Female Sex as a Risk Factor for Glycemic Control and Complications in Iranian Patients with Type One Diabetes Mellitus

por Setoodeh, Aria, Mostafavi, Fereydoun, Rabbani, Ali, Hedayat, Tina
Publicado 2011

Tetrahydrobiopterin responsiveness in a series of 53 cases of phenylketonuria and hyperphenylalaninemia in Iran

por Setoodeh, Aria, Yarali, Bahram, Rabbani, Ali, Khatami, Shohreh, Shams, Sedigheh
Publicado 2015

Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia

por Setoodeh, Aria, Haghighi, Amirreza, Saleh-Gohari, Nasrollah, Ellard, Sian, Haghighi, Alireza
Publicado 2013

A Randomized Clinical Trial of Insulin Glargine and Aspart, Compared to NPH and Regular Insulin in Children with Type 1 Diabetes Mellitus

por Rostami, Parastoo, Setoodeh, Aria, Rabbani, Ali, Nakhaei-Moghadam, Maryam, Najmi-Varzaneh, Farnaz, Rezaei, Nima
Publicado 2014

Assessment of Sexual Maturation Among Girls With Special Needs in Tehran, Iran

por Shabani Mirzaee, Hosein, Mosallanejad, Asieh, Rabbani, Ali, Setoodeh, Aria, Abbasi, Farzaneh, Sayarifard, Fatemeh, Memari, Amir Hosein
Publicado 2016

p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche

por Soveizi, Mahdieh, Mahdieh, Nejat, Setoodeh, Aria, Sayarifard, Fatemeh, Abbasi, Farzaneh, Bose, Himangshu S., Rabbani, Bahareh, Rabbani, Ali
Publicado 2020

Identification of a Novel Mutation in the PAH Gene in an Iranian Phenylketonuria Family: A Case Report

por RAZIPOUR, Masoumeh, KOOSHAVAR, Daniz, ALAVINEJAD, Elaheh, SAJEDI, Seyede Zahra, MOHAJER, Neda, SETOODEH, Aria, TALEBI, Saeed, KERAMATIPOUR, Mohammad
Publicado 2017

A Novel Variant in the PAH Gene Causing Phenylketonuria in an Iranian Pedigree

por Alavinejad, Elaheh, Sajedi, Seyede Zahra, Razipour, Masoumeh, Entezam, Mona, Mohajer, Neda, Setoodeh, Aria, Talebi, Saeed, Keramatipour, Mohammad
Publicado 2017

Diagnosing Mucopolysaccharidosis type IV a by the fluorometric assay of N-Acetylgalactosamine-6-sulfate sulfatase activity

por Shams, Sedigheh, Barazandeh Tehrani, Maliheh, Civallero, Gabriel, Minookherad, Koosha, Giugliani, Roberto, Setoodeh, Aria, Haghi Ashtiani, Mohammad Taghi
Publicado 2017

An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria

por Talebi, Saeed, Entezam, Mona, Mohajer, Neda, Kazemi-sefat, Golnaz-Ensieh, Razipour, Masoumeh, Ahmadloo, Somayeh, Setoodeh, Aria, Keramatipour, Mohammad
Publicado 2016

Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher Patients

por Sardarpour, Negar, Bagherian, Hamideh, Zafarghandi Motlagh, Fatemeh, Shirzadeh, Tina, Asnavandi, Sadaf, Younesikhah, Shahrzad, Salehpour, Shadab, Setoodeh, Aria, Alaei, Mohammad Reza, Zeinali, Sirous
Publicado 2023

Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE...

por Setoodeh, Aria, Panjeh-Shahi, Samareh, Bahmani, Fariba, Vand-Rajabpour, Fatemeh, Jalilian, Nazanin, Sayarifard, Fatemeh, Abbasi, Farzaneh, Sayarifard, Azadeh, Rostami, Parastoo, Parvaneh, Nima, Akhavan-Niaki, Haleh, Ahmadifard, Mohamadreza, Tabrizi, Mina
Publicado 2022

Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica

por Kariminejad, Ariana, Afroozan, Fariba, Bozorgmehr, Bita, Ghanadan, Alireza, Akbaroghli, Susan, Khorram Khorshid, Hamid Reza, Mojahedi, Faezeh, Setoodeh, Aria, Loh, Abigail, Tan, Yu Xuan, Escande-Beillard, Nathalie, Malfait, Fransiska, Reversade, Bruno, Gardeitchik, Thatjana, Morava, Eva
Publicado 2017

Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome

por Habeb, Abdelhadi M., Flanagan, Sarah E., Zulali, Mohamed A., Abdullah, Mohamed A., Pomahačová, Renata, Boyadzhiev, Veselin, Colindres, Lesby E., Godoy, Guillermo V., Vasanthi, Thiruvengadam, Al Saif, Ramlah, Setoodeh, Aria, Haghighi, Amirreza, Haghighi, Alireza, Shaalan, Yomna, Hattersley, Andrew T., Ellard, Sian, De Franco, Elisa
Publicado 2018

Mesenchymal stem cell transplantation in newly diagnosed type-1 diabetes patients: a phase I/II randomized placebo-controlled clinical trial

por Izadi, Mahmoud, Sadr Hashemi Nejad, Anavasadat, Moazenchi, Maedeh, Masoumi, Safdar, Rabbani, Ali, Kompani, Farzad, Hedayati Asl, Amir Abbas, Abbasi Kakroodi, Fatemeh, Jaroughi, Neda, Mohseni Meybodi, Mohammad Ali, Setoodeh, Aria, Abbasi, Farzaneh, Hosseini, Seyedeh Esmat, Moeini Nia, Fatemeh, Salman Yazdi, Reza, Navabi, Roghayeh, Hajizadeh-Saffar, Ensiyeh, Baharvand, Hossein
Publicado 2022

Can untreated PKU patients escape from intellectual disability? A systematic review

por van Vliet, Danique, van Wegberg, Annemiek M. J., Ahring, Kirsten, Bik-Multanowski, Miroslaw, Blau, Nenad, Bulut, Fatma D., Casas, Kari, Didycz, Bozena, Djordjevic, Maja, Federico, Antonio, Feillet, François, Gizewska, Maria, Gramer, Gwendolyn, Hertecant, Jozef L., Hollak, Carla E. M., Jørgensen, Jens V., Karall, Daniela, Landau, Yuval, Leuzzi, Vincenzo, Mathisen, Per, Moseley, Kathryn, Mungan, Neslihan Ö., Nardecchia, Francesca, Õunap, Katrin, Powell, Kimberly K., Ramachandran, Radha, Rutsch, Frank, Setoodeh, Aria, Stojiljkovic, Maja, Trefz, Fritz K., Usurelu, Natalia, Wilson, Callum, van Karnebeek, Clara D., Hanley, William B., van Spronsen, Francjan J.
Publicado 2018