Kinga Salacinska

Lodz, LD, Poland

Last Updated: 09/26/2026

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Found 11 publications

Case Report: Palopegteriparatide as a novel therapeutic option in pediatric autosomal dominant hypocalcemia type 1.

Case Report: Palopegteriparatide as a novel therapeutic option in pediatric autosomal dominant hypocalcemia type 1.

Journal: Frontiers in endocrinology

Published: March 24, 2026

Evaluating the Utility of Fresh Tissue in Molecular Diagnostics of Colorectal Cancer.

Evaluating the Utility of Fresh Tissue in Molecular Diagnostics of Colorectal Cancer.

Journal: Cancers

Published: September 16, 2025

To Test or Not to Test: Routine Thrombophilia Diagnostic Screening of Women with Reproductive Failures.

To Test or Not to Test: Routine Thrombophilia Diagnostic Screening of Women with Reproductive Failures.

Journal: Journal of clinical medicine

Published: October 01, 2023

Clinical significance of polymorphisms of genes encoding collagen (COL1A1, COL5A1) and their correlation with joint laxity and recurrent patellar dislocation in adolescents.

Clinical significance of polymorphisms of genes encoding collagen (COL1A1, COL5A1) and their correlation with joint laxity and recurrent patellar dislocation in adolescents.

Journal: Scientific reports

Published: June 23, 2023

NGS analysis of collagen type I genes in Polish patients with Osteogenesis imperfecta: a nationwide multicenter study.

NGS analysis of collagen type I genes in Polish patients with Osteogenesis imperfecta: a nationwide multicenter study.

Journal: Frontiers in endocrinology

Published: January 23, 2023

Identification of New Copy Number Variation and the Evaluation of a CNV Detection Tool for NGS Panel Data in Polish Familial Hypercholesterolemia Patients.

Identification of New Copy Number Variation and the Evaluation of a CNV Detection Tool for NGS Panel Data in Polish Familial Hypercholesterolemia Patients.

Journal: Genes

Published: July 18, 2022

Identification of New Genetic Determinants in Pediatric Patients with Familial Hypercholesterolemia Using a Custom NGS Panel.

Identification of New Genetic Determinants in Pediatric Patients with Familial Hypercholesterolemia Using a Custom NGS Panel.

Journal: Genes

Published: May 13, 2022

The first glycine-to-tryptophan substitution in the COL1A1 gene identified in a patient with progressively-deforming Osteogenesis imperfecta.

The first glycine-to-tryptophan substitution in the COL1A1 gene identified in a patient with progressively-deforming Osteogenesis imperfecta.

Journal: Molecular genetics & genomic medicine

Published: September 28, 2021

Novel Mutations Within Collagen Alpha1(I) and Alpha2(I) Ligand-Binding Sites, Broadening the Spectrum of Osteogenesis Imperfecta - Current Insights Into Collagen Type I Lethal Regions.

Novel Mutations Within Collagen Alpha1(I) and Alpha2(I) Ligand-Binding Sites, Broadening the Spectrum of Osteogenesis Imperfecta - Current Insights Into Collagen Type I Lethal Regions.

Journal: Frontiers in genetics

Published: April 09, 2021

New findings in oligogenic inheritance of congenital hypogonadotropic hypogonadism.

New findings in oligogenic inheritance of congenital hypogonadotropic hypogonadism.

Journal: Archives of medical science : AMS

Published: June 27, 2020

Identification of gene variants in a cohort of hypogonadotropic hypogonadism: Diagnostic utility of custom NGS panel and WES in unravelling genetic complexity of the disease.

Identification of gene variants in a cohort of hypogonadotropic hypogonadism: Diagnostic utility of custom NGS panel and WES in unravelling genetic complexity of the disease.

Journal: Molecular and cellular endocrinology

Published: April 05, 2020

Showing 1-11 of 11

Last Updated: 09/26/2026