Publicaciones
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Keller R, Chrastina P, Pavlíková M, Gouveia S, Ribes A, Kölker S, Blom HJ, Baumgartner MR, Bártl J, Dionisi-Vici C, Gleich F, Morris AA, Kožich V, Huemer M, and individual contributors of the European Network and Registry for Homocystinu, Baric I, Ben-Omran T, Blasco-Alonso J, Bueno Delgado MA, Carducci C, Cassanello M, Cerone R, Couce ML, Crushell E, Delgado Pecellin C, Dulin E, Espada M, Ferino G, Fingerhut R, Garcia Jimenez I, Gonzalez Gallego I, González-Irazabal Y, Gramer G, Juan Fita MJ, Karg E, Klein J, Konstantopoulou V, la Marca G, Leão Teles E, Leuzzi V, Lilliu F, Lopez RM, Lund AM, Mayne P, Meavilla-Olivas SM, Moat SJ, Okun JG, Pasquini E, Pedron-Giner CC, Racz GZ, Ruiz Gomez MA, Vilarinho L, Yahyaoui R, Zerjav Tansek M, Zetterström RH and Zeyda M.
Newborn screening for homocystinurias: Recent recommendations versus current practice.
JOURNAL OF INHERITED METABOLIC DISEASE . 42(1): 128-139. Nº de citas: 34
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Quintero J, Molera C, Juamperez J, Redecillas S, Meavilla-Olivas SM, Nuñez R, García C, Del Toro M, Garcia Á, Ortega J, Segarra Ó, Martín-de-Carpi J, Bilbao I and Charco R.
The Role of Liver Transplantation in Propionic Acidemia
LIVER TRANSPLANTATION . 24(12): 1736-1745. Nº de citas: 18
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Peña-Quintana L, Scherer G, Curbelo-Estévez ML, Jiménez-Acosta F, Hartmann B, Roche F, Meavilla-Olivas SM, Pérez-Cerdá C, García Segarra N, Giguère Y, Huppke P, Mitchell GA, Mönch E, Trump D, Vianey-Saban C, Trimble ER, Vitoria-Miñana I, Reyes-Suárez D, Ramírez-Lorenzo T and Tugores A.
Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation.
CLINICAL GENETICS . 92(3): 306-317. Nº de citas: 21
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Ruiz-Hernández CJ, Castejón Ponce E, Bossacoma-Busquets F, Hernández DS, Meavilla-Olivas SM, Santacruz EL, Perez-Requena N, De Los Santos Pelegrini M and Villaronga M.
Hypersensitivity reaction to components of parenteral nutrition in pediatrics
Nutrition . 32(11-12): 1303-1305. Nº de citas: 11
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Llorca-Cardeñosa A, Català-Mora J, Garcia-Cazorla A, Meavilla-Olivas SM and Castejón-Ponce E.
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: A case report.
Archivos De La Sociedad Española De Oftalmología . 91(5): 236-239.
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Yubero-Siles D, Montero-Sanchez R, O'Callaghan-Gordo M, Pineda M, Meavilla-Olivas SM, Delgadillo V, Sierra-March C, Altimira L, Navas P, Pope S, Oppenheim M, Neergheen V, Ghosh A, Mills P, Clayton P, Footitt E, Cleary M, Hargreaves I, Jones SA, Heales S and Artuch-Iriberri R.
Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III
JIMD Reports . 25: 1-7. Nº de citas: 10
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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 citas: 19
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Couce ML, Ramos F, Bueno MA, Díaz J, Meavilla-Olivas SM, Bóveda MD, Fernández-Marmiesse A and Garcia-Cazorla A.
Evolution of maple syrup urine disease in patients diagnosed by newborn screening versus late diagnosis
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 19(6): 652-659. Nº de citas: 30
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González Jiménez D, Muñoz Codoceo R, Garriga García M, Molina Arias M, Alvarez Beltran M, García Romero R, Martínez Costa C, Meavilla-Olivas SM, Peña Quintana L, Gallego Gutierrez S, Marugan de Miguelsanz JM, Suarez Cortina L, Castejón Ponce EN, Leis Trabazo R, Martín Cruz F, Díaz Martín JJ and Bousoño García C.
VITAMIN D AND CHRONIC LUNG COLONIZATION IN PEDIATRIC AND YOUNG ADULTS CYSTIC FIBROSIS PATIENTS
NUTRICION HOSPITALARIA . 32(4): 1629-1635. Nº de citas: 3