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There is a page named "Amyloid neuropathies, familial" on Wikipedia

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  • The familial amyloid neuropathies (or familial amyloidotic neuropathies, neuropathic heredofamilial amyloidosis, familial amyloid polyneuropathy) are...
    6 KB (505 words) - 14:56, 27 October 2023
  • Thumbnail for Amyloid
    only a few cases are familial. Others are only familial. Some result from medical treatment. Prions are an infectious form of amyloids that can act as a...
    60 KB (6,536 words) - 06:48, 29 August 2024
  • Thumbnail for Familial amyloid polyneuropathy
    Familial amyloid polyneuropathy, also called transthyretin-related hereditary amyloidosis, transthyretin amyloidosis abbreviated also as ATTR (hereditary...
    14 KB (1,486 words) - 16:53, 7 February 2024
  • autonomic neuropathies. Sensory neuropathy develops in a symmetrical pattern and progresses in a distal to proximal manner. Autonomic neuropathy can present...
    55 KB (5,426 words) - 12:05, 18 September 2024
  • Thumbnail for Cardiac amyloidosis
    less than the Light chain and Familial variants. This is due to the amount of time that it takes to accumulate the amyloid depositions being longer in the...
    30 KB (3,354 words) - 02:30, 21 June 2024
  • "Leber's hereditary optic neuropathy") Diabetic neuropathy, peripheral neuropathy due to diabetes mellitus Familial amyloid neuropathies, a rare group of autosomal...
    2 KB (263 words) - 18:41, 30 September 2024
  • Thumbnail for Ulnar neuropathy
    Ulnar neuropathy is a disorder involving the ulnar nerve. Ulnar neuropathy may be caused by entrapment of the ulnar nerve with resultant numbness and tingling...
    13 KB (1,286 words) - 13:56, 2 September 2024
  • Thumbnail for Familial Amyloidosis, Finnish Type
    Familial Amyloidosis, Finnish Type (FAF), also called hereditary gelsolin amyloidosis and AGel amyloidosis (AGel), is an amyloid condition with a number...
    8 KB (722 words) - 23:14, 3 November 2023
  • Thumbnail for Proteinopathy
    cellulose, "amyloid" actually is rich in protein. Subsequent research has shown that many different proteins can form amyloid, and that all amyloids show birefringence...
    62 KB (4,598 words) - 21:08, 10 September 2024
  • Thumbnail for Transthyretin
    "Familial amyloid polyneuropathy", Wikipedia, 2021-11-02, retrieved 2021-12-05 Andrade C (September 1952). "A peculiar form of peripheral neuropathy;...
    20 KB (2,382 words) - 16:13, 22 January 2024
  • neuropathies. Along with CMT, Reilly has worked on hereditary sensory and autonomic neuropathies and carpal tunnel syndrome in inherited neuropathies...
    15 KB (1,486 words) - 11:25, 17 August 2024
  • as familial amyloid neuropathy, AL amyloidosis, and AA amyloidosis [publication pending]. During the course of AL amyloidosis, peripheral neuropathy occurs...
    41 KB (4,591 words) - 13:05, 28 August 2024
  • Thumbnail for Carpal tunnel syndrome
    et al. (March 2016). ""Red-flag" symptom clusters in transthyretin familial amyloid polyneuropathy". Journal of the Peripheral Nervous System. 21 (1):...
    82 KB (9,502 words) - 22:05, 30 September 2024
  • 452.090.050 – amyloid neuropathies MeSH C18.452.090.050.050 – amyloid neuropathies, familial MeSH C18.452.090.075 – amyloidosis, familial MeSH C18.452...
    47 KB (4,274 words) - 16:49, 9 February 2024
  • disorder 3 Cerebellum agenesis hydrocephaly Cerebral amyloid angiopathy Cerebral amyloid angiopathy, familial Cerebral aneurysm Cerebral autosomal dominant arteriopathy...
    40 KB (3,657 words) - 03:02, 17 August 2024
  • amyloidosis, familial MeSH C16.320.565.100.050 – amyloid neuropathies, familial MeSH C16.320.565.100.160 – cerebral amyloid angiopathy, familial MeSH C16...
    78 KB (6,496 words) - 05:23, 12 April 2022
  • Thumbnail for Microangiopathy
    (CSVDs), which include arteriosclerosis-related CSVD as in hypertension, amyloid-related CSVD as in Alzheimer's disease and other genetic, inflammatory-mediated...
    24 KB (2,501 words) - 20:17, 20 September 2024
  • Thumbnail for Chromosome 21
    amyloid precursor protein (APP) locus (duplicated segment varies in length but includes APP) on Chromosome 21 was found to cause early onset familial...
    34 KB (3,087 words) - 13:30, 30 July 2024
  • Thumbnail for Lattice corneal dystrophy
    et al. (March 2007). "Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case report". Amyloid. 14 (1): 89–95. doi:10.1080/13506120601116393...
    8 KB (849 words) - 23:18, 20 September 2022
  • 829.050 – amyloid neuropathies MeSH C10.668.829.050.050 – amyloid neuropathies, familial MeSH C10.668.829.100 – brachial plexus neuropathies MeSH C10.668...
    109 KB (9,229 words) - 16:51, 9 February 2024
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