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Shahram Savad
33
results:
Search for persons
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Format
Online (33)
Mediatypes
Articles (Online) (17)
OpenAccess-fulltext (16)
Languages
english (30)
Sorted by: Relevance
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1
A Comprehensive Overview of NF1 Mutations in Iranian Patien..:
Savad, Shahram
;
Modarressi, Mohammad-Hossein
;
Younesi, Sarang
...
NeuroMolecular Medicine. 26 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1007/..
?
2
A comprehensive overview of SMN and NAIP copy numbers in Ir..:
Savad, Shahram
;
Ashrafi, Mahmoud Reza
;
Samadaian, Niusha
...
Scientific Reports. 13 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
3
A Novel Exon 2 Deletion Mutation in the GRXCR1 Gene Associa..:
Rastad, Hadith
;
Samimisedeh, Parham
;
Savad, Shahram
.
Annals of Otology, Rhinology & Laryngology. , 2023
Link:
https://doi.org/10.1177/..
?
4
Extreme βHCG levels in first trimester screening are risk f..:
Younesi, Sarang
;
Eslamian, Laleh
;
Khalafi, Nikta
...
Scientific Reports. 13 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
5
Impact of COVID-19 and vaccination on first and second trim..:
Hantoushzadeh, Sedigheh
;
Younesi, Sarang
;
Mahdi Taheri Amin, Mohammad
...
Cytokine. 168 (2023) - p. 156228 , 2023
Link:
https://doi.org/10.1016/..
?
6
Niemann-Pick type A disease with new mutation: a case repor:
Aghamahdi, Fatemeh
;
Nirouei, Matineh
;
Savad, Shahram
Journal of Medical Case Reports. 16 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
7
Molecular Genetic Analysis of Patients with Duchenne/Becker..:
Savad, Shahram
;
Fattah Beigi, Fatemeh
;
Najafi, Laily
...
Precision Medicine and Clinical OMICS. 2 (2022) 1 - p. , 2022
Link:
https://doi.org/10.5812/..
?
8
Clinical and Molecular Findings of Autosomal Recessive Spas..:
Ashrafi, Mahmoud Reza
;
Mohammadi, Pouria
;
Tavasoli, Ali Reza
...
The Cerebellum. 22 (2022) 4 - p. 640-650 , 2022
Link:
https://doi.org/10.1007/..
?
9
Incorporation of second‐tier tests and secondary biomarkers..:
Younesi, Sarang
;
Yazdani, Bahareh
;
Taheri Amin, Mohammad Mahdi
...
Journal of Clinical Laboratory Analysis. 36 (2022) 7 - p. , 2022
Link:
https://doi.org/10.1002/..
?
10
The Role of Thyroid Function Tests in Diagnosing Allan-hern..:
Department of Pediatric Endocrinology and Metabolism, Bahonar Hospital, Alborz University of Medical Sciences, Karaj, Iran.
;
Noorian, Shahab
;
Hamzehlou, Sepideh
...
Basic and Clinical Neuroscience Journal. 12 (2021) 4 - p. 563-568 , 2021
Link:
https://doi.org/10.32598..
?
11
A Family With Novel X-Linked Recessive Homozygous Mutation ..:
Noorian, Shahab
;
Savad, Shahram
;
Khavandegar, Armin
.
AACE Clinical Case Reports. , 2021
Link:
https://doi.org/10.1016/..
?
12
Karyotype analysis of amniotic fluid cells and report of ch..:
Younesi, Sarang
;
Taheri Amin, Mohammad Mahdi
;
Hantoushzadeh, Sedigheh
...
Scientific Reports. 11 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1038/..
?
13
Non-invasive prenatal test to screen common trisomies in tw..:
Motevasselian, Mahtab
;
Saleh Gargari, Soraya
;
Younesi, Sarang
...
Molecular Cytogenetics. 13 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/..
?
14
First-Trimester Contingent Screening for Trisomy 21 by Feta..:
Younesi, Sarang
;
Savad, Shahram
;
Ghafouri-Fard, Soudeh
...
Journal of Fetal Medicine. 5 (2018) 3 - p. 139-143 , 2018
Link:
https://doi.org/10.1007/..
?
15
A novel missense mutation of the HGD gene causes Alkaptonur..:
Noorian, Shahab
;
Dehghan Banadaki, Bahareh
;
Sotoudeh, Arya
..
Meta Gene. 18 (2018) - p. 174-176 , 2018
Link:
https://doi.org/10.1016/..
1-15