Skip to main content

ETHNOS_APP

Home • Search • Journals • List 0

Eusebiu Vlad Gorduza

Biographic Data

ID8253066
NAMEEusebiu Vlad Gorduza
GIVEN NAMESEusebiu Vlad
FAMILY NAMEGorduza
SIGNATUREGORDUZA E V
AFFILIATIONSGrigore T. Popa University of Medicine and Pharmacy
VERIFIEDNo
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2021
LATEST PUBLICATION YEAR2024
H-INDEX0
  • Rare Case of First Permanent Molar Primary Failure of Eruption with Agenesis of Premolars

    Open Access•Arina Vinereanu, Aneta Munteanu et al.•ARTICLE•Children•2024

    Primary failure of eruption (PFE) is a rare non-syndromic condition involving total or partial non-eruption of posterior teeth in the absence of mechanical obstruction. This paper presents the case of a healthy girl referred at age 4 for asymmetry of the upper arch. Clinical examination confirmed a slight shift of the upper midline to the left, with no erupted teeth distal to the upper left canine and a left posterior open bite. Panoramic X-rays …

  • Wolf-Hirschhorn Syndrome

    Open Access•Eva-Cristiana Gavril, Alina-Costina Luca et al.•ARTICLE•Children•2021

    Wolf-Hirschhorn syndrome (WHS), a rare disorder determined by distal 4p deletion, is characterized by a pre and postnatal growth retardation, hypotonia, intellectual disability, epilepsy, craniofacial dysmorphism, and congenital fusion anomalies. The clinical aspects are dependent on the deletion' size. Our aim was to identify rare specific characteristics in a cohort of seven cases with 4p deletion and to assess the utility of Multiplex ligation…

No prominent works on this page.

  • Wolf-Hirschhorn Syndrome

    Open Access•Eva-Cristiana Gavril, Alina-Costina Luca et al.•ARTICLE•Children•2021

    Wolf-Hirschhorn syndrome (WHS), a rare disorder determined by distal 4p deletion, is characterized by a pre and postnatal growth retardation, hypotonia, intellectual disability, epilepsy, craniofacial dysmorphism, and congenital fusion anomalies. The clinical aspects are dependent on the deletion' size. Our aim was to identify rare specific characteristics in a cohort of seven cases with 4p deletion and to assess the utility of Multiplex ligation…

  • Rare Case of First Permanent Molar Primary Failure of Eruption with Agenesis of Premolars

    Open Access•Arina Vinereanu, Aneta Munteanu et al.•ARTICLE•Children•2024

    Primary failure of eruption (PFE) is a rare non-syndromic condition involving total or partial non-eruption of posterior teeth in the absence of mechanical obstruction. This paper presents the case of a healthy girl referred at age 4 for asymmetry of the upper arch. Clinical examination confirmed a slight shift of the upper midline to the left, with no erupted teeth distal to the upper left canine and a left posterior open bite. Panoramic X-rays …

Medicine (2 works) · Agenesis (1 work) · Anatomy (1 work) · Biology (1 work) · Bone and Dental Protein Studies (1 work) · Dental arch (1 work) · dental development and anomalies (1 work) · Dental Trauma and Treatments (1 work) · Dentistry (1 work) · Fetal and Pediatric Neurological Disorders (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