Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

101 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Interference of bromide in determination of serum chloride.
Pressac M, Jardel C, Durand D, Aymard P. Pressac M, et al. Clin Chem. 1987 Mar;33(3):415-6. Clin Chem. 1987. PMID: 3815810 No abstract available.
Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation.
Bataillard M, Chatzoglou E, Rumbach L, Sternberg D, Tournade A, Laforêt P, Jardel C, Maisonobe T, Lombès A. Bataillard M, et al. Neurology. 2001 Feb 13;56(3):405-7. doi: 10.1212/wnl.56.3.405. Neurology. 2001. PMID: 11171912
The pathogenicity of the mutation was shown in single muscle fibers by the correlation between high mutation load and cytochrome c oxidase defect....
The pathogenicity of the mutation was shown in single muscle fibers by the correlation between high mutation load and cytochrome c ox …
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders.
Sternberg D, Chatzoglou E, Laforêt P, Fayet G, Jardel C, Blondy P, Fardeau M, Amselem S, Eymard B, Lombès A. Sternberg D, et al. Brain. 2001 May;124(Pt 5):984-94. doi: 10.1093/brain/124.5.984. Brain. 2001. PMID: 11335700
Direct demonstration of a correlation between the proportion of heteroplasmic sequence variations and the cytochrome c oxidase defect was performed at the single muscle-fibre level. ...
Direct demonstration of a correlation between the proportion of heteroplasmic sequence variations and the cytochrome c oxidase defect …
Functional characterization of novel mutations in the human cytochrome b gene.
Legros F, Chatzoglou E, Frachon P, Ogier De Baulny H, Laforêt P, Jardel C, Godinot C, Lombès A. Legros F, et al. Eur J Hum Genet. 2001 Jul;9(7):510-8. doi: 10.1038/sj.ejhg.5200678. Eur J Hum Genet. 2001. PMID: 11464242
Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor.
Chapiro E, Feldmann D, Denoyelle F, Sternberg D, Jardel C, Eliot MM, Bouccara D, Weil D, Garabédian EN, Couderc R, Petit C, Marlin S. Chapiro E, et al. Eur J Hum Genet. 2002 Dec;10(12):851-6. doi: 10.1038/sj.ejhg.5200894. Eur J Hum Genet. 2002. PMID: 12461693
[Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation].
Auré K, Sternberg D, Maisonobe T, Herson S, Jardel C, Blondy P, Lombès A, Eymard B, Laforêt P. Auré K, et al. Rev Neurol (Paris). 2003 Dec;159(12):1163-8. Rev Neurol (Paris). 2003. PMID: 14978417 French.
Kearns Sayre syndrome: an unusual form of mitochondrial diabetes.
Laloi-Michelin M, Virally M, Jardel C, Meas T, Ingster-Moati I, Lombès A, Massin P, Chabriat H, Tielmans A, Mikol J, Guillausseau PJ. Laloi-Michelin M, et al. Diabetes Metab. 2006 Apr;32(2):182-6. doi: 10.1016/s1262-3636(07)70267-7. Diabetes Metab. 2006. PMID: 16735969
Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1.
Le Ber I, Dubourg O, Benoist JF, Jardel C, Mochel F, Koenig M, Brice A, Lombès A, Dürr A. Le Ber I, et al. Neurology. 2007 Jan 23;68(4):295-7. doi: 10.1212/01.wnl.0000252366.10731.43. Neurology. 2007. PMID: 17242337
101 results
Jump to page
Feedback