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1. El Amrani, B; Barnoussi, M; Fliyou, M; Chaouch, M; Sayouri, S
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2. Oukili, O; Chaouch, M; Rafiq, M; Hadji, M; Hamdi, M; Benlemlih, M
   Bleaching of olive mill wastewater by clay in the presence of hydrogen peroxide
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   CHLORIDE-HYDROGENOPHOSPHATE ION-EXCHANGE INTO THE ZINC-ALUMINUM-CHLORIDE LAYERED DOUBLE HYDROXIDE
   Materials chemistry and physics
   
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4. KHALDI M; DEROY A; CHAOUCH M; BESSE JP
   A NEW STRATEGY FOR SYNTHESIS OF DIFFERENT VARIETIES OF SULFATE INTERCALATED ZINC-CHROMIUM LAMELLAR DOUBLE HYDROXIDES
   Annales de chimie
   
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5. Khaldi, M; Badreddine, M; Legrouri, A; Chaouch, M; Barroug, A; De Roy, A; Besse, JP
   Preparation of a well-ordered layered nanocomposite from zinc-aluminum-chloride layered double hydroxide and hydrogenophosphate by ion exchange
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   INFLUENCE OF THE SUBSTRATE MATERIAL, SUBSTRATE-TEMPERATURE AND SPUTTERED LEAD FLUX ON THE IN-SITU PEROVSKITE PHASE-FORMATION
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7. EYMARD B; ROMERO NB; LETURCQ F; PICCOLO F; CARRIE A; JEANPIERRE M; COLLIN H; DEBURGRAVE N; AZIBI K; CHAOUCH M; MERLINI L; THEMARNOEL C; PENISSON I; MAYER M; TANGUY O; CAMPBELL KP; KAPLAN JC; TOME FMS; FARDEAU M
   PRIMARY ADHALINOPATHY (ALPHA-SARCOGLYCANOPATHY) - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATION IN 20 PATIENTS WITH AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY
   Neurology
   
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8. KHALDI M; DEROY A; CHAOUCH M; BESSE JP
   NEW VARIETIES OF ZINC-CHROMIUM-SULFATE LAMELLAR DOUBLE HYDROXIDES
   Journal of solid state chemistry
   
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   ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS
   Neurology
   
   B. Eymard et al., "ADHALIN-DEFICIENT MUSCULAR-DYSTROPHIES - CLINICAL, PATHOLOGICAL, AND GENETIC CORRELATIONS", Neurology, 46(2), 1996, pp. 68006-68006
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    ABSENCE OF GAMMA-SARCOGLYCAN (35-DAG) IN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY LINKED TO CHROMOSOME 13Q12
    FEBS letters
    
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    PRIMARY ADHALINOPATHY - A COMMON-CAUSE OF AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY OF VARIABLE SEVERITY
    Nature genetics
    
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12. YAMADA H; TOME FMS; HIGUCHI I; KAWAI H; AZIBI K; CHAOUCH M; ROBERDS SL; TANAKA T; FUJITA S; MITSUI T; FUKUNAGA H; MIYOSHI K; OSAME M; FARDEAU M; KAPLAN JC; SHIMIZU T; CAMPBELL KP; MATSUMURA K
    LAMININ ABNORMALITY IN SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY
    Laboratory investigation
    
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    SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH THE DEFICIENCY OF THE 50 KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN MAPS TO CHROMOSOME-13Q12
    Human molecular genetics
    
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