Navarro C - Search Results

1

[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.

2

Presentation, clinical course, and outcome of the congenital form of myotonic dystrophy.

Roig M, Balliu PR, Navarro C, Brugera R, Losada M. Roig M, et al. Among authors: navarro c. Pediatr Neurol. 1994 Oct;11(3):208-13. doi: 10.1016/0887-8994(94)90104-x. Pediatr Neurol. 1994. PMID: 7880334

3

Expression of myogenic regulatory factors (MRFs) in human neuromuscular disorders.

Olivé M, Martinez-Matos JA, Pirretas P, Povedano M, Navarro C, Ferrer I. Olivé M, et al. Among authors: navarro c. Neuropathol Appl Neurobiol. 1997 Dec;23(6):475-82. doi: 10.1111/j.1365-2990.1997.tb01324.x. Neuropathol Appl Neurobiol. 1997. PMID: 9460713

4

Congenital spinal cord haemangioblastoma: another cause of spinal cord section syndrome in the newborn.

Roig M, Ballesca M, Navarro C, Ortega A, Martorell R, Fina A. Roig M, et al. Among authors: navarro c. J Neurol Neurosurg Psychiatry. 1988 Aug;51(8):1091-3. doi: 10.1136/jnnp.51.8.1091. J Neurol Neurosurg Psychiatry. 1988. PMID: 3216212 Free PMC article.

5

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.

6

Peripheral neuropathy in essential mixed cryoglobulinemia.

Garcia-Bragado F, Fernandez JM, Navarro C, Villar M, Bonaventura I. Garcia-Bragado F, et al. Among authors: navarro c. Arch Neurol. 1988 Nov;45(11):1210-4. doi: 10.1001/archneur.1988.00520350048015. Arch Neurol. 1988. PMID: 2847694

7

Clinical and myopathological evaluation of early- and late-onset subtypes of myofibrillar myopathy.

Olivé M, Odgerel Z, Martínez A, Poza JJ, Bragado FG, Zabalza RJ, Jericó I, Gonzalez-Mera L, Shatunov A, Lee HS, Armstrong J, Maraví E, Arroyo MR, Pascual-Calvet J, Navarro C, Paradas C, Huerta M, Marquez F, Rivas EG, Pou A, Ferrer I, Goldfarb LG. Olivé M, et al. Among authors: navarro c. Neuromuscul Disord. 2011 Aug;21(8):533-42. doi: 10.1016/j.nmd.2011.05.002. Epub 2011 Jun 14. Neuromuscul Disord. 2011. PMID: 21676617 Free PMC article.

8

The clinical spectrum of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Pons R, Roig M, Riudor E, Ribes A, Briones P, Ortigosa L, Baldellou A, Gil-Gibernau J, Olesti M, Navarro C, Wanders RJ. Pons R, et al. Among authors: navarro c. Pediatr Neurol. 1996 Apr;14(3):236-43. doi: 10.1016/0887-8994(96)00021-5. Pediatr Neurol. 1996. PMID: 8736409 Review.

9

Skin biopsy findings in glycogenosis III: clinical, biochemical, and electrophysiological correlations.

Sancho S, Navarro C, Fernández JM, Domínguez C, Ortega A, Roig M, Cervera C. Sancho S, et al. Among authors: navarro c. Ann Neurol. 1990 May;27(5):480-6. doi: 10.1002/ana.410270505. Ann Neurol. 1990. PMID: 2360788

10

[Cerebral toxoplasmosis in the acquired immunodeficiency syndrome. Study of the clinical, radiological, and pathological findings in 10 cases].

Bonaventura I, Romero F, Ortega A, Navarro C, Juste C, Codina Puiggrós A. Bonaventura I, et al. Among authors: navarro c. Med Clin (Barc). 1988 May 28;91(1):1-6. Med Clin (Barc). 1988. PMID: 3172889 Spanish. No abstract available.

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