Zobrazeno 1 - 10
of 29
pro vyhledávání: '"sharmeen Nasir"'
Publikováno v:
JLUMHS, Vol 22, Iss 4, Pp 277-281 (2023)
OBJECTIVE: To determine the clinical spectrum of metabolic storage disorders presenting to a public sector tertiary care hospital in Karachi, Pakistan. METHODOLOGY: This retrospective, cross-sectional study was conducted at the Department of Pediatr
Externí odkaz:
https://doaj.org/article/d72aea82b7714928883a252b1fd3c7ed
Publikováno v:
Annals of Abbasi Shaheed Hospital and Karachi Medical & Dental College, Vol 29, Iss 2 (2024)
Objective: Dengue fever, Malaria and Enteric fever are common pediatric acute febrile illnesses, pre- senting with overlapping clinical manifestations. The hematological parameters of these disease may give a clue to the specific diagnosis before def
Externí odkaz:
https://doaj.org/article/ce5f1999569340ddaf8f682108372da7
Autor:
Iqra Rehman Shaikh, Zainab Syyeda Rahmat, Zarmina Islam, Mohammad Arif Mateen Khan, Syed Waqas Ali, Sharmeen Nasir, Sayed Hamid Mousavi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Key Clinical Message Pancreatic pseudocysts are rare in the pediatric population, commonly a result of trauma. Timely diagnosis and adequate management with a multidisciplinary approach are the key to avoid morbidity and mortality. Larger cysts often
Externí odkaz:
https://doaj.org/article/0da6d22c16b44b80a4c4b9ce08d512aa
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 17:410-412
Background: Protein energy malnutrition (PEM) is mainly due to inadequate intake of food both in quantity and quality. Serum magnesium level can be detected to identify magnesium deficiency in malnourished children. Low magnesium level in these child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0d6a79a7476007b7fc76c6992076e3a
https://doi.org/10.53350/pjmhs2023171410
https://doi.org/10.53350/pjmhs2023171410
Publikováno v:
Pakistan Journal of Medical Sciences. 39
Objective: To determine the frequency of inappropriate blood product transfusions in pediatric critically ill patients. Methods: We collected data for this descriptive study from January to December 2020 at the Pediatric Intensive Care Unit (PICU) of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80d601ab2741b814d3461b078cf0dfcf
https://doi.org/10.12669/pjms.39.4.7503
https://doi.org/10.12669/pjms.39.4.7503
Publikováno v:
Ochsner Journal. 22:366-371
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::876847536e2573a825ebeef6539d2647
https://doi.org/10.31486/toj.22.0018
https://doi.org/10.31486/toj.22.0018
We report a case of a four-year-old female child who presented with a massive pancreatic pseudocyst. Pseudocysts >10 cm are at an increased risk of rupture, hence require surgical intervention. Percutaneous external drainage via pig tail catheter was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d61b037f4967b7c84e2712afe79e0a1d
https://doi.org/10.22541/au.166816634.47111708/v1
https://doi.org/10.22541/au.166816634.47111708/v1
Publikováno v:
European journal of emergency medicine : official journal of the European Society for Emergency Medicine. 27(Suppl 1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9eb85354b92433a76e75a00a0598ced
https://pubmed.ncbi.nlm.nih.gov/33555795
https://pubmed.ncbi.nlm.nih.gov/33555795
Publikováno v:
Cureus
Hereditary tyrosinemia type 1 (HT-1) is a rare autosomal recessive disorder caused by a deficiency in the enzyme fumarylacetoacetate hydrolase (FAH), which catalyzes the final step in the tyrosine degradation pathway. Hereditary tyrosinemia is a hete
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c16e4c9ec3aedc04875881acb6f91283
https://doi.org/10.7759/cureus.11541
https://doi.org/10.7759/cureus.11541
Publikováno v:
Cureus
Nonketotic hyperglycinemia (NKH) is an autosomal recessive disorder caused by a defect in glycine cleavage enzyme. It leads to the accumulation of glycine in the body tissues, blood, and cerebrospinal fluid (CSF). Most NKH cases are diagnosed during
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe5a82878bc56f98b9319e798519777e
http://europepmc.org/articles/PMC7145377
http://europepmc.org/articles/PMC7145377