Maciej Borowiec

Bone Resorption After Microvascular Osseous Free-Flap Reconstruction in Pediatric Patients: A Retrospective Study

Maciej Borowiec, Jeremi Matysek, Dominika Lech, Robert Maksymowicz et autres

Unrecognized mitochondrial diabetes cases in a group of patients with type 2 diabetes

Sebastian Skoczylas, Tomasz Płoszaj, Natalia Kapelan, Julia Grzybowska-Adamowicz et autres

BACKGROUND/OBJECTIVES: Maternally Inherited Diabetes and Deafness (MIDD) is a unique form of diabetes caused by β-cell dysfunction. Due to the highly variable symptoms of MIDD, it can be misdiagnosed as either type 1 or type 2 diabetes (T2D). The aim of this …

pl (code pays fourni par la source)

Primordial Odontogenic Tumor of the Maxilla Mimicking Odontogenic Myxoma in a Two-Year-Old Child: A Case Report

Zuzanna Sokolowska, Dawid Rahimi, Maria Magdalena Szwajkowska, Maciej Borowiec et autres

Introduction: Primordial odontogenic tumor (POT) is an exceptionally rare benign mixed odontogenic neoplasm recognized as a distinct entity in the 2017 World Health Organization classification of head and neck tumors. Owing to its rarity and overlapping clinicopathological features with other odontogenic lesions, …

Dendriplexes in alveolar rhabdomyosarcoma therapy

Barbara Ziemba, Marcin Braun, Dietmar Appelhans, Maciej Borowiec et autres

pl, de, us (code pays fourni par la source)

Temperature and developmental stage govern intestinal susceptibility to human coronavirus 229E

Aleksandra Synowiec, Laurensius Kevin Lie, Katarzyna Owczarek, Nina Johannesson et autres

Human coronaviruses have been primarily associated with upper respiratory tract infections, yet cases of gastrointestinal symptoms in COVID-19 patients have highlighted their potential to cause systemic disease. Here, we detail the infection of intestinal epithelia by an endemic, low-pathogenic human coronavirus, human …

pl, us, nl, ca, gb, pt (code pays fourni par la source)

Surgical Management of Pediatric Head and Neck Sarcoma: A Single-Centre Retrospective Analysis over a 10-Year Period

Patryk Kołodziejski, Aleksandra Kołodziejska, Tomasz Brzeski, Maciej Borowiec et autres

Objectives: This study evaluates the epidemiological characteristics and survival, functional, and esthetic outcomes of pediatric patients diagnosed with head and neck sarcoma (PHNS) who underwent individualized surgical treatment for local disease control and/or for defect reconstruction. Methods: A cohort of 45 patients …

us, pl (code pays fourni par la source)

Chirurgia stomatologiczna i szczękowo-twarzowa

Andrzej Marszałek, Andrzej Kurylcio, Grażyna Wyszyńska–Pawelec, Ewelina Grywalska et autres

Search for the most precise diagnosis of monogenic diabetes - the usefulness of short-read NGS method in molecular testing in Polish patients

Tomasz Płoszaj, Sebastian Skoczylas, Karolina Gadzalska, Monika Gorządek et autres

pl (code pays fourni par la source)

Pediatric Head & Neck Free-Flap Reconstruction Outcomes: Score-Based Effectiveness Assessment

Maciej Borowiec, Dominika Maja Lech, Robert Maksymowicz, Jeremi Jan Matysek et autres

Background: Microsurgical free-flap reconstruction has become essential for restoring form and function in pediatric head and neck defects, yet outcome data remain heterogeneous and often limited to technical survival. This single-center retrospective study evaluated 54 free-flap procedures performed in 46 pediatric patients …

pl, us (code pays fourni par la source)

Insights into INS Gene Variation from Seven Years of Monogenic Diabetes Testing—Novel Genetic Variants and Their Clinical Implications

Tomasz Płoszaj, Patrycja Mojsak, Sebastian Skoczylas, Katarzyna Piekarska et autres

Monogenic diabetes (MD) is a rare and heterogeneous group of disorders caused by genetic variants in genes involved in glucose metabolism. Among many MD genes, the insulin gene (INS) deserves special attention, as its variants are responsible for both permanent neonatal diabetes …

pl, hu (code pays fourni par la source)

Neurological manifestations of Allgrove syndrome in patients carrying a potentially founder p.Ser263Pro variant in the AAAS gene

Ewa Juścińska, Karolina Gadzalska, Paulina Jakiel, Monika Gorządek et autres

Allgrove syndrome (AS) is a rare, multisystem, autosomal recessive disorder characterized by the triad of symptoms: achalasia, alacrimia and ACTH-resistant adrenal insufficiency. Various and nonspecific neurological symptoms can also develop over time, "blurring" the typical course of this underdiagnosed condition. The incidence …

pl (code pays fourni par la source)

Mandibular reconstruction with temporomandibular joint prosthesis in the pediatric population

Maciej Borowiec

us (code pays fourni par la source)