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Publications by Shinya Inai

Hereditary Deficiencies of Complement Components. Examination, Frequency and Clinical Features.

SEIBUTSU BUTSURI KAGAKU

1986

English

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Association of Complement Levels and Their Sequential Changes With Clinical Features in Systemic Lupus Erythematosus.

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Hereditary Crystalline Stromal Dystrophy of Schnyder. I. Clinical Features of a Family With Hyperlipoproteinaemia.

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Frequency of Use of Clinical Shoulder Examination Tests by Experienced Shoulder Surgeons

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Complement Metabolism in Man: Hypercatabolism of the Fourth (C4) and Third (C3) Components in Patients With Renal Allograft Rejection and Hereditary Angioedema (HAE)

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Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Shinya Inai

Hereditary Deficiencies of Complement Components. Examination, Frequency and Clinical Features.

Related publications

Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

Molecular Genetic Diagnosis and Clinical Features of Hereditary Neuropathy With Liability to Pressure Palsies

Clinical Features and Molecular Analysis of Seven British Kindreds With Hereditary Hyperferritinaemia Cataract Syndrome

Functional Complement Analysis Can Predict Genetic Testing Results and Long-Term Outcome in Patients With Complement Deficiencies

Genomic Features and Clinical Management of Patients With Hereditary Pancreatic Cancer Syndromes and Familial Pancreatic Cancer

Association of Complement Levels and Their Sequential Changes With Clinical Features in Systemic Lupus Erythematosus.

Hereditary Crystalline Stromal Dystrophy of Schnyder. I. Clinical Features of a Family With Hyperlipoproteinaemia.

Frequency of Use of Clinical Shoulder Examination Tests by Experienced Shoulder Surgeons

Complement Metabolism in Man: Hypercatabolism of the Fourth (C4) and Third (C3) Components in Patients With Renal Allograft Rejection and Hereditary Angioedema (HAE)