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Quoted phrase not found in phrase index: "Amyloidosis of peripheral nerves"
Page 1
Amyloid neuropathies.
Shin SC, Robinson-Papp J. Shin SC, et al. Mt Sinai J Med. 2012 Nov-Dec;79(6):733-48. doi: 10.1002/msj.21352. Mt Sinai J Med. 2012. PMID: 23239211 Free PMC article. Review.
Peripheral neuropathy is a common complication of many of the systemic amyloidoses. ...However, it is important to recognize and distinguish autonomic neuropathy from diseases of the end-organs themselves. This article reviews the inherited and acquired amyloidos …
Peripheral neuropathy is a common complication of many of the systemic amyloidoses. ...However, it is important to recognize a …
Recommendations for the diagnosis and management of transthyretin amyloidosis with gastrointestinal manifestations.
Nakov R, Suhr OB, Ianiro G, Kupcinskas J, Segal JP, Dumitrascu DL, Heinrich H, Mikolasevic I, Stojkovic-Lalosevic M, Barbov I, Sarafov S, Tournev I, Nakov V, Wixner J. Nakov R, et al. Eur J Gastroenterol Hepatol. 2021 May 1;33(5):613-622. doi: 10.1097/MEG.0000000000002030. Eur J Gastroenterol Hepatol. 2021. PMID: 33394808 Review.
Transthyretin amyloid (ATTR) amyloidosis is an adult-onset, rare systemic disorder characterized by the accumulation of misfolded fibrils in the body, including the peripheral nerves, the heart and the gastrointestinal tract. Gastrointestinal manifestations a …
Transthyretin amyloid (ATTR) amyloidosis is an adult-onset, rare systemic disorder characterized by the accumulation of misfolded fib …
Significance of Oligomeric and Fibrillar Species in Amyloidosis: Insights into Pathophysiology and Treatment.
Koike H, Iguchi Y, Sahashi K, Katsuno M. Koike H, et al. Molecules. 2021 Aug 22;26(16):5091. doi: 10.3390/molecules26165091. Molecules. 2021. PMID: 34443678 Free PMC article. Review.
Amyloidosis is a term referring to a group of various protein-misfolding diseases wherein normally soluble proteins form aggregates as insoluble amyloid fibrils. ...As many other agents for amyloidosis will be developed in the future, studies to develop sensitive cl …
Amyloidosis is a term referring to a group of various protein-misfolding diseases wherein normally soluble proteins form aggregates a …
Primary systemic amyloidosis.
Comenzo RL. Comenzo RL. Curr Treat Options Oncol. 2000 Apr;1(1):83-9. doi: 10.1007/s11864-000-0018-9. Curr Treat Options Oncol. 2000. PMID: 12057064 Review.
Patients with unexplained heart failure, hepatomegaly, nephrotic syndrome, or peripheral neuropathy should be evaluated for primary systemic (amyloid light-chain, or AL) amyloidosis by first seeking evidence of a clonal plasma cell disorder with serum and urine immu …
Patients with unexplained heart failure, hepatomegaly, nephrotic syndrome, or peripheral neuropathy should be evaluated for primary s …
The Ultrastructure of Tissue Damage by Amyloid Fibrils.
Koike H, Katsuno M. Koike H, et al. Molecules. 2021 Jul 29;26(15):4611. doi: 10.3390/molecules26154611. Molecules. 2021. PMID: 34361762 Free PMC article. Review.
Amyloidosis is a group of diseases that includes Alzheimer's disease, prion diseases, transthyretin (ATTR) amyloidosis, and immunoglobulin light chain (AL) amyloidosis. The mechanism of organ dysfunction resulting from amyloidosis has been a topic of d …
Amyloidosis is a group of diseases that includes Alzheimer's disease, prion diseases, transthyretin (ATTR) amyloidosis, and im …
Diagnostic yield of nerve biopsy in the evaluation of peripheral neuropathies.
Lee LY, Tan CY, Wong KT, Goh KJ, Shahrizaila N. Lee LY, et al. J Clin Neurosci. 2023 Jan;107:40-47. doi: 10.1016/j.jocn.2022.11.017. Epub 2022 Dec 8. J Clin Neurosci. 2023. PMID: 36502780
The indications for the procedure were vasculitis (34 %), peripheral neuropathy of unknown aetiology (34 %), amyloidosis (14 %) and chronic inflammatory demyelinating polyneuropathy (10 %). ...CONCLUSIONS: With the exception of vasculitis and amyloidosis, the …
The indications for the procedure were vasculitis (34 %), peripheral neuropathy of unknown aetiology (34 %), amyloidosis (14 % …
Strategy for genetic analysis in hereditary neuropathy.
Masingue M, Fernández-Eulate G, Debs R, Tard C, Labeyrie C, Leonard-Louis S, Dhaenens CM, Masson MA, Latour P, Stojkovic T. Masingue M, et al. Rev Neurol (Paris). 2023 Jan-Feb;179(1-2):10-29. doi: 10.1016/j.neurol.2022.11.007. Epub 2022 Dec 22. Rev Neurol (Paris). 2023. PMID: 36566124 Review.
Inherited neuropathies are a heterogeneous group of slowly progressive disorders affecting either motor, sensory, and/or autonomic nerves. Peripheral neuropathy may be the major component of a disease such as Charcot-Marie-Tooth disease or a feature of a more comple …
Inherited neuropathies are a heterogeneous group of slowly progressive disorders affecting either motor, sensory, and/or autonomic nerves …
MRI of pathology-proven peripheral nerve amyloidosis.
McKenzie GA, Broski SM, Howe BM, Spinner RJ, Amrami KK, Dispenzieri A, Ringler MD. McKenzie GA, et al. Skeletal Radiol. 2017 Jan;46(1):65-73. doi: 10.1007/s00256-016-2510-8. Epub 2016 Oct 12. Skeletal Radiol. 2017. PMID: 27730358
OBJECTIVE: To highlight the MRI characteristics of pathologically proven amyloidosis involving the peripheral nervous system (PNS) and determine the utility of MRI in directing targeted biopsy for aiding diagnosis. ...Six of seven patients demonstrated associated mu …
OBJECTIVE: To highlight the MRI characteristics of pathologically proven amyloidosis involving the peripheral nervous system ( …
Long-term efficacy and safety of inotersen for hereditary transthyretin amyloidosis: NEURO-TTR open-label extension 3-year update.
Brannagan TH, Coelho T, Wang AK, Polydefkis MJ, Dyck PJ, Berk JL, Drachman B, Gorevic P, Whelan C, Conceição I, Plante-Bordeneuve V, Merlini G, Obici L, Plana JMC, Gamez J, Kristen AV, Mazzeo A, Gentile L, Narayana A, Olugemo K, Aquino P, Benson MD, Gertz M; NEURO-T. T. R. Open-Label Extension Investigators. Brannagan TH, et al. J Neurol. 2022 Dec;269(12):6416-6427. doi: 10.1007/s00415-022-11276-8. Epub 2022 Jul 31. J Neurol. 2022. PMID: 35908242 Free PMC article.
BACKGROUND: Hereditary transthyretin amyloidosis (hATTR/ATTRv) results from the deposition of misfolded transthyretin (TTR) throughout the body, including peripheral nerves. ...
BACKGROUND: Hereditary transthyretin amyloidosis (hATTR/ATTRv) results from the deposition of misfolded transthyretin (TTR) throughou …
High-resolution ultrasound of peripheral nerves in late-onset hereditary transthyretin amyloidosis with polyneuropathy: similarities and differences with CIDP.
Leonardi L, Di Pietro G, Di Pasquale A, Vanoli F, Fionda L, Garibaldi M, Galosi E, Alfieri G, Lauletta A, Morino S, Salvetti M, Truini A, Antonini G. Leonardi L, et al. Neurol Sci. 2022 May;43(5):3387-3394. doi: 10.1007/s10072-021-05749-3. Epub 2021 Nov 21. Neurol Sci. 2022. PMID: 34802089
In this cross-sectional prospective study, we aimed to investigate the utility of high-resolution ultrasonography of peripheral nerves as a diagnostic tool to differentiate ATTRv-PN from CIDP. METHODS: In 11 treatment-naive patients with genetically confirmed late-o …
In this cross-sectional prospective study, we aimed to investigate the utility of high-resolution ultrasonography of peripheral ne …
74 results