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Mohammed Khattab

Explore the profile of Mohammed Khattab including associated specialties, affiliations and a list of published articles. Areas
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Articles 32
Citations 282
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Recent Articles
1.
Skhoun H, El Fessikh M, Khattab M, Mchich B, Agadr A, Abilkassem R, et al.
Biochem Genet . 2024 Nov; PMID: 39514082
The RAS genes are importantly implicated in oncogenesis and are frequently mutated in childhood acute lymphoblastic leukemia. This study is the first to our knowledge, to determine the mutational status...
2.
Benlhachemi S, Khattab M, Hattoufi K, Abouqal R, Boutayeb S, El Fahime E
Cancer Rep (Hoboken) . 2024 Nov; 7(11):e2158. PMID: 39506861
Background: Wilms tumour (WT), the second most reported childhood cancer in Morocco, is a malignant kidney tumour that affects children under 15 years old. Prognosis has improved with the adoption...
3.
Skhoun H, El Fessikh M, El Alaoui Al Abdallaoui M, Khattab M, Belkhayat A, Chebihi Z, et al.
Arch Pediatr . 2024 Apr; 31(4):238-244. PMID: 38679547
Background: Recurrent genetic abnormalities affecting pivotal signaling pathways are the hallmark of childhood acute lymphoblastic leukemia (ALL). The identification of these aberrations remains clinically important. Therefore, we sought to determine...
4.
Benlhachemi S, Abouqal R, Coleman N, Murray M, Khattab M, El Fahime E
Noncoding RNA Res . 2023 Jun; 8(3):413-425. PMID: 37305178
Background: Wilms tumour (WT) is caused by aberrant embryonic kidney development and associated with dysregulated expression of short, non-protein-coding RNAs termed microRNAs (miRNAs). At present, there is no reliable circulating...
5.
Viprakasit V, Hamdy M, Hassab H, Sherief L, Al-Bagshi M, Khattab M, et al.
Ann Hematol . 2023 May; 102(8):2039-2049. PMID: 37227493
Iron chelation therapy (ICT) is the mainstay of treatment in patients with thalassemia requiring blood transfusions. This phase 2 JUPITER study evaluated patient preference between film-coated tablet (FCT) and dispersible...
6.
Skhoun H, Khattab M, Belkhayat A, Chebihi Z, Bakri Y, Dakka N, et al.
Mol Biol Rep . 2022 Jun; 49(9):8291-8300. PMID: 35705773
Background: TP53 gene plays a pivotal role in maintaining genetic stability and prevention of malignancies. Alterations of this gene are implicated in more than half of human cancers. To the...
7.
Bouhouche A, Tabache Y, Askander O, Charoute H, Mesnaoui N, Belayachi L, et al.
Biomed Res Int . 2022 Mar; 2022:1141280. PMID: 35281597
Leukocyte adhesion deficiency type 1 (LAD1) is a rare autosomal recessive hereditary disorder characterized by recurrent infections, impaired pus formation, delayed wound healing, omphalitis, and delayed separation of the umbilical...
8.
Matthay K, Hylton J, Penumarthy N, Khattab M, Soh S, Nguyen H, et al.
Pediatr Blood Cancer . 2022 Jan; 69(4):e29568. PMID: 35084087
Background: Tumor boards are part of standard care of patients with complex cancers, but appropriate multidisciplinary expertise and infrastructure are often not available in low- and middle-income countries (LMIC) for...
9.
Skhoun H, Khattab M, Chebihi Z, Belkhayat A, Dakka N, El Baghdadi J
Leuk Res Rep . 2022 Jan; 17:100289. PMID: 35079568
Acute leukemias are often of myeloid or lymphoid origin. However, some acute leukemias revealed an undefined differentiation into a single lineage. Mixed phenotype acute leukemia (MPAL) is an uncommon diagnosis...
10.
Salman M, Salman A, Elewa A, Rabiee A, Tourky M, Shaaban H, et al.
Obes Surg . 2022 Jan; 32(4):1141-1148. PMID: 35050483
Purpose: Secondary hyperparathyroidism (SHPT) is linked to obesity. Bariatric surgery may be associated with calcium and vitamin D deficiencies leading to SHPT. This study aimed to detect the prevalence of...