Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

97 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
New type of mutations in three spanish families with choroideremia.
Garcia-Hoyos M, Lorda-Sanchez I, Gómez-Garre P, Villaverde C, Cantalapiedra D, Bustamante A, Diego-Alvarez D, Vallespin E, Gallego-Merlo J, Trujillo MJ, Ramos C, Ayuso C. Garcia-Hoyos M, et al. Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1315-21. doi: 10.1167/iovs.07-1169. Invest Ophthalmol Vis Sci. 2008. PMID: 18385043
Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Dou J, Bakulski K, Guo K, Hur J, Zhao L, Saez-Atienzar S, Stark A, Chia R, García-Redondo A, Rojas-Garcia R, Vázquez Costa JF, Fernandez Santiago R, Bandres-Ciga S, Gómez-Garre P, Periñán MT, Mir P, Pérez-Tur J, Cardona F, Menendez-Gonzalez M, Riancho J, Borrego-Hernández D, Galán-Dávila L, Infante Ceberio J, Pastor P, Paradas C, Dols-Icardo O, Traynor BJ, Feldman EL, Goutman SA; Spanish Neurological Consortium. Dou J, et al. Among authors: gomez garre p. Neurol Genet. 2023 May 31;9(4):e200079. doi: 10.1212/NXG.0000000000200079. eCollection 2023 Aug. Neurol Genet. 2023. PMID: 37293291 Free PMC article.
Author Correction: Peripheral inflammatory immune response differs among sporadic and familial Parkinson's disease.
Muñoz-Delgado L, Macías-García D, Periñán MT, Jesús S, Adarmes-Gómez AD, Bonilla Toribio M, Buiza Rueda D, Jiménez-Jaraba MDV, Benítez Zamora B, Díaz Belloso R, García-Díaz S, Martín-Bórnez M, Pineda Sánchez R, Carrillo F, Gómez-Garre P, Mir P. Muñoz-Delgado L, et al. Among authors: gomez garre p. NPJ Parkinsons Dis. 2023 Feb 17;9(1):27. doi: 10.1038/s41531-023-00471-7. NPJ Parkinsons Dis. 2023. PMID: 36801921 Free PMC article. No abstract available.
Transcriptomic analysis reveals an association of FCGBP with Parkinson's disease.
Gómez-Garre P, Periñán MT, Jesús S, Bacalini MG, Garagnani P, Mollenhauer B, Pirazzini C, Provini F, Trenkwalder C, Franceschi C, Mir P; PROPAG-AGEING consortium. Gómez-Garre P, et al. NPJ Parkinsons Dis. 2022 Nov 12;8(1):157. doi: 10.1038/s41531-022-00415-7. NPJ Parkinsons Dis. 2022. PMID: 36371440 Free PMC article.
Peripheral inflammatory immune response differs among sporadic and familial Parkinson's disease.
Muñoz-Delgado L, Macías-García D, Periñán MT, Jesús S, Adarmes-Gómez AD, Bonilla Toribio M, Buiza Rueda D, Jiménez-Jaraba MDV, Benítez Zamora B, Díaz Belloso R, García-Díaz S, Martín-Bórnez M, Pineda Sánchez R, Carrillo F, Gómez-Garre P, Mir P. Muñoz-Delgado L, et al. NPJ Parkinsons Dis. 2023 Jan 31;9(1):12. doi: 10.1038/s41531-023-00457-5. NPJ Parkinsons Dis. 2023. PMID: 36720879 Free PMC article.
Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.
García-González P, de Rojas I, Moreno-Grau S, Montrreal L, Puerta R, Alarcón-Martín E, Quintela I, Orellana A, Andrade V, Adami PVM, Heilmann-Heimbach S, Gomez-Garre P, Periñán MT, Alvarez I, Diez-Fairen M, Nuñez Llaves R, Olivé Roig C, Garcia-Ribas G, Menéndez-González M, Martínez C, Aguilar M, Buongiorno M, Franco-Macías E, Saez ME, Cano A, Bullido MJ, Real LM, Rodríguez-Rodríguez E, Royo JL, Álvarez V, Pastor P, Piñol-Ripoll G, Mir P, Lara MC, Padilla MM, Sánchez-Juan P, Carracedo A, Valero S, Hernandez I, Tàrraga L, Ramirez A, Boada M, Ruiz A. García-González P, et al. Int J Mol Sci. 2023 Jan 4;24(2):898. doi: 10.3390/ijms24020898. Int J Mol Sci. 2023. PMID: 36674414 Free PMC article.
Turner phenotype in a girl with a 45,X/46,XX/47,XX,+18 mosaicism.
Lorda-Sanchez I, Trujillo MJ, Gomez-Garre P, de Alba MR, Gonzalez-Gonzalez C, García-Hoyos M, Ayuso C, Ramos C. Lorda-Sanchez I, et al. Am J Med Genet A. 2003 Aug 15;121A(1):20-4. doi: 10.1002/ajmg.a.10197. Am J Med Genet A. 2003. PMID: 12900896
Gene symbol: EPM2A.
Trujillo-Tiebas MJ, Gómez-Garré P, Fenolla-Cortés M, Lorda-Sánchez I, Serratosa JM, Ayuso C. Trujillo-Tiebas MJ, et al. Hum Genet. 2007 Apr;121(2):289. Hum Genet. 2007. PMID: 17598204 No abstract available.
Gene symbol: EPM2A.
Trujillo-Tiebas MJ, Gómez-garré P, Arguirre-Lambán J, Lorda-Sánchez I, Serratosa JM, Ayuso C. Trujillo-Tiebas MJ, et al. Hum Genet. 2007 Apr;121(2):289-90. Hum Genet. 2007. PMID: 17598229 No abstract available.
97 results