Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Diana Epure

Biographic Data

ID8253435
NAMEDiana Epure
GIVEN NAMESDiana
FAMILY NAMEEpure
SIGNATUREEPURE D
AFFILIATIONSSpitalul Clinic Dr. Victor Babes
VERIFIEDNo
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2023
LATEST PUBLICATION YEAR2023
H-INDEX0
  • Autosomal Dominant Hypocalcemia Type 1 and Neonatal Focal Seizures

    Open Access•Raluca Ioana Teleanu, Marlene Alexandra Sarman et al.•ARTICLE•Children•2023

    Autosomal dominant hypocalcemia type 1 (ADH1) is a rare form of hypoparathyroidism that is characterized by gain-of-function mutations in the CASR gene, which provides instructions for producing the protein called calcium-sensing receptor (CaSR). Hypocalcemia in the neonatal period has a wide differential diagnosis. We present the case of a female newborn with genetic hypoparathyroidism (L125P mutation of CASR gene), hypocalcemia, and neonatal se…

  • The Importance of Implementing a Transition Strategy for Patients with Muscular Dystrophy

    Open Access•Maria Alina Lupu, Maria Lupu et al.•ARTICLE•Children•2023

    Progress in the field of muscular dystrophy (MD) using a multidisciplinary approach based on international standards of care has led to a significant increase in the life expectancy of patients. The challenge of transitioning from pediatric to adult healthcare has been acknowledged for over a decade, yet it continues to be a last-minute concern. Currently, there is no established consensus on how to evaluate the effectiveness of the transition pr…

No prominent works on this page.

  • Autosomal Dominant Hypocalcemia Type 1 and Neonatal Focal Seizures

    Open Access•Raluca Ioana Teleanu, Marlene Alexandra Sarman et al.•ARTICLE•Children•2023

    Autosomal dominant hypocalcemia type 1 (ADH1) is a rare form of hypoparathyroidism that is characterized by gain-of-function mutations in the CASR gene, which provides instructions for producing the protein called calcium-sensing receptor (CaSR). Hypocalcemia in the neonatal period has a wide differential diagnosis. We present the case of a female newborn with genetic hypoparathyroidism (L125P mutation of CASR gene), hypocalcemia, and neonatal se…

  • The Importance of Implementing a Transition Strategy for Patients with Muscular Dystrophy

    Open Access•Maria Alina Lupu, Maria Lupu et al.•ARTICLE•Children•2023

    Progress in the field of muscular dystrophy (MD) using a multidisciplinary approach based on international standards of care has led to a significant increase in the life expectancy of patients. The challenge of transitioning from pediatric to adult healthcare has been acknowledged for over a decade, yet it continues to be a last-minute concern. Currently, there is no established consensus on how to evaluate the effectiveness of the transition pr…

Internal Medicine (2 works) · Medicine (2 works) · Pediatrics (2 works) · Adolescent and Pediatric Healthcare (1 work) · Adult care (1 work) · Bioinformatics (1 work) · Biology (1 work) · Calcium (1 work) · Calcium metabolism (1 work) · Calcium-sensing receptor (1 work)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae