Zakia Al‐Lamki

Characterization of <i>PRF1</i>, <i>STX11</i> and <i>UNC13D</i> genotype‐phenotype correlations in familial hemophagocytic lymphohistiocytosis

AnnaCarin Horne, Kim Ramme, Eva Rudd et al. · British Journal of Haematology · 2008 · 91 citations

Genetics, Genetic Epidemiology, Immunology +17

A community-based study of common hereditary blood disorders in Oman.

Asya Al‐Riyami, A. J. M. Suleiman, Mustafa Afifi et al. · PubMed · 2001 · 54 citations

Family Medicine, Glucose-6-phosphate Dehydrogenase Deficiency, Genetic Disorder +15

SPLENIC FUNCTION IN OMANI CHILDREN WITH SICKLE CELL DISEASE: Correlation with Severity Index, Hemoglobin Phenotype, Iron Status, and α -Thalassemia Trait

Yasser Wali, Zakia Al‐Lamki, Samir Hussein et al. · Pediatric Hematology and Oncology · 2002 · 35 citations

Immunohematology, Tin Colloid Scintigraphy, Colloid Uptake +12

Ten-Year Prospective Study (Clinical Spectrum) of Childhood Guillain-Barré Syndrome in the Arabian Peninsula: Comparison of Outcome in Patients in the Pre— and Post—Intravenous Immunoglobulin Eras

Roshan Koul, Alexander Chacko, Riaz Ahmed et al. · Journal of Child Neurology · 2003 · 29 citations

Immunodeficiencies, Intravenous Immunoglobulins, Diagnosis +16

Cardiovascular function in Omani children with sickle cell anaemia

Yasser Wali, P Venugopalan, Evangeline Rivera et al. · Annals of Tropical Paediatrics · 2000 · 23 citations

Anemia, Heart Failure, Cardiovascular Disease +15