Search Results - "Cosson, A"

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    Identification and quantification of key phytochemicals in peas – Linking compounds with sensory attributes by Cosson, A., Meudec, E., Ginies, C., Danel, A., Lieben, P., Descamps, N., Cheynier, V., Saint-Eve, A., Souchon, I.

    Published in Food chemistry (15-08-2022)
    “…[Display omitted] Pea protein isolates contain high-quality plant protein. However, they have sensory drawbacks, notably bitterness and astringency, that have…”
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    Journal Article
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    Long-term outcome in methylmalonic aciduria: A series of 30 French patients by Cosson, M.A., Benoist, J.F., Touati, G., Déchaux, M., Royer, N., Grandin, L., Jais, J.P., Boddaert, N., Barbier, V., Desguerre, I., Campeau, P.M., Rabier, D., Valayannopoulos, V., Niaudet, P., de Lonlay, P.

    Published in Molecular genetics and metabolism (01-07-2009)
    “…To better delineate the natural history of patients with methylmalonic aciduria (MMA). Thirty patients with vitamin-B 12-unresponsive MMA (25 aged 1.5 to 22.0…”
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    Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using a 'real time' quantitative RT-PCR assay by PREUDHOMME, C, REVILLION, F, MERLAT, A, HORNEZ, L, ROUMIER, C, DUFLOS-GRARDEL, N, JOUET, J. P, COSSON, A, PEYRAT, J. P, FENAUX, P

    Published in Leukemia (01-06-1999)
    “…Quantitative competitive RT-PCR techniques have been developed to detect BCR-ABL fusion transcripts in CML but they are hardly reproducible. In this work, we…”
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    Increased Trypanosoma cruzi Invasion and Heart Fibrosis Associated with High Transforming Growth Factor β Levels in Mice Deficient in α2-Macroglobulin by WAGHABI, M. C, COUTINHO, C. M. L. M, SOEIRO, M. N. C, PEREIRA, M. C. S, FEIGE, J.-J, KERAMIDAS, M, COSSON, A, MINOPRIO, P, VAN LEUVEN, F, ARAUJO-JORGE, T. C

    Published in Infection and Immunity (01-09-2002)
    “…Classifications Services IAI Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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    Severe form of hereditary neuralgic amyotrophy without SEPT9 gene mutation by Cosson, A, Mathieu, A, Sevrin, P, Nollet, S, Tatu, L

    Published in Revue neurologique (01-02-2011)
    “…Hereditary neuralgic amyotrophy (HNA) is a rare condition characterized by recurrent episodes of painful paralysis preferentially affecting the brachial…”
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    Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria by Cosson, M.A., Touati, G., Lacaille, F., Valayannnopoulos, V., Guyot, C., Guest, G., Verkarre, V., Chrétien, D., Rabier, D., Munnich, A., Benoist, J.F., de Keyzer, Y., Niaudet, P., de Lonlay, P.

    Published in Molecular genetics and metabolism (01-09-2008)
    “…A boy who was diagnosed with methylmalonic aciduria (MMA) at the age of 10 days developed persistent hepatomegaly and raised transaminases from the age of 4…”
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    Emergency department management of maxillofacial trauma by Lynham, Anthony J, Hirst, Julian P, Cosson, John A, Chapman, Pat J, McEniery, Paul

    Published in Emergency medicine (Fremantle, W.A.) (01-02-2004)
    “…This paper highlights critical aspects of examination, diagnosis and early management of the maxillofacial trauma patient…”
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    Arterial vascularization of the human thalamus: extra-parenchymal arterial groups by COSSON, A, TATU, L, VUILLIER, F, PARRATTE, B, DIOP, M, MONNIER, Guy

    “…The problem of the arterial vascularization of the human thalamus has been debated at length. Anatomical references concerning the thalamic arterial groups are…”
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    Névralgie amyotrophiante héréditaire à forme sévère sans mutation du gène SEPT9 by Cosson, A., Mathieu, A., Sevrin, P., Nollet, S., Tatu, L.

    Published in Revue neurologique (01-02-2011)
    “…La névralgie amyotrophiante héréditaire (NAH) est une affection rare caractérisée par des épisodes récidivants de paralysies douloureuses affectant…”
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    The French Hæmovigilance System by Noel, L., Debeir, J., Cosson, A.

    Published in Vox sanguinis (01-06-1998)
    “…Hæmovigilance was part of the reform of the French transfusion system. The hæmovigilance network is now operational with approximately 4600 transfusion…”
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    Journal Article Conference Proceeding
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    Expression of the multidrug resistance‐associated protein in myelodysplastic syndromes by Poulain, Stéphanie, Lepelley, Pascale, Preudhomme, Claude, Cambier, Nathalie, Cornillon, Jérome, Wattel, Eric, Cosson, Alain, Fenaux, Pierre

    Published in British journal of haematology (01-09-2000)
    “…In the myelodysplastic syndromes (MDS), P‐glycoprotein (P‐gp) expression is clinically associated with drug resistance, whereas the clinical significance of…”
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    Good correlation between RT-PCR analysis and relapse in Philadelphia (Ph1)-positive acute lymphoblastic leukemia (ALL) by PREUDHOMME, C, HENIC, N, COSSON, A, FENAUX, P, CAZIN, B, LAÏ, J. L, BERTHEAS, M. F, VANRUMBEKE, M, LEMOINE, F, JOUET, J. P, DECONNINCK, E, NELKEN, B

    Published in Leukemia (01-02-1997)
    “…We sequentially performed cytogenetic analysis and RT-PCR analysis of BCR-ABL transcripts in 17 cases of Ph1-positive ALL who had achieved hematological…”
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    The French Haemovigilance System by Debeir, Joëlle, Noel, Luc, Aullen, Jean-Patrice, Frette, Catherine, Sari, Fatih, Vo Mai, Mai Phuong, Cosson, Alain

    Published in Vox sanguinis (01-01-1999)
    “…Haemovigilance is a national system of surveillance and alarm, from blood collection to the follow–up of the recipients, gathering and analysing all untoward…”
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    Présentation inhabituelle d’une malformation costale by Cosson, M.-A., Breton, S., Aprahamian, A., Grevent, D., Cheron, G.

    “…Les malformations costales et la conduite à tenir devant leur découverte souvent fortuite restent peu connues. Nous rapportons le cas d’une fillette de 4ans et…”
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    bcl-2 expression in myelodysplastic syndromes and its correlation with hematological features, p53 mutations and prognosis by Lepelley, P, Soenen, V, Preudhomme, C, Merlat, A, Cosson, A, Fenaux, P

    Published in Leukemia (01-04-1995)
    “…We looked for bcl-2 protein expression by immunocytochemistry on bone marrow slides from 51 cases of myelodysplastic syndrome (MDS), of whom 25 received some…”
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