Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Buthaina Al-Musalhi"'
Publikováno v:
Oman Medical Journal, Vol 31, Iss 1, Pp 73-76 (2016)
T-cell prolymphocytic leukemia (T-PLL) is a rare and aggressive post-thymic malignancy that is characterized by the proliferation of small- to medium- sized prolymphocytes. The classic clinical features of T-PLL are lymphocytosis, lymphadenopathy, he
Externí odkaz:
https://doaj.org/article/930eefbff90642f492f251ae24ca0f83
Autor:
Buthaina Al-Musalhi, Zainab Al-Balushi
Publikováno v:
Oman Medical Journal, Vol 35, Iss 6, Pp 204-204 (2020)
PHACES syndrome comprises posterior fossa malformations, segmental hemangioma, arterial anomalies, cardiac defects, eye anomalies and less commonly, sternal cleft, or supraumbilical raphe. We report a case of PHACES syndrome associated with intestina
Externí odkaz:
https://doaj.org/article/3f97e311bce244a99d9276b228811c8c
Autor:
Buthaina Al-Musalhi, William Gerstein
Publikováno v:
Oman Medical Journal, Vol 31, Iss 5, Pp 394-395 (2016)
Externí odkaz:
https://doaj.org/article/f4bfdce4791040ba9ce5aba7fa8719a9
Publikováno v:
Oman Medical Journal, Vol 39, Iss 3, Pp e641-e641 (2024)
Externí odkaz:
https://doaj.org/article/9160be484e7b45d6a4e1b6e73c5e03f8
Publikováno v:
JAAD Case Reports, Vol 34, Iss , Pp 61-63 (2023)
Externí odkaz:
https://doaj.org/article/f597368e695a40dda5d8d8819c670587
Autor:
Ghaitha Al Mahruqi, Edwin Stephen, Ibrahim Abdelhedy, Hanan Al Mawaali, Buthaina Al Musalhi, Zainab Al Balushi, Rashid Al Sukeiti, Khalifa Al Wahaibi
Publikováno v:
Oman Medical Journal, Vol 37, Iss 2, Pp e347-e347 (2022)
We present a glimpse of vascular malformations seen at Sultan Qaboos University Hospital from July 2014 to December 2019. The cases are sporadic in nature. Molecular genetic studies can be conducted in patients with a family history of vascular malfo
Externí odkaz:
https://doaj.org/article/e4e13447b11744fd8d3f95632e119a6d
Publikováno v:
Journal of Paediatrics and Child Health.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c14bfe5a14f9b24666a339e3f146ab6
https://doi.org/10.1111/jpc.16292
https://doi.org/10.1111/jpc.16292
Autor:
Denis Khnykin, Nouh Al Mahroqi, Geir J. Braathen, Buthaina Al-Musalhi, Hilde Tveitan Hilmarsen, Hilal Al Mandhari
Publikováno v:
International Journal of Dermatology. 60:368-371
Ichthyosis prematurity syndrome (IPS) is a rare type of syndromic autosomal recessive congenital ichthyosis (ARCI) caused by a mutation in the SLC27A4 gene that encodes the fatty acid transport protein 4 (FATP4), which is responsible for keratinocyte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa0e1fc7c44cc92d06dd7077816d1eec
https://doi.org/10.1111/ijd.15367
https://doi.org/10.1111/ijd.15367
Autor:
Buthaina Al-Musalhi, Raya Qais Alsaid
Publikováno v:
JAAD Case Reports, Vol 6, Iss 6, Pp 572-573 (2020)
JAAD Case Reports
JAAD Case Reports
Minimal or arrested growth hemangiomas are a unique subtype of infantile hemangiomas characterized by a reticulated erythematous patch with multiple fine telangiectasias that do not show a proliferation phase or show minimum growth compared to other
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f1985a58435ad6b4c5c71693a2006c
http://www.sciencedirect.com/science/article/pii/S2352512620303192
http://www.sciencedirect.com/science/article/pii/S2352512620303192
Publikováno v:
NeoReviews. 17:e729-e732
A 1-day-old girl is admitted to the NICU after she is discovered to have crusted skin lesions on her trunk, face, and lower limbs during routine newborn examination. She is born at term by vaginal delivery following a normal pregnancy to a primigravi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::319dab85e402399b09063049aafc547f
https://doi.org/10.1542/neo.17-12-e729
https://doi.org/10.1542/neo.17-12-e729