Pure sensory deficit with crossed orocrural topography after pontine haemorrhage.

Yazar: Combarros, O, Berciano, J, Oterino, A
Baskı/Yayın Bilgisi 1996

Lumbosacral plexopathy due to dermoid cyst of the greater omentum.

Yazar: Leno, C., Combarros, O., Berciano, J.
Baskı/Yayın Bilgisi 1987

Oral dyskinesias associated with bilateral thalamo-capsular infarction.

Yazar: Combarros, O, Gutiérrez, A, Pascual, J, Berciano, J
Baskı/Yayın Bilgisi 1990

Ataxic hemiparesis with cheiro-oral syndrome in capsular infarction.

Yazar: Combarros, O, Díez, C, Cano, J, Berciano, J
Baskı/Yayın Bilgisi 1992

Association of an ataxia indistinguishable from Friedreich's ataxia and congenital glaucoma in a family: a new syndrome.

Yazar: Combarros, O, Calleja, J, Leno, C, Berciano, J
Baskı/Yayın Bilgisi 1988

Giant aneurysm of the intracavernous carotid artery and bilateral carotid fibromuscular dysplasia.

Yazar: Rebollo, M, Quintana, F, Combarros, O, Berciano, J
Baskı/Yayın Bilgisi 1983

Consistency in gene-Alzheimer's disease association studies

Yazar: Llorca, J., Dierssen-Sotos, T., Combarros, O., Berciano, J.
Baskı/Yayın Bilgisi 2005

Hereditary "pure" spastic paraplegia: a study of nine families.

Yazar: Polo, J M, Calleja, J, Combarros, O, Berciano, J
Baskı/Yayın Bilgisi 1993

Hemiageusia from an ipsilateral multiple sclerosis plaque at the midpontine tegmentum

Yazar: COMBARROS, O., SANCHEZ-JUAN, P., BERCIANO, J., DE PABLOS, C.
Baskı/Yayın Bilgisi 2000

Guillain-Barré syndrome associated with idiopathic thrombocytopenic purpura.

Yazar: Combarros, O, Calleja, J, Hernández, L, Polo, J M, Berciano, J
Baskı/Yayın Bilgisi 1991

Diagnosis of the CMT1A duplication by PCR based detection of a novel junction fragment.

Yazar: Combarros, O, Oterino, A, Berciano, J, Benito, A, Fernández-Luna, J L
Baskı/Yayın Bilgisi 1998

Interaction between dopamine β‐hydroxylase and interleukin genes increases Alzheimer's disease risk

Yazar: Mateo, I, Infante, J, Rodríguez, E, Berciano, J, Combarros, O, Llorca, J
Baskı/Yayın Bilgisi 2006

Charcot–Marie–Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles: a long‐term follow‐up study

Yazar: Berciano, J, Gallardo, E, García, A, Infante, J, Mateo, I, Combarros, O
Baskı/Yayın Bilgisi 2006

Ataxic type of Creutzfeldt-Jakob disease with disproportionate enlargement of the fourth ventricle: a serial CT study.

Yazar: Berciano, J, Pascual, J, Polo, J M, Combarros, O, Figols, J, Díez, C
Baskı/Yayın Bilgisi 1997

The Glu298Asp polymorphism in the NOS3 gene is not associated with sporadic Alzheimer's disease

Yazar: SANCHEZ-GUERRA, M, COMBARROS, O, ALVAREZ-ARCAYA, A, MATEO, I, BERCIANO, J, GONZALEZ-GARCIA, J, LLORCA, J
Baskı/Yayın Bilgisi 2001

Autosomal dominant axonal Charcot-Marie-Tooth disease type 2 (CMT2G) maps to chromosome 12q12–q13.3

Yazar: Nelis, E, Berciano, J, Verpoorten, N, Coen, K, Dierick, I, Van Gerwen, V, Combarros, O, De Jonghe, P, Timmerman, V
Baskı/Yayın Bilgisi 2004

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

Yazar: Lambert, J-C, Grenier-Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M A, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz-Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J-F, Tzourio, C, Berr, C, Schrijvers, E M C, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C A, Lannfelt, L, Ingelsson, M, Prince, J A, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez-Garcia, F, Del Zompo, M, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D-A, Williams, J, Amouyel, P
Baskı/Yayın Bilgisi 2013

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

Yazar: Lambert, J-C, Grenier-Boley, B, Harold, D, Zelenika, D, Chouraki, V, Kamatani, Y, Sleegers, K, Ikram, M A, Hiltunen, M, Reitz, C, Mateo, I, Feulner, T, Bullido, M, Galimberti, D, Concari, L, Alvarez, V, Sims, R, Gerrish, A, Chapman, J, Deniz-Naranjo, C, Solfrizzi, V, Sorbi, S, Arosio, B, Spalletta, G, Siciliano, G, Epelbaum, J, Hannequin, D, Dartigues, J-F, Tzourio, C, Berr, C, Schrijvers, E M C, Rogers, R, Tosto, G, Pasquier, F, Bettens, K, Van Cauwenberghe, C, Fratiglioni, L, Graff, C, Delepine, M, Ferri, R, Reynolds, C A, Lannfelt, L, Ingelsson, M, Prince, J A, Chillotti, C, Pilotto, A, Seripa, D, Boland, A, Mancuso, M, Bossù, P, Annoni, G, Nacmias, B, Bosco, P, Panza, F, Sanchez-Garcia, F, Zompo, M Del, Coto, E, Owen, M, O'Donovan, M, Valdivieso, F, Caffara, P, Scarpini, E, Combarros, O, Buée, L, Campion, D, Soininen, H, Breteler, M, Riemenschneider, M, Van Broeckhoven, C, Alpérovitch, A, Lathrop, M, Trégouët, D-A, Williams, J, Amouyel, P
Baskı/Yayın Bilgisi 2013