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1

Problems and Solutions

Maxey Brooke, Huseyin Demir, Joseph D. E. Konhauser, Charles W. Trigg, R. J. Cormier, M. N. S. Swamy, J. S. Vigder, Martin Gorfinkel, Douglas Lind, G. L. N. Rao, Martin J. Cohen, L. Carlitz, Raymond E

Journal:

Mathematics Magazine

Year:

1965

Language:

english

File:

PDF, 880 KB

english, 1965

2

Influences of flavones on cell viability and cAMP-dependent steroidogenic gene regulation in MA-10 Leydig cells

Cormier, Michelle, Ghouili, Firas, Roumaud, Pauline, Bauer, William, Touaibia, Mohamed, Martin, Luc J.

Journal:

Cell Biology and Toxicology

Year:

2017

Language:

english

File:

PDF, 2.06 MB

english, 2017

3

Proximate determinants of tuberculosis in Indigenous peoples worldwide: a systematic review

Cormier, Maxime, Schwartzman, Kevin, N'Diaye, Dieynaba S, Boone, Claire E, dos Santos, Alexandre M, Gaspar, Júlia, Cazabon, Danielle, Ghiasi, Marzieh, Kahn, Rebecca, Uppal, Aashna, Morris, Martin, Oxl

Journal:

The Lancet Global Health

Year:

2019

Language:

english

File:

PDF, 435 KB

english, 2019

4

Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome

Laurence Faivre, Anne-Marie Prieur, Martine Le Merrer, François Hayem, Clothilde Penet, Patricia Woo, Michaël Hofer, Nathalie Dagoneau, Isabelle Sermet, Arnold Munnich, Valérie Cormier-Daire

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 152 KB

english, 2000

5

Nosology and classification of genetic skeletal disorders: 2010 revision

Matthew L. Warman, Valerie Cormier-Daire, Christine Hall, Deborah Krakow, Ralph Lachman, Martine LeMerrer, Geert Mortier, Stefan Mundlos, Gen Nishimura, David L. Rimoin, Stephen Robertson, Ravi Savari

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 180 KB

english, 2011

6

Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

V. Laugel, C. Dalloz, M. Durand, F. Sauvanaud, U. Kristensen, M.C. Vincent, L. Pasquier, S. Odent, V. Cormier-Daire, B. Gener, E.S. Tobias, J.L. Tolmie, D. Martin-Coignard, V. Drouin-Garraud, D. Heron

Journal:

Year:

2010

Language:

english

File:

PDF, 317 KB

english, 2010

7

Maintenance and decline of physical activity during adolescence: insights from a qualitative study

Mathieu Bélanger, Michelle Casey, Marc Cormier, Annie Laflamme Filion, Geneviève Martin, Stéphanie Aubut, Philipe Chouinard, Simon-Pierre Savoie, Jacinthe Beauchamp

Journal:

International Journal of Behavioral Nutrition and Physical Activity

Year:

2011

Language:

english

File:

PDF, 193 KB

english, 2011

8

Contribution of three-dimensional computed tomography in prenatal diagnosis of lethal infantile cortical hyperostosis (Caffey disease)

Véronique Darmency, Christel Thauvin-Robinet, Thierry Rousseau, Nathalie Mejean, Ségolène Charra, Fanny Coron, Cécile Cassini, Frédéric Huet, Martine Le Merrer, Valérie Cormier-Daire, Nicole Laurent,

Journal:

Prenatal Diagnosis

Year:

2009

Language:

english

File:

PDF, 233 KB

english, 2009

9

Microbiology of mandibular third molar pericoronitis: Incidence of β-lactamase-producing bacteria

Jean-Louis Sixou, Christophe Magaud, Anne Jolivet-Gougeon, Michel Cormier, Martine Bonnaure-Mallet

Journal:

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology

Year:

2003

Language:

english

File:

PDF, 79 KB

english, 2003

10

Spectroscopic Characterization of Crocetin Derivatives from Crocus sativus and Gardenia jasminoides

Van Calsteren, Marie-Rose, Bissonnette, Martine C., Cormier, François, Dufresne, Christiane, Ichi, Takahito, LeBlanc, J. C. Yves, Perreault, Daniel, Roewer, Ingeborg

Journal:

Journal of Agricultural and Food Chemistry

Year:

1997

Language:

english

File:

PDF, 316 KB

english, 1997

11

Applications of B -splines in atomic and molecular physics

Bachau, H, Cormier, E, Decleva, P, Hansen, J E, Martín, F

Journal:

Reports on Progress in Physics

Year:

2001

Language:

english

File:

PDF, 1.64 MB

english, 2001

12

Framing constructed action in British Sign Language narratives

Cormier, Kearsy, Smith, Sandra, Zwets, Martine

Journal:

Journal of Pragmatics

Year:

2013

Language:

english

File:

PDF, 3.78 MB

english, 2013

13

Structure activity relationship of caffeic acid phenethyl ester analogs as new 5-lipoxygenase inhibitors

Doiron, Jérémie A., Leblanc, Luc M., Hébert, Martin J. G., Levesque, Natalie A., Paré, Aurélie F., Jean-François, Jacques, Cormier, Marc, Surette, Marc E., Touaibia, Mohamed

Journal:

Chemical Biology & Drug Design

Year:

2016

Language:

english

File:

PDF, 926 KB

english, 2016

14

Influence of flavonols and quercetin derivative compounds on MA-10 Leydig cells steroidogenic genes expressions

Cormier, Michelle, Ghouili, Firas, Roumaud, Pauline, Martin, Luc J., Touaibia, Mohamed

Journal:

Toxicology in Vitro

Year:

2017

Language:

english

File:

PDF, 1.34 MB

english, 2017

15

Developing Proficiency in Standardized Cognitive Assessment Scoring: How Much Is Enough?

Cormier, Damien C., Van Norman, Ethan R., Cheong, Clarissa, Kennedy, Kathleen E., Bulut, Okan, Mrazik, Martin

Journal:

Canadian Journal of School Psychology

Year:

2018

Language:

english

File:

PDF, 121 KB

english, 2018

16

Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome

Cormier-Daire, Valérie, Le Merrer, Martine, Gigarel, Nadine, Morichon, Nicole, Prieur, Marguerite, Lyonnet, Stanislas, Vekemans, Michel, Munnich, Arnold

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 151 KB

english, 1997

17

Osteopathia striata cranial sclerosis: Non-random X-inactivation suggestive of X-linked dominant inheritance

Géraldine Viot, Didier Lacombe, Albert David, Michèle Mathieu, Alain de Broca, Laurence Faivre, Nadine Gigarel, Arnold Munnich, Stanislas Lyonnet, Martine Le Merrer, Valérie Cormier-Daire

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 100 KB

english, 2002

18

Craniosynostosis and kidney malformation in a case of Hennekam syndrome

V. Cormier-Daire, S. Lyonnet, A. Lehnert, D. Martin, R. Salomon, N. Patey, M. Broyer, C. Ricour, A. Munnich

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 409 KB

english, 1995

19

Re-evaluation of kyphomelic dysplasia

Martine Le Merrer, Valerie Cormier Daire, Pierre Maroteaux

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 74 KB

english, 2003

20

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

21

Desbuquois dysplasia, a reevaluation with abnormal and “normal” hands: Radiographic manifestations

Laurence Faivre, Valérie Cormier-Daire, Alison M. Eliott, Fiona Field, Arnold Munnich, Pierre Maroteaux, Martine Le Merrer, Ralph Lachman

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 164 KB

english, 2004

22

Clinical and genetic heterogeneity in Desbuquois dysplasia

Laurence Faivre, Martine Le Merrer, Klaus Zerres, Mongi Ben Hariz, Déborah Scheffer, Ian D. Young, Pierre Maroteaux, Arnold Munnich, Valérie Cormier-Daire

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 175 KB

english, 2004

23

A new osteogenesis imperfecta with improvement over time maps to 11q

Agnès Kamoun-Goldrat, Stéphanie Pannier, Céline Huber, Georges Finidori, Arnold Munnich, Valérie Cormier-Daire, Martine Le Merrer

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 241 KB

english, 2008

24

Expanding the skeletal phenotype of Loeys-Dietz syndrome

Sérgio B. Sousa, Karen Lambot-Juhan, Marlène Rio, Geneviève Baujat, Vicken Topouchian, Nadine Hanna, Martine Le Merrer, Francis Brunelle, Arnold Munnich, Catherine Boileau, Valérie Cormier-Daire

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 193 KB

english, 2011

25

Clinical and molecular overlap in overgrowth syndromes

Geneviève Baujat, Marlène Rio, Sylvie Rossignol, Damien Sanlaville, Stanislas Lyonnet, Martine Le Merrer, Arnold Munnich, Christine Gicquel, Laurence Colleaux, Valérie Cormier-Daire

Journal:

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

Year:

2005

Language:

english

File:

PDF, 176 KB

english, 2005

26

Clinical and molecular overlap in overgrowth syndromes

Geneviève Baujat, Marlène Rio, Sylvie Rossignol, Damien Sanlaville, Stanislas Lyonnet, Martine Le Merrer, Arnold Munnich, Christine Gicquel, Laurence Colleaux, Valérie Cormier-Daire

Journal:

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

Year:

2006

Language:

english

File:

PDF, 52 KB

english, 2006

27

Mutations in two regions of FLNB result in atelosteogenesis I and III

Claire Farrington-Rock, Marc H. Firestein, Louise S. Bicknell, Andrea Superti-Furga, Carlos A. Bacino, Valerie Cormier-Daire, Martine Le Merrer, Clarisse Baumann, Joelle Roume, Patrick Rump, Joke B.G.

Journal:

Year:

2006

Language:

english

File:

PDF, 271 KB

english, 2006

28

Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2

Bertrand Isidor, Martine Le Merrer, G. Ulrich Exner, Olivier Pichon, Gaelle Thierry, Anne Guiochon-Mantel, Albert David, Valérie Cormier-Daire, Cédric Le Caignec

Journal:

Year:

2011

Language:

english

File:

PDF, 156 KB

english, 2011

29

Pseudoachondroplasia and multiple epiphyseal dysplasia: A 7-year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution

Gail C. Jackson, Laureane Mittaz-Crettol, Jacqueline A. Taylor, Geert R. Mortier, Juergen Spranger, Bernhard Zabel, Martine Le Merrer, Valerie Cormier-Daire, Christine M. Hall, Amaka Offiah, Michael J

Journal:

Year:

2012

Language:

english

File:

PDF, 428 KB

english, 2012

30

Design, synthesis, and characterization of peptide nanostructures having ion channel activity

Eric Biron, François Otis, Jean-Christophe Meillon, Martin Robitaille, Julie Lamothe, Patrick Van Hove, Marie-Eve Cormier, Normand Voyer

Journal:

Bioorganic & Medicinal Chemistry

Year:

2004

Language:

english

File:

PDF, 401 KB

english, 2004

31

Ténosynovite aiguë de la cheville due à Capnocytophaga cynodegmi/canimorsus identifié par séquençage du gène 16S rARN

Alexandre Le Meur, Jean-David Albert, Philippe Gautier, Mickael Ropars, Aleth Perdriger, Nicole Gando, Jacques Minet, Michel Cormier, Martine Bonnaure-Mallet, Anne Jolivet-Gougeon

Journal:

Revue du Rhumatisme

Year:

2008

Language:

french

File:

PDF, 198 KB

french, 2008

32

Genetic homogeneity of the Camurati–Engelmann disease

Ana Belinda Cf Xavier, Jorge M Saraiva, Martine Le Merrer, Nathalie Dagoneau, Céline Huber, Clotilde Penet, Arnold Munnich, Valérie Cormier-Daire

Journal:

Clinical Genetics

Year:

2000

Language:

english

File:

PDF, 163 KB

english, 2000

33

Prevalence of oropharyngeal beta-lactamase-producingCapnocytophagaspp. in pediatric oncology patients over a ten-year period

Anne Jolivet-Gougeon, Zohreh Tamanai-Shacoori, Laurent Desbordes, Virginie Gandemer, Jean-Louis Sixou, Nolwenn Morvan-Graveline, Michel Cormier, Martine Bonnaure-Mallet

Journal:

BMC Infectious Diseases

Year:

2005

Language:

english

File:

PDF, 511 KB

english, 2005

34

Phase II study of docetaxel (taxotere) in patients with previously untreated extensive small cell lung cancer

Jean Latreille, Yvon Cormier, Heidi Martins, Glenwood Goss, Bryn Fisher, Elizabeth A. Eisenhauer

Journal:

Investigational New Drugs

Year:

1995-1996

Language:

english

File:

PDF, 195 KB

english, 1995-1996

35

Congenital disorders of glycosylation type I: a rare but new cause of hyperechoic kidneys in infants and children due to early microcystic changes

Lucie Hertz-Pannier, Michele Déchaux, Martine Sinico, Sophie Emond, Valerie Cormier-Daire, Jean-Marie Saudubray, Francis Brunelle, Patrick Niaudet, Nathalie Seta, Pascale de Lonlay

Journal:

Pediatric Radiology

Year:

2006

Language:

english

File:

PDF, 260 KB

english, 2006

36

Spondyloepimetaphyseal dysplasia, short limb-abnormal calcifications type: progressive radiological findings from fetal age to adolescence

Katya Rozovsky, Jacob Sosna, Martine Le Merrer, Natalia Simanovsky, Benjamin Z. Koplewitz, Jacob Bar-Ziv, Valerie Cormier-Daire, Annick Raas-Rothschild

Journal:

Pediatric Radiology

Year:

2011

Language:

english

File:

PDF, 580 KB

english, 2011

37

Presentation of six cases of Stüve-Wiedemann syndrome

Valérie Cormier-Daire, A. Munnich, Stanislas Lyonnet, Pierre Rustin, Anne-Lise Delezoide, Pierre Maroteaux, Martine Le Merrer

Journal:

Pediatric Radiology

Year:

1998

Language:

english

File:

PDF, 590 KB

english, 1998

38

Updated survival analysis in patients with stage IIIB or IV non-small-cell lung cancer receiving BLP25 liposome vaccine (L-BLP25): phase IIB randomized, multicenter, open-label trial

Charles Butts, Andrew Maksymiuk, Glenwood Goss, Denis Soulières, Ernie Marshall, Yvon Cormier, Peter M. Ellis, Allan Price, Ravinder Sawhney, Frank Beier, Martin Falk, Nevin Murray

Journal:

Journal of Cancer Research and Clinical Oncology

Year:

2011

Language:

english

File:

PDF, 225 KB

english, 2011

39

Phenotypic variability at the TGF-β1 locus in Camurati-Engelmann disease

Ana Campos-Xavier, Jorge M. Saraiva, Ravi Savarirayan, Alain Verloes, Josué Feingold, Laurence Faivre, Arnold Munnich, Martine Le Merrer, Valérie Cormier-Daire

Journal:

Year:

2001

Language:

english

File:

PDF, 92 KB

english, 2001

40

Anomalous seismic crustal structure of oceanic fracture zones

Robert S. White, Robert S. Detrick, Martin C. Sinha, Marie H. Cormier

Journal:

Geophysical Journal International

Year:

1984

Language:

english

File:

PDF, 1.07 MB

english, 1984

41

The mutation spectrum in RECQL4 diseases

Siitonen, H Annika, Sotkasiira, Jenni, Biervliet, Martine, Benmansour, Abdelmadjid, Capri, Yline, Cormier-Daire, Valerie, Crandall, Barbara, Hannula-Jouppi, Katariina, Hennekam, Raoul, Herzog, Denise

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 142 KB

english, 2008

42

SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)

Belin, Valérie, Cusin, Veronica, Viot, Géraldine, Girlich, Delphine, Toutain, Annick, Moncla, Anne, Vekemans, Michel, Merrer, Martine Le, Munnich, Arnold, Cormier-Daire, Valérie

Journal:

Nature Genetics

Year:

1998

File:

PDF, 397 KB

1998

43

Mutations within or upstream of the basic helix–loop–helix domain of the TWIST gene are specific to Saethre-Chotzen syndrome

El Ghouzzi, Vincent, Lajeunie, Elisabeth, Le Merrer, Martine, Cormier-Daire, Valérie, Renier, Dominique, Munnich, Arnold, Bonaventure, Jacky

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 372 KB

english, 1999

44

Failure to detect an 8p22–8p23.1 duplication in patients with Kabuki (Niikawa–Kuroki) syndrome

Sanlaville, Damien, Genevieve, David, Bernardin, Céline, Amiel, Jeanne, Baumann, Clarisse, de Blois, Marie-Christine, Cormier-Daire, Valérie, Gerard, Bénédicte, Gerard, Marion, Le Merrer, Martine

Journal:

European Journal of Human Genetics

Year:

2005

Language:

english

File:

PDF, 123 KB

english, 2005

45

Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome

Redon, Richard, Baujat, Geneviève, Sanlaville, Damien, Le Merrer, Martine, Vekemans, Michel, Munnich, Arnold, Carter, Nigel P, Cormier-Daire, Valérie, Colleaux, Laurence

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 370 KB

english, 2006

46

Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia

Heuertz, Solange, Le Merrer, Martine, Zabel, Bernhard, Wright, Michael, Legeai-Mallet, Laurence, Cormier-Daire, Valérie, Gibbs, Linda, Bonaventure, Jacky

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 39 KB

english, 2006

47

Novel FGFR3 mutations creating cysteine residues in the extracellular domain of the receptor cause achondroplasia or severe forms of hypochondroplasia

Heuertz, Solange, Le Merrer, Martine, Zabel, Bernhard, Wright, Michael, Legeai-Mallet, Laurence, Cormier-Daire, Valérie, Gibbs, Linda, Bonaventure, Jacky

Journal:

European Journal of Human Genetics

Year:

2006

Language:

english

File:

PDF, 234 KB

english, 2006

48

Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia?

Bertrand Isidor, Sylvaine Poignant, Georges Picherot, André Mégabarné, Pierre Quartier, Brigitte Bader-Meunier, Cédric Le Caignec, Martine Le Merrer, Geneviève Baujat, Valérie Cormier-Daire, Albert Da

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 230 KB

english, 2012

49

Lung function, diagnosis, and treatment of sleep-disordered breathing in children with achondroplasia

Sébastien Julliand, Michèle Boulé, Geneviève Baujat, Adriana Ramirez, Vincent Couloigner, Nicole Beydon, Michel Zerah, Federico di Rocco, Martine Lemerrer, Valérie Cormier-Daire, Brigitte Fauroux

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 150 KB

english, 2012

50

Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications

Ruth Bargal, Valerie Cormier-Daire, Ziva Ben-Neriah, Martine Le Merrer, Jacob Sosna, Judith Melki, David H. Zangen, Sarah F. Smithson, Zvi Borochowitz, Ruth Belostotsky, Annick Raas-Rothschild

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 690 KB

english, 2009

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