Al-Taei, Omar;

Al-Saadi, Tariq:


Cognitive Deficits in Pediatric Craniopharyngioma: An Updated Review

Anuradha, K. W. D. A.;

Chang, Thashi:


Pediatric Autoimmune Encephalitis in Sri Lanka: A Single-Center Experience over 7 Years

Kenis-Coskun, Ozge;

Deveci, Mehmet;

Ozturk, Gulten;

Karadag-Saygi, Evrim:


Validity and Reliability of Quick Motor Function Test in Ambulatory Duchenne Muscular Dystrophy Patients

Dursun, Nigar;

Gokbel, Tugba;

Cekmece, Cigdem;

Dursun, Erbil:


Improved Sitting Balance in Children with Cerebral Palsy: Body Functions to Activity and Participation

Hattapoğlu, Salih;

Ekici, Faysal:


Value of Magnetic Resonance Spectroscopy for Diagnosis of Creatine Deficiency Syndrome

Maria, Arjun;

Alam, Seema:


Laterotrusion (Side to Side) and Protrusion/Retraction Difficulty of Tongue in Two Children with Wilson’s Disease

Scalia, Gianluca;

Marrone, Salvatore;

Riolo, Carmelo;

Vasta, Giuseppe;

Umana, Giuseppe Emmanuele;

Cicero, Salvatore;

Iacopino, Domenico Gerardo;

Nicoletti, Giovanni Federico:


Neuroendoscopic Navigated One-Step Removal of Crossed Ventricular Catheter Fragments: Technical Note

Ekici, Arzu;

Görükmez, Orhan:


A Novel Heterozygous

ANO3

Mutation in a Child Presenting Tremor with Dystonia and Review of the Literature

Nagabushana, Divya;

M., Pradeep G. C.;

Mangalgi, Sharanabasavesh;

Veerabhadraiah, Krithika Manne:


Congenital Radial Nerve Palsy in a Preterm Baby—A Case Report

Tanaka, Kuniaki;

Iwai, Atsushi;

Taki, Junya;

Kitagawa, Masashi;

Hayashi, Tomoko;

Tsuzuki, Sadatoshi;

Yamamoto, Tetsuro;

Yoshioka, Takako;

Hirato, Junko;

Maihara, Toshiro;

Yamada, Keisuke;

Usami, Ikuya;

Heike, Toshio:


Primary Diffuse Leptomeningeal Atypical Teratoid/Rhabdoid Tumor Initially Masquerading as Guillain–Barré Syndrome: A Case Report and Literature Review

Sharma, Kamal;

Sheikh, Ameera;

Maertens, Paul:


The Novel Use of a Synthetic Amino Acid Analog in the Management of Menkes’ Disease

AlJefri, Abdullah Hussain;

Alsowat, Daad Khalaf:


Abnormal Movement Following Transcobalamin II Deficiency Treatment Responding to Clonazepam: A Case Report

Gadgil, Pradnya;

Seenappa, Venu;

Setty, Phani N.;

Joshi, Vaishali;

Shah, Shailee:


Novel De Novo

TBL1XR1

Variant Causing PIERPONT Syndrome in an Indian Child: A Case Report and Genotype–Phenotype Review of Reported Patients

Malalla, Husain;

Busehail, Mariam:


A Case Report of Two Bahraini Siblings Presenting with Different Rare Neurogenetic Disorders: Congenital Insensitivity to Pain with Anhidrosis and Rigid Spine Muscular Dystrophy

Sastre-Real, María;

Tirado, Pilar;

Díaz-de-Terán, Javier:


Migraine with Brainstem Aura Associated with SCN2A Mutation: A Case Report

Faruq, Mohammed;

Gupta, Ashok;

Shrivastava, Divya;

Shamim, Uzma:


Deletion of 2q22.2q22.3 in Mowat–Wilson Syndrome: A Case Report and Review of the Literature

Siriboriruk, Jukrapun:


Central Nervous System Involvement in Dengue Virus Type 1 Infection: A Pediatric Case Series