top of page

Δημοσιεύσεις του Δρ. Δημήτρη Θ. Παπαδημητρίου

A Greek girl with 11β-hydroxylase deficiency due to compound heterozygosity for two novel mutations in CYP11B1 gene..... Read more

​

A novel heterozygous mutation in the glucokinase gene is responsible for an early-onset mild form of maturity-onset diabetes of the young, type 2... Read more

Acute Bilateral Cataract in Type 1 Diabetes Mellitus... Read more

Anastrozole plus leuprorelin in early maturing girls with compromised growth: the ''GAIL'' study... Read more

Autism spectrum disorder, anxiety and severe depression in a male patient with deletion and duplication in the 21q22.3 region: A case report... Read more

Cerebral Salt Wasting Complicated by Central Diabetes Insipidus and Growth Hormone Deficiency... Read more

Characteristics of the short children referred to an academic paediatric endocrine clinic in Greece... Read more

Combined Growth Hormone-Releasing Hormone and Growth Hormone-Releasing Peptide-6 Test for the Evaluation of Growth Hormone Secretion in Children with Growth Hormone Deficiency and Growth Neurosecretory Dysfunction... Read more

Costitutional Advancement of Growth Is Associated with Early Puberty in Girls... Read more

Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infection... Read more

Greek young men grow taller... Read more

Heterozygous mutations in the cholesterol side-chain cleavage enzyme gene (CYP11A1) can cause transient adrenal insufficiency and life-threatening failure to thrive... Read more

Hypoprolactinemia as a clue to diagnosis of mild central hypothyroidism due to IGSF1 deficiency... Read more

L-Dopa is a Potent Stimulator of Cortisol in Short Children... Read more

L-Dopa Stimulates Cortisol Secretion through Adrenocorticotropic Hormone Release in Short Children... Read more

Low TSH levels are not associated with osteoporosis in childhood... Read more

Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome... Read more

Mineralocorticoid Deficiency in Post-Operative Cerebral Salt Wasting... Read more

Mineralocorticoid Receptor Mutations Are the Principal Cause of Renal Type 1 Pseudohypoaldosteronism ... Read more

bottom of page