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List of works by Barbora Obermannová

Alteration of B cell subsets and the receptor for B cell activating factor (BAFF) in paediatric patients with type 1 diabetes.

scientific article published on 13 April 2017

Five years of improving diabetes control in Czech children after the establishment of the population-based childhood diabetes register ČENDA

scientific article published on 16 October 2019

Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY).

scientific article

Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations

scientific article published on 10 June 2015

HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes

scientific article published on 01 January 2011

High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism

scientific article published on 2 October 2015

High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency

scientific article published on 20 December 2013

Mutations and pituitary morphology in a series of 82 patients with PROP1 gene defects

scientific article published on 18 October 2011

Novel calcium-sensing receptor cytoplasmic tail deletion mutation causing autosomal dominant hypocalcemia: molecular and clinical study

scholarly article by Barbora Obermannova et al published April 2016 in European Journal of Endocrinology

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

Tolerogenic Dendritic Cells from Poorly Compensated Type 1 Diabetes Patients Have Decreased Ability To Induce Stable Antigen-Specific T Cell Hyporesponsiveness and Generation of Suppressive Regulatory T Cells.

scientific article

Treated Autoimmune Thyroid Disease Is Associated with a Decreased Quality of Life among Young Persons with Type 1 Diabetes.

scientific article published on 18 May 2015

Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene

article

Diabetes s nadhledem: průvodce tělem i duší dětí a dospívajících s diabetem

book edition published in 2015

Selhání střeva u dětí: etiopatogeneze a terapie: motolské pediatrické semináře 6

book edition published in 2020

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