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PedAM

Pediatric Disease Annotations & Medicines




Disease narcolepsy
Symptom C0007384|cataplexy
Sentences 180
PubMedID- 26483904 narcolepsy with cataplexy in monozygotic twins.
PubMedID- 20854137 Hypocretin deficiency in narcolepsy with cataplexy is associated with a normal body core temperature modulation.
PubMedID- 21930661 Additionally, the history of tonsillectomy occurring before narcolepsy with cataplexy symptom onset, and biochemical data pertaining to streptococcal infections (anti-streptolysin o titres) were also collected.
PubMedID- 21677900 Measurements and results: there was no difference in risk-taking behavior between narcolepsy with or without cataplexy and the control group, as measured using the bart and the array of questionnaires.
PubMedID- 23950869 Our findings , are supported by studies from sweden and u.k., which reported significant increase in the incidence of narcolepsy with cataplexy in children vaccinated with pandemrix as compared to those in the same age group who were not vaccinated , , .
PubMedID- 21387813 Conclusions: neurophysiological procedures (mslt) and biological markers are necessary in the diagnosis of narcolepsy with cataplexy and hypersomnia without cataplexy.
PubMedID- 24656461 Conclusion: the diagnosis of narcolepsy with cataplexy at onset can be challenging in young children.
PubMedID- 24503475 We aimed to characterize autonomic changes during sleep in narcolepsy with cataplexy (nc) patients to clarify the nature of soremp events and the effect of hypocretin deficiency on sympathetic activity during sleep.
PubMedID- 25142559 The aim is to address the involvement of mirnas in the pathophysiology of central hypersomnias including autoimmune narcolepsy with cataplexy and hypocretin deficiency (type 1 narcolepsy), narcolepsy without cataplexy (type 2 narcolepsy), and idiopathic hypersomnia.
PubMedID- 25264897 Main outcome measures: confirmed narcolepsy with or without cataplexy with onset of excessive daytime sleepiness between january 1st, 2009, and december 31st, 2010.
PubMedID- 24533004 The usual age at onset of narcolepsy with cataplexy is in the second or third decade.
PubMedID- 22259780 In addition, differences in the frequencies of all other alleles except drb1*1501, dqb1*0602, and dqa1*0102 were also observed among the groups; however, none of these differences reached statistical significance between the controls and narcolepsy patients with or without cataplexy (table 1).
PubMedID- 24391530 The orexin system plays a particularly important role in the normal expression of waking and sleep since its disruption underlies the sleep disorder narcolepsy with cataplexy in humans (peyron et al., 2000; thannickal et al., 2000) and produces a narcolepsy phenotype with unstable behavioral states, sleep attacks and cataplexy-like motor arrests in animals (chemelli et al., 1999; lin et al., 1999; hara et al., 2001; willie et al., 2003; beuckmann et al., 2004; mochizuki et al., 2004; kalogiannis et al., 2011).
PubMedID- 23939463 Importance: idiopathic narcolepsy with cataplexy is thought to be an autoimmune disorder targeting hypothalamic hypocretin neurons.
PubMedID- 24727570 Remarkably, narcolepsy with or without cataplexy with low/intermediate or normal cerebrospinal fluid hypocretin-1 is present in both diseases.
PubMedID- 20022299 Rbd was idiopathic in 11 patients (1.6%; 9 men) and symptomatic in 23 patients (3.3%; 18 men) secondary to parkinsonian syndromes (n=11), use of antidepressants (n=7), narcolepsy with cataplexy (n=4), and pontine infarction (n=1).
PubMedID- 25534169 Pseudo-cataplexy, a form of "psychogenic" narcolepsy, "pseudo-parasomnia" and pnes can have a similar presentation.
PubMedID- 21920673 Recent results: antidepressants have long been used in control of narcolepsy with cataplexy, but their sustained efficacy in this role has been in question.
PubMedID- 25286384 Orexins are bioactive peptides, which have been shown to play a pivotal role in vigilance state transitions: the loss of orexin-producing neurons (orexin neurons) leads to narcolepsy with cataplexy in the human.
PubMedID- 25277311 narcolepsy with cataplexy is a sleep disorder caused by the loss of hypocretin-producing neurons in the hypothalamus.
PubMedID- 23646285 Besides, our group has recently reported a clinical trial of oral l-carnitine on narcolepsy with cataplexy and the results suggested that oral l-carnitine can be a promising treatment for narcolepsy with cataplexy (miyagawa et al., 2013; miyagawa et al., 2011).
PubMedID- 21170044 Growing evidence supports the hypothesis that narcolepsy with cataplexy is an autoimmune disease.
PubMedID- 23065655 At the pathophysiological level, it is now clear that most narcolepsy cases with cataplexy, and a minority of cases (5–30 %) without cataplexy or with atypical cataplexy-like symptoms, are caused by a lack of hypocretin (orexin) of likely an autoimmune origin.
PubMedID- 22406785 Mean age at onset of symptoms was 25+/-10 years; 12 (60%) patients had narcolepsy with cataplexy, 4 (20%) patients presented with all cardinal symptoms of narcolepsy, 8 (40%) with 3 symptoms, while 8 (40%) presented with 2 symptoms.
PubMedID- 23496005 The aim of this study was to describe the clinical and psg characteristics of narcolepsy with cataplexy and their genetic predisposition by using the retrospective patient database of the european narcolepsy network (eu-nn).
PubMedID- 22937359 Therefore, while a negative result may be suggestive that the possibility of narcolepsy with associated cataplexy is <10%, a positive result is nonspecific.
PubMedID- 24312261 In summary, our study has demonstrated that brain morphometric abnormalities in the left amygdala, left inferior frontal gyrus, and left postcentral gyrus exist in narcolepsy with cataplexy, but not in narcolepsy without cataplexy.
PubMedID- 24416019 Dko mice display the most profoundly disturbed sleep phenotype of all three models: narcolepsy with cataplexy (transient episodes of behavioral arrest) (kalogiannis et al., 2011).
PubMedID- 26251634 Despite these limitations, the patients demonstrated clear symptoms of narcolepsy with cataplexy that were validated by objective testing.
PubMedID- 26418536 No significant difference in the headache prevalence was observed between the narcolepsy patients with cataplexy (n = 44) and those without cataplexy (n = 24; headache, 45.5% vs. 50.0%: migraine, 25.0% vs. 20.8%; tension-type headache, 18.2% vs. 12.5%).
PubMedID- 20129934 We hypothesized that rapid eye movement sleep behaviour disorder coexists with cataplexy in narcolepsy due to hypocretin deficiency.
PubMedID- 23372264 Study objectives: we analyzed the potential predictive factors for precocious puberty, observed in some cases of childhood narcolepsy with cataplexy (nc) and for obesity, a much more common feature of nc, through a systematic assessment of pubertal staging, body mass index (bmi), and metabolic/endocrine biochemical analyses.
PubMedID- 19955018 Methods: seven narcolepsy with cataplexy patients underwent daytime videopolygraphy using humorous movies or/and jokes to trigger cataplectic attacks.
PubMedID- 23228163 The level of depressive and anxious symptoms in narcolepsy with cataplexy did not differ from the other groups.
PubMedID- 21931493 She also found global loss of hypocretin neurons in the brains of six deceased patients who had suffered from narcolepsy with cataplexy.40 furthermore, thannickal et al found the number of hypocretin neurons to be reduced by 85% to 95% in association with evidence of gliosis.39 these studies collectively suggested that the loss of hypocretin neurons in patients having narcolepsy with cataplexy might be inflammatory in nature.
PubMedID- 20513636 Our results show for the first time that narcolepsy without cataplexy, where the majority of cases have normal csf hypocretin levels, is associated with olfactory dysfunction.
PubMedID- 19555382 Although a close association between human leucocyte antigen (hla) and human narcolepsy with cataplexy suggests an involvement of autoimmune mechanisms, this has not yet been proved.
PubMedID- 24406723 narcolepsy with cataplexy is a sleep dysregulation disorder with alterations of rem sleep, i.e., sleep onset rem periods and rem sleep instability.
PubMedID- 24142146 Clinical and biochemical evidence temporally links the onset of narcolepsy with cataplexy symptoms with an activation of the immune system by infection, either bacterial such as streptococcal (aran et al., 2009), or viral such as h1n1 flu or vaccination (han et al., 2011; partinen et al., 2012), or with an autoimmune response proved by production of self-targeted antibodies (cvetkovic-lopes et al., 2010; kawashima et al., 2010).
PubMedID- 20160349 Elisa analysis showed that sera from narcolepsy patients with cataplexy had higher trib2-specific antibody titers compared with either normal controls or patients with idiopathic hypersomnia, multiple sclerosis, or other inflammatory neurological disorders.
PubMedID- 26090827 Csf orexin levels <110 pg/ml supports a diagnosis of type 1 narcolepsy (narcolepsy with cataplexy).
PubMedID- 23772196 narcolepsy with cataplexy mimicry: the strange case of two sisters.
PubMedID- 23616752 Strong, generally positive emotional stimuli, which might activate the amygdala, are known to trigger cataplexy in narcolepsy-cataplexy patients.
PubMedID- 20927145 According to the new classification, the multiple sleep latency test (mslt) is mandatory for diagnosing narcolepsy without cataplexy, and advisable for diagnosing narcolepsy with cataplexy.
PubMedID- 26074874 In this review, we discuss how rem sleep-control mechanisms underlie the intrusion of rem sleep paralysis during wakefulness in narcolepsy with cataplexy, and how degeneration of this same circuitry could underlie rbd.
PubMedID- 24297759 Methods: we enrolled 181 consecutive patients (108 men, 73 women; mean age 37.6 +/- 16.6 years old; narcolepsy with cataplexy/narcolepsy without cataplexy = 131:50).
PubMedID- 25325489 Patient diagnoses included narcolepsy with cataplexy (28.4%), narcolepsy without cataplexy (8.1%), other hypersomnia conditions (9.5%), delayed sleep phase syndrome (12.2%), behaviorally induced insufficient sleep syndrome (4.1%), other sleep disorders (obstructive sleep apnea, periodic limb movements of sleep; 6.8%), isolated cataplexy (2%), and various diagnoses (29.1%).
PubMedID- 21658163 Background and purpose: the second version of the international classification of sleep disorders suggests narcolepsy with cataplexy can be diagnosed on history alone.
PubMedID- 21210337 Background: narcolepsy with cataplexy (nc) is caused by substantial loss of hypocretin neurons.
PubMedID- 20525256 cataplexy (with or without narcolepsy), usually laughter-induced, is another more specific symptom .

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