Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Ingrid, Brucknerová"'
Autor:
Tatiana Žikavská, Ingrid Brucknerová
Publikováno v:
Potravinarstvo, Vol 7, Iss 1, Pp 202-206 (2013)
Folic acid is an essential vitamin which has been known in recent 50 years. It plays an important role in period of neurogenesis. The substitution of folic acid is one of the important parts in the complex treatment of anaemia in premature newborns.
Externí odkaz:
https://doaj.org/article/0d6bc1ccd8e54b918522dd37ac8c8241
Autor:
Ingrid Brucknerová, Tatiana Žikavská
Publikováno v:
Potravinarstvo, Vol 7, Iss 1, Pp 85-88 (2013)
Folic acid, the essential vitamin, and its active forms are substantial parts of many biochemical processes in the human body. In the period of rapid growth of organism or in cell growth, body’s demands for folate increase. Its impact in neonatal p
Externí odkaz:
https://doaj.org/article/a60ea9a387ad4855b41a42672a3cd055
Publikováno v:
Physiol Res
Congenital lung masses (CLM) the rare group of causes of acute respiratory insufficiency (RI) in newborns include congenital airway pulmonary malformation (CAPM), congenital overinflation, bronchopulmonary sequestration, and bronchial atresia. The pr
Autor:
Alexandra Mc Cullough, Zuzana Pakanová, Anna Hlavatá, A. Salingova, Barbara Siváková, Claudia Šebová, Jan Mucha, Marek Nemčovič, Peter Barath, Ingrid Brucknerová, Vladimir Bzduch, Dimitra-Evanthia Lekka, Jana Ziburová, Martina Skokňová, Sergej Šesták, Jana Bellová, Jana Brucknerová, Mária Ostrožlíková, Gabriela Hrčková
Publikováno v:
American journal of medical genetics. Part A. 185(11)
Congenital disorder of glycosylation type Ig (ALG12-CDG) is a rare inherited metabolic disease caused by a defect in alpha-mannosyltransferase 8, encoded by the ALG12 gene (22q13.33). To date, only 15 patients have been diagnosed with ALG12-CDG globa
Autor:
Sergej Šesták, A. Salingova, Ingrid Brucknerová, M. Ostrozlikova, Barbara Sivakova, J Brucknerova, C. Sebova, M Skoknova, Jana Bellova, Vladimir Bzduch, Jan Mucha, Marek Nemčovič, J. Ziburova, Zuzana Pakanová, D E Lekka, Peter Barath
Publikováno v:
Bratislavske lekarske listy. 122(3)
Aim Congenital disorders of glycosylation (CDG) belong to an expanding group of rare genetic metabolic disorders caused by defects in the complex chemical enzymatic process of glycosylation. The study is aimed at presenting a case report of a prematu
Publikováno v:
Interdisciplinary Toxicology
Interdisciplinary Toxicology, Vol 11, Iss 4, Pp 241-246 (2018)
Interdisciplinary Toxicology, Vol 11, Iss 4, Pp 241-246 (2018)
Zika virus (ZIKV) belongs to the group of viruses called arboviruses. Congenital Zika syndrome is a new disease with infectious teratogenic aetiology. The clinical symptoms are divided into morphological and functional. Most severe complication is th
Publikováno v:
Interdisciplinary Toxicology, Vol 10, Iss 4, Pp 168-171 (2017)
Interdisciplinary Toxicology
Interdisciplinary Toxicology
Despite modern approaches in molecular biology and genetics, we are still not able to identify the actual cause in more than 50% of all congenital defects. One-half of the unidentified cases is referred to as “multifactorial”. Detailed prenatal i
Publikováno v:
Bratislava Medical Journal. 116:417-421
OBJECTIVES To determine whether red blood cell (RBC) folate concentration levels are correlated with the occurrence of neonatal asphyxia and to study the effects of gestational age, gender, and mode of delivery on RBC folate concentration levels in n
Publikováno v:
Biologia. 69:1784-1789
Folate plays one of the most important functions for nucleotide biosynthesis and cellular methylation reactions in cells. Folate-mediated one-carbon metabolism is essential for metabolic processes in the human body. During periods of rapid cell growt
Publikováno v:
Interdisciplinary Toxicology
Teratology is the science that studies the causes, mechanisms, and patterns of abnormal development. The authors present an updated overview of the most important milestones and stages of the development of modern teratology. Development of knowledge