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Publications by Sabrina Fabbri
Autosomal-Dominant Transthyretin (TTR)-related Amyloidosis Is Not a Frequent CMT2 Neuropathy “In Disguise”
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Subcutaneous Immunoglobulins Are a Valuable Treatment Option in Myasthenia Gravis
Journal of Clinical Neurology (Korea
Neurology
Related publications
Fatal TTR Amyloidosis With Neuropathy From Domino Liver p.Val71Ala Transplant
Neurology: Genetics
Neurology
Genetics
Tafamidis for Autonomic Neuropathy in Hereditary Transthyretin (ATTR) Amyloidosis: A Review
Clinical Autonomic Research
Medicine
Endocrine
Neurology
Autonomic Systems
Technetium Pyrophosphate Myocardial Uptake and Peripheral Neuropathy in a Rare Variant of Familial Transthyretin (TTR) Amyloidosis (Ser23Asn): A Case Report and Literature Review
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Internal Medicine
Medicine
Fibroblasts Endocytose and Degrade Transthyretin Aggregates in Transthyretin-Related Amyloidosis
Laboratory Investigation
Forensic Medicine
Pathology
Cell Biology
Molecular Biology
Diagnostic Challenges in Hereditary Transthyretin Amyloidosis With Polyneuropathy: Avoiding Misdiagnosis of a Treatable Hereditary Neuropathy
Journal of Neurology, Neurosurgery and Psychiatry
Psychiatry
Mental Health
Neurology
Surgery
Cardiomyopathy Related to Transthyretin Val30met Mutation in Hereditary Systemic Amyloidosis
ARQUIVOS BRASILEIROS DE CARDIOLOGIA - IMAGEM CARDIOVASCULAR
Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia
Archives of Neurology
TTR Amyloidosis: A Scientific Journey Since Andrade
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
