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1

Is going beyond Rasch analysis necessary to assess the construct validity of a motor function scale?

Guillot, Tiffanie, Roche, Sylvain, Rippert, Pascal, Hamroun, Dalil, Iwaz, Jean, Ecochard, René, Vuillerot, Carole

Journal:

Archives of Physical Medicine and Rehabilitation

Year:

2018

Language:

english

File:

PDF, 4.80 MB

english, 2018

2

The UMD TP53 database and website: update and revisions

Dalil Hamroun, Shunsuke Kato, Chikashi Ishioka, Mireille Claustres, Christophe Béroud, Thierry Soussi

Journal:

Year:

2006

Language:

english

File:

PDF, 346 KB

english, 2006

3

The FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations

Melissa Yana Frédéric, Christine Monino, Christoph Marschall, Dalil Hamroun, Laurence Faivre, Guillaume Jondeau, Hanns-Georg Klein, Luitgard Neumann, Elodie Gautier, Christine Binquet, Cheryl Maslen,

Journal:

Year:

2009

Language:

english

File:

PDF, 340 KB

english, 2009

4

The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients

Jérôme Stirnemann, Marie Vigan, Dalil Hamroun, Djazia Heraoui, Linda Rossi-Semerano, Marc G Berger, Christian Rose, Fabrice Camou, Christine de Roux-Serratrice, Bernard Grosbois, Pierre Kaminsky, Alai

Journal:

Orphanet Journal of Rare Diseases

Year:

2012

Language:

english

File:

PDF, 362 KB

english, 2012

5

Tubulopathie proximale induite par perfusion d’acides aminés dans la radiothérapie interne vectorisée par 177Lu-DOTA0-Tyr3-octréotate

Lenain, R., Georges, L., Hamroun, A., Noel, C., Provot, F.

Journal:

Néphrologie & Thérapeutique

Year:

2017

Language:

french

File:

PDF, 51 KB

french, 2017

6

Dysgammaglobulinémie et maladie de Gaucher : analyse du Registre Français de la Maladie de Gaucher

Nguyen, Y., Stirnemann, J., Lautredoux, F., Cador, B., Hamroun, D., Bengherbia, M., Yousfi, K., Berger, M., Fantin, B., Belmatoug, N.

Journal:

La Revue de Médecine Interne

Year:

2019

Language:

french

File:

PDF, 178 KB

french, 2019

7

The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care

De Antonio, Marie, Dogan, Céline, Daidj, Ferroudja, Eymard, Bruno, Puymirat, Jack, Mathieu, Jean, Gagnon, Cynthia, Katsahian, Sandrine, Hamroun, Dalil, Bassez, Guillaume

Journal:

Orphanet Journal of Rare Diseases

Year:

2019

Language:

english

File:

PDF, 2.64 MB

english, 2019

8

Extremum-Seeking Based Distributed Optimization of Heat Exchangers Network

Zitte, B., Hamroun, B., Couenne, F., Pitault, I.

Journal:

IFAC-PapersOnLine

Year:

2018

Language:

english

File:

PDF, 787 KB

english, 2018

9

A survey on intention analysis: successful approaches and open challenges

Hamroun, Mohamed, Gouider, Mohamed Salah

Journal:

Journal of Intelligent Information Systems

Year:

2020

File:

PDF, 678 KB

2020

10

Impact de la pollution de lâair sur la santÃ© rÃ©naleÂ : revue systÃ©matique et mÃ©ta-analyse

Hamroun, A., Camier, A., Bigna, J.J., Glowacki, F.

Journal:

Néphrologie & Thérapeutique

Year:

2020

File:

PDF, 383 KB

2020

11

UMD (Universal Mutation Database): 2005 update

Christophe Béroud, Dalil Hamroun, Gwenaëlle Collod-Béroud, Catherine Boileau, Thierry Soussi, Mireille Claustres

Journal:

Year:

2005

Language:

english

File:

PDF, 367 KB

english, 2005

12

Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy

Christophe Béroud, Sylvie Tuffery-Giraud, Masafumi Matsuo, Dalil Hamroun, Véronique Humbertclaude, Nicole Monnier, Marie-Pierre Moizard, Marie-Antoinette Voelckel, Laurence Michel Calemard, Pierre Boi

Journal:

Year:

2007

Language:

english

File:

PDF, 292 KB

english, 2007

13

A new locus-specific database (LSDB) for mutations in the TGFBR2 gene: UMD-TGFBR2

Melissa Yana Frederic, Dalil Hamroun, Laurence Faivre, Catherine Boileau, Guillaume Jondeau, Mireille Claustres, Christophe Béroud, Gwenaëlle Collod-Béroud

Journal:

Year:

2008

Language:

english

File:

PDF, 476 KB

english, 2008

14

UMD-USHbases: a comprehensive set of databases to record and analyse pathogenic mutations and unclassified variants in seven Usher syndrome causing genes

David Baux, Valérie Faugère, Lise Larrieu, Sandie Le Guédard-Méreuze, Dalil Hamroun, Christophe Béroud, Sue Malcolm, Mireille Claustres, Anne-Françoise Roux

Journal:

Year:

2008

Language:

english

File:

PDF, 270 KB

english, 2008

15

UMD-predictor, a new prediction tool for nucleotide substitution pathogenicity—application to four genes: FBN1, FBN2, TGFBR1, and TGFBR2

Mélissa Yana Frédéric, Marine Lalande, Catherine Boileau, Dalil Hamroun, Mireille Claustres, Christophe Béroud, Gwenaëlle Collod-Béroud

Journal:

Year:

2009

Language:

english

File:

PDF, 225 KB

english, 2009

16

Genotype–phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD–DMD database: a model of nationwide knowledgebase

Sylvie Tuffery-Giraud, Christophe Béroud, France Leturcq, Rabah Ben Yaou, Dalil Hamroun, Laurence Michel-Calemard, Marie-Pierre Moizard, Rafaëlle Bernard, Mireille Cossée, Pierre Boisseau, Martine Bla

Journal:

Year:

2009

Language:

english

File:

PDF, 389 KB

english, 2009

17

UMD-CFTR: A database dedicated to CF and CFTR-related disorders

Corinne Bareil, Corinne Thèze, Christophe Béroud, Dalil Hamroun, Caroline Guittard, Céline René, Damien Paulet, Marie des Georges, Mireille Claustres

Journal:

Year:

2010

Language:

english

File:

PDF, 616 KB

english, 2010

18

MUT-TP53 2.0: a novel versatile matrix for statistical analysis of TP53 mutations in human cancer

Thierry Soussi, Dalil Hamroun, Linn Hjortsberg, Jean Michel Rubio-Nevado, Jean Louis Fournier, Christophe Béroud

Journal:

Year:

2010

Language:

english

File:

PDF, 240 KB

english, 2010

19

UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene

Gaelle Blandin, Christophe Beroud, Veronique Labelle, Karine Nguyen, Nicolas Wein, Dalil Hamroun, Brad Williams, Nilah Monnier, Laura E. Rufibach, Jon Andoni Urtizberea, Pierre Cau, Marc Bartoli, Nico

Journal:

Year:

2012

Language:

english

File:

PDF, 150 KB

english, 2012

20

Solutions to a nonlinear Poisson–Nernst–Planck system in an ionic channel

L. Hadjadj, K. Hamdache, D. Hamroun

Journal:

Mathematical Methods in the Applied Sciences

Year:

2010

Language:

english

File:

PDF, 210 KB

english, 2010

21

Local solutions to a model of piezoelectric materials

Kamel Hamdache, Djamila Hamroun

Journal:

Mathematical Methods in the Applied Sciences

Year:

2004

Language:

english

File:

PDF, 146 KB

english, 2004

22

Ferromagnets with biquadratic exchange coupling energy. Global existence of weak solutions

K. Hamdache, D. Hamroun

Journal:

Mathematical Methods in the Applied Sciences

Year:

2005

Language:

english

File:

PDF, 186 KB

english, 2005

23

On a model of magnetization switching by spin-polarized current

K. Hamdache, D. Hamroun, M. Tilioua

Journal:

Japan Journal of Industrial and Applied Mathematics

Year:

2006

Language:

english

File:

PDF, 1.02 MB

english, 2006

24

Lattice Boltzmann Model for the Simulation of Flows in Open Channels with Application to Flows in a Submerged Sluice Gate

Marcou, O., Chopard, B., El Yacoubi, S., Hamroun, B., Lefèvre, L., Mendes, E.

Journal:

Journal of Irrigation and Drainage Engineering

Year:

2010

Language:

english

File:

PDF, 1.07 MB

english, 2010

25

Motor and respiratory heterogeneity in Duchenne patients: Implication for clinical trials

Véronique Humbertclaude, Dalil Hamroun, Kamel Bezzou, Carole Bérard, Odile Boespflug-Tanguy, Christine Bommelaer, Emmanuelle Campana-Salort, Claude Cances, Brigitte Chabrol, Marie-Christine Commare, J

Journal:

European Journal of Paediatric Neurology

Year:

2012

Language:

english

File:

PDF, 898 KB

english, 2012

26

The new Ghent criteria for Marfan syndrome: what do they change?

L Faivre, G Collod-Beroud, L Adès, E Arbustini, A Child, BL Callewaert, B Loeys, C Binquet, E Gautier, K Mayer, M Arslan-Kirchner, M Grasso, C Beroud, D Hamroun, C Bonithon-Kopp, H Plauchu, PN Robinso

Journal:

Clinical Genetics

Year:

2012

Language:

english

File:

PDF, 713 KB

english, 2012

27

Introducing the online version of the gene table for neuromuscular disease (nuclear genes only)

Dalil Hamroun, Christophe Béroud, Bertrand Fontaine, Jean-Claude Kaplan

Journal:

Neuromuscular Disorders

Year:

2005

Language:

english

File:

PDF, 45 KB

english, 2005

28

G.P.9.10 Clinical development of the French UMD–DMD database

V. Humbertclaude, S. Tuffery-Giraud, R. Ben Yaou, D. Hamroun, P. Khau Van Kien, F. Leturcq, J. Chelly, M. Claustres, C. Béroud

Journal:

Neuromuscular Disorders

Year:

2007

Language:

english

File:

PDF, 63 KB

english, 2007

29

T.P.3.05 TREAT-NMD global patients’ registries: A unified global source of information about patients with neuromuscular diseases

V. Humbertclaude, S. Tuffery-Giraud, D. Hamroun, F.O. Desmet, S. Baumeister, M. Lalande, G. Collod-Béroud, H. Lochmüller, M. Claustres, C. Béroud

Journal:

Neuromuscular Disorders

Year:

2008

Language:

english

File:

PDF, 45 KB

english, 2008

30

P5.2 The DM-scope project: Promoting myotonic dystrophy care and research

D. Hamroun, C. Dogan, C. Beroud, B. Eymard, s. DM Clinical research network, G. Bassez

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 45 KB

english, 2011

31

P2.43 Revisiting X-linked Emery-Dreifuss muscular dystrophy. New insights into an old story

R. Ben Yaou, C. Beugnet, K. Chikhaoui, D. Hamroun, J.C. Kaplan, C. Béroud, G. Bonne, F. Leturcq, F. French EDMD network

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 48 KB

english, 2011

32

P2.41 From Emery-Dreifuss muscular dystrophy to striated muscle laminopathies. A 12 years retrospective

R. Ben Yaou, L. Demay, K. Chikhaoui, D. Hamroun, C. Béroud, P. Richard, G. Bonne, F. French EDMD network

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 58 KB

english, 2011

33

Banques de données de mutations : enjeux et perspectives pour les maladies génétiques orphelines

V. Humbertclaude, S. Tuffery-Giraud, C. Bareil, C. Thèze, D. Paulet, F.-O. Desmet, D. Hamroun, D. Baux, A. Girardet, G. Collod-Béroud, P. Khau Van Kien, A.-F. Roux, M. des Georges, C. Béroud, M. Claus

Journal:

Pathologie Biologie

Year:

2010

File:

PDF, 456 KB

2010

34

Registre français de la maladie de Gaucher

J. Stirnemann, D. Hamroun, D. Heraoui, L. Rossi, M. Vigan, M. Berger, C. Serratrice, P. Kaminsky, C. Rose, F. Camou, F. Mentré, N. Belmatoug

Journal:

La Revue de Médecine Interne

Year:

2011

Language:

french

File:

PDF, 97 KB

french, 2011

35

Endothelin expression in human megakaryoblastic leukemia cell lines and normal platelet precursors

Marie-Noelle Mathieu, Daniel Vittet, Marie-France Laliberté, François Laliberté, Isabelle Nonotte, Dalil Hamroun, Jean-Marie Launay, Claude Chevillard

Journal:

Regulatory Peptides

Year:

1997

Language:

english

File:

PDF, 707 KB

english, 1997

36

[IEEE 2007 46th IEEE Conference on Decision and Control - New Orleans, LA, USA (2007.12.12-2007.12.14)] 2007 46th IEEE Conference on Decision and Control - Port-based modelling and geometric reduction for open channel irrigation systems

Hamroun, Boussad, Lefevre, Laurent, Mendes, Eduardo

Year:

2007

Language:

english

File:

PDF, 530 KB

english, 2007

37

UMD-CFTR: a database dedicated to CF and CFTR-related diseases

C. Bareil, C. Béroud, C. Thèze, D. Paulet, C. René, D. Hamroun, M. des Georges, M. Claustres

Journal:

Journal of Cystic Fibrosis

Year:

2009

Language:

english

File:

PDF, 66 KB

english, 2009

38

Surgical management of patients with Marfan syndrome: Evolution throughout the years

Alireza Samadi, Delphine Detaint, Carine Roy, Florence Arnoult, Gabriel Delorme, Mathieu Gautier, Olivier Milleron, François Raoux, Catherine Meuleman, Ulrik Hvass, Dalil Hamroun, Christophe Beroud, F

Journal:

Archives of Cardiovascular Diseases

Year:

2012

File:

PDF, 667 KB

2012

39

Change of endothelin receptor subtype in the MEG-01 human megakaryoblastic cell line

Dalil Hamroun, Marie-Noelle Mathieu, Claude Chevillard

Journal:

European Journal of Pharmacology

Year:

1998

Language:

english

File:

PDF, 223 KB

english, 1998

40

Control by Interconnection and Energy-Shaping Methods of Port Hamiltonian Models. Application to the Shallow Water Equations

Hamroun, Boussad, Dimofte, Alexandru, Lefèvre, Laurent, Mendes, Eduardo

Journal:

European Journal of Control

Year:

2010

Language:

english

File:

PDF, 1.42 MB

english, 2010

41

P.10.9 A cross sectional validation study of the English version of the NM-Score in patients with neuromuscular diseases

Vuillerot, C., Rippert, P., Berard, C., Bonnemann, C., Meilleur, K., Jain, M., Waite, M., Payan, C.A.M., Hamroun, D., Poirot, I., Ecochard, R.

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 48 KB

english, 2013

42

The 2014 version of the gene table of monogenic neuromuscular disorders (nuclear genome)

Kaplan, Jean-Claude, Hamroun, Dalil

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 293 KB

english, 2013

43

The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease

Laforêt, P., Laloui, K., Granger, B., Hamroun, D., Taouagh, N., Hogrel, J.-Y., Orlikowski, D., Bouhour, F., Lacour, A., Salort-Campana, E., Penisson-Besnier, I., Sacconi, S., Zagnoli, F., Chapon, F.,

Journal:

Revue Neurologique

Year:

2013

File:

PDF, 944 KB

2013

44

P.10.10 The Rasch-scaled motor function measure for patients with congenital disorders of muscle

Vuillerot, C., Rippert, P., Jain, M., Waite, M., Glanzman, A., Kinet, V., Auh, S., Berard, C., Payan, C.A.M., Hamroun, D., Poirot, I., Ecochard, R., Bonnemann, C.

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 57 KB

english, 2013

45

M - 8 Développements cliniques de la future banque de données nationale des mutations du gène DMD (UMD-DMD)

Humbertclaude, V., Tuffery-Giraud, S., Pages, M., Jonquet, O., Ben Yaou, R., Hamroun, D., Khau Van Kien, P., Claustres, M., Beroud, C.

Journal:

Revue Neurologique

Year:

2007

Language:

french

File:

PDF, 58 KB

french, 2007

46

Variabilité phénotypique et corrélations génotype-phénotype des dystrophinopathies : contribution des banques de données

Humbertclaude, V., Hamroun, D., Picot, M.-C., Bezzou, K., Bérard, C., Boespflug-Tanguy, O., Bommelaer, C., Campana-Salort, E., Cances, C., Chabrol, B., Commare, M.-C., Cuisset, J.-M., de Lattre, C., D

Journal:

Revue Neurologique

Year:

2013

File:

PDF, 1.22 MB

2013

47

P.18.1 The DM-Scope registry: Interfacing myotonic dystrophy clinical care and research

Dogan, C., Hamroun, D., Katsahian, S., Fabbro, M., French, M., Quebec, M., Eymard, B., Puymirat, J., Bassez, G.

Journal:

Neuromuscular Disorders

Year:

2013

Language:

english

File:

PDF, 46 KB

english, 2013

48

Développement et validation de la version anglaise du NM-Score : une classification fonctionnelle pour les patients atteints de maladies neuromusculaires

Vuillerot, C., Meilleur, K.-G., Jain, M., Waite, M., Wu, T., Dastgir, J., Donkervoort, S., Leach, M., Rippert, P., Payan, C., Iwaz, J., Hamroun, D., Berard, C., Poirot, I., Bonnemann, C.

Journal:

Annals of Physical and Rehabilitation Medicine

Year:

2014

Language:

french

File:

PDF, 436 KB

french, 2014

49

English cross-cultural translation and validation of the NM-Score: A system for motor function classification in patients with neuromuscular diseases

Vuillerot, C., Meilleur, K.G., Jain, M., Waite, M., Wu, T., Dastgir, J., Donkervoort, S., Leach, M., Rippert, P., Payan, C., Iwaz, J., Hamroun, D., Berard, C., Poirot, I., Bonnemann, C.

Journal:

Annals of Physical and Rehabilitation Medicine

Year:

2014

Language:

english

File:

PDF, 215 KB

english, 2014

50

Une Rasch analyse de la mesure de fonction motrice chez les patients atteints de dystrophie musculaire congénitale et myopathie congénitale

Vuillerot, C., Rippert, P., Kinet, V., Renders, A., Jain, M., Waite, M., Glanzman, A., Girardot, F., Hamroun, D., Iwaz, J., Quijano-Roy, S., Berard, C., Poirot, I., Bonnemann, C.

Journal:

Annals of Physical and Rehabilitation Medicine

Year:

2014

Language:

french

File:

PDF, 276 KB

french, 2014

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