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Publications by Brett P Monia
Treatment of Transthyretin (TTR) Amyloid Cardiomyopathy With an Antisense Oligonucleotide Inhibitor of TTR Synthesis
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Related publications
A Phase 3 Clinical Trial With ISIS-TTRRx, a 2nd-Generation Antisense Oligonucleotide Targeting Transthyretin (TTR), for the Treatment of TTR Amyloid Cardiomyopathy
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area
Journal of Neuromuscular Diseases
Neurology
Accelerated a Deposition in APPswe/PS1 E9 Mice With Hemizygous Deletions of TTR (Transthyretin)
Journal of Neuroscience
Neuroscience
Late-Onset Transthyretin (TTR)-familial Amyloid Polyneuropathy (FAP) With a Long Disease Duration From Non-Endemic Areas in Japan
Internal Medicine
Internal Medicine
Medicine
The Prevalence and Distribution of the Amyloidogenic Transthyretin (TTR) V122I Allele in Africa
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Refine Penetrance Estimates in the Main Pathogenic Variants of Transthyretin Hereditary (Familial) Amyloid Polyneuropathy (TTR-FAP) Using a New Non-Parametric Approach (NPSE)
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Internal Medicine
Medicine
Autosomal-Dominant Transthyretin (TTR)-related Amyloidosis Is Not a Frequent CMT2 Neuropathy “In Disguise”
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
A Case of Familial Amyloid Polyneuropathy Due to Phe33Val TTR With Vitreous Involvement as the Initial Manifestation
Internal Medicine
Internal Medicine
Medicine
Fatal TTR Amyloidosis With Neuropathy From Domino Liver p.Val71Ala Transplant
Neurology: Genetics
Neurology
Genetics
