Search Page
Save citations to file
Email citations
Email address has not been verified. Go to
My NCBI account settings
to confirm your email and then refresh this page.
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 |
|---|---|
| 2007 | 1 |
| 2008 | 1 |
| 2010 | 1 |
| 2026 | 0 |
Search Results
3 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
Mutations in GCK and HNF-1alpha explain the majority of cases with clinical diagnosis of MODY in Spain.
Clin Endocrinol (Oxf). 2007 Oct;67(4):538-46. doi: 10.1111/j.1365-2265.2007.02921.x. Epub 2007 Jun 15.
Clin Endocrinol (Oxf). 2007.
PMID: 17573900
Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients.
Garin I, Rica I, Estalella I, Oyarzabal M, Rodríguez-Rigual M, San Pedro JI, Pérez-Nanclares G, Fernández-Rebollo E, Busturia MA, Castaño L, Pérez de Nanclares G; Spanish MODY Group.
Garin I, et al.
Clin Endocrinol (Oxf). 2008 Jun;68(6):873-8. doi: 10.1111/j.1365-2265.2008.03214.x. Epub 2008 Feb 1.
Clin Endocrinol (Oxf). 2008.
PMID: 18248649
Item in Clipboard
Heterozygous glucokinase mutations and birth weight in Spanish children.
de Las Heras J, Martínez R, Rica I, de Nanclares GP, Vela A, Castaño L; Spanish MODY group.
de Las Heras J, et al.
Diabet Med. 2010 May;27(5):608-10. doi: 10.1111/j.1464-5491.2010.02953.x.
Diabet Med. 2010.
PMID: 20536962
No abstract available.
Item in Clipboard
Cite
Cite
ARTICLE TYPE
ARTICLE LANGUAGE
AGE
Filters on the sidebar will be reset to the default list and any currently applied filters will be cleared.