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Keyword [fabry disease]
Result: 1 - 16 | Page: 1 of 1
1.
Novel α-galactosidase A Gene Mutation In A Chinese Family With Fabry Disease Mimicking Clinical Features Of Hypertrophic Cardiomyopathy
2.
The Study Of Monoclonal Antibody And Recombinant Protein For Diagnosis And Therapy To Fabry's Disease
3.
Hypertrophic Cardiomyopathy Gene And Phenotype Relationship
4.
The Ivestigation Of Mutations In Patients With Anderson Fabry Disease
5.
Clinical Manifestations And Mutation Study Of Fabry Disease In Chinese People
6.
The Clinical Study Of Fabry Disease In Patients With Hypertrophic Cardiomyopathy
7.
Preliminary Study On The Construction, Expression And Biochemical Characteristics Of A Human Alpha-galactosidase A Mutant
8.
Gene Mutation Study Of GLA In A Family With Fabry Disease
9.
Amissense Mutationof The α-galactosidase A Geneina Chinese Familyof Fabry Disease With Renal Failure
10.
Correlation Between GLA Gene Mutation And Clinical Manifestations Of Fabry Disease
11.
A Case Relate To The Unique Pathological Changes In The Skeletal Muscle Of A Female With Fabry Disease
12.
A Clinical And Genetic Study On Familial Fabry Disease
13.
Clinic-Pathologic Features And Renal Outcome Of Fabry Disease
14.
Clinical Features And Relevant Factors Of Cardiac And Renal Damage In Chinese Fabry Disease Patients
15.
Screening And Diagnosis Of Fabry Disease And Analysis Of Clinical And Genetic Characteristics In Pedigrees
16.
Investigation On The Molecular Mechanism Of GLA Mutation Causing Fabry Disease
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