A case of PURA syndrome in a newborn child (neurodevelopmental disorder syndrome with neonatal respiratory failure, hypotension and feeding difficulties; nEDRIHf(OMIM 616158))
Kravchenko, L. V., Lazareva, K. I., Monat, L. I., Levkovich, M. A.
Published in Medicinskij vestnik Ûga Rossii (01.07.2023)
Published in Medicinskij vestnik Ûga Rossii (01.07.2023)
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A clinical case of a familial form of hereditary metabolic disease from the group of peroxisomal diseases (D-bifunctional protein deficiency) in the neonatal period
Berezhanskaya, S. B., Afonin, A. A., Vostrikh, N. N., Lazareva, K. I., Loginova, I. G., Kravchenko, L. V., Medoyan, A. V., Monat, L. I.
Published in Medicinskij vestnik Ûga Rossii (28.03.2023)
Published in Medicinskij vestnik Ûga Rossii (28.03.2023)
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A case of the amniotic constrictions in a newborn child (Simonart syndrome)
Lebedenko, A. A., Afonin, A. A., Kozureva, T. B., Monat, L. I.
Published in Medicinskij vestnik Ûga Rossii (02.09.2019)
Published in Medicinskij vestnik Ûga Rossii (02.09.2019)
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