Τρίτη 7 Μαρτίου 2017

Promoting global action on hearing loss: World hearing day.

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Promoting global action on hearing loss: World hearing day.

Int J Audiol. 2017 Mar;56(3):145-147

Authors: Chadha S, Cieza A

PMID: 28262049 [PubMed - in process]



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Promoting global action on hearing loss: World hearing day.

Related Articles

Promoting global action on hearing loss: World hearing day.

Int J Audiol. 2017 Mar;56(3):145-147

Authors: Chadha S, Cieza A

PMID: 28262049 [PubMed - in process]



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Promoting global action on hearing loss: World hearing day.

Related Articles

Promoting global action on hearing loss: World hearing day.

Int J Audiol. 2017 Mar;56(3):145-147

Authors: Chadha S, Cieza A

PMID: 28262049 [PubMed - in process]



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via IFTTT

Promoting global action on hearing loss: World hearing day.

Related Articles

Promoting global action on hearing loss: World hearing day.

Int J Audiol. 2017 Mar;56(3):145-147

Authors: Chadha S, Cieza A

PMID: 28262049 [PubMed - in process]



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Asystole During Direct Laryngoscopy for Vocal Fold Injection in a Healthy Patient

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Publication date: Available online 6 March 2017
Source:Journal of Voice
Author(s): Zahrah Taufique, Gregory R. Dion, Milan R. Amin
ObjectivesThis study aims (1) to present a case of asystole during direct laryngoscopy in an otherwise healthy patient at an outpatient surgery center and (2) to review literature on cardiac complications, specifically asystole and bradycardia, during direct laryngoscopy.MethodsA 67-year-old woman with no prior cardiac history underwent induction with succinylcholine and remifentanil for direct laryngoscopy and vocal fold augmentation. During suspension laryngoscopy, the patient became asystolic, and advanced care life support measures were started. The patient regained a cardiac rhythm after chest compressions and epinephrine and was transferred to a tertiary care hospital for further treatment. She remained intubated overnight, requiring pressors, and regained normal cardiac function over the next few days.ResultsA structured literature review uncovered few reports of asystole during suspension laryngoscopy. Although bradycardia is common during suspension laryngoscopy, likely secondary to stimulation of afferent visceral sensory parasympathetic fibers of the vagus nerve, asystole is rare.ConclusionsCardiac complications are possible in otolaryngologic surgery, especially with activation of the oculocardiac or trigeminocardiac reflexes. Asystole during direct laryngoscopy, although rare, is not always predictable from medicine or cardiac risk indices. Awareness, rapid recognition, and early implementation of advanced care life support are crucial to avoid further complications.



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Supporting cells remove and replace sensory receptor hair cells in a balance organ of adult mice.

Supporting cells remove and replace sensory receptor hair cells in a balance organ of adult mice.

Elife. 2017 Mar 06;6:

Authors: Bucks SA, Cox BC, Vlosich BA, Manning JP, Nguyen TB, Stone JS

Abstract
Vestibular hair cells in the inner ear encode head movements and mediate the sense of balance. These cells undergo cell death and replacement (turnover) throughout life in non-mammalian vertebrates. However, there is no definitive evidence that this process occurs in mammals. We used fate-mapping and other methods to demonstrate that utricular type II vestibular hair cells undergo turnover in adult mice under normal conditions. We found that supporting cells phagocytose both type I and II hair cells. Plp1-CreER(T2)-expressing supporting cells replace type II hair cells. Type I hair cells are not restored by Plp1-CreER(T2)-expressing supporting cells or by Atoh1-CreER(TM)-expressing type II hair cells. Destruction of hair cells causes supporting cells to generate 6 times as many type II hair cells compared to normal conditions. These findings expand our understanding of sensorineural plasticity in adult vestibular organs and further elucidate the roles that supporting cells serve during homeostasis and after injury.

PMID: 28263708 [PubMed - in process]



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Supporting cells remove and replace sensory receptor hair cells in a balance organ of adult mice.

Supporting cells remove and replace sensory receptor hair cells in a balance organ of adult mice.

Elife. 2017 Mar 06;6:

Authors: Bucks SA, Cox BC, Vlosich BA, Manning JP, Nguyen TB, Stone JS

Abstract
Vestibular hair cells in the inner ear encode head movements and mediate the sense of balance. These cells undergo cell death and replacement (turnover) throughout life in non-mammalian vertebrates. However, there is no definitive evidence that this process occurs in mammals. We used fate-mapping and other methods to demonstrate that utricular type II vestibular hair cells undergo turnover in adult mice under normal conditions. We found that supporting cells phagocytose both type I and II hair cells. Plp1-CreER(T2)-expressing supporting cells replace type II hair cells. Type I hair cells are not restored by Plp1-CreER(T2)-expressing supporting cells or by Atoh1-CreER(TM)-expressing type II hair cells. Destruction of hair cells causes supporting cells to generate 6 times as many type II hair cells compared to normal conditions. These findings expand our understanding of sensorineural plasticity in adult vestibular organs and further elucidate the roles that supporting cells serve during homeostasis and after injury.

PMID: 28263708 [PubMed - in process]



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Light shed on evolutionary change in bones of middle ear of non-mammals, new study reveals

Researchers at King's College London have begun to uncover the cellular and molecular drivers underlying a key anatomical change during the evolution of mammals.

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Light shed on evolutionary change in bones of middle ear of non-mammals, new study reveals

Researchers at King's College London have begun to uncover the cellular and molecular drivers underlying a key anatomical change during the evolution of mammals.

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Light shed on evolutionary change in bones of middle ear of non-mammals, new study reveals

Researchers at King's College London have begun to uncover the cellular and molecular drivers underlying a key anatomical change during the evolution of mammals.

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MYH9-related disorder, a probable May-Hegglin anomaly case series: A tertiary care experience.

http:--linkinghub.elsevier.com-ihub-imag Related Articles

MYH9-related disorder, a probable May-Hegglin anomaly case series: A tertiary care experience.

Hematol Oncol Stem Cell Ther. 2016 Dec;9(4):137-140

Authors: Kamath V, Gnanasekaran KK, Mammen J

Abstract
OBJECTIVE/BACKGROUND: May-Hegglin anomaly (MHA) is a rare familial bleeding disorder characterized by a triad of thrombocytopenia, giant platelets, and Döhle-like inclusion bodies within the leukocytes. The clinical spectrum as well as the pathophysiology of this entity is not well defined. The objective of this work is to present a series of three cases of MHA diagnosed in our hospital, where the patients presented with variable bleeding manifestations, thrombocytopenia, and giant platelets.
MATERIALS AND METHODS: We studied three cases of possible MHA. In addition to the clinical examination, complete hemogram, and peripheral blood smear examination, these patients were also subjected to coagulation studies. Although bleeding symptoms varied among these patients, platelet aggregation tests with various agonists showed a normal response.
RESULTS: Consistent findings of this entity noted in our patients were mild-to-moderate thrombocytopenia, giant platelets, and Döhle-like inclusions within the leukocytes.
CONCLUSION: A diagnosis of MHA could be made based on a thorough peripheral blood smear examination, which also helps to avoid a misdiagnosis of immune thrombocytopenia.

PMID: 27614228 [PubMed - indexed for MEDLINE]



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Book Review.

No abstract available

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