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peyman eshraghi
peyman eshraghi
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引用次数
年份
Noonan syndrome–a new survey
A Tafazoli, P Eshraghi, ZK Koleti, M Abbaszadegan
Archives of Medical Science 13 (1), 215-220, 2017
632017
Recommendations for infantile-onset and late-onset Pompe disease: An Iranian consensus
F Fatehi, MR Ashrafi, M Babaee, B Ansari, M Beiraghi Toosi, R Boostani, ...
Frontiers in Neurology 12, 739931, 2021
202021
Impact of intravenous trehalose administration in patients with niemann–pick disease types A and B
M Mobini, S Radbakhsh, F Kubaski, P Eshraghi, S Vakili, R Vakili, ...
Journal of Clinical Medicine 11 (1), 247, 2022
192022
Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencing
A Tafazoli, P Eshraghi, F Pantaleoni, R Vakili, M Moghaddassian, ...
Advances in medical sciences 63 (1), 87-93, 2018
192018
Comparison of parenting related stress and depression symptoms in mothers of children with and without autism spectrum disorders (ASD)
F Kiani, MR Khodabakhsh, HK Hashjin, H Rahbardar, MA Abbasi, ...
International J of Pediatrics 2 (3.3), 31-7, 2014
182014
Characteristics of patients with phenylketonuria in Mazandaran Province, northern, Iran
P Eshraghi, A Abaskhanian, AR MOHAMMADHASANI
Caspian Journal of Internal Medicine 1 (2), 72-74, 2010
162010
Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of< 5 years in the Iranian population
H Yaghootkar, F Abbasi, N Ghaemi, A Rabbani, MN Wakeling, P Eshraghi, ...
Diabetic Medicine 36 (12), 1694-1702, 2019
152019
Evaluation of nutritional status and growth in phenylketonuria patients in Mazandaran Province Iran
P Eshraghi, A Abbaskhanian, A Bijani, S Hosseinzadeh
Journal of Babol University of Medical Sciences 13 (5), 58-62, 2011
122011
Effectiveness of group cognitive-behavioral therapy on anxiety, depression and glycemic control in children with type 1 diabetes
S Ahmadi, Z Tabibi, A Mashhadi, P Eshraghi, F Faroughi, P Ahmadi
International Journal of Pediatrics 2 (3.1), 165-171, 2014
102014
Congenital rickets: report of four cases
R Vakili, P Eshraghi, A Ataei Nakhaei, S Vakili, A Khakshour, M Saeidi, ...
International Journal of Pediatrics 2 (1), 101-105, 2014
102014
Non-thyroidal illness syndrome and cardiopulmonary bypass in children with congenital heart disease
K Babazadeh, A Tabib, P Eshraghi, H Bakhshandeh, H Zamani
Caspian Journal of Internal Medicine 5 (4), 235, 2014
102014
Response to sapropterin hydrochloride (Kuvan®) in children with phenylketonuria (PKU): a clinical trial
P Eshraghi, S Noroozi Asl, S Bagheri, V Chalak
Journal of Pediatric Endocrinology and Metabolism 32 (8), 885-888, 2019
82019
Association of pediatric stress hyperglycemia with insulin metabolism disorders
P Eshraghi, S Bagheri, S Kamel
International Journal of Pediatrics 2 (1), 83-87, 2014
82014
Investigating genetic mutations in a large cohort of Iranian patients with congenital hyperinsulinism
M Razzaghy-Azar, S Saeedi, SB Dayani, S Enayati, F Abbasi, ...
Journal of Clinical Research in Pediatric Endocrinology 14 (1), 87, 2022
72022
The report of three rare cases of the Niemann-pick disease in Birjand, South Khorasan, Eastern Iran
SN Asl, R Vakili, N Ghaemi, P Eshraghi
Iranian journal of child neurology 11 (3), 53, 2017
72017
Niemann-pick diseases: the largest Iranian cohort with genetic analysis
S Hashemian, P Eshraghi, N Dilaver, H Galehdari, B Shalbafan, R Vakili, ...
Iranian Journal of Child Neurology 13 (2), 155, 2019
62019
Association of dietary pattern and body size with early menarche among elementary school girls in west of Iran
A Rahimi, M Rahimi, A Norouzy, H Esmaily, P Eshraghi, SAR Mohajeri, ...
Int J Pediatr 7 (12), 10583-10593, 2019
52019
Hypercalciuria, a promoting factor to urinary tract infection in children
A Gheissari, TS Adjoodani, P Eshraghi
Urology Annals 1 (2), 52-55, 2009
42009
Optimal Frequency to Screen Celiac Disease amongst Patients with Type 1 Diabetes Mellitus: A Multicenter Study
H Moravej, D Zamanfar, F Aghamahdi, M Hashemipour, FS Mirrashidi, ...
Primary Care Diabetes 15 (6), 1100-1103, 2021
32021
Genotyping of ABCC8, KCNJ11, and HADH in Iranian Infants with Congenital Hyperinsulinism
S Hashemian, RJ Esfehani, S Karimdadi, N Ghaemi, P Eshraghi, ...
Case Reports in Endocrinology 2021 (1), 8826174, 2021
32021
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