Publicaciones
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Paredes-Fuentes AJ, César-Díaz S, Montero-Sanchez R, Latre C, Genovés-Escarré J, Martorell-Sampol L, Cuadras-Palleja D, Colom H, Pineda M, O'Callaghan-Gordo M, Sarquella-Brugada G, Darling A and Artuch-Iriberri R.
Plasma idebenone monitoring in Friedreich's ataxia patients during a long-term follow-up
BIOMEDICINE & PHARMACOTHERAPY . 143: 112143-112143. Nº de citas: 8
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Martorell-Sampol L, Tondo M, García-Fructuoso G, Naudo-Lahoz M, Alegre C, Gamez J, Genovés-Escarré J and Poo P.
Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgia
CLINICAL RHEUMATOLOGY . 31(11): 1611-1615. Nº de citas: 7
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Tondo M, Poo P, Naudo-Lahoz M, Ferrando T, Genovés-Escarré J, Molero M and Martorell-Sampol L.
Predisposition to epilepsy in fragile X syndrome: Does the Va166Met polymorphism in the BDNF gene play a role?
EPILEPSY & BEHAVIOR . 22(3): 581-583. Nº de citas: 11
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Martorell-Sampol L, Nascimento MT, Colomé-Roura R, Genovés-Escarré J, Naudo-Lahoz M and Nascimento-Osorio A.
Four sisters compound heterozygotes for the pre- and full mutation in fragile X syndrome and a complete inactivation of X-functional chromosome: implications for genetic counseling
JOURNAL OF HUMAN GENETICS . 56(1): 87-90. Nº de citas: 4