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1 function (normosmia > hyposmia > functional anosmia).
2 (range, 0-6; lower score indicating greater anosmia).
3 % CI, 0.005-0.062) m/s slower for those with anosmia.
4 humans may be involved in CRSwNP-associated anosmia.
5 ents, or of the loss of sensory input due to anosmia.
6 al intervention for improving post-traumatic anosmia.
7 various therapeutics for SARS-CoV-2-related anosmia.
8 e has been little exploration of hyposmia or anosmia.
9 nificantly associated with increased odds of anosmia.
10 e exhibited prodepression phenotypes without anosmia.
11 e 15 men who had a sustained reversal, 4 had anosmia.
12 UBR3-/- mice had female-specific behavioral anosmia.
13 ndividuals with BBS have partial or complete anosmia.
14 les, 22 to 36 years of age, with and without anosmia.
15 O4, as generally practiced, does not produce anosmia.
16 cluding 321 (23.0%) with severe microsmia or anosmia.
17 ncluding 128 (8.2%) with severe microsmia or anosmia.
18 ans leads to profound pain insensitivity and anosmia.
19 igns of clinical disease, it did not prevent anosmia.
20 0.007-0.013) m/s/year faster for those with anosmia.
21 One patient suffered from anosmia.
23 ce, 4%; 95% CI, 1% to 6%) and have objective anosmia (15% vs 13%; difference, 2%; 95% CI, 0.1% to 4%)
24 sisting of 25 with post-traumatic functional anosmia, 16 with post-traumatic hyposmia, and 22 healthy
25 he symptoms with the highest prevalence were anosmia (43.1% (95% CI 35.2% to 51.3%), n=15 975, 63 stu
27 t symptoms among non-hospitalized women were anosmia [63% pregnant, 92% non-pregnant] and headache [7
28 ousal, and neuro-COVID-19 complex (headache, anosmia, ageusia, chemesthesis, vertigo, presyncope, par
34 pite ethnic differences in the prevalence of anosmia/ageusia, our study highlights similar clinical p
39 mitter release is the principal mechanism of anosmia and analgesia in mouse and human Nav1.7-null mut
44 ann syndrome (KS), which is characterized by anosmia and pubertal failure due to hypogonadotropic hyp
45 tely strong correlation between the level of anosmia and the score of histological damage within the
46 tely strong correlation between the level of anosmia and the thickness of the olfactory epithelium, p
48 y symptoms of fatigue, headache, dyspnea and anosmia and was more likely with increasing age and body
49 45% in the lowest quartile of UPSIT scores (anosmia) and 18% in the highest quartile of UPSIT scores
50 amilies, one with Kallmann syndrome (IHH and anosmia) and another with normosmic IHH, in which a sing
51 (range, 0-14; lower score indicating greater anosmia) and NASAL-3 (range, 0-6; lower score indicating
52 in olfactory sensory neurons (OSNs) leads to anosmia, and is a newly recognized clinical manifestatio
53 thic hypogonadotropic hypogonadism (IHH) and anosmia, and is most commonly due to KAL1 or FGFR1 mutat
54 a of the olfactory bulb, likely resulting in anosmia, are reminiscent of the symptoms of Kallmann syn
55 te accuracy in identifying participants with anosmia as defined by UPSIT (NASAL-7 area under the rece
56 ctory system function in COVID-19-associated anosmia, as opposed to neuronal infection or neuroinvasi
58 % CI, 1.17-3.48) times higher for those with anosmia at the year 8 visit and 2.73 (95% CI, 1.40-5.35)
59 ported neurological complications (including anosmia, ataxia, epilepsy, and neuropsychiatric and cogn
60 to vocalizing pups, as peripherally induced anosmia attenuated maternal proximal orientation toward
62 = 34), individuals with isolated congenital anosmia (born without olfactory bulbs) were used as a le
63 ignal transduction occur too late to trigger anosmia, but may contribute to the duration of the olfac
65 e period with a significantly higher risk of anosmia, cardiac dysrhythmia, diabetes, genitourinary di
66 re more likely to be found to have objective anosmia compared with participants with no history of he
67 (such as rapid eye movement sleep disorder, anosmia, constipation and depression) appear at prodromi
68 pared to controls, individuals with acquired anosmia displayed significantly stronger dynamic functio
69 ction, fatigue and muscle weakness, anxiety, anosmia, dysgeusia, headaches, difficulty in concentrati
70 preceding the PCR testing date, we identify anosmia/dysgeusia (27.1-fold), fever/chills (2.6-fold),
71 positive population, 81.2% of subjects with anosmia/dysgeusia and fever were SARS-CoV-2 infected, in
72 he week prior to PCR testing, in addition to anosmia/dysgeusia, constitutes the earliest EHR-derived
77 the angular gyrus, individuals with acquired anosmia had stronger connectivity from the angular gyrus
78 the emergence of Omicron, the prevalence of anosmia has dropped, reducing interest for Omicron patho
80 though olfactory cilia dysfunction can cause anosmia, how their differentiation is programmed at the
81 and additional features (fatigue, insomnia, anosmia, hypersalivation and rapid-eye-movement sleep be
83 g in patients with CA or idiopathic acquired anosmia (IA) in comparison to normosmia controls (NC) du
86 Y maze and a new method to induce peripheral anosmia in ferrets, we assessed the contribution of cons
88 r matches a known locus mediating a specific anosmia, indicating the anosmia may be due directly to t
91 dies have suggested mechanisms driving acute anosmia, it remains unclear how SARS-CoV-2 causes persis
93 hic hypogonadotropic hypogonadism (IHH) with anosmia (Kallmann syndrome; KS) or with a normal sense o
97 mediating a specific anosmia, indicating the anosmia may be due directly to the loss of receptors.
99 ization of mammalian ciliated cells and that anosmia might be a useful determinant of other pleiotrop
100 may experience persistent severe hyposmia or anosmia more than 1 year from the onset of symptoms, sug
101 s positively associated only with persistent anosmia (odds ratio, 2.72; 95% CI, 1.66-4.46), even when
104 fever 37.8 C, cough, shortness of breath, or anosmia or ageusia) more than 14 days after the second d
106 these defects are not secondary responses to anosmia or developmental defects, we generated a conditi
107 Furthermore, COVID-19-like symptoms, but not anosmia or dysgeusia alone, were associated with subsequ
112 ; hypertension, OR, 1.29; 95% CI, 1.26-1.31; anosmia, OR, 2.16; 95% CI, 1.59-2.93; and parasomnias (i
114 or symptoms, sometimes by years, and include anosmia, problems with gastrointestinal motility, sleep
115 e imaging (fMRI) studies consistent with the anosmia reported in Na(v)1.7 loss-of-function patients.
116 lidate 45 household items into 2 short Novel Anosmia Screening at Leisure (NASAL) assessments, NASAL-
117 terized by adult-onset retinitis pigmentosa, anosmia, sensory neuropathy and phytanic acidaemia.
119 common presentation, and many patients with anosmia show no or only minor respiratory symptoms(1).
120 syndrome (hypogonadotropic hypogonadism and anosmia), stereotyped midface hypoplasia, intellectual d
121 ing patients with COVID-19 range widely from anosmia, stroke, encephalopathy/encephalitis, and seizur
122 sociated with PD: sensory impairments beyond anosmia, such as hearing loss (OR, 1.14; 95% CI, 1.09-1.
123 ior to threat conditioning (without inducing anosmia), suggesting that both regions are critical for
124 c hypogonadism, which may be associated with anosmia (the Kallmann syndrome) or with a normal sense o
128 riate modeling demonstrated severe microsmia/anosmia was associated with 1.75 (95% CI, 1.09-2.80) tim
129 12 [31.1%] vs 36 [11.7%]; P < .001), whereas anosmia was more prevalent among nonhospitalized than am
131 mes were not significantly different, except anosmia, which was more common after COVID-19 (odds rati
132 mptomatic forms of SARS-CoV-2 (identified by anosmia with either fever, breathlessness or cough) pres