Zeynep Y. Yildirmak
Sisli, Turkey
Last Updated: 09/26/2026
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Found 13 publications
Comment on: Novel Findings in Pediatric and Adolescent Patients With Cancer and a Germline SMARCA4 Variant. First Familial Case of Neuroblastoma in a Mother-Daughter Pair With a Shared Germline SMARCA4 Variant: First Familial Case of Neuroblastoma in a Mother-Daughter Pair With a Shared Germline SMARCA4 Variant.
Journal: Pediatric blood & cancer
Published: July 09, 2025
Evaluation of anemia at diagnosis and during follow-up in childhood inflammatory bowel diseases.
Journal: European journal of pediatrics
Published: April 28, 2025
Clinical Evaluation and Outcomes of Mesenteric Lymphadenopathy in Children: A Cross-Sectional Analysis.
Journal: Sisli Etfal Hastanesi tip bulteni
Published: January 17, 2025
Status of IKZF1 Deletions in Diagnose and Relapsed Pediatric B-ALL Patients.
Journal: Biochemical genetics
Published: August 26, 2024
Severe hepatic sinusoidal obstruction syndrome in a patient with Wilms tumor and hereditary spherocytosis.
Journal: International cancer conference journal
Published: September 28, 2023
Clinical Characteristics and Treatment Outcome of Hereditary Spherocytosis: A Single Center's Experience.
Journal: Sisli Etfal Hastanesi tip bulteni
Published: April 09, 2023
Seroprevalence of Hepatitis A, B, and C in Syrian Refugee Children Newly Diagnosed With Cancer.
Journal: Journal of pediatric hematology/oncology
Published: December 17, 2022
Prolonged Bleeding After Dental Extraction Due to Decreased Serum Level of Von Willebrand Factor Caused by Untreated Profound Hypothyroidism.
Journal: Journal of pediatric hematology/oncology
Published: October 03, 2022
Diagnostic challenges during the COVID-19 pandemic: A child with tuberculosis-induced haemophagocytic lymphohistiocytosis misdiagnosed as multi-inflammatory syndrome in children.
Journal: Journal of paediatrics and child health
Published: March 18, 2022
Renal Ultrasonographic Abnormalities at Initial Presentation of Children Diagnosed with Acute Lymphoblastic Leukemia and Long-Term Renal Functions and Prognosis in Survivors.
Journal: Sisli Etfal Hastanesi tip bulteni
Published: December 11, 2021
Assessment of Serum Spexin Levels in Obese Adolescents with Metabolic Syndrome Antecedents: Preliminary Results.
Journal: Hormone research in paediatrics
Published: September 02, 2021
Amyloidosis in a Patient With Congenital Neutropenia Because of G6PC3 Deficiency.
Journal: Journal of pediatric hematology/oncology
Published: January 01, 2021
Last Updated: 09/26/2026