I agree that this site is using cookies. You can find further informations here.
X
Eshraghi, Peyman
56  results:
Search for persons X
?
1

Identified PAH V230A and PAH V230I mutations in a family wi..:

Khaghani, Faeze ; Eshraghi, Peyman ; Hamzehloei, Tayebeh
Clinical Case Reports.  12 (2024)  3 - p. , 2024
Link: https://doi.org/10.1002/..
 
?
2

Care Needs of Children with Inborn Errors of Metabolism and..:

Shirdelzade, Sara ; Ramezani, Monir ; Eshraghi, Peyman.
Jundishapur Journal of Chronic Disease Care.  13 (2024)  3 - p. , 2024
Link: https://doi.org/10.5812/..
 
?
3

Mothers' lived experience of caring for children with inbor..:

Shirdelzade, Sara ; Ramezani, Monir ; Eshraghi, Peyman.
BMC Pediatrics.  23 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
?
4

Correction: Mothers' lived experience of caring for childre..:

Shirdelzade, Sara ; Ramezani, Monir ; Eshraghi, Peyman.
BMC Pediatrics.  23 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
?
5

Genetic evaluation of hyperphenylalaninemia patients with t..:

Sadat Fatemi, Seyedeh Helia ; Eshraghi, Peyman ; Ghanei, Mahmoud.
Molecular Genetics & Genomic Medicine.  10 (2022)  12 - p. , 2022
Link: https://doi.org/10.1002/..
 
?
6

Molecular characterization of a large cohort of mucopolysac..:

Ghaffari, Saeed R. ; Rafati, Maryam ; Shadnoush, Mahdi...
Human Mutation.  43 (2022)  4 - p. , 2022
Link: https://doi.org/10.1002/..
 
?
7

Impact of Intravenous Trehalose Administration in Patients ..:

Mobini, Moein ; Radbakhsh, Shabnam ; Kubaski, Francyne...
Journal of Clinical Medicine.  11 (2022)  1 - p. 247 , 2022
Link: https://doi.org/10.3390/..
 
?
8

Tetrahydrobiopterin responsiveness in Phenylalanine hydroxy..:

Khaghani, Faeze ; Eshraghi, Peyman ; Hamzehloei, Tayebeh
European Journal of Medical Genetics.  65 (2022)  9 - p. 104536 , 2022
Link: https://doi.org/10.1016/..
 
?
9

Recommendations for Infantile-Onset and Late-Onset Pompe Di..:

Fatehi, Farzad ; Ashrafi, Mahmoud Reza ; Babaee, Marzieh...
Frontiers in Neurology.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
?
10

Optimal Frequency to Screen Celiac Disease amongst Patients..:

Moravej, Hossein ; Zamanfar, Daniel ; Aghamahdi, Fatemeh...
Primary Care Diabetes.  15 (2021)  6 - p. 1100-1103 , 2021
Link: https://doi.org/10.1016/..
 
?
11

Genotyping of ABCC8, KCNJ11, and HADH in Iranian Infants wi..:

Hashemian, Somayyeh ; Esfehani, Reza Jafarzadeh ; Karimdadi, Siroos...
Case Reports in Endocrinology.  2021 (2021)  - p. 1-6 , 2021
Link: https://doi.org/10.1155/..
 
?
12

Novel mutations and their genotype-phenotype correlations i..:

Tafazoli, Alireza ; Eshraghi, Peyman ; Pantaleoni, Francesca...
Advances in Medical Sciences.  63 (2018)  1 - p. 87-93 , 2018
Link: https://doi.org/10.1016/..
 
?
13

Identification of mutations in Iranian patients' DAX-1 gene..:

Davoodnejad, Mahdieh ; Eshraghi, Peyman ; vakili, Rahim.
Egyptian Journal of Medical Human Genetics.  18 (2017)  2 - p. 165-172 , 2017
Link: https://doi.org/10.1016/..
 
?
14

Correction: Mothers' lived experience of caring for childre..:

Shirdelzade, Sara ; Ramezani, Monir ; Eshraghi, Peyman.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10278250/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
?
15

Mothers' lived experience of caring for children with inbor..:

Shirdelzade, Sara ; Ramezani, Monir ; Eshraghi, Peyman.
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244838/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
1-15