Marton Doleschall

Budapest, BU, Hungary

Last Updated: 09/26/2026

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Found 16 publications

Familial medullary thyroid carcinoma secondary to an SLC30A9 intragenic deletion and translation reinitiation.

Familial medullary thyroid carcinoma secondary to an SLC30A9 intragenic deletion and translation reinitiation.

Journal: medRxiv : the preprint server for health sciences

Published: March 18, 2026

Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation.

Quantitative PCR from human genomic DNA: The determination of gene copy numbers for congenital adrenal hyperplasia and RCCX copy number variation.

Journal: PloS one

Published: March 16, 2022

Role and function of granin proteins in diabetes mellitus.

Role and function of granin proteins in diabetes mellitus.

Journal: World journal of diabetes

Published: January 27, 2021

Regular chromogranin A monitoring facilitated the early detection of a gastrointestinal neuroendocrine tumour in a patient with type 1 diabetes.

Regular chromogranin A monitoring facilitated the early detection of a gastrointestinal neuroendocrine tumour in a patient with type 1 diabetes.

Journal: Endokrynologia Polska

Published: June 17, 2020

Lower serum chromogranin B level is associated with type 1 diabetes and with type 2 diabetes patients with intensive conservative insulin treatment.

Lower serum chromogranin B level is associated with type 1 diabetes and with type 2 diabetes patients with intensive conservative insulin treatment.

Journal: Diabetology & metabolic syndrome

Published: May 12, 2020

Serum chromogranin A level continuously rises with the progression of type 1 diabetes, and indicates the presence of both enterochromaffin-like cell hyperplasia and autoimmune gastritis.

Serum chromogranin A level continuously rises with the progression of type 1 diabetes, and indicates the presence of both enterochromaffin-like cell hyperplasia and autoimmune gastritis.

Journal: Journal of diabetes investigation

Published: September 06, 2019

Chromogranin A and its role in the pathogenesis of diabetes mellitus.

Chromogranin A and its role in the pathogenesis of diabetes mellitus.

Journal: Endokrynologia Polska

Published: May 04, 2018

Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia

Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia

Journal: Orvosi hetilap

Published: February 13, 2018

A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics.

A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics.

Journal: European journal of human genetics : EJHG

Published: June 10, 2016

Increased Thyroid Hormone Activation Accompanies the Formation of Thyroid Hormone-Dependent Negative Feedback in Developing Chicken Hypothalamus.

Increased Thyroid Hormone Activation Accompanies the Formation of Thyroid Hormone-Dependent Negative Feedback in Developing Chicken Hypothalamus.

Journal: Endocrinology

Published: January 19, 2016

Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels.

Common genetic variants of the human steroid 21-hydroxylase gene (CYP21A2) are related to differences in circulating hormone levels.

Journal: PloS one

Published: April 14, 2014

NFκB induces overexpression of bovine FcRn: a novel mechanism that further contributes to the enhanced immune response in genetically modified animals carrying extra copies of FcRn.

NFκB induces overexpression of bovine FcRn: a novel mechanism that further contributes to the enhanced immune response in genetically modified animals carrying extra copies of FcRn.

Journal: mAbs

Published: February 05, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026