Navarro C - Search Results

1

Mutational spectrum of Duchenne muscular dystrophy in Spain: Study of 284 cases.

Vieitez I, Gallano P, González-Quereda L, Borrego S, Marcos I, Millán JM, Jairo T, Prior C, Molano J, Trujillo-Tiebas MJ, Gallego-Merlo J, García-Barcina M, Fenollar M, Navarro C. Vieitez I, et al. Among authors: navarro c. Neurologia. 2017 Jul-Aug;32(6):377-385. doi: 10.1016/j.nrl.2015.12.009. Epub 2016 Mar 9. Neurologia. 2017. PMID: 26968818 Free article. English, Spanish.

2

Myoadenylate deaminase deficiency: clinico-pathological and molecular study of a series of 27 Spanish cases.

Teijeira S, San Millán B, Fernández JM, Rivas E, Viéitez I, Miranda S, González F, Navarro C. Teijeira S, et al. Among authors: navarro c. Clin Neuropathol. 2009 Mar-Apr;28(2):136-42. doi: 10.5414/npp28136. Clin Neuropathol. 2009. PMID: 19353846 Free article.

3

Molecular and clinical study of McArdle's disease in a cohort of 123 European patients. Identification of 20 novel mutations.

Vieitez I, Teijeira S, Fernandez JM, San Millan B, Miranda S, Ortolano S, Louis S, Laforet P, Navarro C. Vieitez I, et al. Among authors: navarro c. Neuromuscul Disord. 2011 Dec;21(12):817-23. doi: 10.1016/j.nmd.2011.07.002. Epub 2011 Jul 29. Neuromuscul Disord. 2011. PMID: 21802952

4

Phenotypic variability in a Spanish family with a Caveolin-3 mutation.

González-Pérez P, Gallano P, González-Quereda L, Rivas-Infante E, Teijeira S, Navarro C, Bautista-Lorite J. González-Pérez P, et al. Among authors: navarro c. J Neurol Sci. 2009 Jan 15;276(1-2):95-8. doi: 10.1016/j.jns.2008.09.009. Epub 2008 Oct 19. J Neurol Sci. 2009. PMID: 18930476

5

[Congenital muscular dystrophy: report on 10 cases].

Olivé M, Roig M, Bonaventura I, Navarro C. Olivé M, et al. Among authors: navarro c. Neurologia. 1994 Nov;9(9):387-92. Neurologia. 1994. PMID: 7811489 Spanish.

6

Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.

Viéitez I, Teijeira S, Millán BS, Navarro C. Viéitez I, et al. Among authors: navarro c. Hum Genet. 2009 Apr;125(3):338. Hum Genet. 2009. PMID: 19309802 No abstract available.

7

Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.

Viéitez I, Teijeira S, Millán BS, Navarro C. Viéitez I, et al. Among authors: navarro c. Hum Genet. 2009 Apr;125(3):343. Hum Genet. 2009. PMID: 19320018 No abstract available.

8

Chorionic villi ultrastructure in the prenatal diagnosis of glycogenosis type II.

San Millan B, Teijeira S, Domínguez C, Vieitez I, Navarro C. San Millan B, et al. Among authors: navarro c. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S105-11. doi: 10.1007/s10545-009-9033-6. Epub 2010 Feb 16. J Inherit Metab Dis. 2010. PMID: 20157781

9

Novel human pathological mutations. Gene symbol: PYGM. Disease: McArdle disease.

Viéitez I, Teijeira S, San Millán B, Navarro C. Viéitez I, et al. Among authors: navarro c. Hum Genet. 2009 Apr;125(3):349. Hum Genet. 2009. PMID: 19320035 No abstract available.

10

[Myopathology. New concept. New laboratory].

Navarro C, Teijeira S. Navarro C, et al. Neurologia. 2004 May;19(4):168-82. Neurologia. 2004. PMID: 15131736 Review. Spanish.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,261 results

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

1,261 results