Dimitrios T Papadimitriou

Biographic Data

ID7606218
NAMEDimitrios T Papadimitriou
GIVEN NAMESDimitrios T
FAMILY NAMEPapadimitriou
SIGNATUREPAPADIMITRIOU D T
AFFILIATIONSNational and Kapodistrian University of Athens
ORCID0000-0002-6083-3560
VERIFIEDYes
TOTAL WORKS4
TOTAL CITATIONS0
WORKS AS AUTHOR4
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2022
LATEST PUBLICATION YEAR2023
H-INDEX0

  • Secondary Prevention of Diabetes Type 1 with Oral Calcitriol and Analogs, the PRECAL Study

    Open AccessDimitrios T Papadimitriou, Eleni Dermitzaki et al.ARTICLEChildren2023

    Screening for Type 1 Diabetes (T1D, incidence 1:300) with T1D autoantibodies (T1Ab) at ages 2 and 6, while sensitive, lacks a preventive strategy. Cholecalciferol 2000 IU daily since birth reduced T1D by 80% at 1 year. T1D-associated T1Ab negativized within 0.6 years with oral calcitriol in 12 children. To further investigate secondary prevention of T1D with calcitriol and its less calcemic analog, paricalcitol, we initiated a prospective interve…

  • A Novel Variant in the TP53 Gene Causing Li–Fraumeni Syndrome

    Open AccessDimitrios T Papadimitriou, Constantine A Stratakis et al.ARTICLEChildren2023

    Li-Fraumeni syndrome (LFS) is an autosomal dominant hereditary cancer syndrome associated with germline pathogenic variants in the tumor protein p53 ( TP53 ) gene and elevated risk of a broad range of early-onset malignancies. Patients with LFS are at risk of a second and third primary tumor. A 15-month-old girl consulted for clitoromegaly and pubic hair. Adrenal ultrasound detected a large left adrenal tumor. Left total adrenalectomy confirmed a…

  • Identification of the Rare Ala871Glu Mutation in the Androgen Receptor Gene Leading to Complete Androgen Insensitivity Syndrome in an Adolescent Girl with Primary Amenorrhea

    Open AccessAikaterini Kapama, Dimitrios T Papadimitriou et al.ARTICLEChildren2022

    Complete Androgen Insensitivity Syndrome (CAIS) is a rare genetic condition by mutations in the androgen receptor (AR) gene resulting in target issue resistance to androgens and a female phenotype in genetically male individuals. A 16-year-old phenotypically female individual presented to our clinic with primary amenorrhea. Her clinical evaluation showed normal female external genitalia, Tanner III breast development and sparse pubic and axillary…

  • A Mixed-Longitudinal Study of Height Velocity of Greek Schoolchildren and the Milestones of the Adolescent Growth Spurt

    Open AccessKleanthis Neokleous, Kleanthis Kleanthous et al.ARTICLEChildren2022

    Height velocity (HV) growth charts constructed from longitudinal studies are scarce as they have inherent difficulties, e.g., time, and costs. These difficulties can be partly overcome by a mixed-longitudinal study that covers the entire age range within 3-6 years. To construct HV charts of Greek children and to estimate the milestones of the adolescent growth spurt (AGS), i.e., the onset of AGS (take-off), peak HV, and total pubertal growth (TPG…