REVISTE MEDICALE NEINSTITUȚIONALE

Recent Submissions

  • Rodoman, Iulia; Sacara, Victoria; Palii, Ina (Asociația de Biosiguranță și Biosecuritate din Republica Moldova, 2026)
    Introduction. Duchenne muscular dystrophy (DMD) is a genetic disorder that significantly affects growth and development, characterised by progressive degeneration of skeletal and cardiac muscles, typically beginning in ...
  • Gongladze, Nino; Pitskhelauri, Nato (Asociația de Biosiguranță și Biosecuritate din Republica Moldova, 2026)
    Introduction. The informed consent process is crucial in ensuring patient autonomy and ethical medical practice. The study aimed to assess understanding, experiences, and perceptions of informed consent among hospital ...
  • Corețchi, Liuba; Overcenco, Ala; Ababii, Aurelia; Gîncu, Mariana; Capatîna, Angela (Asociația de Biosiguranță și Biosecuritate din Republica Moldova, 2026)
    Introduction. Radon is a naturally occurring radioactive gas, recognized as a leading cause of lung cancer among non-smokers. The level of public radon awareness remains low in many countries. The study presents the ...
  • Sajin, Octavian; Țurcanu, Adela; Guțu, Veaceslav; Iziumov, Nina; Blaj, Valentina (Asociația de Biosiguranță și Biosecuritate din Republica Moldova, 2026)
    Introduction. Hepatitis E virus (HEV) represents a significant public health concern during pregnancy, being associated with severe maternal and fetal complications. This meta-analysis aimed to estimate the global seroprevalence ...
  • Rahmaddian, Tosi; Huvaid, Sevilla Ukhtil; Hidayat, Hilda; Yulianita, Yulianita; Oktarina, Sri (Asociația de Biosiguranță și Biosecuritate din Republica Moldova, 2026)
    Introduction. Medication management is a complex, high-risk component of healthcare and remains vulnerable to errors that might affect patient safety and operational efficiency. This systematic review aimed to evaluate risk ...
  • Villani, Simona (Asociația de Biosiguranță și Biosecuritate din Republica Moldova, 2026)
    According to the World Health Organization “One Health is an integrated, unifying approach that aims to sustainably balance and optimize the health of people, animals and ecosystems. (...) By linking humans, animals and ...
  • Cabac-Pogorevici, Irina; Cheibaș, Dorina; Revenco, Valeriu (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Epidermolysis bullosa (EB) is a rare genetic disorder characterized by skin fragility and the recurrent formation of blisters on the skin, oral mucosa, and esophagus. The disease is caused by genetic mutations ...
  • Utchina, Olesea; Draganel, Andrei; Boian, Veaceslav (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Extrinsic neuronal lesions in congenital malformations in children lead to the development of Neurogenic Colonic Dysfunction (NCD). It is well known that anorectal malformations (ARMs), with a frequency of ...
  • Railean, Silvia; Poștaru, Cristina; Ursu, Dănis; Rusu-Radzichevici, Natalia (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Congenital malformations rank second in the causes of death among children worldwide. Those who survive often face aesthetic, functional, and psychological difficulties throughout their growth and ...
  • Bernic, Jana; Pisarenco, Aliona; Litovcenco, Anatolii; Petrovici, Vergil; Bajurea, Ala; Gudumac, Eva (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Material and methods. We present the case of a nweborn, born at 33 weeks of gestation. The purpoze of the study. Familiarization with a rare pathology – multichistic kydney on the left against the background of purulent ...
  • Barbova, Natalia; Egorov, Vladimir; Halabudenco, Elena; Opalco, Igor (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Congenital anomalies (CA) are structural disorders that occur during the intrauterine development of the fetus. In the Republic of Moldova (RM), the CM ranks annually on the second place among the causes ...
  • Petrov, Victor; Bursacovscaia, Natalia; Castraveț, Irina (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Wilson’s disease is a hereditary condition caused by the mutation of the ATP7B gene, responsible for normal copper metabolism, with a frequency of approximately 1 in 30,000 people. The mutation leads to ...
  • Stamati, Adela; Ușurelu, Natalia (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Dilated cardiomyopathy (DCM) is the most common cardiomyopathy phenotype, characterized by dilation and systolic dysfunction of the left ventricle. The prevalence of pediatric DCM is 0.57-1.13/100,000 children. ...
  • Cabac-Pogorevici, Irina; Creangă, Iuliana; Revenco, Valeriu (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Hypertrophic cardiomyopathy (HCM) is a hereditary cardiovascular pathology with a prevalence of 1:500 to 1:200, inherited in an autosomal dominant manner. The primary presentation may be sudden cardiac death, ...
  • Răilean, Gheorghe (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Relevance: In the past five years, we have observed a significant increase in the frequency of severe neurological disorders based on the age of the child. Available data indicate that clinical manifestations predominantly ...
  • Șciuca, Svetlana; Tomacinschii, Cristina (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Cystic fibrosis (CF) is the most common monogenic disease in the European population, with a prevalence that varies by region: 1:1000-1800 in Europe, 1:2000-2500 in Romania and Moldova, 1:10000 in Russia, and 1:90000 ...
  • Cepraga, Victoria; Golubenco, Elena; Iacomi, Vladimir; Foca, Silvia; Barbova, Natalia; Revenco, Ninel (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introducere: Artrita juvenilă idiopatică, forma sistemică este o afecțiune autoinflamatorie sistemică rară, ce se caracterizează prin febră, rash cutanat evanescent și artrită, în asociere cu leucocitoză și creșterea ...
  • Constantin, Olga; Calcîi, Cornelia; Calistru, Iulia; Capestru, Elena; Istratuc, Irina; Hadjiu, Svetlana (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introducere: Sindromul Dravet (SD) este o encefalopatie epileptică și de dezvoltare cu debut infantil, caracterizată printr-o evoluție polimorfă a convulsiilor și rezistență la medicația antiepileptică. Scopul: Evaluarea ...
  • Țurcanu, Adela; Revenco, Ninel; Cumpătă, Veronica (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Actuality: Advances in the management of rare liver disease including and liver transplantation in children have allowed them to survive into adulthood with or without a native liver. Young adults with pediatric-onset liver ...
  • Palega, Daniela; Ciuhrii, Olga; Rodoman, Iulia; Eșanu, Veronica; Pîrțu, Lucia; Palii, Ina (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction. Pulmonary hypertension (PH) is a severe condition characterized by increased pressure in the pulmonary arteries, leading to right ventricular overload and heart failure. Early diagnosis is crucial for ...

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