Education History
| Undergraduate |
University of Damascus, College of Science |
BS |
|---|---|---|
| Professional Medical |
Damascus University |
MD |
| Internship |
Jordan Royal Medical Services |
Intern |
| Residency |
Jordan Royal Medical Services |
Resident |
| Residency |
William Beaumont Hospital Medical Center |
Resident |
| Fellowship |
William Beaumont Hospital Medical Center |
Fellow |
| Clerkship |
Fred Hutchinson Cancer Research Center |
Clinical Clerkship |
Selected Publications
Journal Article
- Yaish HM, Christensen RD, Agarwal (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. Journal of perinatology, 33(5), 404-6.
- Christensen RD, Yaish HM, Johnson CB, Bianchi P, Zanella (2011). Six children with pyruvate kinase deficiency from one small town: molecular characterization of the PK-LR gene. The Journal of pediatrics, 159(4), 695-7.
- Grace RF, Rose C, Layton DM, Galactéros 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 (2019). Safety and Efficacy of Mitapivat in Pyruvate Kinase Deficiency. The New England journal of medicine, 381(10), 933-944.
- Bahr TM, Christensen RD, Ward DM, Meng F, Jackson LK, Doyle K, Christensen DR, Harvey AG, Yaish H (2019). Ferritin in serum and urine: A pilot study. Blood cells, molecules & diseases, 76, 59-62.
- Christensen RD, Agarwal AM, George TI, Bhutani VK, Yaish H (2018). Acute neonatal bilirubin encephalopathy in the State of Utah 2009-2018. Blood cells, molecules & diseases, 72, 10-13.
- Yaish H, Matsushita T, Belhani M, Jiménez-Yuste V, Kavakli K, Korsholm L, Matytsina I, Philipp C, Reichwald K, Wu (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,
Case Report
- Christensen RD, Yaish H (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. Journal of perinatology, 32(3), 238-40.
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, Pospí¿ilová 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 R (2019). Prevalence and management of iron overload in pyruvate kinase deficiency: report from the Pyruvate Kinase Deficiency Natural History Study. Haematologica, 104(2), e51-e53.
Abstract
- Yaish H, Rodgers (2010). Alloantibodies in type 3 VWD: report of two cases and review of the literature. Haemophilia, 16(Suppl 4), 156.