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Shahram Savad
33  Ergebnisse:
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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/..
 
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2

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/..
 
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3

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/..
 
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4

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/..
 
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5

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/..
 
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6

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/..
 
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7

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/..
 
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8

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/..
 
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9

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/..
 
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10

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/..
 
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11

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/..
 
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12

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..
 
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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/..
 
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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/..
 
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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/..
 
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