Lista de obras -

Detection of the Bcl I polymorphism of the glucocorticoid receptor gene by single-tube allele-specific polymerase chain reaction.

artículo científico publicado en 2006

Gene Expression in Mouse Thyrotrope Adenoma: Transcription Elongation Factor Stimulates Proliferation.

artículo científico publicado en 2016

Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency

artículo científico publicado en 2018

Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

artículo científico publicado en 2016

Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.

artículo científico publicado en 2009

ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism

artículo científico publicado en 2015

ISL1-based LIM complexes control Slit2 transcription in developing cranial motor neurons.

artículo científico publicado en 2016

Increased total scavenger capacity and decreased liver fat content in rats fed dehydroepiandrosterone and its sulphate on a high-fat diet

artículo científico publicado en 2010

Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.

artículo científico publicado en 2015

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1

artículo científico publicado en 2007

Methods for the analysis of large gene deletions and their application in some hereditary diseases

artículo científico publicado en 2009

Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene.

artículo científico publicado en 2007

Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.

artículo científico publicado en 2005

Parathyroid hormone-dependent hypercalcemia.

scientific article published on January 2009

Pituitary gland development and disease: from stem cell to hormone production

artículo científico publicado en 2013

Rapid re-enlargement of a macroprolactinoma after initial shrinkage in a young woman treated with bromocriptine.

artículo científico publicado en 2005

Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family

article

Serum chromogranin A reflects regression of metastatic carcinoid during prolonged octreotide treatment

The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndrome

artículo científico publicado en 2010

The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model

artículo científico publicado en 2015

[Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients]

scientific article published on 01 October 2005

[Extracellular calcium sensing under normal and pathological conditions]

artículo científico publicado en 2009

[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity].

artículo científico publicado en 2006

Lista de obras de

Detection of the Bcl I polymorphism of the glucocorticoid receptor gene by single-tube allele-specific polymerase chain reaction.

Gene Expression in Mouse Thyrotrope Adenoma: Transcription Elongation Factor Stimulates Proliferation.

Genetic factors in hypopituitarism. The role of transcription factors in pituitary hormone deficiency

Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.

ISL1 Is Necessary for Maximal Thyrotrope Response to Hypothyroidism

ISL1-based LIM complexes control Slit2 transcription in developing cranial motor neurons.

Increased total scavenger capacity and decreased liver fat content in rats fed dehydroepiandrosterone and its sulphate on a high-fat diet

Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.

MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1

Methods for the analysis of large gene deletions and their application in some hereditary diseases

Neonatal severe hyperparathyroidism associated with a novel de novo heterozygous R551K inactivating mutation and a heterozygous A986S polymorphism of the calcium-sensing receptor gene.

Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency: demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.

Parathyroid hormone-dependent hypercalcemia.

Pituitary gland development and disease: from stem cell to hormone production

Rapid re-enlargement of a macroprolactinoma after initial shrinkage in a young woman treated with bromocriptine.

Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL gene in an extended Hungarian von Hippel-Lindau family

Serum chromogranin A reflects regression of metastatic carcinoid during prolonged octreotide treatment

The 83,557insA variant of the gene coding 11β-hydroxysteroid dehydrogenase type 1 enzyme associates with serum osteocalcin in patients with endogenous Cushing's syndrome

The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model

[Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients]

[Extracellular calcium sensing under normal and pathological conditions]

[Nucleotide sequence variants of the glucocorticoid receptor gene and their significance in determining glucocorticoid sensitivity].