Publicacions
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Izquierdo-Renau M, Martinez-Monseny T, Pociello N, Gonzalez P, del Río-Florentino R, Iriondo-Sanz M and Iglesias-Platas I.
Changes in Parenteral Nutrition During the First Week of Life Influence Early but Not Late Postnatal Growth in Very Low-Birth-Weight Infants
NUTRITION IN CLINICAL PRACTICE . 31(5): 666-672. Nº de cites: 8
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Fernández-Torrón R, García-Puga M, Emparanza JI, Maneiro M, Cobo AM, Poza JJ, Espinal JB, Zulaica M, Ruiz I, Martorell-Sampol L, Otaegui D, Matheu A and López de Munain A.
Cancer risk in DM1 is sex-related and linked to miRNA-200/141 downregulation
Neurology . 87(12): 1250-1257. Nº de cites: 40
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Margarit Soler A, Martínez-Sánchez L, Martinez-Monseny T, Trenchs-Sainz de la Maza V, Picouto MD, Villar F and Luaces-Cubells C.
Epidemiological characteristics in suicidal adolescents seen in the Emergency Department
ANALES DE PEDIATRIA . 85(1): 13-17. Nº de cites: 5
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Mollá B, Riveiro F, Bolinches-Amorós A, Muñoz-Lasso DC, Palau F and González-Cabo P.
Two different pathogenic mechanisms, dying-back axonal neuropathy and pancreatic senescence, are present in the YG8R mouse model of Friedreich's ataxia
DISEASE MODELS & MECHANISMS . 9(6): 647-657. Nº de cites: 13
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Yubero-Siles D, Brandi-Tarrau N, Ormazabal-Herrero A, Garcia-Cazorla A, Pérez-Dueñas B, Campistol-Plana J, Ribes A, Palau F, Artuch-Iriberri R, Armstrong-Moron J and Working Group.
Targeted Next Generation Sequencing in Patients with Inborn Errors of Metabolism
PLoS One . 11(5): . Nº de cites: 40
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Ponce G, Quiñones-Lombraña A, Martín-Palanco NG, Rubio-Solsona E, Jiménez-Arriero MÁ, Palomo T and Hoenicka J.
The Addiction-Related Gene Ankk1 is Oppositely Regulated by D1R-and D2R-Like Dopamine Receptors
NEUROTOXICITY RESEARCH . 29(3): 345-350. Nº de cites: 16
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Sáez MA, Fernández-Rodríguez J, Moutinho C, Sanchez-Mut JV, Gomez A, Vidal E, Petazzi P, Szczesna K, Lopez-Serra P, Lucariello M, Lorden P, Delgado-Morales R, de la Caridad OJ, Huertas D, Gelpí JL, Orozco M, López-Doriga A, Milà M, Perez-Jurado LA, Pineda M, Armstrong-Moron J, Lázaro C and Esteller M.
Mutations in JMJD1C are involved in Rett syndrome and intellectual disability.
GENETICS IN MEDICINE . 18(4): 378-385. Nº de cites: 36
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Sevilla T, Lupo V, Martínez-Rubio D, Sancho P, Sivera R, Chumillas MJ, García-Romero M, Pascual-Pascual SI, Muelas N, Dopazo J, Vílchez JJ, Palau F and Espinós C.
Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth disease
BRAIN . 139: 62-72. Nº de cites: 74
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Prieto J, León M, Ponsoda X, García-García F, Bort R, Serna E, Barneo-Muñoz M, Palau F, Dopazo J, López-García C and Torres J.
Dysfunctional mitochondrial fission impairs cell reprogramming
Cell Cycle . 15(23): 3240-3250. Nº de cites: 34
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Cassis L, Cortés-Saladelafont E, Molero M, Yubero-Siles D, González MJ, Ormazabal-Herrero A, Fons-Estupina C, Jou-Munoz C, Sierra-March C, Castejón Ponce E, Ramos F, Armstrong-Moron J, O'Callaghan-Gordo M, Casado-Rio M, Montero-Sanchez R, Meavilla-Olivas SM, Artuch-Iriberri R, Baric I, Bartoloni F, Bellettato CM, Bonifazi F, Ceci A, Cvitanovic-Šojat L, Dali CI, D'Avanzo F, Fumic K, Giannuzzi V, Lampe C, Scarpa M and Garcia-Cazorla A.
Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders
ORPHANET JOURNAL OF RARE DISEASES . 10: 164-164. Nº de cites: 19