Viswanathan, Venkataraman;

Shah, Harshuti:


A Review of the Prevalence, Etiology, Diagnosis, and Management of Pediatric Epilepsies in India

Atıcı, Emine;

Razaei, Derya Azim;

Saldıran, Tülay Çevik:


Effectiveness of Robot-Assisted Gait Training on Functional Skills in Children with Cerebral Palsy

Nagula, Karthikeya;

Taksande, Amar:


Modified Glasgow Coma Scale and the Alert Verbal Painful Unresponsive Scale for Assessing the Level of Consciousness in Pediatric Critical Care Patients—A Comparative Study

Yildizdas, Dincer;

Ekinci, Faruk;

Ozgur Horoz, Ozden;

Mert, Gulen Gul:


Comparison of the Full Outline of Unresponsiveness Score with the Glasgow Coma Scale as a Coma Assessment Scale in Pediatric Intensive Care

Agarwal, Ekta;

Rajadhyaksha, Surekha:


Resurgence of Subacute Sclerosing Panencephalitis: Case Series and Global Epidemiological Trends

Schneider, Joanna;

Eismann, Caroline;

Ryczek, Monika;

Potratz, Cornelia;

Kaindl, Angela M.:


Psychosocial and Socioeconomic Factors in Children with Neurofibromatosis Type 1

Jain, Rajendra S.;

Agarwal, Jitesh:


Denosumab-Induced Proximal Myopathy in a Child

Brown, Amy;

Peters, Heidi:


Cognitive and Behavioral Profiles of Children with Aspartylglucosaminuria: A Case Series

Shah, Piyush;

Seenappa, Venu;

Kalyankar, Jayashree;

Hingwala, Divyata:


Exome Sequencing Reveals Diagnosis of LAMA2-Muscular Dystrophy and Possibility of Coexisting Bethlem Myopathy in a Neonate

Hegde, Pranoy;

Palassery, Rasmi;

Karunakara, B. P.:


Factor XIII Deficiency and Intracranial Bleed: Surgical Management and Prophylaxis with Cryoprecipitate

Minamikawa, Shogo;

Ishida, Yusuke;

Maruyama, Azusa;

Nakagishi, Yasuo:


A Case of Influenza Virus-Induced Acute Cerebellitis Treated with Steroid Pulse Therapy

Buchmann, Johannes:


Case of Steroid-Sensitive Neuronopathy as a Differential Diagnosis to Dissociative Paralysis in Conversion Disorder

Nashi, Saraswati;

P., Srijithesh Rajendran;

Arunachal, Gautham;

Christopher, Rita;

Kulkarni, Girish B.;

Alladi, Survarna:


Screening for Inherited Metabolic Disorders by Tandem Mass Spectrometry May Miss L-2 Hydroxy Glutaric Aciduria: A Report of Two Cases

Bas, Hasan;

Celik, Gokalp;

Cilingir, Oguz;

Carman, Kursat Bora;

Artan, Sevilhan:


Identification of a Homozygous Deletion within

FGD4

in a Charcot-Marie-Tooth type 4H Family by Exome Sequencing

Villarreal, Enrique G.;

Diaz-Arizpe, Oscar;

Vazquez-Mena, Jesus;

Lozano-Lee, Francisco;

Tambasco, Nicola:


Atypical Case of Early-Onset Shapiro Syndrome: Diagnostic Approach and Therapeutic Challenges

Presenza, Thomas;

Scattergood, Emily;

Solomon, Jason:


Multifocal Calvarial Infarction with Epidural Hemorrhage in a Patient with Sickle Cell Vaso-Occlusive Crisis: A Case Report

Peña Segura, José Luis;

López Lafuente, Amparo;

López Pisón, Javier;

Lafuente Hidalgo, Miguel;

Pérez Delgado, Raquel:


Spastic Paraplegia Type 57: A Cerebral Palsy Mimic