(Q82094701)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18821042%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

title

Electrophysiological features of late-onset transthyretin Met30 familial amyloid polyneuropathy unrelated to endemic foci (English)

1 reference

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14 January 2020

1

1 reference

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14 January 2020

Masaaki Hirayama

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18821042%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

5

Naoki Hattori

1 reference

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14 January 2020

author name string

Yuichi Kawagashira

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18821042%20AND%20SRC:MED&resulttype=core&format=json

14 January 2020

Masahiro Iijima

3

1 reference

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14 January 2020

Masahiko Yamamoto

4

1 reference

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14 January 2020

Fumiaki Tanaka

6

1 reference

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14 January 2020

Shu-ichi Ikeda

9

1 reference

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14 January 2020

Gen Sobue

10

1 reference

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14 January 2020

Yukio Ando

8

1 reference

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14 January 2020

publication date

24 September 2008

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14 January 2020

1 reference

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14 January 2020

volume

255

1 reference

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14 January 2020

issue

10

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14 January 2020

page(s)

1526-1533

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https://scigraph.springernature.com/pub.10.1007/s00415-008-0962-z

14 January 2020

exact match

0 references

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Endothelial dysfunction precedes C-fiber abnormalities in primary (AL) amyloidosis

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Anticipation in early- but not late-onset familial amyloid polyneuropathy (TTR met 30) in Japan

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Transthyretin gene analysis in European patients with suspected familial amyloid polyneuropathy

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Interobserver agreement for the assessment of handicap in stroke patients.

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Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form

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Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features

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Alcoholic neuropathy is clinicopathologically distinct from thiamine-deficiency neuropathy.

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Geographical distribution of TTR met30 carriers in northern Sweden: discrepancy between carrier frequency and prevalence rate

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12 December 2020

Postgastrectomy polyneuropathy with thiamine deficiency is identical to beriberi neuropathy

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12 December 2020

Clinical variability in type I familial amyloid polyneuropathy (Val30Met): comparison between late- and early-onset cases in Portugal.

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12 December 2020

Dissociated sensation in amylidosis. Compound action potential, quantitative histologic and teased-fiber, and electron microscopic studies of sural nerve biopsies

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12 December 2020

Peripheral nerve pathological findings in familial amyloid polyneuropathy: a correlative study of proximal sciatic nerve and sural nerve lesions

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12 December 2020

Familial amyloidotic polyneuropathy type 1 in Kumamoto, Japan: A clinicopathologic, histochemical, immunohistochemical, and ultrastructural study

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12 December 2020

Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy

1 reference

12 December 2020

Diflunisal stabilizes familial amyloid polyneuropathy-associated transthyretin variant tetramers in serum against dissociation required for amyloidogenesis

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12 December 2020

Ataxic vs painful form of paraneoplastic neuropathy

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12 December 2020

Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP)

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12 December 2020

Postgastrectomy polyneuropathy with thiamine deficiency

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12 December 2020

Age associated axonal features in HNPP with 17p11.2 deletion in Japan

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12 December 2020

Immunization in familial amyloidotic polyneuropathy: counteracting deposition by immunization with a Y78F TTR mutant.

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12 December 2020

Painful alcoholic polyneuropathy with predominant small-fiber loss and normal thiamine status.

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12 December 2020

The wide spectrum of clinical manifestations in Sjögren's syndrome-associated neuropathy.

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12 December 2020

Length-dependent degeneration of fibers in Portuguese amyloid poly neuropathy: A clinicopathologic study

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12 December 2020

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

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12 December 2020

Nonmyelinating Schwann cell involvement with well-preserved unmyelinated axons in Charcot-Marie-Tooth disease type 1A

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12 December 2020

Early involvement of motor nerve dysfunction in atypical cases with familial amyloidotic polyneuropathy (FAP) type I

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12 December 2020

Genetic epidemiology of familial amyloidotic polyneuropathy (FAP)-type I in Póvoa do Varzim and Vila do Conde (north of Portugal).

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12 December 2020

1 reference

12 December 2020

Evidence for early cytotoxic aggregates in transgenic mice for human transthyretin Leu55Pro

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12 December 2020

Type I familial amyloidotic polyneuropathy in Japan

1 reference

12 December 2020

Pathology of early- vs late-onset TTR Met30 familial amyloid polyneuropathy

1 reference

12 December 2020

Is familial amyloid polyneuropathy rare? DNA testing is changing the concept of this disease

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12 December 2020

Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity.

1 reference

12 December 2020

Deposition of transthyretin in early stages of familial amyloidotic polyneuropathy: evidence for toxicity of nonfibrillar aggregates

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12 December 2020

A study of 159 Portuguese patients with familial amyloidotic polyneuropathy (FAP) whose parents were both unaffected

1 reference

12 December 2020

Type I familial amyloid polyneuropathy. A pathological study of the peripheral nervous system

1 reference

12 December 2020