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Saudi Medical Journal, ISSN 0379-5284, 02/2018, Volume 39, Issue 2, pp. 209 - 212
Herein, we report a case of a 27-year-old man with Ebstein’s anomaly and a history of unexplained recurrent venous thrombosis despite adequate anticoagulation.... 
Venous thrombosis | Recurrent | Blood stasis | Ebstein’s anomaly | Case Report | blood stasis | recurrent | venous thrombosis
Journal Article
npj Genomic Medicine, ISSN 2056-7944, 12/2019, Volume 4, Issue 1, pp. 4 - 7
Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding disorder. Around 490 mutations in and genes were reported. We aimed to use targeted... 
Mutation
Journal Article
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 12/2018, Volume 16, Issue 6, p. 773
Mitochondrial neurogastrointestinal encephalomyopathy syndrome is a rare autosomal recessive multisystem disorder caused by nuclear TYMP gene mutations, which... 
Journal Article
Experimental and Clinical Transplantation, ISSN 1304-0855, 12/2016, Volume 14, Issue 6, pp. 660 - 664
Objectives: Fanconi anemia is a congenital bone marrow failure syndrome that is associated with congenital anomalies and increased risk of cancer.... 
Adult | Bone marrow failure | Anemia | Transplant | LOW-DOSE CYCLOPHOSPHAMIDE | MYELODYSPLASIA | EUROPEAN GROUP | TRANSPLANTATION | EXPERIENCE | UPDATE | MARROW-TRANSPLANTATION | LEUKEMIA | BLOOD | T?p | Index Medicus
Journal Article
SAUDI MEDICAL JOURNAL, ISSN 0379-5284, 02/2018, Volume 39, Issue 2, pp. 209 - 212
Herein, we report a case of a 27-year-old man with Ebstein's anomaly and a history of unexplained recurrent venous thrombosis despite adequate anticoagulation.... 
MEDICINE, GENERAL & INTERNAL | DISEASE | Recurrence | Venous Thrombosis - drug therapy | Humans | Ebstein Anomaly - complications | Adult | Anticoagulants - therapeutic use | Male | Ebstein Anomaly - surgery | Venous Thrombosis - etiology | Venous thrombosis | Research | Ebstein's anomaly | Risk factors | Index Medicus
Journal Article
JOURNAL OF CLINICAL ONCOLOGY, ISSN 0732-183X, 05/2016, Volume 34, Issue 15, pp. e18504 - e18504
Conference Proceeding
Clinical Lymphoma, Myeloma and Leukemia, ISSN 2152-2650, 09/2018, Volume 18, pp. S225 - S225
Journal Article
Biotechnology research international, ISSN 2090-3138, 2016, Volume 2016, pp. 8589270 - 6
Background. We studied DNA chimerism in cell-free DNA (cfDNA) in patients treated with HSCT. Methods. Chimerism analysis was performed on CD3+ cells,... 
Care and treatment | Relapse | Prognosis | Leukemia | Physiological aspects | Transplantation | Genetic aspects | Research | Diagnosis | Risk factors | Hematopoietic stem cells | Diseases
Journal Article
Journal of Applied Hematology, ISSN 1658-5127, 01/2018, Volume 9, Issue 1, pp. 33 - 36
We report an atypical manifestation of Antiphospholipid syndrome (APS) in a 40-year-old male with nonartertic anterior ischemic optic neuropathy (NAION)... 
nonartertic anterior ischemic optic neuropathy | Antiphospholipid syndrome | optic neuritis
Journal Article
Journal of Applied Hematology, ISSN 1658-5127, 01/2014, Volume 5, Issue 4, pp. 168 - 168
Journal Article
Journal of Applied Hematology, ISSN 1658-5127, 01/2018, Volume 9, Issue 4, pp. 111 - 119
BACKGROUND: Histiocytic disease is a diverse disease, characterized by multisystem involvement, diagnosis and management can be challenging. Guidelines are... 
histiocytic disease | Erdheium chester | hemophagocytic lymhohistiocytosis
Journal Article
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, ISSN 1304-0855, 12/2018, Volume 16, Issue 6, pp. 773 - 778
Mitochondrial neurogastrointestinal encephalomyopathy syndrome is a rare autosomal recessive multisystem disorder caused by nuclear TYMP gene mutations, which... 
Failure to thrive | Autosomal recessive disorder | Thymidine phosphorylase | TRANSPLANTATION
Journal Article
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