Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Maya, Mukhopadhyay"'
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 6, Iss 3, Pp 1-9 (2017)
The value of ophthalmological examination is often overlooked when we deal with disorders of hepatobiliary system. There is a wide spectrum of genetic, metabolic and other acquired disorders in infants and children that have ocular changes along with
Externí odkaz:
https://doaj.org/article/f0154f024239498ba3cbd61c5d478d7f
Autor:
Aniruddha Ghosh, Sumon Poddar, Sushmita Banerjee, Jaydeep Choudhury, Maya Mukhopadhyay, Jaydeb Ray
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 1, Pp SC05-SC08 (2018)
Introduction: Antibiotic resistance is an increasing global problem which hampers appropriate treatment of Urinary Tract Infection (UTI) in paediatric population, rendering the developing kidneys vulnerable for scarring and long-term complications. T
Externí odkaz:
https://doaj.org/article/3c6d557205bd42bc932af841839cdc96
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
Autor:
Sushmita Banerjee, Sumon Poddar, Aniruddha Ghosh, Jaydeb Ray, Jaydeep Choudhury, Maya Mukhopadhyay
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 1, Pp SC05-SC08 (2018)
Introduction: Antibiotic resistance is an increasing global problem which hampers appropriate treatment of Urinary Tract Infection (UTI) in paediatric population, rendering the developing kidneys vulnerable for scarring and long-term complications. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d4f1cb1cc3b1157c80236d05dbce533
https://doi.org/10.7860/jcdr/2018/30228.11106
https://doi.org/10.7860/jcdr/2018/30228.11106
Publikováno v:
Sri Lanka Journal of Child Health. 48:82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc938759102a1d5a2f00ec3e83fb8a04
https://doi.org/10.4038/sljch.v48i1.8660
https://doi.org/10.4038/sljch.v48i1.8660
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
Publikováno v:
International Journal of Research in Medical Sciences. 5:1726
Electroencephalogram has long been an integral part of evaluation of a child with first episode of afebrile seizure. Several studies have backed up its routine use in pediatric neurology till date and management guidelines also have adopted it. But a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::532f55a592a1b0b72a53a70724c58fae
https://doi.org/10.18203/2320-6012.ijrms20171586
https://doi.org/10.18203/2320-6012.ijrms20171586
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:
Indian pediatrics. 45(4)
Spontaneous rupture of malarial spleen is uncommon even in highly endemic areas of malaria. We report an eight year old girl who presented with spontaneous splenic rupture following malaria. She recovered with conservative management.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::69df11dd2c1fb7a3228d6af457afb8bc
https://pubmed.ncbi.nlm.nih.gov/18451457
https://pubmed.ncbi.nlm.nih.gov/18451457
Publikováno v:
Indian journal of pediatrics. 73(7)
Nager acrofacial dysostosis comprises defects of cranio facial region and limbs (mostly upper) with variable associated anomalies. The cranio- facial complex is indistinguishable from the mandibulo facial dysostosis (Treacher Collins syndrome). About
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::226f74da86b095f3604ffe0e40867915
https://pubmed.ncbi.nlm.nih.gov/16877861
https://pubmed.ncbi.nlm.nih.gov/16877861