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51

SPIE Proceedings [SPIE SPIE Advanced Lithography - San Jose, California, United States (Sunday 21 February 2016)] Extreme Ultraviolet (EUV) Lithography VII - Recent progress in nanoparticle photoresists development for EUV lithography

Panning, Eric M., Goldberg, Kenneth A., Kasahara, Kazuki, Kosma, Vasiliki, Odent, Jeremy, Xu, Hong, Yu, Mufei, Giannelis, Emmanuel P., Ober, Christopher K.

Year:

2016

Language:

english

File:

PDF, 1.48 MB

english, 2016

52

Surgical Treatment of Destructive Cervical Spondyloarthropathy With Neurologic Impairment in Hemodialysis Patients

Van Driessche, Stéphane, Goutallier, Daniel, Odent, Thierry, Piat, Christophe, Legendre, C, Buisson, C, Drucke, T, Kuntz, Daniel, Allain, Jérome, Bardin, Thierry

Journal:

Year:

2006

Language:

english

File:

PDF, 633 KB

english, 2006

53

Outcomes of intra-detrusor injections of botulinum toxin in patients with spina bifida: A systematic review

Hascoet, Juliette, Manunta, Andrea, Brochard, Charlène, Arnaud, Alexis, Damphousse, Mireille, Menard, Hélène, Kerdraon, Jacques, Journel, Hubert, Bonan, Isabelle, Odent, Sylvie, Fremond, Benjamin, Sip

Journal:

Neurourology and Urodynamics

Year:

2016

Language:

english

File:

PDF, 180 KB

english, 2016

54

Reliability and Validity of the French-Canadian Version of the Scoliosis Research Society 22 Questionnaire in France

Lonjon, Guillaume, Ilharreborde, Brice, Odent, Thierry, Moreau, Sébastien, Glorion, Christophe, Mazda, Keyvan

Journal:

Year:

2014

Language:

english

File:

PDF, 1.77 MB

english, 2014

55

Ischiovertebral Dysplasia

Aurégan, Jean-Charles, Odent, Thierry, Coyle, Ryan M., Miladi, Lotfi, Wicart, Philippe, Dubousset, Jean, Le Merrer, Martine, Padovani, Jean-Paul, Glorion, Christophe

Journal:

Year:

2014

Language:

english

File:

PDF, 11.79 MB

english, 2014

56

Cobb-1 versus cobb-to-cobb anterior fusion for adolescent idiopathic scoliosis Lenke 5C curves: a radiological comparative study

Dubory, Arnaud, Miladi, Lotfi, Ilharreborde, Brice, Gennari, Jean-Marie, Rouissi, Jihane, Glorion, Christophe, Flouzat Lachaniette, Charles Henri, Odent, Thierry

Journal:

European Spine Journal

Year:

2017

Language:

english

File:

PDF, 3.34 MB

english, 2017

57

Epifisiólisis femoral proximal

Klein, C., Odent, T., Glorion, C.

Journal:

EMC - Aparato Locomotor

Year:

2016

File:

PDF, 486 KB

2016

58

SPIE Proceedings [SPIE SPIE Advanced Lithography - San Jose, California, United States (Sunday 26 February 2017)] Extreme Ultraviolet (EUV) Lithography VIII - Nanoparticle photoresist studies for EUV lithography

Panning, Eric M., Goldberg, Kenneth A., Kasahara, Kazuki, Xu, Hong, Kosma, Vasiliki, Odent, Jeremy, Giannelis, Emmanuel P., Ober, Christopher K.

Year:

2017

Language:

english

File:

PDF, 4.66 MB

english, 2017

59

Psychiatric adult-onset of urea cycle disorders: A case-series

Bigot, Adrien, Brunault, Paul, Lavigne, Christian, Feillet, François, Odent, Sylvie, Kaphan, Elsa, Thauvin, Christel, Leguy, Vanessa, Broué, Pierre, Tchan, Michel C., Maillot, François

Journal:

Molecular Genetics and Metabolism Reports

Year:

2017

Language:

english

File:

PDF, 265 KB

english, 2017

60

Recent Progress in EUV Metal Oxide Photoresists

Kasahara, Kazuki, Xu, Hong, Kosma, Vasiliki, Odent, Jeremy, Giannelis, Emmanuel P., Ober, Christopher K.

Journal:

Journal of Photopolymer Science and Technology

Year:

2017

Language:

english

File:

PDF, 4.54 MB

english, 2017

61

Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy

Robert, Cyrille, Pasquier, Laurent, Cohen, David, Fradin, Mélanie, Canitano, Roberto, Damaj, Léna, Odent, Sylvie, Tordjman, Sylvie

Journal:

International Journal of Molecular Sciences

Year:

2017

Language:

english

File:

PDF, 1.10 MB

english, 2017

62

Antimicrobial Usage and Resistance in Companion Animals: A Cross-Sectional Study in Three European Countries

Joosten, Philip, Ceccarelli, Daniela, Odent, Evelien, Sarrazin, Steven, Graveland, Haitske, Van Gompel, Liese, Battisti, Antonio, Caprioli, Andrea, Franco, Alessia, Wagenaar, Jaap A., Mevius, Dik, Dew

Journal:

Year:

2020

Language:

english

File:

PDF, 1.01 MB

english, 2020

63

Dynamic Thermal-Regulating Textiles with Metallic Fibers Based on a Switchable Transmittance

Abebe, Muluneh G., Rosolen, Gilles, Khousakoun, Eric, Odent, Jeremy, Raquez, Jean-Marie, Desprez, Sylvain, Maes, Bjorn

Journal:

Physical Review Applied

Year:

2020

File:

PDF, 2.01 MB

2020

64

Segregation analysis in nonsyndromic holoprosencephaly

Odent, Sylvie, Le Marec, Bernard, Munnich, Arnold, Le Merrer, Martine, Bona�ti-Pelli�, Catherine

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 101 KB

english, 1998

65

Heterotaxy-neural tube defect and holoprosencephaly occurring independently in two sib fetuses

Bonneau, Dominique, Mar�chaud, Martine, Odent, Sylvie, Piegay, Isabelle, Godard, Alain, Amati, Patrizia

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 247 KB

english, 1999

66

Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome

Briault, Sylvain, Odent, Sylvie, Lucas, Josette, Le Merrer, Martine, Turleau, Catherine, Munnich, Arnold, Moraine, Claude

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 158 KB

english, 1999

67

1q32-q41 microdeletion with reference to van der Woude syndrome and allied clefting entities

Houdayer, Claude, Soupre, V�ronique, Karcenty, Bruno, Vazquez, Marie-Paule, Odent, Sylvie, Lacombe, Didier, Le Bouc, Yves, Munnich, Arnold, Bahuau, Michel

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 80 KB

english, 2000

68

Short Communication. Prenatal detection of a congenital pancreatic cyst and Beckwith–Wiedemann Syndrome

B. Fremond, P. Poulain, S. Odent, J. Milon, C. Treguier, J. M. Babut

Journal:

Prenatal Diagnosis

Year:

1997

Language:

english

File:

PDF, 412 KB

english, 1997

69

Identification of novel L1CAM mutations using fluorescence-assisted mismatch analysis

Pascale Saugier-Veber, Cosette Martin, Nathalie Le Meur, Stanislas Lyonnet, Arnold Munnich, Albert David, Alain Hénocq, Delphine Héron, Philippe Jonveaux, Sylvie Odent, Sylvie Manouvrier, Anne Moncla,

Journal:

Year:

1998

Language:

english

File:

PDF, 314 KB

english, 1998

70

Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure

Christèle Dubourg, Sylvie Odent, Patricia Fergelot, Jean-Yves Le Gall, Véronique David, Martine Blayau

Journal:

Year:

1999

Language:

english

File:

PDF, 115 KB

english, 1999

71

Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: A second FG locus [FGS2]?

Sylvain Briault, Laurent Villard, Ute Rogner, Johannes Coy, Sylvie Odent, Josette Lucas, Edith Passage, Danping Zhu, Antony Shrimpton, Marcus Pembrey, Marianne Till, Agnès Guichet, Sabine Dessay, Mich

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 1.85 MB

english, 2000

72

Multi-minicore disease–searching for boundaries: Phenotype analysis of 38 cases

Ana Ferreiro, Brigitte Estournet, Danielle Chateau, Norma B. Romero, Cécile Laroche, Sylvie Odent, Annick Toutain, Ana Cabello, Daniel Fontan, Heloísa G. Dos Santos, Charles-Antoine Haenggeli, Enrico

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 4.81 MB

english, 2000

73

Mosaic trisomy 9 and lobar holoprosencephaly

Marion Gérard-Blanluet, Claude Danan, Martine Sinico, Françoise Lelong, Elsa Borghi, Gilles Dassieu, Jean-Claude Janaud, Sylvie Odent, Férechté Encha-Razavi

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 207 KB

english, 2002

74

Molecular analysis of 53 fragile X families with the probe StB12.3

Dr. H. Puissant, M. C. Malinge, A. Larget-Piet, D. Martin, P. Chauveau, S. Odent, G. Plessis, Ph. Parent, B. Lemarec, L. Larget-Piet

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 442 KB

english, 1994

75

Opitz GBBB syndrome: Chromosomal evidence of an X-linked form

Dr Alain Verloes, Albert David, Sylvie Odent, Annick Toutain, Marie-Joseph André, Josette Lucas, Bernard Le Marec

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 462 KB

english, 1995

76

Perinatal-lethal Gaucher disease

C. Mignot, A. Gelot, B. Bessières, F. Daffos, M. Voyer, F. Menez, C. Fallet Bianco, S. Odent, D. Le Duff, P. Loget, P. Fargier, J. Costil, P. Josset, J. Roume, MT. Vanier, I. Maire, T. Billette de Vil

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 98 KB

english, 2003

77

Long-term outcome in desbuquois dysplasia: A follow-up in four adult patients

Laurence Faivre, Valérie Cormier-Daire, Ian Young, Henri Bracq, Georges Finidori, Jean Paul Padovani, Sylvie Odent, Ralph Lachman, Arnold Munnich, Pierre Maroteaux, Martine Le Merrer

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 250 KB

english, 2004

78

Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: Genotypic and phenotypic analysis

Delphine Feldmann, Françoise Denoyelle, Pierre Chauvin, Eréa-Noël Garabédian, Rémy Couderc, Sylvie Odent, Alain Joannard, Sébastien Schmerber, Bruno Delobel, Jacques Leman, Hubert Journel, Hélène Catr

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 71 KB

english, 2004

79

Solitary median maxillary central incisor syndrome: Clinical case with a novel mutation of sonic hedgehog

Livia Garavelli, C. Zanacca, G. Caselli, G. Banchini, C. Dubourg, V. David, S. Odent, F. Gurrieri, G. Neri

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 112 KB

english, 2004

80

Phenotypic and molecular variability of the holoprosencephalic spectrum

Leila Lazaro, Christéle Dubourg, Laurent Pasquier, Franck Le Duff, Martine Blayau, Marie-Renée Durou, Armelle Thomas de la Pintière, Céline Aguilella, Véronique David, Sylvie Odent

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 128 KB

english, 2004

81

Mild phenotypes in a series of patients with Opitz GBBB syndrome with MID1 mutations

Joyce So, Vanessa Suckow, Zofia Kijas, Vera Kalscheuer, Bettina Moser, Jennifer Winter, Marieke Baars, Helen Firth, Peter Lunt, Ben Hamel, Peter Meinecke, Claude Moraine, Sylvie Odent, Albert Schinzel

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 193 KB

english, 2005

82

Search for a gene responsible for Floating-Harbor syndrome on chromosome 12q15q21.1

Estelle Lopez, Patrick Callier, Valérie Cormier-Daire, Didier Lacombe, Anne Moncla, Armand Bottani, Sandy Lambert, Alice Goldenberg, Bérénice Doray, Sylvie Odent, Damien Sanlaville, Lucie Gueneau, Lau

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 303 KB

english, 2012

83

Analysis of genotype–phenotype correlations in human holoprosencephaly

Benjamin D. Solomon, Sandra Mercier, Jorge I. Vélez, Daniel E. Pineda-Alvarez, Adrian Wyllie, Nan Zhou, Christèle Dubourg, Veronique David, Sylvie Odent, Erich Roessler, Maximilian Muenke

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2010

Language:

english

File:

PDF, 239 KB

english, 2010

84

Holoprosencephaly flashcards: A summary for the clinician

Benjamin D. Solomon, Daniel E. Pineda-Alvarez, Sandra Mercier, Manu S. Raam, Sylvie Odent, Maximilian Muenke

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2010

Language:

english

File:

PDF, 691 KB

english, 2010

85

Introduction to the American Journal of Medical Genetics Part C on holoprosencephaly

Maximilian Muenke, Benjamin D. Solomon, Sylvie Odent

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2010

Language:

english

File:

PDF, 42 KB

english, 2010

86

OPA1 R445H mutation in optic atrophy associated with sensorineural deafness

Patrizia Amati-Bonneau, Agnès Guichet, Aurélien Olichon, Arnaud Chevrollier, Frédérique Viala, Stéphanie Miot, Carmen Ayuso, Sylvie Odent, Catherine Arrouet, Christophe Verny, Marie-Noelle Calmels, Gi

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 2.07 MB

english, 2005

87

Hereditary optic neuropathies share a common mitochondrial coupling defect

Arnaud Chevrollier, Virginie Guillet, Dominique Loiseau, Naïg Gueguen, Marie-Anne Pou de Crescenzo, Christophe Verny, Marc Ferre, Hélène Dollfus, Sylvie Odent, Dan Milea, Cyril Goizet, Patrizia Amati-

Journal:

Annals of Neurology

Year:

2008

Language:

english

File:

PDF, 205 KB

english, 2008

88

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype–phenotype correlations

Christèle Dubourg, Leïla Lazaro, Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, Marie-Renée Durou, Sylvie Odent, Véronique David

Journal:

Year:

2004

Language:

english

File:

PDF, 225 KB

english, 2004

89

The full spectrum of holoprosencephaly-associated mutations within the ZIC2 gene in humans predicts loss-of-function as the predominant disease mechanism

Erich Roessler, Felicitas Lacbawan, Christèle Dubourg, Aimee Paulussen, Jos Herbergs, Ute Hehr, Claude Bendavid, Nan Zhou, Maia Ouspenskaia, Sherri Bale, Sylvie Odent, Vèronique David, Maximilian Muen

Journal:

Year:

2009

Language:

english

File:

PDF, 254 KB

english, 2009

90

Phenotypic spectrum of STRA6 mutations: from Matthew-Wood syndrome to non-lethal anophthalmia

Nicolas Chassaing, Christelle Golzio, Sylvie Odent, Léopoldine Lequeux, Adeline Vigouroux, Jelena Martinovic-Bouriel, Francesco Danilo Tiziano, Lucia Masini, Francesca Piro, Giovanna Maragliano, Anne-

Journal:

Year:

2009

Language:

english

File:

PDF, 205 KB

english, 2009

91

Non-USH2A mutations in USH2 patients

Thomas Besnard, Christel Vaché, David Baux, Lise Larrieu, Caroline Abadie, Catherine Blanchet, Sylvie Odent, Patricia Blanchet, Patrick Calvas, Christian Hamel, Hélène Dollfus, Geneviève Lina-Granade,

Journal:

Year:

2012

Language:

english

File:

PDF, 304 KB

english, 2012

92

Mutation analysis of the tyrosinase gene in oculocutaneous albinism

Olivier Camand, Dominique Marchant, Sandrine Boutboul, Marie Péquignot, Sylvie Odent, Hélène Dollfus, Joanne Sutherland, Alex Levin, Maurice Menasche, Cécile Marsac, Jean-Louis Dufier, Elise Heon, Mar

Journal:

Year:

2001

Language:

english

File:

PDF, 33 KB

english, 2001

93

Micro-computed tomography evaluation of vertebral end-plate trabecular bone changes in a porcine asymmetric vertebral tether

Jean-Michel Laffosse, Thierry Odent, Franck Accadbled, Thibault Cachon, Charles Kinkpe, Eric Viguier, Jérôme Sales de Gauzy, Pascal Swider

Journal:

Journal of Orthopaedic Research

Year:

2010

Language:

english

File:

PDF, 192 KB

english, 2010

94

Cyclosporin enhances diabetes induced by low-dose streptozotocin treatment in mice

C. Sestier, S. Odent-Pogu, M. Bonneville, C. Maurel, F. Lang, P. Sai

Journal:

Immunology Letters

Year:

1985

Language:

english

File:

PDF, 428 KB

english, 1985

95

La chondrodysplasie ponctuée (CDP) des enfants nés de mère lupique

N. Gando-Cocley, M. Ferry, A. Biraben, M. Laurent, S. Odent, M. Kouakou-Nzue, G. Chalès, A. Perdriger

Journal:

Revue du Rhumatisme

Year:

2007

Language:

french

File:

PDF, 137 KB

french, 2007

96

Can water immersion stop labor?

Journal:

Journal of Nurse-Midwifery

Year:

1997

Language:

english

File:

PDF, 271 KB

english, 1997

97

Role of HOXA7 to HOXA13 and PBX1 genes in various forms of MRKH syndrome (congenital absence of uterus and vagina)

Agnès Burel, Thomas Mouchel, Sylvie Odent, Filiz Tiker, Bertrand Knebelmann, Isabelle Pellerin, Daniel Guerrier

Journal:

Journal of Negative Results in BioMedicine

Year:

2006

Language:

english

File:

PDF, 532 KB

english, 2006

98

Embryology of neural tube defects: information provided by associated malformations

A. S. Cabaret, P. Loget, L. Loeuillet, S. Odent, P. Poulain

Journal:

Prenatal Diagnosis

Year:

2007

Language:

english

File:

PDF, 70 KB

english, 2007

99

Fetal ascites and oligohydramnios: Prenatal diagnosis of a sialic acid storage disease (index case)

P. Poulain, S. Odent, I. Maire, J. Milon, J. F. Proudhon, H. Jouan, B. Le Marec

Journal:

Prenatal Diagnosis

Year:

1995

Language:

english

File:

PDF, 833 KB

english, 1995

100

Prenatal diagnosis of a complete sternal cleft in a child with PHACES syndrome—a case report

Nathalie Thébault, Hélène Le Guern, Bernard Le Fiblec, Mathilde Ferry, Sylvie Odent

Journal:

Prenatal Diagnosis

Year:

2009

Language:

english

File:

PDF, 86 KB

english, 2009