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1

Modèle à hasard proportionnel pour la fiabilité des composants mécaniques

Lanternier, Brice, Lyonnet, Patrick, Toscano, Rosario

Journal:

Mécanique & Industries

Year:

2008

File:

PDF, 291 KB

2008

2

Robust PID controller tuning based on the heuristic Kalman algorithm

Rosario Toscano, Patrick Lyonnet

Journal:

Year:

2009

Language:

english

File:

PDF, 3.67 MB

english, 2009

3

Microsatellite DNA markers detects 95% of chromosome 22q11 deletions

Bonnet, Damien, Cormier-Daire, Valérie, Kachaner, Jean, Szezepanski, Isabelle, Souillard, Patrick, Sidi, Daniel, Munnich, Arnold, Lyonnet, Stanislas

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 97 KB

english, 1997

4

Apparent genetic homogeneity of the treacher Collins-Franceschetti syndrome

Patrick Edery, Yves Manach, Martine Le Merrer, Marianne Till, Alain Vignal, Stanislas Lyonnet, Arnold Munnich

Journal:

American Journal of Medical Genetics Part A

Year:

1994

Language:

english

File:

PDF, 310 KB

english, 1994

5

Ret in human development and oncogenesis

Patrick Edery, Arnold Munnich, Stanislas Lyonnet, Charis Eng

Journal:

Year:

1997

Language:

english

File:

PDF, 821 KB

english, 1997

6

PAX2 mutations in oligomeganephronia

Salomon, Remi, Tellier, Anne-Lorraine, Attie-Bitach, Tania, Amiel, Jeanne, Vekemans, Michel, Lyonnet, Stanislas, Dureau, Pascal, Niaudet, Patrick, Gubler, Marie-Claire, Broyer, Michel

Journal:

Kidney International

Year:

2001

Language:

english

File:

PDF, 1.74 MB

english, 2001

7

A novel polymorphism in the coding sequence of the human RET proto-oncogene

Patrick Edery, Tania Attié, Lois M. Mulligan, Anna Pelet, Charis Eng, Brace A. J. Ponder, Arnold Munnich, Stanislas Lyonnet

Journal:

Year:

1994

Language:

english

File:

PDF, 111 KB

english, 1994

8

Mutations of the RET proto-oncogene in Hirschsprung's disease

Edery, Patrick, Lyonnet, Stanislas, Mulligan, Lois M., Pelet, Anna, Dow, Eleanore, Abel, Laurent, Holder, Susan, Nihoul-Fékété, Claire, Ponder, Bruce A. J., Munnich, Arnold

Journal:

Year:

1994

File:

PDF, 420 KB

1994

9

A duplication in the L1CAM gene associated with X–linked hydrocephalus

Camp, Guy Van, Vits, Lieve, Coucke, Paul, Lyonnet, Stanislas, Schrander-Stumpel, Connie, Darby, John, Holden, Jeanette, Munnich, Arnold, Willems, Patrick J.

Journal:

Nature Genetics

Year:

1993

File:

PDF, 576 KB

1993

10

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

Edery, Patrick, Attie, Tania, Amiel, Jeanne, Pelet, Anna, Eng, Charis, Hofstra, Robert M.W., Martelli, Helene, Bidaud, Christelle, Munnich, Arnold, Lyonnet, Stanislas

Journal:

Nature Genetics

Year:

1996

File:

PDF, 319 KB

1996

11

The multiple endocrine neoplasia type 2 syndromes and Hirschsprung disease are due to different mutations in the receptor tyrosine kinase ret

Bruce Ponder, Lois Mulligan, Charis Eng, Patrick Edery, Stanislas Lyonnet, Darrin Smith, Alan Tunnacliffe, John Kwok

Journal:

Cancer Genetics and Cytogenetics

Year:

1994

Language:

english

File:

PDF, 102 KB

english, 1994

12

[IEEE 2008 4th International IEEE Conference "Intelligent Systems" (IS) - Varna, Bulgaria (2008.09.6-2008.09.8)] 2008 4th International IEEE Conference Intelligent Systems - A methodological approach ball bearing damage prediction under fretting wear conditions.

Kolodziejczyk, Tomasz, Toscano, Rosario, Fillon, Cyril, Fouvry, Siegfried, Poloni, Carlo, Morales-Espejel, Guillermo, Lyonnet, Patrick

Year:

2008

Language:

english

File:

PDF, 618 KB

english, 2008

13

Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus family

Coucke, Paul, Vits, Lleve, Camp, Guy Van, Serville, Francoise, Lyonnet, Stanislas, Kenwrick, Susan, Rosenthal, André, Wehnert, Manfred, Munnich, Arnold, Willems, Patrick J.

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 1.81 MB

english, 1994

14

Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease

Attié, Tania, Till, Marianne, Pelet, Anna, Amiel, Jeanne, Edery, Patrick, Boutrand, Laetitia, Munnich, Arnold, Lyonnet, Stanislas

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 1.82 MB

english, 1995

15

Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease

Attié, Tania, Pelet, Anna, Edery, Patrick, Eng, Charis, Mulligan, Lois M., Amiel, Jeanne, Boutrand, Laetitia, Beldjord, Chérif, Nihoul-Fékété, Claire, Munnich, Arnold, Ponder, Bruce A.J., Lyonnet, Sta

Journal:

Human Molecular Genetics

Year:

1995

Language:

english

File:

PDF, 637 KB

english, 1995

16

A 7 bp deletion of the RET proto-oncogene in familial Hirschsprung‘s disease

Attle, Tanla, Pelet, Anna, Sarda, Pierre, Eng, Chads, Edery, Patrick, Mulligan, Lois M., Ponder, Bruce A.J., Munnich, Arnold, Lyonnet, Stanislas

Journal:

Human Molecular Genetics

Year:

1994

Language:

english

File:

PDF, 3.54 MB

english, 1994

17

Dynamic Preventive Maintenance, Optimization of Time between Overhaul

Lyonnet, Patrick, Toscano, Rosario

Journal:

Advanced Materials Research

Year:

2012

Language:

english

File:

PDF, 257 KB

english, 2012

18

Hereditary diffuse gastric cancer syndrome: improved performances of the 2015 testing criteria for the identification of probands with a CDH1 germline mutation

Benusiglio, Patrick R, Colas, Chystelle, Rouleau, Etienne, Uhrhammer, Nancy, Romero, Pierre, Remenieras, Audrey, Moretta, Jessica, Wang, Qing, De Pauw, Antoine, Buecher, Bruno, Stoppa-Lyonnet, Dominiq

Journal:

Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 137 KB

english, 2015

19

Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith-Wiedemann Syndrome: Clinical Spectrum and Functional Characterization

Brioude, Frederic, Netchine, Irène, Praz, Francoise, Le Jule, Marilyne, Calmel, Claire, Lacombe, Didier, Edery, Patrick, Catala, Martin, Odent, Sylvie, Isidor, Bertrand, Lyonnet, Stanislas, Sigaudy, S

Journal:

Year:

2015

Language:

english

File:

PDF, 854 KB

english, 2015

20

Design for electronic equipment reliability in complex systems

Poncelin, Guillaume, Cauvin, Aline, Glade, Mathieu, Lyonnet, Patrick, Dufrene, Denis

Journal:

International Journal of Product Development

Year:

2010

Language:

english

File:

PDF, 441 KB

english, 2010

21

RPL10 mutation segregating in a family with X-linked syndromic Intellectual Disability

Thevenon, Julien, Michot, Caroline, Bole, Christine, Nitschke, Patrick, Nizon, Mathilde, Faivre, Laurence, Munnich, Arnold, Lyonnet, Stanislas, Bonnefont, Jean-Paul, Portes, Vincent Des, Amiel, Jeanne

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 400 KB

english, 2015

22

Isolated generalized dystonia in biallelic missense mutations of the ATM gene

Meissner, Wassilios G., Fernet, Marie, Couturier, Jérôme, Hall, Janet, Laugé, Anthony, Henry, Patrick, Stoppa-Lyonnet, Dominique, Tison, François

Journal:

Movement Disorders

Year:

2013

Language:

english

File:

PDF, 250 KB

english, 2013

23

MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence

Gordon, Christopher T., Chopra, Maya, Oufadem, Myriam, Alibeu, Olivier, Bras, Marc, Boddaert, Nathalie, Bole-Feysot, Christine, Nitschké, Patrick, Abadie, Véronique, Lyonnet, Stanislas, Amiel, Jeanne

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 824 KB

english, 2017

24

Ethical, Social and Economic Issues in Familial Breast Cancer: A Compilation of Views from the E.C. Biomed II Demonstration Project

Steel, Michael, Smyth, Elizabeth, Vasen, Hans, Eccles, Diana, Evans, Gareth, Møller, Pål, Hodgson, Shirley, Stoppa-Lyonnet, Dominique, Chang-Claude, Jenny, Caligo, Maria, Morrison, Patrick, Haites, Ne

Journal:

Disease Markers

Year:

1999

Language:

english

File:

PDF, 2.92 MB

english, 1999

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