Search Results - "Amsallem, D."

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    An adaptive and efficient greedy procedure for the optimal training of parametric reduced-order models by Paul-Dubois-Taine, A., Amsallem, D.

    “…SummaryAn adaptive and efficient approach for constructing reduced‐order models (ROMs) that are robust to changes in parameters is developed. The approach is…”
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    Journal Article
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    A posteriori error estimators for linear reduced-order models using Krylov-based integrators by Amsallem, D., Hetmaniuk, U.

    “…SummaryReduced‐order models for linear time‐invariant dynamical systems are considered, and the error between the full‐order model and the reduced‐order model…”
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    Journal Article
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    Rett‐like phenotypes: expanding the genetic heterogeneity to the KCNA2 gene and first familial case of CDKL5‐related disease by Allou, L., Julia, S., Amsallem, D., El Chehadeh, S., Lambert, L., Thevenon, J., Duffourd, Y., Saunier, A., Bouquet, P., Pere, S., Moustaïne, A., Ruaud, L., Roth, V., Jonveaux, P., Philippe, C.

    Published in Clinical genetics (01-03-2017)
    “…Several genes have been implicated in Rett syndrome (RTT) in its typical and variant forms. We applied next‐generation sequencing (NGS) to evaluate for…”
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    Journal Article
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    Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females by Philippe, C, Amsallem, D, Francannet, C, Lambert, L, Saunier, A, Verneau, F, Jonveaux, P

    Published in Journal of medical genetics (01-01-2010)
    “…The FOXG1 gene has been recently implicated in the congenital form of Rett syndrome (RTT). It encodes the fork-head box protein G1, a winged-helix…”
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    Journal Article
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    RELN and VLDLR mutations underlie two distinguishable clinico-radiological phenotypes by Valence, S., Garel, C., Barth, M., Toutain, A., Paris, C., Amsallem, D., Barthez, M.-A., Mayer, M., Rodriguez, D., Burglen, L.

    Published in Clinical genetics (01-12-2016)
    “…Pontocerebellar hypoplasias (PCH) are characterized by lack of development and/or early neurodegeneration of cerebellum and brainstem. We report five patients…”
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    Journal Article
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    Vertebral-artery dissection following a judo session: a case report by Lannuzel, A, Moulin, T, Amsallem, D, Galmiche, J, Rumbach, L

    Published in Neuropediatrics (01-04-1994)
    “…A few days after a judo session, an 11-year-old boy presented with an ischemic stroke with dizziness, aphasia and ataxia. CCT scan revealed a left thalamic…”
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    Journal Article
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    Empirical treatment of fever in neutropenic children: the role of the carbapenems by COMETTA, ALAIN, VISCOLI, CLAUDIO, CASTAGNOLA, ELIO, MASSIMO, LUISA, GIACCHINO, RAFFAELE, GIBSON, BRENDA, GIACCHINO, MAREVA, BALBO, LUCIANO, ENGELHARD, DAN, SHAPIRO, MERRWYN, AMSALLEM, DANIEL, ESTAVOYER, JEAN-MARIE, FERSTER, ALINA, GLAUSER, MICHEL P

    Published in The Pediatric infectious disease journal (01-08-1996)
    “…The occurrence of fever during periods of neutropenia in children with cancer presents a difficult problem for the clinician. Neutropenic patients are at high…”
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    Journal Article Conference Proceeding
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    Four-Component Reactions for a New Diastereoselective Synthesis of Chiral Quaternary Centers by Sklute, Genia, Amsallem, Deborah, Shabli, Amal, Varghese, Jos P, Marek, Ilan

    Published in Journal of the American Chemical Society (01-10-2003)
    “…The one-pot preparation of chiral homoallylic alcohol and amine derivatives was easily achieved by carbocupration of alkynyl sulfoxides followed by an in situ…”
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    Journal Article
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    Why Did Infection with Aeromonas hydrophila Occur When Water Contains So Many Other Microorganisms? by Cailleaux, Vincent, Dupont, Marie-Jeanne, Dory, Bernard, Amsallem, Daniel, Michel-Briand, Yvon

    Published in Clinical infectious diseases (01-01-1993)
    “…Aeromonas hydrophila is a gram-negative bacillus commonly found in water. It is responsible for a number of diseases in cold-blooded animals (e.g., fish,…”
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    Journal Article
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    A detailed analysis of the MECP2 gene : prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients by BOURDON, Violaine, PHILIPPE, Christophe, LABRUNE, Orianne, AMSALLEM, Daniel, ARNOULD, Cécile, JONVEAUX, Philippe

    Published in Human genetics (01-01-2001)
    “…Mutations in the X-linked methyl-CpG-binding protein 2 gene (MECP2) have been found to be a cause of Rett syndrome (RTT). In order to provide further insights…”
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    Journal Article
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    SFP P-072 – Encéphalopathie épileptique précoce: à propos de 3 cas by Goffeney, J., Dumont, P., Neumann, F., Chelabi, R., Comte, A., Amsallem, D., Altuzarra, C.

    “…Les crises convulsives chez le nouveau-né et le nourrisson de moins de 2 mois peuvent être un signe précoce d’encéphalopathie. Nous rapportons 3 observations…”
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    Journal Article
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