Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Mohammed A Albalwi"'
Autor:
Zheng Wang, Aritoshi Iida, Noriko Miyake, Koji M Nishiguchi, Kosuke Fujita, Toru Nakazawa, Abdulrahman Alswaid, Mohammed A Albalwi, Ok-Hwa Kim, Tae-Joon Cho, Gye-Yeon Lim, Bertrand Isidor, Albert David, Cecilie F Rustad, Else Merckoll, Jostein Westvik, Eva-Lena Stattin, Giedre Grigelioniene, Ikuyo Kou, Masahiro Nakajima, Hirohumi Ohashi, Sarah Smithson, Naomichi Matsumoto, Gen Nishimura, Shiro Ikegawa
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0150555 (2016)
Axial spondylometaphyseal dysplasia (axial SMD) is an autosomal recessive disease characterized by dysplasia of axial skeleton and retinal dystrophy. We conducted whole exome sequencing and identified C21orf2 (chromosome 21 open reading frame 2) as a
Externí odkaz:
https://doaj.org/article/b6da7a20f1984f7b853b2aabf45cb344
Autor:
Ikram Ullah, Imtiaz Ahmad, Nigar Ali, Ihtisham Ul Haq, Mohammad Idrees, Mohammed Daher Albalwi, Mehmet Yavuz
Publikováno v:
Mathematical and Computational Applications, Vol 29, Iss 5, p 94 (2024)
This study implements a minded approach to studying Ebola virus disease (EVD) by dividing the infected population into aware and unaware groups and including a hospitalized compartment. This offers a more detailed understanding of illness distributio
Externí odkaz:
https://doaj.org/article/fcc53c5da7544bc1a5e0db1fe28c5fad
Autor:
Ibad Ullah, Nigar Ali, Ihtisham Ul Haq, Imtiaz Ahmad, Mohammed Daher Albalwi, Md. Haider Ali Biswas
Publikováno v:
International Journal of Mathematics and Mathematical Sciences, Vol 2024 (2024)
The SEIQHR model, introduced in this study, serves as a valuable tool for anticipating the emergence of various infectious diseases, such as COVID-19 and illnesses transmitted by insects. An analysis of the model’s qualitative features was conducte
Externí odkaz:
https://doaj.org/article/a40becd55e8b4ed285bf52f215429678
Autor:
Musa Alzahrani, Saeed Al Turki, Waleed Al Rajban, Fatimah Alshalati, Fahad Almodaihsh, Khadega A. Abuelgasim, Bader Alahmari, Thamer Al Bogami, Osama Ali, Talal Al Harbi, Mohammed A. AlBalwi, Maram Alotaibi, Aamer Aleem, Ahmed Al Asker, Areej Al Mugairi
Publikováno v:
Platelets, Vol 33, Iss 8, Pp 1220-1227 (2022)
The P106L mutation in the human myeloproliferative leukemia virus oncogene (MPL) was shown to be associated with hereditary thrombocythemia in Arabs. The clinical and bone marrow (BM) features of P106L mutation are unknown. Genetic databases at two t
Externí odkaz:
https://doaj.org/article/b3dfdcf067bd4384bbe486c95c270452
Publikováno v:
Case Reports in Dermatology, Vol 13, Iss 3, Pp 470-473 (2021)
Ichthyosis prematurity syndrome is a rare autosomal recessive genodermatosis that is associated with mutations in the SLC27A4 gene. Its onset occurs in early childhood and presents with the clinical triad of premature birth, thick caseous desquamatin
Externí odkaz:
https://doaj.org/article/9ff3d4d350394a72882c36d0c6906300
Autor:
Raghad Alharthi, Muhannad A. Alnahdi, Ahad Alharthi, Seba Almutairi, Sultan Al-Khenaizan, Mohammed A. AlBalwi
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Epidermolysis bullosa (EB) is a rare heterogeneous genetic mechanobullous skin disorder that is characterized by increased skin fragility leading to blistering following minor trauma. EB may be inherited as an autosomal dominant or an autosomal reces
Externí odkaz:
https://doaj.org/article/5ce8dd4ea16146fbbc9a2e1a7df5b1b8
Autor:
Anis Khan, Mohammed A. AlBalwi, Ibraheem AlAbdulkareem, Abdulrahman AlMasoud, Abdulrahman AlAsiri, Wardah AlHarbi, Faisal AlSehile, Aiman El-Saed, Hanan H. Balkhy
Publikováno v:
Journal of Infection and Public Health, Vol 12, Iss 4, Pp 557-567 (2019)
Background: The triple assortment influenza A(H1N1) virus emerged in spring 2009 and disseminated worldwide, including Saudi Arabia. This study was carried out to characterize Saudi influenza isolates in relation to the global strains and to evaluate
Externí odkaz:
https://doaj.org/article/4b7884c6ae34497ca710ea329fcd0f12
Autor:
Mohammad M. Al-Qattan, Ali Hadadi, Abdullah M. Al-Thunayan, Ahmed A. Eldali, Mohammed A. AlBalwi
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-7 (2018)
Abstract Background Scientists have previously described an overgrowth syndrome in Saudi patients and named it ‘Upper limb muscle overgrowth with hypoplasia of the index finger’ syndrome. Case presentation We describe a new case and document that
Externí odkaz:
https://doaj.org/article/da25e8359cb842c7913c6f58e62dbaac
