalized Muscle Contraction in Siblings with Molybdenum Cofactor Deficiency Type A

  • 130
    Rezaei, Zahra; Hosseinpour, Sareh; Ashrafi, Mahmoud Reza; Mahdieh, Nejat; Alizadeh, Houman; Mohammadpour, Masoud; Khosroshahi, Nahideh; Amanat, Man; Tavasoli, Ali Reza:

    Hypomyelinating Leukodystrophy with Spinal Cord Involvement Caused by a Novel Variant in RARS: Report of Two Unrelated Patients

    • Images in Neuropediatrics

  • 135
    Dhawan, Sumeet R.; Saini, Lokesh; Verma Attri, Savita; Kumar, Ajay; Sankhyan, Naveen:

    Owl's Eye Sign in a Reversible Etiology of Spastic Quadriparesis