Search Results - "Lazareva, K. I."

A case of PURA syndrome in a newborn child (neurodevelopmental disorder syndrome with neonatal respiratory failure, hypotension and feeding difficulties; nEDRIHf(OMIM 616158)) by Kravchenko, L. V., Lazareva, K. I., Monat, L. I., Levkovich, M. A.

“…   A clinical observation of a newborn child with an extremely rare disease - PURA syndrome is presented. In the world scientific literature, there is a…”
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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 by Berezhanskaya, S. B., Afonin, A. A., Vostrikh, N. N., Lazareva, K. I., Loginova, I. G., Kravchenko, L. V., Medoyan, A. V., Monat, L. I.

“…A clinical case of a familial form of peroxisomal D-bifunctional protein (DBP) deficiency (OMIM 261515) with an unfavorable (fatal) outcome caused by a…”
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A case of hyperplasia of the adrenal cortex in the newborn child by A. A. Afonin, A. A. Lebedenko, A. V. Shokarev, T. B. Kozireva, T. D. Tarakanova, K. I. Lazareva, S. E. Avilov, N. N. Sinanova

“…Clinical observation of a hyperplasia of the adrenal cortex in the newborn is presented. Main feature of this observation is the complicated course of this…”
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A case of congenital malformation of the brain in a newborn on the background of hereditary metabolic disorders by A. A. Lebedenko, A. A. Afonin, T. B. Kozyreva, K. I. Lazareva, L. I. Monat

“…A clinical observation of congenital malformation of the brain in a newborn child is presented. Diagnosis and comprehensive treatment of newborns with such…”
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