Eda G. Utine
Ankara, Turkey
Last Updated: 09/26/2026
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Found 25 publications
In memory of Prof. Enver Hasanoğlu: Honoring a legacy.
Journal: The Turkish journal of pediatrics
Published: April 25, 2026
AP-1-dependent fibrosis: Exploring its potential role in the pathogenesis of placental transmogrification of the lung (PTL) via tissue-level transcriptome analysis.
Journal: Pathology, research and practice
Published: January 04, 2024
A Long-Term Follow-Up of a Patient with a Novel PORCN Variant and Additional Clinical Features.
Journal: Molecular syndromology
Published: October 05, 2023
Allele-specific antisense oligonucleotides for the treatment of BEST1-related dominantly inherited retinal diseases: An in vitro model.
Journal: Experimental eye research
Published: June 08, 2023
Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand abnormal calcification type: Further expanding the mutational spectrum and dental findings of three new patients.
Journal: European journal of medical genetics
Published: December 15, 2022
Recurrent squamous cell carcinoma and a novel mutation in a patient with xeroderma pigmentosum: a case report.
Journal: Journal of medical case reports
Published: April 24, 2022
Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review.
Journal: Pediatric gastroenterology, hepatology & nutrition
Published: April 20, 2022
Apparent mineralocorticoid excess: A diagnosis beyond classical causes of severe hypertension in a child.
Journal: Blood pressure monitoring
Published: January 19, 2022
Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features.
Journal: American journal of medical genetics. Part A
Published: January 17, 2021
Spondyloepimetaphyseal dysplasia EXTL3-deficient type: Long-term follow-up and review of the literature.
Journal: American journal of medical genetics. Part A
Published: January 08, 2021
A rare cause of syndromic short stature: 3M syndrome in three families.
Journal: American journal of medical genetics. Part A
Published: June 15, 2020
Poikiloderma with Neutropenia, Clericuzio-Type Accompanied by Loss of Digits Due to Severe Osteomyelitis.
Journal: Journal of clinical immunology
Published: April 02, 2020
Last Updated: 09/26/2026