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Asadollah Habib
Asadollah Habib
Islamic Azad University, Kazerun Branch
在 doctorhabib.com 的电子邮件经过验证 - 首页
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引用次数
引用次数
年份
Alterations in TSH and thyroid hormones following mobile phone use
S Mortavazi, A Habib, A Ganj-Karami, R Samimi-Doost, A Pour-Abedi, ...
Oman medical journal 24 (4), 274, 2009
1562009
Incidence of phenylketonuria in Southern Iran
A Habib, MH Fallahzadeh, HR Kazeroni, AH Ganjkarimi
Iranian Journal of Medical Sciences 35 (2), 137-139, 2010
662010
Pharmacogenetic variation of SLC47A1 gene and metformin response in type2 diabetes patients
S Mousavi, L Kohan, M Yavarian, A Habib
Molecular biology research communications 6 (2), 91, 2017
282017
Elevated serum TSH concentrations are associated with higher BMI Z-scores in southern Iranian children and adolescents
A Habib, M Molayemat, A Habib
Thyroid research 13, 1-8, 2020
182020
Prevalence and predictive factors of transient and permanent congenital hypothyroidism in Fars province, Iran
A Habib, A Shojazadeh, M Molayemat, A Habib, M Jeddi, R Arabsolghar, ...
BMC pediatrics 21 (1), 264, 2021
142021
Association of G-2548A polymorphism in the promoter of leptin gene with plasma leptin level and risk of type 2 diabetes
L Kohan, M Nasiri, A Habib, A Bolhasani
SSU_Journals 21 (1), 70-77, 2013
132013
Association of lipid profile and BMI Z-score in southern Iranian children and adolescents
A Habib, M Molayemat, A Habib
Journal of Pediatric Endocrinology and Metabolism 32 (8), 827-835, 2019
102019
No association between subclinical hypothyroidism and dyslipidemia in children and adolescents
A Habib, A Habib
BMC pediatrics 20, 1-7, 2020
52020
Vitamin D and Zinc are interlinked but affected by different growth factors in Iranian children and adolescents: Vitamin D and Zinc in Iranian children and adolescents
A Habib, M Molayemat, A Habib, Z Hejrati, Z Kheirandish
Iranian Journal of Pediatrics 32 (6), 2022
42022
Epidemiology of neonatal congenital hypothyroidism during 2011-2017
M Amiri, M NaderiLordejani, H Askarpour, R Yahyapour, D Bastam, ...
Journal of critical reviews 7 (2), 175-179, 2020
32020
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
A Habib, A Shojazadeh, M Molayemat, H Jafari Khamirani, S Zoghi, ...
Human Genome Variation 8 (1), 31, 2021
2021
Association of BMI Z-score and Subclinical Hypothyroidism in Children and Adolescents
A Habib, A Habib
Thyroid 3, 255, 2019
2019
The Effect of Time Passage on False Positive Urinary Nitrite Test
SH Nabavizadeh, M Nabavi, A Habib, SH BARAZANDEH
IRANIAN JOURNAL OF PEDIATRICS 13 (1), 17-21, 2003
2003
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