Dana Zemkova

Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene.

Journal: Endocrine connections

Published: May 04, 2024

Analysis of children with familial short stature: who should be indicated for genetic testing?

Journal: Endocrine connections

Published: June 13, 2023

A comprehensive validation study of the latest version of BoneXpert on a large cohort of Caucasian children and adolescents.

Journal: Frontiers in endocrinology

Published: December 23, 2022

Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

Journal: Frontiers in endocrinology

Published: November 19, 2022

Tubuloglomerular Disease With Cone-Shaped Epiphyses Associated With Hypomorphic Variant and a Novel p.Cys14Arg in the TTC21B Gene: A Case Report.

Journal: Frontiers in pediatrics

Published: August 03, 2021

Familial Short Stature-A Novel Phenotype of Growth Plate Collagenopathies.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 27, 2020

NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy.

Journal: The Journal of clinical endocrinology and metabolism

Published: September 24, 2019

High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 23, 2018

Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt.

Journal: American journal of medical genetics. Part A

Published: May 30, 2018

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? .

Journal: Hormone research in paediatrics

Published: August 30, 2016

A Rare Variant of Turner Syndrome in Four Sequential Generations: Effect of the Interplay of Growth Hormone Treatment and Estrogens on Body Proportion.

Journal: Hormone research in paediatrics

Published: March 10, 2016

Cost-of-illness analysis and regression modeling in cystic fibrosis: a retrospective prevalence-based study.

Journal: The European journal of health economics : HEPAC : health economics in prevention and care

Published: September 22, 2015

Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene.

Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene.

Analysis of children with familial short stature: who should be indicated for genetic testing?

Analysis of children with familial short stature: who should be indicated for genetic testing?

A comprehensive validation study of the latest version of BoneXpert on a large cohort of Caucasian children and adolescents.

A comprehensive validation study of the latest version of BoneXpert on a large cohort of Caucasian children and adolescents.

Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

Tubuloglomerular Disease With Cone-Shaped Epiphyses Associated With Hypomorphic Variant and a Novel p.Cys14Arg in the TTC21B Gene: A Case Report.

Tubuloglomerular Disease With Cone-Shaped Epiphyses Associated With Hypomorphic Variant and a Novel p.Cys14Arg in the TTC21B Gene: A Case Report.

Familial Short Stature-A Novel Phenotype of Growth Plate Collagenopathies.

Familial Short Stature-A Novel Phenotype of Growth Plate Collagenopathies.

NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy.

NPR2 Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy.

High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH.

High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH.

Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt.

Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt.

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? .

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? .

A Rare Variant of Turner Syndrome in Four Sequential Generations: Effect of the Interplay of Growth Hormone Treatment and Estrogens on Body Proportion.

A Rare Variant of Turner Syndrome in Four Sequential Generations: Effect of the Interplay of Growth Hormone Treatment and Estrogens on Body Proportion.

Cost-of-illness analysis and regression modeling in cystic fibrosis: a retrospective prevalence-based study.

Cost-of-illness analysis and regression modeling in cystic fibrosis: a retrospective prevalence-based study.

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? .

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? .