Publications
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Quijano-Roy S, Mbieleu B, Bönnemann CG, Jeannet PY, Colomer J, Clarke NF, Cuisset JM, Roper H, De Meirleir L, D'Amico A, Ben Yaou R, Nascimento-Osorio A, Barois A, Demay L, Bertini E, Ferreiro A, Sewry CA, Romero NB, Ryan M, Muntoni F, Guicheney P, Richard P, Bonne G and Estournet B.
De novo LMNA mutations cause a new form of congenital muscular dystrophy
ANNALS OF NEUROLOGY . 64(2): 177-186. Number of citations: 217
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Garcia-Cazorla A, Duarte S, Serrano M, Nascimento-Osorio A, Ormazabal-Herrero A, Carrilho I, Briones P, Montoya J, Garesse R, Sala-Castellvi P, Pineda M and Artuch-Iriberri R.
Mitochondrial diseases mimicking neuro transmitter defects
MITOCHONDRION . 8(3): 273-278. Number of citations: 42
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Colomer J, Gooding R, Angelicheva D, King RH, Guillén-Navarro E, Parman Y, Nascimento-Osorio A, Conill J and Kalaydjieva L.
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2
NEUROMUSCULAR DISORDERS . 16(7): 449-453. Number of citations: 48
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Colomer J, Müller JS, Vernet A, Nascimento-Osorio A, Pons-Odena M, Gonzalez V, Abicht A and Lochmüller H.
Long-term improvement of slow-channel congenital myasthenic syndrome with fluoxetine
NEUROMUSCULAR DISORDERS . 16(5): 329-333. Number of citations: 33
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Pineda M, Ormazabal-Herrero A, López-Gallardo E, Nascimento-Osorio A, Solano A, Herrero MD, Vilaseca MA, Briones P, Ibañez-Toda L, Montoya J and Artuch-Iriberri R.
Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion
ANNALS OF NEUROLOGY . 59(2): 394-398. Number of citations: 97
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Nascimento-Osorio A, Navarro, R, Colomer J, Gómez, F and Sola-Martinez T.
Síndrome de Moyamoya asociado al síndrome de Down. Hallazgos clínicos y radiológicos
SD, Revista Medica Internacional sobre el Sindrome de Down . 10(3): 41-45.
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Montero-Sanchez R, Artuch-Iriberri R, Briones P, Nascimento-Osorio A, Garcia-Cazorla A, Vilaseca MA, Sánchez-Alcázar JA, Navas P, Montoya J and Pineda M.
Muscle coenzyme Q10 concentrations in patients with probable and definite diagnosis of respiratory chain disorders
BIOFACTORS . 25(1-4): 109-115. Number of citations: 39
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Villar-Quiles RN, Foley AR, Metay C, Orbach R, Donkervoort S, Labella B, Natera-de Benito D, Nascimento-Osorio A, Estévez-Arias B, Jimenez-Mallebrera C, Ortez-Gonzalez CI, Domínguez-González C, Horga A, Marti Carrera MI, Fernandez Torron R, Kurbatov S, Chausova P, Murtazina A, Subbotin D, Kuchina A, Frezzati R, Carvalho A, Waschbisch A, Allamand V, Zou Y, Richard P, Bönnemann CG and Stojkovic T.
Expanding the phenotypic spectrum of COL6-related diseases: Motor neuropathy-like and neuromyopathy associated with COL6A3 c.7447A>G.
Journal of Neuromuscular Diseases . : .