Works by Setoodeh, Aria

Results: 31

Long‐Term Outcomes of Hematopoietic Stem Cell Transplantation in Mucopolysaccharidoses Patients Without Radiation.

Published in:

Clinical Transplantation, 2025, v. 39, n. 6, p. 1, doi. 10.1111/ctr.70188

By:

Jahanpanah, Mohammad;
Jafari, Leila;
Behfar, Maryam;
Alipour, Nadia;
Ahad, Farah;
Mohseni, Rashin;
Mohsenipour, Reihaneh;
Setoodeh, Aria;
Heidari, Morteza;
Ashrafi, Mahmoud Reza;
Badv, Reza Shervin;
Mokaram, Mina;
Eshghi, Shirin;
Hamidieh, Amir Ali

Publication type:

Article

Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE‐diagnosis study (IMPRESsion).

Published in:

Human Mutation, 2022, v. 43, n. 4, p. e1, doi. 10.1002/humu.24328

By:

Ghaffari, Saeed R.;
Rafati, Maryam;
Shadnoush, Mahdi;
Pourbabaee, Shokooh;
Aghighi, Mohammad;
Mirab Samiee, Siamak;
Kermanchi, Jamshid;
Alaei, Mohammad R.;
Salehpour, Shadab;
Amirkashani, Davoud;
Setoodeh, Aria;
Sarkhail, Peymaneh;
Badv, Reza Shervin;
Aminzadeh, Majid;
Shiva, Siamak;
Eshraghi, Peyman;
Moravej, Hossein;
Hashemipour, Mahin;
Rostampour, Noushin;
Hamidieh, َAmir Ali

Publication type:

Article

Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome.

Published in:

Diabetologia, 2018, v. 61, n. 5, p. 1027, doi. 10.1007/s00125-018-4554-x

By:

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;
International Neonatal Diabetes Consortium;
Hattersley, Andrew T.;
Ellard, Sian;
De Franco, Elisa

Publication type:

Article

A Rare Case of ACTH‐Secreting Pituitary Adenoma in a Pediatric Patient. Diagnosis and Management: Case Report and Literature Review.

Published in:

2025

By:

Niliyeh, Shadi;
Sayarifard, Fatemeh;
Moradi, Ali;
Setoodeh, Aria;
Ebrahimi, Pouya

Publication type:

Case Study

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

Published in:

Stem Cell Research & Therapy, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s13287-022-02941-w

By:

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

Publication type:

Article

The Effect of Metformin as an Adjunct Therapy in Adolescents with Type 1 Diabetes.

Published in:

Journal of Clinical & Diagnostic Research, 2017, v. 11, n. 4, p. 1, doi. 10.7860/JCDR/2017/24901.9725

By:

SETOODEH, ARIA;
DIDBAN, ABDOLLAH;
RABBANI, ALI;
SAYARIFARD, AZADEH;
ABBASI, FARZANEH;
SAYARIFARD, FATEMEH;
HOSEINZADE, FATEMEH

Publication type:

Article

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

Published in:

Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-021-02170-z

By:

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

Publication type:

Article

Early and delayed puberty among Iranian children with obesity.

Published in:

Minerva Endocrinology, 2022, v. 47, n. 2, p. 167, doi. 10.23736/S2724-6507.20.03168-5

By:

MOHSENIPOUR, Reihaneh;
ABBASI, Farzaneh;
SETOODEH, Aria;
FARD, Fatemeh SAYARI;
ROSTAMI, Parastoo;
MOINFAR, Zeinab;
AMOLI, Mahsa M.;
TAJDINI, Parisa;
RABBANI, Ali

Publication type:

Article

Molecular investigation of mutations in androgen receptor and 5‐alpha‐reductase‐2 genes in 46,XY Disorders of Sex Development with normal testicular development.

Published in:

Andrologia, 2019, v. 51, n. 5, p. N.PAG, doi. 10.1111/and.13250

By:

Ahmadifard, Mohamadreza;
Kajbafzadeh, Abdolmohamad;
Panjeh‐Shahi, Samareh;
Vand‐Rajabpour, Fatemeh;
Ahmadi‐Beni, Reza;
Arshadi, Hamid;
Setoodeh, Aria;
Rostami, Parastoo;
Tavakkoly‐Bazzaz, Javad;
Tabrizi, Mina

Publication type:

Article

A Novel Missense Mutation of c.965C>T (p.Ala322Val) in the Human GALNS Gene Results in Severe Mucopolysaccharidosis Type IVA.

Published in:

Iranian Journal of Pathology, 2025, v. 20, n. 1, p. 138, doi. 10.30699/ijp.2024.2025376.3278

By:

Safavi, Moeinadin;
Setoodeh, Aria;
Ghoddoosi, Mahdiieh

Publication type:

Article

Glycemic Control in Iranian Children with Type 1 Diabetes Mellitus: Effect of Gender.

Published in:

Indian Journal of Pediatrics, 2012, v. 79, n. 7, p. 896, doi. 10.1007/s12098-011-0613-8

By:

Setoodeh, Aria;
Mostafavi, Fereydoun;
Hedayat, Tina

Publication type:

Article

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.

Published in:

Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1159, doi. 10.1007/s10545-018-0228-6

By:

Shirzadeh, Tina;
Saeidian, Amir Hossein;
Bagherian, Hamideh;
Salehpour, Shadab;
Setoodeh, Aria;
Alaei, Mohammad Reza;
Youssefian, Leila;
Samavat, Ashraf;
Touati, Andrew;
Fallah, Mohammad‐Sadegh;
Vahidnezhad, Hassan;
Karimipoor, Morteza;
Azadmehr, Sarah;
Raeisi, Marzieh;
Bandehi Sarhadi, Ameneh;
Zafarghandi Motlagh, Fatemeh;
Jamali, Mojdeh;
Zeinali, Zahra;
Abiri, Maryam;
Zeinali, Sirous

Publication type:

Article

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population.

Published in:

Journal of Inherited Metabolic Disease, 2018, v. 41, n. 6, p. 1159, doi. 10.1007/s10545-018-0228-6

By:

Shirzadeh, Tina;
Saeidian, Amir Hossein;
Bagherian, Hamideh;
Salehpour, Shadab;
Setoodeh, Aria;
Alaei, Mohammad Reza;
Youssefian, Leila;
Samavat, Ashraf;
Touati, Andrew;
Fallah, Mohammad-Sadegh;
Vahidnezhad, Hassan;
Karimipoor, Morteza;
Azadmehr, Sarah;
Raeisi, Marzieh;
Bandehi Sarhadi, Ameneh;
Zafarghandi Motlagh, Fatemeh;
Jamali, Mojdeh;
Zeinali, Zahra;
Abiri, Maryam;
Zeinali, Sirous

Publication type:

Article

Safety and effectiveness of a biosimilar somatropin (Cinnatropin®) in children and adolescents receiving growth hormone therapy over 1 year: a registry-based phase IV study.

Published in:

European Journal of Pediatrics, 2025, v. 184, n. 3, p. 1, doi. 10.1007/s00431-025-06056-1

By:

Rabbani, Ali;
Razzaghy-Azar, Maryam;
Karamizadeh, Zohreh;
Hashemipour, Mahin;
Vakili, Rahim;
Setoodeh, Aria;
Alaei, Mohammadreza;
Ghergherehchi, Robabeh;
Salehpour, Shadab;
Aminzadeh, Majid;
Talea, Ali;
Zaeri, Hossein;
Ghasemi, Mahmoud;
Saki, Forough;
Sabzvari, Araz;
Kafi, Hamidreza

Publication type:

Article

Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486*) causing severe Wolfram syndrome and first report of male fertility.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 3, p. 347, doi. 10.1038/ejhg.2012.154

By:

Haghighi, Amirreza;
Haghighi, Alireza;
Setoodeh, Aria;
Saleh-Gohari, Nasrollah;
Astuti, Dewi;
Barrett, Timothy G

Publication type:

Article

Identification of Novel Mutations in the MMAA and MUT Genes among Methylmalonic Aciduria Families.

Published in:

Iranian Biomedical Journal, 2023, v. 27, n. 6, p. 397, doi. 10.61186/ibj.3782

By:

Jafari, Mahboobeh;
Karami, Fatemeh;
Setoodeh, Aria;
Rahmanifar, Ali;
Bagherian, Hamideh;
Alaei, Mohammad Reza;
Rohani, Farzaneh;
Zeinali, Sirous

Publication type:

Article

The treatment and clinical follow-up outcome in Iranian patients with tetrahydrobiopterin deficiency.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2021, v. 34, n. 9, p. 1157, doi. 10.1515/jpem-2021-0155

By:

Khani, Soghra;
Barzegari, Mina;
Esmaeilizadeh, Zahra;
Farsian, Pantea;
Alaei, Mohammadreza;
Salehpour, Shadab;
Setoodeh, Aria;
Rohani, Farzaneh;
Samavat, Ashraf;
Zekri, Ali;
Mirzazadeh, Roghieh;
Sadeghi, Sedigheh;
Khatami, Shohreh

Publication type:

Article

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: report of three cases from Iran.

Published in:

Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 8, p. 979, doi. 10.1515/jpem-2016-0017

By:

Seifi-Alan, Mahnaz;
Shamsi, Roshanak;
Setoodeh, Aria;
Sayarifard, Fatemeh;
Aghasi, Parisa;
Kompani, Farzad;
Ghafouri-Fard, Soudeh;
Abbasi, Farzaneh

Publication type:

Article

Identification of eleven different mutations including six novel, in the arylsulfatase B gene in Iranian patients with mucopolysaccharidosis type VI.

Published in:

Molecular Biology Reports, 2019, v. 46, n. 3, p. 3417, doi. 10.1007/s11033-019-04804-9

By:

Jafaryazdi, Rokhsareh;
Shams, Sedigheh;
Isaian, Anna;
Setoodeh, Aria;
Teimourian, Shahram

Publication type:

Article

Endocrine and Metabolic Disorders in Children With Cancer Treatment.

Published in:

Zahedan Journal of Research in Medical Sciences, 2016, v. 18, n. 3, p. 1, doi. 10.17795/zjrms-6244

By:

Nakhaei-Moghadam, Maryam;
Setoodeh, Aria;
Noori, Noormohammad;
Rostami, Parastoo;
Teimouri, Alireza

Publication type:

Article

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

Published in:

Cell Journal (Yakhteh), 2016, v. 18, n. 2, p. 229

By:

Talebi, Saeed;
Entezam, Mona;
Mohajer, Neda;
Kazemi-Sefat, Golnaz-Ensieh;
Razipour, Masoumeh;
Ahmadloo, Somayeh;
Setoodeh, Aria;
Keramatipour, Mohammad

Publication type:

Article

Health-related quality of life of parents of children with phenylketonuria in Tehran Province, Islamic Republic of Iran.

Published in:

Eastern Mediterranean Health Journal, 2020, v. 26, n. 3, p. 331, doi. 10.26719/emhj.19.045

By:

Etemad, Koorosh;
Heidari, Alireza;
Setoodeh, Aria;
Shayeganrad, Amir;
Akhlaghi, Atoosa;
Azizi, Maryam;
Nejatbakhsh, Roya;
Beglar, Maryam Beheshti;
Lotfi, Mansoureh

Publication type:

Article

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

Published in:

International Journal of Molecular Sciences, 2017, v. 18, n. 3, p. 635, doi. 10.3390/ijms18030635

By:

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

Publication type:

Article

Assessment of Vitamin D Status and Response to Vitamin D3 in Obese and Non-Obese Iranian Children.

Published in:

2016

By:

Motlaghzadeh, Yasaman;
Sayarifard, Fatemeh;
Allahverdi, Bahar;
Rabbani, Ali;
Setoodeh, Aria;
Sayarifard, Azadeh;
Abbasi, Farzaneh;
Haghi-Ashtiani, Mohammad-Taghi;
Rahimi-Froushani, Abbas

Publication type:

journal article

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

Published in:

Avicenna Journal of Medical Biotechnology, 2017, v. 9, n. 3, p. 146

By:

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

Publication type:

Article

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

Published in:

International Journal of Endocrinology, 2020, p. 1, doi. 10.1155/2020/4329791

By:

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

Publication type:

Article

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

Published in:

International Journal of Endocrinology, 2020, p. 1, doi. 10.1155/2020/4329791

By:

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

Publication type:

Article

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

Published in:

International Journal of Endocrinology, 2020, p. 1, doi. 10.1155/2020/4329791

By:

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

Publication type:

Article

Transient Neonatal Diabetes as a Presentation of Fanconi- Bickel Syndrome.

Published in:

Acta Medica Iranica, 2012, v. 50, n. 12, p. 836

By:

Setoodeh, Aria;
Rabbani, Ali

Publication type:

Article

Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort.

Published in:

Metabolic Brain Disease, 2018, v. 33, n. 5, p. 1689, doi. 10.1007/s11011-018-0277-4

By:

Shafaat, Mehdi;
Alaee, Mohammad Reza;
Rahmanifar, Ali;
Setoodeh, Aria;
Razzaghy-Azar, Maryam;
Bagherian, Hamideh;
Bagheri, Samira Dabbagh;
Zafarghandi Motlagh, Fatemeh;
Hashemi, Mehrdad;
Abiri, Maryam;
Zeinali, Sirous

Publication type:

Article

Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes.

Published in:

Metabolic Brain Disease, 2017, v. 32, n. 5, p. 1685, doi. 10.1007/s11011-017-0048-7

By:

Razipour, Masoumeh;
Alavinejad, Elaheh;
Sajedi, Seyede;
Talebi, Saeed;
Entezam, Mona;
Mohajer, Neda;
Kazemi-sefat, Golnaz-Ensieh;
Gharesouran, Jalal;
Setoodeh, Aria;
Mohaddes Ardebili, Seyyed;
Keramatipour, Mohammad

Publication type:

Article