Raguer N - Search Results

1

Late-onset metachromatic leukodystrophy clinically presenting as isolated peripheral neuropathy: compound heterozygosity for the IVS2+1G-->A mutation and a newly identified missense mutation (Thr408Ile) in a Spanish family.

Comabella M, Waye JS, Raguer N, Eng B, Domínguez C, Navarro C, Borrás C, Krivit W, Montalbán X. Comabella M, et al. Among authors: raguer n. Ann Neurol. 2001 Jul;50(1):108-12. Ann Neurol. 2001. PMID: 11456299

2

Lower motor neuron disease in a HIV-2 infected woman.

Sastre-Garriga J, Tintoré M, Raguer N, Ruíz I, Montalban X, Codina A. Sastre-Garriga J, et al. Among authors: raguer n. J Neurol. 2000 Sep;247(9):718-9. doi: 10.1007/s004150070121. J Neurol. 2000. PMID: 11081817 No abstract available.

3

Phenotypic variability in a Spanish family with MNGIE.

Gamez J, Ferreiro C, Accarino ML, Guarner L, Tadesse S, Martí RA, Andreu AL, Raguer N, Cervera C, Hirano M. Gamez J, et al. Among authors: raguer n. Neurology. 2002 Aug 13;59(3):455-7. doi: 10.1212/wnl.59.3.455. Neurology. 2002. PMID: 12177387

4

A novel thymidine phosphorylase mutation in a Spanish MNGIE patient.

Gamez J, Lara MC, Mearin F, Oliveras-Ley C, Raguer N, Olive M, Leist AT, Perello A, Perona M, Cervera C, Andreu AL, Martí R, Hirano M. Gamez J, et al. Among authors: raguer n. J Neurol Sci. 2005 Jan 15;228(1):35-9. doi: 10.1016/j.jns.2004.09.034. Epub 2004 Nov 12. J Neurol Sci. 2005. PMID: 15607208

5

Lambert-Eaton Myasthenic syndrome associated with sarcoidosis.

Purroy García F, Comabella M, Raguer N, Majó J, Montalban X. Purroy García F, et al. Among authors: raguer n. J Neurol. 2005 Sep;252(9):1127-8. doi: 10.1007/s00415-005-0807-y. Epub 2005 Apr 20. J Neurol. 2005. PMID: 15834646 No abstract available.

6

SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement.

Manole A, Horga A, Gamez J, Raguer N, Salvado M, San Millán B, Navarro C, Pittmann A, Reilly MM, Houlden H. Manole A, et al. Among authors: raguer n. Neurogenetics. 2017 Jan;18(1):63-67. doi: 10.1007/s10048-016-0505-1. Epub 2016 Dec 22. Neurogenetics. 2017. PMID: 28005197

7

Myasthenia gravis following alemtuzumab therapy for multiple sclerosis.

Midaglia L, Gratacòs M, Caronna E, Raguer N, Sastre-Garriga J, Montalban X, Tintoré M. Midaglia L, et al. Among authors: raguer n. Neurology. 2018 Sep 25;91(13):622-624. doi: 10.1212/WNL.0000000000006251. Epub 2018 Aug 24. Neurology. 2018. PMID: 30143565 Free PMC article. No abstract available.

8

MRI findings in Möbius syndrome: correlation with clinical features.

Pedraza S, Gámez J, Rovira A, Zamora A, Grive E, Raguer N, Ruscalleda J. Pedraza S, et al. Among authors: raguer n. Neurology. 2000 Oct 10;55(7):1058-60. doi: 10.1212/wnl.55.7.1058. Neurology. 2000. PMID: 11061273

9

Mutational analysis of the Cu/Zn superoxide dismutase gene in a Catalan ALS population: should all sporadic ALS cases also be screened for SOD1?

Gamez J, Corbera-Bellalta M, Nogales G, Raguer N, García-Arumí E, Badia-Canto M, Lladó-Carbó E, Alvarez-Sabín J. Gamez J, et al. Among authors: raguer n. J Neurol Sci. 2006 Aug 15;247(1):21-8. doi: 10.1016/j.jns.2006.03.006. Epub 2006 May 3. J Neurol Sci. 2006. PMID: 16674979

10

Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients.

Gamez J, Also E, Alias L, Corbera-Bellalta M, Barceló MJ, Centeno M, Raguer N, Gratacós M, Baiget M, Tizzano EF. Gamez J, et al. Among authors: raguer n. Clin Neurol Neurosurg. 2007 Dec;109(10):844-8. doi: 10.1016/j.clineuro.2007.07.019. Epub 2007 Sep 11. Clin Neurol Neurosurg. 2007. PMID: 17850955

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