Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Sai Chandar Dudipala"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 5, Pp SD03-SD04 (2020)
Myasthenia Gravis (MG) is most commonly caused by antibodies to acetylcholine receptor (AChRs). MG can present as respiratory failure during the late course of the disease, known as a myasthenia crisis. Mostly, this crisis develops in adult patients
Externí odkaz:
https://doaj.org/article/ff3c4143ea6e4c1ca86dc5d33191b472
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92b191bfa168f758dd29332d5ee64d0e
https://doi.org/10.7759/cureus.38082
https://doi.org/10.7759/cureus.38082
Publikováno v:
Cureus. 14(11)
Background This study aims to examine the clinico-etiological profile of children with the first episode of a seizure and categorize seizure types based on age groups in a tertiary care hospital. Methodology This was a prospective observational study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3ecda2d2cedc13092226f56c167e401
https://pubmed.ncbi.nlm.nih.gov/36514607
https://pubmed.ncbi.nlm.nih.gov/36514607
Publikováno v:
Journal of Neurosciences in Rural Practice, Vol 12, Iss 01, Pp 112-115 (2021)
Journal of Neurosciences in Rural Practice
Journal of Neurosciences in Rural Practice
Objective Eucalyptus oil (EO)-induced seizures (EOIS) in children is a less recognized entity and a rare cause of acute symptomatic seizures. The purpose of this review outlines the clinical features and outcomes of EOIS with observed cases. Patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::553cd116787dcf15a9abcf948072318e
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1721199
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0040-1721199
Publikováno v:
Pediatric Review: International Journal of Pediatric Research. 7:442-445
A congenital variant of rett syndrome or Forkhead box G1 (FOXG1) syndrome is a rareneurodevelopmental disorder characterized by global developmental delay, microcephaly, autisticfeatures, early-onset dyskinesia, and seizures. Once it was described as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdfb79ea880ea60beb7f969235d14007
https://doi.org/10.17511/ijpr.2020.i08.09
https://doi.org/10.17511/ijpr.2020.i08.09
Publikováno v:
Journal of Pediatric Neurosciences
Dengue fever is a common viral infection in the tropical areas, especially in India. The clinical manifestations of dengue infection are broad-spectrum, ranging from asymptomatic to life-threatening dengue shock syndrome. Usually, the dengue virus do
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::152e705b2f74a337405afa3514fed51e
http://europepmc.org/articles/PMC7847127
http://europepmc.org/articles/PMC7847127
Publikováno v:
Indian Journal of Child Health. :220-222
Background: Acute dystonic reactions are the most common type of extrapyramidal reactions associated with the use of certain drugs. Drug-induced dystonic reactions (DIDRs) are diagnosed based on the detailed history and physical examination. Objectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::471f168fa63037cfd0ba08267c5c1f47
https://doi.org/10.32677/ijch.2020.v07.i05.007
https://doi.org/10.32677/ijch.2020.v07.i05.007
Publikováno v:
Journal of Pediatric Epilepsy. :048-050
Idiopathic ketotic hypoglycemia (IKH) is characterized by recurrent neurohypoglycemic symptoms with ketosis. Hypoglycemic episodes typically occur during early mornings, especially either with illness and/or prolonged fasting. We reported a case of I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2a3b42c274db4728a225173638830f5
https://doi.org/10.1055/s-0040-1710043
https://doi.org/10.1055/s-0040-1710043
Publikováno v:
Cureus
3-Methylglutaconic aciduria type I (3-MGA I) is a rare inherited disorder of the leucine metabolism pathway due to mutations in the AUH gene for 3-methylglutaconyl-CoA hydratase enzyme and enzyme deficiency. It has a variable phenotypic presentation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47c7ccb9345702b36b594da9317c0d9e
https://doi.org/10.7759/cureus.11951
https://doi.org/10.7759/cureus.11951
Publikováno v:
Pediatric Oncall. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97bf5972c2676c90fdbf11e9ff5ddeaa
https://doi.org/10.7199/ped.oncall.2020.25
https://doi.org/10.7199/ped.oncall.2020.25