2017
DOI: 10.1186/s12883-017-0879-1
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The association between lunar phase and intracranial aneurysm rupture: Myth or reality? Own data and systematic review

Abstract: BackgroundIt is a common belief in medical community that lunar phases have an impact on human health. A growing body of evidence indicates that lunar phases can predict the risk to develop acute neurological and vascular disorders. The goal of present report was to present our institution data and to perform systematic review of studies examining the association of intracranial aneurysm rupture with moon phases.MethodsWe identified all patients admitted to our department for ruptured intracranial aneurysms in… Show more

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Cited by 11 publications
(12 citation statements)
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“…Bunevicius et al . have found no relationship between intracranial aneurysm rupture across all lunar phases . Outside of cardiovascular pathologies, Eisenbach et al .…”
mentioning
confidence: 93%
“…Bunevicius et al . have found no relationship between intracranial aneurysm rupture across all lunar phases . Outside of cardiovascular pathologies, Eisenbach et al .…”
mentioning
confidence: 93%
“…Bunevicius and Karla looked at the effect of the lunar cycle on human health, and there is growing evidence that there is a common belief in the medical community that the phases of the moon may predict the risk of the development of acute neurological and vascular disorders [30,31]. This is important in terms of the early diagnosis of diseases.…”
Section: The Effect Of the Moon And Planets On The Biological Clockmentioning
confidence: 99%
“…SAO is a hereditary haematological condition common in Southeast Asia and Melanesia with a prevalence as high as 30% in some areas. [1][2][3] It presents as macrocytosis with stomatocytes on blood film and may confer some protection against Plasmodium falciparum, but is otherwise clinically benign. 2 Genetically, SAO is an autosomal dominant variant of the SLC4A1/AE1 gene on chromosome 17: a p. Ala400_Ala408 deletion variant (a deletion of codons 400-408 known as B3SAO).…”
mentioning
confidence: 99%
“…4 It is characterised by the inability of α-intercalated cells of the collecting duct to secrete H + ions into urine and an associated metabolic acidosis caused by a non-functional chloride-bicarbonate anion exchanger in α-intercalated cells. [2][3][4] Familial dRTA may result from a simple autosomal recessive variant on the SLC4A1/AE1 gene of chromosome 17 in which a p.G701D loss-of function mutation occurs. 1 This may either occur in homozygosity, or due to compound heterozygosity with SAO gene mutations.…”
mentioning
confidence: 99%
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