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共收录本刊相关文章索引340
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Agnieszka M Zdzienicka-Chyła,Krystyna Mitosek-Szewczyk Agnieszka M Zdzienicka-Chyła
Wstęp: Noworodki urodzone przed czasem stanowią blisko 7% wszystkich urodzonych dzieci i jednocześnie przybywa dzieci urodzonych jako ekstremalnie małe wcześniaki. W Parlamencie Europejskim już w roku 2011 priorytet...
Maria Kostro,Natalia Jacyna,Ewa Głuszczak-Idziakowska et al. Maria Kostro et al.
Objective: Objective: The purpose of the study was to identify the features of both the labor and the assisting physicians when evaluating the newborn according to the Apgar score and how these correlate with the biochemi...
Maria Respondek-Liberska Maria Respondek-Liberska
The article underlined the role of perinatal cardiology in contributing to the medical care of the pregnant woman taking into consideration the technical and medical progress which has made it possible to save not only human life but also i...
Maria Respondek-Liberska Maria Respondek-Liberska
The article underlined the role of perinatal cardiology in contributing to the medical care of the pregnant woman taking into consideration the technical and medical progress which has made it possible to save not only human life but also i...
Agnieszka Kowalik,Danuta Gajewska,Jolanta Sykut-Cegielska Agnieszka Kowalik
3-Methylcrotonylglycinuria (3-MCG) is an autosomal recessive inborn error of leucine metabolism caused by the deficiency of 3-methylocrotonyl-CoA carboxylase (3-MCC deficiency). It is the most commonly detected organic aciduria in newborn s...
Agnieszka Kowalik,Danuta Gajewska,Jolanta Sykut-Cegielska Agnieszka Kowalik
3-Methylcrotonylglycinuria (3-MCG) is an autosomal recessive inborn error of leucine metabolism caused by the deficiency of 3-methylocrotonyl-CoA carboxylase (3-MCC deficiency). It is the most commonly detected organic aciduria in newborn s...
Katarzyna Jobs,Magda Rakowska,Aleksandra Paturej Katarzyna Jobs
Urolithiasis, a condition in which calculi are found in the urinary tract, has been known for centuries. Although the disease was considered casuistic in the pediatric population, its prevalence is rising among both children and infants. Th...
Katarzyna Jobs,Magda Rakowska,Aleksandra Paturej Katarzyna Jobs
Urolithiasis, a condition in which calculi are found in the urinary tract, has been known for centuries. Although the disease was considered casuistic in the pediatric population, its prevalence is rising among both children and infants. Th...