Suchergebnisse - "Setoodeh, Aria"

PubPharm (72)

1

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

enthalten in: Iranian biomedical journal | 2023

von Jafari, M. | Karami, F. | Setoodeh, A. | +5

2

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

enthalten in: International journal of molecular and cellular medicine | 2023

von Sardarpour, N. | Bagherian, H. | Zafarghandi Motlagh, F. | +7

3

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

enthalten in: Stem cell research & therapy | 2022

von Izadi, M. | Sadr Hashemi Nejad, A. | Moazenchi, M. | +15

4

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

enthalten in: Stem cell research & therapy | 2022

von Izadi, M. | Sadr Hashemi Nejad, A. | Moazenchi, M. | +15

5

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

enthalten in: Stem cell research & therapy | 2022

von Izadi, M. | Sadr Hashemi Nejad, A. | Moazenchi, M. | +15

6

Early and delayed puberty among Iranian children with obesity

enthalten in: Minerva endocrinology | 2022

von Mohsenipour, R. | Abbasi, F. | Setoodeh, A. | +6

7

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

enthalten in: Human mutation | 2022

von Ghaffari, S. | Rafati, M. | Shadnoush, M. | +36

8

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

enthalten in: Orphanet journal of rare diseases | 2022

von Setoodeh, A. | Panjeh-Shahi, S. | Bahmani, F. | +10

9

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

enthalten in: Orphanet journal of rare diseases | 2022

von Setoodeh, A. | Panjeh-Shahi, S. | Bahmani, F. | +10

10

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

enthalten in: Orphanet journal of rare diseases | 2022

von Setoodeh, A. | Panjeh-Shahi, S. | Bahmani, F. | +10

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