Zobrazeno 1 - 10
of 301
pro vyhledávání: '"Bahig M, Shehata"'
Publikováno v:
Journal of Electrocardiology. 70:75-78
The specific electrocardiographic (ECG) pattern of left main coronary artery ischemia is exceptionally rare in children and under recognized. Occasional reports are bereft of a detailed mechanistic ECG description and limited to dissection, spasm, or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daac4430ec60999536746f1667cde216
https://doi.org/10.1016/j.jelectrocard.2021.12.002
https://doi.org/10.1016/j.jelectrocard.2021.12.002
Autor:
Eric Chang, Anna Maria Hadjilambris, Bahig M. Shehata, Hany Eskarous, Janet Poulik, Mena Abdo, Rania Daboul, Abdul Hanan
Publikováno v:
Fetal and Pediatric Pathology. 41:909-918
Background: Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia is an inherited cardiomyopathy, characterized by replacement of the RV muscle wall with fibrofatty tissue. The diagnosis is challenging, due to the absence of a unique presentation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49c9d699d62ee1429fa37ad6c7bd4cb2
https://doi.org/10.1080/15513815.2021.2008564
https://doi.org/10.1080/15513815.2021.2008564
Publikováno v:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
Hirschsprung disease (HD) is characterized by circumferential aganglionosis of the rectum with variable proximal bowel involvement. The underlying pathogenesis is due to failure of caudal migration of neural crest cells during pre-natal development,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36e8d6394bd1f5a16737e3fb8252c1fc
https://pubmed.ncbi.nlm.nih.gov/36457257
https://pubmed.ncbi.nlm.nih.gov/36457257
Autor:
Kasey McCollum, Iman William, Janet Poulik, Adina Alazraki, Eman Al-Haddad, Bahig M. Shehata, Renee Dhar-Dass, Abdul Hanan, Alyssa Kalsbeek, Aya Almashad
Publikováno v:
Fetal and Pediatric Pathology. 41:749-758
BACKGROUND Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a lethal congenital disorder characterized by a large, non-obstructed bladder, microcolon, and lack of proper peristalsis. MATERIALS AND METHODS Five cases of MMIHS were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12d4ba4a362d34822b68ea1fe99a0d2c
https://doi.org/10.1080/15513815.2021.1964656
https://doi.org/10.1080/15513815.2021.1964656
Autor:
Thomas Cash, Hong Yin, Courtney McCracken, Zhi Geng, Steven G. DuBois, Bahig M. Shehata, Thomas A. Olson, Howard M. Katzenstein, Cynthia Wetmore
Publikováno v:
Sarcoma, Vol 2017 (2017)
Background. Ezrin is a membrane-cytoskeleton linker protein that has been associated with metastasis and poor outcomes in osteosarcoma and high-grade soft tissue sarcomas. The prognostic value of ezrin expression in Ewing sarcoma is unknown. Methods.
Externí odkaz:
https://doaj.org/article/d059f513979348e9b8eb959389b513c1
Autor:
Bahig M. Shehata, Sarah S. Kappa
Publikováno v:
Pediatric Oncology ISBN: 9783030920708
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2ecc5072730dd409a58a5e587aaa8ea
https://doi.org/10.1007/978-3-030-92071-5_23
https://doi.org/10.1007/978-3-030-92071-5_23
Publikováno v:
Fetal and pediatric pathology. 41(6)
Background: While much is known about the channelopathy disorder Long QT Syndrome (LQTS), the histopathological findings and their implications on the disease have remained largely unexplored to date. In this review, we discuss the background of LQTS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15a07eef1617c9a43181deb6c54b23a1
https://pubmed.ncbi.nlm.nih.gov/34766536
https://pubmed.ncbi.nlm.nih.gov/34766536
Autor:
Nadeen Zaiat, Eric Chang, Scott Baker, Ereny Demian, Jasmine Vickery, Eman Sallam, Bahig M. Shehata, Janet Poulik, Mohamed Alhamar, Abdul Hanan
Publikováno v:
Fetal and pediatric pathology. 41(5)
Background CRMO is a sterile auto inflammatory bone disease that affects the pediatric population. Recently, single gene mutations in LPIN2, DIRA, and IL1RN have been reported in murine models of CRMO. Materials and methods The medical records and hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::250897d436082a9466c311a75f2a5d9f
https://pubmed.ncbi.nlm.nih.gov/34542007
https://pubmed.ncbi.nlm.nih.gov/34542007
Publikováno v:
Fetal and pediatric pathology. 41(5)
BACKGROUND Urothelial rests, also known as Walthard rests, are benign nests of epithelial cells that most often are found in the female gynecologic tract. Only four of these urothelial rests have been described in the appendix. Case report: A 10-year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::996af704787c9a83813d67cfc61abc9a
https://pubmed.ncbi.nlm.nih.gov/34338594
https://pubmed.ncbi.nlm.nih.gov/34338594
Autor:
Arshawn Mohseni, Shriprasad R. Deshpande, Bahig M. Shehata, Felipe O. Giuste, May D. Wang, Yuanda Zhu, Sahar Ibrahim, Ali Mirzazadeh
Publikováno v:
BHI
Cardiac allograft rejection is a life-threatening complication that can occur in patients following heart transplantation. Endomyocardial biopsies, the current gold-standard for monitoring rejection, require manual identification of samples by expert
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acde3e46acc46ccb4b2ffd8706bb313a
https://doi.org/10.1109/bhi50953.2021.9508532
https://doi.org/10.1109/bhi50953.2021.9508532