about
Coinheritance of Gaucher disease and α-thalassemia resulting in confusion between two inherited hematologic diseasesSingle course of high dose dexamethasone is more effective than conventional prednisolone therapy in the treatment of primary newly diagnosed immune thrombocytopenia.Human Cytomegalovirus in Oral Squamous Cell Carcinoma in Southeast of Iran.Role of Thr399Ile and Asp299Gly polymorphisms of toll-like receptor-4 gene in acute dental abscess.C677T and A1298C polymorphisms of methylene tetrahydrofolate reductase in non-Hodgkin lymphoma: southeast Iran.Duffy blood group genotypes among malaria Plasmodium vivax patients of Baoulch population in Southeastern Iran.Decisions Regarding Pregnancy Termination Due to β-Thalassemia Major: a Mixed-Methods Study in Sistan and Baluchestan, Iran.Apoptosis and reduced cell proliferation of HL-60 cell line caused by human telomerase reverse transcriptase inhibition by siRNA.Downregulation of telomerase activity in human promyelocytic cell line using RNA interference.Sistani population: a different spectrum of β-thalassemia mutations from other ethnic groups of Iran.Health-related Quality of Life and Associated Factors Among Thalassemia Major Patients, Southeast of Iran.Methylenetetrahydrofolate reductase C677T and A1298C gene polymorphisms in oral squamous cell carcinoma in south-east Iran.Molecular Characterization of β-Thalassemia Intermedia in Southeast Iran.Intracranial hemorrhage pattern in the patients with factor XIII deficiency.Hematological phenotype of the IVS-I-5 (G > C) beta-thalassemia mutation and assessment of Iran's national screening criteria.Successful delivery in patients with FXIII deficiency receiving prophylaxis: report of 17 cases in Iran.Prevalence and molecular identification of the mediterranean variant among G6PD-deficient Sistani and Balouch males in Southeastern Iran.A local equation for differential diagnosis of β-thalassemia trait and iron deficiency anemia by logistic regression analysis in Southeast Iran.Profile of β-thalassemia and its prenatal diagnosis in Khorasan-e-Jonobi Province, Iran.Major histocompatibility complex class I and II antigens frequencies in Baloch ethnic group living in the southeast region of IranMolecular analysis of sixteen unrelated factor XIIIA deficient families from south-east of IranMolecular basis and prenatal diagnosis of β-thalassemia among Balouch population in IranTramadol and the occurrence of seizures: a systematic review and meta-analysisIdentification and In Silico Characterization of a Novel Point Mutation within the Phosphatidylinositol Glycan Anchor Biosynthesis Class G Gene in an Iranian Family with Intellectual DisabilityAssociation of Glutathione-S-Transferases M1 and T1 Deletional Variants with Development of Oral Squamous Cell Carcinoma: A Study in the South-East of Iran
P50
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P50
description
hulumtues
@sq
researcher
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wetenschapper
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հետազոտող
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name
Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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type
label
Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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prefLabel
Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
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Ebrahim Miri-Moghaddam
@nl
Ebrahim Miri-Moghaddam
@sl
P106
P1153
55887158900
P21
P31
P496
0000-0001-9435-2450