Mayumi Mizukami

A novel age-related venous amyloidosis derived from EGF-containing fibulin-like extracellular matrix protein 1.

Journal: The Journal of pathology

Published: June 02, 2018

Identification of amyloid precursor protein from autopsy and biopsy specimens using LMD-LC-MS/MS: the experience at Kumamoto University.

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

Published: April 25, 2017

A late-onset case of hereditary transthyretin amyloidosis with a novel compound heterozygous mutation.

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

Published: April 25, 2017

Clinicopathological and biochemical findings of late-onset hereditary transthyretin amyloidosis 16 years after liver transplantation: an autopsy case study.

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

Published: April 25, 2017

Clinicopathological and biochemical findings of thyroid amyloid in hereditary transthyretin amyloidosis with and without liver transplantation.

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

Published: January 14, 2017

A novel age-related venous amyloidosis derived from EGF-containing fibulin-like extracellular matrix protein 1.

A novel age-related venous amyloidosis derived from EGF-containing fibulin-like extracellular matrix protein 1.

Identification of amyloid precursor protein from autopsy and biopsy specimens using LMD-LC-MS/MS: the experience at Kumamoto University.

Identification of amyloid precursor protein from autopsy and biopsy specimens using LMD-LC-MS/MS: the experience at Kumamoto University.

A late-onset case of hereditary transthyretin amyloidosis with a novel compound heterozygous mutation.

A late-onset case of hereditary transthyretin amyloidosis with a novel compound heterozygous mutation.

Clinicopathological and biochemical findings of late-onset hereditary transthyretin amyloidosis 16 years after liver transplantation: an autopsy case study.

Clinicopathological and biochemical findings of late-onset hereditary transthyretin amyloidosis 16 years after liver transplantation: an autopsy case study.

Clinicopathological and biochemical findings of thyroid amyloid in hereditary transthyretin amyloidosis with and without liver transplantation.

Clinicopathological and biochemical findings of thyroid amyloid in hereditary transthyretin amyloidosis with and without liver transplantation.

Early skin denervation in hereditary and iatrogenic transthyretin amyloid neuropathy.

Early skin denervation in hereditary and iatrogenic transthyretin amyloid neuropathy.

Serum amyloid P component: A novel potential player in vessel degeneration in CADASIL.

Serum amyloid P component: A novel potential player in vessel degeneration in CADASIL.

Sushi repeat-containing protein 1: a novel disease-associated molecule in cerebral amyloid angiopathy.

Sushi repeat-containing protein 1: a novel disease-associated molecule in cerebral amyloid angiopathy.