Ahlem Achour
Overview
Explore the profile of Ahlem Achour including associated specialties, affiliations and a list of published articles.
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Articles
11
Citations
48
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0
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Recent Articles
1.
Yehia M, Askri A, Achour A, Prus J, Ouellet V, Alnahhas N
Poult Sci
. 2025 Jan;
104(2):104748.
PMID: 39756110
This study aimed to characterize body temperature in finishing broiler chickens and to explore heat transfer dynamics under thermoneutral (TN) and heat stress (HS) conditions. To achieve this, 900 Ross...
2.
Harteveld C, Achour A, Fairuz Mohd Hasan N, Legebeke J, Arkesteijn S, Ter Huurne J, et al.
Int J Mol Sci
. 2024 Aug;
25(16).
PMID: 39201615
It is well known that modifiers play a role in ameliorating or exacerbating disease phenotypes in patients and carriers of recessively inherited disorders such as sickle cell disease and thalassemia....
3.
Younsi M, Achour A, Kraoua L, Nesrine M, Sayari T, Abderrahim E, et al.
Pediatr Nephrol
. 2024 Aug;
40(1):103-116.
PMID: 39138691
Background: Alport syndrome is a genetic disorder affecting the kidneys, ears, and eyes, causing chronic kidney disease, sensorineural hearing loss, and ocular abnormalities. It results from pathogenic variants in the...
4.
Achour A, Knijnenburg J, Koopmann T, Raz A, Tischkowitz M, Coates T, et al.
Am J Hematol
. 2024 May;
99(8):1655-1658.
PMID: 38817045
No abstract available.
5.
Akrout F, Achour A, Tops C, Gallon R, Meddeb R, Achoura S, et al.
Front Oncol
. 2023 Sep;
13:1195814.
PMID: 37664053
Constitutional mismatch repair deficiency (CMMRD) syndrome is a rare autosomal recessive genetic disorder caused by biallelic germline mutations in one of the mismatch repair genes. Carriers are at exceptionally high...
6.
Harteveld C, Achour A, Arkesteijn S, Ter Huurne J, Verschuren M, Bhagwandien-Bisoen S, et al.
Int J Lab Hematol
. 2022 Sep;
44 Suppl 1:28-36.
PMID: 36074711
Hemoglobinopathies are the most common monogenic disorders in the world with an ever increasing global disease burden each year. As most hemoglobinopathies show recessive inheritance carriers are usually clinically silent....
7.
Kraoua L, Jaouadi H, Allouche M, Achour A, Kaouther H, Ben Ahmed H, et al.
Mol Genet Genomic Med
. 2022 Jun;
10(7):e1954.
PMID: 35656879
Background: Genetic cardiac diseases are the main trigger of sudden cardiac death (SCD) in young adults. Hypertrophic cardiomyopathy (HCM) is the most prevalent cardiomyopathy and accounts for 0.5 to 1%...
8.
Younsi M, Trabelsi M, Ben Youssef S, Ouertani I, Hammi Y, Achour A, et al.
Pediatr Nephrol
. 2022 Apr;
38(1):119-129.
PMID: 35445972
Background: Nephropathic cystinosis is an autosomal recessive disease caused by a mutation in the CTNS gene which encodes cystinosin, a lysosomal cystine transporter. The spectrum of mutations in the CTNS...
9.
Achour A, Koopmann T, Baas F, Harteveld C
Front Physiol
. 2021 Aug;
12:686689.
PMID: 34385932
During the last few years, next-generation sequencing (NGS) has undergone a rapid transition from a research setting to a clinical application, becoming the method of choice in many clinical genetics...
10.
Achour A, Koopmann T, Castel R, Santen G, den Hollander N, Knijnenburg J, et al.
Blood
. 2020 Jun;
136(15):1789-1793.
PMID: 32589702
No abstract available.