Determination of Bone Density by DEXA Method Based on Bone Age and its Comparison with Chronological Age in Chronic Patients
Katebi, Leyla, Rabbani, Ali, Sayarifard, Fatemeh, Mehdizadeh, Mehrzad, Sayarifard, Azadeh, Sotoudeh, Arya, Abbasi, Farzaneh, Rostami, Parastoo
Published in Mediterranean journal of rheumatology (01.03.2023)
Published in Mediterranean journal of rheumatology (01.03.2023)
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Journal Article
The Role of Thyroid Function Tests in Diagnosing Allan-herndon-dudley Syndrome Revisited: A Novel Iran-based Mutation
Noorian, Shahab, Hamzehlou, Sepideh, Rabbani, Ali, Sotoudeh, Arya, Pour Rostami, Kioumars, Savad, Shahram
Published in Basic and clinical neuroscience (01.07.2021)
Published in Basic and clinical neuroscience (01.07.2021)
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Journal Article
Pericentric Inversion of Chromosome 9 in an Infant With Ambiguous Genitalia
Sotoudeh, Arya, Rostami, Parastoo, Nakhaeimoghadam, Maryam, Mohsenipour, Reihaneh, Rezaei, Nima
Published in Acta medica Iranica (01.10.2017)
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Published in Acta medica Iranica (01.10.2017)
Journal Article
Altered Suppressor Function of Regulatory T Cells in Type 1 Diabetes
Aghili, Babak, Amirzargar, Ali Akbar, Rajab, Asadollah, Rabbani, Ali, Sotoudeh, Arya, Assadiasl, Sara, Larijani, Bagher, Massoud, Ahmad
Published in Iranian journal of immunology (01.12.2015)
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Published in Iranian journal of immunology (01.12.2015)
Journal Article
Insulin edema in a child with diabetes mellitus type 1
Rostami, Parastoo, Sotoudeh, Arya, Nakhaeimoghadam, Maryam, Rabbani, Ali, Rezaei, Nima
Published in Turkish journal of pediatrics (01.05.2012)
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Published in Turkish journal of pediatrics (01.05.2012)
Journal Article
AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndrome
Rostami, Parastoo, Nakhaeimoghadam, Maryam, Bijani, Faezeh-Moghimpour, Sotoudeh, Arya, Rabbani, Ali, Hilbert, Pascale, Rezaei, Nima
Published in Annales d'endocrinologie (01.02.2013)
Published in Annales d'endocrinologie (01.02.2013)
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Journal Article
Pubertal Development in a Random Sample of 4,020 Urban Iranian Girls
Rabbani, A., Khodai, S., Mohammad, K., Sotoudeh, A., Karbakhsh, M., Nouri, K., Salavati, A., Parvaneh, N.
Published in Journal of Pediatric Endocrinology and Metabolism (01.07.2008)
Published in Journal of Pediatric Endocrinology and Metabolism (01.07.2008)
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Journal Article
A novel missense mutation of the HGD gene causes Alkaptonuria
Noorian, Shahab, Dehghan Banadaki, Bahareh, Sotoudeh, Arya, Savad, Shahram, Modarressi, Mohammad Hossein
Published in Meta Gene (01.12.2018)
Published in Meta Gene (01.12.2018)
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Journal Article
The Role of Thyroid Function Tests in Diagnosing Allan-herndon-dudley Syndrome Revisited: A Novel Iran-based Mutation
Noorian, Shahab, Hamzehlou, Sepideh, Rabbani, Ali, Sotoudeh, Arya, Pour Rostami, Kioumars, Savad, Shahram
Published in Basic and clinical neuroscience (01.07.2021)
Published in Basic and clinical neuroscience (01.07.2021)
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