Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Debadatta Mukhopadhyay"'
Publikováno v:
Indian Journal of Rheumatology, Vol 17, Iss 1, Pp 24-29 (2022)
Background: Kawasaki disease, the commonest cause of multisystem vasculitis in children, was believed initially as a one-time disease. Long-term follow-up reveals that endothelial dysfunction persists in post-Kawasaki disease patients with and withou
Externí odkaz:
https://doaj.org/article/c42e36825ee143d0afbae78726866bd2
Publikováno v:
Indian Journal of Dermatology, Vol 59, Iss 5, Pp 502-504 (2014)
Biotinidase is a ubiquitous mammalian cell enzyme occurring in liver, serum and kidney. It cleaves biotin from biocytin, which is a cofactor for biotin dependent enzymes, namely the human carboxylases. Biotinidase deficiency is associated with a wide
Externí odkaz:
https://doaj.org/article/6e71be629728443b915faf0950d60702
Publikováno v:
Journal of Nepal Paediatric Society. 41:454-457
Adenoviruses are DNA viruses that typically cause mild self-limited disease mostly involving the respiratory tract, gastrointestinal tract or conjunctiva. Typical respiratory symptoms include fever, pharyngitis, tonsillitis, cough, and sore throat bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::603ef753d428e4cb1eb40d41596fed6f
https://doi.org/10.3126/jnps.v41i3.38138
https://doi.org/10.3126/jnps.v41i3.38138
Publikováno v:
Pediatric Infectious Disease. 3:43-45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a71584dc5faf7f13346c378f269236c
https://doi.org/10.5005/jp-journals-10081-1268
https://doi.org/10.5005/jp-journals-10081-1268
Publikováno v:
International Journal of Contemporary Pediatrics. 8:1612
Neonatal fungal endocarditis (FE) remains a rare condition associated with prematurity. It often puts us in diagnostic and therapeutic dilemma as there are no specific guidelines. We described our successful journey with a 26 days old neonate with as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b92aa5258238abc9de7e77a5ba42e43b
https://doi.org/10.18203/2349-3291.ijcp20213329
https://doi.org/10.18203/2349-3291.ijcp20213329
Publikováno v:
CSI: Cardiology Update 2015 (2 Volumes)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3328402b179b1c4b6a233351bde8900
https://doi.org/10.5005/jp/books/12785_85
https://doi.org/10.5005/jp/books/12785_85
Autor:
Seema Kapoor, Sharmila Banerjee Mukherjee, Daraius Shroff, Ritu Arora, Debadatta Mukhopadhyay, Apurba Ghosh, Maya Mukhopadhyay, J. P. Narayan, P. Garg, G. Pareek, S. Narayan, Seema Thakur, Sarah E. Flanagan, Sian Ellard, I. C. Verma, Rakesh Mondal, Madhumita Nandi, Astha Tiwari, Swati Chakravorti
Publikováno v:
Indian Pediatrics. 48:727-736
A 6 year old boy presented with mental retardation, hypotonia, abnormal facies, impaired hearing, protuberant eyes, visual impairment, short stature, Axenfeld-Rieger anomaly, a bicuspid aortic valve, and bilateral sensorineural deafness. CT scan of h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd7ff2aa24630a8b9bbc482dcaa0247b
https://doi.org/10.1007/s13312-011-0108-8
https://doi.org/10.1007/s13312-011-0108-8
Autor:
Debadatta Mukhopadhyay, Mihir Sarkar
Publikováno v:
Journal of Pediatric Critical Care. 5:118
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc07ad83665887be172da4962cac6767
https://doi.org/10.21304/2018.0501.00355
https://doi.org/10.21304/2018.0501.00355
Publikováno v:
Indian pediatrics. 48(9)
Satoyoshi syndrome is a rare autoimmune disease characterized by alopecia, painful muscle spasms, diarrhea and secondary skeletal changes. We report a 11 year old girl presenting with the typical features of alopecia totalis, severe muscle spasm and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::469ea99c288f07d3a4591118001a72e9
https://pubmed.ncbi.nlm.nih.gov/21992906
https://pubmed.ncbi.nlm.nih.gov/21992906
Publikováno v:
Journal of the Indian Medical Association. 105(7)
Joubert syndrome is a rare genetic disorder characterised by dysplasia of the cerebellar vermis and a malformed brainstem causing ataxia, tachypnoea, nystagmus, hypotonia and mental retardation. An early case of a two-month-old infant presenting with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec96b562dc920e4bf085c46b9efe45a6
https://pubmed.ncbi.nlm.nih.gov/18178993
https://pubmed.ncbi.nlm.nih.gov/18178993