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CNKI学位论文(17)
知网期刊论文(79)
在“
Elsevier电子期刊
”中,
命中:
19
条,耗时:小于0.01 秒
在所有数据库中总计命中:
96
条
1.
Screening, diagnosis, and management of patients with
Fabry
disease: conclusions from a “Kidney Disease: Improving Global Outcomes” (KDIGO) Controversies Conference
作者:
Raphael Schiffmann
1
;
raphael.schiffmann@baylorhealth.edu
;
Derralynn A. Hughes
2
;
Gabor E. Linthorst
3
;
Alberto Ortiz
4
;
Einar Svarstad
5
;
6
;
David G. Warnock
7
;
Michael L. West
8
;
Christoph Wanner
9
;
wanner_c@ukw.de
;
for Conference Participants
10
;
Daniel G. Bichet
;
Erik Ilsø
;
Christensen
;
Ricardo Correa-Rotter
;
Perry M. Elliott
;
Sandro Feriozzi
;
Agnes B. Fogo
;
Dominique P. Germain
;
Carla E.M. Hollak
;
Robert J. Hopkin
;
Jack Johnson
;
Ilkka Kantola
;
Jeffrey B. Kopp
;
Jü
;
rgen Krö
;
ner
;
Ale&scaron
;
Linhart
;
Ana Maria Martins
;
Dietrich Matern
;
Atul B. Mehta
;
Renzo Mignani
;
Behzad Najafian
;
Ichiei Narita
;
Kathy Nicholls
;
Greg T. Obrador
;
Joã
;
o Paulo Oliveira
;
Antonio Pisani
;
Juan Politei
;
Uma Ramaswami
;
Markus Ries
;
Wim Terryn
;
Camilla Tø
;
ndel
;
Roser Torra
;
Bojan Vujkovac
;
Stephen Waldek
;
Jerry Walter
关键词:
chronic kidney disease
;
enzyme replacement therapy
;
Fabry
disease
;
Fabry
nephropathy
;
standard of care
刊名:Kidney International
出版年:2017
2.
Differential response of glomerular parietal epithelial cells and podocytes to enzyme replacement therapy in
Fabry
nephropathy
作者:
Fu-Pang Chang
a
;
b
;
Michael Mauer
c
;
Alexey Sokolovskiy
a
;
Camilla Tø
;
ndel
d
;
e
;
Einar Svarstad
d
;
e
;
Behzad Najafian
a
刊名:Molecular Genetics and Metabolism
出版年:2016
3.
Clinical-pathological correlation in
Fabry
nephropathy
in Mexican children based on ISGFN
作者:
Circe Gó
;
mez-Tenorio
a
;
Virgilia Soto-Abraham
b
;
Carmen Dí
;
az-Leal C
a
;
Juan Antonio Garcí
;
a-Bello
a
;
Karen Ordaz-Ló
;
pez
a
;
Norma E. Guerra-Herná
;
ndez
a
;
Miguel Arturo Má
;
rquez-Gutierrez
a
;
Sergio Franco-Ornelas
a
刊名:Molecular Genetics and Metabolism
出版年:2016
4.
Urinary type IV collagen: Better than albuminuria to identify incipient
Fabry
nephropathy
作者:
Patricio Aguiar
a
;
Rui Pinto
b
;
Olga Azevedo
c
;
Jacira Marino
d
;
Rob Baker
d
;
Carlos Cardoso
b
;
Jose Luis Ducla Soares
a
;
Derralynn Hughes
d
刊名:Molecular Genetics and Metabolism
出版年:2016
5.
Anti-proteinuric therapy and
Fabry
nephropathy
; factors associated with preserved kidney function during agalsidase-beta therapy
作者:
David G. Warnock
a
;
Christie P. Thomas
b
;
Bojan Vujkovac
c
;
Ruth C. Campbell
d
;
Joel Charrow
e
;
Dawn A. Laney
f
;
Leslie L. Jackson
a
;
William R. Wilcox
f
;
Christoph Wanner
g
刊名:Molecular Genetics and Metabolism
出版年:2016
6.
Fabry
disease and membranous
nephropathy
: Case report
作者:
Jose T. Monte Neto
a
;
Daniel Santos Rocha Sobral Filho
a
;
Roosevelt Valente Chaves
a
;
Nayze L.S. Aldeman
a
;
Marlene Antonia Reis
b
;
Semiramis J. Hadad Monte
a
刊名:Molecular Genetics and Metabolism
出版年:2016
7.
Clinical, Histological and Molecular Characteristics of Mexican Patients with
Fabry
Disease and Significant Renal Involvement
作者:
Manuel Ramos-Kuri
a
;
b
;
c
;
David Olvera
d
;
Juan J. Morales
e
;
Benjamin A. Rodriguez-Espino
c
;
Alejandra Lara-Mejí
;
a
f
;
Diana De Los Rí
;
os
g
;
Gregorio T. Obrador
c
;
Julio Granados
f
;
julgrate@yahoo.com" class="auth_mail
;
Ricardo Correa-Rotter
d
关键词:
Fabry
disease
;
伪-galactosidase A
;
伪-GLA-A enzyme
;
Fabry
nephropathy
刊名:Archives of Medical Research
出版年:April 2014
8.
Podocyturia correlates with proteinuria in patients with
Fabry
disease (FD) and is a potential biomarker of Fabry
nephropathy
作者:
Cecilia Ponchiardi
a
;
Brent Fall
a
;
Ronald Scott
a
;
Stefanie Uhrich
a
;
Michael Mauer
b
;
Chester Whitley
b
;
Jeffrey Pippin
a
;
Stuart Shankland
a
;
Jonathan Jefferson
a
;
Behzad Najafian
a
刊名:Molecular Genetics and Metabolism
出版年:2013
9.
Renal structural-functional relationship (SFR) studies suggest that podocyte GL-3 accumulation predicts urine protein creatinine ratio in
Fabry
disease (FD)
nephropathy
(FDN)
作者:
Behzad Najafian
a
;
Chester Whitley
b
;
Beth Thurberg
c
;
Einar Svarstad
d
;
Camilla Tondel
d
;
Marie Claire Gubler
e
;
Michael West
f
;
Michael Mauer
b
刊名:Molecular Genetics and Metabolism
出版年:2013
10.
No accumulation of globotriaosylceramide in the heart of a patient with the E66Q mutation in the ¦Á-galactosidase A gene
作者:
Masahisa Kobayashi
a
;
masa-koba@jikei.ac.jp
;
Toya Ohashi
a
;
b
;
g
;
Takahiro Fukuda
c
;
Tomoyoshi Yanagisawa
d
;
Takayuki Inomata
d
;
Takashi Nagaoka
e
;
Teruo Kitagawa
f
;
Yoshikatsu Eto
g
;
Hiroyuki Ida
a
;
b
;
g
;
Eiji Kusano
h
关键词:
Fabry
disease
;
¦Á-galactosidase A
;
Globotriaosylceramide (GL3)
;
E66Q mutation
;
Pseudo-deficiency
;
Polymorphism
刊名:Molecular Genetics and Metabolism
出版年:2012
1
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