Siham Chafai Elalaoui
Overview
Explore the profile of Siham Chafai Elalaoui including associated specialties, affiliations and a list of published articles.
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Articles
40
Citations
347
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Recent Articles
1.
Amllal N, Lyahyai J, Afif L, Kriouile Y, Sefiani A, Elalaoui S
Epileptic Disord
. 2024 Nov;
27(1):114-116.
PMID: 39513746
No abstract available.
2.
Amllal N, Lyahyai J, Elalaoui S, El Kadiri Y, Sefiani A
Mol Syndromol
. 2024 Oct;
15(5):421-426.
PMID: 39359953
Introduction: Pathogenic variants in the gene are associated to a large spectrum of severe early onset developmental and epileptic encephalopathies (OMIM #612164). They were also identified in various other neurodevelopmental...
3.
Benyahya N, Amllal N, Elalaoui S, El Alloussi M, Sefiani A, Lyahyai J
Int J Dev Neurosci
. 2024 Sep;
84(8):1006-1009.
PMID: 39300047
Background: SATB2-associated syndrome (SAS) also known as Glass syndrome is characterized by/intellectual disability and/or developmental delay coupled with absent or limited speech development. Other abnormalities can be noticed including craniofacial...
4.
Amllal N, Zerkaoui M, Jdioui W, Elalaoui S, Sefiani A, Lyahyai J
Mol Biol Rep
. 2024 Aug;
51(1):885.
PMID: 39096335
Background: Sotos syndrome is a rare and complex genetic disorder caused by haploinsufficiency of the NSD1 gene. This syndrome is characterized by rapid early childhood growth, distinct facial features, a...
5.
El Mouhi H, Amllal N, Abbassi M, Nedbour A, Jalte M, Lyahyai J, et al.
Mol Biol Rep
. 2024 Jan;
51(1):233.
PMID: 38282049
Dravet syndrome is a severe form of epilepsy characterised by recurrent seizures and cognitive impairment. It is mainly caused by variant in the SCN1A gene in 90% of cases, which...
6.
Amllal N, Elalaoui S, Zerkaoui M, Chiguer A, Afif L, Izgua A, et al.
Ann Lab Med
. 2023 Sep;
44(1):110-117.
PMID: 37665295
No abstract available.
7.
El Amrani Z, Elalaoui S, Jdioui W, Sbiti A, Ratbi I, Liehr T, et al.
Ophthalmic Genet
. 2022 Jun;
43(5):689-692.
PMID: 35658784
Background: Retinoblastoma (RB) is the most common malignant intraocular tumor in children; it affects their eyes often even prenatally. RB may be sporadic or familial, due to germinal mutation in...
8.
Elalaoui S, Laarabi F, Afif L, Lyahyai J, Ratbi I, Cherkaoui Jaouad I, et al.
Breast Cancer Res Treat
. 2022 May;
194(1):187-198.
PMID: 35578052
Purpose: Breast cancer (BC) is the most common form of female cancer around the world. BC is mostly sporadic, and rarely hereditary. These hereditary forms are mostly BRCA1- and BRCA2-associated...
9.
Elalaoui S, Smaili W, Van-Gils J, Fergelot P, Ratbi I, Tajir M, et al.
Afr Health Sci
. 2021 Nov;
21(2):960-967.
PMID: 34795756
Background: Rubinstein-Taybi syndrome (RSTS; OMIM 180849) is a rare autosomal dominant developmental disorder with an estimated prevalence of one case per 125,000 live births. RSTS is characterized by typical face,...
10.
Doubaj Y, Zrhidri A, Elalaoui S, Lyahyai J, El Kadiri Y, Elkassimi N, et al.
Pan Afr Med J
. 2021 Aug;
39:72.
PMID: 34422195
Introduction: Fanconi anemia (FA) is a rare inherited hematological disease due to a defect in the DNA repair pathway resulting in congenital abnormalities and high susceptibility to develop cancers. The...