Format
Sort by

Send to

Choose Destination

Search results

Items: 3

  • Showing results for a modified search because your search retrieved no results.
1.

Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease.

Andrade-Campos M, Alfonso P, Irun P, Armstrong J, Calvo C, Dalmau J, Domingo MR, Barbera JL, Cano H, Fernandez-Galán MA, Franco R, Gracia I, Gracia-Antequera M, Ibañez A, Lendinez F, Madruga M, Martin-Hernández E, O'Callaghan MDM, Del Soto AP, Del Prado YR, Sancho-Val I, Sanjurjo P, Pocovi M, Giraldo P.

Orphanet J Rare Dis. 2017 May 3;12(1):84. doi: 10.1186/s13023-017-0627-z.

2.

Differences in the toxin profiles of Alexandrium ostenfeldii (Dinophyceae) strains isolated from different geographic origins: Evidence of paralytic toxin, spirolide, and gymnodimine.

Salgado P, Riobó P, Rodríguez F, Franco JM, Bravo I.

Toxicon. 2015 Sep;103:85-98. doi: 10.1016/j.toxicon.2015.06.015. Epub 2015 Jun 18.

PMID:
26093028
3.

Hyperlipoproteinaemia(a) is a common cause of autosomal dominant hypercholesterolaemia.

Meriño-Ibarra E, Puzo J, Jarauta E, Cenarro A, Recalde D, García-Otín AL, Ros E, Martorell E, Pintó X, Franco M, Zambón D, Brea A, Pocoví M, Civeira F.

J Inherit Metab Dis. 2007 Nov;30(6):970-7. Epub 2007 Oct 20.

PMID:
17955342

Supplemental Content

Loading ...
Support Center