Sule Kamıs
Adana, Turkey
Last Updated: 09/26/2026
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Found 12 publications
Congenital Ichthyosis and Jordans' Anomaly: A Diagnostic Clue to Chanarin-Dorfman Syndrome.
Journal: Journal of paediatrics and child health
Published: July 22, 2026
Serum ferritin levels in non-anemic children and adolescents with attention-deficit/hyperactivity disorder: associations with clinical presentations and symptom severity.
Journal: Frontiers in psychiatry
Published: May 08, 2026
Maxillary mesenchymal chondrosarcoma harboring HEY1::NCOA2 fusion in a 13-year-old girl: a rare case report and literature review.
Journal: Frontiers in pediatrics
Published: December 01, 2025
Computed tomography-derived sarcopenia, enteral nutritional support, and febrile neutropenia burden in children with acute lymphoblastic leukemia: a retrospective cohort study.
Journal: Frontiers in pediatrics
Published: November 23, 2025
Diagnostic Value of CA-125 and Other Tumor Biomarkers in Children with Suspected Malignancy: A Retrospective Cohort Study.
Journal: Diagnostics (Basel, Switzerland)
Published: November 20, 2025
Childhood lymphadenopathy: ultrasonographic predictors of malignancy in a retrospective cohort of 500 patients.
Journal: Frontiers in pediatrics
Published: July 10, 2025
Metastatic pediatric alveolar soft part sarcoma: a rare case report highlighting multidisciplinary treatment, molecular diagnostics, and novel therapeutic approaches.
Journal: Frontiers in pediatrics
Published: May 30, 2025
Pediatric tonsillar synovial sarcoma: extremely rare case report.
Journal: Frontiers in pediatrics
Published: May 28, 2025
Evaluation of iron accumulation during childhood cancer treatment.
Journal: Frontiers in pediatrics
Published: April 28, 2025
Recurrent T-lymphoblastic lymphoma in a pediatric patient with bilateral breast and skin involvement: A rare clinical presentation.
Journal: Annals of medicine and surgery (2012)
Published: March 18, 2025
Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report.
Journal: Case reports in hematology
Published: December 23, 2024
Hoyeraal-Hreidarsson syndrome: a case report of dyskeratosis congenita with a novel PARN gene mutation.
Journal: Annals of medicine and surgery (2012)
Published: August 06, 2024
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Last Updated: 09/26/2026