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51

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

52

Development of a Sensitive Radioimmunoassay for Fab Fragments: Application to Fab Pharmacokinetics in Humans

Corinne Vo Thanh-Barthet, Michel Urtizberea, Alain E. Sabouraud, Nathalie J. Cano, Jean-Michel G. Scherrmann

Journal:

Pharmaceutical Research

Year:

1993

File:

PDF, 797 KB

1993

53

Note: A sample holder design for sensitive magnetic measurements at high temperatures in a magnetic properties measurement system

Arauzo, A., Guerrero, E., Urtizberea, A., Stankiewicz, J., Rillo, C.

Journal:

Review of Scientific Instruments

Year:

2012

Language:

english

File:

PDF, 650 KB

english, 2012

54

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

55

Reversal of advanced colchicine toxicity in mice with goat colchicine-specific antibodies

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

Journal:

Toxicology and Applied Pharmacology

Year:

1990

Language:

english

File:

PDF, 644 KB

english, 1990

56

Autosomal-Dominant Distal Myopathy Associated with a Recurrent Missense Mutation in the Gene Encoding the Nuclear Matrix Protein, Matrin 3

Jan Senderek, Sean M. Garvey, Michael Krieger, Velina Guergueltcheva, Andoni Urtizberea, Andreas Roos, Miriam Elbracht, Claudia Stendel, Ivailo Tournev, Violeta Mihailova, Howard Feit, Jeff Tramonte,

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 1.03 MB

english, 2009

57

Operational Oceanography System applied to the Prestige oil-spillage event

Manuel González, Luis Ferrer, Adolfo Uriarte, Agurtzane Urtizberea, Ainhoa Caballero

Journal:

Journal of Marine Systems

Year:

2008

Language:

english

File:

PDF, 1.05 MB

english, 2008

58

Surface effects in maghemite nanoparticles

A. Millan, A. Urtizberea, N.J.O. Silva, F. Palacio, V.S. Amaral, E. Snoeck, V. Serin

Journal:

Journal of Magnetism and Magnetic Materials

Year:

2007

Language:

english

File:

PDF, 394 KB

english, 2007

59

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

60

Induction of supernumerary Ribs with sodium salicylate

Olivier Foulon, Helene Girard, Catherine Pallen, Michel Urtizberea, Marina Repetto–Larsay, Ann M. Blacker

Journal:

Reproductive Toxicology

Year:

1999

Language:

english

File:

PDF, 628 KB

english, 1999

61

Relationship between Red Blood Cell Potassium and Plasma Digitoxin Concentrations in Intoxicated Patients

M. Urtizberea, M. Rochdi, A. Sabouraud, C. Bismuth, J. M. Scherrmann

Journal:

Basic & Clinical Pharmacology & Toxicology

Year:

1991

Language:

english

File:

PDF, 550 KB

english, 1991

62

Toxicokinetics of envenomations and anlivenom therapy

V. Choumet, F. Audebert, G. Riviere, M. Sorkine, M. Urtizberea, A. Sabouraud, J.-M. Scherrmann, C. Bon

Journal:

Year:

1995

Language:

english

File:

PDF, 193 KB

english, 1995

63

New approaches in antivenom therapy

F. Audebert, C. Bon, V. Choumet, G. Rivière, A. Robbe-Vincent, M. Sorkine, A. Sabouraud, J.-M. Scherrmann, M. Urtizberea

Journal:

Year:

1996

Language:

english

File:

PDF, 117 KB

english, 1996

64

Toxicokinetics of envenomations and antivenom therapy

V. Choumet, F. Audebert, G. Rivière, M. Sorkine, A. Sabouraud, M. Urtizberea, J.M. Scherrmann, C. Bon

Journal:

Year:

1996

Language:

english

File:

PDF, 116 KB

english, 1996

65

Dystrophies musculaires congénitales. À propos des formes avec déficience en mérosine

J.A. Urtizberea, A. Barois, B. Estournet-Matthiaud

Journal:

Archives de Pédiatrie

Year:

1995

File:

PDF, 138 KB

1995

66

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

67

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

68

Clinical, pathological and molecular findings in two siblings with giant axonal neuropathy (GAN): Report from India

A. Nalini, N. Gayathri, T.C. Yasha, S. Ravishankar, A. Urtizberea, Kathrin Huehne, Bernd Rautenstrauss

Journal:

European Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 1.16 MB

english, 2008

69

A comparative study of the sensitivity of the 3-induction and 9-induction Buehler test procedures for assessing skin sensitisation potential

P. Botham, M. Urtizberea, C. Wiemann, X. Manciaux, L. Tilbury, H.-W. Vohr, S. Allen, N.G. Carmichael, S. de Jouffrey

Journal:

Food and Chemical Toxicology

Year:

2005

Language:

english

File:

PDF, 295 KB

english, 2005

70

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

71

‘Cap myopathy’: Case report of a family

J.M. Cuisset, C.A. Maurage, J.F. Pellissier, A. Barois, J.A. Urtizberea, N. Laing, H. Tajsharghi, L. Vallée

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 370 KB

english, 2006

72

G.P.8 12 Centronuclear myopathy: clinical and morphological phenotype/genotype correlations

J.A. Bevilacqua, M. Bitoun, A. Oldfors, F. Lubieniecki, S. Monges, A.L. Taratuto, A. Urtizberea, L. Cartier, E. Uro-Coste, C. Cances, M. Fardeau, P. Guicheney, N.B. Romero

Journal:

Neuromuscular Disorders

Year:

2006

Language:

english

File:

PDF, 45 KB

english, 2006

73

G.P.4.01 Mutational spectrum of the DYSF gene based on a large cohort of dysferlin deficient patients

M. Krahn, R. Bernard, K. Nguyen, V. Labelle, G. Bassez, D. Figarella-Branger, J. Pouget, E. Di Salvo, E. Hammouda, C. Béroud, B. Eymard, J.A. Urtizberea, F. Leturcq, N. Lévy

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 51 KB

english, 2007

74

G.P.4.15 CAPN3 mutations in patients with idiopathic eosinophilic myositis: A predystrophic stage of LGMD2A?

M. Krahn, F. Hanisch, M. Goicoechea, E. Groen, C. Pécheux, F. Garcia-Bragado, R. Layzer, F. Leturcq, J. Strober, J.A. Urtizberea, A. Sáenz, K. Bushby, N. Lévy, A. Lopez de Munain

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 63 KB

english, 2007

75

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

76

C.P.3.05 MDC1D due to a large genomic insertion in LARGE that causes abnormal gene splicing

N. Clarke, S. Maugenre, J.A. Urtizberea, F. Gray, C. Bouchet, N. Seta, A. Mégarbané, P. Guicheney

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 51 KB

english, 2007

77

Phenotypic variability in giant axonal neuropathy

Meriem Tazir, Sonia Nouioua, Laurent Magy, Kathrin Huehne, Salima Assami, Andoni Urtizberea, Djamel Grid, Tarik Hamadouche, Bernd Rautenstrauss, Jean-Michel Vallat

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 443 KB

english, 2009

78

G.O.5 A new autosomal dominant distal vacuolar myopathy associated with mutation of the nuclear matrix protein, matrin 3

J. Senderek, S.M. Garvey, M. Krieger, I. Tournev, M. Elbracht, A. Roos, C. Stendel, A. Urtizberea, V. Guergueltcheva, V. Mihailova, H. Feit, J. Tramonte, P. Hedera, C. Bergmann, S. Rudnik-Schöneborn,

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 43 KB

english, 2009

79

G.P.10.09 Description of a family associating a calpainopathy and a Duchenne myopathy

S. Nouioua, A.M. Cobo, T. Benhassine, A. Urtizberea, S. Slimani, N. Terki, S. Assami, M. Tazir

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 41 KB

english, 2009

80

Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity

Kristl G. Claeys, Jean-François Pellissier, Federico Garcia-Bragado, Joachim Weis, Andoni Urtizberea, Juan-Jose Poza, Ana-Maria Cobo, Gisela Stoltenburg, Dominique Figarella-Branger, Patrick J. Willem

Journal:

Neuromuscular Disorders

Year:

2010

Language:

english

File:

PDF, 871 KB

english, 2010

81

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

82

Rachis et maladies neuromusculaires de l'adulte

C Gilardeau, H Rivière, JA Urtizberea

Journal:

Annales de Réadaptation et de Médecine Physique

Year:

1997

File:

PDF, 113 KB

1997

83

Apport diagnostique de la biologie moléculaire dans les dystrophies musculaires

J.A. Urtizberea

Journal:

Archives de Pédiatrie

Year:

2000

Language:

french

File:

PDF, 236 KB

french, 2000

84

Quoi de neuf en rééducation neurologique infantile ?

V Leroy-Malherbe, A Laurent-Vannier, D.G Brugel, J.A Urtizberea

Journal:

Archives de Pédiatrie

Year:

2002

Language:

french

File:

PDF, 200 KB

french, 2002

85

Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with ‘de novo’ duplication of dystrophin gene

Norma Beatriz Romero, Pascale De Lonlay, Stéphane Llense, France Leturcq, Guy Touati, J-Andoni Urtizberea, Jean Marie Saudubray, Arnold Munnich, Jean Claude Kaplan, Dominique Récan

Journal:

Neuromuscular Disorders

Year:

2001

Language:

english

File:

PDF, 576 KB

english, 2001

86

Bethlem myopathy (BETHLEM) 86th ENMC International Workshop, 10–11 November 2000, Naarden, The Netherlands

Guglielmina Pepe, Marianne de Visser, Enrico Bertini, Kate Bushby, Olga Camacho Vanegas, Mon-Li Chu, Giovanna Lattanzi, Luciano Merlini, Francesco Muntoni, Andoni Urtizberea

Journal:

Neuromuscular Disorders

Year:

2002

Language:

english

File:

PDF, 108 KB

english, 2002

87

Refined mapping of the HMSNR critical gene region—construction of a high-density integrated genetic and physical map

Janina Hantke, Tamara Rogers, Lisa French, Ivailo Tournev, Velina Guergueltcheva, Jon Andoni Urtizberea, Jaume Colomer, Axinia Corches, Constantin Lupu, Luciano Merlini, P.K Thomas, Luba Kalaydjieva

Journal:

Neuromuscular Disorders

Year:

2003

Language:

english

File:

PDF, 321 KB

english, 2003

88

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

89

Penetrance of the FSHD mutation differs according to the D4Z4 repeat number

C. de Toma, S. Chiron, P. Laforet, J.A. Urtizberea, B. Eymard, M. Fardeau, J-C. Kaplan, M. Jeanpierre

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 130 KB

english, 1997

90

Calpain-3 deficiency: a mild muscular dystrophy in childhood: molecular and clinical findings

P. Dinçer, I. Richard, M.Z. Akçören, J.A. Urtizberea, J.S. Beckmann, H. Topaloglu

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 136 KB

english, 1997

91

A family with severe pseudo-dominant Emery-Dreifuss muscular dystrophy due to emerin deficiency

D. Récan, S. Llense, J.-C. Barbot, F. Leturcq, N. Deburgrave, J.-M. Dupont, P. Warrot, C. Giraudet, F. Fraisse, D. Amsallem, J. Bensaid, J.A. Urtizberea, G.E. Morris, J.-C. Kaplan

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 130 KB

english, 1997

92

Limb girdle muscular dystrophy with calpain deficiency in Guipuzcoa (Basque country, Spain)

J.A. Urtizberea, M. Urtasun, I. Richard, A. Saenz, J.J. Poza, A.M. Cobo, A. Lopez de Munain, J.S. Beckmann

Journal:

Neuromuscular Disorders

Year:

1997

Language:

english

File:

PDF, 136 KB

english, 1997

93

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

94

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

95

66th/67th ENMC Sponsored International Workshop: The Limb-Girdle Muscular Dystrophies 26–28 March 1999, Naarden, The Netherlands

J.S Beckmann, R.H Brown, F Muntoni, A Urtizberea, C Bonnemann, K.M.D Bushby

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 87 KB

english, 1999

96

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

Carina Wallgren-Pettersson, Katarina Pelin, Pirta Hilpelä, Kati Donner, Berardino Porfirio, Claudio Graziano, Kathryn J. Swoboda, Michel Fardeau, J.Andoni Urtizberea, Francesco Muntoni, Caroline Sewry

Journal:

Neuromuscular Disorders

Year:

1999

Language:

english

File:

PDF, 286 KB

english, 1999

97

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

98

Fibrodysplasia Ossificans Progressiva, a Heritable Disorder of Severe Heterotopic Ossification, Maps to Human Chromosome 4q27-31

George Feldman, Ming Li, Shelden Martin, Margrit Urbanek, J. Andoni Urtizberea, Michel Fardeau, Martine LeMerrer, J. Michael Connor, James Triffitt, Roger Smith, Maximilian Muenke, Frederick S. Kaplan

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 214 KB

english, 2000

99

A mass-balanced pelagic ecosystem model with size-structured behaviourally adaptive zooplankton and fish

Castellani, Marco, Rosland, Rune, Urtizberea, Agurtzane, Fiksen, Øyvind

Journal:

Ecological Modelling

Year:

2013

Language:

english

File:

PDF, 1.58 MB

english, 2013

100

Inefficacy of cytarabine in progressive multifocal leucoencephalopathy in AIDS

Pierre de Truchis, Marie Flament-Saillour, Jon-Andoni Urtizberea, Daniel Hassine, Bernard Clair

Journal:

Year:

1993

Language:

english

File:

PDF, 340 KB

english, 1993