Infante J - Search Results

1

Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1.

Peeters K, Palaima P, Pelayo-Negro AL, García A, Gallardo E, García-Barredo R, Mateiu L, Baets J, Menten B, De Vriendt E, De Jonghe P, Timmerman V, Infante J, Berciano J, Jordanova A. Peeters K, et al. Among authors: infante j. Ann Neurol. 2016 Dec;80(6):823-833. doi: 10.1002/ana.24775. Epub 2016 Sep 30. Ann Neurol. 2016. PMID: 27686364

2

[Progressive anarthria: one case without lingual apraxia].

Infante J, Sánchez Guerra M, Polo JM, Carril JM, Berciano J, Oterino A. Infante J, et al. Neurologia. 2000 May;15(5):208-10. Neurologia. 2000. PMID: 10850122 Spanish.

3

Celiac disease and idiopathic cerebellar ataxia.

Combarros O, Infante J, López-Hoyos M, Bartolomé MJ, Berciano J, Corral J, Volpini V. Combarros O, et al. Among authors: infante j. Neurology. 2000 Jun 27;54(12):2346. doi: 10.1212/wnl.54.12.2346. Neurology. 2000. PMID: 10881272 No abstract available.

4

Akinetic mutism from frontal lobe damage responding to levodopa.

Combarros O, Infante J, Berciano J. Combarros O, et al. Among authors: infante j. J Neurol. 2000 Jul;247(7):568-9. doi: 10.1007/s004150070161. J Neurol. 2000. PMID: 10993505 No abstract available.

5

[Neurologic complications of herpes zoster. A retrospective study in 100 patients].

Sánchez-Guerra M, Infante J, Pascual J, Berciano J, Polo J. Sánchez-Guerra M, et al. Among authors: infante j. Neurologia. 2001 Mar;16(3):112-7. Neurologia. 2001. PMID: 11333780 Spanish.

6

Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletion.

Infante J, García A, Combarros O, Mateo JI, Berciano J, Sedano MJ, Gutiérrez-Rivas EJ, Palau F. Infante J, et al. Muscle Nerve. 2001 Sep;24(9):1149-55. doi: 10.1002/mus.1126. Muscle Nerve. 2001. PMID: 11494267

7

Case-control study and meta-analysis of low density lipoprotein receptor-related protein gene exon 3 polymorphism in Alzheimer's disease.

Sánchez-Guerra M, Combarros O, Infante J, Llorca J, Berciano J, Fontalba A, Fernández-Luna JL, Peña N, Fernández-Viadero C. Sánchez-Guerra M, et al. Among authors: infante j. Neurosci Lett. 2001 Dec 4;316(1):17-20. doi: 10.1016/s0304-3940(01)02342-4. Neurosci Lett. 2001. PMID: 11720768

8

[Hereditary ataxias and paraplegias: a clinicogenetic review].

Berciano J, Infante J, Mateo I, Combarros O. Berciano J, et al. Among authors: infante j. Neurologia. 2002 Jan;17(1):40-51. Neurologia. 2002. PMID: 11834196 Review. Spanish.

9

Lack of association between cathepsin D genetic polymorphism and Alzheimer disease in a Spanish sample.

Mateo I, Sánchez-Guerra M, Combarros O, Llorca J, Infante J, González-García J, del Molino JP, Berciano J. Mateo I, et al. Among authors: infante j. Am J Med Genet. 2002 Jan 8;114(1):31-3. doi: 10.1002/ajmg.1623. Am J Med Genet. 2002. PMID: 11840502

10

The myeloperoxidase gene in Alzheimer's disease: a case-control study and meta-analysis.

Combarros O, Infante J, Llorca J, Peña N, Fernández-Viadero C, Berciano J. Combarros O, et al. Among authors: infante j. Neurosci Lett. 2002 Jun 21;326(1):33-6. doi: 10.1016/s0304-3940(02)00303-8. Neurosci Lett. 2002. PMID: 12052532

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