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Meretoja syndrome

Known as: Meretoja's syndrome, Amyloidosis, Finnish Type, Amyloidosis 5 
National Institutes of Health

Related topics

Related topics

6 relations

Broader (2)

AmyloidosisHereditary corneal dystrophy
Cerebral Amyloid Angiopathy, Gsn-RelatedGSN geneGSN, ASP187ASN

Narrower (1)

Lattice Corneal Dystrophy, Type II

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2020
Highly Cited
2020
Single‐Dose Pharmacokinetics and Pharmacodynamics of Transthyretin Targeting N‐acetylgalactosamine–Small Interfering Ribonucleic Acid Conjugate, Vutrisiran, in Healthy Subjects
Vutrisiran (ALN‐TTRsc02) is a liver‐directed, investigational, small interfering ribonucleic acid drug for the treatment of… 
Review
2017
Review
2017
Diagnostic challenges in hereditary transthyretin amyloidosis with polyneuropathy: avoiding misdiagnosis of a treatable hereditary neuropathy
Hereditary transthyretin (ATTR) amyloidosis is a debilitating highly penetrant autosomal dominant disease leading to motor… 
Review
2016
Review
2016
Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis
Transthyretin (TTR) transports the retinol-binding protein–vitamin A complex and is a minor transporter of thyroxine in blood… 
Review
2015
Review
2015
Hereditary ATTR amyloidosis: a single-institution experience with 266 patients
Abstract Background: Hereditary transthyretin amyloidosis (ATTR amyloidosis) is a rare, clinically heterogeneous disease due to… 
Highly Cited
2014
Highly Cited
2014
IGF2 Ameliorates Amyloidosis, Increases Cholinergic Marker Expression and Raises BMP9 and Neurotrophin Levels in the Hippocampus of the APPswePS1dE9 Alzheimer’s Disease Model Mice
The development of an effective therapy for Alzheimer’s disease (AD) is a major challenge to biomedical sciences. Because much of… 
Highly Cited
2014
Highly Cited
2014
New mouse model of Alzheimer's.
Amyloid β-peptide (Aβ) accumulation is a key characteristic of Alzheimer's disease (AD); therefore, mouse models of AD exhibiting… 
Review
2012
Review
2012
Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention
Protein misassembly into aggregate structures, including cross-β-sheet amyloid fibrils, is linked to diseases characterized by… 
Highly Cited
2008
Highly Cited
2008
Overexpression of Neprilysin Reduces Alzheimer Amyloid-β42 (Aβ42)-induced Neuron Loss and Intraneuronal Aβ42 Deposits but Causes a Reduction in cAMP-responsive Element-binding Protein-mediated…
The amyloid-β42 (Aβ42) peptide has been suggested to play a causative role in Alzheimer disease (AD). Neprilysin (NEP) is one of… 
Review
2001
Review
2001
Transthyretin amyloidosis: a tale of weak interactions
Highly Cited
1990
Highly Cited
1990
Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene
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