Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Hani Almalki"'
Autor:
Sami Mukhdari Mushta, Riyad Alghamdi, Hani Almalki, Saadia Waqas, Adel Alawwadh, Osamah Barasheed, Mohammad Garnan, Sarah McIntyre, Harunor Rashid, Nadia Badawi, Gulam Khandaker
Publikováno v:
Journal of Epidemiology and Global Health, Vol 14, Iss 2, Pp 453-461 (2024)
Abstract This protocol presents a comprehensive proposal for the establishment of the Saudi Cerebral Palsy Register (SCPR), a crucial project for investigating and addressing the prevalence, etiology, and management of cerebral palsy (CP) in Saudi Ar
Externí odkaz:
https://doaj.org/article/efc20f0e89c3476dbb8992a71582dabb
Publikováno v:
Journal of Applied Hematology, Vol 9, Iss 3, Pp 104-107 (2018)
Atypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy representing A, p.(Asp1115Asn). The early recognition and administration of eculizumab are a lifesaving measure. C3 gene mutations are an autosomal dominant inheri
Externí odkaz:
https://doaj.org/article/2f930b25b8d64caaa97173423b9ba520
Publikováno v:
Journal of Applied Hematology, Vol 10, Iss 3, Pp 103-105 (2019)
Griscelli syndrome (GS) is a rare autosomal recessive disorder. It features with clinical constellation of skin hypopigmentation, silvery-gray hair, associated with neurological involvement (type I), or defective cell-mediated immunity with hemophago
Externí odkaz:
https://doaj.org/article/ab88688bbeed41f7afe9bb0c70428fc7
Publikováno v:
Pediatric Reports, Vol 10, Iss 2 (2018)
Systemic primary carnitine deficiency (SPCD) is an autosomal recessive inborn error of fatty acid metabolism caused by a defect in the transporter responsible for moving carnitine across plasma membrane. The clinical features of SPCD vary widely base
Externí odkaz:
https://doaj.org/article/4092b1c6f7814c30bb1f99af8cde20cf
Autor:
Abdullah A Baothman, Hani Almalki
Publikováno v:
Archives of Medicine and Health Sciences, Vol 6, Iss 2, Pp 304-305 (2018)
Externí odkaz:
https://doaj.org/article/a84a38de68724f5eaa0681524602b605
Publikováno v:
JAMA Network Open
Key Points Question Do patients with cancer understand the treatment plans to which they consent? Findings In this cross-sectional study of 151 adult patients with cancer and 20 treating physicians only 13.7% of patients had full concordance with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b280a2b0fe703c0b05e1d566756bf92
http://europepmc.org/articles/PMC7054829
http://europepmc.org/articles/PMC7054829
Publikováno v:
Journal of Applied Hematology, Vol 9, Iss 3, Pp 104-107 (2018)
Atypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy representing A, p.(Asp1115Asn). The early recognition and administration of eculizumab are a lifesaving measure. C3 gene mutations are an autosomal dominant inheri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f901364e857b921f752281f22a765f0e
http://www.jahjournal.org/article.asp?issn=1658-5127
http://www.jahjournal.org/article.asp?issn=1658-5127
Publikováno v:
Cureus
Familial hemophagocytic lymphohistiocytosis (HLH) is a fatal autosomal recessive disorder resulting in an exaggerated and ineffective immune response. Genetic defects in familial HLH can lead to the impaired function of the secretory lysosome-depende
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cfb87fa2d350433af6299c27954709a
https://doi.org/10.7759/cureus.6246
https://doi.org/10.7759/cureus.6246
Autor:
Abdurrahman Abdullah Alghamdi, Mohammed Khan, Ahmad Almohanad Absi, Hani Almalki, Mohammed Alsalmi
Publikováno v:
Abstracts.
Background The journey towards better patient safety starts with effective patient–physician communication. This is true for cancer patients, in whom treatments are complex and patients’ understanding might be compromised. Multiple factors can re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b0c6caacb0026e04aae1f5d3bb677c2
https://doi.org/10.1136/bmjoq-2019-psf.17
https://doi.org/10.1136/bmjoq-2019-psf.17
Publikováno v:
Pediatric Reports
Volume 10
Issue 2
Pediatric Reports, Vol 10, Iss 2 (2018)
Volume 10
Issue 2
Pediatric Reports, Vol 10, Iss 2 (2018)
Systemic primary carnitine deficiency (SPCD) is an autosomal recessive inborn error of fatty acid metabolism caused by a defect in the transporter responsible for moving carnitine across plasma membrane. The clinical features of SPCD vary widely base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1c7dfc8a9e5c9d0e50105293c443e81