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  • Approccio multidisciplinare ai disturbi dell’equilibrio nell’anziano – 14 Novembre 2015 Ostia Lido (RM) Vertigini | Dott. Giuseppe Nola
    clicca qui Locandina clicca qui Related Posts No related posts maggio 2016 L M M G V S D Set 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 Partner Pubblicazioni Approccio multidisciplinare ai disturbi dell equilibrio nell anziano 14 Novembre 2015 Ostia Lido RM Day case stapedotomy

    Original URL path: http://www.vertigini.me/approccio-multidisciplinare-ai-disturbi-dellequilibrio-nellanziano-14-novembre-2015-ostia-lido-rm/ (2016-05-02)
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  • Day-case stapedotomy: is it a viable option? Vertigini | Dott. Giuseppe Nola
    it decreases the likelihood of late cancellation and hospital acquired morbidity A prospective study was performed to determine whether stapes surgery for otosclerosis could be performed safely in an outpatient setting METHODS We present a series of stapes surgery cases for otosclerosis performed on a day case basis We performed a classic stapedotomy in 9 patients a reverse classic step stapedotomy in 2 patients a partial reverse classic step stapedotomy in 11 patients and a hemi stapedectomy in two patients RESULTS Three of 24 patients 12 5 treated with classic stapedotomy 1 patient with partial reverse classic step stapedotomy and 1 patient with hemi stapedectomy were formally admitted to the hospital after surgery length of stay 23 h The indications were vertigo two patients and asthenia one patient These patients were treated under general anesthesia Two of these patients resided more than 250 km away from the hospital Ralli G Mora R Nola G Guastini L ENT Department University of Rome La Sapienza Italy PMID 22074449 PubMed indexed for MEDLINE Related Posts No related posts maggio 2016 L M M G V S D Set 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15

    Original URL path: http://www.vertigini.me/day-case-stapedotomy-is-it-a-viable-option/ (2016-05-02)
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  • Vestibular evoked myogenic potential in vestibular neuritis Vertigini | Dott. Giuseppe Nola
    from symmetrical sites over the upper half of each sternocleidomastoid muscle with a reference electrode on the lateral end of the upper sternum During the acute attack 8 days 1 month and 3 months after the beginning of the acute attack all the patients underwent the following examinations Dix Hallpike manoeuvre Pagnini McClure manoeuvre head shaking test pure tone audiometry tympanometry caloric labyrinth stimulation according to the Fitzgerald Hallpike method and VEMP At the last visit the 11 patients diagnosed with superior branch vestibular neuritis did not show any improvement at the caloric labyrinth stimulation and presented VEMP on both sides with normal amplitude and latency in the 9 cases diagnosed with inferior branch vestibular neuritis there was an improvement of the VEMP reflex and normal caloric test Our experience highlights that VEMP recording is applicable for patients with VN as a screening test Nola G Guastini L Crippa B Deiana M Mora R Ralli G ENT Department G B Grassi Hospital Ostia Rome Italy PMID 21448610 PubMed indexed for MEDLINE Related Posts No related posts maggio 2016 L M M G V S D Set 1 2 3 4 5 6 7 8 9 10 11 12 13 14

    Original URL path: http://www.vertigini.me/vestibular-evoked-myogenic-potential-in-vestibular-neuritis/ (2016-05-02)
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  • Validity of Italian adaptation of the Dizziness Handicap Inventory (DHI) and evaluation of the quality of life in patients with acute dizziness Vertigini | Dott. Giuseppe Nola
    the QoL of patients with acute dizziness The study population consisted of 50 patients 76 females and 24 males mean age 51 6 years range 25 85 years SD 14 5 A cross sectional design was used to examine the internal consistency Cronbach s α and concurrent validity Pearson s product moment correlation r The application followed the stages of translation from English to Italian and linguistic adaptation grammatical and idiomatic equivalence review To confirm the external validity of DHI I the Pearson correlation test between the total score and single subscales of DHI I and the 8 scales of the Short Form Health Survey SF 36 was performed The Cronbach α coefficients for internal consistency were 0 92 for the DHI I and 0 82 0 84 and 0 75 for the sub scale functional emotional and physical respectively The frequency distribution of no one item showed a percentage higher than 75 in a single possible answer 0 2 4 excluding a ceiling or floor effect Correlations with the total score of DHI I were consistent and the correlation between total score of DHI I and total score on SF 36 was 0 593 Of the single subscales the emotional scale showed a closer correlation with almost all scales of the SF 36 The correlation between the total score of SF 36 and the single sub scale of DHI I functional emotional physical were respectively 0 599 0 563 0 398 The DHI was culturally and linguistically adapted for its application in the Italian population The DHI I demonstrated a good reliability and is recommended as a measure of disability in patients with dizziness and unsteadiness According to the DHI I patients with acute dizziness and with a clinical diagnosis of vestibular syndrome presented a decreased QoL the physical

    Original URL path: http://www.vertigini.me/validity-of-italian-adaptation-of-the-dizziness-handicap-inventory-dhi-and-evaluation-of-the-quality-of-life-in-patients-with-acute-dizziness/ (2016-05-02)
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  • Clinical and audiological follow up of a family with the 8363G>A mutation in the mitochondrial DNA Vertigini | Dott. Giuseppe Nola
    in individuals bearing other mtDNA mutations We performed a 4 year clinical and audiological follow up in a family carrying the 8363G A mutation in the mitochondrial transfer ribonucleic acid lysine tRNA Lys gene who displayed a progressive neuromuscular disease In addition to pure tone audiometry we considered distortion products of otoacoustic emissions a sensitive indicator of cochlear dysfunction as well as brainstem auditory evoked responses A generalized increase in the auditory threshold at follow up indicating a cochlear impairment in three cases was noted Distortion products of otoacoustic emissions may reveal sub clinical cochlear dysfunction even in oligosymptomatic patients A complete and periodical assessment of the hearing function should be encouraged in asymptomatic relatives of patients carrying the tRNA Lys 8363G A mutation DiFabio R Santorelli FM Nola G Cricchi F Masi R Ingrosso A Fattori F Carrozzo R Vanacore N Pierelli F Ralli G Casali C Department of Neurology and ORL Sapienza University of Rome ICOT Polo Pontino 04100 Latina Italy rob dif tiscali it PMID 19233651 PubMed indexed for MEDLINE Related Posts No related posts maggio 2016 L M M G V S D Set 1 2 3 4 5 6 7 8 9 10 11 12

    Original URL path: http://www.vertigini.me/clinical-and-audiological-follow-up-of-a-family-with-the-8363ga-mutation-in-the-mitochondrial-dna/ (2016-05-02)
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  • 2013 novembre Vertigini | Dott. Giuseppe Nola
    scale showed a closer correlation with almost all scales of the SF 36 The correlation between the total score of SF 36 and the single sub scale of DHI I functional emotional physical were respectively 0 599 0 563 0 398 The DHI was culturally and linguistically adapted for its application in the Italian population The DHI I demonstrated a good reliability and is recommended as a measure of disability in patients with dizziness and unsteadiness According to the DHI I patients with acute dizziness and with a clinical diagnosis of vestibular syndrome presented a decreased QoL the physical aspects were the most compromised Nola G Mostardini C Salvi C Ercolani AP Ralli G Operative Unit ENT G B Grassi Hospital Rome Italy Link PMC Article Leggi tutto 20 Nov Clinical and audiological follow up of a family with the 8363G A mutation in the mitochondrial DNA Dr Nola in Pubblicazioni Commenti disabilitati su Clinical and audiological follow up of a family with the 8363G A mutation in the mitochondrial DNA Hearing loss is relatively common in mtDNA related disorders While auditory function has been assessed fully in the syndrome of mitochondrial encephalomyopathy lactic acidosis and stroke like episodes few studies have investigated the degree of progressive hearing deficit in individuals bearing other mtDNA mutations We performed a 4 year clinical and audiological follow up in a family carrying the 8363G A mutation in the mitochondrial transfer ribonucleic acid lysine tRNA Lys gene who displayed a progressive neuromuscular disease In addition to pure tone audiometry we considered distortion products of otoacoustic emissions a sensitive indicator of cochlear dysfunction as well as brainstem auditory evoked responses A generalized increase in the auditory threshold at follow up indicating a cochlear impairment in three cases was noted Distortion products of otoacoustic emissions may reveal sub clinical cochlear dysfunction even in oligosymptomatic patients A complete and periodical assessment of the hearing function should be encouraged in asymptomatic relatives of patients carrying the tRNA Lys 8363G A mutation DiFabio R Santorelli FM Nola G Cricchi F Masi R Ingrosso A Fattori F Carrozzo R Vanacore N Pierelli F Ralli G Casali C Department of Neurology and ORL Sapienza University of Rome ICOT Polo Pontino 04100 Latina Italy rob dif tiscali it PMID 19233651 PubMed indexed for MEDLINE Leggi tutto 20 Nov Otoacoustic emissions a new method for newborn hearing screening Dr Nola in Pubblicazioni Commenti disabilitati su Otoacoustic emissions a new method for newborn hearing screening Pediatric deafness is a handicap affecting approximately 2 1000 newborns Currently its diagnosis is markedly delayed since it occurs approximately at 24 to 36 months of age at this age rehabilitation procedures i e acoustic prosthesis speech therapy psychological interventions on the family or cochlear implants in the most serious situations are unable to ensure a complete development of both the voice and the speech thus preventing the full participation of the deaf child in social living The turning point has taken place when methods and techniques were developed

    Original URL path: http://www.vertigini.me/2013/11/ (2016-05-02)
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  • Vertigini Vertigini | Dott. Giuseppe Nola
    completo dell evento clicca qui Locandina clicca qui Leggi tutto maggio 2016 L M M G V S D Set 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 Partner Pubblicazioni Approccio multidisciplinare ai disturbi dell equilibrio nell anziano 14 Novembre 2015 Ostia Lido RM Day case stapedotomy

    Original URL path: http://www.vertigini.me/category/vertigini/ (2016-05-02)
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  • Dr. Nola Vertigini | Dott. Giuseppe Nola
    and the correlation between total score of DHI I and total score on SF 36 was 0 593 Of the single subscales the emotional scale showed a closer correlation with almost all scales of the SF 36 The correlation between the total score of SF 36 and the single sub scale of DHI I functional emotional physical were respectively 0 599 0 563 0 398 The DHI was culturally and linguistically adapted for its application in the Italian population The DHI I demonstrated a good reliability and is recommended as a measure of disability in patients with dizziness and unsteadiness According to the DHI I patients with acute dizziness and with a clinical diagnosis of vestibular syndrome presented a decreased QoL the physical aspects were the most compromised Nola G Mostardini C Salvi C Ercolani AP Ralli G Operative Unit ENT G B Grassi Hospital Rome Italy Link PMC Article Leggi tutto 20 Nov Clinical and audiological follow up of a family with the 8363G A mutation in the mitochondrial DNA Dr Nola in Pubblicazioni Commenti disabilitati su Clinical and audiological follow up of a family with the 8363G A mutation in the mitochondrial DNA Hearing loss is relatively common in mtDNA related disorders While auditory function has been assessed fully in the syndrome of mitochondrial encephalomyopathy lactic acidosis and stroke like episodes few studies have investigated the degree of progressive hearing deficit in individuals bearing other mtDNA mutations We performed a 4 year clinical and audiological follow up in a family carrying the 8363G A mutation in the mitochondrial transfer ribonucleic acid lysine tRNA Lys gene who displayed a progressive neuromuscular disease In addition to pure tone audiometry we considered distortion products of otoacoustic emissions a sensitive indicator of cochlear dysfunction as well as brainstem auditory evoked responses A generalized increase in the auditory threshold at follow up indicating a cochlear impairment in three cases was noted Distortion products of otoacoustic emissions may reveal sub clinical cochlear dysfunction even in oligosymptomatic patients A complete and periodical assessment of the hearing function should be encouraged in asymptomatic relatives of patients carrying the tRNA Lys 8363G A mutation DiFabio R Santorelli FM Nola G Cricchi F Masi R Ingrosso A Fattori F Carrozzo R Vanacore N Pierelli F Ralli G Casali C Department of Neurology and ORL Sapienza University of Rome ICOT Polo Pontino 04100 Latina Italy rob dif tiscali it PMID 19233651 PubMed indexed for MEDLINE Leggi tutto 20 Nov Otoacoustic emissions a new method for newborn hearing screening Dr Nola in Pubblicazioni Commenti disabilitati su Otoacoustic emissions a new method for newborn hearing screening Pediatric deafness is a handicap affecting approximately 2 1000 newborns Currently its diagnosis is markedly delayed since it occurs approximately at 24 to 36 months of age at this age rehabilitation procedures i e acoustic prosthesis speech therapy psychological interventions on the family or cochlear implants in the most serious situations are unable to ensure a complete development of both the voice and the speech

    Original URL path: http://www.vertigini.me/author/admin/ (2016-05-02)
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