4 research outputs found
Whatβs happening to the locomotive of global economy, or The myths about the recovery of China
The COVID-19 pandemic has caused irreparable damage to all economies. Coping with the consequences by the leading players in the global economy is only expected. However, the worldβs leading organizations have been trumpeting about overcoming the crisis in China. The aim of the research is to analyze the current state of the Chinese economy and answer the question whether it has overcome all the crisis phenomena. As part of the study, the authors analyzed indicators such as GDP, debt level, level of domestic demand, activity in the financial market and the M&A market, as well as technological and social policies of China and the structure of trade. For the analysis of quantitative indicators, a combination of comparison and classification methods, media scanning, and crowdsourcing was used. The information base was grounded on annual reference books published by official institutions in Π‘hina, World Bank, International Monetary Fund, statistical data from international publications devoted to Chinese economy. The analysis showed the presence of trigger situations in the stock market, in the market for innovative investments and the banking sector. The state of the credit system is also a matter of concern. The authors have proven that enthusiastic statements about the rapid recovery of the Chinese economy are more an encouraging myth than a fait accompli. Today, China is only at the beginning of its recovery from the crisis caused by the pandemic. Will it be able to become the locomotive of global economic growth again, as in 2008? The answer to this question remains open.ΠΠ°Π½Π΄Π΅ΠΌΠΈΡ COVID-19 Π½Π°Π½Π΅ΡΠ»Π° Π½Π΅ΠΏΠΎΠΏΡΠ°Π²ΠΈΠΌΡΠΉ ΡΡΠ΅ΡΠ± ΡΠΊΠΎΠ½ΠΎΠΌΠΈΠΊΠ°ΠΌ Π²ΡΠ΅Ρ
ΡΡΡΠ°Π½. ΠΡΠ΅Π΄ΠΏΠΎΠ»Π°Π³Π°Π΅ΡΡΡ, ΡΡΠΎ Π²Π΅Π΄ΡΡΠΈΠ΅ ΠΈΠ³ΡΠΎΠΊΠΈ ΠΌΠΈΡΠΎΠ²ΠΎΠΉ ΡΠΊΠΎΠ½ΠΎΠΌΠΈΠΊΠΈ ΡΠΎΠ»ΡΠΊΠΎ Π½Π°ΡΠΈΠ½Π°ΡΡ ΡΠΏΡΠ°Π²Π»ΡΡΡΡΡ Ρ Π΅Π΅ ΠΏΠΎΡΠ»Π΅Π΄ΡΡΠ²ΠΈΡΠΌΠΈ. ΠΠ΄Π½Π°ΠΊΠΎ Π²Π΅Π΄ΡΡΠΈΠ΅ ΠΌΠΈΡΠΎΠ²ΡΠ΅ ΠΎΡΠ³Π°Π½ΠΈΠ·Π°ΡΠΈΠΈ ΡΠΆΠ΅ ΡΠΎΠΎΠ±ΡΠ°ΡΡ ΠΎ ΠΏΡΠ΅ΠΎΠ΄ΠΎΠ»Π΅Π½ΠΈΠΈ ΠΊΡΠΈΠ·ΠΈΡΠ° Π² ΠΠΈΡΠ°Π΅. Π¦Π΅Π»Ρ ΡΡΠ°ΡΡΠΈ - ΠΏΡΠΎΠ°Π½Π°Π»ΠΈΠ·ΠΈΡΠΎΠ²Π°ΡΡ ΡΠ΅ΠΊΡΡΠ΅Π΅ ΡΠΎΡΡΠΎΡΠ½ΠΈΠ΅ ΡΠΊΠΎΠ½ΠΎΠΌΠΈΠΊΠΈ ΠΠΈΡΠ°Ρ ΠΈ ΠΎΡΠ²Π΅ΡΠΈΡΡ Π½Π° Π²ΠΎΠΏΡΠΎΡ, ΠΏΡΠ΅ΠΎΠ΄ΠΎΠ»Π΅Π»Π° Π»ΠΈ ΠΎΠ½Π° Π²ΡΠ΅ ΠΊΡΠΈΠ·ΠΈΡΠ½ΡΠ΅ ΡΠ²Π»Π΅Π½ΠΈΡ. Π ΡΠ°ΠΌΠΊΠ°Ρ
ΠΈΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΈΡ ΠΏΡΠΎΠ°Π½Π°Π»ΠΈΠ·ΠΈΡΠΎΠ²Π°Π½Ρ ΡΠ°ΠΊΠΈΠ΅ ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»ΠΈ, ΠΊΠ°ΠΊ ΠΠΠ, ΡΡΠΎΠ²Π΅Π½Ρ Π΄ΠΎΠ»Π³Π°, ΡΡΠΎΠ²Π΅Π½Ρ Π²Π½ΡΡΡΠ΅Π½Π½Π΅Π³ΠΎ ΡΠΏΡΠΎΡΠ°, Π°ΠΊΡΠΈΠ²Π½ΠΎΡΡΡ Π½Π° ΡΠΈΠ½Π°Π½ΡΠΎΠ²ΠΎΠΌ ΡΡΠ½ΠΊΠ΅ ΠΈ ΡΡΠ½ΠΊΠ΅ ΡΠ»ΠΈΡΠ½ΠΈΠΉ ΠΈ ΠΏΠΎΠ³Π»ΠΎΡΠ΅Π½ΠΈΠΉ, Π° ΡΠ°ΠΊΠΆΠ΅ ΡΠ΅Ρ
Π½ΠΎΠ»ΠΎΠ³ΠΈΡΠ΅ΡΠΊΠ°Ρ ΠΈ ΡΠΎΡΠΈΠ°Π»ΡΠ½Π°Ρ ΠΏΠΎΠ»ΠΈΡΠΈΠΊΠ° ΠΠΈΡΠ°Ρ ΠΈ ΡΡΡΡΠΊΡΡΡΠ° ΡΠΎΡΠ³ΠΎΠ²Π»ΠΈ. ΠΠ»Ρ Π°Π½Π°Π»ΠΈΠ·Π° ΠΊΠΎΠ»ΠΈΡΠ΅ΡΡΠ²Π΅Π½Π½ΡΡ
ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»Π΅ΠΉ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π»ΠΎΡΡ ΡΠΎΡΠ΅ΡΠ°Π½ΠΈΠ΅ ΠΌΠ΅ΡΠΎΠ΄ΠΎΠ² ΡΡΠ°Π²Π½Π΅Π½ΠΈΡ ΠΈ ΠΊΠ»Π°ΡΡΠΈΡΠΈΠΊΠ°ΡΠΈΠΈ, ΠΌΠ΅Π΄ΠΈΠ°ΡΠΊΠ°Π½ΠΈΡΠΎΠ²Π°Π½ΠΈΡ ΠΈ ΠΊΡΠ°ΡΠ΄ΡΠΎΡΡΠΈΠ½Π³Π°. ΠΠ½ΡΠΎΡΠΌΠ°ΡΠΈΠΎΠ½Π½Π°Ρ Π±Π°Π·Π° ΠΎΡΠ½ΠΎΠ²Π°Π½Π° Π½Π° Π΅ΠΆΠ΅Π³ΠΎΠ΄Π½ΡΡ
ΡΠΏΡΠ°Π²ΠΎΡΠ½ΠΈΠΊΠ°Ρ
, ΠΈΠ·Π΄Π°Π²Π°Π΅ΠΌΡΡ
ΠΎΡΠΈΡΠΈΠ°Π»ΡΠ½ΡΠΌΠΈ ΡΡΡΠ΅ΠΆΠ΄Π΅Π½ΠΈΡΠΌΠΈ ΠΠΈΡΠ°Ρ, ΠΡΠ΅ΠΌΠΈΡΠ½ΠΎΠ³ΠΎ Π±Π°Π½ΠΊΠ°, ΠΠ΅ΠΆΠ΄ΡΠ½Π°ΡΠΎΠ΄Π½ΠΎΠ³ΠΎ Π²Π°Π»ΡΡΠ½ΠΎΠ³ΠΎ ΡΠΎΠ½Π΄Π°, ΡΡΠ°ΡΠΈΡΡΠΈΡΠ΅ΡΠΊΠΈΡ
Π΄Π°Π½Π½ΡΡ
ΠΈΠ· ΠΌΠ΅ΠΆΠ΄ΡΠ½Π°ΡΠΎΠ΄Π½ΡΡ
ΠΈΠ·Π΄Π°Π½ΠΈΠΉ, ΠΏΠΎΡΠ²ΡΡΠ΅Π½Π½ΡΡ
ΡΠΊΠΎΠ½ΠΎΠΌΠΈΠΊΠ΅ ΠΠΈΡΠ°Ρ. ΠΠ½Π°Π»ΠΈΠ· ΠΏΠΎΠΊΠ°Π·Π°Π» Π½Π°Π»ΠΈΡΠΈΠ΅ ΡΡΠΈΠ³Π³Π΅ΡΠ½ΡΡ
ΡΠΈΡΡΠ°ΡΠΈΠΉ Π½Π° ΡΠΎΠ½Π΄ΠΎΠ²ΠΎΠΌ ΡΡΠ½ΠΊΠ΅, Π½Π° ΡΡΠ½ΠΊΠ΅ ΠΈΠ½Π½ΠΎΠ²Π°ΡΠΈΠΎΠ½Π½ΡΡ
ΠΈΠ½Π²Π΅ΡΡΠΈΡΠΈΠΉ ΠΈ Π² Π±Π°Π½ΠΊΠΎΠ²ΡΠΊΠΎΠΌ ΡΠ΅ΠΊΡΠΎΡΠ΅. Π‘ΠΎΡΡΠΎΡΠ½ΠΈΠ΅ ΠΊΡΠ΅Π΄ΠΈΡΠ½ΠΎΠΉ ΡΠΈΡΡΠ΅ΠΌΡ ΡΠ°ΠΊΠΆΠ΅ Π²ΡΠ·ΡΠ²Π°Π΅Ρ ΠΎΠ·Π°Π±ΠΎΡΠ΅Π½Π½ΠΎΡΡΡ. ΠΠΎΠΊΠ°Π·Π°Π½ΠΎ, ΡΡΠΎ Π²ΠΎΡΡΠΎΡΠΆΠ΅Π½Π½ΡΠ΅ Π·Π°ΡΠ²Π»Π΅Π½ΠΈΡ ΠΎ Π±ΡΡΡΡΠΎΠΌ Π²ΠΎΡΡΡΠ°Π½ΠΎΠ²Π»Π΅Π½ΠΈΠΈ ΠΊΠΈΡΠ°ΠΉΡΠΊΠΎΠΉ ΡΠΊΠΎΠ½ΠΎΠΌΠΈΠΊΠΈ ΡΠ²Π»ΡΡΡΡΡ ΡΠΊΠΎΡΠ΅Π΅ ΠΎΠ±Π½Π°Π΄Π΅ΠΆΠΈΠ²Π°ΡΡΠΈΠΌ ΠΌΠΈΡΠΎΠΌ, ΡΠ΅ΠΌ ΡΠ²Π΅ΡΡΠΈΠ²ΡΠΈΠΌΡΡ ΡΠ°ΠΊΡΠΎΠΌ. Π‘Π΅Π³ΠΎΠ΄Π½Ρ ΠΠΈΡΠ°ΠΉ Π½Π°Ρ
ΠΎΠ΄ΠΈΡΡΡ ΡΠΎΠ»ΡΠΊΠΎ Π² Π½Π°ΡΠ°Π»Π΅ Π²ΡΡ
ΠΎΠ΄Π° ΠΈΠ· ΠΊΡΠΈΠ·ΠΈΡΠ°, Π²ΡΠ·Π²Π°Π½Π½ΠΎΠ³ΠΎ ΠΏΠ°Π½Π΄Π΅ΠΌΠΈΠ΅ΠΉ. Π‘ΠΌΠΎΠΆΠ΅Ρ Π»ΠΈ ΠΎΠ½ ΡΠ½ΠΎΠ²Π° ΡΡΠ°ΡΡ Π»ΠΎΠΊΠΎΠΌΠΎΡΠΈΠ²ΠΎΠΌ Π³Π»ΠΎΠ±Π°Π»ΡΠ½ΠΎΠ³ΠΎ ΡΠΊΠΎΠ½ΠΎΠΌΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΡΠΎΡΡΠ°, ΠΊΠ°ΠΊ Π² 2008 Π³ΠΎΠ΄Ρ? ΠΡΠ²Π΅Ρ Π½Π° ΡΡΠΎΡ Π²ΠΎΠΏΡΠΎΡ ΠΎΡΡΠ°Π΅ΡΡΡ ΠΎΡΠΊΡΡΡΡΠΌ
The structure of interstitial lung diseases in children of the first two years of life
For the first time in Russia, the article provides data on interstitial lung diseases structure in children of the first two years of life, based on a series of observations of 68 patients with these rare diseases, as a part of multi-center ambispective study. Interstitial lung diseases in observed children included: Wilson-Mikity syndrome (23,4%), neuroendocrine hyperplasia of infancy (22%), bronchiolitis obliterans with organizing pneumonia (7,4%), primary pulmonary hypoplasia (1,5%), secondary pulmonary hypoplasia with Jeune syndrome (10,3%), secondary pulmonary hypoplasia with Edwards syndrome (2,9%), secondary pulmonary hypoplasia with other associated pathology (omphalocele - 1,5%, non-immune fetal hydrops - 1,5%), subpleural cysts in patients with Down syndrome (5,9%), congenital deficiency of surfactant protein B (1,5%), brain-lung- thyroid syndrome (2,9%), congenital alveolar-capillary dysplasia (1,5%), interstitial lung diseases with systemic diseases (Langerhans cell histiocytosis - 16,2%, Niemann-Pick disease - 1,5%). The article summarizes clinical features, the results of image diagnosis and disease outcomes. Β© 2015, Pediatria Ltd. All rights reserved
The structure of interstitial lung diseases in children of the first two years of life
For the first time in Russia, the article provides data on interstitial lung diseases structure in children of the first two years of life, based on a series of observations of 68 patients with these rare diseases, as a part of multi-center ambispective study. Interstitial lung diseases in observed children included: Wilson-Mikity syndrome (23,4%), neuroendocrine hyperplasia of infancy (22%), bronchiolitis obliterans with organizing pneumonia (7,4%), primary pulmonary hypoplasia (1,5%), secondary pulmonary hypoplasia with Jeune syndrome (10,3%), secondary pulmonary hypoplasia with Edwards syndrome (2,9%), secondary pulmonary hypoplasia with other associated pathology (omphalocele - 1,5%, non-immune fetal hydrops - 1,5%), subpleural cysts in patients with Down syndrome (5,9%), congenital deficiency of surfactant protein B (1,5%), brain-lung- thyroid syndrome (2,9%), congenital alveolar-capillary dysplasia (1,5%), interstitial lung diseases with systemic diseases (Langerhans cell histiocytosis - 16,2%, Niemann-Pick disease - 1,5%). The article summarizes clinical features, the results of image diagnosis and disease outcomes. Β© 2015, Pediatria Ltd. All rights reserved