Search Results - "Normuradova, Nodira M."

  • Showing 1 - 5 results of 5
Refine Results
  1. 1

    Aortic Isthmus Retrograde Blood Flow in Intrauterine Child as a Sign of the Terminal Stage of Placental Dysfunction: Clinical Observation by Normuradova, Nodira M.

    Published in Voprosy sovremennoĭ pediatrii (07-05-2023)
    “…Background . Aortic isthmus retrograde blood flow in intrauterine children with growth delay and centralization of blood circulation in the late stages of…”
    Get full text
    Journal Article
  2. 2

    Prenatal Ultrasound Diagnostics of Autosomal Recessive Polycystic Kidney Disease in Fetus: Clinical Case by Normuradova, Nodira M., Pardaev, Mirtalim А.

    Published in Voprosy sovremennoĭ pediatrii (01-05-2022)
    “…Background. Autosomal recessive polycystic kidney disease is a rare congenital anomaly with poor prognosis. It characterized by the development of cysts in…”
    Get full text
    Journal Article
  3. 3

    Ultrasound Differential Diagnosis and Prognosis of Right Main Bronchus Atresia in Fetus: Clinical Case by Normuradova, Nodira M., Kurbanova, Vusala V.

    Published in Voprosy sovremennoĭ pediatrii (18-05-2021)
    “…Background. Obstructive lesion of upper respiratory tract in fetus is extremely rare pathology with adverse perinatal outcomes. Clinical Case Description…”
    Get full text
    Journal Article
  4. 4

    Hypoplastic Left Heart Syndrome: Diagnostic Difficulties in Prenatal Period by Normuradova, Nodira M., Fazilov, Аkram A., Rasulova, Munisa M.

    “…The article discusses the possible diagnostic errors in the hypoplastic left heart syndrome (HLHS) with mitral atresia and intact interventricular septum…”
    Get full text
    Journal Article
  5. 5

    Prenatal Ultrasound Signs of Cornelia de Lange Syndrome in Monochorionic Twins: Case Study by Normuradova, Nodira M., Khujakulov, Odil A., Ergasheva, Mahliyo Sh, Ollanazarov, Eshdavlat R., Majidov, Bekhruz B.

    Published in Voprosy sovremennoĭ pediatrii (03-03-2022)
    “…Background . Cornelia de Lange syndrome is rare genetic disease manifested by short stature, limb abnormalities, craniofacial dysmorphies, and developmental…”
    Get full text
    Journal Article