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Publications by Yuka Shibata

Pseudo-Homozygous Mutation Due to a Primer Site Polymorphism in Hereditary ATTR Amyloidosis: A Pitfall of PCR-based Genetic Testing

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Internal Medicine

English

Related publications

Tafamidis for Autonomic Neuropathy in Hereditary Transthyretin (ATTR) Amyloidosis: A Review

Clinical Autonomic Research

Autonomic Systems

English

A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro Amyloidosis

Mayo Clinic Proceedings

English

Kidney Dysfunction in Renal Amyloidosis: Does the Complement System Play a Part in Hereditary ATTRV30M and Iatrogenic ATTR Amyloidosis?

Portuguese Journal of Nephrology & Hypertension

English

Congenital Central Hypothyroidism Due to a Homozygous Mutation in theTSHβSubunit Gene

Case Reports in Pediatrics

English

APOE Polymorphism in ATTR Amyloidosis Patients Treated With Lipid Nanoparticle siRNA

Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Internal Medicine

English

Cardiomyopathy Related to Transthyretin Val30met Mutation in Hereditary Systemic Amyloidosis

ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR

English

Mutation in Gelsolin Gene in Finnish Hereditary Amyloidosis

Journal of Experimental Medicine

English

Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)

Internal Medicine

Internal Medicine

English

Screening for Fabry Disease and Hereditary ATTR Amyloidosis in Idiopathic Small Fiber and Mixed Neuropathy

Muscle and Nerve

Molecular Neuroscience

English