A. Afenjar : rechercher sur Z-Library

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Don't use scam websites

Livres
Articles (78)
Les plus populaires
Liste
- Liste
- Tableau

1

Stratégie d’exploration d’une déficience intellectuelle inexpliquée

A. Verloes, D. Héron, T. Billette de Villemeur, A. Afenjar, C. Baumann, N. Bahi-Buisson, P. Charles, A. Faudet, A. Jacquette, C. Mignot, M.-L. Moutard, S. Passemard, M. Rio, L. Robel, C. Rougeot, D. V

Journal:

Archives de Pédiatrie

Année:

2012

Fichier:

PDF, 478 KB

2012

2

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Wolff, Markus, Johannesen, Katrine M., Hedrich, Ulrike B. S., Masnada, Silvia, Rubboli, Guido, Gardella, Elena, Lesca, Gaetan, Ville, Dorothée, Milh, Mathieu, Villard, Laurent, Afenjar, Alexandra, Cha

Journal:

Année:

2017

Langue:

english

Fichier:

PDF, 976 KB

english, 2017

3

MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype

Smol, T., Petit, F., Piton, A., Keren, B., Sanlaville, D., Afenjar, A., Baker, S., Bedoukian, E. C., Bhoj, E. J., Bonneau, D., Boudry-Labis, E., Bouquillon, S., Boute-Benejean, O., Caumes, R., Chatron

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 7.33 MB

english, 2018

4

Exome sequencing in congenital ataxia identifies two new candidate genes and highlights a pathophysiological link between some congenital ataxias and early infantile epileptic encephalopathies

Valence, Stéphanie, Cochet, Emmanuelle, Rougeot, Christelle, Garel, Catherine, Chantot-Bastaraud, Sandra, Lainey, Elodie, Afenjar, Alexandra, Barthez, Marie-Anne, Bednarek, Nathalie, Doummar, Diane, F

Journal:

Genetics in Medicine

Année:

2018

Langue:

english

Fichier:

PDF, 1.80 MB

english, 2018

5

Heterogeneity of NSD1 alterations in 116 patients with Sotos syndrome

Pascale Saugier-Veber, Céline Bonnet, Alexandra Afenjar, Valérie Drouin-Garraud, Christine Coubes, Séverine Fehrenbach, Muriel Holder-Espinasse, Joëlle Roume, Valérie Malan, Marie-France Portnoi, Nico

Journal:

Année:

2007

Langue:

english

Fichier:

PDF, 354 KB

english, 2007

6

The three stages of epilepsy in patients with CDKL5 mutations

Nadia Bahi-Buisson, Anna Kaminska, Nathalie Boddaert, Marlène Rio, Alexandra Afenjar, Marion Gérard, Fabienne Giuliano, Jacques Motte, Delphine Héron, Marie Ange N'Guyen Morel, Perrine Plouin, Christi

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 608 KB

english, 2008

7

Spectrum of pontocerebellar hypoplasia in 13 girls and boys withCASKmutations: confirmation of a recognizable phenotype and first description of a male mosaic patient

Lydie Burglen, Sandra Chantot-Bastaraud, Catherine Garel, Mathieu Milh, Renaud Touraine, Ginevra Zanni, Florence Petit, Alexandra Afenjar, Cyril Goizet, Sabina Barresi, Aurélie Coussement, Christine I

Journal:

Orphanet Journal of Rare Diseases

Année:

2012

Langue:

english

Fichier:

PDF, 949 KB

english, 2012

8

The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 ofSRCAP

Nikkel, Sarah M, Dauber, Andrew, de Munnik, Sonja, Connolly, Meghan, Hood, Rebecca L, Caluseriu, Oana, Hurst, Jane, Kini, Usha, Nowaczyk, Malgorzata J, Afenjar, Alexandra, Albrecht, Beate, Allanson, J

Journal:

Orphanet Journal of Rare Diseases

Année:

2013

Langue:

english

Fichier:

PDF, 5.33 MB

english, 2013

9

Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE

Nava, C, Lamari, F, Héron, D, Mignot, C, Rastetter, A, Keren, B, Cohen, D, Faudet, A, Bouteiller, D, Gilleron, M, Jacquette, A, Whalen, S, Afenjar, A, Périsse, D, Laurent, C, Dupuits, C, Gautier, C, G

Journal:

Translational Psychiatry

Année:

2012

Langue:

english

Fichier:

PDF, 1.18 MB

english, 2012

10

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations

Passemard, S., Titomanlio, L., Elmaleh, M., Afenjar, A., Alessandri, J. -L., Andria, G., de Villemeur, T. B., Boespflug-Tanguy, O., Burglen, L., Del Giudice, E., Guimiot, F., Hyon, C., Isidor, B., Meg

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 429 KB

english, 2009

11

HER2 status in advanced or metastatic gastric, esophageal, or gastro-esophageal adenocarcinoma for entry to the TRIO-013/LOGiC trial of lapatinib

Press, M. F., Ellis, C. E., Gagnon, R. C., Grob, T. J., Buyse, M., Villalobos, I., Liang, Z., Wu, S., Bang, Y.-J., Qin, S.-K., Chung, H. C., Xu, J., Park, J. O., Jeziorski, K., Afenjar, K., Ma, Y., Es

Journal:

Molecular Cancer Therapeutics

Année:

2016

Langue:

english

Fichier:

PDF, 7.90 MB

english, 2016

12

Whole exome sequencing in non progressive congenital ataxia consanguineous families: 3 genes lumping with early infantile epileptic encephalopathies

Valence, Stéphanie, Garel, Catherine, Chantot Bastaraud, Sandra, Afenjar, Alexandra, Barthez, Marie Anne, Bednarek, Nathalie, Goizet, Cyril, Lacombe, Didier, Milh, Mathieu, Moutard, Marie Laure, Robin

Journal:

European Journal of Paediatric Neurology

Année:

2017

Langue:

english

Fichier:

PDF, 173 KB

english, 2017

13

Defining the phenotypic spectrum of SLC6A1 mutations

Johannesen, Katrine M., Gardella, Elena, Linnankivi, Tarja, Courage, Carolina, de Saint Martin, Anne, Lehesjoki, Anna-Elina, Mignot, Cyril, Afenjar, Alexandra, Lesca, Gaetan, Abi-Warde, Marie-Thérèse,

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 2.51 MB

english, 2018

14

16p13.11 microduplication in 45 new patients: refined clinical significance and genotype–phenotype correlations

Allach El Khattabi, Laïla, Heide, Solveig, Caberg, Jean-Hubert, Andrieux, Joris, Doco Fenzy, Martine, Vincent-Delorme, Caroline, Callier, Patrick, Chantot-Bastaraud, Sandra, Afenjar, Alexandra, Boute-

Journal:

Journal of Medical Genetics

Année:

2018

Langue:

english

Fichier:

PDF, 588 KB

english, 2018

15

Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature

Torti, Erin, Keren, Boris, Palmer, Elizabeth E., Zhu, Zehua, Afenjar, Alexandra, Anderson, Ilse. J., Andrews, Marisa V., Atkinson, Celia, Au, Margaret, Berry, Susan A., Bowling, Kevin M., Boyle, Jacki

Journal:

Genetics in Medicine

Année:

2019

Langue:

english

Fichier:

PDF, 1.18 MB

english, 2019

16

Expanding the phenotypic spectrum of Allan–Herndon–Dudley syndrome in patients with SLC 16A2 mutations

Remerand, Ganaelle, Boespflug‐Tanguy, Odile, Tonduti, Davide, Touraine, Renaud, Rodriguez, Diana, Curie, Aurore, Perreton, Nathalie, Des Portes, Vincent, Sarret, Catherine, Afenjar, Alexandra, Burglen

Journal:

Developmental Medicine & Child Neurology

Année:

2019

Langue:

english

Fichier:

PDF, 671 KB

english, 2019

17

CDK5RAP2 primary microcephaly is associated with hypothalamic, retinal and cochlear developmental defects

Nasser, Hala, Vera, Liza, Elmaleh-BergÃ¨s, Monique, Steindl, Katharina, Letard, Pascaline, Teissier, Natacha, Ernault, Anais, Guimiot, Fabien, Afenjar, Alexandra, Moutard, Marie Laure, HÃ©ron, Delphin

Journal:

Journal of Medical Genetics

Année:

2020

Fichier:

PDF, 2.83 MB

2020

18

Novel comprehensive diagnostic strategy in Pitt–Hopkins syndrome: Clinical score and further delineation of the TCF4 mutational spectrum

Sandra Whalen, Delphine Héron, Thierry Gaillon, Oana Moldovan, Massimiliano Rossi, Françoise Devillard, Fabienne Giuliano, Gabriela Soares, Michelle Mathieu-Dramard, Alexandra Afenjar, Perrine Charles

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 356 KB

english, 2012

19

Infantile hypokinetic-hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene

Diane Doummar, Fabienne Clot, Marie Vidailhet, Alexandra Afenjar, Alexandra Durr, Alexis Brice, Cyril Mignot, Agnès Guet, Thierry Billette de Villemeur, Diana Rodriguez

Journal:

Movement Disorders

Année:

2009

Langue:

english

Fichier:

PDF, 302 KB

english, 2009

20

CDKL5 and ARX mutations are not responsible for early onset severe myoclonic epilepsy in infancy

Rima Nabbout, Christel Depienne, Mathilde Chipaux, Benoit Girard, Isabelle Souville, Oriane Trouillard, Olivier Dulac, Jamel Chelly, Alexandra Afenjar, Delphine Héron, Eric Leguern, Cherif Beldjord, T

Journal:

Epilepsy Research

Année:

2009

Langue:

english

Fichier:

PDF, 157 KB

english, 2009

21

Treatment by oral creatine, L-arginine and L-glycine in six severely affected patients with creatine transporter defect

Vassili Valayannopoulos, Nathalie Boddaert, Allel Chabli, Valerie Barbier, Isabelle Desguerre, Anne Philippe, Alexandra Afenjar, Michel Mazzuca, David Cheillan, Arnold Munnich, Yves de Keyzer, Corneli

Journal:

Journal of Inherited Metabolic Disease

Année:

2012

Langue:

english

Fichier:

PDF, 203 KB

english, 2012

22

Spectrum of epilepsy in terminal 1p36 deletion syndrome

Nadia Bahi-Buisson, Eva Guttierrez-Delicado, Christine Soufflet, Marlène Rio, Valérie Cormier Daire, Didier Lacombe, Delphine Héron, Alain Verloes, Sameer Zuberi, Lydie Burglen, Alexandra Afenjar, Mar

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 380 KB

english, 2008

23

Deletion of filamin A in two female patients with periventricular nodular heterotopia

Jodi Warman Chardon, Cyril Mignot, Swaroop Aradhya, Boris Keren, Alexandra Afenjar, Anna Kaminska, Cherif Beldjord, Delphine Héron, Kym M. Boycott

Journal:

American Journal of Medical Genetics Part A

Année:

2012

Langue:

english

Fichier:

PDF, 259 KB

english, 2012

24

Early neurological phenotype in 4 children with biallelic PRODH mutations

Alexandra Afenjar, Marie-Laure Moutard, Diane Doummar, Agnés Guët, Daniel Rabier, Anne-Isabelle Vermersch, Cyril Mignot, Lydie Burglen, Delphine Heron, Elizabeth Thioulouse, Thierry Billette de Villem

Journal:

Brain and Development

Année:

2007

Langue:

english

Fichier:

PDF, 114 KB

english, 2007

25

Phénotype psychiatrique des maladies neuromusculaires de l’enfant : revue de la littérature

M. Douniol, J. Xavier, A. Jacquette, A. Afenjar, N. Angeard, D. Heron, D. Cohen

Journal:

Neuropsychiatrie de l'Enfance et de l'Adolescence

Année:

2008

Fichier:

PDF, 247 KB

2008

26

L'HHV-6, une cause de leucoencéphalite aiguë disséminée du nourrisson : à propos de 1 observation

A. Afenjar, D. Rodriguez, F. Rozenberg, N. Dorison, A. Guët, C. Mignot, D. Doummar, T. Billette de Villemeur, G. Ponsot

Journal:

Archives de Pédiatrie

Année:

2007

Langue:

french

Fichier:

PDF, 412 KB

french, 2007

27

Netrin G1 Mutations Are an Uncommon Cause of Atypical Rett Syndrome With or Without Epilepsy

Juliette Nectoux, Benoit Girard, Nadia Bahi-Buisson, Fabienne Prieur, Alexandra Afenjar, Haydee Rosas-Vargas, Jamel Chelly, Thierry Bienvenu

Journal:

Pediatric Neurology

Année:

2007

Langue:

english

Fichier:

PDF, 225 KB

english, 2007

28

P-566 Vinflunine (VFL) in combination with carboplatin (CBDCA) for treatment of advanced non-small cell lung cancer (NSCLC) in chemonaive patients (pts): Phase I and pharmacokinetic study

Robinet, G., Afenjar, K., Gouva, S., Planchard, D., Zorza, G., Tourani, J.

Journal:

Année:

2005

Langue:

english

Fichier:

PDF, 139 KB

english, 2005

29

Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort

Catherine Sarret, Mélanie Rigal, Catherine Vaurs-Barrière, Imen Dorboz, Eléonore Eymard-Pierre, Patricia Combes, Geneviève Giraud, Ronald J.A. Wanders, Alexandra Afenjar, Christine Francannet, Odile B

Journal:

Journal of the Neurological Sciences

Année:

2012

Langue:

english

Fichier:

PDF, 475 KB

english, 2012

30

Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders

Nava, Caroline, Keren, Boris, Mignot, Cyril, Rastetter, Agnès, Chantot-Bastaraud, Sandra, Faudet, Anne, Fonteneau, Eric, Amiet, Claire, Laurent, Claudine, Jacquette, Aurélia, Whalen, Sandra, Afenjar,

Journal:

European Journal of Human Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 2.50 MB

english, 2014

31

Phénotype clinique reconnaissable des neurodegeneration with brain iron accumulation (NBIA) liées aux mutations du gène C19ORF12

Afenjar, A., Billette De Villemeur, T., Chabrol, B., Gras, D., Legall, A., Mochel, F., Sedel, F., Rodriguez, D., Burglen, L.

Journal:

Archives de Pédiatrie

Année:

2013

Fichier:

PDF, 78 KB

2013

32

Retinal involvement in two unrelated patients with Myhre syndrome

Al Ageeli, Essam, Mignot, Cyril, Afenjar, Alexandra, Whalen, Sandra, Dorison, Nathalie, Mayer, Michèle, Esteva, Blandine, Dubern, Béatrice, Momtchilova, Marta, Le Gargasson, Jean-François, Bursztyn, J

Journal:

European Journal of Medical Genetics

Année:

2012

Langue:

english

Fichier:

PDF, 747 KB

english, 2012

33

6584 A phase III study of CapeOx +/− lapatinib in HER2 positive locally-advanced/metastatic upper gastrointestinal adenocarcinoma: interim safety results

Hecht, J., Bang, Y., Sobrero, A., Elme, A., Patel, G., Park, J., Kemner, A., Afenjar, K., Koehler, M.

Journal:

European Journal of Cancer Supplements

Année:

2009

Langue:

english

Fichier:

PDF, 47 KB

english, 2009

34

O9 – 2019 Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2

Milh, M, Boutry-Kryza, N, Sutera-Sardo, J, Mignot, C, Auvin, S, Villeneuve, N, Roubertie, A, Héron, B, Kaminska, A, Altuzara, C, Blanchard, G, Ville, D, Barthez, H, Héron, D, Afenjar, A, Dorison, N, B

Journal:

European Journal of Paediatric Neurology

Année:

2013

Langue:

english

Fichier:

PDF, 82 KB

english, 2013

35

Key clinical features to identify girls with CDKL5 mutations

Bahi-Buisson, N., Nectoux, J., Rosas-Vargas, H., Milh, M., Boddaert, N., Girard, B., Cances, C., Ville, D., Afenjar, A., Rio, M., Heron, D., N'Guyen Morel, M. A., Arzimanoglou, A., Philippe, C., Jonve

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 1010 KB

english, 2008

36

Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations

Dupre, T., Vuillaumier-Barrot, S., Chantret, I., Yaye, H. S., Le Bizec, C., Afenjar, A., Altuzarra, C., Barnerias, C., Burglen, L., de Lonlay, P., Feillet, F., Napuri, S., Seta, N., Moore, S. E. H.

Journal:

Journal of Medical Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 609 KB

english, 2010

37

Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome

Le Goff, Carine, Mahaut, Clémentine, Abhyankar, Avinash, Le Goff, Wilfried, Serre, Valérie, Afenjar, Alexandra, Destrée, Anne, di Rocco, Maja, Héron, Delphine, Jacquemont, Sébastien, Marlin, Sandrine,

Journal:

Nature Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 696 KB

english, 2011

38

Myhre and LAPS syndromes: clinical and molecular review of 32 patients

Michot, Caroline, Le Goff, Carine, Mahaut, Clémentine, Afenjar, Alexandra, Brooks, Alice S, Campeau, Philippe M, Destree, Anne, Di Rocco, Maja, Donnai, Dian, Hennekam, Raoul, Heron, Delphine, Jacquemo

Journal:

European Journal of Human Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 937 KB

english, 2014

39

Floating-Harbor Syndrome

Arpin, Stéphanie, Afenjar, Alexandra, Dubern, Béatrice, Toutain, Annick, Cabrol, Sylvie, Héron, Delphine

Journal:

Clinical Dysmorphology

Année:

2012

Langue:

english

Fichier:

PDF, 195 KB

english, 2012

40

Xp21 deletion in female patients with intellectual disability: Two new cases and a review of the literature

Heide, Solveig, Afenjar, Alexandra, Edery, Patrick, Sanlaville, Damien, Keren, Boris, Rouen, Alexandre, Lavillaureix, Alinoë, Hyon, Capucine, Doummar, Diane, Siffroi, Jean-Pierre, Chantot-Bastaraud, S

Journal:

European Journal of Medical Genetics

Année:

2015

Langue:

english

Fichier:

PDF, 457 KB

english, 2015

41

A recurrent KCNQ2 pore mutation causing early onset epileptic encephalopathy has a moderate effect on M current but alters subcellular localization of Kv7 channels

Abidi, Affef, Devaux, Jérôme J., Molinari, Florence, Alcaraz, Gisèle, Michon, François-Xavier, Sutera-Sardo, Julie, Becq, Hélène, Lacoste, Caroline, Altuzarra, Cécilia, Afenjar, Alexandra, Mignot, Cyr

Journal:

Neurobiology of Disease

Année:

2015

Langue:

english

Fichier:

PDF, 3.29 MB

english, 2015

42

Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females

Depienne, Christel, Bouteiller, Delphine, Keren, Boris, Cheuret, Emmanuel, Poirier, Karine, Trouillard, Oriane, Benyahia, Baya, Quelin, Chloé, Carpentier, Wassila, Julia, Sophie, Afenjar, Alexandra, G

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 1.11 MB

english, 2009

43

GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia

Coutelier, M., Burglen, L., Mundwiller, E., Abada-Bendib, M., Rodriguez, D., Chantot-Bastaraud, S., Rougeot, C., Cournelle, M.-A., Milh, M., Toutain, A., Bacq, D., Meyer, V., Afenjar, A., Deleuze, J.-

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 900 KB

english, 2015

44

Myhre and LAPS syndromes: clinical and molecular review of 32 patients

Michot, Caroline, Le Goff, Carine, Mahaut, Clémentine, Afenjar, Alexandra, Brooks, Alice S, Campeau, Philippe M, Destree, Anne, Di Rocco, Maja, Donnai, Dian, Hennekam, Raoul, Heron, Delphine, Jacquemo

Journal:

European Journal of Human Genetics

Année:

2014

Langue:

english

Fichier:

PDF, 63 KB

english, 2014

45

Recessive hereditary methaemoglobinaemia, type II: delineation of the clinical spectrum

Ewenczyk, C., Leroux, A., Roubergue, A., Laugel, V., Afenjar, A., Saudubray, J. M., Beauvais, P., de Villemeur, T. B., Vidailhet, M., Roze, E.

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 270 KB

english, 2008

46

The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD

Richard, Anne Claire, Rovelet-Lecrux, Anne, Delaby, Elsa, Charbonnier, Camille, Thiruvahindrapuram, Bhooma, Hatchwell, Eli, Eis, Peggy S., Afenjar, Alexandra, Dussardier, Brigitte Gilbert, Scherer, St

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Année:

2016

Langue:

english

Fichier:

PDF, 104 KB

english, 2016

47

Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases

Di Meglio, Chloé, Lesca, Gaetan, Villeneuve, Nathalie, Lacoste, Caroline, Abidi, Affef, Cacciagli, Pierre, Altuzarra, Cécilia, Roubertie, Agathe, Afenjar, Alexandra, Renaldo-Robin, Florence, Isidor, B

Journal:

Année:

2015

Langue:

english

Fichier:

PDF, 729 KB

english, 2015

48

A Distinct Class of Chromoanagenesis Events Characterized by Focal Copy Number Gains

Masset, Heleen, Hestand, Matthew S., Van Esch, Hilde, Kleinfinger, Pascale, Plaisancié, Julie, Afenjar, Alexandra, Molignier, Romain, Schluth-Bolard, Caroline, Sanlaville, Damien, Vermeesch, Joris R.

Journal:

Année:

2016

Langue:

english

Fichier:

PDF, 1.34 MB

english, 2016

49

Variable clinical expression in patients with mosaicism for KCNQ2 mutations

Milh, Mathieu, Lacoste, Caroline, Cacciagli, Pierre, Abidi, Affef, Sutera-Sardo, Julie, Tzelepis, Ilias, Colin, Estelle, Badens, Catherine, Afenjar, Alexandra, Coeslier, Anne Dieux, Dailland, Thomas,

Journal:

American Journal of Medical Genetics Part A

Année:

2015

Langue:

english

Fichier:

PDF, 181 KB

english, 2015

50

ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability

Mignot, Cyril, Moutard, Marie-Laure, Rastetter, Agnès, Boutaud, Lucile, Heide, Solveig, Billette, Thierry, Doummar, Diane, Garel, Catherine, Afenjar, Alexandra, Jacquette, Aurélia, Lacombe, Didier, Ve

Journal:

Année:

2016

Langue:

english

Fichier:

PDF, 445 KB

english, 2016