Huseyin B. Senol
Dokuz Eylul, Turkey
Last Updated: 09/26/2026
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Found 15 publications
Acute-Phase Amantadine Treatment in Children with Severe Traumatic Brain Injury: A Dual-Center Cohort Study.
Journal: Turkish archives of pediatrics
Published: July 02, 2026
Effects of newborn screening and nusinersen on survival and functional outcomes in spinal muscular atrophy with two SMN2 copies: A nationwide multicentre real-world study from Turkey.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: March 15, 2026
Urine protein/osmolality and creatinine/osmolality ratios for assessing proteinuria and motor function in children with spinal muscular atrophy.
Journal: Brain & development
Published: February 09, 2026
THUMPD1-Related Neurodevelopmental Disorder: A Novel Homozygous Loss-of-Function Variant with an Unusual Skeletal Phenotype - A Case Report.
Journal: Molecular syndromology
Published: January 15, 2026
An Artificial Intelligence-Assisted Decision Support Tool Developed Using Real Patient Data: Classification of Normal and Neuropathic Findings in Pediatric Nerve Conduction Studies.
Journal: Pediatric neurology
Published: December 27, 2025
Challenging Mild Hypoxic-Ischemic Encephalopathy: Insights Into Neurological Outcomes.
Journal: Turkish archives of pediatrics
Published: September 17, 2025
Ataxia-telangiectasia in pediatric neurology clinics: A retrospective multicenter study.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: August 21, 2025
Clinical and laboratory characteristics of children with leukemia: a 34-year single-center experience.
Journal: The Turkish journal of pediatrics
Published: April 12, 2025
Single sural nerve response: A reliable and practical method for diagnosis of diabetic peripheral neuropathy in children with type 1 diabetes.
Journal: Journal of diabetes investigation
Published: January 29, 2025
A Novel HERC2 Variant in Two Siblings with Autosomal Recessive Intellectual Developmental Disorder-38 and Cardiomyopathy.
Journal: Molecular syndromology
Published: September 27, 2024
Symptomatic and Prophylactic Dantrolene Treatment in a Case of RYR1 -Related Congenital Myopathy.
Journal: Annals of Indian Academy of Neurology
Published: July 12, 2024
An Unusual Presentation of Leber Hereditary Optic Neuropathy-Plus Case Caused by a Novel DNAJC30 Variant.
Journal: American journal of medical genetics. Part A
Published: April 13, 2024
Last Updated: 09/26/2026