Search Page
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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2006 | 1 |
2010 | 2 |
2011 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Caracterización molecular de la nueva entidad clínica relacionada con la hiperplasia suprarrenal congénita, síndrome CAH-X en población española.
Adv Lab Med. 2023 Jul 4;4(3):268-278. doi: 10.1515/almed-2023-0050. eCollection 2023 Sep.
Adv Lab Med. 2023.
PMID: 38075178
Free PMC article.
Spanish.
LEOPARD syndrome (PTPN11, T468M) in three boys fulfilling neurofibromatosis type 1 clinical criteria.
Carcavilla A, Pinto I, Muñoz-Pacheco R, Barrio R, Martin-Frías M, Ezquieta B.
Carcavilla A, et al. Among authors: munoz pacheco r.
Eur J Pediatr. 2011 Aug;170(8):1069-74. doi: 10.1007/s00431-011-1418-5. Epub 2011 Mar 2.
Eur J Pediatr. 2011.
PMID: 21365175
Item in Clipboard
Gene duplications in 21-hydroxylase deficiency: the importance of accurate molecular diagnosis in carrier detection and prenatal diagnosis.
Ezquieta B, Beneyto M, Muñoz-Pacheco R, Barrio R, Oyarzabal M, Lechuga JL, Luzuriaga C, Hermoso F, Quinteiro S, Martinez S.
Ezquieta B, et al. Among authors: munoz pacheco r.
Prenat Diagn. 2006 Dec;26(12):1172-8. doi: 10.1002/pd.1584.
Prenat Diagn. 2006.
PMID: 17042033
Item in Clipboard
Carrier detection and prenatal diagnosis of congenital adrenal hyperplasia must identify 'apparently mild' CYP21A2 alleles which associate neonatal salt-wasting disease.
Ezquieta B, Santomé L, Barrio R, Barrionuevo JL, López-Siguero JP, Oliver A, Ramírez J, Rodríguez I, Muñoz-Pacheco R.
Ezquieta B, et al. Among authors: munoz pacheco r.
Prenat Diagn. 2010 Aug;30(8):758-63. doi: 10.1002/pd.2537.
Prenat Diagn. 2010.
PMID: 20661889
Item in Clipboard
[Simple virilizing forms of congenital adrenal hyperplasia: adaptation and prospective validation of the molecular screening].
Santomé Collazo JL, Cirujano Segura A, Ferreiro Fernández B, Casado Fúnez C, Muñoz-Pacheco R, Ezquieta Zubicaray B.
Santomé Collazo JL, et al. Among authors: munoz pacheco r.
Med Clin (Barc). 2010 Jul 10;135(5):195-201. doi: 10.1016/j.medcli.2009.11.039. Epub 2010 Feb 19.
Med Clin (Barc). 2010.
PMID: 20171703
Spanish.
Item in Clipboard
Cite
Cite