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Author/Creator Ali, Bassam R

2. Correlation of SIN3A genomic variants with β-hemoglobinopathies disease severity and hydroxyurea treatment efficacy. (November 2016)

Authors:
Gravia, Aikaterini; Chondrou, Vasiliki; Kolliopoulou, Alexandra; Kourakli, Alexandra; John, Anne; Symeonidis, Argyris; Ali, Bassam R; Sgourou, Argyro; Papachatzopoulou, Adamantia; Katsila, Theodora; Patrinos, George P
Journal:
Pharmacogenomics
Issue:
Volume 17:Number 16(2016)
Page Start:
1785
Record Type:
Journal Article
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3. Defect in phosphoinositide signalling through a homozygous variant in PLCB3 causes a new form of spondylometaphyseal dysplasia with corneal dystrophy. Issue 2 (9th November 2017)

Authors:
Ben-Salem, Salma; Robbins, Sarah M; LM Sobreira, Nara; Lyon, Angeline; Al-Shamsi, Aisha M; Islam, Barira K; Akawi, Nadia A; John, Anne; Thachillath, Pramathan; Al Hamed, Sania; Valle, David; Ali, Bassam R; Al-Gazali, Lihadh
Journal:
Journal of medical genetics
Issue:
Volume 55:Issue 2(2018)
Page Start:
122
Record Type:
Journal Article
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4. Genomic variants in the ASS1 gene, involved in the nitric oxide biosynthesis and signaling pathway, predict hydroxyurea treatment efficacy in compound sickle cell disease/β-thalassemia patients. (March 2016)

Authors:
Chalikiopoulou, Constantina; Tavianatou, Anastasia-Gerasimoula; Sgourou, Argyro; Kourakli, Alexandra; Kelepouri, Dimitra; Chrysanthakopoulou, Maria; Kanelaki, Vasiliki-Kaliopi; Mourdoukoutas, Evangelos; Siamoglou, Stavroula; John, Anne; Symeonidis, Argyris; Ali, Bassam R; Katsila, Theodora; Papac...
Journal:
Pharmacogenomics
Issue:
Volume 17:Number 4(2016)
Page Start:
393
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗