Search the collection

32 results for Setoodeh,+Aria

Sort by:

Sort by

Limit results to:

20 per page

32 results for Setoodeh,+Aria

Export to excel

Export record to excel

File type to download

Beta version

Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 1
ArticlesPeer ReviewedFull Text
Mesenchymal stem cell transplantation in newly diagnosed type-1 diabetes patients: a phase I/II randomized placebo-controlled clinical trial
Author / Creator: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
Publisher:London: BioMed Central Ltd
Journal title:Stem cell research & therapy, 2022-06, Vol.13 (1), p.1-264, Article 264
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 2
ArticlesPeer ReviewedFull Text
A Rare Case of ACTH‐Secreting Pituitary Adenoma in a Pediatric Patient. Diagnosis and Management: Case Report and Literature Review
Author / Creator:Niliyeh, Shadi ; Sayarifard, Fatemeh ; Moradi, Ali ; Setoodeh, Aria ; Ebrahimi, Pouya
Publisher:England: John Wiley & Sons, Inc
Journal title:Clinical case reports, 2025-04, Vol.13 (4), p.e70385-n/a
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 3
ArticlesPeer ReviewedFull Text
Can untreated PKU patients escape from intellectual disability? A systematic review
Author / Creator: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.
Publisher:England: BioMed Central
Journal title:Orphanet journal of rare diseases, 2018-08, Vol.13 (1), p.149-149, Article 149
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 4
ArticlesPeer ReviewedFull Text
Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic var...
Author / Creator: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
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2022-01, Vol.17 (1), p.10-10, Article 10
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 5
ArticlesPeer ReviewedFull Text
p.Gln318X and p.Val281Leu as the Major Variants of CYP21A2 Gene in Children with Idiopathic Premature Pubarche
Author / Creator:Rabbani, Ali ; Bose, Himangshu S. ; Abbasi, Farzaneh ; Sayarifard, Fatemeh ; Setoodeh, Aria ; Mahdieh, Nejat ; Soveizi, Mahdieh ; Rabbani, Bahareh
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:International journal of endocrinology, 2020, Vol.2020 (2020), p.1-9
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 6
ArticlesPeer ReviewedFull Text
A Randomized Clinical Trial of Insulin Glargine and Aspart, Compared to NPH and Regular Insulin in Children with Type 1 Diabetes Mellitus
Author / Creator:Rostami, Md, Parastoo ; Setoodeh, Md, Aria ; Rabbani, Md, Ali ; Nakhaei-Moghadam, Md, Maryam ; Najmi-Varzaneh, Md, Farnaz ; Rezaei, Md PhD, Nima
Publisher:Iran: Tehran University of Medical Sciences
Journal title:Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2014-04, Vol.24 (2), p.173-178
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 7
ArticlesPeer ReviewedFull Text
Identification of eleven different mutations including six novel, in the arylsulfatase B gene in Iranian patients with mucopolysaccharidosis type VI
Author / Creator:Jafaryazdi, Rokhsareh ; Shams, Sedigheh ; Isaian, Anna ; Setoodeh, Aria ; Teimourian, Shahram
Publisher:Dordrecht: Springer Netherlands
Journal title:Molecular biology reports, 2019-06, Vol.46 (3), p.3417-3426
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 8
ArticlesPeer ReviewedFull Text
Identification of Novel Mutations in the MMAA and MUT Genes among Methylmalonic Aciduria Families
Author / Creator:Jafari, Mahboobeh ; Karami, Fatemeh ; Setoodeh, Aria ; Rahmanifar, Ali ; Bagherian, Hamideh ; Alaei, Mohammad Reza ; Rohani, Farzaneh ; Zeinali, Sirous
Publisher:Iran: Pasteur Institute of Iran
Journal title:Iranian biomedical journal, 2023-11, Vol.27 (6), p.397-403
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 9
ArticlesPeer ReviewedFull Text
Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome
Author / Creator: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
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Diabetologia, 2018-05, Vol.61 (5), p.1027-1036
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 10
ArticlesPeer ReviewedFull Text
Health-related quality of life of parents of children with phenylketonuria in Tehran Province, Islamic Republic of Iran
Author / Creator:Etemad, Koorosh ; Heidari, Alireza ; Setoodeh, Aria ; Shayeganrad, Amir ; Akhlaghi, Atoosa ; Azizi, Maryam ; Nejatbakhsh, Roya ; Beheshti Beglar, Maryam ; Lotfi, Mansoureh
Publisher:Alexandria: World Health Organization
Journal title:Eastern Mediterranean health journal, 2020-03, Vol.26 (3), p.331-339
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 11
ArticlesPeer ReviewedFull Text
Transient neonatal diabetes as a presentation of Fanconi- Bickel Syndrome
Author / Creator:Setoodeh, Aria ; Rabbani, Ali
Publisher:Iran: Tehran University of Medical Sciences
Journal title:Acta medica Iranica, 2012, Vol.50 (12), p.836-838
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 12
ArticlesPeer ReviewedFull Text
Growth Failure in a Series of Iranian Patients with Juvenile Idiopathic Arthritis
Author / Creator:Aghamahdi, Fatemeh ; Setoodeh, Aria ; Ziaee, Vahid ; Rabbani, Ali
Publisher:Tehran: Tehran University of Medical Sciences
Journal title:Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2018-06, Vol.28 (3)
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 13
ArticlesPeer ReviewedFull Text
Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica
Author / Creator:Kariminejad, Ariana ; Afroozan, Fariba ; Bozorgmehr, Bita ; Ghanadan, Alireza ; Akbaroghli, Susan ; Khorram Khorshid, Hamid ; Mojahedi, Faezeh ; Setoodeh, Aria ; Loh, Abigail ; Tan, Yu ; Escande-Beillard, Nathalie ; Malfait, Fransiska ; Reversade, Bruno ; Gardeitchik, Thatjana ; Morava, Eva
Publisher:Switzerland: MDPI
Journal title:International journal of molecular sciences, 2017-03, Vol.18 (3), p.635-635
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 14
ArticlesPeer ReviewedFull Text
Transient Neonatal Diabetes as a Presentation of Fanconi- Bickel Syndrome Transient Neonatal Diabetes as a Presentation of Fanconi- Bickel Syndrome
Author / Creator:Aria Setoodeh ; Ali Rabbani
Publisher:Tehran University of Medical Sciences
Journal title:Acta medica Iranica, 2012-12, Vol.50 (12), p.836-838
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 15
ArticlesPeer ReviewedFull Text
Transient Neonatal Diabetes as a Presentation of Fanconi- Bickel Syndrome Transient Neonatal Diabetes as a Presentation of Fanconi- Bickel Syndrome
Author / Creator:Aria Setoodeh ; Ali Rabbani
Publisher:Tehran University of Medical Sciences
Journal title:Acta medica Iranica, 2012-12, Vol.50 (12)
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 16
ArticlesPeer ReviewedFull Text
Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population
Author / Creator: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
Publisher:Dordrecht: Springer Netherlands
Journal title:Journal of inherited metabolic disease, 2018-11, Vol.41 (6), p.1159-1167
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 17
ArticlesPeer ReviewedFull Text
Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort
Author / Creator: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
Publisher:New York: Springer US
Journal title:Metabolic brain disease, 2018-10, Vol.33 (5), p.1689-1697
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 18
ArticlesPeer ReviewedFull Text
Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes
Author / Creator:Razipour, Masoumeh ; Alavinejad, Elaheh ; Sajedi, Seyede Zahra ; Talebi, Saeed ; Entezam, Mona ; Mohajer, Neda ; Kazemi-sefat, Golnaz-Ensieh ; Gharesouran, Jalal ; Setoodeh, Aria ; Mohaddes Ardebili, Seyyed Mojtaba ; Keramatipour, Mohammad
Publisher:New York: Springer US
Journal title:Metabolic brain disease, 2017-10, Vol.32 (5), p.1685-1691
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 19
ArticlesPeer ReviewedFull Text
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy: report of three cases from Iran
Author / Creator:Seifi-Alan, Mahnaz ; Shamsi, Roshanak ; Setoodeh, Aria ; Sayarifard, Fatemeh ; Aghasi, Parisa ; Kompani, Farzad ; Ghafouri-Fard, Soudeh ; Abbasi, Farzaneh
Publisher:Germany: De Gruyter
Journal title:Journal of Pediatric Endocrinology & Metabolism, 2016-08, Vol.29 (8), p.979-983
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.
Export this record
Export to excel
Print
Export record to excel
File type to download
Beta version
Select record 20
ArticlesPeer ReviewedFull Text
Inborn Errors of Metabolism-Clinical Findings and Laboratory Tests at the Children’s Medical Center, Tehran, Iran
Author / Creator:Abbasi, Farzaneh ; Setoodeh, Aria ; Sayarifard, Fatemeh ; Rostami, Parastoo ; Rabbani, Ali
Journal title:Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2016-12, Vol.In Press (In Press)
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.

Showing 1 to 20 of 32 results

Export record to excel

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome

Export this record

Export record to excel

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

Export this record

Export record to excel

Transient neonatal diabetes as a presentation of Fanconi- Bickel Syndrome

Export this record

Export record to excel

Growth Failure in a Series of Iranian Patients with Juvenile Idiopathic Arthritis

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

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

Export this record

Export record to excel

Inborn Errors of Metabolism-Clinical Findings and Laboratory Tests at the Children’s Medical Center, Tehran, Iran

Refine your search