Inflammatory cytokines, C reactive protein, and procalcitonin as early predictors of necrosis infection in acute necrotizing pancreatitis
Riché, Florence C., Cholley, Bernard P., Laisné, Marie-Josèphe C., Vicaut, Eric, Panis, Yves H., Lajeunie, Elisabeth J., Boudiaf, Mourad, Valleur, Patrice D.
Published in Surgery (01.03.2003)
Published in Surgery (01.03.2003)
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Mutations within or upstream of the basic helix-loop-helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome
El Ghouzzi, V, Lajeunie, E, Le Merrer, M, Cormier-Daire, V, Renier, D, Munnich, A, Bonaventure, J
Published in European journal of human genetics : EJHG (01.01.1999)
Published in European journal of human genetics : EJHG (01.01.1999)
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Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome
LAJEUNIE, Elisabeth, HEUERTZ, Solange, EL GHOUZZI, Vincent, MARTINOVIC, Jelena, RENIER, Dominique, LE MERRER, Martine, BONAVENTURE, Jacky
Published in European journal of human genetics : EJHG (01.03.2006)
Published in European journal of human genetics : EJHG (01.03.2006)
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Journal Article
Mutations of the TWIST gene in the Saethre-Chotzene syndrome
Renier, Dominique, Bolcato-Bellemin, Anne-Laure, Munnich, Arnold, Bourgeois, Patrice, Bonaventure, Jacky, Merrer, Martine Le, Perrin-Schmitt, Fabienne, Ghouzzi, Vincent El, Lajeunie, Elisabeth, Benit, Paule
Published in Nature genetics (01.01.1997)
Published in Nature genetics (01.01.1997)
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Journal Article
Mutations of the TWIST gene in the Saethre-Chotzen syndrome
EL GHOUZZI, V, LE MERRER, M, PERRIN-SCHMITT, F, LAJEUNIE, E, BENIT, P, RENIER, D, BOURGEOIS, P, BOLCATO-BELLEMIN, A.-L, MUNNICH, A, BONAVENTURE, J
Published in Nature genetics (1997)
Published in Nature genetics (1997)
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Journal Article
Mutations in the basic domain and the loop–helix II junction of TWIST abolish DNA binding in Saethre–Chotzen syndrome
El Ghouzzi, Vincent, Legeai-Mallet, Laurence, Benoist-Lasselin, Catherine, Lajeunie, Elisabeth, Renier, Dominique, Munnich, Arnold, Bonaventure, Jacky
Published in FEBS letters (09.03.2001)
Published in FEBS letters (09.03.2001)
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Journal Article
Clinical variability in patients with Apert's syndrome
Lajeunie, E, Cameron, R, El Ghouzzi, V, de Parseval, N, Journeau, P, Gonzales, M, Delezoide, A L, Bonaventure, J, Le Merrer, M, Renier, D
Published in Journal of neurosurgery (01.03.1999)
Published in Journal of neurosurgery (01.03.1999)
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FGFR2 mutations in Pfeiffer syndrome
Renier, Dominique, Munnich, Arnold, Bonaventure, Jacky, Le Merrer, Martine, Lajeunie, Elisabeth, Ma, Hong Wei
Published in Nature genetics (1995)
Published in Nature genetics (1995)
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Journal Article
Sex related expressivity of the phenotype in coronal craniosynostosis caused by the recurrent P250R FGFR3 mutation
Lajeunie, Elisabeth, El Ghouzzi, Vincent, Le Merrer, Martine, Munnich, Arnold, Bonaventure, Jacky, Renier, Dominique
Published in Journal of medical genetics (01.01.1999)
Published in Journal of medical genetics (01.01.1999)
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Journal Article
Somatostatin receptor scintigraphy in pituitary adenomas: A somatostatin receptor denisty index can predict hormonal and tumoral efficacy of octreotide in vivo
Duet, Michele, Ajzenberg, Christiane, Benelhadj, Salah, Lajeunie, Elisabeth
Published in The Journal of nuclear medicine (1978) (01.08.1999)
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Published in The Journal of nuclear medicine (1978) (01.08.1999)
Journal Article
Somatostatin Receptor Scintigraphy in Pituitary Adenomas: A Somatostatin Receptor Density Index Can Predict Hormonal and Tumoral Efficacy of Octreotide In Vivo
Duet, Michele, Ajzenberg, Christiane, Benelhadj, Salah, Lajeunie, Elisabeth, Lormeau, Boris, Guillausseau, Pierre-Jean, Rohmer, Vincens, Vilain, Didier, Mundler, Olivier, Warnet, Andre
Published in The Journal of nuclear medicine (1978) (01.08.1999)
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Published in The Journal of nuclear medicine (1978) (01.08.1999)
Journal Article
Clinical variability in patients with Apert's syndrome
Lajeunie, Elisabeth, Cameron, Rhoda, Ghouzzi, Vincent El, de Parseval, Nathalie, Journeau, Pierre, Gonzales, Marie, Delezoide, Anne-Lise, Bonaventure, Jacky, Le Merrer, Martine, Renier, Dominique
Published in Neurosurgical focus (01.01.1999)
Published in Neurosurgical focus (01.01.1999)
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Journal Article
No evidence of genetic heterogeneity in Crouzon craniofacial dysostosis
Ma, H W, Lajeunie, E, Le Merrer, M, de Parseval, N, Serville, F, Weissenbach, J, Munnich, A, Renier, D
Published in Human genetics (01.12.1995)
Published in Human genetics (01.12.1995)
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Possible genetic heterogeneity in the Saethre-Chotzen syndrome
Ma, H W, Lajeunie, E, de Parseval, N, Munnich, A, Renier, D, Le Merrer, M
Published in Human genetics (01.08.1996)
Published in Human genetics (01.08.1996)
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Shrinkage of a primary thyrotropin-secreting pituitary adenoma treated with the long-acting somatostatin analogue octreotide (SMS 201-995)
Warnet, A, Lajeunie, E, Gelbert, F, Duet, M, Chanson, P, Cophignon, J, Harris, A G
Published in Acta endocrinologica (Copenhagen) (01.05.1991)
Published in Acta endocrinologica (Copenhagen) (01.05.1991)
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Journal Article
Saethre-Chotzen syndrome: notable intrafamilial phenotypic variability in a large family with Q28X TWIST mutation
Dollfus, Hélène, Biswas, Partha, Kumaramanickavel, Govindsamy, Stoetzel, Corinne, Quillet, Renaud, Biswas, Jyotirmay, Lajeunie, Elisabeth, Renier, Dominique, Perrin-Schmitt, Fabienne
Published in American journal of medical genetics (01.05.2002)
Published in American journal of medical genetics (01.05.2002)
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A Novel Phenotypic Pattern in X-Linked Inheritance: Craniofrontonasal Syndrome Maps to Xp22
Feldman, George J., Ward, Deeann E., Lajeunie-Renier, Elisabeth, Saavedra, Dolores, Robin, Nathaniel H., Proud, Virginia, Robb, Laura J., Der Kaloustian, Vazken, Carey, John C., Cohen, M. Michael, Cormier, Valerie, Munnich, Arnold, Zackai, Elaine H., Wilkie, Andrew O. M., Arlen Price, R., Muenke, Maximilian
Published in Human molecular genetics (01.10.1997)
Published in Human molecular genetics (01.10.1997)
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Journal Article
Pfeiffer syndrome type 2: further delineation and review of the literature
Plomp, A S, Hamel, B C, Cobben, J M, Verloes, A, Offermans, J P, Lajeunie, E, Fryns, J P, de Die-Smulders, C E
Published in American journal of medical genetics (23.01.1998)
Published in American journal of medical genetics (23.01.1998)
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