Romero NB - Search Results

1

Congenital Nemaline Myopathy with Dense Protein Masses.

Bevilacqua JA, Malfatti E, Labasse C, Brochier G, Madelaine A, Lacène E, Doray B, Laforêt P, Eymard B, Rendu J, Romero NB. Bevilacqua JA, et al. Among authors: romero nb. J Neuropathol Exp Neurol. 2022 Mar 29;81(4):304-307. doi: 10.1093/jnen/nlab139. J Neuropathol Exp Neurol. 2022. PMID: 35139532 No abstract available.

2

[Clinical and electrophysiologic study of the peripheral nerve in 28 cases of mitochondrial disease].

Eymard B, Penicaud A, Leger JM, Romero N, Marsac C, Fardeau M, Brunet P. Eymard B, et al. Rev Neurol (Paris). 1991;147(6-7):508-12. Rev Neurol (Paris). 1991. PMID: 1660183 French.

3

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: genetic, biochemical and morphological studies.

Degoul F, Nelson I, Lestienne P, Francois D, Romero N, Duboc D, Eymard B, Fardeau M, Ponsot G, Paturneau-Jouas M, et al. Degoul F, et al. J Neurol Sci. 1991 Feb;101(2):168-77. doi: 10.1016/0022-510x(91)90042-6. J Neurol Sci. 1991. PMID: 1851820

4

[Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy].

Marsac C, Degoul F, Bonne G, Romero N, Nelson I, Fardeau M, François D, Ponsot G, Harpey JP, Eymard B, et al. Marsac C, et al. Rev Neurol (Paris). 1991;147(6-7):462-6. Rev Neurol (Paris). 1991. PMID: 1962051 French.

5

Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.

Eymard B, Romero NB, Leturcq F, Piccolo F, Carrié A, Jeanpierre M, Collin H, Deburgrave N, Azibi K, Chaouch M, Merlini L, Thémar-Noël C, Penisson I, Mayer M, Tanguy O, Campbell KP, Kaplan JC, Tomé FM, Fardeau M. Eymard B, et al. Among authors: romero nb. Neurology. 1997 May;48(5):1227-34. doi: 10.1212/wnl.48.5.1227. Neurology. 1997. PMID: 9153448

6

Gallium-67 scintigraphy in macrophagic myofasciitis.

Chérin P, Authier FJ, Gherardi RK, Romero N, Laforêt P, Eymard B, Herson S, Caillat-Vigneron N. Chérin P, et al. Arthritis Rheum. 2000 Jul;43(7):1520-6. doi: 10.1002/1529-0131(200007)43:7<1520::AID-ANR16>3.0.CO;2-Q. Arthritis Rheum. 2000. PMID: 10902755 Free article.

7

[Exploration of exercise intolerance by 31P NMR spectroscopy of calf muscles coupled with MRI and ergometry].

Laforêt P, Wary C, Duteil S, de Kerviler E, Carlier PG, Lombès A, Romero NB, Fardeau M, Eymard B, Leroy-Willig A. Laforêt P, et al. Among authors: romero nb. Rev Neurol (Paris). 2003 Jan;159(1):56-67. Rev Neurol (Paris). 2003. PMID: 12618654 Clinical Trial. French.

8

Clinical and histologic findings in autosomal centronuclear myopathy.

Jeannet PY, Bassez G, Eymard B, Laforêt P, Urtizberea JA, Rouche A, Guicheney P, Fardeau M, Romero NB. Jeannet PY, et al. Among authors: romero nb. Neurology. 2004 May 11;62(9):1484-90. doi: 10.1212/01.wnl.0000124388.67003.56. Neurology. 2004. PMID: 15136669 Review.

9

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey.

Charron P, Villard E, Sébillon P, Laforêt P, Maisonobe T, Duboscq-Bidot L, Romero N, Drouin-Garraud V, Frébourg T, Richard P, Eymard B, Komajda M. Charron P, et al. Heart. 2004 Aug;90(8):842-6. doi: 10.1136/hrt.2003.029504. Heart. 2004. PMID: 15253947 Free PMC article.

10

Progression despite replacement of a myopathic form of coenzyme Q10 defect.

Auré K, Benoist JF, Ogier de Baulny H, Romero NB, Rigal O, Lombès A. Auré K, et al. Among authors: romero nb. Neurology. 2004 Aug 24;63(4):727-9. doi: 10.1212/01.wnl.0000134607.76780.b2. Neurology. 2004. PMID: 15326254

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