Neveen A Soliman
Overview
Explore the profile of Neveen A Soliman including associated specialties, affiliations and a list of published articles.
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68
Citations
2634
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Recent Articles
1.
Schneider R, Shril S, Buerger F, Deutsch K, Yousef K, Frank C, et al.
Genes Dis
. 2024 Nov;
12(2):101280.
PMID: 39584075
No abstract available.
2.
Karimi K, Weis D, Aukrust I, Hsieh T, Horackova M, Paulsen J, et al.
Eur J Hum Genet
. 2024 Oct;
32(12):1574-1582.
PMID: 39424669
Developmental Delay with Gastrointestinal, Cardiovascular, Genitourinary, and Skeletal Abnormalities syndrome (DEGCAGS, MIM #619488) is caused by biallelic, loss-of-function (LoF) ZNF699 variants, and is characterized by variable neurodevelopmental disability, discordant organ...
3.
Deutsch K, Klambt V, Kitzler T, Jobst-Schwan T, Schneider R, Buerger F, et al.
Genes Dis
. 2024 Jun;
11(5):101111.
PMID: 38868576
No abstract available.
4.
Amer K, Soliman N, Soror S, Gad Y, Moustafa A, Elmonem M, et al.
J Adv Res
. 2024 Jun;
PMID: 38844121
Background: Studying the human genome is crucial to embrace precision medicine through tailoring treatment and prevention strategies to the unique genetic makeup and molecular information of individuals. After human genome...
5.
Elmonem M, Soliman N, Moustafa A, Gad Y, Hassan W, Taha T, et al.
Nat Genet
. 2024 Apr;
56(6):1035-1037.
PMID: 38684896
No abstract available.
6.
Naguib S, Mansour L, Soliman N, El-Hanafy H, Fahmy Y, Elmonem M, et al.
Genet Test Mol Biomarkers
. 2024 Apr;
28(4):151-158.
PMID: 38657121
Approximately 80% of primary hyperoxaluria cases are caused by primary hyperoxaluria type 1 (PH1, OMIM# 259900), which is characterized by pathogenic variants in the gene, resulting in deficiency of the...
7.
Salman M, Elgebaly A, Soliman N
Pediatr Nephrol
. 2024 Jan;
39(9):2569-2578.
PMID: 38261064
The incidence of rare diseases is expected to be comparatively higher in the Middle East and North Africa (MENA) region than in other parts of the world, attributed to the...
8.
Omar M, El Hawary R, Eldash A, Sadek K, Soliman N, Hanna M, et al.
Lab Med
. 2023 Jun;
55(2):153-161.
PMID: 37352143
Background: While we strive to live with SARS-CoV-2, defining the immune response that leads to recovery rather than severe disease remains highly important. COVID-19 has been associated with inflammation and...
9.
Groothoff J, Metry E, Deesker L, Garrelfs S, Acquaviva C, Almardini R, et al.
Nat Rev Nephrol
. 2023 Jan;
19(3):194-211.
PMID: 36604599
Primary hyperoxaluria (PH) is an inherited disorder that results from the overproduction of endogenous oxalate, leading to recurrent kidney stones, nephrocalcinosis and eventually kidney failure; the subsequent storage of oxalate...
10.
Wu C, Lim T, Wang C, Seltzsam S, Zheng B, Schierbaum L, et al.
Eur Urol Open Sci
. 2022 Oct;
44:106-112.
PMID: 36185583
Background: Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease among children and adults younger than 30 yr. In our previous...