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1

Persistence of Dominant T Cell Clones in Accepted Solid Organ Transplants

Baron, C., McMorrow, I., Sachs, D. H., LeGuern, C.

Journal:

The Journal of Immunology

Year:

2001

Language:

english

File:

PDF, 205 KB

english, 2001

2

The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5q

H. Z. Ring, H. Chang, Angèle Guilbot, Alexis Brice, Eric LeGuern, Uta Francke

Journal:

Year:

1999

Language:

english

File:

PDF, 228 KB

english, 1999

3

Magmatic He distribution around Unzen volcano inferred from intensive investigation of helium isotopes in groundwater

N. Morikawa, K. Kazahaya, E. Fourre, H.A. Takahashi, P. Jean-Baptiste, M. Ohwada, F.J. LeGuern, A. Nakama

Journal:

Journal of Volcanology and Geothermal Research

Year:

2008

Language:

english

File:

PDF, 1.41 MB

english, 2008

4

Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormality

N. Collongues, C. Depienne, N. Boehm, A. Echaniz-Laguna, B. Samama, A. Dürr, G. Stevanin, E. Leguern, A. Brice, P. Labauge, J. de Seze

Journal:

European Journal of Neurology

Year:

2012

Language:

english

File:

PDF, 647 KB

english, 2012

5

X-linked Charcot-Marie-Tooth disease with connexin 32 mutations: Clinical and electrophysiologic study

Birouk, N., LeGuern, E., Maisonobe, T., Rouger, H., Gouider, R., Tardieu, S., Gugenheim, M., Routon, M. C., Leger, J. M., Agid, Y., Brice, A., Bouche, P.

Journal:

Year:

1998

Language:

english

File:

PDF, 1.10 MB

english, 1998

6

Screening of theTHAP1gene in patients with early-onset dystonia: myoclonic jerks are part of the dystonia 6 phenotype

Fabienne Clot, David Grabli, Pierre Burbaud, Magali Aya, Pascal Derkinderen, Luc Defebvre, Philippe Damier, Pierre Krystkowiak, Pierre Pollak, Eric Leguern, Chan San, Agnès Camuzat, Emmanuel Roze, Mar

Journal:

Year:

2011

Language:

english

File:

PDF, 71 KB

english, 2011

7

Primary Vascularization of Allografts Governs Their Immunogenicity and Susceptibility to Tolerogenesis

Kant, C. D., Akiyama, Y., Tanaka, K., Shea, S., Connolly, S. E., Germana, S., Winn, H. J., LeGuern, C., Tocco, G., Benichou, G.

Journal:

The Journal of Immunology

Year:

2013

Language:

english

File:

PDF, 1.17 MB

english, 2013

8

Génétique des encéphalopathies épileptiques : l’exemple du syndrome de Dravet

Journal:

Revue Neurologique

Year:

2013

Language:

french

File:

PDF, 171 KB

french, 2013

9

SPOT satellite monitoring of the eruption of Nevado Sabancaya volcano (Southern Peru)

J. Chorowicz, B. Deffontaines, D. Huaman-Rodrigo, R. Guillande, F. Leguern, J.C. Thouret

Journal:

Remote Sensing of Environment

Year:

1992

Language:

english

File:

PDF, 927 KB

english, 1992

10

Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?

Amiet, Claire, Gourfinkel-An, Isabelle, Laurent, Claudine, Bodeau, Nicolas, Génin, Bérengère, Leguern, Eric, Tordjman, Sylvie, Cohen, David

Journal:

Molecular Autism

Year:

2013

Language:

english

File:

PDF, 606 KB

english, 2013

11

Recurrent polyradiculoneuropathy with the 17p11.2 deletion

Nadine Le Forestier, Eric LeGuern, Philippe Coullin, Nazha Birouk, Thierry Maisonobe, Alexis Brice, Jean Marc Léger, Pierre Bouche

Journal:

Year:

1997

Language:

english

File:

PDF, 24 KB

english, 1997

12

Comparison of the thermal performance between conventional and cob building

Zeghari, Kaoutar, Louahlia, Hasna, Leguern, Malo, Boutouil, Mohamed, Gualous, Hamid, Marion, Michael, Schaetzel, Pierre, Goodhew, Steeve, Streif, François, Tanabe, S.I, Zhang, H., Kurnitski, J., Gamei

Journal:

E3S Web of Conferences

Year:

2019

Language:

english

File:

PDF, 2.40 MB

english, 2019

13

Three novel patients with epileptic encephalopathy due to biallelic mutations in the PLCB1 gene

Desprairies, Camille, Valence, Stéphanie, Maurey, Hélène, Helal, Suzette Ibrahim, Weckhuysen, Sarah, Soliman, Hala, Mefford, Heather C., Spentchian, Myrtille, Héron, Delphine, Leguern, Eric, Nava, Car

Journal:

Clinical Genetics

Year:

2019

File:

PDF, 2.11 MB

2019

14

Glial cell line-derived neurotrophic factor (GDNF) gene expression in the human brain: A post mortem in situ hybridization study with special reference to Parkinson's disease

S. Hunot, V. Bernard, B. Faucheux, F. Boissière, E. Leguern, C. Brana, P. P. Gautris, J. Guérin, B. Bloch, Y. Agid, E. C. Hirsch

Journal:

Journal of Neural Transmission

Year:

1996

Language:

english

File:

PDF, 1.26 MB

english, 1996

15

Expression of IL-17B in neurons and evaluation of its possible role in the chromosome 5q-linked form of Charcot–Marie–Tooth disease

Emma E. Moore, Scott Presnell, Ursula Garrigues, Angele Guilbot, Eric LeGuern, Deborah Smith, Lena Yao, Theodore E. Whitmore, Teresa Gilbert, Theo D. Palmer, Philip J. Horner, Rolf E. Kuestner

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 737 KB

english, 2002

16

Recessive sensory and motor hereditary neuropathy associated with juvenile glaucoma

R. Gouider, T. Dogui, M. Fredj, E. Leguern, S. Ben Ammou, A. Mrabet

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 256 KB

english, 1997

17

A rat model for LGI1-related epilepsies

Baulac, S., Ishida, S., Mashimo, T., Boillot, M., Fumoto, N., Kuwamura, M., Ohno, Y., Takizawa, A., Aoto, T., Ueda, M., Ikeda, A., LeGuern, E., Takahashi, R., Serikawa, T.

Journal:

Human Molecular Genetics

Year:

2012

Language:

english

File:

PDF, 558 KB

english, 2012

18

BU-29 - Impact de l’allergie à la pénicilline chez la femme enceinte

Catteau, C., Poitrenaud, D., Granbastien, B., Richart, P., Leguern, R., Vuotto, F., Mambie, A., Weyrich, P., Subtil, D., Faure, K.

Journal:

Médecine et Maladies Infectieuses

Year:

2016

Language:

french

File:

PDF, 98 KB

french, 2016

19

Silencing of the Charcot–Marie–Tooth associated MTMR2 gene decreases proliferation and enhances cell death in primary cultures of Schwann cells

Alexandre Chojnowski, Nicole Ravisé, Corinne Bachelin, Christel Depienne, Merle Ruberg, Bernard Brugg, Jocelyn Laporte, Anne Baron-Van Evercooren, Eric LeGuern

Journal:

Neurobiology of Disease

Year:

2007

Language:

english

File:

PDF, 1.05 MB

english, 2007

20

Grossesse et syndrome des antiphospholipides

N. Costedoat-Chalumeau, G. Guettrot-Imbert, V. Leguern, G. Leroux, D. Le Thi Huong, B. Wechsler, N. Morel, D. Vauthier-Brouzes, M. Dommergues, A. Cornet, O. Aumaître, O. Pourrat, J.-C. Piette, J. Niza

Journal:

La Revue de Médecine Interne

Year:

2012

Language:

french

File:

PDF, 374 KB

french, 2012

21

In Vitro Granuloma-like Formations in Bronchoalveolar Cell Cultures from Patients with Sarcoidosis

ANNIE G. ARNOUX, FRANÇIS JAUBERT, GISÈLE STANISLAS-LEGUERN, CLAIRE DANEL, JACQUES CHRÉTIEN

Journal:

Annals of the New York Academy of Sciences

Year:

1986

Language:

english

File:

PDF, 690 KB

english, 1986

22

Epilepsy in Simplex Autism Pedigrees is Much Lower Than the Rate in Multiplex Autism Pedigrees

Amiet, Claire, Gourfinkel-An, Isabelle, Laurent, Claudine, Carayol, Jérôme, Génin, Bérengère, Leguern, Eric, Tordjman, Sylvie, Cohen, David

Journal:

Biological Psychiatry

Year:

2013

Language:

english

File:

PDF, 124 KB

english, 2013

23

Epilepsy Gene LGI1 Regulates Postnatal Developmental Remodeling of Retinogeniculate Synapses

Zhou, Y.-D., Zhang, D., Ozkaynak, E., Wang, X., Kasper, E. M., Leguern, E., Baulac, S., Anderson, M. P.

Journal:

Journal of Neuroscience

Year:

2012

Language:

english

File:

PDF, 1.41 MB

english, 2012

24

Homologous DNA Exchanges in Humans Can Be Explained by the Yeast Double-Strand Break Repair Model: A Study of 17p11.2 Rearrangements Associated with CMT1A and HNPP

Lopes, J., Tardieu, S., Silander, K., Blair, I., Vandenberghe, A., Palau, F., Ruberg, M., Brice, A., LeGuern, E.

Journal:

Human Molecular Genetics

Year:

1999

Language:

english

File:

PDF, 349 KB

english, 1999

25

Regulation of T-cell functions by MHC class II self-presentation

Christian LeGuern

Journal:

Trends in Immunology

Year:

2003

Language:

english

File:

PDF, 596 KB

english, 2003

26

Abrogation of Renal Allograft Tolerance in MGH Miniature Swine: The Role of Intra-Graft and Peripheral Factors in Long-Term Tolerance

Scalea, J. R., Okumi, M., Villani, V., Shimizu, A., Nishimura, H., Gillon, B. C., Torabi, R., Cormack, T., Moran, S., LeGuern, C., Sachs, D. H., Yamada, K.

Journal:

American Journal of Transplantation

Year:

2014

Language:

english

File:

PDF, 1.51 MB

english, 2014

27

Expression of a swine class II gene in murine bone marrow hematopoietic cells by retroviral-mediated gene transfer.

Shafer, G. E., Emery, D. W., Gustafsson, K., Germana, S., Anderson, W. F., Sachs, D. H., LeGuern, C.

Journal:

Proceedings of the National Academy of Sciences

Year:

1991

Language:

english

File:

PDF, 1.33 MB

english, 1991

28

The first de novo mutation of the connexin 32 gene associated with X linked Charcot-Marie-Tooth disease.

Meggouh, F, Benomar, A, Rouger, H, Tardieu, S, Birouk, N, Tassin, J, Barhoumi, C, Yahyaoui, M, Chkili, T, Brice, A, LeGuern, E

Journal:

Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 515 KB

english, 1998

29

PADS 1-09 - Streptococcus agalactiae est-il uropathogène pendant la grossesse ?

Douaud, M., Leguern, R., Dessein, R., Grandbastien, B., Subtil, D., Faure, K.

Journal:

Médecine et Maladies Infectieuses

Year:

2016

Language:

french

File:

PDF, 113 KB

french, 2016

30

Autosomal recessive hereditary neuropathy with focally folded myelin sheaths and linked to chromosome 11q23: a distinct and homogeneous entity

M.A.M Salih, T Maisonobe, M Kabiraj, M Al Rayess, M.H.S Al-Turaiki, M Akbar, A Tahan, J.A Urtizberea, D Grid, T Hamadouche, A Guilbot, A Brice, E Leguern

Journal:

Neuromuscular Disorders

Year:

2000

Language:

english

File:

PDF, 398 KB

english, 2000

31

Genetic analysis of SS18L1 in French amyotrophic lateral sclerosis

Teyssou, Elisa, Vandenberghe, Nadia, Moigneu, Carine, Boillée, Séverine, Couratier, Philippe, Meininger, Vincent, Pradat, Pierre-François, Salachas, François, LeGuern, Eric, Millecamps, Stéphanie

Journal:

Neurobiology of Aging

Year:

2014

Language:

english

File:

PDF, 968 KB

english, 2014

32

Familial cortical myoclonic tremor with epilepsy (FCMTE): Clinical characteristics and exclusion of linkages to 8q and 2p in a large French family

Magnin, E., Vidailhet, M., Depienne, C., Saint-Martin, C., Bouteiller, D., LeGuern, E., Apartis, E., Rumbach, L., Labauge, P.

Journal:

Revue Neurologique

Year:

2009

Language:

english

File:

PDF, 366 KB

english, 2009

33

Molecular identification of porcine interleukin 10: regulation of expression in a kidney allograft model.

Blancho, G., Gianello, P., Germana, S., Baetscher, M., Sachs, D. H., LeGuern, C.

Journal:

Proceedings of the National Academy of Sciences

Year:

1995

Language:

english

File:

PDF, 1.31 MB

english, 1995

34

Ultrastructural PMP22 expression in inherited demyelinating neuropathies

Dr Jean-Michel Vallat, Philippe Sindou, Pierre-Marie Preux, Fransois Tabaraud, André-Michel Milor, Philippe Couratier, Eric Leguern, Alexis Brice

Journal:

Annals of Neurology

Year:

1996

Language:

english

File:

PDF, 485 KB

english, 1996

35

The mechanism of specific prolongation of class I-mismatched skin grafts induced by retroviral gene therapy

Robin Stanton Mayfield, Hideki Hayashi, Tokihiko Sawada, Kate Bergen, Christian Leguern, Megan Sykes, David H. Sachs, John Iacomini

Journal:

European Journal of Immunology

Year:

1997

Language:

english

File:

PDF, 469 KB

english, 1997

36

New intra-renal graft genes associated with tolerance or rejection

Mcmorrow, Isabel M., Narayan, Kavitha, Sachs, David H., Leguern, Christian

Journal:

Kidney International

Year:

2002

Language:

english

File:

PDF, 1.08 MB

english, 2002

37

Molecular evidence for five distinct MHC class II α genes in the rabbit

Christian LeGuern, Patrice N. Marche, Thomas J. Kindt

Journal:

Year:

1985

Language:

english

File:

PDF, 477 KB

english, 1985

38

Molecular analysis of a ring chromosome X in a family with fragile X syndrome

Etienne Mornet, Any Bogyo, Christiane Deluchat, Brigitte Simon-Bouy, Michèle Mathieu, François Thépot, Marie -Claude Grisard, Eric Leguern, Joelle Boué, André Boué

Journal:

Year:

1993

Language:

english

File:

PDF, 791 KB

english, 1993

39

Human Fas-ligand expression on porcine endothelial cells does not protect against xenogeneic natural killer cytotoxicity

Ulrike B. Matter-Reissmann, Kai-Christian Sonntag, Urs O. Gilli, Christian Leguern, Mårten K. J. Schneider, Jörg D. Seebach

Journal:

Xenotransplantation

Year:

2004

Language:

english

File:

PDF, 475 KB

english, 2004

40

The Autosomal Recessive Form of CMT Disease Linked to 5q31-q33

A. GUILBOT, M. KESSALI, N. RAVISÉ, T. HAMMADOUCHE, A. BOUHOUCHE, T. MAISONOBE, D. GRID, A. BRICE, E. LEGUERN

Journal:

Annals of the New York Academy of Sciences

Year:

1999

File:

PDF, 1.34 MB

1999

41

Tremblement cortical familial associé à une épilepsie : localisation génétique en 5p

Depienne, C., Magnin, E., Bouteiller, D., Stevanin, G., Saint-Martin, C., Vidailhet, M., Apartis, E., LeGuern, E., Labauge, P., Rumbach, L.

Journal:

Revue Neurologique

Year:

2010

Language:

french

File:

PDF, 223 KB

french, 2010

42

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa

Coullin, P., Diatta, A.L., Boufettal, H., Feingold, J., Leguern, E., Candelier, J.J.

Journal:

Year:

2015

Language:

english

File:

PDF, 880 KB

english, 2015

43

738. Influence of the Major Histocompatibility Complex on Immunological Rejection of Skin Grafts Expressing a Gene Therapy Reporter Gene

DOWN, J, LEGUERN, C

Journal:

Molecular Therapy

Year:

2005

Language:

english

File:

PDF, 87 KB

english, 2005

44

Lafora progressive myoclonus epilepsy:NHLRC1mutations affect glycogen metabolism

Philippe Couarch, Santiago Vernia, Isabelle Gourfinkel-An, Gaëtan Lesca, Svetlana Gataullina, Estelle Fedirko, Oriane Trouillard, Christel Depienne, Olivier Dulac, Dominique Steschenko, Eric Leguern,

Journal:

Journal of Molecular Medicine

Year:

2011

Language:

english

File:

PDF, 624 KB

english, 2011

45

Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33

E. LeGuern, A. Guilbot, M. Kessali, N. Ravise, J. Tassin, T. Maisonobe, D. Grid, A. Brice

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 265 KB

english, 1997

46

SERUM ANGIOTENSIN-CONVERTING ENZYME AND BRONCHOALVEOLAR LAVAGE IN SARCOIDOSIS

Stanislas-Leguern, G., Marsac, J., Arnoux, A., Lecossier, D.

Journal:

Year:

1979

Language:

english

File:

PDF, 150 KB

english, 1979

47

Données récentes sur l’implications des canaux ioniques dans les formes familiales d’épilepsies généralisées idiopathiques associées ou non à des convulsions fébriles

Gourfinkel-An, I., Baulac, S., Nabbout, R., Brice, A., Baulac, M., Leguern, E.

Journal:

Revue Neurologique

Year:

2004

Language:

french

File:

PDF, 172 KB

french, 2004

48

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

Depienne, C, Trouillard, O, Saint-Martin, C, Gourfinkel-An, I, Bouteiller, D, Carpentier, W, Keren, B, Abert, B, Gautier, A, Baulac, S, Arzimanoglou, A, Cazeneuve, C, Nabbout, R, LeGuern, E

Journal:

Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 2.62 MB

english, 2008

49

[IEEE 2010 5th Advanced Satellite Multimedia Systems Conference and the 11th Signal Processing for Space Communications Workshop (ASMS/SPSC) - Cagliari, Italy (2010.09.13-2010.09.15)] 2010 5th Advanced Satellite Multimedia Systems Conference and the 11th Signal Processing for Space Communications Workshop - HD Video Broadcasting using Scalable Video Coding combined with DVB-S2 Variable Coding and Modulation

Mirta, S., Schierl, T., Wiegand, T., Inigo, P., LeGuern, C., Moreau, C., Guarnieri, L., Tronc, J.

Year:

2010

Language:

english

File:

PDF, 876 KB

english, 2010

50

LGI1 acts presynaptically to regulate excitatory synaptic transmission during early postnatal development

Boillot, Morgane, Lee, Chun-Yao, Allene, Camille, Leguern, Eric, Baulac, Stéphanie, Rouach, Nathalie

Journal:

Scientific Reports

Year:

2016

Language:

english

File:

PDF, 1.11 MB

english, 2016

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