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Asthme aigu grave : épidémiologie, facteur de risque et reconnaissance

Perfectionnement en Pédiatrie, 2021-05, Vol.4 (2), p.E33-E34

2021

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L’otite externe nécrosante chez le diabétique : quelles particularités ?

Annales d'endocrinologie, 2023-10, Vol.84 (5), p.632-633

2023

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First-principles calculation of the structural and elastic properties of ternary metal nitrides TaxMo1-xN and TaxW1-xN

Journal of physics. Conference series, 2015, Vol.640 (1)

2015

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Structural and elastic properties of ternary metal nitrides TixTa1−xN alloys: First-principles calculations versus experiments

Surface & coatings technology, 2013-01, Vol.215, p.199-208

2013

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Corrélations phénotype-génotype des patients pédiatriques porteurs de mutations bi-alléliques du gène lié au surfactant ABCA3

Revue des maladies respiratoires actualités, 2024-01, Vol.16 (1), p.21-22

2024

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Bronchiolite : faire aussi bien en prescrivant moins

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2016-12, Vol.23 (12), p.1296-1296

2016

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Influence of contact coefficients on vibrational behavior of PM machines in a complete study

International journal of applied electromagnetics and mechanics, 2018-04, Vol.57, p.95-106

2018

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First-principles calculation of the structural and elastic properties of ternary metal nitrides Ta x Mo 1-x N and Ta x W 1-x N

Journal of physics. Conference series, 2015-09, Vol.640, p.12022

2015

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Computational Study of Mechanical and Electronic Properties of Transition Metal Carbides Ti x M 1– x C with M = Nb, V and Zr

Journal of nanoelectronics and optoelectronics, 2019-05, Vol.14 (5), p.622-625

2019

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International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome

Journal of the neurological sciences, 1997-02, Vol.145 (2), p.205-211

1997

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Locked posterior dislocation of the shoulder: A report of three cases

Chirurgie de la main, 2015-04, Vol.34 (2), p.98-101

2015

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Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

Science (American Association for the Advancement of Science), 1995-11, Vol.270 (5237), p.819-822

1995

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Ceramic Femoral Head Fracture and Severe Wear of the Cone: A Case Report and Review of the Literature

Journal of Medical Diagnostic Methods, 2016, Vol.5 (1)

2016

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Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein

Nature genetics, 1995-02, Vol.9 (2), p.141-145

1995

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Pericytic Tumors of the Kidney – A Clinicopathologic Analysis of 17 Cases

Human pathology, 2017-06, Vol.64, p.106-117

2017

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Large wind turbine generators: State-of-the-art review

2018 XIII International Conference on Electrical Machines (ICEM), 2018, p.2205-2211

2018

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Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

Nature genetics, 1993-10, Vol.5 (2), p.195-200

1993

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Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35

Nature genetics, 1994-07, Vol.7 (3), p.425-428

1994

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Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

Neurology, 1995-04, Vol.45 (4), p.768-772

1995

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Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

Brain (London, England : 1878), 1990-04, Vol.113 (2), p.347-363

1990

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Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q

Nature genetics, 1992-12, Vol.2 (4), p.315-317

1992

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Reluctance network - Lumped mechanical & thermal models for the modeling of concentrated flux synchronous machine

2017 18th International Symposium on Electromagnetic Fields in Mechatronics, Electrical and Electronic Engineering (ISEF) Book of Abstracts, 2017, p.1-2

2017

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Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease

Journal of rheumatology, 1994-12, Vol.21 (12), p.2301

1994

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Friedreich's ataxia with isolated vitamin E deficiency : a neuropathological study of a Tunisian patient

Acta neuropathologica, 1997-06, Vol.93 (6), p.633-637

1997

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Vibrational behavior investigation approach and Influence of contact coefficient on stator natural frequencies

2017 18th International Symposium on Electromagnetic Fields in Mechatronics, Electrical and Electronic Engineering (ISEF) Book of Abstracts, 2017, p.1-2

2017

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Asthme aigu grave : épidémiologie, facteur de risque et reconnaissance

L’otite externe nécrosante chez le diabétique : quelles particularités ?

First-principles calculation of the structural and elastic properties of ternary metal nitrides TaxMo1-xN and TaxW1-xN

Structural and elastic properties of ternary metal nitrides TixTa1−xN alloys: First-principles calculations versus experiments

Corrélations phénotype-génotype des patients pédiatriques porteurs de mutations bi-alléliques du gène lié au surfactant ABCA3

Bronchiolite : faire aussi bien en prescrivant moins

Influence of contact coefficients on vibrational behavior of PM machines in a complete study

First-principles calculation of the structural and elastic properties of ternary metal nitrides Ta x Mo 1-x N and Ta x W 1-x N

Computational Study of Mechanical and Electronic Properties of Transition Metal Carbides Ti x M 1– x C with M = Nb, V and Zr

International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome

Locked posterior dislocation of the shoulder: A report of three cases

Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy

Ceramic Femoral Head Fracture and Severe Wear of the Cone: A Case Report and Review of the Literature

Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein

Pericytic Tumors of the Kidney – A Clinicopathologic Analysis of 17 Cases

Large wind turbine generators: State-of-the-art review

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q

Reluctance network - Lumped mechanical & thermal models for the modeling of concentrated flux synchronous machine

Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease

Friedreich's ataxia with isolated vitamin E deficiency : a neuropathological study of a Tunisian patient

Vibrational behavior investigation approach and Influence of contact coefficient on stator natural frequencies

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