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Page 1
Plasma levels of nitrates in patients with Parkinson's disease.
Molina JA, Jiménez-Jiménez FJ, Navarro JA, Ruiz E, Arenas J, Cabrera-Valdivia F, Vázquez A, Fernández-Calle P, Ayuso-Peralta L, Rabasa M, et al. Molina JA, et al. Among authors: rabasa m. J Neurol Sci. 1994 Dec 1;127(1):87-89. doi: 10.1016/0022-510x(94)90139-2. J Neurol Sci. 1994. PMID: 7699396
Serum and urinary manganese levels in patients with Parkinson's disease.
Jiménez-Jiménez FJ, Molina JA, Aguilar MV, Arrieta FJ, Jorge-Santamaría A, Cabrera-Valdivia F, Ayuso-Peralta L, Rabasa M, Vázquez A, García-Albea E, et al. Jiménez-Jiménez FJ, et al. Among authors: rabasa m. Acta Neurol Scand. 1995 May;91(5):317-20. doi: 10.1111/j.1600-0404.1995.tb07014.x. Acta Neurol Scand. 1995. PMID: 7639058
Peripheral iron metabolism in patients with Parkinson's disease.
Cabrera-Valdivia F, Jiménez-Jiménez FJ, Molina JA, Férnandez-Calle P, Vázquez A, Cañizares-Liébana F, Larumbe-Lobalde S, Ayuso-Peralta L, Rabasa M, Codoceo R. Cabrera-Valdivia F, et al. Among authors: rabasa m. J Neurol Sci. 1994 Aug;125(1):82-6. doi: 10.1016/0022-510x(94)90246-1. J Neurol Sci. 1994. PMID: 7964893
Metrics of progression and prognosis in untreated adults with thymidine kinase 2 deficiency: An observational study.
Domínguez-González C, Hernández-Voth A, de Fuenmayor-Fernández de la Hoz CP, Guerrero LB, Morís G, García-García J, Muelas N, León Hernández JC, Rabasa M, Lora D, Blázquez A, Arenas J, Martin MÁ. Domínguez-González C, et al. Among authors: rabasa m. Neuromuscul Disord. 2022 Sep;32(9):728-735. doi: 10.1016/j.nmd.2022.07.399. Epub 2022 Jul 16. Neuromuscul Disord. 2022. PMID: 35907766 Free article.
Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI).
Serrano-Lorenzo P, Rabasa M, Esteban J, Hidalgo Mayoral I, Domínguez-González C, Blanco-Echevarría A, Garrido-Moraga R, Lucia A, Blázquez A, Rubio JC, Palma-Milla C, Arenas J, Martín MA. Serrano-Lorenzo P, et al. Among authors: rabasa m. Genes (Basel). 2022 Oct 11;13(10):1835. doi: 10.3390/genes13101835. Genes (Basel). 2022. PMID: 36292720 Free PMC article.
Prognostic value of X-chromosome inactivation in symptomatic female carriers of dystrophinopathy.
Juan-Mateu J, Rodríguez MJ, Nascimento A, Jiménez-Mallebrera C, González-Quereda L, Rivas E, Paradas C, Madruga M, Sánchez-Ayaso P, Jou C, González-Mera L, Munell F, Roig-Quilis M, Rabasa M, Hernández-Lain A, Díaz-Manera J, Gallardo E, Pascual J, Verdura E, Colomer J, Baiget M, Olivé M, Gallano P. Juan-Mateu J, et al. Among authors: rabasa m. Orphanet J Rare Dis. 2012 Oct 23;7:82. doi: 10.1186/1750-1172-7-82. Orphanet J Rare Dis. 2012. PMID: 23092449 Free PMC article.
Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.
Gutiérrez Gutiérrez G, Díaz-Manera J, Almendrote M, Azriel S, Eulalio Bárcena J, Cabezudo García P, Camacho Salas A, Casanova Rodríguez C, Cobo AM, Díaz Guardiola P, Fernández-Torrón R, Gallano Petit MP, García Pavía P, Gómez Gallego M, Gutiérrez Martínez AJ, Jericó I, Kapetanovic García S, López de Munaín Arregui A, Martorell L, Morís de la Tassa G, Moreno Zabaleta R, Muñoz-Blanco JL, Olivar Roldán J, Pascual Pascual SI, Peinado Peinado R, Pérez H, Poza Aldea JJ, Rabasa M, Ramos A, Rosado Bartolomé A, Rubio Pérez MÁ, Urtizberea JA, Zapata-Wainberg G, Gutiérrez-Rivas E. Gutiérrez Gutiérrez G, et al. Among authors: rabasa m. Med Clin (Barc). 2019 Jul 19;153(2):82.e1-82.e17. doi: 10.1016/j.medcli.2018.10.028. Epub 2019 Jan 24. Med Clin (Barc). 2019. PMID: 30685181 English, Spanish.
20 results