Migliore, Marcello;

Polizzi, Agata;

Bragazzi, Nicola L.;

Martini, Mariano;

Ruggieri, Martino;

Praticò, Andrea D.;

Vecchio, Ignazio:


Reconstructive Surgery in Children with Down Syndrome: Bioethical Implications

Ajite, Adebukola;

Oluwayemi, Oluwadare Isaac;

Olatunya, Oladele Simeon;

Ogundare, Ezra Olatunde;

Abdulraheem, Fadlulai Olaoluwa:


Malaria Infection as a Leading Cause of Febrile Seizures among Children with Seizures in Ekiti State University Teaching Hospital, Ado Ekiti, Nigeria

Bilgiç, Ayhan;

Derin, Hatice;

Eroğlu, Arzu;

Akça, Ömer Faruk;

Çaksen, Hüseyin:


Comparison of Children with Migraine and Those with Tension-Type Headache for Psychiatric Symptoms and Quality of Life

Mahfooz, Naeem;

Ostwani, Waseem:


A 17-Year-Old Male with Large Retropharyngeal Neurofibroma as the Only Symptom of Neurofibromatosis Type 1 (NF1): A Case Report and Review of Literature

Roy, Shuvendu:


ALG-9 Congenital Disorder of Glycosylation: A Patient with Novel Variants and No Dysmorphism

Smith, David F.;

Sarber, Kathleen M.;

Turner, Michele;

Dye, Thomas J.:


Vagus Nerve Stimulator–Associated Sleep Disordered Breathing: Identification, Treatment, and Outcomes in a Pediatric Patient

Mordekar, Santosh R.;

Matthai, Sona:


Mutation in

KCNJ2

Gene in a Boy with Atypical Features of Andersen–Tawil Syndrome, ADHD, and ASD: An Expanding Phenotype

Bandyopadhyay, Tapas:


Extremely Elevated Cerebrospinal Fluid Protein and Glucose Level in a Neonate with Hypernatremic Dehydration

Kılıç, Zeynep;

Mercen, Yezdanşer;

Karaoğlan, Emel;

Öztarhan, Kazım:


A Rare Cause of Facial Paralysis in Children: A Case of Ramsay Hunt Syndrome

Willoughby, Colin Eric;

Lacruz- Rengel, María Angelina;

Bertini, Enrico Silvio;

Callea, Michele:


Pierquin Syndrome: Report of a New Case

Moarefzadeh, Mohammad;

Alavi-Moghaddam, Hamideh;

Morovvati, Saeid:


A Novel Mutation in Aicardi–Goutières’ Syndrome: A Case Report

Kamoun, Fatma;

Charfi, Slim;

Nsir, Siham Ben;

Bouchaala, Wafa;

Boudawara, Tahya;

Triki, Chahnez:


Neurological Nuance: Sporadic Burkitt’s Lymphoma Presenting with Guillain–Barre Syndrome

Friedman, Neil;

Rodriguez, Ricardio J.:


Utility of Rapid Exome Sequencing in the Diagnosis of a Rare Congenital Myasthenic Syndromes in a Preterm Infant