Urtizberea, J.-A.: search on Z-Library

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1

Folklore, museums and identity politics in Spain: 1931 to present

Arrieta Urtizberea, Iñaki, Seguí, Joan, Roigé, Xavier

Journal:

International Journal of Heritage Studies

Year:

2019

Language:

english

File:

PDF, 1.16 MB

english, 2019

2

Diagnostic des maladies musculaires

Petiot, P., Urtizberea, J. Andoni

Journal:

EMC - Neurologie

Year:

2004

Language:

french

File:

PDF, 394 KB

french, 2004

3

Bilan et prise en charge des maladies neuromusculaires

Urtizberea, Jon Andoni, Miranda, Alain

Journal:

EMC - Kinésithérapie - Médecine physique - Réadaptation

Year:

2006

Language:

french

File:

PDF, 326 KB

french, 2006

4

Quand tous les chemins mènent à l’Afrique…

Urtizberea, J. Andoni, Alrohaif, Hadil, Gouda, Sayed A., Bastaki, Laila

Journal:

médecine/sciences

Year:

2019

Language:

french

File:

PDF, 6.20 MB

french, 2019

5

Deciphering the complexity of the 4q and 10q subtelomeres by molecular combing in healthy individuals and patients with facioscapulohumeral dystrophy

Nguyen, Karine, Broucqsault, Natacha, Chaix, Charlene, Roche, Stephane, Robin, Jérôme D, Vovan, Catherine, Gerard, Laurene, Mégarbané, André, Urtizberea, Jon Andoni, Bellance, Remi, Barnérias, Christi

Journal:

Journal of Medical Genetics

Year:

2019

Language:

english

File:

PDF, 1013 KB

english, 2019

6

Maladies neuromusculaires : évolution des concepts médicoscientifiques et des pratiques de soins

J.-A. Urtizberea, W. Boucharef, M. Frischmann

Journal:

Neuropsychiatrie de l'Enfance et de l'Adolescence

Year:

2008

Language:

french

File:

PDF, 114 KB

french, 2008

7

Evaluación y tratamiento de las enfermedades neuromusculares

Urtizberea, J.A., Miranda, A.

Journal:

EMC - Kinesiterapia - Medicina Física

Year:

2001

File:

PDF, 362 KB

2001

8

Le ptosis dans les maladies rares du muscle et de la jonction neuromusculaire : revue bibliographique et stratégie diagnostique

Brignol, T.N., Urtizberea, J.A.

Journal:

Journal Français d'Ophtalmologie

Year:

2015

Language:

french

File:

PDF, 204 KB

french, 2015

9

Natural history of LGMD2A for delineating outcome measures in clinical trials

Richard, Isabelle, Hogrel, Jean-Yves, Stockholm, Daniel, Payan, Christine A. M., Fougerousse, Françoise, Eymard, Bruno, Mignard, Claude, Lopez de Munain, Adolfo, Fardeau, Michel, Urtizberea, Jon Andon

Journal:

Annals of Clinical and Translational Neurology

Year:

2016

Language:

english

File:

PDF, 2.03 MB

english, 2016

10

Relief from episodic weakness with pyridostigmine in paramyotonia congenita: A family study

Satish V. Khadilkar, R.K. Singh, K.A. Mansukhani, J.A. Urtizberea, D. Sternberg

Journal:

Year:

2010

Language:

english

File:

PDF, 187 KB

english, 2010

11

Dealing with invasive alien species in the French overseas territories: results and benefits of a 7-year Initiative

Soubeyran, Yohann, Meyer, Jean-Yves, Lebouvier, Marc, De Thoisy, Benoit, Lavergne, Christophe, Urtizberea, Frank, Kirchner, Florian

Journal:

Biological Invasions

Year:

2015

Language:

english

File:

PDF, 344 KB

english, 2015

12

Reversal of murine colchicine toxicity by colchicine-specific Fab fragments

Urtizberea, M., Sabouraud, A., Cano, N., Grandgeorge, M., Rouzioux, J.M., Scherrmann, J.M.

Journal:

Toxicology Letters

Year:

1991

Language:

english

File:

PDF, 381 KB

english, 1991

13

A novel INPP5K mutation in a sibship from the Reunion Island

Nelson, I., Jacquemont, M., Urtizberea, A., Renouil, M., Boland, A., Masson, C., Ben Yaou, R., Bonne, G.

Journal:

Neuromuscular Disorders

Year:

2017

Language:

english

File:

PDF, 255 KB

english, 2017

14

Brown-Vialetto-Van Laere syndrome in a large inbred Lebanese family: Confirmation of autosomal recessive inheritance?

M�garban�, A., Desguerres, I., Rizkallah, E., Delague, V., Nabbout, R., Barois, A., Urtizberea, A.

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 614 KB

english, 2000

15

Morphine pharmacokinetics and pain assessment after intracerebroventricular administration in patients with terminal cancer

Sandouk, Pierre, Serrie, Alain, Urtizberea, Michel, Debray, Marcel, Got, Pierre, Scherrmann, Jean Michel

Journal:

Clinical Pharmacology & Therapeutics

Year:

1991

Language:

english

File:

PDF, 521 KB

english, 1991

16

Diagnostic des maladies musculaires

P Petiot, J.Andoni Urtizberea

Journal:

EMC - Neurologie

Year:

2004

Language:

french

File:

PDF, 768 KB

french, 2004

17

Clinical and pathological features in 15 Chinese patients with calpainopathy

Su-Shan Luo, Jian-Ying Xi, Jia-Hong Lu, Chong-Bo Zhao, Wen-Hua Zhu, Jie Lin, Yin Wang, Hui-Min Ren, Bo Yin, Urtizberea J. Andoni

Journal:

Year:

2011

Language:

english

File:

PDF, 279 KB

english, 2011

18

Actininopathy – a new muscular dystrophy caused by ACTN2 dominant mutations

Savarese, Marco, Palmio, Johanna, Poza, Juan José, Weinberg, Jan, Olive, Montse, Cobo, Ana Maria, Vihola, Anna, Jonson, Per Harald, Sarparanta, Jaakko, García‐Bragado, Federico, Urtizberea, Jon Andoni

Journal:

Annals of Neurology

Year:

2019

Language:

english

File:

PDF, 1.62 MB

english, 2019

19

Development and validation of a motor function classification in patients with neuromuscular disease: The NM-Score

Vuillerot, C., Rippert, P., Roche, S., Bérard, C., Margirier, F., de Lattre, C., Poirot, I., Berruyer, A., Tiffreau, V., Fournier-Mehouas, M., Bouhour, F., Urtizberea, J.-A., Renders, A., Ecochard, R.

Journal:

Annals of Physical and Rehabilitation Medicine

Year:

2013

File:

PDF, 893 KB

2013

20

New autosomal recessive cerebellar ataxia disorder in a large inbred Lebanese family

A. Mégarbané, V. Delague, M.M. Ruchoux, E. Rizkallah, C.A. Maurage, L. Viollet, N. Rouaix-Emery, A. Urtizberea

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 323 KB

english, 2001

21

Spectrum of HSPG2 (Perlecan) mutations in patients with Schwartz-Jampel syndrome

Morgane Stum, Claire-Sophie Davoine, Savine Vicart, Léna Guillot-Noël, Haluk Topaloglu, Francisco Javier Carod-Artal, Hülya Kayserili, Fayçal Hentati, Luciano Merlini, Jon Andoni Urtizberea, EL-Hadi H

Journal:

Year:

2006

Language:

english

File:

PDF, 507 KB

english, 2006

22

Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)

M-Q Xu, G Feldman1,, M Le Merrer, YY Shugart, DL Glaser, JA Urtizberea, M Fardeau, JM Connor, J Triffitt, R Smith, EM Shore, FS Kaplan

Journal:

Clinical Genetics

Year:

2000

Language:

english

File:

PDF, 209 KB

english, 2000

23

High Incidence of Sudden Death with Conduction System and Myocardial Disease Due to Lamins A and C Gene Mutation

HENRI-MARC BÉCANE, GISÈLE BONNE, SHAIDA VARNOUS, ANTOINE MUCHIR, VÉRONIQUE ORTEGA, EL HADI HAMMOUDA, J-ANDONI URTIZBEREA, THOMAS LAVERGNE, MICHEL FARDEAU, BRUNO EYMARD, SIMON WEBER, KETTY SCHWARTZ, DE

Journal:

Pacing and Clinical Electrophysiology

Year:

2000

Language:

english

File:

PDF, 287 KB

english, 2000

24

Report on the 124th ENMC International Workshop. Treatment of Duchenne muscular dystrophy; defining the gold standards of management in the use of corticosteroids 2–4 April 2004, Naarden, The Netherlands

K. Bushby, F. Muntoni, A. Urtizberea, R. Hughes, R. Griggs

Journal:

Neuromuscular Disorders

Year:

2004

Language:

english

File:

PDF, 108 KB

english, 2004

25

Apport diagnostique de la biologie moléculaire dans les dystrophies musculaires

J.A. Urtizberea

Journal:

Journal de Pédiatrie et de Puériculture

Year:

2000

File:

PDF, 227 KB

2000

26

Specific Anti-digoxin Fab Fragments: an Available Antidote for Proscillaridin and Scilliroside Poisoning?

Sabouraud, A., Urtizberea, M., Cano, N., Garnier, R., Scherrmann, J.M.

Journal:

Human & Experimental Toxicology

Year:

1990

Language:

english

File:

PDF, 185 KB

english, 1990

27

Evoked Potentials in Spinal Muscular Atrophy

Cheliout-Heraut, F., Barois, A., Urtizberea, A., Viollet, L., Estournet-Mathiaud, B.

Journal:

Journal of Child Neurology

Year:

2003

Language:

english

File:

PDF, 134 KB

english, 2003

28

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

G. Bonne, E. Mercuri, A. Muchir, A. Urtizberea, H. M. Bécane, D. Recan, L. Merlini, M. Wehnert, R. Boor, U. Reuner, M. Vorgerd, E. M. Wicklein, B. Eymard, D. Duboc, I. Penisson-Besnier, J. M. Cuisset,

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 1.61 MB

english, 2000

29

C-terminal titin deletions cause a novel early-onset myopathy with fatal cardiomyopathy

Virginie Carmignac, Mustafa A. M. Salih, Susana Quijano-Roy, Sylvie Marchand, Molham M. Al Rayess, Maowia M. Mukhtar, Jon A. Urtizberea, Siegfried Labeit, Pascale Guicheney, France Leturcq, Mathias Ga

Journal:

Annals of Neurology

Year:

2007

Language:

english

File:

PDF, 1.35 MB

english, 2007

30

Removal of heavy metals from tap water by a cation exchanger

E. Korngold, S. Belfer, C. Urtizberea

Journal:

Year:

1996

Language:

english

File:

PDF, 254 KB

english, 1996

31

10.1038/1682

Brown, Robert H., Liu, Jing, Aoki, Masashi, Illa, Isabel, Wu, Chenyan, Fardeau, Michel, Angelini, Corrado, Serrano, Carmen, Urtizberea, J. Andoni, Hentati, Faycal, Hamida, Mongi Ben, Bohlega, Saeed, C

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 443 KB

english, 1998

32

Phenotypic Study in 40 Patients With Dysferlin Gene Mutations: High Frequency of Atypical Phenotypes

Nguyen, K., Bassez, G., Krahn, M., Bernard, R., Laforet, P., Labelle, V., Urtizberea, J. A., Figarella-Branger, D., Romero, N., Attarian, S.

Journal:

Archives of Neurology

Year:

2007

Language:

english

File:

PDF, 152 KB

english, 2007

33

A novel CRYAB mutation resulting in multisystemic disease

Sabrina Sacconi, Léonard Féasson, Jean Christophe Antoine, Christophe Pécheux, Rafaelle Bernard, Ana Maria Cobo, Alberto Casarin, Leonardo Salviati, Claude Desnuelle, Andoni Urtizberea

Journal:

Neuromuscular Disorders

Year:

2012

Language:

english

File:

PDF, 562 KB

english, 2012

34

Immunotoxicothérapie : stratégie dans la préparation et l'administration des anticorps spécifiques

Urtizberea, M., Sabouraud, A., Terrien, N., Scherrmann, J.M.

Journal:

Immuno-analyse & Biologie Spécialisée

Year:

1989

File:

PDF, 764 KB

1989

35

Encapsulation of magnetic nanoparticles in a pH-sensitive poly(4-vinyl pyridine) polymer: a step forward to a multi-responsive system

Arizaga, Ana, Ibarz, Gemma, Piñol, Rafael, Urtizberea, Ainhoa

Journal:

Journal of Experimental Nanoscience

Year:

2014

Language:

english

File:

PDF, 607 KB

english, 2014

36

Self-assembled trityl radical capsules – implications for dynamic nuclear polarization

Marin-Montesinos, I., Paniagua, J. C., Vilaseca, M., Urtizberea, A., Luis, F., Feliz, M., Lin, F., Van Doorslaer, S., Pons, M.

Journal:

Physical Chemistry Chemical Physics

Year:

2015

Language:

english

File:

PDF, 2.37 MB

english, 2015

37

Influence of goat colchicine specific antibodies on murine colchicine disposition

N. Terrien, M. Urtizberea, J.M. Scherrmann

Journal:

Year:

1989

Language:

english

File:

PDF, 593 KB

english, 1989

38

Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay

M Krahn, C Pécheux, F Chapon, C Béroud, V Drouin-Garraud, P Laforet, NB Romero, I Penisson-Besnier, R Bernard, JA Urtizberea, F Leturcq, N Lévy

Journal:

Clinical Genetics

Year:

2007

Language:

english

File:

PDF, 600 KB

english, 2007

39

Prise en charge des enfants porteurs de maladies neuromusculaires: bilan de 10 années de réseau

Journal:

Archives de Pédiatrie

Year:

1996

File:

PDF, 168 KB

1996

40

À propos d'un cas de dystrophie musculaire congénitale de type occidental avec mutation ponctuelle dans le gène condant pour la mérosine

J.A. Urtizberea, B. Estournet-Mathiaud, A. Barois, F. Tomé, M. Fardeau, P. Guicheney

Journal:

Archives de Pédiatrie

Year:

1996

File:

PDF, 282 KB

1996

41

The phenotypes of autosomal recessive HSMN linked to chromosomes 5q and 11q

M.A. Salih, M. Kessali, T. Hammadouche, M. Kabira, A. Tahan, M. Al Rayes, T. Maisonobe, E. Le Guern, J.A. Urtizberea, D. Grid

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 129 KB

english, 1997

42

Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression

Daoud, F., Angeard, N., Demerre, B., Martie, I., Benyaou, R., Leturcq, F., Cossee, M., Deburgrave, N., Saillour, Y., Tuffery, S., Urtizberea, A., Toutain, A., Echenne, B., Frischman, M., Mayer, M., De

Journal:

Human Molecular Genetics

Year:

2009

Language:

english

File:

PDF, 254 KB

english, 2009

43

Modelling growth of larval anchovies including diel feeding patterns, temperature and body size

Urtizberea, A., Fiksen, O., Folkvord, A., Irigoien, X.

Journal:

Journal of Plankton Research

Year:

2008

Language:

english

File:

PDF, 846 KB

english, 2008

44

G.P.8.12 Molecular characterization and clinical update on one of the earliest described families with severe childhood autosomal recessive muscular dystrophy (SCARMD)

M. Salih, J.A. Urtizberea, F. Leturcq, M. Mukhtar, L. Anderson, K. Bushby

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

45

Looking under every rock: Duchenne muscular dystrophy and traditional Chinese medicine

J. Andoni Urtizberea, Qi-Shi Fan, Elizabeth Vroom, Dominique Récan, Jean-Claude Kaplan

Journal:

Neuromuscular Disorders

Year:

2003

Language:

english

File:

PDF, 53 KB

english, 2003

46

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

47

Intake of total omega-3 fatty acids, eicosapentaenoic acid and docosahexaenoic acid and risk of coronary heart disease in the Spanish EPIC cohort study

Amiano, P., Machón, M., Dorronsoro, M., Dolores Chirlaque, M., Barricarte, A., Sánchez, M.-J., Navarro, C., Huerta, J.M., Molina-Montes, E., Sánchez-Cantalejo, E., Urtizberea, M., Arriola, L., Larraña

Journal:

Nutrition, Metabolism and Cardiovascular Diseases

Year:

2014

Language:

english

File:

PDF, 250 KB

english, 2014

48

Immunotoxicotherapy: Present status and future trends

Scherrmann, Jean-Michel, Terrien, Nicole, Urtizberea, Michel, Pierson, Pascale, Denis, HÉLÈNe, Bourre, Jean-Marie

Journal:

Clinical Toxicology (Informa Healthcare)

Year:

1989

Language:

english

File:

PDF, 1.23 MB

english, 1989

49

The Ability of the Association Francaise Contre les Myopathies to Promote Research in Neuromuscular Diseases

Urtizberea, J. A.

Journal:

Therapeutic Innovation & Regulatory Science

Year:

2000

Language:

english

File:

PDF, 263 KB

english, 2000

50

Analytical Control Procedures of Immunoreactivity for IgG and Fab Fragments Specific to Haptens

Nathalie J. Cano, Alain E. Sabouraud, Michel Urtizberea, Jean Carcagne, Michel Grandgeorge, Jean Michel G. Scherrmann

Journal:

Pharmaceutical Research

Year:

1992

File:

PDF, 841 KB

1992

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