Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Samiya Al-Hashmi"'
Publikováno v:
Case Reports in Pediatrics, Vol 2023 (2023)
The Vogt–Koyanagi–Harada syndrome (VKHS) is a unique form of granulomatous autoimmune disease that mostly impacts the pigmented tissues of the body. The main feature is bilateral granulomatous panuveitis, which is detected on ophthalmologic exami
Externí odkaz:
https://doaj.org/article/4d4e705395b6497b864496ea76a2a690
Autor:
Abdulhamid Al‐Hinai, Samiya Al‐Hashmi, Anuradha Ganesh, Nadia Al‐Hashmi, Abeer Al‐Saegh, Watfa Al‐Mamari, Fathiya Al‐Murshedi, Khalid Al‐Thihli, Adila Al‐Kindi, Almundher Al‐Maawali
Publikováno v:
American Journal of Medical Genetics Part A. 188:2485-2490
Autor:
Samiuddin Shaikh, Nawal Al Maskari, Ahmad ElKhamisy, Nuha Al Tahir, Samiya Al-Hashmi, Kholoud Al-Mukhaini
Publikováno v:
Sultan Qaboos University Medical Journal [SQUMJ]. 22:129-133
Measles is a highly contagious infectious disease. Despite aggressive national initiatives to eradicate measles, outbreaks have occurred in recent years. We report three infants who presented to a tertiary care hospital in Muscat, Oman, in 2019 with
Publikováno v:
Global Journal of Medical Research. :23-27
Gallbladder stones in children is one complication that is mostly seen in diseases such as hemolytic diseases, liver disease, and obesity. It can also be a secondary complication of long-duration use of antibiotics like ceftriaxone. However, gallblad
Publikováno v:
Case Reports in Pediatrics. 10/26/2023, p1-6. 6p.
Severe Pneumonitis in Omani Infants During An In-Hospital Measles Outbreak: A report of three cases.
Autor:
Al-Hashmi, Samiya1, Al-Mukhaini, Kholoud2, Shaikh, Samiuddin2, ElKhamisy, Ahmad2, Al Tahir, Nuha1, Al Maskari, Nawal1 nawal.almaskari@gmail.com
Publikováno v:
Sultan Qaboos University Medical Journal. Feb2022, Vol. 22 Issue 1, p129-133. 5p.
Autor:
Al‐Hinai, Abdulhamid, Al‐Hashmi, Samiya, Ganesh, Anuradha, Al‐Hashmi, Nadia, Al‐Saegh, Abeer, Al‐Mamari, Watfa, Al‐Murshedi, Fathiya, Al‐Thihli, Khalid, Al‐Kindi, Adila, Al‐Maawali, Almundher
Publikováno v:
American Journal of Medical Genetics. Part A; Aug2022, Vol. 188 Issue 8, p2485-2490, 6p