Found: 28
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A Patient With Coinheritance of Alpha-Globin Gene Triplication and IVSI-5 Mutation of Beta-Globin Gene.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
Prevalence of Diabetes and Impaired Glucose Tolerance Test in Patients with Thalassemia Major.
- Published in:
- Zahedan Journal of Research in Medical Sciences, 2014, v. 16, n. 1, p. 86
- By:
- Publication type:
- Article
Premarital Screening Program for Congenital Factor XIII Deficiency in Iran.
- Published in:
- Clinical Laboratory, 2020, n. 8, p. 1495, doi. 10.7754/Clin.Lab.2020.191133
- By:
- Publication type:
- Article
Congenital Factor V Deficiency: Comparison of the Severity of Clinical Presentations among Patients with Rare Bleeding Disorders.
- Published in:
- Acta Haematologica, 2015, v. 133, n. 2, p. 148, doi. 10.1159/000363598
- By:
- Publication type:
- Article
Cutaneous and mucosal manifestations in patients with beta major thalassemia.
- Published in:
- Dermatology & Cosmetic, 2013, v. 4, n. 1, p. 27
- By:
- Publication type:
- Article
How to Assess Founder Effect in Patients with Congenital Factor XIII Deficiency.
- Published in:
- International Journal of Hematology-Oncology & Stem Cell Research, 2020, v. 14, n. 4, p. 248
- By:
- Publication type:
- Article
Reference interval of antithrombin, protein C, and protein S activities in healthy adults in Iran, the effect of age, sex, oral contraceptive intake, and menopause.
- Published in:
- International Journal of Laboratory Hematology, 2022, v. 44, n. 3, p. 626, doi. 10.1111/ijlh.13804
- By:
- Publication type:
- Article
Do congenital bleeding disorders have a protective effect against COVID‐19? A prospective study.
- Published in:
- International Journal of Laboratory Hematology, 2021, v. 43, n. 3, p. e124, doi. 10.1111/ijlh.13413
- By:
- Publication type:
- Article
Persistent hiccups in a patient with mild congenital factor V deficiency and COVID‐19; clinical and laboratory finding of a rare bleeding disorder.
- Published in:
- 2021
- By:
- Publication type:
- Letter to the Editor
Gastrointestinal bleeding in a newborn infant with congenital factor X deficiency and COVID‐19—A common clinical feature between a rare disorder and a new, common infection.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
Molecular and clinical profile of congenital fibrinogen disorders in Iran, identification of two novel mutations.
- Published in:
- International Journal of Laboratory Hematology, 2020, v. 42, n. 5, p. 619, doi. 10.1111/ijlh.13258
- By:
- Publication type:
- Article
Hemostasis critical values among Iranian clinical laboratories "National Survey of 157 Clinical Laboratories".
- Published in:
- International Journal of Laboratory Hematology, 2019, v. 41, n. 6, p. 778, doi. 10.1111/ijlh.13109
- By:
- Publication type:
- Article
Molecular and clinical profile of type 2 von Willebrand disease in Iran: a thirteen-year experience.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Congenital Combined Bleeding Disorders, a Comprehensive Study of a Large Number of Iranian Patients.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2021, v. 27, p. 1, doi. 10.1177/1076029621996813
- By:
- Publication type:
- Article
Molecular Basis of Congenital Factor XIII Deficiency in Iran.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2018, v. 24, n. 2, p. 210, doi. 10.1177/1076029616680473
- By:
- Publication type:
- Article
Health‐related quality of life in persons with haemophilia in Afghanistan.
- Published in:
- Haemophilia, 2023, v. 29, n. 3, p. 770, doi. 10.1111/hae.14772
- By:
- Publication type:
- Article
Inhibitor development in patients with type 3 Von Willebrand disease, a comprehensive study on 99 Iranian patients.
- Published in:
- Haemophilia, 2021, v. 27, n. 4, p. 520, doi. 10.1111/hae.14266
- By:
- Publication type:
- Article
Miscarriage and recurrent miscarriage in patients with congenital factor V deficiency: a report of six cases in Iran.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Clinical manifestations and management of life-threatening bleeding in the largest group of patients with severe factor XIII deficiency.
- Published in:
- International Journal of Hematology, 2014, v. 100, n. 5, p. 443, doi. 10.1007/s12185-014-1664-1
- By:
- Publication type:
- Article
Rare bleeding disorders: a narrative review of epidemiology, molecular and clinical presentations, diagnosis and treatment.
- Published in:
- Journal of Pediatrics Review, 2014, v. 2, n. 2, p. 31, doi. 10.7508/JPR-V2-N2-31-46
- By:
- Publication type:
- Article
Anemia and Thrombocytopenia in Acute and Chronic Renal Failure.
- Published in:
- International Journal of Hematology-Oncology & Stem Cell Research, 2013, v. 7, n. 4, p. 34
- By:
- Publication type:
- Article
Public Health Problems related to factor V deficiency in southeast of Iran.
- Published in:
- Medical Journal of the Islamic Republic of Iran, 2014, v. 28, p. 1
- By:
- Publication type:
- Article
Childhood acute lymphoblastic leukemia: refusal and abandonment of treatment in the southeast of Iran.
- Published in:
- Turkish Journal of Medical Sciences, 2016, v. 46, n. 3, p. 706, doi. 10.3906/sag-1412-42
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- Publication type:
- Article
Effect of Social Factors on the Highest Global Incidence of Congenital Faxtor XIII Deficiency in Southeast of Iran.
- Published in:
- Archives of Iranian Medicine (AIM), 2015, v. 18, n. 5, p. 331
- By:
- Publication type:
- Article
Comparison of 2 Methods of Clot Solubility Testing in Detection of Factor XIII Deficiency.
- Published in:
- Laboratory Medicine, 2016, v. 47, n. 4, p. 283, doi. 10.1093/labmed/lmw046
- By:
- Publication type:
- Article
Laboratory Diagnosis of Factor XIII Deficiency in Developing Countries: An Iranian Experience.
- Published in:
- Laboratory Medicine, 2016, v. 47, n. 3, p. 220, doi. 10.1093/labmed/lmw021
- By:
- Publication type:
- Article
Genetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian population.
- Published in:
- Thrombosis Journal, 2015, v. 13, p. 1, doi. 10.1186/s12959-015-0064-y
- By:
- Publication type:
- Article
Indirect Molecular Diagnosis of Congenital Factor XIII Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms.
- Published in:
- Iranian Journal of Pediatric Hematology & Oncology, 2020, v. 10, n. 2, p. 114
- By:
- Publication type:
- Article