Stayko Sarafov - Publications

Clinical trials in pediatric ALS: a TRICALS feasibility study.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: February 17, 2022

Characterization of population genetic structure of hereditary transthyretin amyloidosis in Bulgaria.

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

Published: June 02, 2021

Recommendations for the diagnosis and management of transthyretin amyloidosis with gastrointestinal manifestations.

Journal: European journal of gastroenterology & hepatology

Published: January 04, 2021

Cardiac involvement, morbidity and mortality in hereditary transthyretin amyloidosis because of p.Glu89Gln mutation.

Journal: Journal of cardiovascular medicine (Hagerstown, Md.)

Published: August 03, 2020

Transthyretin amyloidosis: Testing strategies and model for center of excellence support.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: April 16, 2020

Fecal calprotectin concentrations in patients with hereditary transthyretin amyloidosis and gastrointestinal symptoms.

Journal: European journal of gastroenterology & hepatology

Published: April 07, 2020

Fecal calprotectin levels are elevated in transthyretin amyloidosis patients with gastrointestinal manifestations.

Journal: Medicine

Published: March 17, 2020

Transthyretin Amyloidosis with Gastrointestinal Manifestation: a Case Report.

Journal: Journal of gastrointestinal and liver diseases : JGLD

Published: September 10, 2019

Gastrointestinal Manifestations in Hereditary Transthyretin Amyloidosis associated with Glu89Gln Mutation.

Journal: Journal of gastrointestinal and liver diseases : JGLD

Published: August 17, 2019

Founder effect of the Glu89Gln TTR mutation in the Bulgarian population.

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

Published: July 30, 2019

Early diagnosis of ATTR amyloidosis through targeted follow-up of identified carriers of TTR gene mutations.

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

Published: February 23, 2019

Monoallelic expression of the TTR gene as a contributor to the age at onset and penetrance of TTR-related amyloidosis.

Journal: Gene

Published: October 22, 2018