Ceren Alavanda

Istanbul, 34093, Turkey

Last Updated: 09/26/2026

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Found 38 publications

Synergistic Contribution of HFE H63D Mutation to Secondary Polycythemia Pathogenesis at Moderate-High Altitude: A Retrospective Cohort Study.

Synergistic Contribution of HFE H63D Mutation to Secondary Polycythemia Pathogenesis at Moderate-High Altitude: A Retrospective Cohort Study.

Journal: Diagnostics (Basel, Switzerland)

Published: May 03, 2026

Clinical course of proteinuria due to cubilin variants: a large multicenter pediatric cohort.

Clinical course of proteinuria due to cubilin variants: a large multicenter pediatric cohort.

Journal: Pediatric nephrology (Berlin, Germany)

Published: November 14, 2025

Clinical and Molecular Spectrum of Infantile Hypercalcemia Type I: Insights Into CYP24A1 Variants.

Clinical and Molecular Spectrum of Infantile Hypercalcemia Type I: Insights Into CYP24A1 Variants.

Journal: Clinical endocrinology

Published: September 09, 2025

Benign proximal tubular albuminuria due to AMN mutation: A challenging presentation of Imerslund-Gräsbeck syndrome.

Benign proximal tubular albuminuria due to AMN mutation: A challenging presentation of Imerslund-Gräsbeck syndrome.

Journal: Pediatric nephrology (Berlin, Germany)

Published: April 30, 2025

Predictors of kidney survival in children with autosomal recessive polycystic kidney disease.

Predictors of kidney survival in children with autosomal recessive polycystic kidney disease.

Journal: Clinical and experimental nephrology

Published: April 21, 2025

A New Family with X-Linked Intellectual Disability 90: A Case Report of a Novel DLG3 Variant and Literature Review.

A New Family with X-Linked Intellectual Disability 90: A Case Report of a Novel DLG3 Variant and Literature Review.

Journal: Molecular syndromology

Published: April 05, 2025

Genetic Characterization of Turkish Patients with Pituitary Neuroendocrine Tumors.

Genetic Characterization of Turkish Patients with Pituitary Neuroendocrine Tumors.

Journal: Turkish neurosurgery

Published: March 25, 2025

Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in Türkiye

Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in Türkiye

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: January 06, 2025

Comprehensive Assessment of Dermatologic and Dysmorphic Manifestations in Patients With Down Syndrome.

Comprehensive Assessment of Dermatologic and Dysmorphic Manifestations in Patients With Down Syndrome.

Journal: Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI)

Published: September 06, 2024

Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings

Expanding the Clinical Features of Schimke Immuno-osseous Dysplasia: a New Patient with a Novel Variant and Novel Clinical Findings

Journal: Journal of clinical research in pediatric endocrinology

Published: August 08, 2024

Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.

Clinical and Molecular Genetic Characteristics of Patients with Hereditary Hypophosphatemia.

Journal: The Journal of clinical endocrinology and metabolism

Published: August 08, 2024

Comprehensive analysis of genotypic and phenotypic characteristics of biotinidase deficiency patients in the eastern region of Türkiye.

Comprehensive analysis of genotypic and phenotypic characteristics of biotinidase deficiency patients in the eastern region of Türkiye.

Journal: The Turkish journal of pediatrics

Published: July 09, 2024

Showing 1-12 of 38

Last Updated: 09/26/2026