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A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site.
Hum Genome Var. 2021 Jul 21;8(1):31. doi: 10.1038/s41439-021-00160-y.
Hum Genome Var. 2021.
PMID: 34290232
Free PMC article.
Recurrent Infections and Immunodeficiency Caused by Severe Pancytopenia Associated with a Novel Life-Threatening Mutation in Hypoxia-Upregulated Protein 1.
Jafari Khamirani H, Dianatpour M, Zoghi S, Mohammadi S, Habib A, Dastgheib SA, Tabei SMB, Molayemat M, Shirazi Yeganeh B.
Jafari Khamirani H, et al. Among authors: molayemat m.
Immunol Invest. 2022 Aug;51(6):1883-1894. doi: 10.1080/08820139.2022.2072736. Epub 2022 May 12.
Immunol Invest. 2022.
PMID: 35549617
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Elevated serum TSH concentrations are associated with higher BMI Z-scores in southern Iranian children and adolescents.
Habib A, Molayemat M, Habib A.
Habib A, et al. Among authors: molayemat m.
Thyroid Res. 2020 Jun 13;13:9. doi: 10.1186/s13044-020-00084-9. eCollection 2020.
Thyroid Res. 2020.
PMID: 32547643
Free PMC article.
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Association of lipid profile and BMI Z-score in southern Iranian children and adolescents.
Habib A, Molayemat M, Habib A.
Habib A, et al. Among authors: molayemat m.
J Pediatr Endocrinol Metab. 2019 Aug 27;32(8):827-835. doi: 10.1515/jpem-2019-0002.
J Pediatr Endocrinol Metab. 2019.
PMID: 31219798
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Prevalence and predictive factors of transient and permanent congenital hypothyroidism in Fars province, Iran.
Habib A, Shojazadeh A, Molayemat M, Habib A, Jeddi M, Arabsolghar R, Nahas M, Rahimi N, Ardekani FM.
Habib A, et al. Among authors: molayemat m.
BMC Pediatr. 2021 Jun 5;21(1):264. doi: 10.1186/s12887-021-02729-6.
BMC Pediatr. 2021.
PMID: 34090374
Free PMC article.
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