Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Flavia Chisavu

Biographic Data

ID8256248
NAMEFlavia Chisavu
GIVEN NAMESFlavia
FAMILY NAMEChisavu
SIGNATURECHISAVU F
AFFILIATIONSVictor Babeș University of Medicine and Pharmacy Timișoara
ORCID0000-0001-9456-4517
VERIFIEDYes
TOTAL WORKS3
TOTAL CITATIONS0
WORKS AS AUTHOR3
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2023
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Nephrogenic Diabetes Insipidus Affecting Three Males in Two Generations—Case Report and Review of the Literature

    Open Access•Ramona Stroescu, Adela Chiriţă-Emandi et al.•ARTICLE•Children•2025

    Background: Nephrogenic diabetes insipidus (NDI) is defined as the inability of the kidney to concentrate urine owing to the insensitivity of the distal nephron to the antidiuretic hormone, arginine vasopressin. NDI is a heterogeneous rare autosomal dominant or X-linked disease. Objective: We present a family with nephrogenic diabetes affecting three males in two generations. Methods: We report two boys with NDI: a 4-month-old infant who was trea…

  • Acute Glomerulonephritis Following Systemic Scabies in Two Brothers

    Open Access•Flavia Chisavu, Mihai Gafencu et al.•ARTICLE•Children•2024

    Scabies is a parasitic infestation of the skin with high prevalence in crowded spaces. In some instances, scabies becomes the underlying factor for complicated skin-borne opportunistic pathogens infections in both children and adults. Geographic area and socio-economic factors are determinants of the endemic pattern of this disease. Currently, the treatment of scabies has been under special attention. A combination of oral therapy with Ivermectin…

  • Phenotype of Idiopathic Infantile Hypercalcemia Associated with the Heterozygous Pathogenic Variant of SLC34A1 and CYP24A1

    Open Access•Teofana Bizerea, Flavia Chisavu et al.•ARTICLE•Children•2023

    Idiopathic infantile hypercalcemia (IIH) is a rare genetic disease, also called hypersensitivity to vitamin D3. The molecular heterogeneity allows for the differentiation between the two forms; IIH type 1 caused by CYP24A1 genetic variants and IIH type 2 associated with SLC34A1 mutations. The affected individuals express a variety of symptoms: hypercalcemia, hypercalciuria, suppressed intact parathormone levels (PTH), nephrocalcinosis, elevated l…

No prominent works on this page.

  • Phenotype of Idiopathic Infantile Hypercalcemia Associated with the Heterozygous Pathogenic Variant of SLC34A1 and CYP24A1

    Open Access•Teofana Bizerea, Flavia Chisavu et al.•ARTICLE•Children•2023

    Idiopathic infantile hypercalcemia (IIH) is a rare genetic disease, also called hypersensitivity to vitamin D3. The molecular heterogeneity allows for the differentiation between the two forms; IIH type 1 caused by CYP24A1 genetic variants and IIH type 2 associated with SLC34A1 mutations. The affected individuals express a variety of symptoms: hypercalcemia, hypercalciuria, suppressed intact parathormone levels (PTH), nephrocalcinosis, elevated l…

  • Acute Glomerulonephritis Following Systemic Scabies in Two Brothers

    Open Access•Flavia Chisavu, Mihai Gafencu et al.•ARTICLE•Children•2024

    Scabies is a parasitic infestation of the skin with high prevalence in crowded spaces. In some instances, scabies becomes the underlying factor for complicated skin-borne opportunistic pathogens infections in both children and adults. Geographic area and socio-economic factors are determinants of the endemic pattern of this disease. Currently, the treatment of scabies has been under special attention. A combination of oral therapy with Ivermectin…

  • Nephrogenic Diabetes Insipidus Affecting Three Males in Two Generations—Case Report and Review of the Literature

    Open Access•Ramona Stroescu, Adela Chiriţă-Emandi et al.•ARTICLE•Children•2025

    Background: Nephrogenic diabetes insipidus (NDI) is defined as the inability of the kidney to concentrate urine owing to the insensitivity of the distal nephron to the antidiuretic hormone, arginine vasopressin. NDI is a heterogeneous rare autosomal dominant or X-linked disease. Objective: We present a family with nephrogenic diabetes affecting three males in two generations. Methods: We report two boys with NDI: a 4-month-old infant who was trea…

Internal Medicine (3 works) · Medicine (3 works) · Biology (2 works) · Endocrinology (2 works) · Kidney (2 works) · Acute kidney injury (1 work) · Amino Acid Enzymes and Metabolism (1 work) · Aquaporin 2 (1 work) · Blood pressure (1 work) · Body Image and Dysmorphia Studies (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