ライフサイエンスコーパス: anosmia

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1 nificantly associated with increased odds of anosmia.

2 e 15 men who had a sustained reversal, 4 had anosmia.

3 UBR3-/- mice had female-specific behavioral anosmia.

4 ndividuals with BBS have partial or complete anosmia.

5 les, 22 to 36 years of age, with and without anosmia.

6 O4, as generally practiced, does not produce anosmia.

7 e exhibited prodepression phenotypes without anosmia.

8 lead to Kallmann syndrome, characterized by anosmia and hypogonadotrophic hypogonadism.

9 ann syndrome (KS), which is characterized by anosmia and pubertal failure due to hypogonadotropic hyp

10 Furthermore, treatments used to induce anosmia and to disrupt magneto-reception in displacement

11 45% in the lowest quartile of UPSIT scores (anosmia) and 18% in the highest quartile of UPSIT scores

12 amilies, one with Kallmann syndrome (IHH and anosmia) and another with normosmic IHH, in which a sing

13 in olfactory sensory neurons (OSNs) leads to anosmia, and is a newly recognized clinical manifestatio

14 thic hypogonadotropic hypogonadism (IHH) and anosmia, and is most commonly due to KAL1 or FGFR1 mutat

15 a of the olfactory bulb, likely resulting in anosmia, are reminiscent of the symptoms of Kallmann syn

16 ported neurological complications (including anosmia, ataxia, epilepsy, and neuropsychiatric and cogn

17 to vocalizing pups, as peripherally induced anosmia attenuated maternal proximal orientation toward

18 248 (29.9%) were normosmic and 78 (9.4%) had anosmia (B-SIT score < 6).

19 and additional features (fatigue, insomnia, anosmia, hypersalivation and rapid-eye-movement sleep be

20 Apathy, REM sleep behaviour disorder, anosmia, hypersalivation, and cognitive decline were all

21 Isolated congenital anosmia (ICA) is a rare condition that is associated wit

22 Y maze and a new method to induce peripheral anosmia in ferrets, we assessed the contribution of cons

23 r matches a known locus mediating a specific anosmia, indicating the anosmia may be due directly to t

24 hic hypogonadotropic hypogonadism (IHH) with anosmia (Kallmann syndrome; KS) or with a normal sense o

25 hypogonadotropic hypogonadism (nIHH) or with anosmia [Kallmann syndrome (KS)].

26 mediating a specific anosmia, indicating the anosmia may be due directly to the loss of receptors.

27 ization of mammalian ciliated cells and that anosmia might be a useful determinant of other pleiotrop

28 these defects are not secondary responses to anosmia or developmental defects, we generated a conditi

29 occurring only in individuals with specific anosmias, perhaps only to androstenone.

30 or symptoms, sometimes by years, and include anosmia, problems with gastrointestinal motility, sleep

31 terized by adult-onset retinitis pigmentosa, anosmia, sensory neuropathy and phytanic acidaemia.

32 carriers and non-carriers were screened for anosmia, severe hyposmia, and dementia.

33 syndrome (hypogonadotropic hypogonadism and anosmia), stereotyped midface hypoplasia, intellectual d

34 c hypogonadism, which may be associated with anosmia (the Kallmann syndrome) or with a normal sense o

35 Metyrapone-induced anosmia was restricted to the pheromone detectors in P.

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