Child Neurology Open: 2022, vol: 9, issue:
- 1)- Maya Eid, Sonal Bhatia. Novel De Novo Heterozygous Variants in the Gene Causing ZTTK Syndrome: A Case Report of Two Patients and Review of Neurological Findings. Child neurology open. 2022, 9: 2329048X221119658
Cited : 0Read More - 2)- Douglas R Nordli, Chethan K Rao, Antonio V Delgado-Escueta, Fernando Galan. A Novel Mutation in Lafora Disease and Update on Pathophysiology and Future Treatments. Child neurology open. 2022, 9: 2329048X221126361Cited : 0Read More
- 3)- Abdulla Alawadhi, Chantal Poulin. Spontaneous Resolution of Drug-Resistant Epilepsy in Patients with Sturge-Weber Syndrome. Child neurology open. 2022, 9: 2329048X221129678Cited : 1Read More
- 4)- Abdulhafeez M Khair, Stephen Falchek, Rahul Nikam, Gurcharanjeet Kaur. Epilepsy and Electroencephalogram Characteristics in Children with Neurofibromatosis Type 1, What We Have Learned from a Tertiary Center Five Years' Experience. Child neurology open. 2022, 9: 2329048X221131445Cited : 3Read More
- 5)- Ingrid Frydson, Sreenivas Avula, Samiya Fatima Ahmad. A Case of a Seven-Year-old boy with Epilepsy with Myoclonic Absence: Importance of Seizure Semiology, Genetic Etiology, and Electroencephalogram Correlation for Timely Intervention. Child neurology open. 2022, 9: 2329048X221131738Cited : 0Read More
- 6)- Luciana de Paula Souza, Beatriz Bagatin Bermudez, Danielle Caldas Bufara, Ana Chrystina de Souza Crippa. A Retrospective Cohort Study of Combined Therapy in West Syndrome associated with Trisomy 21. Child neurology open. 2022, 9: 2329048X221132639Cited : 0Read More
- 7)- Rebecca Silverstein, Michael Kuwabara, Brian Appavu. Neonatal Aneurysm Rupture in a Child with a De Novo Variant to ANKRD17. Child neurology open. 2022, 9: 2329048X221134600Cited : 1Read More
- 8)- Jay Lodhia, Hilary Chipongo, Adnan Sadiq, Khadija Khelef, Kenan Bosco, Marieke Dekker. An Unusual Cause of Cerebral Infarction in a Tanzanian School Child. Child neurology open. 2022, 9: 2329048X221139411Cited : 1Read More
- 9)- Siddiqa Ozaal, Subashinie Jayasena, Surani Jayakody, Sabine Schröder, Anura Jayawardana, Eresha Jasinge. Clinical Presentation and Genetic Heterogeneity Including Two Novel Variants in Sri Lankan Patients With Infantile Sandhoff Disease. Child neurology open. 2022, 9: 2329048X221139495Cited : 2Read More
- 10)- Grace Bryant, Steven A Moore, James S Nix, Grace Rice, Murat Gokden, Aravindhan Veerapandiyan. Miyoshi Muscular Dystrophy Due to Novel Splice Site Variants in Gene. Child neurology open. 2022, 9: 2329048X221140298Cited : 0Read More
- 11)- Sarah Mingels, Marita Granitzer. Cross-Sectional Study of Headache in Flemish Children and Adolescents. Child neurology open. 2022, 9: 2329048X221140783Cited : 1Read More
- 12)- Roxanne M Miller, Anthony Zarka, Samiya F Ahmad. The Case of the Rare Malformation and Rare Variant: An Infant with a Self-Embolized Torcular Dural Sinus Malformation and a Concomitant Prothrombin Variant. Child neurology open. 2022, 9: 2329048X221140784Cited : 0Read More
- 13)- Fernando Galan, Douglas R Nordli, Milad Yazdani, Jessica Klein. A Favorable Treatment Outcome in and Influenza Associated Acute Necrotizing Encephalitis. Child neurology open. 2022, 9: 2329048X221143689Cited : 1Read More
- 14)- Mekka R Garcia, Lena Bell, Claire Miller, Devorah Segal. A Case of Infant-Type Hemispheric Glioma with Fusion. Child neurology open. 2022, 9: 2329048X221146982Cited : 1Read More
