Repository of Research and Investigative Information

Repository of Research and Investigative Information

Zabol University of Medical Sciences

Items where Author is "Dorgalaleh, A."

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Number of items: 8.

Article

(2020) Indirect Molecular Diagnosis of Congenital Factor XIII Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms. Iranian Journal of Pediatric Hematology and Oncology. pp. 114-130. ISSN 2008-8892

(2020) Indirect molecular diagnosis of congenital factor ΧIII deficiency by candidate microsatellites and single nucleotide polymorphisms. Iranian Journal of Pediatric Hematology and Oncology. pp. 114-130. ISSN 20088892 (ISSN)

(2019) Correlation of bleeding score with frequency and severity of bleeding symptoms in FXIII deficiency assessing by the ISTH Bleeding Assessment Tool. Transfusion and Apheresis Science. pp. 495-497. ISSN 1473-0502

(2019) A retrospective study on clinical manifestations of neonates with FXIII-A deficiency. Blood Cells Molecules and Diseases. pp. 78-81. ISSN 1079-9796

(2016) Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency. Blood Coagulation & Fibrinolysis. pp. 324-327. ISSN 0957-5235

(2014) Congenital factor V deficiency, comparison the severity of clinical presentations among patients with rare bleeding disorders. Haemophilia. p. 107. ISSN 1351-8216

(2014) Long term two central follow up study on a large group of patients with congenital factor XIII deficiency treated prophylactically with Fibrogammin P (R). Haemophilia. p. 107. ISSN 1351-8216

(2014) Molecular analysis, clinical manifestations and management of factor XIII deficiency in Southeast of Iran. Haemophilia. p. 108. ISSN 1351-8216

This list was generated on Sun May 19 13:56:23 2024 IRDT.