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Publications by Svein Ivar Mellgren
Screening for Fabry Disease and Hereditary ATTR Amyloidosis in Idiopathic Small Fiber and Mixed Neuropathy
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
Primary Sjögren's Syndrome Associated Neuropathy
Canadian Journal of Neurological Sciences
Medicine
Neurology
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Tafamidis for Autonomic Neuropathy in Hereditary Transthyretin (ATTR) Amyloidosis: A Review
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A Patient With Hereditary ATTR and a Novel AGel p.Ala578Pro Amyloidosis
Mayo Clinic Proceedings
Medicine
Author Response: Small Fiber Neuropathy and Wilson Disease
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Kidney Dysfunction in Renal Amyloidosis: Does the Complement System Play a Part in Hereditary ATTRV30M and Iatrogenic ATTR Amyloidosis?
Portuguese Journal of Nephrology & Hypertension
Hereditary ATTR Amyloidosis With Cardiomyopathy Caused by the Novel Variant Transthyretin Y114S (p.Y134S)
Internal Medicine
Internal Medicine
Medicine
Association of Small Fiber Neuropathy and Post Treatment Lyme Disease Syndrome
PLoS ONE
Multidisciplinary
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
Newborn Screening for Fabry Disease in Japan: Prevalence and Genotypes of Fabry Disease in a Pilot Study
Journal of Human Genetics
Genetics
Screening, Diagnosis and Treatment of Fabry Disease
Clinical pharmacology and therapy