ライフサイエンスコーパス: familial amyloid polyneuropathy

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1 tations of TTR such as L55P (associated with familial amyloid polyneuropathy).

2 00 mutations in the TTR gene are involved in familial amyloid polyneuropathy.

3 as Alzheimer's and Parkinson's diseases and familial amyloid polyneuropathy.

4 a useful prognostic marker in transthyretin familial amyloid polyneuropathy.

5 on detected by MIBG imaging in transthyretin familial amyloid polyneuropathy.

6 ly the only medication approved to treat TTR familial amyloid polyneuropathy.

7 ing, while several TTR mutants are linked to familial amyloid polyneuropathy.

8 tively cause senile systemic amyloidosis and familial amyloid polyneuropathy.

9 the course of senile systemic amyloidosis or familial amyloid polyneuropathy.

10 the diseases senile systemic amyloidosis and familial amyloid polyneuropathy.

11 nsidered part of the syndrome of TTR-related familial amyloid polyneuropathy.

12 ibits the amyloidogenesis of the most common familial amyloid polyneuropathy and familial amyloid car

13 ween TTR amyloid deposition and the onset of familial amyloid polyneuropathy and senile systemic amyl

14 fibril formation is observed systemically in familial amyloid polyneuropathy and senile systemic amyl

15 e, transthyretin V30M mutant associated with familial amyloid polyneuropathy, and Abeta42 associated

16 yloid diseases: senile systemic amyloidosis, familial amyloid polyneuropathy, and familial amyloid ca

17 associated with senile systemic amyloidosis, familial amyloid polyneuropathy, and familial amyloid ca

18 oid diseases, including Alzheimer's disease, familial amyloid polyneuropathy, and senile systemic amy

19 opic hepatic transplantation is effective in familial amyloid polyneuropathy associated with variant

20 The L55P transthyretin (TTR) familial amyloid polyneuropathy-associated variant is di

21 eripheral nervous system which characterizes familial amyloid polyneuropathy caused by variant TTR.

22 Interestingly, the L55P and V30M familial amyloid polyneuropathy (FAP) associated variant

23 Familial amyloid polyneuropathy (FAP) associated with mu

24 Autonomic neuropathy is a major component of familial amyloid polyneuropathy (FAP) due to mutated tra

25 Familial amyloid polyneuropathy (FAP) is a neurodegenera

26 sthyretin gene (TTR) in Indian patients with familial amyloid polyneuropathy (FAP) is described.

27 ino liver transplant in which a patient with familial amyloid polyneuropathy (FAP) received an orthot

28 In the most common familial amyloid polyneuropathy (FAP), transthyretin (TT

29 ansthyretin (senile systemic amyloidosis and familial amyloid polyneuropathy), immunoglobulin light c

30 TTR mutation is the most prevalent cause of familial amyloid polyneuropathy in heterozygotes, wherea

31 Transthyretin familial amyloid polyneuropathy is a hereditary form of

32 at tolcapone, already in clinical trials for familial amyloid polyneuropathy, is a strong candidate f

33 Familial amyloid polyneuropathy may respond to liver tra

34 The most common example is that of familial amyloid polyneuropathy, of particular concern f

35 loid diseases senile systemic amyloidosis or familial amyloid polyneuropathy, respectively.

36 an Medicines Agency for the treatment of TTR familial amyloid polyneuropathy, the most common familia

37 elay neurologic progression of transthyretin familial amyloid polyneuropathy, there are no approved p

38 ials for the treatment of Transthyretin Type Familial Amyloid Polyneuropathy (TTR-FAP) and demonstrat

39 FN) is an important feature of transthyretin familial amyloid polyneuropathy (TTR-FAP).

40 Familial amyloid polyneuropathy type I is an autosomal d

41 presentations of the disease: transthyretin familial amyloid polyneuropathy, which primarily affects

42 ATTR patients after LTx, as reported to the Familial Amyloid Polyneuropathy World Transplant Registr

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