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/vufind/Search/Results?lookfor=%22Bouhouche%2C+Ahmed%22&type=Person&sort=year
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PubPharm (72)
1
Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans : implications for a North African Neanderthal connection
enthalten in:
Archives of virology
| 2024
von
Yousfi, F.
|
Haroun, A.
|
Nebhani, C.
| +8
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2
Prevalence of the protective OAS1 rs10774671-G allele against severe COVID-19 in Moroccans: implications for a North African Neanderthal connection
enthalten in:
Archives of virology
| 2024
von
Yousfi, F.
|
Haroun, A.
|
Nebhani, C.
| +8
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3
Association of Renin-angiotensin pathway gene polymorphisms with COVID-19 susceptibility and severity in the Moroccan cohort
enthalten in:
ResearchSquare.com
| 2024
von
Yousfi, F.
|
Hilali, S.
|
Belayachi, J.
| +4
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4
Study of the protective
OAS1
rs10774671-G allele against severe COVID-19 in Moroccans suggests a North African origin for Neanderthals
enthalten in:
bioRxiv.org
| 2023
von
Youssfi, F.
|
Haroun, A.
|
Nebhani, C.
| +8
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5
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson’s Disease in Sporadic Moroccan Patients
enthalten in:
Journal of molecular neuroscience
| 2023
von
Smaili, I.
|
Tibar, H.
|
Rahmani, M.
| +7
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6
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson’s Disease in Sporadic Moroccan Patients
enthalten in:
Journal of molecular neuroscience
| 2023
von
Smaili, I.
|
Tibar, H.
|
Rahmani, M.
| +7
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7
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson’s Disease in Sporadic Moroccan Patients
enthalten in:
Journal of molecular neuroscience
| 2023
von
Smaili, I.
|
Tibar, H.
|
Rahmani, M.
| +7
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8
PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability
enthalten in:
Brain : a journal of neurology
| 2023
von
Fevga, C.
|
Tesson, C.
|
Carreras Mascaro, A.
| +118
CommentIn: Brain. 2023 Dec 1;146(12):e125-e127. - PMID 37448355
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9
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients
enthalten in:
Journal of molecular neuroscience : MN
| 2023
von
Smaili, I.
|
Tibar, H.
|
Rahmani, M.
| +7
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10
Novel ITGB2 Mutation Is Responsible for a Severe Form of Leucocyte Adhesion Deficiency Type 1
enthalten in:
BioMed research international
| 2022
von
Bouhouche, A.
|
Tabache, Y.
|
Askander, O.
| +11
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3
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3
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3
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3
Hereditary Spastic Paraplegia
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Erscheinungszeitraum
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