Lucia Galan
Madrid, MD, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 21 publications
Real-world effectiveness and clinical predictors of response to first-generation TTR silencers in variant ATTR amyloidosis with polyneuropathy.
Journal: Scientific reports
Published: March 03, 2026
Phenotype and clinical outcomes of Glu89Lys hereditary transthyretin amyloidosis: a new endemic variant in Spain.
Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: November 07, 2022
Hereditary transthyretin amyloidosis caused by p.Ser43Asn variant. A new endemic variant in Ecuador.
Hereditary transthyretin amyloidosis caused by p.Ser43Asn variant. A new endemic variant in Ecuador.
Journal: Revista espanola de cardiologia (English ed.)
Published: July 26, 2022
Estimating the annual economic burden for the management of patients with transthyretin amyloid polyneuropathy in Spain.
Journal: Expert review of pharmacoeconomics & outcomes research
Published: March 16, 2021
Assessment of patients with hereditary transthyretin amyloidosis - understanding the impact of management and disease progression.
Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: July 25, 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
Notch Signalling in the Hippocampus of Patients With Motor Neuron Disease.
Journal: Frontiers in neuroscience
Published: December 10, 2018
Collagen XIX Alpha 1 Improves Prognosis in Amyotrophic Lateral Sclerosis.
Journal: Aging and disease
Published: July 25, 2018
Inhibition impairment in frontotemporal dementia, amyotrophic lateral sclerosis, and Alzheimer's disease: clinical assessment and metabolic correlates.
Journal: Brain imaging and behavior
Published: May 12, 2018
Analysis of known amyotrophic lateral sclerosis and frontotemporal dementia genes reveals a substantial genetic burden in patients manifesting both diseases not carrying the C9orf72 expansion mutation.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: July 06, 2017
Cerebrospinal fluid cytotoxicity in amyotrophic lateral sclerosis and sample size.
Journal: Acta neurologica Scandinavica
Published: June 03, 2017
Last Updated: 09/26/2026