ライフサイエンスコーパス: neuroaxonal dystrophy

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1 on may produce aberrant axonal sprouting and neuroaxonal dystrophy.

2 l childhood genetic disorders categorized as neuroaxonal dystrophies.

3 A2G6 mutations are associated with infantile neuroaxonal dystrophy and have been reported previously

4 questions of pathogenesis and prevention of neuroaxonal dystrophy can be addressed.

5 y complete normalization of the frequency of neuroaxonal dystrophy in both sites without altering the

6 Neuroaxonal dystrophy in brainstem, spinal cord tracts,

7 or affect the ultrastructural appearance of neuroaxonal dystrophy in diabetic or age-matched control

8 processes in the development of sympathetic neuroaxonal dystrophy in diabetic rats.

9 Thus, fetal-onset neuroaxonal dystrophy in dogs, a species with well-devel

10 cently identified in patients with infantile neuroaxonal dystrophy (INAD) and neurodegeneration with

11 We mapped a locus for infantile neuroaxonal dystrophy (INAD) and neurodegeneration with

12 esions homologous to that of human infantile neuroaxonal dystrophy (INAD), most commonly caused by mu

13 Neuroaxonal dystrophy (NAD), a distinctive axonopathy ch

14 Neuroaxonal dystrophy (NAD), a distinctive axonopathy in

15 associated with disorders such as infantile neuroaxonal dystrophy, neurodegeneration with brain iron

16 In diabetes, sympathetic neuroaxonal dystrophy occurs in prevertebral celiac/supe

17 iabetic humans and experimental animals show neuroaxonal dystrophy of autonomic nerve terminals, part

18 frequency of ganglionic or mesenteric nerve neuroaxonal dystrophy or the severity of diabetes.

19 Neuroaxonal dystrophy similar to that observed in lysoso

20 f chronically diabetic rats with established neuroaxonal dystrophy (the neuropathological hallmark of

21 The frequency of neuroaxonal dystrophy, the neuropathological hallmark of

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