Education History
Clerkship |
Fred Hutchinson Cancer Research Center |
Clinical Clerkship |
---|---|---|
William Beaumont Hospital Medical Center |
Fellow | |
Residency |
William Beaumont Hospital Medical Center |
Resident |
Jordan Royal Medical Services |
Resident | |
Internship |
Jordan Royal Medical Services |
Intern |
Damascus University |
MD | |
Undergraduate |
University of Damascus, College of Science |
BS |
Selected Publications
Journal Article
- Yaish H, Matsushita T, Belhani M, Jimnez-Yuste V, Kavakli K, Korsholm L, Matytsina I, Philipp C, Reichwald K, Wu R (2019). Safety and efficacy of turoctocog alfa in the prevention and treatment of bleeds in previously untreated paediatric patients with severe haemophilia A: Results from the guardian 4 multinational clinical trial. Haemophilia. (Read full article)
- Grace RF, Rose C, Layton DM, Galactros F, Barcellini W, Morton DH, van Beers EJ, Yaish H, Ravindranath Y, Kuo KHM, Sheth S, Kwiatkowski JL, Barbier AJ, Bodie S, Silver B, Hua L, Kung C, Hawkins P, Jouvin MH, Bowden C, Glader B (2019). Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency. N Engl J Med, 381(10), 933-944. (Read full article)
- Bahr TM, Christensen RD, Ward DM, Meng F, Jackson LK, Doyle K, Christensen DR, Harvey AG, Yaish HM (2019). Ferritin in serum and urine: A pilot study. Blood Cells Mol Dis, 76, 59-62. (Read full article)
- Christensen RD, Agarwal AM, George TI, Bhutani VK, Yaish HM (2018). Acute neonatal bilirubin encephalopathy in the State of Utah 2009-2018. Blood Cells Mol Dis, 72, 10-13. (Read full article)
- Yaish HM, Christensen RD, Agarwal A (2013). A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency. J Perinatol, 33(5), 404-6. (Read full article)
- Christensen RD, Yaish HM, Johnson CB, Bianchi P, Zanella A (2011). Six children with pyruvate kinase deficiency from one small town: molecular characterization of the PK-LR gene. J Pediatr, 159(4), 695-7. (Read full article)
Case Report
- Christensen RD, Yaish HM (2012). A neonate with the Pelger-Huet anomaly, cleft lip and palate, and agenesis of the corpus callosum, with a chromosomal microdeletion involving 1q41 to 1q42.12. J Perinatol, 32(3), 238-40. (Read full article)
Letter
- van Beers EJ, van Straaten S, Morton DH, Barcellini W, Eber SW, Glader B, Yaish HM, Chonat S, Kwiatkowski JL, Rothman JA, Sharma M, Neufeld EJ, Sheth S, Despotovic JM, Kollmar N, Pospilov D, Knoll CM, Kuo K, Pastore YD, Thompson AA, Newburger PE, Ravindranath Y, Wang WC, Wlodarski MW, Wang H, Holzhauer S, Breakey VR, Verhovsek M, Kunz J, McNaull MA, Rose MJ, Bradeen HA, Addonizio K, Li A, Al-Sayegh H, London WB, Grace RF (2018). Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study. [Letter to the editor]. Haematologica, 104(2), e51-e53. (Read full article)
Abstract
- Yaish H, Rodgers G (2010). Alloantibodies in type 3 VWD: report of two cases and review of the literature [Abstract]. Haemophilia, 16(Suppl 4), 156.