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Application of direct contact membrane distillation for textile wastewater treatment and fouling study

Separation and purification technology, 2019-01, Vol.209, p.815-825

2019

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Dépression et anxiété chez des patients tunisiens atteints de cancers colorectaux : spécificités et ampleur

Psycho-oncologie, 2019-06, Vol.13 (2), p.105-111

2019

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Robotic colectomy with CME versus laparoscopic colon resection with or without CME for colon cancer: a systematic review and meta-analysis

Annals of the Royal College of Surgeons of England, 2023-02, Vol.105 (2), p.113

2023

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Wood thermodegradation: experimental analysis and modeling of mass loss kinetics

Maderas, 2014, Vol.16 (ahead), p.133-148

2014

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5610131 A STANDARDISED LANGUAGE TAG PROTOCOL AND WORKFLOW FOR DEVELOPING AND MANAGING MULTILINGUAL ONTOLOGIES: SHOWCASING THE FRENCH SICKLE CELL DISEASE ONTOLOGY (SCDO)

HemaSphere, 2023-04, Vol.7 (S1), p.42-43

2023

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Atypical pantothenate kinase-associated neurodegeneration: Clinical description of two brothers and a review of the literature

Revue neurologique, 2017-12, Vol.173 (10), p.658-662

2017

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Experimental and numerical analysis of wood thermodegradation: Mass loss kinetics

Journal of thermal analysis and calorimetry, 2012-08, Vol.109 (2), p.907-914

2012

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Production of the Bioenergy from the Industrial Waste

Materials today : proceedings, 2019, Vol.13, p.607-614

2019

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Lichnerowicz inequality on foliated manifold with a parallel 2-form

Bulletin of the Belgian Mathematical Society, Simon Stevin, 2012-04, Vol.19 (2), p.229-237

Chaouch, M.A

2012

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Le profil clinique, évolutif, électrophysiologique et anatomopathologique de la maladie de Charcot-Marie-Tooth (CMT) à transmission autosomale récessive liée aux gènes GDAP1, MTMR2 et FGD4/FRABIN

Revue neurologique, 2013-04, Vol.169, p.A48-A48

2013

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Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C

Brain (London, England : 1878), 2004-01, Vol.127 (1), p.154-163

2004

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Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa

Annals of human genetics, 2008-09, Vol.72 (5), p.590-597

2008

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The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene

Neuromuscular disorders : NMD, 2003-01, Vol.13 (1), p.60-67

2003

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Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays

Journal of neurology, 2011, Vol.258 (1), p.56-67

2011

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LATENT CLASS ANALYSIS IN DIAGNOSTIC TESTS EVALUATION FOR CANINE LEISHMANIA INFANTUM INFECTION

Archives de l'Institut Pasteur de Tunis, 2014, Vol.91 (1-4), p.51

2014

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Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11

Journal of medical genetics, 2005-03, Vol.42 (3), p.260-265

2005

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Théorèmes de type Obata pour certains feuilletages riemanniens

Comptes rendus. Mathématique, 2013-02, Vol.351 (3-4), p.123-126

Chaouch, M.A.

2013

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Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

American journal of human genetics, 2002-03, Vol.70 (3), p.726-736

2002

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G.P.10.01 DMD and SGCG molecular analysis in 200 Algerian patients affected with progressive muscular dystrophies

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.620-620

2009

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Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H

American journal of human genetics, 2007-07, Vol.81 (1), p.1-16

2007

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Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations

Journal of medical genetics, 2003-07, Vol.40 (7), p.e87-87

2003

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Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Nature genetics, 1995-06, Vol.10 (2), p.243-245

1995

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Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy

Neurology, 1997-05, Vol.48 (5), p.1227

1997

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Transulnar versus transradial artery approach for coronary angioplasty: The PCVI-CUBA study

Catheterization and cardiovascular interventions, 2006-05, Vol.67 (5), p.711-720

2006

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Limiting law results for a class of conditional mode estimates for functional stationary ergodic data

Mathematical methods of statistics, 2016-07, Vol.25 (3), p.168-195

2016

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Application of direct contact membrane distillation for textile wastewater treatment and fouling study

Dépression et anxiété chez des patients tunisiens atteints de cancers colorectaux : spécificités et ampleur

Robotic colectomy with CME versus laparoscopic colon resection with or without CME for colon cancer: a systematic review and meta-analysis

Wood thermodegradation: experimental analysis and modeling of mass loss kinetics

5610131 A STANDARDISED LANGUAGE TAG PROTOCOL AND WORKFLOW FOR DEVELOPING AND MANAGING MULTILINGUAL ONTOLOGIES: SHOWCASING THE FRENCH SICKLE CELL DISEASE ONTOLOGY (SCDO)

Atypical pantothenate kinase-associated neurodegeneration: Clinical description of two brothers and a review of the literature

Experimental and numerical analysis of wood thermodegradation: Mass loss kinetics

Production of the Bioenergy from the Industrial Waste

Lichnerowicz inequality on foliated manifold with a parallel 2-form

Le profil clinique, évolutif, électrophysiologique et anatomopathologique de la maladie de Charcot-Marie-Tooth (CMT) à transmission autosomale récessive liée aux gènes GDAP1, MTMR2 et FGD4/FRABIN

Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C

Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa

The phenotypic manifestations of autosomal recessive axonal Charcot-Marie-Tooth due to a mutation in Lamin A/C gene

Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays

LATENT CLASS ANALYSIS IN DIAGNOSTIC TESTS EVALUATION FOR CANINE LEISHMANIA INFANTUM INFECTION

Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11

Théorèmes de type Obata pour certains feuilletages riemanniens

Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

G.P.10.01 DMD and SGCG molecular analysis in 200 Algerian patients affected with progressive muscular dystrophies

Mutations in FGD4 Encoding the Rho GDP/GTP Exchange Factor FRABIN Cause Autosomal Recessive Charcot-Marie-Tooth Type 4H

Phenotypic and genetic exploration of severe demyelinating and secondary axonal neuropathies resulting from GDAP1 nonsense and splicing mutations

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy

Transulnar versus transradial artery approach for coronary angioplasty: The PCVI-CUBA study

Limiting law results for a class of conditional mode estimates for functional stationary ergodic data

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