Ruiz-Pesini E - Search Results

1

Pathological Features in Paediatric Patients with TK2 Deficiency.

Jou C, Nascimento A, Codina A, Montoya J, López-Gallardo E, Emperador S, Ruiz-Pesini E, Montero R, Natera-de Benito D, Ortez CI, Marquez J, Zelaya MV, Gutierrez-Mata A, Badosa C, Carrera-García L, Expósito-Escudero J, Roldán M, Camara Y, Marti R, Ferrer I, Jimenez-Mallebrera C, Artuch R. Jou C, et al. Among authors: ruiz pesini e. Int J Mol Sci. 2022 Sep 20;23(19):11002. doi: 10.3390/ijms231911002. Int J Mol Sci. 2022. PMID: 36232299 Free PMC article.

2

Correlation of sperm motility with mitochondrial enzymatic activities.

Ruiz-Pesini E, Diez C, Lapeña AC, Pérez-Martos A, Montoya J, Alvarez E, Arenas J, López-Pérez MJ. Ruiz-Pesini E, et al. Clin Chem. 1998 Aug;44(8 Pt 1):1616-20. Clin Chem. 1998. PMID: 9702947

3

Direct and highly species-specific detection of pork meat and fat in meat products by PCR amplification of mitochondrial DNA.

Montiel-Sosa JF, Ruiz-Pesini E, Montoya J, Roncalés P, López-Pérez MJ, Pérez-Martos A. Montiel-Sosa JF, et al. J Agric Food Chem. 2000 Jul;48(7):2829-32. doi: 10.1021/jf9907438. J Agric Food Chem. 2000. PMID: 10898631

4

Mitochondrial DNA content of human spermatozoa.

Díez-Sánchez C, Ruiz-Pesini E, Lapeña AC, Montoya J, Pérez-Martos A, Enríquez JA, López-Pérez MJ. Díez-Sánchez C, et al. Biol Reprod. 2003 Jan;68(1):180-5. doi: 10.1095/biolreprod.102.005140. Biol Reprod. 2003. PMID: 12493711

5

Mitochondria from ejaculated human spermatozoa do not synthesize proteins.

Díez-Sánchez C, Ruiz-Pesini E, Montoya J, Pérez-Martos A, Enríquez JA, López-Pérez MJ. Díez-Sánchez C, et al. FEBS Lett. 2003 Oct 9;553(1-2):205-8. doi: 10.1016/s0014-5793(03)01013-5. FEBS Lett. 2003. PMID: 14550574 Free article.

6

[Deletions of the mitochondrial DNA associated to chronic progressive external ophthalmoplegia with ragged-red fibers in 2 Brazilian patients].

Carod-Artal FJ, López-Gallardo E, Solano A, Dahmani Y, Ruiz-Pesini E, Montoya J. Carod-Artal FJ, et al. Med Clin (Barc). 2006 Apr 1;126(12):457-60. doi: 10.1016/s0025-7753(06)71972-8. Med Clin (Barc). 2006. PMID: 16620733 Spanish.

7

Mitochondrial DNA transcription and diseases: past, present and future.

Montoya J, López-Pérez MJ, Ruiz-Pesini E. Montoya J, et al. Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1179-89. doi: 10.1016/j.bbabio.2006.03.023. Epub 2006 Apr 7. Biochim Biophys Acta. 2006. PMID: 16697348 Free article. Review.

8

[Diseases of the human mitochondrial oxidative phosphorylation system].

Ruiz-Pesini E, López-Gallardo E, Dahmani Y, Herrero MD, Solano A, Díez-Sánchez C, López-Pérez M, Montoya J. Ruiz-Pesini E, et al. Rev Neurol. 2006 Oct 1-15;43(7):416-24. Rev Neurol. 2006. PMID: 17006861 Free article. Review. Spanish.

9

Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation.

Carod-Artal FJ, Herrero MD, Lara MC, López-Gallardo E, Ruiz-Pesini E, Martí R, Montoya J. Carod-Artal FJ, et al. Eur J Neurol. 2007 May;14(5):581-5. doi: 10.1111/j.1468-1331.2007.01720.x. Eur J Neurol. 2007. PMID: 17437622

10

A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT-CO1).

Herrero-Martín MD, Pineda M, Briones P, López-Gallardo E, Carreras M, Benac M, Angel Idoate M, Vilaseca MA, Artuch R, López-Pérez MJ, Ruiz-Pesini E, Montoya J. Herrero-Martín MD, et al. Hum Mutat. 2008 Aug;29(8):E112-22. doi: 10.1002/humu.20800. Hum Mutat. 2008. PMID: 18484665

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

141 results

Search Page