Metin Eser

Istanbul, Turkey

Last Updated: 09/26/2026

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Found 38 publications

Familial Low-Phospholipid-Associated Cholelithiasis Syndrome Presenting with Recurrent Intrahepatic Stones After Cholecystectomy with a Heterozygous ABCB4 Variant.

Familial Low-Phospholipid-Associated Cholelithiasis Syndrome Presenting with Recurrent Intrahepatic Stones After Cholecystectomy with a Heterozygous ABCB4 Variant.

Journal: The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology

Published: July 20, 2026

Mismatch Repair Deficiency and Programmed Death-Ligand 1 Expression in Treatment-Naïve High-Risk and Very High-Risk Locally Advanced Prostate Cancer: Histomorphological Associations and Prognostic Value.

Mismatch Repair Deficiency and Programmed Death-Ligand 1 Expression in Treatment-Naïve High-Risk and Very High-Risk Locally Advanced Prostate Cancer: Histomorphological Associations and Prognostic Value.

Journal: International journal of surgical pathology

Published: April 23, 2026

Risk Tier, Variant Certainty, and Real-World Care Patterns in Breast Cancer Patients with Germline Alterations in Breast Cancer Susceptibility Genes.

Risk Tier, Variant Certainty, and Real-World Care Patterns in Breast Cancer Patients with Germline Alterations in Breast Cancer Susceptibility Genes.

Journal: Cancers

Published: April 12, 2026

Oculo-auricular syndrome caused by a novel HMX1 frameshift variant: a case report.

Oculo-auricular syndrome caused by a novel HMX1 frameshift variant: a case report.

Journal: Ophthalmic genetics

Published: February 24, 2026

Next-Generation Sequencing-Based Detection of KRAS G12D Variants in Colorectal Cancer: A Retrospective Cohort Study.

Next-Generation Sequencing-Based Detection of KRAS G12D Variants in Colorectal Cancer: A Retrospective Cohort Study.

Journal: Genes

Published: January 09, 2026

Breast cancer surgery in the era of genetic uncertainty: real-world outcomes in BRCA1/2 pathogenic variants and variants of uncertain significance.

Breast cancer surgery in the era of genetic uncertainty: real-world outcomes in BRCA1/2 pathogenic variants and variants of uncertain significance.

Journal: BMC cancer

Published: January 01, 2026

Paediatric macrophage activation syndrome: clinical features and outcomes across diverse aetiologies.

Paediatric macrophage activation syndrome: clinical features and outcomes across diverse aetiologies.

Journal: Rheumatology (Oxford, England)

Published: December 30, 2025

Effective interleukin-6 inhibition in a pediatric patient with mevalonate kinase deficiency and chronic nonbacterial osteomyelitis-like bone lesions under interleukin-1 blockade.

Effective interleukin-6 inhibition in a pediatric patient with mevalonate kinase deficiency and chronic nonbacterial osteomyelitis-like bone lesions under interleukin-1 blockade.

Journal: The Turkish journal of pediatrics

Published: December 01, 2025

Neonatal-onset genetic epilepsies: Insights from a large multicentre cohort.

Neonatal-onset genetic epilepsies: Insights from a large multicentre cohort.

Journal: Seizure

Published: October 28, 2025

From Synovial Fluid to Musculoskeletal Ultrasound: A Portrayal of Joint Involvement in Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: A Case Series.

From Synovial Fluid to Musculoskeletal Ultrasound: A Portrayal of Joint Involvement in Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome: A Case Series.

Journal: Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

Published: October 15, 2025

Pediatric-Onset Polyarteritis Nodosa and Deficiency of Adenosine Deaminase 2: Clinical Overlap and Divergence.

Pediatric-Onset Polyarteritis Nodosa and Deficiency of Adenosine Deaminase 2: Clinical Overlap and Divergence.

Journal: Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases

Published: August 15, 2025

Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1.

Clinical and molecular results in 15 Turkish patients with Wiedemann-Steiner syndrome: identification of eight novel KMT2A variants and a case of dual molecular diagnosis in the CSNK2A1.

Journal: European journal of pediatrics

Published: June 17, 2025

Showing 1-12 of 38

Last Updated: 09/26/2026