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Journal Article
Kidney International, ISSN 0085-2538, 04/2017, Volume 91, Issue 4, pp. 964 - 971
Journal Article
Journal of the American Society of Nephrology, ISSN 1046-6673, 02/2017, Volume 28, Issue 2, pp. 431 - 438
Lysozyme amyloidosis (ALys) is a rare form of hereditary amyloidosis that typically manifests with renal impairment, gastrointestinal (GI) symptoms, and sicca... 
HETEROGENEITY | RENAL AMYLOIDOSIS | GENE | DISEASE | UROLOGY & NEPHROLOGY | SYMPTOMS | SYSTEMIC AMYLOIDOSIS | MUTATIONS | FAMILY | Phenotype | Amyloidosis, Familial - genetics | Pedigree | Humans | Adult | Male | Muramidase - metabolism | Amyloidosis, Familial - enzymology | Index Medicus | malfolding proteins | Up Front Matters | amyloidosis | lysozyme | hereditary amyloid
Journal Article
Amyloid, ISSN 1350-6129, 01/2018, Volume 25, Issue 1, pp. 54 - 61
Journal Article
Journal Article
Journal Article
Clinical Neurophysiology, ISSN 1388-2457, 06/2019, Volume 130, Issue 6, pp. 903 - 910
To elucidate Aδ-fiber dysfunction at the trunk in patients with hereditary transthyretin (ATTRm) amyloidosis using intra-epidermal electrical stimulation... 
Hereditary transthyretin amyloidosis | Truncal polyneuropathy | Aδ-fiber | Intra-epidermal electrical stimulation | Transthyretin familial amyloid polyneuropathy | Quantitative sensory testing | POLYNEUROPATHY | DETECTION THRESHOLDS | HUMANS | NEUROSCIENCES | CLINICAL NEUROLOGY | DEGENERATION | PERCEPTION | PAIN | NEUROPATHY | A delta-fiber
Journal Article
Circulation, ISSN 0009-7322, 09/2009, Volume 120, Issue 13, pp. 1203 - 1212
Journal Article
JACC: Cardiovascular Imaging, ISSN 1936-878X, 06/2011, Volume 4, Issue 6, pp. 659 - 670
In a cohort of patients with hereditary transthyretin-related amyloidosis (ATTR), we aimed to assess the role of Tc-3,3-diphosphono-1,2-propanodicarboxylic... 
cardiac amyloidosis | hereditary transthyretin-related amyloidosis | diagnosis | 99mTc-DPD scintigraphy | prognosis | Tc-DPD scintigraphy
Journal Article
Indian Dermatology Online Journal, ISSN 2229-5178, 2013, Volume 4, Issue 4, pp. 344 - 346
Amyloidosis cutis dyschromica is a very rare form of primary cutaneous amyloidosis characterized by prepubertal onset of hyper and hypopigmented spots and... 
genetic | dyschromica | Amyloidosis
Journal Article