Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sataroopa Mishra"'
Publikováno v:
Current Medical Issues, Vol 21, Iss 4, Pp 196-200 (2023)
Background: Adolescent sleep deprivation affects their mental health, cardiovascular health, academic performance, and safety while on the road. This study analyzed sleep quality, hygiene, and daytime sleepiness among adolescents attending a tertiary
Externí odkaz:
https://doaj.org/article/419fc46c795c4090aa4568ef14974600
Autor:
Sataroopa Mishra, Saurabh Kumar Gupta, Sivasubramanian Ramakrishnan, Shyam Sunder Kothari, Anita Saxena, Sanjeev Kumar
Publikováno v:
Annals of Pediatric Cardiology, Vol 16, Iss 2, Pp 122-126 (2023)
Organ-specific vasculitis is an uncommon, delayed complication of COVID-19 infection. It is usually seen in mildly symptomatic or asymptomatic patients. Underlying endothelitis is the most likely pathophysiological mechanism for such a manifestation.
Externí odkaz:
https://doaj.org/article/e3bb6e15b6e04bf28e7f79183cf76190
Autor:
Saurabh Kumar Gupta, Sataroopa Mishra, Palleti Rajashekar, Sanjeev Kumar, Shyam Sunder Kothari
Publikováno v:
Annals of Pediatric Cardiology, Vol 16, Iss 1, Pp 77-78 (2023)
Despite optimal medical management, an 8-year-old boy had persistent pleural drainage following total cavopulmonary connection. Detailed evaluation, including computed tomography angiography, confirmed obstruction at the lower end of the circuit due
Externí odkaz:
https://doaj.org/article/51b6390789494ebf889ec4e55aba103e
Publikováno v:
Asian Journal of Transfusion Science, Vol 12, Iss 1, Pp 85-88 (2018)
Hemophagocytic lymphohistiocytosis (HLH) is a disorder of immune dysregulation secondary to a massive unregulated cytokine storm and its downstream consequences. HLH is being increasingly recognized as a cause of pyrexia of unknown origin, unexplaine
Externí odkaz:
https://doaj.org/article/147e41d77e9145a59d926d48620aa3ff
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 17, Iss 2, Pp 225-228 (2017)
Langerhans cell histiocytosis (LCH) is a rare proliferative disorder of the Langerhans cells, which are part of the mononuclear phagocytic system. The disorder varies in terms of the extent of the disease, its natural course and patient outcomes. Whi
Externí odkaz:
https://doaj.org/article/a30b6fb21d924431bedd99a654069c61
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 9, Pp SR01-SR02 (2017)
Autoimmune Haemolytic Anaemias (AIHAs) are rare in children. They can be either a primary disease or secondary to/triggered by a host of other clinical conditions. We present five interesting cases of paediatric AIHA associated with infections (vira
Externí odkaz:
https://doaj.org/article/8a1752e6e8c2427585b22f91a362d337
Publikováno v:
Annals of Pediatric Cardiology. 16:77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d464ae7958e0adf32321938a728fdcd
https://doi.org/10.4103/apc.apc_85_22
https://doi.org/10.4103/apc.apc_85_22
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 17, Iss 2, Pp 225-228 (2017)
Langerhans cell histiocytosis (LCH) is a rare proliferative disorder of the Langerhans cells, which are part of the mononuclear phagocytic system. The disorder varies in terms of the extent of the disease, its natural course and patient outcomes. Whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b820cd9268bc6437f6fd06490f19c67a
https://pubmed.ncbi.nlm.nih.gov/28690898
https://pubmed.ncbi.nlm.nih.gov/28690898
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 9, Pp SR01-SR02 (2017)
Autoimmune Haemolytic Anaemias (AIHAs) are rare in children. They can be either a primary disease or secondary to/triggered by a host of other clinical conditions. We present five interesting cases of paediatric AIHA associated with infections (viral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d224e9ba6811160389e35d5dc257df
https://doi.org/10.7860/jcdr/2017/27895.10646
https://doi.org/10.7860/jcdr/2017/27895.10646
Publikováno v:
Journal of Clinical Neonatology. 8:120
Calcinosis cutis is a disorder characterized by the deposition of insoluble calcium salts in the skin and subcutaneous tissue. It is separated into five subtypes, namely dystrophic calcification, metastatic calcification, idiopathic calcification, ia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d34aaa2e8dee7a7f222e808782b40f8c
https://doi.org/10.4103/jcn.jcn_67_18
https://doi.org/10.4103/jcn.jcn_67_18