Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hareesh Sanikam"'
Publikováno v:
Asian Journal of Medical Sciences, Vol 14, Iss 4, Pp 143-146 (2023)
Background: Dengue is a rapidly increasing global public health problem especially in tropical countries. Dengue is a benign and self-limiting febrile illness in the majority of children but in some children, it can progress to severe dengue (SD) res
Externí odkaz:
https://doaj.org/article/f7e9caae011241b0b3d53ff1340ca607
Autor:
Hareesh Sanikam, Basavaraj Bheeman
Publikováno v:
Indian Journal of Child Health. 6:375-378
Background: Wilson disease (WD) is a rare autosomal recessive disorder characterized by the accumulation of copper in the liver, brain, cornea, and kidneys. Asymptomatic nature of disease at earlier stages leads to diagnostic enigma. Objective: The o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::31766fa2ba19a141098efe885fad2fa8
https://doi.org/10.32677/ijch.2019.v06.i07.011
https://doi.org/10.32677/ijch.2019.v06.i07.011
Publikováno v:
Asian Journal of Clinical Pediatrics and Neonatology. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::069684073785b14b2e9d453db605cb9e
https://doi.org/10.21276/ajcpn.2019.7.2.2
https://doi.org/10.21276/ajcpn.2019.7.2.2
Publikováno v:
International Journal of Contemporary Pediatrics. 8:314
Background: Febrile seizures are seizures that occur in children between 6 months and 60 months of age , with body temperature of 38ºC or higher not resulting from Central Nervous System (CNS) infection or any metabolic imbalance without any prior a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03ba613dbd7128d4ec3ab3c732d37a51
https://doi.org/10.18203/2349-3291.ijcp20210120
https://doi.org/10.18203/2349-3291.ijcp20210120
Autor:
Vidya Krishnamurthy, Hareesh Sanikam, Udayakumar Seetharam Rao, Pushpalatha Kariyappa, Abdus Subhan Sohail
Publikováno v:
International Journal of Contemporary Pediatrics. 7:2387
Alymphoid cystic thymic dysgenesis is a severe combined immunodeficiency (SCID) syndrome caused b y a mutation in fork head box N1 gene (FOXN1) on chromosome 17. It is a transcriptional factor regulating the development, differentiation and function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10bb16bca7f7265f058d08a7fb9f76d2
https://doi.org/10.18203/2349-3291.ijcp20205102
https://doi.org/10.18203/2349-3291.ijcp20205102
Autor:
S. Udaya Kumar, Hareesh Sanikam, Pavan Pujar, Sujatha Ramabhatta, Pavan Anilkumar Kittagaly, Pushpalatha Kariyappa
Publikováno v:
Sri Lanka Journal of Child Health. 48:117
Objective: To identify the aetiology of children presenting with fever of unknown origin (FUO). Method: A prospective study of children between 6 months to 18 years admitted for FUO at Employees State Insurance Corporation Medical College and Post Gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6bdb5265827eef5157dfb3b9857c981
https://doi.org/10.4038/sljch.v48i2.8703
https://doi.org/10.4038/sljch.v48i2.8703
Autor:
Pushpalatha Kariyappa, Hareesh Sanikam, Bharathi Kondappa, Sujatha Ramabhatta, Udaya Kumar Rao
Publikováno v:
Sri Lanka Journal of Child Health. 47:146
Objective: To establish the possible aetiology of febrile children presenting with thrombocytopenia. Method: In this observational study, all children, aged 1 month to 18 years, admitted to paediatric wards of the ESIC Medical College & Postgraduate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54c5cdc54f488723a890e97c3194acab
https://doi.org/10.4038/sljch.v47i2.8481
https://doi.org/10.4038/sljch.v47i2.8481
Autor:
Sanikam, Hareesh1, Bheeman, Basavaraj2 basavaraj16382@gmail.com, Ramabhatta, Sujatha2, Kariyappa, Pushpalatha3
Publikováno v:
Asian Journal of Medical Sciences. Apr2023, Vol. 14 Issue 4, p143-146. 4p.