Genetics of hypophosphatasia
Mornet, E.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2017)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.05.2017)
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Tissue-nonspecific alkaline phosphatase is an anti-inflammatory nucleotidase
Bessueille, L., Briolay, A., Como, J., Mebarek, S., Mansouri, C., Gleizes, M., El Jamal, A., Buchet, R., Dumontet, C., Matera, E.L., Mornet, E., Millan, J.L., Fonta, C., Magne, D.
Published in Bone (New York, N.Y.) (01.04.2020)
Published in Bone (New York, N.Y.) (01.04.2020)
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Haemangioma of the temporal bone
Roubaud, J.-C., Leclere, J.-C., Mornet, E., Marianowski, R.
Published in European annals of otorhinolaryngology, head and neck diseases (01.01.2021)
Published in European annals of otorhinolaryngology, head and neck diseases (01.01.2021)
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Neurosurgical aspects of childhood hypophosphatasia
Collmann, H, Mornet, E, Gattenlöhner, S, Beck, C, Girschick, H
Published in Child's nervous system (01.02.2009)
Published in Child's nervous system (01.02.2009)
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Enzyme-replacement therapy in perinatal hypophosphatasia: Case report and review of the literature
Rougier, H., Desrumaux, A., Bouchon, N., Wroblewski, I., Pin, I., Nugues, F., Mornet, E., Baujat, G.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.10.2018)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.10.2018)
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Intralabyrinthine sporadic endolymphatic sac tumour
Lucas, C., Leclère, J.-C., Mornet, E., Marianowski, R.
Published in European annals of otorhinolaryngology, head and neck diseases (01.04.2018)
Published in European annals of otorhinolaryngology, head and neck diseases (01.04.2018)
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A new mechanism of dominance in hypophosphatasia: the mutated protein can disturb the cell localization of the wild-type protein
Lia-Baldini, A. S., Brun-Heath, I., Carrion, C., Simon-Bouy, B., Serre, J. L., Nunes, M. E., Mornet, E.
Published in Human genetics (01.05.2008)
Published in Human genetics (01.05.2008)
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Assessment of chronic childhood dysphonia
Mornet, E, Coulombeau, B, Fayoux, P, Marie, J.-P, Nicollas, R, Robert-Rochet, D, Marianowski, R
Published in European annals of otorhinolaryngology, head and neck diseases (01.11.2014)
Published in European annals of otorhinolaryngology, head and neck diseases (01.11.2014)
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Outpatient hemithyroidectomy
Lacroix, C, Potard, G, Clodic, C, Mornet, E, Valette, G, Marianowski, R
Published in European annals of otorhinolaryngology, head and neck diseases (01.02.2014)
Published in European annals of otorhinolaryngology, head and neck diseases (01.02.2014)
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Recurrent neuroendocrine adenoma of the middle ear: A case report
Gobel, Y, La Croix, C, Mornet, E, Marianowski, R
Published in European annals of otorhinolaryngology, head and neck diseases (01.09.2014)
Published in European annals of otorhinolaryngology, head and neck diseases (01.09.2014)
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Interpretation of suspect head and neck fixations seen on PET/CT in lung cancer
Gobel, Y, Valette, G, Abgral, R, Clodic, C, Mornet, E, Potard, G, Salaun, P.-Y, Marianowski, R
Published in European annals of otorhinolaryngology, head and neck diseases (01.09.2014)
Published in European annals of otorhinolaryngology, head and neck diseases (01.09.2014)
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P-006 Polymorphisms of placental alkaline phosphatase gene are associated with recurrent pregnancy loss
Bouvier, S, Vatin, M, Bellazi, L, Montagutelli, X, Laissue, P, Ziyyat, A, Serres, C, Dieudonné, M.N, de Mazancourt, P, Mornet, E, Vaiman, D, Gris, J.-C
Published in Thrombosis research (2013)
Published in Thrombosis research (2013)
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Correlations of Genotype and Phenotype in Hypophosphatasia
Zurutuza, L., Muller, F., Gibrat, J.F., Taillandier, A., Simon-Bouy, B., Serre, L., Mornet, E.
Published in Human molecular genetics (01.06.1999)
Published in Human molecular genetics (01.06.1999)
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Genome wide expression profile in human HTR-8/Svneo trophoblastic cells in response to overexpression of placental alkaline phosphatase gene
Bellazi, L, Mornet, E, Meurice, G, Pata-Merci, N, De Mazancourt, P, Dieudonné, M.-N
Published in Placenta (Eastbourne) (01.10.2011)
Published in Placenta (Eastbourne) (01.10.2011)
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A molecular approach to dominance in hypophosphatasia
Lia-Baldini, A S, Muller, F, Taillandier, A, Gibrat, J F, Mouchard, M, Robin, B, Simon-Bouy, B, Serre, J L, Aylsworth, A S, Bieth, E, Delanote, S, Freisinger, P, Hu, J C, Krohn, H P, Nunes, M E, Mornet, E
Published in Human genetics (01.07.2001)
Published in Human genetics (01.07.2001)
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Childhood Hypophosphatasia Due to a de Novo Missense Mutation in the Tissue-Nonspecific Alkaline Phosphatase Gene
Taillandier, A, Sallinen, S.-L, Brun-Heath, I, De Mazancourt, P, Serre, J.-L, Mornet, E
Published in The journal of clinical endocrinology and metabolism (01.04.2005)
Published in The journal of clinical endocrinology and metabolism (01.04.2005)
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A sequence variation in the promoter of the placental alkaline phosphatase gene ( ALPP) is associated with allele-specific expression in human term placenta
Bellazi, L, Germond, S, Dupont, C, Brun-Heath, I, Taillandier, A, De Mazancourt, P, Dieudonné, M.N, Mornet, E
Published in Placenta (Eastbourne) (01.09.2010)
Published in Placenta (Eastbourne) (01.09.2010)
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L’étude de la muqueuse sphénoïdale par analyse anatomopathologique a-t-elle un intérêt en cas de chirurgie par voie basse des adénomes hypophysaires ?
Rabbo, F. Abed, Sonnet, E, Quintin-Roué, I, Mornet, E, Kerlan, V, Seizeur, R
Published in Annales d'endocrinologie (01.09.2016)
Published in Annales d'endocrinologie (01.09.2016)
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Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic images
Sinico, M., Levaillant, J. M., Vergnaud, A., Blondeau, J. R., Encha-Razavi, F., Mornet, E., Le Merrer, M., Gerard-Blanluet, M.
Published in Prenatal diagnosis (01.03.2007)
Published in Prenatal diagnosis (01.03.2007)
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