Overexpression and Secretion of the Soluble CTLA-4 Splice Variant in Various Autoimmune Diseases and in Cases with Overlapping Autoimmunity

Por AlFadhli, Suad
Publicado em 2013

Influence of Endothelial Nitric Oxide Synthase Gene Intron-4 27bp Repeat Polymorphism on Its Expression in Autoimmune Diseases

Por AlFadhli, Suad
Publicado em 2013

Violating the Theory of Single Gene-Single Disorder: Inhibitor Development in Hemophilia

Por AlFadhli, Suad, Nizam, Rasheeba
Publicado no Indian J Hematol Blood Transfus (2014)

Prevalence of Cytomegalovirus DNA in Cord Blood and Voided Urine Obtained from Pregnant Women at the End of Pregnancy

Por Al-Awadhi, Rana, Al-Harmi, Jehad, AlFadhli, Suad
Publicado no Med Princ Pract (2013)

Novel crystallin gamma B mutations in a Kuwaiti family with autosomal dominant congenital cataracts reveal genetic and clinical heterogeneity

Por AlFadhli, Suad, Abdelmoaty, Sidky, Al-Hajeri, Amal, Behbehani, Abdulmutalib, Alkuraya, Fowzan
Publicado em 2012

The Effects of HFE Polymorphisms on Biochemical Parameters of Iron Status in Arab Beta-Thalassemia Patients

Por AlFadhli, Suad, Salem, Matra, Shome, D. K., Mahdi, Najat, Nizam, Rasheeba
Publicado no Indian J Hematol Blood Transfus (2017)

The Effect of UGT1A1 Promoter Polymorphism in the Development of Hyperbilirubinemia and Cholelithiasis in Hemoglobinopathy Patients

Por AlFadhli, Suad, Al-Jafer, Hassan, Hadi, Mays, Al-Mutairi, Mashael, Nizam, Rasheeba
Publicado em 2013

Mutations in the RNA Granule Component TDRD7 Cause Cataract and Glaucoma

Por Lachke, Salil A., Alkuraya, Fowzan S., Kneeland, Stephen C., Ohn, Takbum, Aboukhalil, Anton, Howell, Gareth R., Saadi, Irfan, Cavallesco, Resy, Yue, Yingzi, Tsai, Anne C-H., Nair, K. Saidas, Cosma, Mihai I., Smith, Richard S., Hodges, Emily, AlFadhli, Suad M., Al-Hajeri, Amal, Shamseldin, Hanan E., Behbehani, AbdulMutalib, Hannon, Gregory J., Bulyk, Martha L., Drack, Arlene V., Anderson, Paul J., John, Simon W. M., Maas, Richard L.
Publicado em 2011