Pineda M - Search Results

1

New agents and approaches to treatment in Niemann-Pick type C disease.

Pérez-Poyato MS, Pineda M. Pérez-Poyato MS, et al. Among authors: pineda m. Curr Pharm Biotechnol. 2011 Jun;12(6):897-901. doi: 10.2174/138920111795542697. Curr Pharm Biotechnol. 2011. PMID: 21235443 Review.

2

Hypokinetic-rigid syndrome in children and inborn errors of metabolism.

García-Cazorla A, Ortez C, Pérez-Dueñas B, Serrano M, Pineda M, Campistol J, Fernández-Álvarez E. García-Cazorla A, et al. Among authors: pineda m. Eur J Paediatr Neurol. 2011 Jul;15(4):295-302. doi: 10.1016/j.ejpn.2011.04.013. Epub 2011 May 25. Eur J Paediatr Neurol. 2011. PMID: 21612960 Review.

3

Oxidative stress in Rett syndrome.

Sierra C, Vilaseca MA, Brandi N, Artuch R, Mira A, Nieto M, Pineda M. Sierra C, et al. Among authors: pineda m. Brain Dev. 2001 Dec;23 Suppl 1:S236-9. doi: 10.1016/s0387-7604(01)00369-2. Brain Dev. 2001. PMID: 11738881

4

[Familiar chronic progressive external ophthalmoplegia of mitochondrial origin].

Pineda M, Playán-Ariso A, Alcaine-Villarroya MJ, Vernet AM, Serra-Castanera A, Solano A, Vilaseca MA, Artuch R, López-Pérez M, Briones-Godino MP, Andreu A, Montoya J. Pineda M, et al. Rev Neurol. 2004 Jun 1-15;38(11):1023-7. Rev Neurol. 2004. PMID: 15202078 Spanish.

5

[Hallervorden-Spatz disease: presentation of a new case].

Pedrola D, Pineda M, Fernández Alvarez E. Pedrola D, et al. Among authors: pineda m. Rev Neurol. 1995 Jan-Feb;23(119):51-3. Rev Neurol. 1995. PMID: 8548643 Spanish.

6

Miglustat in patients with Niemann-Pick disease Type C (NP-C): a multicenter observational retrospective cohort study.

Pineda M, Wraith JE, Mengel E, Sedel F, Hwu WL, Rohrbach M, Bembi B, Walterfang M, Korenke GC, Marquardt T, Luzy C, Giorgino R, Patterson MC. Pineda M, et al. Mol Genet Metab. 2009 Nov;98(3):243-9. doi: 10.1016/j.ymgme.2009.07.003. Epub 2009 Aug 4. Mol Genet Metab. 2009. PMID: 19656703

7

Long-term evolution of eight Spanish patients with CDG type Ia: typical and atypical manifestations.

Pérez-Dueñas B, García-Cazorla A, Pineda M, Poo P, Campistol J, Cusí V, Schollen E, Matthijs G, Grunewald S, Briones P, Pérez-Cerdá C, Artuch R, Vilaseca MA. Pérez-Dueñas B, et al. Among authors: pineda m. Eur J Paediatr Neurol. 2009 Sep;13(5):444-51. doi: 10.1016/j.ejpn.2008.09.002. Epub 2008 Oct 22. Eur J Paediatr Neurol. 2009. PMID: 18948042

8

Vanishing white matter disease associated with progressive macrocephaly.

Pineda M, R-Palmero A, Baquero M, O'Callaghan M, Aracil A, van der Knaap M, Scheper GC. Pineda M, et al. Neuropediatrics. 2008 Feb;39(1):29-32. doi: 10.1055/s-2008-1076738. Neuropediatrics. 2008. PMID: 18504679

9

Niemann-Pick C disease in Spain: clinical spectrum and development of a disability scale.

Iturriaga C, Pineda M, Fernández-Valero EM, Vanier MT, Coll MJ. Iturriaga C, et al. Among authors: pineda m. J Neurol Sci. 2006 Nov 1;249(1):1-6. doi: 10.1016/j.jns.2006.05.054. Epub 2006 Jun 30. J Neurol Sci. 2006. PMID: 16814322

10

Study of a fetal brain affected by a severe form of tyrosine hydroxylase deficiency, a rare cause of early parkinsonism.

Tristán-Noguero A, Díez H, Jou C, Pineda M, Ormazábal A, Sánchez A, Artuch R, Garcia-Cazorla À. Tristán-Noguero A, et al. Among authors: pineda m. Metab Brain Dis. 2016 Jun;31(3):705-9. doi: 10.1007/s11011-015-9780-z. Epub 2015 Dec 21. Metab Brain Dis. 2016. PMID: 26686676

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

Search Page

Search Results