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Laila Bouguenouch
92
results:
Search for persons
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Online (92)
Mediatypes
Articles (Online) (44)
OpenAccess-fulltext (48)
Sorted by: Relevance
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1
RAS Mutations Predict Recurrence-Free Survival and Recurren..:
El Agy, Fatima
;
El Bardai, Sanae
;
Boukansa, Sara
...
Cancer Control. 31 (2024) - p. , 2024
Link:
https://doi.org/10.1177/..
?
2
Identification of novel and de novo variant in the SCN1A ge..:
El Mouhi, Hinde
;
Amllal, Nada
;
Abbassi, Meriame
...
Molecular Biology Reports. 51 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1007/..
?
3
Genotypic and Allelic Distribution of the CD36 rs1761667 Po..:
El Ouali, El Mokhtar
;
Kartibou, Jihan
;
Del Coso, Juan
...
Genes. 15 (2024) 4 - p. 419 , 2024
Link:
https://doi.org/10.3390/..
?
4
Update on prostate cancer epidemiology in Morocco:
Samtal, Chaimae
;
Bouguenouch, Laila
;
Ismaili, Nabil
...
African Journal of Urology. 30 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
5
Clinicopathological and prognostic implications of EGFR mut..:
Boukansa, Sara
;
Mouhrach, Ismail
;
El Agy, Fatima
...
PLOS ONE. 19 (2024) 6 - p. e0298721 , 2024
Link:
https://doi.org/10.1371/..
?
6
Exploring Splice-Site Mutations in LAMA2-Related Muscular D..:
Nmer, Samira
;
Ameli, Amina
;
Trhanint, Said
...
Cureus. , 2024
Link:
https://doi.org/10.7759/..
?
7
The Genetic Facets of Dravet Syndrome: Recent Insights:
Mouhi, Hinde El
;
Abbassi, Meriame
;
Jalte, Meryem
...
Annals of Child Neurology. 32 (2024) 2 - p. 67-82 , 2024
Link:
https://doi.org/10.26815..
?
8
The burden of cystic fibrosis in North Africa:
El Makhzen, Nada
;
Daimi, Houria
;
Bouguenouch, Laila
.
Frontiers in Genetics. 14 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
9
A novel homozygous missense variant identified in the myosi..:
Ouarhache, Maryem
;
Kettani, Oussama
;
Fizazi, Khawla El
..
Molecular Biology Reports. 51 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1007/..
?
10
The Diagnosis and Genetic Mechanisms of Prader-Willi Syndro..:
Ahakoud, Mohamed
;
Daha Belghiti, Hanae
;
Nedbour, Ayoub
...
Cureus. , 2023
Link:
https://doi.org/10.7759/..
?
11
P046: Involvement of MLH1 and MSH2 genes in hereditary susc..:
Bouramtane, Abdelhamid
;
Moufid, Fatima Zahra
;
Ahakoud, Mohamed
..
Genetics in Medicine Open. 1 (2023) 1 - p. 100065 , 2023
Link:
https://doi.org/10.1016/..
?
12
Rare and Atypical Case of Turner Syndrome With Three Cell L..:
Essouabni, Amal
;
Ahakoud, Mohamed
;
Aynaou, Hayat
...
Cureus. , 2023
Link:
https://doi.org/10.7759/..
?
13
P048: Novel frameshift MLH1 germline mutation in a Moroccan..:
Bouramtane, Abdelhamid
;
Moufid, Fatima Zohra
;
Ahakoud, Mohamed
..
Genetics in Medicine Open. 1 (2023) 1 - p. 100067 , 2023
Link:
https://doi.org/10.1016/..
?
14
Jacob's Syndrome and Deficiency of 11-Beta-Hydroxylase Enzy..:
Aitifali, Wafa
;
Lahmamssi, Fatima Zahra
;
Abourazzak, Sana
..
Case Reports in Clinical Medicine. 12 (2023) 6 - p. 207-211 , 2023
Link:
https://doi.org/10.4236/..
?
15
A Mosaic PIK3CA Mutation in a Moroccan Female: Exploring th..:
Ahakoud, Mohamed
;
Daha Belghiti, Hanae
;
Ihlal, Hajar
.
Cureus. , 2023
Link:
https://doi.org/10.7759/..
1-15