Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Talib Y. Surve"'
Autor:
Talib Y. Surve, Ashok D. Rathod
Publikováno v:
Journal of Tropical Pediatrics. 52:451-453
Background: Human immunodeficiency virus (HIV) infection predisposes to various opportunistic infections like tuberculosis, Pneumocystis carinii (P. carinii) pneumonia, toxoplasmosis and fungal infections. Naso-gastric aspirate (NGA) is utilized to d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c02a18a1e0a005eb6d0b16662d2a3cc0
https://doi.org/10.1093/tropej/fml022
https://doi.org/10.1093/tropej/fml022
Publikováno v:
Tropical Doctor. 36:59-61
Congenital TB has varied clinical manifestations, and may mimic septicaemia in neonates. Congenital TB is transmitted through the infected placenta via the umbilical vein or inhalation and ingestion of infected amniotic fluid. Endometrial TB usually
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a64df1f55b0d1218588f6e7f6798207
https://doi.org/10.1258/004947506775599021
https://doi.org/10.1258/004947506775599021
Publikováno v:
Indian journal of pediatrics. 73(2)
Epilepsy with myoclonic absences is a rare seizure disorder with intellectual impairment and resistance to conventional anti-convulsants. It is essential to diagnose epilepsy with myoclonic absences earlier for a better outcome. The authors present a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce8b365ee984b76f7ee730f895ee71e3
https://pubmed.ncbi.nlm.nih.gov/16514226
https://pubmed.ncbi.nlm.nih.gov/16514226
Publikováno v:
Indian journal of pediatrics. 66(1)
We report three brothers with Allgrove syndrome. All three had evidence of adrenal insufficiency and deficient tear production, though neither of them had achalasia, the third component of the disorder at the time of this report. Neurological abnorma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc41a9b50cc9bbd3da3c70cd203d6097
https://pubmed.ncbi.nlm.nih.gov/10798051
https://pubmed.ncbi.nlm.nih.gov/10798051
Publikováno v:
The Indian Journal of Pediatrics. 72:353-354
Wolman disease is a rare fatal autosomal recessive disorder caused by absence of acid lipase enzyme leading to accumulation of cholesterol ester. Hepatosplenomegaly is a constant feature and occurs as early as fourth day of life. Progressive mental d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::372dc832eb978c2ae5276bc44fa2e865
https://doi.org/10.1007/bf02724020
https://doi.org/10.1007/bf02724020