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Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.
Published in:
Multiple Sclerosis Journal, 2012, v. 18, n. 10, p. 1395, doi. 10.1177/1352458512440832
By:
- Al Jumah, M;
- Al Balwi, M;
- Hussein, M;
- Kojan, S;
- Al Khathaami, A;
- Al Fawaz, M;
- Al Muzaini, B;
- Jawhary, A;
- Al Abdulkareem, I
Publication type:
Article
Congenital Duplication of the Palm Syndrome: Gene Analysis and the Molecular Basis of its Clinical Features.
Published in:
Journal of Hand Surgery (17531934), 2009, v. 34, n. 2, p. 247, doi. 10.1177/1753193408099828
By:
- AL-QATTAN, M. M.;
- AL-BALWI, M.;
- EYAID, W.;
- AL-ABDULKARIM, I.;
- AL-TURKI, S.
Publication type:
Article
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies.
Published in:
Brain: A Journal of Neurology, 2013, v. 136, n. 10, p. 3096, doi. 10.1093/brain/awt218
By:
- Webb, Emma A.;
- AlMutair, Angham;
- Kelberman, Daniel;
- Bacchelli, Chiara;
- Chanudet, Estelle;
- Lescai, Francesco;
- Andoniadou, Cynthia L.;
- Banyan, Abdul;
- Alsawaid, Al;
- Alrifai, Muhammad T.;
- Alahmesh, Mohammed A.;
- Balwi, M.;
- Mousavy-Gharavy, Seyedeh N.;
- Lukovic, Biljana;
- Burke, Derek;
- McCabe, Mark J.;
- Kasia, Tessa;
- Kleta, Robert;
- Stupka, Elia;
- Beales, Philip L.
Publication type:
Article
HLA class II polymorphism in Saudi patients with multiple sclerosis.
Published in:
HLA: Immune Response Genetics, 2018, v. 91, n. 1, p. 17, doi. 10.1111/tan.13173
By:
- Al Jumah, M.;
- Kojan, S.;
- Al Shehri, A. M.;
- Al Balwi, M.;
- Al Abdulkarim, I.;
- Masuadi, E. M.;
- Alhaidan, Y.;
- Alabdulrahman, A.;
- Fakhoury, H. M.;
- Hajeer, A. H.
Publication type:
Article
The prevalence of CCR5-Δ32 mutation in a cohort of Saudi stem cell donors.
Published in:
HLA: Immune Response Genetics, 2017, v. 90, n. 5, p. 292, doi. 10.1111/tan.13100
By:
- Alarifi, M.;
- Al‐Amro, F.;
- Alalwan, A.;
- Al‐Turki, A.;
- Fakhoury, H.;
- Atallah, N.;
- Al‐Muallimi, M.;
- Al‐Balwi, M.;
- Alzahrani, M.;
- Alaskar, A.;
- Hajeer, A.;
- Jawdat, D.
Publication type:
Article
Risk factors predicting disease severity and mortality in coronavirus disease 2019 Saudi Arabian patients.
Published in:
Annals of Thoracic Medicine, 2023, v. 18, n. 2, p. 98, doi. 10.4103/atm.atm_435_22
By:
- Al Balwi, Wala M.;
- AlGhamdi, Nouf;
- Alshahrani, Reem;
- Abdelrahman, Ihssan H.;
- Mahmoud, Sami;
- Al-Hamad, Ali;
- Al Hamzah, Salma;
- Al Jraid, Fahad;
- Al Turki, Maha;
- Al Balwi, Mohammed A.
Publication type:
Article
PRF1 gene mutation in a Saudi patient with haemophagocytic lymphohistiocytosis.
Published in:
British Journal of Biomedical Science, 2010, v. 67, n. 2, p. 88, doi. 10.1080/09674845.2010.11978194
By:
- Al Balwi, M. A.;
- Al Harbi, T.;
- Al Abdulkareem, I.;
- Hajeer, A. H.
Publication type:
Article

Found: 7

Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.

Congenital Duplication of the Palm Syndrome: Gene Analysis and the Molecular Basis of its Clinical Features.

ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies.

HLA class II polymorphism in Saudi patients with multiple sclerosis.

The prevalence of CCR5-Δ32 mutation in a cohort of Saudi stem cell donors.

Risk factors predicting disease severity and mortality in coronavirus disease 2019 Saudi Arabian patients.

PRF1 gene mutation in a Saudi patient with haemophagocytic lymphohistiocytosis.