コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 n Zero gene (MPZ, P0) cause various forms of hereditary neuropathy.
2 thin the P0 gene (MPZ) underlie a variety of hereditary neuropathies.
3 derations in the management of patients with hereditary neuropathies.
4 drial myopathy, spinal muscular atrophy, and hereditary neuropathies.
5 the subtypes of this heterogeneous group of hereditary neuropathies and in differentiating them from
6 mutation in a molecular chaperonin causing a hereditary neuropathy and raises the possibility that mi
10 g1/RTP/Rit42 gene are commonly identified in hereditary neuropathies of the motor and sensory systems
11 advances in our understanding of rare human hereditary neuropathies, peripheral nervous system tumor
12 type I (HSAN I) is the most frequent type of hereditary neuropathy that primarily affects sensory neu
13 e majority of genes causally associated with hereditary neuropathies were highly enriched in DRG.
14 final two cases were shown to be examples of hereditary neuropathy with focally folded myelin sheaths
15 most common CMT subtypes were CMT1A, CMT1X, hereditary neuropathy with liability to pressure palsies
16 e compression in an authentic mouse model of hereditary neuropathy with liability to pressure palsies
17 e type 1A (CMT1A), whereas deletions lead to hereditary neuropathy with liability to pressure palsies
19 h healthy controls (n = 7) and patients with Hereditary Neuropathy with liability to Pressure Palsies
20 ological features of a neuropathy similar to hereditary neuropathy with liability to pressure palsies
21 duplication) and decreased in patients with hereditary neuropathy with liability to pressure palsies
22 me features present in neuropathies, such as hereditary neuropathy with liability to pressure palsies
23 Charcot-Marie-Tooth disease type 1A (CMT1A), hereditary neuropathy with liability to pressure palsies
25 associated with the peripheral neuropathies, hereditary neuropathy with liability to pressure palsies
27 duplication in chromosome 17p11.2-p12, while hereditary neuropathy with liability to pressure palsies
28 type 1A (CMT1A) and deleted in patients with hereditary neuropathy with liability to pressure palsies
29 ous group of genetic disorders that includes hereditary neuropathy with liability to pressure palsies
30 eature of brachial neuropathy is shared with hereditary neuropathy with liability to pressure palsies
31 A) and a reciprocal deletion associated with hereditary neuropathy with liability to pressure palsies
32 m duplication in chromosome 17p11.2-p12, and hereditary neuropathy with liability to pressure palsies
33 ooth disease type 1A (CMT1A) duplication and hereditary neuropathy with liability to pressure palsies
34 peripheral myelin protein 22 (PMP22) causes hereditary neuropathy with liability to pressure palsies
35 n types of inherited neuropathies, including hereditary neuropathy with liability to pressure palsies
36 MP22 leads to another peripheral neuropathy, hereditary neuropathy with liability to pressure palsies
37 rcot-Marie-Tooth disease type 1A (CMT1A) and hereditary neuropathy with liability to pressure palsy (
38 CMT2A/MFN2 mutation, CMT1B/MPZ mutation, and hereditary neuropathy with liability to pressure palsy/P
39 r deletions, causing the reciprocal disorder hereditary neuropathy with pressure palsies (HNPP), were
40 previously been recognized in patients with hereditary neuropathy, with uncharacterized genetic defe
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。