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Proton conducting membranes composed of sulfonated poly(etheretherketone) and zirconium phosphate nanosheets for fuel cell applications

Solid state ionics, 2010-03, Vol.181 (5), p.348-353

2010

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Enzymatic and molecular strategies to diagnose Pompe disease

Expert opinion on medical diagnostics, 2010-01, Vol.4 (1), p.79-89

2010

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Galactose Stabilizes Various Missense Mutants of α-Galactosidase in Fabry Disease

Biochemical and biophysical research communications, 1995-09, Vol.214 (3), p.1219-1224

1995

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Unrecognised iron deficiency in critical illness

The Lancet (British edition), 1999-03, Vol.353 (9155), p.842-843

1999

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Proton-Conducting Properties of Sulfonated Poly(etheretherketone) with Layered Double Hydroxides at Intermediate Temperatures

Journal of the Electrochemical Society, 2010, Vol.157 (6), p.B798

2010

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Fabry disease : correlation between structural changes in a-galactosidase, and clinical and biochemical phenotypes

Human genetics, 2005-08, Vol.117 (4), p.317-328

2005

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A new diagnostic assay for glycogen storage disease type II in mixed leukocytes

Molecular genetics and metabolism, 2006-05, Vol.88 (1), p.22-28

2006

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Fabry disease

Nihon rinshō, 2001-03, Vol.59 Suppl 3, p.313

2001

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Abnormally decreased HbA1c can be assessed with erythrocyte creatine in patients with a shortened erythrocyte age

Diabetes care, 1998-10, Vol.21 (10), p.1732-1735

1998

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Two novel mutations in the α-galactosidase gene in Japanese classical hemizygotes with Fabry disease

Jinrui idengaku zasshi. Japanese journal of human genetics, 1996-09, Vol.41 (3), p.313-321

1996

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Evaluation of Intravascular Hemolysis With Erythrocyte Creatine in Patients With Cardiac Valve Prostheses

Chest, 2004-06, Vol.125 (6), p.2115-2120

2004

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Update of the pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants

Human mutation, 2012-08, Vol.33 (8), p.1161-1165

2012

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alpha-Galactosidase gene mutation and its expression product in Fabry disease (alpha-galactosidase deficiency)

Rinsho byori. The Japanese journal of clinical pathology, 1997-02, Vol.45 (2), p.127

1997

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Imbalanced substrate specificity of mutant β-galactosidase in patients with Morquio B disease

Molecular genetics and metabolism, 2003, Vol.78 (1), p.51-58

2003

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Clinical Factors Associated With Persistent Pericardial Effusion After Successful Primary Coronary Angioplasty

Chest, 2005-08, Vol.128 (2), p.798-803

2005

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From sample collection to testing. D. Designing of a transcutaneous blood-collecting tube

Rinsho byori. The Japanese journal of clinical pathology, 1996-11, Vol.Suppl 103, p.35

1996

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From sample collection to testing. B. Evaluation of sample condensation in a container without a cover

Rinsho byori. The Japanese journal of clinical pathology, 1996-11, Vol.Suppl 103, p.21

1996

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Stroke risk and antihypertensive drug treatment in the general population: the Japan arteriosclerosis longitudinal study

Journal of hypertension, 2009-02, Vol.27 (2), p.357-364

2009

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Fabry disease: correlation between structural changes in alpha-galactosidase, and clinical and biochemical phenotypes

Human genetics, 2005-08, Vol.117 (4), p.317-328

2005

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Clinical usefulness of measurement of creatine contents in human erythrocytes as an index of erythropoiesis

Rinsho byori. The Japanese journal of clinical pathology, 1992-02, Vol.40 (2), p.165

1992

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Aggregation of the Inactive Form of Human α-Galactosidase in the Endoplasmic Reticulum

Biochemical and biophysical research communications, 1996-03, Vol.220 (3), p.812-815

1996

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A colorimetric method for determination of delta-bilirubin in serum using bilirubin oxidase (Trachyderma tsunodae)

Rinsho byori. The Japanese journal of clinical pathology, 1989-08, Vol.37 (8), p.905

1989

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Estimation of corrected plasma fructosamine by plasma protein concentration

Rinsho byori. The Japanese journal of clinical pathology, 1989-05, Vol.37 (5), p.537

1989

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Highly sensitive analysis of guanidino compounds using linear gradient elution HPLC

Rinsho byori. The Japanese journal of clinical pathology, 1988-03, Vol.36 (3), p.313

1988

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Erythrocyte creatine as a marker of excessive erythrocyte destruction due to hypersplenism in patients with liver cirrhosis

Clinical biochemistry, 2001-07, Vol.34 (5), p.395-398

2001

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Proton conducting membranes composed of sulfonated poly(etheretherketone) and zirconium phosphate nanosheets for fuel cell applications

Enzymatic and molecular strategies to diagnose Pompe disease

Galactose Stabilizes Various Missense Mutants of α-Galactosidase in Fabry Disease

Unrecognised iron deficiency in critical illness

Proton-Conducting Properties of Sulfonated Poly(etheretherketone) with Layered Double Hydroxides at Intermediate Temperatures

Fabry disease : correlation between structural changes in a-galactosidase, and clinical and biochemical phenotypes

A new diagnostic assay for glycogen storage disease type II in mixed leukocytes

Fabry disease

Abnormally decreased HbA1c can be assessed with erythrocyte creatine in patients with a shortened erythrocyte age

Two novel mutations in the α-galactosidase gene in Japanese classical hemizygotes with Fabry disease

Evaluation of Intravascular Hemolysis With Erythrocyte Creatine in Patients With Cardiac Valve Prostheses

Update of the pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants

alpha-Galactosidase gene mutation and its expression product in Fabry disease (alpha-galactosidase deficiency)

Imbalanced substrate specificity of mutant β-galactosidase in patients with Morquio B disease

Clinical Factors Associated With Persistent Pericardial Effusion After Successful Primary Coronary Angioplasty

From sample collection to testing. D. Designing of a transcutaneous blood-collecting tube

From sample collection to testing. B. Evaluation of sample condensation in a container without a cover

Stroke risk and antihypertensive drug treatment in the general population: the Japan arteriosclerosis longitudinal study

Fabry disease: correlation between structural changes in alpha-galactosidase, and clinical and biochemical phenotypes

Clinical usefulness of measurement of creatine contents in human erythrocytes as an index of erythropoiesis

Aggregation of the Inactive Form of Human α-Galactosidase in the Endoplasmic Reticulum

A colorimetric method for determination of delta-bilirubin in serum using bilirubin oxidase (Trachyderma tsunodae)

Estimation of corrected plasma fructosamine by plasma protein concentration

Highly sensitive analysis of guanidino compounds using linear gradient elution HPLC

Erythrocyte creatine as a marker of excessive erythrocyte destruction due to hypersplenism in patients with liver cirrhosis

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