Skip navigation
Home
Browse
Communities
& Collections
Browse Items by:
Issue Date
Author
Title
Subject
Item Type
Advanced Search
Help
About DSpace
Sign on to:
My DSpace
Receive email
updates
Edit Profile
Saved Searches
Favorites
Repository of UOI "Olympias"
Repository of OAI
Saved Searches
Save this search
Go!
Discover
Author
10
Kitsos, G.
10
Psilas, K.
7
Petersen, M. B.
6
Grigoriadou, M.
4
Economou-Petersen, E.
3
Aperis, G.
3
Georgiou, I.
3
Syrrou, M.
3
Wirtz, M. K.
2
Aspiotis, M.
.
next >
Subject
34
Humans
29
Male
25
Female
16
Adult
11
Middle Aged
10
Greece
8
Aged
8
Infant
6
Child
5
Adolescent
.
next >
Item Type
34
journalArticle
Date
1
2010 - 2011
22
2000 - 2009
7
1990 - 1999
3
1980 - 1989
1
1974 - 1979
.
next >
Search
Search:
All of DSpace
ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
Σχολή Επιστημών Υγείας
Τμήμα Ιατρικής
Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
for
Search only items with full text availability
Current filters:
Title
Author
Subject
Date Issued
Item Type
Date
Has File(s)
???jsp.search.filter.original_bundle_filenames???
???jsp.search.filter.original_bundle_descriptions???
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Clear current filters
or
Add more filters
Title
Author
Subject
Date Issued
Item Type
Date
Has File(s)
???jsp.search.filter.original_bundle_filenames???
???jsp.search.filter.original_bundle_descriptions???
Equals
Contains
ID
Not Equals
Not Contains
Not ID
View Option
Results/Page
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
Sort items by
Relevance
Title
Issue Date
In order
Ascending
Descending
Authors/record
All
1
5
10
15
20
25
30
35
40
45
50
Results 1-10 of 34 (Search time: 0.004 seconds).
previous
1
2
3
4
next
Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis (Journal article)
Phenotypic and molecular genetic aspects of pseudohypoparathyroidism type Ib in a Greek kindred: evidence for enhanced uric acid excretion due to parathyroid hormone resistance (Journal article)
Juvenile open-angle glaucoma: a report of a pedigree (Journal article)
PGD for autosomal dominant polycystic kidney disease type 1 (Journal article)
Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation (Journal article)
Prevalence of GJB2 mutations in prelingual deafness in the Greek population (Journal article)
Prolonged jaundice and hypothyroidism as the presenting symptoms in a neonate with a novel Prop1 gene mutation (Q83X) (Journal article)
Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's disease (Journal article)
On the use of EEG features towards person identification via neural networks (Journal article)
Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia (Journal article)