Serwa Ghasemi
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Explore the profile of Serwa Ghasemi including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
24
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Recent Articles
1.
Hesami H, Ghasemi S, Houshmand G, Nilipour Y, Hesami M, Biglari A, et al.
BMC Musculoskelet Disord
. 2024 Mar;
25(1):241.
PMID: 38539162
Background: Limb girdle muscular dystrophies (LGMDs) constitute a heterogeneous group of neuromuscular disorders with a very variable clinical presentation and overlapping traits. The clinical symptoms of LGMD typically appear in...
2.
Ghaffari Jolfayi A, Kohansal E, Ghasemi S, Naderi N, Hesami M, MozafaryBazargany M, et al.
Sci Rep
. 2024 Mar;
14(1):5313.
PMID: 38438525
The giant protein titin (TTN) is a sarcomeric protein that forms the myofibrillar backbone for the components of the contractile machinery which plays a crucial role in muscle disorders and...
3.
Ghaffari Jolfayi A, Naderi N, Ghasemi S, Salmanipour A, Adimi S, Maleki M, et al.
BMC Cardiovasc Disord
. 2024 Jan;
24(1):1.
PMID: 38166572
Background: Primary carnitine deficiency (PCD) denotes low carnitine levels with an autosomal recessive pattern of inheritance. Cardiomyopathy is the most common cardiac symptom in patients with PCD, and early diagnosis...
4.
Ghasemi S, Mahdavi M, Maleki M, Salahshourifar I, Kalayinia S
BMC Med Genomics
. 2023 Dec;
16(1):334.
PMID: 38129817
Background: Dilated cardiomyopathy (DCM) is a major cause of sudden cardiac death and heart failure. Up to 50% of all DCM cases have a genetic background, with variants in over...
5.
Sadeghipour P, Valuian M, Ghasemi S, Rafiee F, Pourirahim M, Mahmoodian M, et al.
Lab Med
. 2023 Dec;
55(4):447-453.
PMID: 38113391
Background: Thoracic aortic aneurysm (TAA) is a multifactorial disorder. Familial TAA, which is more clinically aggressive, is associated with a high risk of lethal dissection or rupture. Genetic evaluation can...
6.
Mahdavi M, Mohsen-Pour N, Maleki M, Ghasemi S, Tabib A, Houshmand G, et al.
Lab Med
. 2023 May;
55(1):62-70.
PMID: 37246508
Objective: We studied the clinical and molecular features of a family with hypertrophic cardiomyopathy (HCM). Background: A very heterogeneous disease affecting the heart muscle, HCM is mostly caused by variants...
7.
Heshmatzad K, Naderi N, Maleki M, Abbasi S, Ghasemi S, Ashrafi N, et al.
J Cell Mol Med
. 2023 May;
27(12):1621-1636.
PMID: 37183561
Cardiovascular diseases (CVDs) constitute one of the significant causes of death worldwide. Different pathological states are linked to CVDs, which despite interventions and treatments, still have poor prognoses. The genetic...
8.
Tabib A, Talebi T, Ghasemi S, Pourirahim M, Naderi N, Maleki M, et al.
Eur J Med Res
. 2022 Dec;
27(1):286.
PMID: 36496429
Background: Congenital heart defects (CHDs) are the most common congenital malformations, including structural malformations in the heart and great vessels. CHD complications such as low birth weight, prematurity, pregnancy termination,...
9.
Ghasemi S, Mahdavi M, Maleki M, Salahshourifar I, Kalayinia S
BMC Med Genomics
. 2022 Nov;
15(1):234.
PMID: 36344977
Background: Familial dilated cardiomyopathy (DCM) is a genetic heart disorder characterized by progressive heart failure and sudden cardiac death. Over 250 genes have been reported in association with DCM; nonetheless,...
10.
Mohsen-Pour N, Naderi N, Ghasemi S, Hesami M, Maleki M, Kalayinia S
Lab Med
. 2022 Jun;
53(6):640-650.
PMID: 35686496
Objective: Solute carrier family 19 member 2 (SLC19A2, OMIM *603941) encodes thiamine human transporter 1 (THTR-1), which contributes to bringing thiamine (vitamin B1) into cells. Mutations in SLC19A2 lead to...