Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Malay Kumar Sinha"'
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 17, Iss 3, Pp 209-211 (2016)
Mastocytosis is a group of a disorder characterized by infiltration of mast cell in various organs, e.g. skin, bone marrow, liver, spleen, gastrointestinal tract, lymph node, etc., The term bullous mastocytosis is generally used to describe the varie
Externí odkaz:
https://doaj.org/article/6b7655a758104eeda5ff524663e81d7c
Autor:
Anirban Chatterjee, Malay Kumar Sinha
Publikováno v:
Panacea Journal of Medical Sciences. 12:215-220
Tuberous sclerosis complex (TSC) is a rare genetic disease, belongs to the group of neurocutaneous syndrome. The consequence of genetic mutation is inadequate inhibition of the mammalian target of rapamycin (mTOR) signal pathway that results in inact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc0f64564ce1fb11a5fff612579ccbc3
https://doi.org/10.18231/j.pjms.2022.040
https://doi.org/10.18231/j.pjms.2022.040
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :76-80
Background: Nephrotic syndrome is a common renal disease in children characterised by massive proteinuria,hypoalbuminemia(serum albumin 200mg/dl) and edema.It has high propensity for relapse.Approximately 80-90%of steroid sensitive nephrotic syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90d8c2fb0bb245e70cbe2ab6fa821382
https://doi.org/10.36106/ijsr/7410824
https://doi.org/10.36106/ijsr/7410824
Autor:
Malay Kumar Sinha, Anirban Chatterjee
Publikováno v:
Nepal Journal of Neuroscience. 18:49-54
Introduction: Sturge Weber syndrome (SWS) is a rare, nonhereditary genetic disorder. SWS belongs to a diverse group of Neurocutaneous disorders. A somatic mutation in the early development of cells in SWS patients causes the formation of a congenital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a1d31c42621efb2666fd55de5c0fdbc
https://doi.org/10.3126/njn.v18i3.34969
https://doi.org/10.3126/njn.v18i3.34969
Publikováno v:
INDIAN JOURNAL OF APPLIED RESEARCH. :81-83
INTRODUCTION: Clinically silent pulmonary thromboembolism is commoner than symptomatic one in children with nephrotic syndrome. The present study was done to look for the occurrence of asymptomatic pulmonary thromboembolism in children with nephrotic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e64b19823f8ae1db906603b6ca2cba77
https://doi.org/10.36106/1603050
https://doi.org/10.36106/1603050
Publikováno v:
Journal of tropical pediatrics. 67(1)
Introduction Pericardial effusion may be due to various causes. With the changing scenario of newer generation antibiotics and robust immunization program our aim is to identify the change, if any, in etiology and disease menifestations. Methodology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d05a43f19860721f1f61a4bdf4e5cceb
https://pubmed.ncbi.nlm.nih.gov/33346812
https://pubmed.ncbi.nlm.nih.gov/33346812
Publikováno v:
INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH. :66-67
Hepatoblastoma is the most common tumour in children under the age of 5 years. Diagnosis is made usually by combination of clinical, laboratory and radiological ndings. Biopsy is the gold standard for diagnosis. We present a case of hepatoblastoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::434b3a02ce1ace680e9530f2076b266b
https://doi.org/10.36106/ijsr/8424842
https://doi.org/10.36106/ijsr/8424842
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 31:1057-1060
Background Van Wyk-Grumbach syndrome (VWGS) is characterized by juvenile primary hypothyroidism, delayed bone age and isosexual incomplete precocious puberty with reversal to the prepubertal state following thyroid hormone replacement. Case presentat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3106dc5559669f5b0af47c0ce5bbc95b
https://doi.org/10.1515/jpem-2018-0049
https://doi.org/10.1515/jpem-2018-0049
Autor:
Sumantra Sarkar, Avijit Hazra, Malay Kumar Sinha, Mrinal Kanti Das, Arpan Saha, Suprit Basu, Supratim Datta, Ranjabati Datta, Sumana Datta Kanjilal
Publikováno v:
Journal of Tropical Pediatrics. 65:139-146
The aim of this study was to assess the clinico-laboratory parameters, complications and therapeutic responses in children with scrub typhus in Eastern India.In this prospective, observational study, all children (age,12 years) with suspected scrub t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d751fe65e05a309596df2259cca4171
https://doi.org/10.1093/tropej/fmy027
https://doi.org/10.1093/tropej/fmy027
Autor:
Suprit Basu, Sarbani Misra (Roy), Tanushree Mondal, Maidul Islam, Sumantra Sarkar, Mrinal Kanti Das, Malay Kumar Sinha, Sumana Datta (Kanjilal), Supratim Datta
Publikováno v:
Sri Lanka Journal of Child Health. 50:610
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d927b04a14505dae61d7791774f1f6bc
https://doi.org/10.4038/sljch.v50i4.9847
https://doi.org/10.4038/sljch.v50i4.9847