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Ghandil, Pegah
49  results:
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1

Association Study of Polymorphisms in Folate Metabolism and..:

Heydari, Atefeh ; Aminzadeh, Majid ; Momen, Ali Akbar...
Jundishapur Journal of Chronic Disease Care.  13 (2024)  2 - p. , 2024
Link: https://doi.org/10.5812/..
 
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2

Genetic features of patients with MPS type IIIB: Descriptio..:

Nasir Shalal, Mahzad ; Aminzadeh, Majid ; Saberi, Alihossein...
Gene.  913 (2024)  - p. 148354 , 2024
Link: https://doi.org/10.1016/..
 
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3

Association of DRD2, DRD4 and COMT genes variants and their..:

Taheri, Narges ; Pirboveiri, Rokhshid ; Sayyah, Mehdi..
BMC Psychiatry.  23 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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4

Clinical and Molecular Spectrum of Muscular Dystrophies (MD..:

Mohamadian, Malihe ; Rastegar, Mandana ; Pasamanesh, Negin...
Journal of Molecular Neuroscience.  72 (2021)  1 - p. 9-23 , 2021
Link: https://doi.org/10.1007/..
 
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5

Genetic association study of CTLA4 and FCεRIα polymorphisms..:

Roshanizadeh, Zahra ; Ghandil, Pegah ; Khodadadi, Ali...
Nucleosides, Nucleotides & Nucleic Acids.  40 (2021)  9 - p. 914-925 , 2021
Link: https://doi.org/10.1080/..
 
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6

Molecular diagnosis of maturity onset diabetes of the young..:

Davoudi, Fatemeh ; Aminzadeh, Majid ; Shahbazian, Hajiye Bibi...
Journal of Diabetes & Metabolic Disorders.  20 (2021)  2 - p. 1369-1374 , 2021
Link: https://doi.org/10.1007/..
 
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7

Clinical features and tubulin folding cofactor E gene analy..:

Aminzadeh, Majid ; Galehdari, Hamid ; Shariati, Gholamreza..
Jornal de Pediatria.  96 (2020)  1 - p. 60-65 , 2020
Link: https://doi.org/10.1016/..
 
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8

Identification of Cytochrome b‐245, beta‐chain gene mutatio..:

Heydari, Atefeh ; Abolnezhadian, Farhad ; Sadeghi‐Shabestari, Mahnaz...
Journal of Clinical Laboratory Analysis.  35 (2020)  2 - p. , 2020
Link: https://doi.org/10.1002/..
 
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9

Association of vascular endothelial growth factor A polymor..:

Sajjadi, Maryam S. ; Ghandil, Pegah ; Shahbazian, Nahid.
Journal of Obstetrics and Gynaecology Research.  46 (2020)  3 - p. 369-375 , 2020
Link: https://doi.org/10.1111/..
 
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10

Association Metabolic Obesity Phenotypes with Cardiometabol..:

Abolnezhadian, Farhad ; Hosseini, Seyed Ahmad ; Alipour, Meysam...
Vascular Health and Risk Management.  16 (2020)  - p. 249-256 , 2020
Link: https://doi.org/10.2147/..
 
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11

Clinical features and tubulin folding cofactor E gene analy..:

Aminzadeh, Majid ; Galehdari, Hamid ; Shariati, Gholamreza..
Jornal de Pediatria (Versão em Português).  96 (2020)  1 - p. 60-65 , 2020
Link: https://doi.org/10.1016/..
 
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12

A novel homozygous variant in an Iranian pedigree with cere..:

Mohamadian, Malihe ; Ghandil, Pegah ; Naseri, Mohsen..
Journal of Clinical Laboratory Analysis.  34 (2020)  11 - p. , 2020
Link: https://doi.org/10.1002/..
 
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13

The first report of two homozygous sequence variants in FKR..:

Mohamadian, Malihe ; Naseri, Mohsen ; Ghandil, Pegah..
The Journal of Gene Medicine.  22 (2020)  12 - p. , 2020
Link: https://doi.org/10.1002/..
 
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14

Identification of arylsulfatase B gene mutations and clinic..:

Aminzadeh, Majid ; Malekpour, Nasrin ; Ghandil, Pegah
Gene.  706 (2019)  - p. 1-5 , 2019
Link: https://doi.org/10.1016/..
 
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15

Corrigendum: IRAK4 Deficiency in a Patient with Recurrent P..:

Gobin, Karina S. ; Hintermeyer, Mary ; Boisson, Bertrand...
Frontiers in Pediatrics.  6 (2018)  - p. , 2018
Link: https://doi.org/10.3389/..
 
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