Shahram Savad
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Explore the profile of Shahram Savad including associated specialties, affiliations and a list of published articles.
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22
Citations
97
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Recent Articles
1.
Noorian S, Soltani H, Aghamahdi F, Savad S, Alan M
Clin Case Rep
. 2025 Feb;
13(2):e70234.
PMID: 39980897
Isolated growth hormone deficiency (IGHD) IA is inherited autosomal recessively and occurs due to GH1 gene deletions. This study emphasizes the importance of clinical diagnosis and molecular examination for detecting...
2.
Motevasselian M, Omrani M, Saleh Gargari S, Younesi S, Taheri Amin M, Saadati P, et al.
Mol Cytogenet
. 2024 Dec;
17(1):33.
PMID: 39707390
The advent of non-invasive prenatal testing (NIPT) in the screening of fetal abnormalities has optimized prenatal care and decreased the rate of invasive diagnostic tests. In this retrospective descriptive study,...
3.
Savad S, Modarressi M, Younesi S, Seifi-Alan M, Samadaian N, Masoomy M, et al.
Neuromolecular Med
. 2024 Jul;
26(1):28.
PMID: 38954284
Neurofibromatosis type 1 (NF1) is a genetic disorder caused by mutations in the NF1 gene. This disorder shows nearly complete penetrance and high phenotypic variability. We used the whole-exome sequencing...
4.
Hantoushzadeh S, Younesi S, Taheri Amin M, Saadati P, Jamali S, Nassiri S, et al.
Cytokine
. 2023 May;
168:156228.
PMID: 37224577
COVID-19 has been shown to affect pregnant women. Since pregnant women are at risk of this infection, vaccination against COVID-19 has been suggested as an imperative way to diminish rate...
5.
Rastad H, Samimisedeh P, Savad S, Alan M
Ann Otol Rhinol Laryngol
. 2023 Apr;
132(11):1493-1495.
PMID: 37009772
Background: About 80% of congenital hearing loss cases have genetic causes, often autosomal recessive and non-syndromic. Autosomal Recessive Non-syndromic hearing loss is characterized by extreme genetic heterogeneity. Objectives: To report...
6.
Savad S, Ashrafi M, Samadaian N, Heidari M, Modarressi M, Zamani G, et al.
Sci Rep
. 2023 Feb;
13(1):3202.
PMID: 36828874
Spinal muscular atrophy (SMA) is among the most common autosomal recessive disorders with different incidence rates in different ethnic groups. In the current study, we have determined SMN1, SMN2 and...
7.
Younesi S, Eslamian L, Khalafi N, Taheri Amin M, Saadati P, Jamali S, et al.
Sci Rep
. 2023 Jan;
13(1):1228.
PMID: 36681713
Multiples of the normal median (MoM) of free βHCG is a valuable parameter in evaluation of risk of adverse pregnancy outcomes. In the current retrospective study, we assessed the maternal...
8.
Aghamahdi F, Nirouei M, Savad S
J Med Case Rep
. 2022 Jul;
16(1):288.
PMID: 35883096
Background: Niemann-Pick type A (NP-A) is a congenital, hereditary disease caused by a deficiency in acid sphingomyelinase, a lysosomal enzyme. This deficiency results in an accumulation of sphingomyelin in lysosomes,...
9.
Ashrafi M, Mohammadi P, Tavasoli A, Heidari M, Hosseinpour S, Rasulinejad M, et al.
Cerebellum
. 2022 Jun;
22(4):640-650.
PMID: 35731353
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS) is now increasingly identified from all countries over the world, possibly rendering it one of the most common autosomal recessive ataxias. Here,...
10.
Younesi S, Yazdani B, Taheri Amin M, Saadati P, Jamali S, Modarresi M, et al.
J Clin Lab Anal
. 2022 May;
36(7):e24471.
PMID: 35500172
Background: Nowadays, neonatal screening has become an essential part of routine newborn care in the world. This is a non-invasive evaluation that evaluated inborn errors of metabolisms (IEMs) using tandem...