Gender Identity in Patients with Congenital Adrenal Hyperplasia

Por Razzaghy-Azar, Maryam, Karimi, Sakineh, Shirazi, Elham
Publicado no Int J Endocrinol Metab (2017)

Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome

Por Behnam, Babak, Shakiba, Marjan, Ahani, Ali, Razzaghy Azar, Maryam
Publicado em 2013

Identification of a novel nonsense mutation and a missense substitution in the AGPAT2 gene causing congenital generalized lipodystrophy type 1

Por Haghighi, Amirreza, Razzaghy-Azar, Maryam, Talea, Ali, Sadeghian, Mahnaz, Ellard, Sian, Haghighi, Alireza
Publicado em 2012

An Evaluation of Acylated Ghrelin and Obestatin Levels in Childhood Obesity and Their Association with Insulin Resistance, Metabolic Syndrome, and Oxidative Stress

Por Razzaghy-Azar, Maryam, Nourbakhsh, Mitra, Pourmoteabed, Abdolreza, Nourbakhsh, Mona, Ilbeigi, Davod, Khosravi, Mohsen
Publicado no J Clin Med (2016)

Effects of extremely low frequency electromagnetic fields on paraoxonase serum activity and lipid peroxidation metabolites in rat

Por Seifirad, Soroush, Farzampour, Shahrokh, Nourbakhsh, Mitra, Amoli, Mahsa Mohammad, Razzaghy-Azar, Maryam, Larijani, Bagher
Publicado em 2014

Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development

Por Shojaei, Azadeh, Ebrahimzadeh-Vesal, Reza, Ahani, Ali, Razzaghy-Azar, Maryam, khakpour, Golnaz, Ghazi, Farideh, Tavakkoly-Bazzaz, Javad
Publicado no Rep Biochem Mol Biol (2017)

Ethnic Specific Distribution of Mutations in 716 Patients with Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency

Por Wilson, Robert C., Nimkarn, Saroj, Dumic, Miro, Obeid, Jihad, Razzaghy Azar, Maryam, Najmabadi, Hossein, Saffari, Fatemeh, New, Maria I.
Publicado em 2007

Genotype–phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency

Por New, Maria I., Abraham, Moolamannil, Gonzalez, Brian, Dumic, Miroslav, Razzaghy-Azar, Maryam, Chitayat, David, Sun, Li, Zaidi, Mone, Wilson, Robert C., Yuen, Tony
Publicado em 2013

Efficacy and safety of Samtropin™ recombinant human growth hormone; a double-blind randomized clinical trial

Por Tabatabaei-Malazy, Ozra, Mohajeri-Tehrani, Mohammad Reza, Heshmat, Ramin, Taheri, Eghbal, Shafiee, Gita, Razzaghy-Azar, Maryam, Rabbani, Ali, Qorbani, Mostafa, Adibi, Hossein, Shahbazi, Samimeh, Karimi, Farzaneh, Rezaian, Sheema, Larijani, Bagher
Publicado no J Diabetes Metab Disord (2014)

Identification and Treatment of Patients with Homozygous Familial 
Hypercholesterolaemia: Information and Recommendations from a 
Middle East Advisory Panel

Por Al-Ashwal, Abdullah, Alnouri, Fahad, Sabbour, Hani, Al-Mahfouz, Abdulraof, Al-Sayed, Nasreen, Razzaghy-Azar, Maryam, Al-Allaf, Faisal, Al-Waili, Khalid, Banerjee, Yajnavalka, Genest, Jacques, Santos, Raul D., Al-Rasadi, Khalid
Publicado no Curr Vasc Pharmacol (2015)

Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency

Por Yau, Mabel, Haider, Shozeb, Khattab, Ahmed, Ling, Chen, Mathew, Mehr, Zaidi, Samir, Bloch, Madison, Patel, Monica, Ewert, Sinead, Abdullah, Wafa, Toygar, Aysenur, Mudryi, Vitalii, Al Badi, Maryam, Alzubdi, Mouch, Wilson, Robert C., Al Azkawi, Hanan Said, Ozdemir, Hatice Nur, Abu-Amer, Wahid, Hertecant, Jozef, Razzaghy-Azar, Maryam, Funder, John W., Al Senani, Aisha, Sun, Li, Kim, Se-Min, Yuen, Tony, Zaidi, Mone, New, Maria I.
Publicado no Proc Natl Acad Sci U S A (2017)