KCH Search
  • Contact KCH
العربية
Our Doctors
Dr. Ibrahim Al Harbi
Book Appointment

Dr. Ibrahim Al Harbi

Consultant Pediatric Hematology Oncology

Paediatric, Oncology | 18 years of experience | Speaks English, Arabic

Areas of Expertise:

  • Bleeding disorders
  • Coagulations Defects
  • Febrile Neutropenia
    • +more
  • Education & Training
  • Books & Publications
  • Professional Affiliations
  • Areas of Expertise

Education & Training

  • MD Ottawa University 2004
  • Canadian Fellowship in Pediatrics 2008
  • Canadian Fellowship in Pediatric Hematology and Oncology – 2011

Books & Publications

  1. Ibrahim Al_Harbi, Yvonne Yau, Upton Allen, Tal Schechter, Wendy Lau, Astrid Petrich, Adam Gasses, Elizabeth McDougall and John J Doyle “Herpesvirus Viremia and Engraftment Status of Umbilical Cord Blood in Children Undergoing Allogeneic Hematopoietic Stem Cell Transplant”, Blood 2011 118:3021; http://www.bloodjournal.org/content/118/21/3021?sso-checked=true
  2. Ibrahim Al-Harbi , Abdulaziz Saleh Althobaiti , Enas Hasan Alahmadi, Saudi boy with Factor XII Deficiency, International Journal of Healthcare Sciences ISSN 2348-5728
  3. I Alharbi, A Algethami, and T Almteri, “Management of Congenital Afibrinogenemia: Report of Two Cases” Clin Med Rev Case Rep 2017, 4:196
  4. Ibrahim Al-Harbi1, Enas Hasan Alahmadi, Abdulaziz Saleh Althobaiti and Ranad Jafar Medhir “A Prekallikrein Deficiency Case Report”; A Saudi boy with Prekallikrein Deficiency, Pediatrics 2.4(2016): 201-204.
  5. Ibrahim Alharbi, Mariyyah A. Algethami, Norah A. Almalki, Glanzmann’s thrombasthenia due to a novel mutation in ITGA2B gene, International Journal of Medicine in Developing Countries, , 2019;3(12):1128–1130
  6. Imtinan K. Alsahafi, Ibrahim Al-Harbi, Shahad M. Aldor, Bilqis Albarakati Ghaida Alahmadi, A point mutation in Phe71Ser in glycoprotein IX as agentic cause of Bernard–Soulier syndrome: case report, Clinical Case Reports 2018; 6(4): 686–689
  7. Ghaida Bakoar Alahmadi, Ibrahim Alharbi , Imtinan kh.Alsahafi , Bilqis Ahmed Albarakati and Shahad M Aldor, Rare case of Fanconi anemia associated with polydactly , Clinical Case Reports and Reviews , ISSN: 2059-0393, Clin Case Rep Rev, November 28, 2017
  8. Ibrahim Alharbi, Wijdan Al Zamzami, Elham Alharbi, A Rare Case of Saudi Girl with Recurrent Strokes and Abnormal Multiple Thrombophilia, Blood Disorders & Transfusion, Volume 9 • Issue 3 • 1000404, s 2018, 9:3
  9. Ibrahim al-harbi, Khawlah Nafadi, Abdullah Banani, A Case of Schimke Immunoosseous Dysplasia, Hemophilia C and Hyperlipoproteinemia (a), Medical Case Reports, Vol.4 No.4:80, 2018

Professional Affiliations

  • American Society of Hematology
  • American Society of Pediatric Hematology
  • Bleeding disorders
  • Coagulations Defects
  • Febrile Neutropenia
  • Hemophilia
  • Iton Deficiency Anemia
  • Leukemia
  • Lymphoma
  • Mediastinal Mass
  • Pediatric Hematology
  • Pediatric Oncology
  • Sickle Cell Disease
  • Solid tumors
  • Spinal Cord Compression Due To Malignancy
  • Thalassemia
  • Tumor lysis Syndrome

Slot Unavailable!

The requested doctor’s slot is not available for appointment. Please try again later.

Menu

Enquire Now