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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 1 |
2011 | 1 |
2013 | 1 |
2014 | 1 |
2017 | 2 |
2020 | 1 |
2021 | 1 |
2023 | 0 |
Search Results
6
results
Results by year
Page 1
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries.
Neurol Genet. 2020 Dec 24;7(1):e536. doi: 10.1212/NXG.0000000000000536. eCollection 2021 Feb.
Neurol Genet. 2020.
PMID: 33376799
Free PMC article.
γ-sarcoglycan and dystrophin mutation spectrum in an Algerian cohort.
Dalichaouche I, Sifi Y, Roudaut C, Sifi K, Hamri A, Rouabah L, Abadi N, Richard I.
Dalichaouche I, et al. Among authors: sifi y.
Muscle Nerve. 2017 Jul;56(1):129-135. doi: 10.1002/mus.25443. Epub 2017 Feb 10.
Muscle Nerve. 2017.
PMID: 27759885
Item in Clipboard
Clinical Analysis of Algerian Patients with Pompe Disease.
Sifi Y, Medjroubi M, Froissart R, Taghane N, Sifi K, Benhabiles A, Lemai S, Semra S, Benmekhebi H, Bouderda Z, Abadi N, Hamri A.
Sifi Y, et al.
J Neurodegener Dis. 2017;2017:9427269. doi: 10.1155/2017/9427269. Epub 2017 Feb 6.
J Neurodegener Dis. 2017.
PMID: 28265479
Free PMC article.
Item in Clipboard
Multiple sclerosis: progression rate and severity in a multicenter cohort from Algeria.
Hecham N, Nouioua S, Sifi Y, Toubal N, Aissa LA, Hattab S, Batsi D, Hamimed A, Berkane F, Oudrer N, Aidi A, Abrouk S, Daoudi S, Hamri A, Assami S, Tazir M.
Hecham N, et al. Among authors: sifi y.
Mult Scler. 2014 Dec;20(14):1923-4. doi: 10.1177/1352458514543343. Epub 2014 Aug 13.
Mult Scler. 2014.
PMID: 25122474
No abstract available.
Item in Clipboard
Clinical and Genetic Study of Algerian Patients with Spinal Muscular Atrophy.
Sifi Y, Sifi K, Boulefkhad A, Abadi N, Bouderda Z, Cheriet R, Magen M, Bonnefont JP, Munnich A, Benlatreche C, Hamri A.
Sifi Y, et al.
J Neurodegener Dis. 2013;2013:903875. doi: 10.1155/2013/903875. Epub 2013 Mar 24.
J Neurodegener Dis. 2013.
PMID: 26317002
Free PMC article.
Item in Clipboard
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays.
H'mida-Ben Brahim D, M'zahem A, Assoum M, Bouhlal Y, Fattori F, Anheim M, Ali-Pacha L, Ferrat F, Chaouch M, Lagier-Tourenne C, Drouot N, Thibaut C, Benhassine T, Sifi Y, Stoppa-Lyonnet D, N'Guyen K, Poujet J, Hamri A, Hentati F, Amouri R, Santorelli FM, Tazir M, Koenig M.
H'mida-Ben Brahim D, et al. Among authors: sifi y.
J Neurol. 2011 Jan;258(1):56-67. doi: 10.1007/s00415-010-5682-5. Epub 2010 Aug 27.
J Neurol. 2011.
PMID: 20798953
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