Repository of Research and Investigative Information

Repository of Research and Investigative Information

Shahid Sadoughi University of Medical Sciences

Items where Author is "Hadadzadeh, M."

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Number of items: 15.

Article

(2023) Novel missense mutation in<i> NKX2.6</i> gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease. Gene Reports. p. 10.

(2022) Mitochondrial Mutations in Protein Coding Genes of Respiratory Chain Including Complexes Iv, V, And Mt-Trna Genes Are Associated Risk Factors for Congenital Heart Disease. EXCLI Journal. pp. 1306-1330.

(2022) Novel Point Mutations in 3'-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Current Medical Science. pp. 129-143.

(2022) Novel Point Mutations in 3�-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Current Medical Science. pp. 129-143.

(2022) Novel Point Mutations in 3′-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Current Medical Science. pp. 129-143. ISSN 20965230 (ISSN)

(2020) Novel Point Mutations in Mitochondrial <i>MT-CO2</i> Gene May Be Risk Factors for Coronary Artery Disease. Applied Biochemistry and Biotechnology. pp. 1326-1339. ISSN 0273-2289

(2020) Novel Point Mutations of <i>CITED2</i> Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients. Applied Biochemistry and Biotechnology. pp. 896-906. ISSN 0273-2289

(2020) Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis. Journal of cardiovascular and thoracic research. pp. 214-221. ISSN 2008-5117

(2019) Comparison of Short-Term Results between Patients Undergoing Coronary Artery Bypass Graft with a Stent-Placement History and Patients Undergoing Primary Coronary Artery Surgery. The journal of Tehran Heart Center. pp. 53-58. ISSN 1735-5370 (Print) 2008-2371 (Electronic) 1735-5370 (Linking)

(2019) Development of One-Step Tetra-primer ARMS-PCR for Simultaneous Detection of the Angiotensin Converting Enzyme (ACE) I/D and rs4343 Gene Polymorphisms and the Correlation with CAD Patients. Avicenna Journal of Medical Biotechnology. pp. 118-123. ISSN 2008-2835 (Print) 2008-4625 (Electronic) 2008-2835 (Linking)

(2018) Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome. Cardiology Journal. pp. 113-119. ISSN 1897-5593

(2017) Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR. Iranian Journal of Public Health. pp. 811-819. ISSN 2251-6085

(2016) Polymorphisms in NOS3, MTHFR, APOB and TNF-alpha Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients. Research in cardiovascular medicine. e29134. ISSN 2251-9572 (Print) 2251-9580 (Electronic) 2251-9572 (Linking)

(2011) Perioperative predictors and clinical outcome in early and late ICU discharge after off-pump coronary artery bypass surgery. Acta Medica Iranica. pp. 307-309. ISSN 17359694 (ISSN)

(2010) Risk factors of blood transfusion in patients undergoing off-pump coronary artery bypass. Tehran University Medical Journal. pp. 522-526. ISSN 16831764 (ISSN)

This list was generated on Wed Feb 5 13:16:57 2025 +0330.