Threatening Blindness in a Child With Typical Hemolytic Uremic Syndrome

Anaïs Corgier-Pattberg(Hôpital de la Timone), Béatrice Desnous(Inserm), Stéphanie Clave, M. Beylerian(Hôpital Nord), Benoît Testud(Hôpital de la Timone), Mathilde Cailliez(Hôpital de la Timone)

Pediatric Neurology

June 25, 2021

10.1016/j.pediatrneurol.2021.06.008

Cited by 1

Related Papers

Diagnosis delay in West syndrome: misdiagnosis and consequences

|European Journal of Pediatrics|2012|88

Molecular and clinical descriptions of patients with <scp>GABA<sub>A</sub></scp> receptor gene variants (<i><scp>GABRA1</scp>, <scp>GABRB2</scp>, <scp>GABRB3</scp>, <scp>GABRG2</scp></i>): A cohort study, review of literature, and genotype–phenotype correlation

|Epilepsia|2022|80

Challenges and new perspectives of developmental cognitive EEG studies

|NeuroImage|2022|49

De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy

|Journal of Medical Genetics|2017|41

Slow Titration of Cannabidiol Add-On in Drug-Resistant Epilepsies Can Improve Safety With Maintained Efficacy in an Open-Label Study

|Frontiers in Neurology|2020|39