IRMS - Nicolae Testemitanu SUMPh: Recent submissions

  • Guzun, Gheorghe; Turchin, Radu (CEP Medicina, 2026)
    Background. Decreased tone of the anterolateral abdominal wall muscles, actually is considered the main etiological factor in the appearance of inguinal hernia. Taking into consideration that the spinal nerves have the ...
  • Satheswaran, Maharajan; Cebotari, Dionisie; Railean, Nadejda; Tagadiuc, Olga; Sardari, Veronica (CEP Medicina, 2026)
    Introduction. Transplantation is a vital treatment for organ failure, degenerative diseases and severe tissue injuries. Challenge being, the poor function, survival of transplanted cells caused by oxidative stress. During ...
  • Grusac, Evgheni; Cebotari, Dionisie; Railean, Nadejda; Oboroc, Sandu; Sardari, Veronica (CEP Medicina, 2026)
    Background. Ischemic heart disease, myocardial infarction, ischemic stroke, and peripheral arterial disease are non-communicable, highly disabling conditions with high incidence and mortality rates. It is well recognized ...
  • Grusac, Evgheni; Pantea, Valeriana; Railean, Nadejda; Stratulat, Silvia; Sardari, Veronica (CEP Medicina, 2026)
    Background. In disease conditions, the goal of therapeutic targeting of the angiogenic process is to normalize vasculature in target tissues by enhancing angiogenesis, where reduced vascularity and blood flow occur, such ...
  • Secu, Doina; Blăniță, Daniela; Ușurelu, Natalia; Sacară, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Mitochondrial diseases (MD) are a group of rare, genetically inherited disorders caused by defects in mitochondrial function, particularly in oxidative phosphorylation, leading to impaired cellular energy ...
  • Sacară, Victoria; Coliban, Iulia; Secu, Doina; Dorif, Alexandr; Boiciuc, Constantin; Egorov, Vladimir (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introduction: Molecular diagnosis represents an essential frontier in modern medicine, offering promising perspectives for managing genetic and hereditary diseases. Its relevance is growing in the context of expanding ...
  • Ciobanu, Sergiu; Marcu, Diana; Roman, Ion; Musteață, Olesea (Instituţia Publică Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu” din Republica Moldova, 2026)
  • Rotaru, Ludmila; Rotaru, Tudor (CEP Medicina, 2026)
    Introduction. Cystic fibrosis (CF) is an autosomal recessive genetic disorder caused by mutations in the CFTR gene, affecting multiple organs, particularly the lungs, and leading to progressive respiratory failure. Despite ...
  • Potînga, Irina; Protopop, Svetlana (CEP Medicina, 2026)
    Introduction. Metabolic syndrome (MetS) is a multifactorial disease, and the gut microbiota plays an important role in its pathogenesis. Moreover, recent studies suggest associations between gut dysbiosis and components ...
  • Pîrțac, Mihail; Berliba, Sergiu; Chira, Inga; Ciobanu, Lorina (CEP Medicina, 2026)
    Introduction. In the management of chronic pancreatitis (CP), pancreatic pseudocyst (PCP) is a complication that requires the attention of surgeons, provided that it is non-neoplastic, recurrent, >6 cm in size, persists ...
  • Negarî, Nadejda; Minchevici, Delia; Cazacov, Vladimir; Nacu, Viorel (CEP Medicina, 2026)
    Introduction: Liver cirrhotic patients often face surgical and interventional procedures, such as hepatectomy with modulation of future liver remnant, portoenterostomy in cases of biliary atresia, transjugular intrahepatic ...
  • Neagu, Anastasia (CEP Medicina, 2026)
    Introduction. Non-immune fetal hydrops (NIHF) represents one of the most severe conditions in fetal medicine, characterized by the pathological accumulation of fluid in at least two fetal compartments and associated with ...
  • Mudzhuk, Alona; Nacu, Viorel (CEP Medicina, 2026)
    Introduction. The preservation of perinatal biological materials - umbilical cord blood, umbilical cord tissue, and placental tissue - has become one of the most important developments in modern preventive and regenerative ...
  • Minchevici, Delia; Negarî, Nadejda; Bour, Alin; Gîlea, Angela; Nacu, Viorel (CEP Medicina, 2026)
    Introduction: Post-thyroidectomy hypothyroidism is a common complication of total thyroid removal, traditionally managed with lifelong hormone replacement therapy. Thyroid models developed through tissue engineering ...
  • Mihalachi-Anghel, Maria; Bacinschi-Gheorghița, Stela; Bacinschi, Nicolae (CEP Medicina, 2026)
    Introduction. In organ transplant patients, new onset diabetes mellitus after transplantation (NODAT) has been found to be a frequent and serious complication. The use of immunosuppressive drugs after transplantation has ...
  • Nacu, Viorel; Stepa, Serghei; Cospormac, Igor; Cociug, Adrian; Cobzac, Vitalie; Țîmbalari, Tatiana (CEP Medicina, 2026)
    Introduction. Tissue transplantation represents an essential component of modern regenerative and reconstructive medicine. In the Republic of Moldova, this field has evolved progressively since the 1960s, beginning with ...
  • Colța, Olga; Harea, Dumitru; Șeremet, Aristia (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Sindroamele de lipodistrofie (SL) se caracterizează prin lipsa generalizată sau parțială a țesutului adipos, în absența deprivării nutriționale sau catabolismului accelerat. Se identifică 4 forme: lipodistrofia generalizată ...
  • Gangan, Diana (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introducere: Neoplazii endocrine multiple subtipul 2A este sindromul genetic care se manifestă prin feocromocitom, carcinom medular a glandei tiroide și hiperparatiroidism. Scopul lucrării: Analiza particularităților ...
  • Clipii, Olga (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Introducere: Sindromul Down (SD) este asociat cu o serie de disfuncții endocrine care influențează semnificativ starea și dezvoltarea copiilor. Cele mai frecvente tulburări endocrine sunt dereglările tiroidiene, boala ...
  • Bauchina, Alisa; Porosencov, Egor; Dolapciu, Elena; Tutueva, Tatyana; Sacara, Victoria (Instituţia Medico-Sanitară Publică Institutul Mamei și Copilului, 2025)
    Papillon-Lefèvre Syndrome (PLS), a rare autosomal recessive disorder (1/1,000,000) caused by cathepsin C gene mutation with severe periodontitis following early tooth loss. Methods involved a thorough clinical evaluation ...