Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Nida Ansari"'
Autor:
Sacide S. Ozgur MD, Nida Ansari DO, Yezin Shamoon MD, Sherif Elkattway DO, Rachel Abboud DO, Fayez Shamoon MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 12 (2024)
Systemic lupus erythematosus (SLE) is an autoimmune disease targeting multiple organs through immune complexes. Pericarditis and pericardial effusions are often encountered; however, cases of biventricular failure are notably less common in the setti
Externí odkaz:
https://doaj.org/article/e0e6fcd50e7345d6b60f9988b32f3b4a
Autor:
Sacide S. Ozgur MD, Nida Ansari DO, Alan Alcantara MD, Angela Pais Vidreiro BS, Ryan Rahman, Yezin Shamoon MD, Sherif Elkattawy DO, Rachel Abboud DO, Rajkumar Doshi MD, Fayez Shamoon MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 12 (2024)
Perimyocarditis and myopericarditis are inflammatory conditions of the pericardium and myocardium, often of idiopathic or infectious etiology, with viral infections being the most common. Nonrheumatic streptococcal myopericarditis (NSM) is a rare con
Externí odkaz:
https://doaj.org/article/07e8ebfba5054aef9f7d3f8bb8a7b42d
Autor:
Sacide S. Ozgur, Arielle Aiken, Lefika Bathobakae, Nida Ansari, Patrick Michael, Mourad Ismail
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message Mounier‐Kuhn syndrome, characterized by tracheal dilatation due to the loss of elastic fibers and smooth muscle cells, is a rare condition, often leading to recurrent respiratory infections from impaired mucociliary clearance.
Externí odkaz:
https://doaj.org/article/1b32c95be1834c5fbf76066cc14d3c21
Publikováno v:
Clinical Case Reports, Vol 12, Iss 7, Pp n/a-n/a (2024)
Key Clinical Message Isolated spontaneous superior mesenteric artery (SMA) dissection is relatively rare. Often found incidentally on cross‐sectional imaging, often managed non‐operatively. We present a patient who presented with chest pain and w
Externí odkaz:
https://doaj.org/article/668fcd78f605451689b2b772460f1d92
Publikováno v:
Clinical Case Reports, Vol 12, Iss 3, Pp n/a-n/a (2024)
Key Clinical Message Isolated agenesis of pulmonary arteries with congenital lung hypoplasia is rare. It can be found in childhood or adulthood if asymptomatic. We present a patient with congenital right lung hypoplasia with an absent right pulmonary
Externí odkaz:
https://doaj.org/article/1089677fbca24856a5c2d9bbc038b594
Autor:
Sacide S. Ozgur MD, Muhammad Adil Afzal MD, Dhruv Patel DO, Nida Ansari DO, Arielle Aiken MD, Yezin Shamoon MD, Rachel Abboud DO, Fayez Shamoon MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 12 (2024)
Lyme disease, caused by Borrelia burgdorferi and transmitted via Ixodes ticks, is a common vector-borne illness in the United States, with an estimated 476,000 annual cases. While primarily known for its neurological and rheumatological manifestation
Externí odkaz:
https://doaj.org/article/ed64afc2108a4ab2b17e38f5df696d83
Publikováno v:
GastroHep, Vol 2024 (2024)
Conclusion: We intend to educate providers on the appropriate time to intervene to reduce mortality and subsequent hospitalizations for those with advanced liver disease.
Externí odkaz:
https://doaj.org/article/57131c390150461fa55ac0f5741a316f
Autor:
Lefika Bathobakae, Nida Ansari, Anas Mahmoud, Shayee Hasan, Ruhin Yuridullah, Sohail Qayyum, Sam Rae
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2024 (2024)
Familial Mediterranean fever (FMF) is a hereditary disorder characterized by episodes of fever, polyserositis, or cutaneous inflammation. The FMF attacks last 1–3 days and have no apparent triggers. Recurrent deposition of the serum amyloid A (SAA)
Externí odkaz:
https://doaj.org/article/45be1cb64175446a83a3dbe026cc9b63
Publikováno v:
Sensors, Vol 23, Iss 23, p 9470 (2023)
The present study tests the feasibility, acceptability, and utility of the novel smartphone application—Time2Feel—to monitor family members’ emotional experiences, at the experiential and physiological level, and their context. To our knowledge
Externí odkaz:
https://doaj.org/article/f73189ebfa0348779e9e14c6d7bb3859
Publikováno v:
Case Reports in Hematology, Vol 2022 (2022)
Splenomegaly is manifested by a variety of etiologies, one of which is macrocytic anemia. Macrocytic anemia has multiple causes in itself that include; folate (Vitamin B9) and Cobalamin (vitamin B12) deficiencies. In this case report, we present a pa
Externí odkaz:
https://doaj.org/article/a29a9ec9299146e29caa7bc12610ba2d