ADA2 deficiency: case report of a new phenotype and novel mutation in two sisters
Uettwiller, F, Sarrabay, G, Rodero, M P, Rice, G I, Lagrue, E, Marot, Y, Deiva, K, Touitou, I, Crow, Y J, Quartier, P
Published in Rheumatic & musculoskeletal diseases open (01.01.2016)
Published in Rheumatic & musculoskeletal diseases open (01.01.2016)
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Journal Article
Cerebrospinal fluid metabolomics to explore West Syndrome: Central role of serine pathways
Lagrue, E, Rullier, C, Blasco, H, Emond, P, Castelnau, P
Published in European journal of paediatric neurology (01.06.2017)
Published in European journal of paediatric neurology (01.06.2017)
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Journal Article
Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia
Furby, A, Vicart, S, Camdessanché, J.P, Fournier, E, Chabrier, S, Lagrue, E, Paricio, C, Blondy, P, Touraine, R, Sternberg, D, Fontaine, B
Published in Neuromuscular disorders : NMD (01.11.2014)
Published in Neuromuscular disorders : NMD (01.11.2014)
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Journal Article
Corticosteroid treatment in early-onset lamin A/C related muscular dystrophies
Dabaj, I., Ben Yaou, R., Bönnemann, C., Nascimento, A., Rutkowski, A., Erazo Torricelli, R., Muntoni, F., Lagrue, E., Dowling, J., Bushby, K., Casteglioni, C., Kleinsteuber, K., Lorenzo, M., Ishiyama, A., Sejersen, T., Gurgel-Giannetti, J., Monges, S., Bonne, G., Quijano-roy, S.
Published in NEUROMUSCULAR DISORDERS (01.10.2017)
Published in NEUROMUSCULAR DISORDERS (01.10.2017)
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Journal Article
Conference Proceeding
Congenital myasthenic syndromes in childhood: Drug therapeutic strategies
de la Vaissière, S, Toutain, A, Chêne, M-A, Lagrue, E, Cantagrel, S, Provost, S, Eymard, B, Castelnau, P
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.07.2015)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.07.2015)
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Journal Article
N-methyl-D-aspartate receptor antibody encephalitis: value of immunomodulatory therapy
Le Moigno, L, Ternant, D, Paintaud, G, Thibault, G, Cloarec, S, Tardieu, M, Lagrue, E, Castelnau, P
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.06.2014)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.06.2014)
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Journal Article
Promoting the use of Motor Function Measure (MFM) as outcome measure in patients with Duchenne Muscular Dystrophy (DMD) treated by corticosteroids
Schreiber-Bontemps, A, Brochard, S., Dr, Fontaine-Carbonnel, S., Dr, Chabrier, S., Dr, Gautheron, V., Dr, Peudenier, S., Dr, Rippert, P, Rauscent, H., Dr, Rivier, F., Dr, Andoni Urtizberea, J., Dr, Fournier-Mehouas, M., Dr, Mahé, J.Y., Dr, Tiffreau, V., Dr, Lagrue, E., Dr, Hamroun, D, Poirot, I., Dr, Ragot-Mandry, S., Dr, Sacconi, S., Dr, Puy Haubert, B, Fafin, C, Vuillerot, C., Dr
Published in Annals of physical and rehabilitation medicine (01.09.2015)
Published in Annals of physical and rehabilitation medicine (01.09.2015)
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Journal Article
Basal ganglia neuroprotection with anticonvulsants after energy stress: a comparative study
Arpin, S, Lagrue, E, Bodard, S, Chalon, S, Castelnau, P
Published in Metabolic brain disease (01.09.2009)
Published in Metabolic brain disease (01.09.2009)
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Journal Article
MPTP intoxication in mice: a useful model of Leigh syndrome to study mitochondrial diseases in childhood
Lagrue, E, Abert, B, Nadal, L, Tabone, L, Bodard, S, Medja, F, Lombes, A, Chalon, S, Castelnau, P
Published in Metabolic brain disease (01.06.2009)
Published in Metabolic brain disease (01.06.2009)
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Journal Article
A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management
Published in Neurology
(03.03.2020)
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Journal Article
Encéphalite à anticorps anti-récepteurs N-méthyl-d-aspartate (NMDA-R) : place des immunomodulateurs
Le Moigno, L., Ternant, D., Paintaud, G., Thibault, G., Cloarec, S., Tardieu, M., Lagrue, E., Castelnau, P.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.06.2014)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.06.2014)
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Journal Article
P.266 - A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management
Lagrue, E., Dogan, C., De Antonio, M., Bassez, G., Hamroun, D., Gherardi, R.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management
Lagrue, E., Dogan, C., De Antonio, M., Bassez, G., Hamroun, D., Gherardi, R.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
PB0323 Preliminary Analysis of ATHN 16: Real-World Safety of Eptacog Beta
Singleton, T., Acharya, S., Ahuja, S., Amos, L., Bonzo, D., Eason, A., Escobar, M., Knoll, C., Kuriakose, P., Lagrue, E., Recht, M., Sullivan, S., Quon, D., Reding, M.
Published in Research and practice in thrombosis and haemostasis (01.10.2023)
Published in Research and practice in thrombosis and haemostasis (01.10.2023)
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Journal Article
Corticosteroids in Duchenne muscular dystrophy: impact on the motor function measure sensitivity to change and implications for clinical trials
Schreiber, Audrey, Brochard, Sylvain, Rippert, Pascal, Fontaine‐Carbonnel, Stephanie, Payan, Christine, Poirot, Isabelle, Hamroun, Dalil, Vuillerot, Carole, Peudenier, Sylviane, Ropars, Juliette, Urtizberea, Andoni, Tiffreau, Vincent, Puyhaubert, Blandine, Fournier Mehouas, Manuella, Sacconi, Sabrina, Lagrue, Emmanuelle, Chabrier, Stéphane
Published in Developmental medicine and child neurology (01.02.2018)
Published in Developmental medicine and child neurology (01.02.2018)
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Journal Article
Cas clinique de radiologie
Lagrue, E., Martinerie, L., Adamsbaum, C.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (2003)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (2003)
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Journal Article
P.137 - Corticosteroid treatment in early-onset lamin A/C related muscular dystrophies
Dabaj, I., Ben Yaou, R., Bönnemann, C., Nascimento, A., Rutkowski, A., Erazo Torricelli, R., Muntoni, F., Lagrue, E., Dowling, J., Bushby, K., Casteglioni, C., Kleinsteuber, K., Lorenzo, M., Ishiyama, A., Sejersen, T., Gurgel-Giannetti, J., Monges, S., Bonne, G., Quijano-roy, S.
Published in Neuromuscular disorders : NMD (01.10.2017)
Published in Neuromuscular disorders : NMD (01.10.2017)
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Journal Article
The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care
de Antonio, M, Dogan, C, Eymard, B, Puymirat, J, Mathieu, J, Gagnon, C, Attarian, S, Aube-Nathier, Ac, Audic, F, Bach, N, Barnerias, C, Bedat-Millet, Al, Behin, A, Bellance, R, Ben Yaou, R, Bombard, V, Bouhour, F, Boutte, C, Boyer, F, Cances, C, Chabrol, B, Chanson, Jb, Chapon, F, Chasseriau, R, Cintas, P, Cobo, Am, Colombert, V, Cruz, Mc, Cuisset, Jm, Deschamps, R, Desguerre, I, Durigneux, J, Duval, F, Espil, C, Fafin, C, Feasson, L, Fradin, M, Furby, A, Goldenberg, A, Grotto, S, Ghorab, K, Guyant-Marechal, L, Heron, D, Isapof, A, Jacquin-Piques, A, Journel, H, Laforet, P, Lagrue, E, Laroche-Raynaud, C, Laugel, V, Lebeau, F, Magot, A, Manel, V, Mayer, M, Mercier, S, Menard, D, Michaud, M, Minot, Mc, Morales, Rj, Nadaj-Pakleza, A, Noury, Jb, Pasquier, L, Pellieux, S, Pereon, Y, Perrier, J, Peudenier, S, Preudhomme, M, Pouget, J, Quijano-Roy, S, Ragot-Mandry, S, Richelme, C, Rivier, F, Sabouraud, P, Sacconi, S, Salort-Campana, E, Sarret, C, Schaeffer, S, Sole, G, Stojkovic, T, Taithe, F, Testard, H, Tiffereau, V, Urtizberea, A, Vanhulle, C, Vial, C, Walther-Louvier, U, Zagnoli, F, Hamroun, D, Bassez, G
Published in Orphanet journal of rare diseases (01.06.2019)
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Published in Orphanet journal of rare diseases (01.06.2019)
Journal Article