Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Muhamad Alhaj Moustafa, MD"'
Autor:
Benjamin J. McCormick MD, MS, Daniel Zieman MD, Jason C. Sluzevich MD, Muhamad Alhaj Moustafa MD, MS
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 12 (2024)
Cutaneous paraneoplastic syndromes due to Hodgkin lymphoma present with a wide spectrum of clinical manifestations from generalized pruritus to exfoliative erythroderma. We summarize the clinical findings and outcomes of 14 patients with Hodgkin lymp
Externí odkaz:
https://doaj.org/article/f04c2f7bc9594f5da763ed9699ef4d03
Autor:
Emily B. Wolf MD, David Li MD, Andre J. Fernandez MPAS, PA-C, Lindsay B. Gardner MD, Candido E. Rivera MD, Ewa M. Wysokinska MD, Marwan E. Shaikh MD, Han W. Tun MD, Vivek Roy MD, Muhamad Alhaj Moustafa MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 11 (2023)
Factor VII (FVII) is an important, vitamin K-dependent clotting factor. Acquired FVII deficiency is a rare entity that is associated with serious bleeding complications. We report a case of acquired FVII deficiency in a patient with recurrent chronic
Externí odkaz:
https://doaj.org/article/128a25ad03e74b48badd6609083a9599
Autor:
Omran Saifi, MD, Scott C. Lester, MD, William Rule, MD, Bradley J. Stish, MD, Scott Stafford, MD, Deanna H. Pafundi, PhD, Liuyan Jiang, MD, David Menke, MD, Muhamad Alhaj Moustafa, MD, Allison Rosenthal, MD, Taimur Sher, MD, Ayala Ernesto, MD, Han W. Tun, MD, Bradford S. Hoppe, MD, Jennifer L. Peterson, MD
Publikováno v:
Advances in Radiation Oncology, Vol 6, Iss 4, Pp 100714- (2021)
Purpose: This study compares reduced (
Externí odkaz:
https://doaj.org/article/d4f14c6d278c4de0994673c5b221b6f1
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 7 (2019)
Pulmonary veno-occlusive disease (PVOD) is a rare entity that is usually mistaken with pulmonary arterial hypertension (PAH) but is considered class I′ of PAH. It is important to subclassify PVOD and distinguish it from PAH as treatment with vasodi
Externí odkaz:
https://doaj.org/article/675eab6b9a9c4f8095d6eca1af8d17e9
Autor:
Muhammad Usman Mirza MBBS, John Van Taunay MD, Muhammad Waleed MBBS, Shiva Shankar Vangimalla MBBS, Sharana Hegde MBBS, Muhamad Alhaj Moustafa MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 7 (2019)
Xanthogranulomatous pyelonephritis (XGP) is a rare chronic granulomatous destructive process of the renal parenchyma. It is caused by a chronic inflammatory process due to recurrent urinary tract infections and/or obstructing renal calculi. Rarely, i
Externí odkaz:
https://doaj.org/article/eafaf6ff9d3f44d5aa785278be44a395
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 6 (2018)
Stent migration is an uncommon complication of endovascular stenting procedures. It could cause serious cardiovascular complications. In this article, we describe an interesting case of acute heart failure as a result of stent embolization from the l
Externí odkaz:
https://doaj.org/article/eb2816ca6a1e438889b2b98b3981c147
Autor:
Anusha Vakiti MD, Ravi Pilla MD, Muhamad Alhaj Moustafa MD, Jacinth J. Joseph MD, Aarthi G. Shenoy MD
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 6 (2018)
Ifosfamide, an alkylating agent used in cancer treatments, can cause neurotoxicity. The clinical presentation can range from mild symptoms such as acute confusion to non-convulsive seizures, severe irreversible coma, and death. The benefit of methyle
Externí odkaz:
https://doaj.org/article/64e47f7b58d74ce0b88036cf5f843b7f
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 5 (2017)
Pseudohyperkalemia is an uncommon finding in chronic lymphocytic leukemia. It is a misleading condition that could lead to iatrogenic hypokalemia when unwarranted treatment is administered. We describe an interesting case of pseudohyperkalemia in sev
Externí odkaz:
https://doaj.org/article/0ba1cfef3b6a4232b21c8b3f147192b2
Publikováno v:
Journal of Investigative Medicine High Impact Case Reports, Vol 1 (2013)
The findings of hypercalcemia, skull lytic lesions, and renal failure are usually characteristic for multiple myeloma. We herein describe an interesting case of B-cell follicular lymphoma that presented with many features mimicking multiple myeloma.
Externí odkaz:
https://doaj.org/article/8cba625dce6b4e25839c30c7582dccf4
Autor:
Melody, Megan1 (AUTHOR), Parrondo, Ricardo2 (AUTHOR), Alhaj Moustafa, Muhamad2 (AUTHOR), Wu, Kevin3 (AUTHOR), Menke, David3 (AUTHOR), Seim, Lynsey1 (AUTHOR), Tun, Han W.2 (AUTHOR) Tun.Han@mayo.edu
Publikováno v:
Clinical Case Reports. Oct2020, Vol. 8 Issue 10, p2003-2006. 4p.