Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Anupam Sibal"'
Autor:
Raju Vaishya, Dhananjaya Sharma, Anupam Sibal, Bipin Puri, Muralidharan Manikesi, Abhishek Vaish
Publikováno v:
National Board of Examinations Journal of Medical Sciences, Vol Volume 2, Iss Issue 9, Pp 919-932 (2024)
There is a pressing need to address the noticeable disparity in biomedical research output between High-Income Countries (HICs) and Low-Middle Income Countries (LMICs). This imbalance raises urgent concerns about equity and the impact on global healt
Externí odkaz:
https://doaj.org/article/f2a1f6a80191474f87b8d664b2cad246
Autor:
Sujoy Kar, Rajesh Chawla, Sai Praveen Haranath, Suresh Ramasubban, Nagarajan Ramakrishnan, Raju Vaishya, Anupam Sibal, Sangita Reddy
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract In Coronavirus disease 2019 (COVID-19), early identification of patients with a high risk of mortality can significantly improve triage, bed allocation, timely management, and possibly, outcome. The study objective is to develop and validate
Externí odkaz:
https://doaj.org/article/4bb232ea10b045828e4c97aab2c2c3d3
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 27, Iss 1, Pp 115-117 (2022)
Septic thrombophlebitis of the portal vein or pylephlebitis is a rare cause of morbidity and mortality in children. The common causes include infective intra-abdominal pathology (acute appendicitis or diverticulitis) or inflammatory conditions (acute
Externí odkaz:
https://doaj.org/article/4c96570d91194aaf80237069707290c7
Publikováno v:
Apollo Medicine, Vol 20, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/c5539da6415440a7b09f1b26bb004194
Publikováno v:
Asia Pacific Journal of Medical Toxicology, Vol 10, Iss 1, Pp 29-32 (2021)
Ayurvedic and Herbal medicine induced liver injury is rarely reported in children. The injury can range from mild asymptomatic elevation of liver enzymes to severe presentation with acute liver failure leading to death. The diagnosis is by exclusion
Externí odkaz:
https://doaj.org/article/fff05e94c2f34a9cbbba558ad53d9875
Novel Variant ATP8B1 mutation in a child with progressive familial intrahepatic cholestasis (type 1)
Publikováno v:
Journal of Biochemical and Clinical Genetics, Vol 3, Iss 1, Pp 32-35 (2020)
Background: Progressive familial intrahepatic cholestasis (PFIC) is a group of heterogeneous autosomal recessive disorders attributed to hepatocellular cholestasis, characterized by low serum γ-glutamyl transferase (GGT) levels due to mutation in AT
Externí odkaz:
https://doaj.org/article/620a78e23ef84f69be94a63f4b709119
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 19, Iss 3, Pp 156-161 (2014)
The presentation and management of ureterocele has been rarely reported from India and is limited to an odd case report. They can be detected antenatally, may have incidental diagnosis or present with consequences of obstructive uropathy. They always
Externí odkaz:
https://doaj.org/article/7f74d243d0c44e74a53c260605762595
Publikováno v:
Journal of Indian Association of Pediatric Surgeons, Vol 19, Iss 3, Pp 162-165 (2014)
Neuropathic bladder in children is most commonly secondary to spina bifida. The management starts early in life. The modalities of treatment vary depending on the severity of the symptoms. A proportion of children inspite of adequate medical manageme
Externí odkaz:
https://doaj.org/article/fe76240c08724609bcb3af4d72cf5993
Autor:
Anupam Sibal, Vidyut Bhatia, Akshay Kapoor, Sarath Gopalan, Nameet Jerath, Manav Wadhawan, Subash Gupta
Publikováno v:
Journal of Pediatric Critical Care, Vol 1, Iss 1, Pp 34-39 (2014)
Externí odkaz:
https://doaj.org/article/a04a1f509aaa4ed583d0d88840995604
Publikováno v:
BMJ case reports. 15(7)
Systemic primary carnitine deficiency (PCD) is an autosomal recessive disorder caused by mutations in the SLC22A5 gene that encodes carnitine transporter, OCTN2. Transporter deficiency leads to defective fatty acid oxidation. Signs and symptoms rangi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87481b4f3360eea92d7741fe4a81d4bb
https://pubmed.ncbi.nlm.nih.gov/35853679
https://pubmed.ncbi.nlm.nih.gov/35853679