Glycemic variability in continuous glucose monitoring negatively correlates with gestational age in very low birth weight infants
Szymońska, Izabela, Jagła, Mateusz, Starzec, Katarzyna, Kwinta, Przemko
Published in The journal of maternal-fetal & neonatal medicine (01.09.2020)
Published in The journal of maternal-fetal & neonatal medicine (01.09.2020)
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Paternal uniparental disomy of chromosome 2 resulting in a concurrent presentation of Crigler–Najjar syndrome type I and long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency
Knapp, Anna, Jagła, Mateusz, Madetko‐Talowska, Anna, Szewczyk, Katarzyna, Książek, Teofila, Końska, Katarzyna, Kwinta, Przemko
Published in American journal of medical genetics. Part A (01.06.2022)
Published in American journal of medical genetics. Part A (01.06.2022)
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Preterm Glycosuria - New Data from a Continuous Glucose Monitoring System
Jagła, Mateusz, Szymońska, Izabela, Starzec, Katarzyna, Kwinta, Przemko
Published in Neonatology (Basel, Switzerland) (01.01.2018)
Published in Neonatology (Basel, Switzerland) (01.01.2018)
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Defining Glycemic Variability in Very Low-Birthweight Infants: Data from a Continuous Glucose Monitoring System
Jagła, Mateusz, Szymońska, Izabela, Starzec, Katarzyna, Gach, Olga, Włodarczyk, Aneta, Kwinta, Przemko
Published in Diabetes technology & therapeutics (01.11.2018)
Published in Diabetes technology & therapeutics (01.11.2018)
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Sonographic findings in a neonate with cobb syndrome
Jagła, Mateusz, Szymońska, Izabela, Kruczek, Piotr
Published in Journal of clinical ultrasound (01.05.2013)
Published in Journal of clinical ultrasound (01.05.2013)
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From a Regional Cohort of Extremely Low Birth Weight Infants: Cardiac Function at the Age of 7 Years
Kwinta, Przemko, Jagła, Mateusz, Grudzień, Andrzej, Klimek, Małgorzata, Zasada, Magdalena, Pietrzyk, Jacek Jozef
Published in Neonatology (Basel, Switzerland) (01.01.2013)
Published in Neonatology (Basel, Switzerland) (01.01.2013)
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Gene expression profiling in preterm infants: new aspects of bronchopulmonary dysplasia development
Pietrzyk, Jacek J, Kwinta, Przemko, Wollen, Embjorg J, Bik-Multanowski, Mirosław, Madetko-Talowska, Anna, Günther, Clara-Cecilie, Jagła, Mateusz, Tomasik, Tomasz, Saugstad, Ola D
Published in PloS one (23.10.2013)
Published in PloS one (23.10.2013)
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Specification and guideline for technical aspects and scanning parameter settings of neonatal lung ultrasound examination
Liu, Jing, Guo, Guo, Kurepa, Dalibor, Volpicelli, Giovanni, Sorantin, Erich, Lovrenski, Jovan, Alonso-Ojembarrena, Almudena, Hsieh, Kai-Sheng, Lodha, Abhay, Yeh, Tsu F., Jagła, Mateusz, Shah, Heli, Yan, Wei, Hu, Cai-Bao, Zhou, Xiao-Guang, Guo, Rui-Jun, Cao, Hai-Ying, Wang, Yan, Zong, Hai-Feng, Shang, Li-Li, Ma, Hai-Ran, Liu, Ying, Fu, Wei, Shan, Rui-Yan, Qiu, Ru-Xin, Ren, Xiao-Ling, Copetti, Roberto, Rodriguez-Fanjul, Javier, Feletti, Francesco
Published in The journal of maternal-fetal & neonatal medicine (04.03.2022)
Published in The journal of maternal-fetal & neonatal medicine (04.03.2022)
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Assessment of long-term renal complications in extremely low birth weight children
Kwinta, Przemko, Klimek, Małgorzata, Drozdz, Dorota, Grudzień, Andrzej, Jagła, Mateusz, Zasada, Magdalena, Pietrzyk, Jacek Jozef
Published in Pediatric nephrology (Berlin, West) (01.07.2011)
Published in Pediatric nephrology (Berlin, West) (01.07.2011)
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A novel mutation in MTM1 gene in newborn, resulting in centronuclear myopathy phenotype: a case report
Dudzik, Aleksandra, Nedza, Weronika, Końska, Katarzyna, Starzec, Katarzyna, Tomasik, Tomasz, Grudzień, Andrzej, Jagła, Mateusz, Durlak, Wojciech, Kwinta, Przemko
Published in Egyptian Journal of Medical Human Genetics (15.03.2021)
Published in Egyptian Journal of Medical Human Genetics (15.03.2021)
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New insight into the pathogenesis of retinopathy of prematurity: assessment of whole-genome expression
Pietrzyk, Jacek J, Kwinta, Przemko, Bik-Multanowski, Mirosław, Madetko-Talowska, Anna, Jagła, Mateusz, Tomasik, Tomasz, Mitkowska, Zofia, Wollen, Embjørg J, Nygård, Ståle, Saugstad, Ola D
Published in Pediatric research (01.04.2013)
Published in Pediatric research (01.04.2013)
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Impact of antenatal glucocorticosteroids on whole-genome expression in preterm babies
Saugstad, Ola Didrik, Kwinta, Przemko, Wollen, Embjørg Julianne, Bik - Multanowski, Mirosław, Madetko - Talowska, Anna, Jagła, Mateusz, Tomasik, Tomasz, Pietrzyk, Jacek Józef
Published in Acta Paediatrica (01.04.2013)
Published in Acta Paediatrica (01.04.2013)
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Novel mutation-deletion in the PHOX2B gene of the patient diagnosed with Neuroblastoma, Hirschsprung's Disease, and Congenital Central Hypoventilation Syndrome (NB-HSCR-CCHS) Cluster
Szymońska, Izabela, Borgenvik, Thore Langfeldt, Karlsvik, Tina Margrethe, Halsen, Anders, Malecki, Bianka Kathryn, Saetre, Sindre Ervik, Jagła, Mateusz, Kruczek, Piotr, Talowska, Anna Madetko, Drabik, Grażyna, Zasada, Magdalena, Malecki, Marek
Published in Journal of genetic syndrome & gene therapy (01.12.2015)
Published in Journal of genetic syndrome & gene therapy (01.12.2015)
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PP-182. Impact of intrauterine growth on renal function and renal size at the age of 7 years of extremely low birth weight infants (ELBW)
Kwinta, Przemko, Klimek, Malgorzata, Grudzien, Andrzej, Jagla, Mateusz, Drozdz, Dorota, Pietrzyk, Jacek Jozef
Published in Early human development (01.11.2010)
Published in Early human development (01.11.2010)
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