Search Results - "Amiour, M"

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  1. 1

    Apel: A Graphical Yet Executable Formalism for Process Modeling by Dami, S, Estublier, J, Amiour, M

    Published in Automated software engineering (01-01-1998)
    “…Software process improvement requires high level formalisms for describing project-specific, organizational and quality aspects. These formalisms must be…”
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    Journal Article
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    Macrolides, Pseudomonas aeruginosa and cystic fibrosis by Guillot, M, Amiour, M, El Hachem, C, Harchaoui, S, Ribault, V, Paris, C

    “…Long-term low dose azithromycin treatment in cystic fibrosis patients with chronic Pseudomonas aeruginosa infection is safe and reduces the decline in lung…”
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  3. 3

    A furoncular ankle cellulitis in a teenager with a difference: Dermatobia hominis by Flandrois, M, El Hachem, C, Amiour, M, Ribault, V, Harchaoui, S, Mellah, D, Roth, F X, Dolezon, M L, Al Khoury, M, Vaillant, J M, Paris, C, Guillot, M

    “…We report a case of botfly myiasis presenting as an ankle cellulitis in a teenager returning from Guyana. Main clinical features and therapeutic approaches are…”
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  4. 4

    Hurler syndrome. Early diagnosis and successful enzyme replacement therapy: a new therapeutic approach. Case report by Dupont, C, El Hachem, C, Harchaoui, S, Ribault, V, Amiour, M, Guillot, M, Maire, I, Froissart, R, Guffon-Fouilhoux, N

    “…Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder due to alpha-L-iduronidase deficiency. Its severe prognosis has been significantly…”
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  5. 5

    Mucopolysaccharidose de type I : intérêt d’un diagnostic et d’une enzymothérapie substitutive précoces. À propos d’un cas by Dupont, C., Hachem, C. El, Harchaoui, S., Ribault, V., Amiour, M., Guillot, M., Maire, I., Froissart, R., Guffon-Fouilhoux, N.

    “…La mucopolysaccharidose de type I (MPS I) est une maladie de surcharge lysosomiale due à un déficit en α-L-iduronidase, dont le pronostic a été amélioré par…”
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  6. 6

    Un passager clandestin à ne pas méconnaître : Dermatobia hominis, à propos d’un cas by Flandrois, M., El Hachem, C., Amiour, M., Ribault, V., Harchaoui, S., Mellah, D., Roth, F.X., Dolezon, M.L., Al Khoury, M., Vaillant, J.M., Paris, C., Guillot, M.

    Published in Archives de pédiatrie (Paris) (2009)
    “…Dermatobia hominis est une mouche américaine responsable en pathologie humaine d’une zoonose inhabituelle. Les présentations cliniques principales ainsi que…”
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    Journal Article Conference Proceeding
  7. 7

    Œdème angioneurotique héréditaire : à propos d'une observation chez un enfant de trois ans by El-Hachem, C., Amiour, M., Guillot, M., Laurent, J.

    “…L'œdème angioneurotique héréditaire est une maladie autosomique dominante exceptionnelle (1/150 000) qu'il importe de reconnaître car elle peut mettre en jeu…”
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    Varicelle, artériopathie aiguë post-infectieuse et infarctus cérébral artériel de l'enfant : Un cadre clinique et étiologique à ne pas méconnaître by Guillot, M., El Hachem, C., Amiour, M., Harchaoui, S., Bessière, A., Lasjaunias, P., Mafoufi, N., Tardieu, M.

    Published in Archives de pédiatrie (Paris) (01-04-2005)
    “…Les artériopathies aiguës sont responsables du quart des infarctus cérébraux artériels de l'enfant; les accidents vasculaires qu'elles induisent présentent des…”
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    Journal Article Conference Proceeding
  10. 10

    Méningite bactérienne à Haemophilus influenzae : le risque résiduel ; à propos d’un cas by Guillot, M, Eckart, P, Amiour, M, El-Hachem, C, Paris, C, Dabernat, H

    “…La survenue d’une méningite bactérienne à Haemophilus influenzae, depuis la généralisation de la vaccination contre ce germe pathogène, est un événement rare…”
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  11. 11

    Amylose rénale secondaire et mucoviscidose by Guillot, M., Drut-Desombre, B., Amiour, M., Aljazayri, Z., Eckart, P., Dominique, S., Grateau, G.

    Published in Archives de pédiatrie (Paris) (01-08-1998)
    “…L'amélioration de la prise en charge de patients atteints de mucoviscidose a permis un allongement de l'espérance de vie favorisant l'émergence de nouvelles…”
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    Journal Article Conference Proceeding
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    Hereditary angioneurotic edema: a case report in a 3-year-old child by El-Hachem, C, Amiour, M, Guillot, M, Laurent, J

    “…Hereditary angioneurotic edema is a dominant autosomal disease (incidence 1/150,000), whose diagnosis is crucial as this condition can lead to fatal asphyxia…”
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  14. 14

    Varicella, acute postinfectious arteriopathy and cerebral arterial thrombosis in childhood: a unique clinical and etiologic framework to be fully acknowledged by Guillot, M, El Hachem, C, Amiour, M, Harchaoui, S, Bessière, A, Lasjaunias, P, Mafoufi, N, Tardieu, M

    “…Acute arteriopathies are the etiological factor of 25% of all the cerebral arterial thrombosis cases in childhood; they give way to ischemic strokes which have…”
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  15. 15

    Aspergillosis in cystic fibrosis patients by Guillot, M, El Hachem, C, Amiour, M, Delaisi, B, Reinert, P

    “…Allergic bronchopulmonary aspergillosis (ABPA) should be suspected in any CF patient whose pulmonary disease deteriorates precipitously, suddenly or…”
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  16. 16

    Haemophilus influenzae bacterial meningitis: residual risk; case report by Guillot, M, Eckart, P, Amiour, M, el-Hachem, C, Paris, C, Dabernat, H

    “…Bacterial meningitis due to Haemophilus influenzae has become a rare, albeit not exceptional occurrence since generalized vaccination against that pathogen was…”
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  17. 17

    Pseudotumoral presentation of cat scratch disease by Eckart, P, Tournade, G, Amiour, M, Guillot, M, Courthéoux, P, Rousselot, P

    “…A frequent cause of chronic benign lymphadenopathy, cat-scratch disease (CSD) occurs mainly in children and young adults. Bartonella henselae is the agent…”
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  18. 18

    Home environment and acute propylene glycol intoxication in a two-year old. An unusual case report by Guillot, M, Bocquet, G, Eckart, P, Amiour, M, el-Hachem, C, Garnier, R, Galliot-Guilley, M, Haguenoer, J M

    “…Acute propylene glycol intoxication in a two-year-old toddler underlines the potentially serious toxicity in children of this chemical agent present as a…”
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  19. 19

    Osteogenesis imperfecta: a new, early therapeutic approach with biphosphonates. A case report by Guillot, M, Eckart, P, Desrosieres, H, Amiour, M, al-Jazayri, Z

    “…Management of type III osteogenesis imperfecta (O.I.) (brittle bone disease) is primarily supportive; early introduction of cyclic intravenous pamidronate…”
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  20. 20

    Secondary kidney amyloidosis and mucoviscidosis by Guillot, M, Drut-Desombre, B, Amiour, M, Aljazayri, Z, Eckart, P, Dominique, S, Grateau, G

    “…Due to the improvement in cystic fibrosis management, life expectancy has risen; on the other hand, longer survival has led to new complications, including…”
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