Items where Author is "Hosseinzadeh, M."

Article

(2022) Adherence to Mediterranean diet and attention-deficit/hyperactivity disorder in children: A case control study. CLINICAL NUTRITION ESPEN. pp. 346-350. ISSN 2405-4577 J9 - CLIN NUTR ESPEN

(2022) Dietary phytochemical index and attention-deficit/hyperactivity disorder in Iranian children: a case control study. Eur J Clin Nutr. pp. 456-461. ISSN 0954-3007

(2022) The association between dairy products and the risk of COVID-19. Eur J Clin Nutr. pp. 1-7. ISSN 0954-3007 (Print) 0954-3007

(2022) A plant-based dietary score and attention deficit/hyperactivity disorder in Iranian children: A case-control study. JOURNAL OF AFFECTIVE DISORDERS. pp. 27-31. ISSN 0165-0327 1573-2517 J9 - J AFFECT DISORDERS

(2021) Dietary phytochemical index and attention-deficit/hyperactivity disorder in Iranian children: a case control study. Eur J Clin Nutr. ISSN 0954-3007

(2021) Dysregulation of RNA interference components in COVID-19 patients. BMC RESEARCH NOTES. ISSN 1756-0500 J9 - BMC RES NOTES

(2021) The effects of high fructose fruits and honey on the serum level of metabolic factors and nonalcoholic fatty liver disease. JOURNAL OF DIABETES AND METABOLIC DISORDERS. pp. 1647-1654. ISSN 2251-6581 J9 - J DIABETES METAB DIS

(2020) Effect of flaxseed oil on glycemic control and inflammatory markers in overweight adults with pre-diabetes: A double-blind randomized controlled clinical trial. Journal of Herbal Medicine. ISSN 2210-8033

(2020) Errors in Meta-Analysis Should Be Corrected: Comment on "Effects of a Paleolithic Diet on Cardiovascular Disease Risk Factors: A Systematic Review and Meta-Analysis of Randomized Controlled Trials" Reply. Advances in Nutrition. pp. 1048-1050. ISSN 2161-8313

(2020) Reply to X Chen et al. Adv Nutr. pp. 1048-1050. ISSN 2161-8313 (Print) 2161-8313

(2020) The commencement of congenital heart diseases registry in Isfahan, Iran: Methodology and design. ARYA Atherosclerosis. pp. 244-247. ISSN 1735-3955

(2019) Effects of a Paleolithic Diet on Cardiovascular Disease Risk Factors: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Adv Nutr. ISSN 2156-5376 (Electronic) 2161-8313 (Linking)

(2019) Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome. Iranian Journal of Child Neurology. pp. 25-34. ISSN 1735-4668

(2019) Psychological disorders and dietary patterns by reduced-rank regression. European Journal of Clinical Nutrition. pp. 408-415. ISSN 0954-3007

(2018) Estimating the Risk for Chromosomal Abnormalities and Heteromorphic Variants in Azoospermic and Severe Oligozoospermic Men. Crescent Journal of Medical and Biological Sciences. pp. 101-106. ISSN 2148-9696

(2018) Population structures of Leishmania infantum and Leishmania tropica the causative agents of kala-azar in Southwest Iran. Parasitology Research. pp. 3447-3458. ISSN 0932-0113

(2018) A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features. Journal of Human Genetics. pp. 487-491. ISSN 1434-5161

(2016) Empirically derived dietary patterns in relation to psychological disorders. Public Health Nutrition. pp. 204-217. ISSN 1368-9800

(2016) Reciprocal 22q11.2 deletion and duplication in siblings with karyotypically normal parents. Cytogenetic and Genome Research. pp. 1-5. ISSN 14248581 (ISSN)

(2015) Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia. BMC research notes. p. 350. ISSN 1756-0500 (Electronic) 1756-0500 (Linking)

(2015) Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication. Genetics Research International. ISSN 2090-3154

(2015) Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran. International Journal of Pediatric Otorhinolaryngology. pp. 1892-1895. ISSN 0165-5876

(2015) Significant association between nonsyndromic cleft lip with or without cleft palate and IRF6rs2235371 polymorphism in Iranian familiar population. Molecular Biology. pp. 848-851. ISSN 0026-8933

(2015) A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family. International Journal of Pediatric Otorhinolaryngology. pp. 553-556. ISSN 0165-5876