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Possible association of 3′ UTR+ 357 A> G, IVS11-nt 93 T> C, c. 1311 C> T polymorphism with G6PD deficiency

Sirdah, Mahmoud; Shubair, Mohammad E.; Al-Kahlout, Mustafa S; Al-Tayeb, Jamal M; Prchal, Josef T; Reading, N Scott (Taylor & Francis, 2017)

Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked inherited enzymopathic disorder affecting more than 500 million people worldwide. It has so far been linked to 217 distinct genetic ...

Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community

Reading, N Scott; Sirdah, Mahmoud; Shubair, Mohammad E.; Nelson, Benjamin E; Al-Kahlout, Mustafa S; Al-Tayeb, Jamal M; Aboud, Lina; Abu Shaban, Maysaa; Luzzatto, Lucio; Prchal, Josef T (Academic Press, 2016)

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common genetic abnormality known to predispose to acute hemolytic anemia (AHA), which can be triggered by certain drugs or infection. However, the commonest trigger ...

Clinical Significance of G6PD Variants among Palestinians

Reading, N Scott; Sirdah, Mahmoud; Shubair, Mohammad E.; Nelson, Benjamin E; Al-Kahlout, Mustafa S; Al-Tayeb, Jamal M; Aboud, Lina; Abu Shaban, Maysaa; Luzzatto, Lucio; Prchal, Josef T (ELSEVIER SCIENCE INC, 2016)

Conclusion: We conclude that children with G6PD A-deficiency are also susceptible to AHA, but demonstrate in direct comparison within this same population that G6PD Mediterranean and G6PD Cairo are more severe forms of ...

Parathyroid Hormone, Calcium and Phosphorus Levels in Hemodialysis Patients at Al-Shifa Hospital, Gaza-Palestine

Shubair, Mohammad E.; Abo Shamala, Hosam; Sirdah, Mahmoud (الجامعة الإسلامية - غزة, 2014)

Secondary hyperparathyroidism is one of the common complications among patients suffering from chronic kidney disease (CKD). This condition is accompanied by hypocalcaemia, hyperphosphatemia, and many other consequences.The ...

Assessment of liver and kidney functions in patients receiving antipsychotic and antiepileptic drugs in Gaza strip

Shubair, Mohammad E.; EL Massri, Raisa; Sirdah, Mahmoud (الجامعة الإسلامية - غزة, 2013)

Background: many drugs affect liver and kidney functions, among these, drugs used to treat psychotic patients such as chlorpromazine (CPZ) which is used to treat schizophrenia and Trihexyphenidyl- hydrochloride ( T.H.P) ...

Blood Levels of Protein C Among Intensive Care Unit(ICU )Patients in Gaza

Shubair, Mohammad E.; Nabulsyia, F; Sirdah, Mahmoud (O Sarsour, F Nabulsyia, M Sirdah, ME Shubair, 2013)

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians

Sirdah, Mahmoud; Vankayalapati, Hariprasad; Perkins, Sherrie L; Shubair, Mohammad E.; Aboud, Lina; Roper, David; Prchal, Josef T (Academic Press, 2012)

Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency, affecting more than 500 million people worldwide, is one of the most common of inherited disorders. There are 186 G6PD mutations published, with mutational ...

G6PD Deficient Variants Differ in Risk of Hospitalization Among Gaza Strip Palestinian Children

Reading, Noel S; Sirdah, Mahmoud; Perkins, Sherrie L; Wilson, Andrew R; Shubair, Mohammad E.; Aboud, Lina; Prchal, Josef T (American Society of Hematology, 2012)

Glucose-6-phosphate dehydrogenase (G6PD) deficiency, affecting more than 500 million people worldwide, is one of the most common inherited disorders. There are 186 G6PD mutations published, with some that cluster within ...

Hemolysis and Mediterranean G6PD mutation (c. 563 C> T) and c. 1311 C> T polymorphism among Palestinians at Gaza Strip

Sirdah, Mahmoud; Perkins, Sherrie L; Shubair, Mohammad E.; Aboud, Lina; Prchal, Josef T (Academic Press, 2012)

Background The G6PD c.563 C > T deficient mutation is endemic among Mediterranean populations but its clinical significance is not well delineated. We set up to estimate the proportion of G6PD deficient children presenting ...

G6PD Deficiency in Palestinian children increases risk of hospitalization which differs according to G6PD variant

Reading, N Scott; Reading, Noel S; Sirdah, Mahmoud; Perkins, Sherrie L; Wilson, Andrew R; Shubair, Mohammad E.; Aboud, Lina; Prchal, Josef T

Glucose-6-phosphate dehydrogenase (G6PD) deficiency, affecting more than 500 million people worldwide, is one of the most common inherited red blood cell disorders. There are 186 G6PD mutations published, with some that ...