Completeness: 57 (82.61%)
Cited: 2 (1.65%)
All atributes instances: 65 (7.96%)
Identification (url, isbn, doi, issn, jstor, pmc, pmid, arxiv, oclc, website): 2 (66.67%)
Filled attributes and number of instances
title
X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a 'European Community Alport Syndrome Concerted Action' study
1
X-Linked Alport Syndrome: Natural History and Genotype-Phenotype Correlations in Girls and Women Belonging to 195 Families: A \
1
last1
Jais
1
first1
J. P.
1
last2
Knebelmann
1
first2
B
1
last3
Giatras
1
first3
I
1
last4
De Marchi
1
first4
M
1
last5
Rizzoni
1
first5
G
1
last6
Renieri
1
first6
A
1
last7
Weber
1
first7
M
1
last8
Gross
1
first8
O
1
last9
Netzer
1
first9
K. O.
1
year
2003
2
pages
2603–10
2
journal
Journal of the American Society of Nephrology
2
volume
14
2
issue
10
2
doi
10.1097/01.ASN.0000090034.71205.74
2
last20
Carvalho
1
last21
Saus
1
last22
Antignac
1
last23
Smeets
1
last24
Gubler
1
first23
H
1
first22
C
1
first21
J
1
first20
M. F.
1
first24
M. C.
1
vauthors
Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Dahan K, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC
1
pmid
14514738
2
last15
Tryggvason
1
last14
Persson
1
last17
Hertz
1
last16
Martin
1
last11
Pirson
1
last10
Flinter
1
last13
Wieslander
1
last12
Dahan
1
last19
Sanak
1
last18
Schröder
1
first19
M
1
first18
C
1
first12
K
1
first13
J
1
first10
F
1
first11
Y
1
first16
P
1
first17
J. M.
1
first14
U
1
first15
K
1
Points based on comparison of each characteristics of the source with a median of each relevant characteristics of the TOP1000 corresponding sources In English Wikipedia:
| Characteristics | Median* |
|---|---|
| Completeness | 69 |
| Cited | 121 |
| All atributes instances | 817 |
* - as of August 2016
