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I Feki

Showing results (11-20 of 17) with videos related to

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Gynecologie, Obstetrique, Fertilite & Senologie|July 29, 2017
[Post-partum depressive symptoms: Prevalence, risk factors and relationship with quality of life]R Cherif, I Feki, H Gassara, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34B Fontaine, C S Davoine, A Dürr, et al.
Revue Neurologique|March 1, 1997
[Lupic spinal cord diseases and antiphospholipid antibodies]I Feki, M Ben Hmida, H Masmoudi, et al.
Archives of Neurology|March 14, 2000
Frequency of the DYT1 mutation in primary torsion dystonia without family historyD Brassat, A Camuzat, M Vidailhet, et al.
La Revue De Medecine Interne|March 17, 2009
[Cardiac involvement in Steinert myotonic dystrophy]M I Miladi, H Charfeddine, I Feki, et al.
Clinical Genetics|May 15, 2009
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneityA Boukhris, G Stevanin, I Feki, et al.
Human Molecular Genetics|March 4, 2000
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegiaN Fonknechten, D Mavel, P Byrne, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Gynecologie, Obstetrique, Fertilite & Senologie|July 29, 2017
[Post-partum depressive symptoms: Prevalence, risk factors and relationship with quality of life]R Cherif, I Feki, H Gassara, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34B Fontaine, C S Davoine, A Dürr, et al.
Revue Neurologique|March 1, 1997
[Lupic spinal cord diseases and antiphospholipid antibodies]I Feki, M Ben Hmida, H Masmoudi, et al.
Archives of Neurology|March 14, 2000
Frequency of the DYT1 mutation in primary torsion dystonia without family historyD Brassat, A Camuzat, M Vidailhet, et al.
La Revue De Medecine Interne|March 17, 2009
[Cardiac involvement in Steinert myotonic dystrophy]M I Miladi, H Charfeddine, I Feki, et al.
Clinical Genetics|May 15, 2009
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneityA Boukhris, G Stevanin, I Feki, et al.
Human Molecular Genetics|March 4, 2000
Spectrum of SPG4 mutations in autosomal dominant spastic paraplegiaN Fonknechten, D Mavel, P Byrne, et al.
Pageof 2