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在“
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394
条
1.
Iduronate-2-sulfatase proteome isolation from mouse brain and identification of changes in the proteomic profiling in murine model for
Hunter
syndrome
作者:
Carolina Cardona
a
;
Luisa Natalia Pimentel
a
;
Edwin Alexander Rodrí
;
guez
a
;
Luis Humberto Reyes
a
;
Luis Alejandro Barrera
b
;
Carlos J Almé
;
ciga-Diaz
a
刊名:Molecular Genetics and Metabolism
出版年:2017
2.
Short term impact from enzyme replacement therapy on patients with attenuated
Hunter
syndrome
(MPS II) showing complex heart disease
作者:
Lina J Moreno
;
Adalberto Sanchez
;
José
;
M Satizá
;
bal
刊名:Molecular Genetics and Metabolism
出版年:2017
3.
Successful use of spinal anesthesia for inguinal hernia repair in a child with
Hunter
syndrome
with difficult airway
作者:
Kanil Ranjith Kumar
;
MD
;
kanil.aiims@gmail.com" class="auth_mail" title="E-mail the corresponding author
;
Hem Kumar
;
MD
;
Dalim Kumar Baidya
;
MD
;
Mahesh Kumar Arora
;
MD
关键词:
Congenital
syndrome
;
difficult airway
;
regional anesthesia
;
pediatric spinal
;
Hunter
syndrome
;
Mucopolysaccharidoses
刊名:Journal of Clinical Anesthesia
出版年:2016
4.
Validation of the shortened "
Hunter
Syndrome
-Functional Outcomes for Clinical Understanding Scale" (HS-FOCUS) questionnaire
刊名:Molecular Genetics and Metabolism
出版年:2017
5.
Neurocognitive profiles of untreated
Hunter
syndrome
刊名:Molecular Genetics and Metabolism
出版年:2017
6.
The challenge of using Hospital Episode Statistics (HES) to identify a
Hunter
syndrome
cohort in the UK
刊名:Molecular Genetics and Metabolism
出版年:2017
7.
Health care resource utilization by patients with
Hunter
syndrome
in the UK hospital episode statistics (HES) database
刊名:Molecular Genetics and Metabolism
出版年:2017
8.
Structural basis of
Hunter
syndrome
and construction of a database of mutant iduronate 2-sulfatase
刊名:Molecular Genetics and Metabolism
出版年:2017
9.
Correction of central nervous system deficits in the mouse model of
Hunter
syndrome
by recombinant iduronate 2-sulfatase crossing the blood-brain barrier
刊名:Molecular Genetics and Metabolism
出版年:2017
10.
Pathogenic mutation at IDS gene on a newborn girl with clinical symptoms of
Hunter
syndrome
(MPS II)
刊名:Molecular Genetics and Metabolism
出版年:2017
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