Filtros de búsqueda

Lista de obras de

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

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2010

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

artículo científico publicado en 2015

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

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

artículo científico publicado en 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.

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

article

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda