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1

L’auteur est dans l’escalier. Une relecture de La Promesse de l’aube de Romain Gary

Allamand, Carole

Journal:

Les Lettres Romanes

Année:

2007

Langue:

french

Fichier:

PDF, 114 KB

french, 2007

2

A Tooth for a Private Eye: James Ellroy's Detective Fiction

CAROLE ALLAMAND

Journal:

The Journal of Popular Culture

Année:

2006

Langue:

english

Fichier:

PDF, 89 KB

english, 2006

3

The Genealogy of Lettrism

Jacques Allamand and Julia Bowe

Journal:

Année:

1947

Langue:

english

Fichier:

PDF, 328 KB

english, 1947

4

Selenoprotein N in skeletal muscle: from diseases to function

Castets, Perrine, Lescure, Alain, Guicheney, Pascale, Allamand, Valérie

Journal:

Journal of Molecular Medicine

Année:

2012

Langue:

english

Fichier:

PDF, 932 KB

english, 2012

5

Compound heterozygous mutations of the TNXB gene cause primary myopathy

Pénisson-Besnier, Isabelle, Allamand, Valérie, Beurrier, Philippe, Martin, Ludovic, Schalkwijk, Joost, van Vlijmen-Willems, Ivonne, Gartioux, Corine, Malfait, Fransiska, Syx, Delfien, Macchi, Laurent,

Journal:

Neuromuscular Disorders

Année:

2013

Langue:

english

Fichier:

PDF, 2.14 MB

english, 2013

6

Du Sommaire au Moindre : L’Humanité en Fuite

Allamand, Carole

Journal:

Contemporary French and Francophone Studies

Année:

2012

Fichier:

PDF, 105 KB

2012

7

Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution

Deconinck, N., Richard, P., Allamand, V., Behin, A., Laforet, P., Ferreiro, A., de Becdelievre, A., Ledeuil, C., Gartioux, C., Nelson, I., Carlier, R. Y., Carlier, P., Wahbi, K., Romero, N., Zabot, M.

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Année:

2014

Langue:

english

Fichier:

PDF, 4.18 MB

english, 2014

8

Au défaut des mères: Yourcenar, Duras et la création littéraire

Carole Allamand

Journal:

The French Review

Année:

2002

Fichier:

PDF, 1.45 MB

2002

9

Management of Eisenmenger Syndrome in Pregnancy With Sildenafil and l-arginine

Lacassie, Héctor J., Germain, Alfredo M., Valdés, Gloria, Fernández, M Soledad, Allamand, Francisco, López, Héctor

Journal:

Obstetrics & Gynecology

Année:

2004

Langue:

english

Fichier:

PDF, 237 KB

english, 2004

10

ANNIE ERNAUX: À LA SERPE, À L'AIGUILLE ET AU COUTEAU

Allamand, Carole

Journal:

The Romanic Review

Année:

2006

Langue:

english

Fichier:

PDF, 680 KB

english, 2006

11

Génétique : Une mutation du gène TNPO3 impliquée dans la LGMD D2 confère une protection à l’infection par le VIH-1

Allamand, Valérie

Journal:

médecine/sciences

Année:

2019

Fichier:

PDF, 597 KB

2019

12

Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy

Volker Straub, Kathleen M. Donahue, Valérie Allamand, Robin L. Davisson, Young R. Kim, Kevin P. Campbell

Journal:

Magnetic Resonance in Medicine

Année:

2000

Langue:

english

Fichier:

PDF, 391 KB

english, 2000

13

ChemInform Abstract: Novel Biphenol Phosphoramidite Ligands for the Enantioselective Copper-Catalyzed Conjugated Addition of Dialkyl Zincs.

Alexandre Alexakis, Stephane Rosset, Janik Allamand, Sebastien March, Frederic Guillen, Cyril Benhaim

Journal:

Année:

2002

Fichier:

PDF, 31 KB

2002

14

A mutation in the SEPN1 selenocysteine redefinition element (SRE) reduces selenocysteine incorporation and leads to SEPN1-related myopathy

Baijayanta Maiti, Sandrine Arbogast, Valérie Allamand, Mark W. Moyle, Christine B. Anderson, Pascale Richard, Pascale Guicheney, Ana Ferreiro, Kevin M. Flanigan, Michael T. Howard

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 226 KB

english, 2009

15

Drug-induced readthrough of premature stop codons leads to the stabilization of laminin α2 chain mRNA in CMD myotubes

Valérie Allamand, Laure Bidou, Masayuki Arakawa, Célia Floquet, Masataka Shiozuka, Marion Paturneau-Jouas, Corine Gartioux, Gillian S. Butler-Browne, Vincent Mouly, Jean-Pierre Rousset, Ryoichi Matsud

Journal:

The Journal of Gene Medicine

Année:

2008

Langue:

english

Fichier:

PDF, 354 KB

english, 2008

16

Selenoprotein N is dynamically expressed during mouse development and detected early in muscle precursors

Perrine Castets, Svetlana Maugenre, Corine Gartioux, Mathieu Rederstorff, Alain Krol, Alain Lescure, Shahragim Tajbakhsh, Valérie Allamand, Pascale Guicheney

Journal:

BMC Developmental Biology

Année:

2009

Langue:

english

Fichier:

PDF, 1.51 MB

english, 2009

17

ColVI myopathies: where do we stand, where do we go?

Valérie Allamand, Laura Briñas, Pascale Richard, Tanya Stojkovic, Susana Quijano-Roy, Gisèle Bonne

Journal:

Skeletal Muscle

Année:

2011

Langue:

english

Fichier:

PDF, 4.28 MB

english, 2011

18

Surgical treatment of the hepatic hydatid cyst

R. G. Jove, L. H. Allamand, H. F. Fernandez, F. H. Fonseca, M. A. Lopez

Journal:

World Journal of Surgery

Année:

1981

Fichier:

PDF, 91 KB

1981

19

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

Lim, Leland E., Duclos, Franck, Broux, Odile, Bourg, Nathalie, Sunada, Yoshihide, Allamand, Valérie, Meyer, Jon, Richard, Isabelle, Moomaw, Carolyn, Slaughter, Clive

Journal:

Nature Genetics

Année:

1995

Fichier:

PDF, 1.07 MB

1995

20

A single homozygous point mutation in a 3′untranslated region motif of selenoprotein N mRNA causes SEPN1-related myopathy

Allamand, Valérie, Richard, Pascale, Lescure, Alain, Ledeuil, Céline, Desjardin, Delphine, Petit, Nathalie, Gartioux, Corine, Ferreiro, Ana, Krol, Alain, Pellegrini, Nadine, Urtizberea, J Andoni, Guic

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 130 KB

english, 2006

21

Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice

Allamand, V, Donahue, K M, Straub, V, Davisson, R L, Davidson, B L, Campbell, K P

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 1.01 MB

english, 2000

22

Premature stop codons involved in muscular dystrophies show a broad spectrum of readthrough efficiencies in response to gentamicin treatment

Bidou, L, Hatin, I, Perez, N, Allamand, V, Panthier, J-J, Rousset, J-P

Journal:

Année:

2004

Langue:

english

Fichier:

PDF, 196 KB

english, 2004

23

Method of preventing oxydation of iron

M.F.L. Allamand

Journal:

Journal of the Franklin Institute

Année:

1842

Langue:

english

Fichier:

PDF, 137 KB

english, 1842

24

2FC2.4 A survey of Collagen VI myopathies at Hôpital Pitié-Salpêtrière: the natural history and genetic description of 26 patients

N. Deconinck, A. Ferreiro, C. Ledeuil, C. Gartioux, P. Richard, V. Allamand, T. Stojkovic

Journal:

European Journal of Paediatric Neurology

Année:

2011

Langue:

english

Fichier:

PDF, 52 KB

english, 2011

25

Targeted Development of Microsatellite Markers from Inter-Alu Amplification of YAC Clones

Anete Pereira de Souza, Valérie Allamand, Isabelle Richard, Lydie Brenguier, Ilya Chumakov, Daniel Cohen, Jacques S. Beckmann

Journal:

Année:

1994

Fichier:

PDF, 199 KB

1994

26

Regional Localization of Human Chromosome 15 Loci

Isabelle Richard, Odile Broux, Nuchanard Chiannilkulchai, Françoise Fougerousse, Valérie Allamand, Nathalie Bourg, Lydie Brenguier, Catherine Devaud, Patricia Pasturaud, Carinne Roudaut, Frederic Lore

Journal:

Année:

1994

Fichier:

PDF, 455 KB

1994

27

Low-Molecular-Weight, Calcium-Dependent Phospholipase A2Genes Are Linked and Map to Homologous Chromosome Regions in Mouse and Human

Jay A. Tischfield, Yu-Rong Xia, Diana M. Shih, Ivana Klisak, Ju Chen, Sandra J. Engle, Aristotle N. Siakotos, Michelle V. Winstead, Jeffrey J. Seilhamer, Valérie Allamand, Gabor Gyapay, Aldons J. Lusi

Journal:

Année:

1996

Langue:

english

Fichier:

PDF, 107 KB

english, 1996

28

Identification of muscle-specific calpain and β-sarcoglycan genes in progressive autosomal recessive muscular dystrophies

J.S. Beckmann, I. Richard, O. Broux, F. Fougerousse, N. Bourg, L. Brenguier, V. Allamand, N. Chiannilkulchai, C. Roudaut, F. Duclos, L.E. Lim, Y. Sunada, J. Meyer, C. Moomaw, C. Slaughter, F.M.S. Tomé

Journal:

Neuromuscular Disorders

Année:

1996

Langue:

english

Fichier:

PDF, 113 KB

english, 1996

29

β-sarcoglycan : Characterization and role in limb-girdle muscular dystrophy linked to 4q12

O. Broux, F. Duclos, L.E. Lim, N. Bourg, Y. Sunada, V. Allamand, J. Meyer, I. Richard, C. Moomaw, C. Slaughter, F.M.S. Tomé, M. Fardeau, C.E. Jackson, K.P. Campbell, J.S. Beckmann

Journal:

Neuromuscular Disorders

Année:

1996

Langue:

english

Fichier:

PDF, 128 KB

english, 1996

30

Selenoprotein function and muscle disease

Alain Lescure, Mathieu Rederstorff, Alain Krol, Pascale Guicheney, Valérie Allamand

Journal:

Biochimica et Biophysica Acta (BBA) - General Subjects

Année:

2009

Langue:

english

Fichier:

PDF, 477 KB

english, 2009

31

First molecular characterization and immunolocalization of keratoepithelin in adult human skeletal muscle

Francesca Sciandra, Simona Morlacchi, Valérie Allamand, Giacomo De Benedetti, Gianfranco Macchia, Tamara C. Petrucci, Manuela Bozzi, Andrea Brancaccio

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 2.33 MB

english, 2008

32

P.P.1 03 A clinical, morphological and genetic study of congenital muscular dystrophies in Algeria

S. Makri, N. Terki, S. Belarbi, S. Assami, S. Maugenre, C. Gartioux, V. Allamand, P. Richard, N.B. Romero, M. Ait Kaci-Ahmed, D. Grid, P. Guicheney, M. Tazir

Journal:

Neuromuscular Disorders

Année:

2006

Langue:

english

Fichier:

PDF, 61 KB

english, 2006

33

P.P.7 04 A homozygous COL6A1 splice site mutation in siblings with Ullrich congenital muscular dystrophy

S. Makri, V. Allamand, P. Richard, C. Gartioux, N. Terki, S. Maugenre, M. Ait-Kaci, P. Guicheney

Journal:

Neuromuscular Disorders

Année:

2006

Langue:

english

Fichier:

PDF, 46 KB

english, 2006

34

T.O. 3 Rescue of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a homozygous mutation in the selenocysteine codon of SEPN1

V. Allamand, P. Richard, C. Ledeuil, D. Chaigne, P. Guicheney, A. Krol, A. Lescure

Journal:

Neuromuscular Disorders

Année:

2006

Langue:

english

Fichier:

PDF, 48 KB

english, 2006

35

C.P.2.06 Spectrum of COL6A1 mutations in patients with Ullrich congenital muscular dystrophy

P. Richard, C. Ledeuil, C. Gartioux, L. Torrieri, L. Briñas, A. Ferreiro, A. Toutain, S. Makri, E. Ollagnon, B. Eymard, S. Quijano-Roy, B. Estournet, P. Guicheney, V. Allamand

Journal:

Neuromuscular Disorders

Année:

2007

Langue:

english

Fichier:

PDF, 49 KB

english, 2007

36

C.O.3 Endoplasmic reticulum retention of COL6 chains in Ullrich congenital muscular dystrophy

V. Allamand, C. Gartioux, E. Lacène, J. Lainé, C. Ledeuil, S. Quijano-Roy, S. Makri, L. Viollet, P. Jeannet, D. Herlicoviez, M. Penniello-Valette, P. Richard, B. Estournet, N. Romero, P. Guicheney

Journal:

Neuromuscular Disorders

Année:

2007

Langue:

english

Fichier:

PDF, 51 KB

english, 2007

37

C.P.2.11 Expression of selenoprotein N in mice during development and in muscle regeneration

P. Castets, S. Maugenre, M. Rederstorff, A. Lescure, A. Krol, V. Allamand, P. Guicheney

Journal:

Neuromuscular Disorders

Année:

2007

Langue:

english

Fichier:

PDF, 48 KB

english, 2007

38

C.P.2.15 Cib2 in muscular dystrophy

M. Häger, Å. Mikael, V. Allamand, M. Dubeej-Hjalt

Journal:

Neuromuscular Disorders

Année:

2007

Langue:

english

Fichier:

PDF, 49 KB

english, 2007

39

C.P.2.03 Predictive factors of severity and management of respiratory and orthopaedic complications in 16 Ullrich CMD patients

S. Quijano-Roy, V. Allamand, N. Riahi, C. Gartioux, L. Briñas, D. Leclair-Richard, R. Zeller, C. Ledeuil, M. Commare, L. Viollet, C. Bönnemann, M. Mayer, D. Chaigne, N. Essid, F. Renault, A. Barois, A

Journal:

Neuromuscular Disorders

Année:

2007

Langue:

english

Fichier:

PDF, 51 KB

english, 2007

40

C.P.2.16 Novel recessive and dominant mutations in collagen VI causing Ullrich congenital muscular dystrophy and correlation with mRNA degradation

L. Briñas, C. Gartioux, C. Ledeuil, S. Quijano-Roy, S. Makri, L. Merlini, H. Topaloglu, F. Roelens, V. Hovers, P. Jeannet, B. Estournet, P. Richard, P. Guicheney, V. Allamand

Journal:

Neuromuscular Disorders

Année:

2007

Langue:

english

Fichier:

PDF, 65 KB

english, 2007

41

G.P.1.03 Important variability in clinical severity in a family with Col VI-related myopathy: Potential implication of digenism?

F. Chapon, C. Gartioux, C. Ledeuil, L. Demay, L. Brinas, D. Herlicoviez, S. Allouche, A. Ferreiro, F. Leturcq, P. Richard, V. Allamand, G. Bonne

Journal:

Neuromuscular Disorders

Année:

2008

Langue:

english

Fichier:

PDF, 48 KB

english, 2008

42

G.P.6.03 Specific CT scanner muscle pattern helps to differentiate contractural lamin A/C and collagen VI related myopathies

N. Deconinck, E. Dion, A. Ferreiro, B. Eymard, P. Richard, V. Allamand, R. Benyaou, G. Bonne, T. Stojkovic

Journal:

Neuromuscular Disorders

Année:

2008

Langue:

english

Fichier:

PDF, 49 KB

english, 2008

43

T.O.1 Cyclosporin A as a potential treatment for collagen VI-related muscular dystrophy: A cellular study of mitochondrial dysfunction and its rescue

D. Hicks, A.K. Lampe, S.H. Laval, V. Allamand, C. Jimenez-Mallebrera, M. Walter, F. Muntoni, S. Quijano-Roy, P. Richard, V. Straub, H. Lochmuller, K.M.D. Bushby

Journal:

Neuromuscular Disorders

Année:

2008

Langue:

english

Fichier:

PDF, 46 KB

english, 2008

44

Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern

N. Deconinck, E. Dion, R. Ben Yaou, A. Ferreiro, B. Eymard, L. Briñas, C. Payan, T. Voit, P. Guicheney, P. Richard, V. Allamand, G. Bonne, T. Stojkovic

Journal:

Neuromuscular Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 699 KB

english, 2010

45

O.3 Satellite cell loss is the pathomechanism leading to muscle atrophy in selenoprotein N deficiency

P. Castets, A.T. Bertrand, M. Beuvin, A. Ferry, F. Le Grand, M. Castets, G. Chazot, M. Rederstorff, A. Krol, A. Lescure, N.B. Romero, P. Guicheney, V. Allamand

Journal:

Neuromuscular Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 41 KB

english, 2010

46

P1.10 A survey of collagen VI myopathies at Hôpital Pitié-Salpêtrière

N. Deconinck, A. Ferreiro, B. Eymard, A. Behin, P. Laforêt, C. Ledeuil, C. Gartioux, P. Richard, V. Allamand, T. Stojkovic

Journal:

Neuromuscular Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 39 KB

english, 2010

47

166th ENMC International Workshop on Collagen type VI-related Myopathies, 22–24 May 2009, Naarden, The Netherlands

Valérie Allamand, Luciano Merlini, Kate Bushby

Journal:

Neuromuscular Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 199 KB

english, 2010

48

P1.15 DNA micro-arrays for revisiting molecular pathology in neuromuscular disorders

M. Cossée, M. Bartoli, V. Allamand, C. Guittard, V. Delague, M. Krahn, C. Ledeuil, I. Marey, I. Nelson, P. Richard, P. Bourgeois, G. Bonne, F. Leturcq, T. Voit, C. Béroud, J. Chelly, N. Lévy

Journal:

Neuromuscular Disorders

Année:

2010

Langue:

english

Fichier:

PDF, 39 KB

english, 2010

49

P5.62 Garches muscle Whole-Body MRI protocol: Pattern recognition in early onset neuromuscular disorders

D. Avila-Smirnow, S. Quijano-Roy, V. Allamand, G. Bonne, V. Biancalana, O. Dubourg, N. Essid, A. Ferreiro, P. Guicheney, C. Lebreton, M. Hamida, C. Ioos, F. Leturcq, N. Monnier, R. Rubinsztajn, N.B. R

Journal:

Neuromuscular Disorders

Année:

2011

Langue:

english

Fichier:

PDF, 61 KB

english, 2011

50

P2.4 Searching for pulmonary outcome measures in ’Early Onset’ COL6-related myopathy

S. Wehbi, N. Essid, L. Briñas, D. Leclair-Richard, L. Viollet, N.B. Romero, P. Richard, V. Allamand, B. Estournet, S. Quijano-Roy

Journal:

Neuromuscular Disorders

Année:

2011

Langue:

english

Fichier:

PDF, 61 KB

english, 2011