| scholarly article | Q13442814 |
| P50 | author | Christopher J. Klein | Q55233106 |
| Morie A Gertz | Q57052163 | ||
| P2093 | author name string | P James B Dyck | |
| Paola Sandroni | |||
| Phillip A Low | |||
| Wolfgang Singer | |||
| Michelle L Mauermann | |||
| Adam J Loavenbruck | |||
| P2860 | cites work | Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis | Q55670644 |
| Varied patterns of inaugural light-chain (AL) amyloid polyneuropathy: a monocentric study of 24 patients | Q58292197 | ||
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| Primary systemic amyloidosis: multivariate analysis for prognostic factors in 168 cases | Q69540739 | ||
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| Composite autonomic scoring scale for laboratory quantification of generalized autonomic failure | Q70465661 | ||
| Dissociated sensation in amylidosis. Compound action potential, quantitative histologic and teased-fiber, and electron microscopic studies of sural nerve biopsies | Q72502976 | ||
| Use of percentiles and normal deviates to express nerve conduction and other test abnormalities | Q73882354 | ||
| Ten years of international experience with liver transplantation for familial amyloidotic polyneuropathy: results from the Familial Amyloidotic Polyneuropathy World Transplant Registry | Q75265488 | ||
| Progressive cardiac amyloidosis following liver transplantation for familial amyloid polyneuropathy: implications for amyloid fibrillogenesis | Q77078349 | ||
| Progressive wild-type transthyretin deposition after liver transplantation preferentially occurs onto myocardium in FAP patients | Q79296603 | ||
| Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP) | Q80796069 | ||
| Hereditary amyloidosis of the Finnish type in a German family: clinical and electrophysiological presentation | Q83189922 | ||
| Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas | Q83196192 | ||
| Operative risks of domino liver transplantation for the familial amyloid polyneuropathy liver donor and recipient: a double analysis | Q83741982 | ||
| Immunoglobulin light chain amyloidosis: 2013 update on diagnosis, prognosis, and treatment | Q26827340 | ||
| A peculiar form of peripheral neuropathy; familiar atypical generalized amyloidosis with special involvement of the peripheral nerves | Q28207316 | ||
| Classification of amyloidosis by laser microdissection and mass spectrometry-based proteomic analysis in clinical biopsy specimens | Q33508070 | ||
| Mass spectrometric-based proteomic analysis of amyloid neuropathy type in nerve tissue. | Q33715284 | ||
| Patterns of neuropathy and autonomic failure in patients with amyloidosis | Q33743816 | ||
| Review: immunoglobulin light chain amyloidosis--the archetype of structural and pathogenic variability. | Q34001302 | ||
| Primary amyloidosis presenting as upper limb multiple mononeuropathies | Q34162936 | ||
| Primary systemic amyloidosis: clinical and laboratory features in 474 cases. | Q34320169 | ||
| Hereditary and acquired amyloid neuropathies | Q34379234 | ||
| Current trends in diagnosis and management of cardiac amyloidosis | Q34556410 | ||
| APOA1 related amyloidosis: a case report and literature review | Q35592671 | ||
| Rapid progression of familial amyloidotic polyneuropathy: a multinational natural history study | Q36005668 | ||
| Ten years of experience with liver transplantation for familial amyloid polyneuropathy in Japan: outcomes of living donor liver transplantations. | Q36343179 | ||
| Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France | Q36536822 | ||
| Isolated amyloidosis presenting with lumbosacral radiculoplexopathy: description of two cases and pathogenic review | Q36659347 | ||
| The molecular biology and clinical features of amyloid neuropathy | Q36842534 | ||
| Generalized amyloid in a family of Swedish origin. A study of 426 family members in seven generations of a new kinship with neuropathy, nephropathy, and central nervous system involvement | Q37391084 | ||
| Lattice corneal dystrophy, gelsolin type (Meretoja's syndrome). | Q37615476 | ||
| Cardiac amyloidosis: approaches to diagnosis and management | Q37654514 | ||
| Familial amyloid polyneuropathy | Q37957492 | ||
| Amyloidosis (AL). Clinical and laboratory features in 229 cases | Q40158440 | ||
| The natural history of peripheral neuropathy in primary systemic amyloidosis | Q40271871 | ||
| Cervical amyloidoma of C2. Case report and review of the literature | Q41699276 | ||
| Clinical presentations and skin denervation in amyloid neuropathy due to transthyretin Ala97Ser. | Q42942105 | ||
| Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trials | Q44432566 | ||
| Familial amyloid polyneuropathy: a clinico-pathologic study | Q47730369 | ||
| Peripheral nerve changes in amyloid neuropathy | Q48553390 | ||
| Amyloidomas of the nervous system: a monoclonal B-cell disorder with monotypic amyloid light chain lambda amyloid production | Q48554047 | ||
| Effect of age and gender on sudomotor and cardiovagal function and blood pressure response to tilt in normal subjects. | Q50920455 | ||
| Amyloid neuropathy: a peculiar form of peripheral neuropathy. | Q53485917 | ||
| Progression of cardiomyopathy after liver transplantation in patients with familial amyloidotic polyneuropathy, Portuguese type. | Q54160889 | ||
| P433 | issue | 3 | |
| P921 | main subject | amyloid neuropathy | Q54911710 |
| P304 | page(s) | 401-411 | |
| P577 | publication date | 2016-07-25 | |
| P1433 | published in | Annals of Neurology | Q564414 |
| P1476 | title | Transthyretin amyloid neuropathy has earlier neural involvement but better prognosis than primary amyloid counterpart: an answer to the paradox? | |
| P478 | volume | 80 |
| Q41123192 | Autonomic Neuropathy and Albuminocytologic Dissociation in Cerebrospinal Fluid As the Presenting Features of Primary Amyloidosis: A Case Report |
| Q52670605 | Autonomic involvement in hereditary transthyretin amyloidosis (hATTR amyloidosis). |
| Q92885198 | Orthostatic hypotension in hereditary transthyretin amyloidosis: epidemiology, diagnosis and management |
| Q47562649 | Transthyretin familial amyloid polyneuropathy: an update |
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