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Our experience in the treatment of acute deafness

Author(s): Mihailović-Kokić Branka | Todorović Aleksandar J. | Kokić Zoran
MERRF Case Report

Author(s): Ayten Ceyhan DİRİCAN | Yavuz ALTUNKAYNAK | Arzu Şanlı TÜRK | Belgin MUTLUAY | Sevim BAYBAŞ
THE BENEFIT OF EARLY EXPOSURE TO SIGN LANGUAGE

Author(s): Ljubica PRIBANIKJ | Marina MILKOIVKJ
Speech Perception and Audiometry Thresholds in Nucleus Cochlear 22 and Nucleus 24 Implant Users

Author(s): Samuel, Paola Angelica | Gomez, Maria Valéria Schmidt Goffi | Lopes, Débora Maria Befi | Matas, Carla Gentile | Tsuji, Robinson Koji | Brito Neto, Rubens Vuono de | Bento, Ricardo Ferreira
Meningitis as cochlear implant complication

Author(s): Kosanović Rade | Ivanković Zoran | Babac Snežana | Stojanović Sandra | Petrović-Lazić Mirjana | Ječmenica Jovana
Deafness and motor abilities level

Author(s): A Zwierzchowska | K Gawlik | M Grabara
Comparison of Indicators of Risk of Deafness in Newborns Studied in the Years 1995 and 2005

Author(s): Lopes, Monique Kelly Duarte | Santos, Teresa Maria Momensohn
LEV S. VIGOTSKI AND THE MODERN SPECIAL PSYCHOLOGY

Author(s): Daniela VARDULAKI | Petar S. PETROV
Wildervanck syndrome associated with cleft palate and short stature

Author(s): Kumar Anand | Sahu Anupam | Shetty Shashikant | Vijayalakshmi P
Marinesco-Sjogren Syndrome With Sensori Neural Deafness And Primary Optic Atrophy

Author(s): Aleem M A | Raveendran D | Meikandan D | Ramasubramanian D
Cortical Deafness - A Clinical, Audiological, Electrophysiological, Radiological And Follow Up Study

Author(s): Sinha S | Shasikala H R | Arunodaya G R | Shivashankar N | Taly A B
Cockayne syndrome - A Clinical, Radiological, Audiological And Chromosomal Study

Author(s): Ashraff V V | Sinha S | Hegde Sridevi | Kovoor JME | Arunodaya G R | Taly A B
Cockayne Syndrome

Author(s): Sharma Nand Lal | Mahajan Vikram K | Sharma Ramesh Chander | Sharma Ashok K
Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy

Author(s): Wang Da-Yong | Wang Yi-Chen | Weil Dominique | Zhao Ya-Li | Rao Shao-Qi | Zong Liang | Ji Yu-Bin | Liu Qiong | Li Jian-Qiang | Yang Huan-Ming | Shen Yan | Benedict-Alderfer Cindy | Zheng Qing-Yin | Petit Christine | Wang Qiu-Ju
Cochlear implant application with postlingually deaf patients

Author(s): Kosanović Rade | Ivanković Zoran | Stojanović Sandra
A Case Report: Usher Syndrome and Psychosis Comorbidity

Author(s): Latif Alpkan | Nezih Eradamlar | Neslihan Ergen | Neşe Üstün | Mustafa Karagöz | A. Umut Dalanay
Study of Deafness Associated with DFNB59 Gene (pejvakin) Mutation in Fars Province

Author(s): Raeisi S | Farokhi E | Taherzadeh M | Azadegan F | Abolhasani M | Raeisi M | Banitalebi G | Esmaili A | Zaker R | Hashemzadeh M
Ophthalmologic abnormalities among deaf students in Kaduna, Northern Nigeria

Author(s): Abah E | Oladigbolu K | Samaila E | Merali H | Ahmed A | Abubakar T
Sudden Hearing Loss as the Initial Manifestation of Chronic Myeloid Leukemia in a Child.

Author(s): Ching-Chung Tsai | Chung-Bin Huang | Jiunn-Ming Sheen | Hsiu-Hui Wei | Chih-Cheng Hsiao
Usher syndrome associated with Fuchs’ heterochromic uveitis: a case report

Author(s): Turan-Vural E | Torun-Acar B | Tükenmez N | Sevim S | Buttanri B | Acar S
Experiences with bimodal hearing and bilateral cochlear implantation in the elderly

Author(s): E.M. Schedlbauer | R. Götze | S. Scholz | I. Todt | A. Ernst
RNA profiles of rat olfactory epithelia: individual and age related variations

Author(s): Rimbault Maud | Robin Stéphanie | Vaysse Amaury | Galibert Francis
Conditions of Personality Predicting Results with Cochlear Implant in Post-lingual Patients with Long-time Hearing Deprivation

Author(s): Nasralla, Heloisa Romeiro | Goffi, Valeria | Rigamonti, Carla | Peralta, Cristina Ornelas | Tsuji, Robinson Koji | Brito Neto, Rubens Vuono de | Bento, Ricardo Ferreira
HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Hirschsprung Disease

Author(s): Mohsen Akhavan Sepahi | Behrouz Baraty | Fatemeh Khalifeh Shooshtary
Passing otoacustic emissions as a complementar method in the topodiagnosis of the neurosensories hearing loss

Author(s): Franceschi, Cacineli Marion de | Tochetto, Tania | Lautenschlager, Larissa
Surdez: um território de fronteiras/Deafness: a territory of boundaries

Author(s): Madalena Klein e | Márcia Lise Lunardi
Olmsted Syndrome

Author(s): Mukhopadhyay Piyali | Biswas Nibir | Dutta R.N | Pal S
Mastoiditis aguda: estudio epidemiológico de una década Acute mastoiditis: one-decade long epidemiological study

Author(s): C. Suárez Castañón | M. Morán Poladura | R. Pardo de la Vega | C. Pérez Méndez
Streptococcus suis infection: Clinical manifestations

Author(s): Dragojlović Julijana | Milošević Branko | Šašić Neda | Pelemiš Miomir | Šašić Milan
The role of current audiological tests in the early diagnosis of hearing impairment in children

Author(s): Lemajić-Komazec Slobodanka | Komazec Zoran | Vlaški Ljiljana
Cochlear implantation at the ear, nose and throat clinic of the Clinical center of Vojvodina

Author(s): Komazec Zoran | Dankuc Dragan | Vlaški Ljiljana | Lemajić-Komazec Slobodanka | Nedeljkov Spomenka | Sokolovac Ivana
Current and emerging treatments for the management of osteogenesis imperfecta

Author(s): Elena Monti | Monica Mottes | Paolo Fraschini | et al
Autosomal Recessive Deafness is Heterogeneous in Pakistani Pakhtun Population

Author(s): S.M. Ibrahim | S. Ahmad | R. Tareen | F.U. Amin
Current options for the treatment of Paget’s disease of the bone

Author(s): Daniela Merlotti | Luigi Gennari | Giuseppe Martini | et al
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome

Author(s): Riazuddin Saima | Ahmed Zubair | Hegde Rashmi | Khan Shaheen | Nasir Idrees | Shaukat Uzma | Riazuddin Sheikh | Butman John | Griffith Andrew | Friedman Thomas | Choi Byung
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics

Author(s): Shen Zhisen | Zheng Jing | Chen Bobei | Peng Guanghua | Zhang Ting | Gong Shasha | Zhu Yi | Zhang Chuqin | Li Ronghua | Yang Li | Zhou Jianjin | Cai Ting | Jin Lihua | Lu Jianxin | Guan Min-Xin
Prevalence of the GJB2 IVS1+1G >A mutation in Chinese hearing loss patients with monoallelic pathogenic mutation in the coding region of GJB2

Author(s): Yuan Yongyi | Yu Fei | Wang Guojian | Huang Shasha | Yu Ruili | Zhang Xin | Huang Deliang | Han Dongyi | Dai Pu
Long-Term follow up after intra-Uterine transfusionS; the LOTUS study

Author(s): Verduin Esther | Lindenburg Irene | Smits-Wintjens Vivianne | van Klink Jeanine | Schonewille Henk | van Kamp Inge | Oepkes Dick | Walther Frans | Kanhai Humphrey | Doxiadis Ilias | Lopriore Enrico | Brand Anneke
Maternally Inherited Diabetes and Deafness (MIDD) Syndrome: A Clinical and Molecular Genetic Study of a Taiwanese Family.

Author(s): Yung-Nien Chen | Chia-Wei Liou | Chin-Chang Huang | Tsu-Kung Lin | Yau-Huei Wei
Universal neonatal audiological screening: experience of the University Hospital of Pisa

Author(s): Ghirri Paolo | Liumbruno Annalisa | Lunardi Sara | Forli Francesca | Boldrini Antonio | Baggiani Angelo | Berrettini Stefano
Libyan cochlear implant programme: achievements, difficulties, and future goals

Author(s): Ali Salamat | Anwer Esriti | Asia Ehtuish | Samya El-Ogbi
Waardenburg syndrome type I- a rare case report

Author(s): Gurmit Singh | Kunal Ahya | Dhananjay Y Shrikhande | Suhas Patil | Apurva Desai | Niranjan Bommisetti Kurukuti | Sankalp Yadav | Rajiv Girdhar
Basic Circuit for Silicon Cochlea

Author(s): Daniela Durackova | Peter Kruzlic
Early detection of hearing loss

Author(s): Schade, Götz
"Osteogenesis Imperfecta: Report of a new pedigree in Iran "

Author(s): "Farhoud D | Mohammadi Asl J | Derakhshandeh P "
Wolfram syndrome: Endocrinological features in a case series study and review of the literature

Author(s): Ali Rabbani; Abdolmajid Kajbafzadeh; Reza Shabanian; Aria Setoodeh; Feridoon Mostafavi; Morteza Rezv
HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Hirschsprung Disease

Author(s): Mohsen Akhavan Sepahi | Behrouz Baraty | Fatemeh Khalifeh Shooshtary
A Repot of Surgical Complications in a Series of 262 Consecutive Pediatric Cochlear Implantations in Iran

Author(s): Mohammad Ajalloueyan | Susan Amirsalari | Jaleh Yousefi | Mohammad-Ali Raeessi | Shokofeh Radfar | Mahdieh Hassanalifard
Basic Circuit for Silicon Cochlea

Author(s): Daniela Durackova | Peter Kruzlic
A HYBRID WIRELESS NETWORK MODEL FOR POST DISASTER RELIEF OPERATIONS

Author(s): SK Dwivedi | NK Shukla | Sudhakar Pandey
Risk Behaviour of lead-exposed Workers and Hearing Impairment

Author(s): Salma Galal | Gamal H El-Samra | Manal Mazhar | Fatma El-Kholy | Amel Hegazy
The First Survey of Distribution of Inherited Deafness Patterns in Individuals Referred to Genetic Center of Ahvaz Welfare Organization, Southern Iran

Author(s): Ali Mohammad Foroughmand | Hamid Galehdari | Gholamreza Mohammadian | Abdolrahman Rasekh | Jasem Ghavabesh
Experiences with bimodal hearing and bilateral cochlear implantation in the elderly

Author(s): E.M. Schedlbauer | R. Götze | S. Scholz | I. Todt | A. Ernst
Intratympanic injection of dexamethasone for treatment of tinnitus in patients with sudden sensorineural hearing loss

Author(s): Tadao Yoshida | Masaaki Teranishi | Tomoyuki Iwata | Hironao Otake | Tsutomu Nakashima
Bloch wave deafness and modal conversion at a phononic crystal boundary

Author(s): Vincent Laude | Rayisa P. Moiseyenko | Sarah Benchabane | Nico F. Declercq
JERVELL AND LANGE-NIELSEN SYNDROME;

Author(s): AMMAR ANWER | M. HAMAYUN IKRAM | ALI SHAKEEL | Shahroona Masud Zaman
Firefly Clock Synchronization in an 802.15.4 Wireless Network

Author(s): Leidenfrost Robert | Elmenreich Wilfried
Genetic mutations in non-syndromic deafness patients of uyghur and han chinese ethnicities in xinjiang, China: a comparative study

Author(s): Chen Yu | Tudi Mayila | Sun Jie | He Chao | Lu Hong-li | Shang Qing | Jiang Di | Kuyaxi Pilidong | Hu Bin | Zhang Hua
Unique phenotype in a patient with CHARGE syndrome

Author(s): Jain Shobhit | Kim Hyung-Goo | Lacbawan Felicitas | Meliciani Irene | Wenzel Wolfgang | Kurth Ingo | Sharma Josefina | Schoeneman Morris | Ten Svetlana | Layman Lawrence | Jacobson-Dickman Elka
Prevalence of head and neck abnormalities among people with consanguineous parents

Author(s): Razmpa E | Azimi C | Soltan Sanjarei M | Nazari H | Ghasempoure A | Yousefi M
Prevalence of hearing loss among high risk newborns hospitalized in hospitals affiliated to Tehran University of Medical Sciences

Author(s): Ali Zamani | Alireza Karimi | Mohsen Naseri | Elaheh Amini | Mohammad Milani | Amir Arvin Sazgar | Seyed Mousa Sadr Hosseini | Mohammad Sadeghi Hassan Abadi | Fatemeh Nayeri | Firouzeh Nili | Mamak Shariat | Mostafa Vasigh | Fariba Nasaj | Fatemeh Zamani | Narges Zamani
Keratitis-Ichthyosis-Deafness Syndrome, Atypical Connexin GJB2 Gene Mutation, and Peripheral T-Cell Lymphoma: More Than a Random Association?

Author(s): Claudio Fozza | Fausto Poddie | Salvatore Contini | Antonio Galleu | Francesca Cottoni | Maurizio Longinotti | Francesco Cucca
"Deafness –Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population"

Author(s): M Hashemzadeh Chaleshtori | DD Farhud | R Taylor | V Hadavi | MA Patton | AR Afzal
"Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations "

Author(s): R Sasanfar | A Tolouei | A Hoseinipour | DD Farhud | M Dolati | L Hoghooghi Rad | M Montazer Zohour | M Ghadami | H Pour-Jafari | M Hashemzadeh Chaleshtori
"Two Novel Mutations and Predominant 35delG Mutation in the Connexin 26 Gene (GJB2) in Iranian Populations"

Author(s): "M Hashemzadeh Chaleshtori | M Dowlati | DD Farhud | L Hoghooghi Rad | R Sasanfar A Hoseinipour | M Montazer Zohour | A Tolooi | M Ghadami | HR Pourjafari | MA Oshaghi | MA Patton "
Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz)

Author(s): M Hashemzadeh Chaleshtori | L Hoghooghi Rad | M Dolati | R Sasanfar | A Hoseinipour | M Montazer Zohour | H Pourjafari | A Tolooi | M Ghadami | DD Farhud | MA Patton
Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran

Author(s): M Hashemzadeh Chaleshtori | M Montazer Zohour | L Hoghooghi Rad | H Pour-Jafari | DD Farhud | M Dolati | K Safa Chaleshtori | R Sasanfar | A Hosseinipour | L Andonian | A Tolouei | M Ghadami | MA Patton
Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases

Author(s): M Hashemzadeh Chaleshtori | DD Farhud | AH Crosby | E Farrokhi | H Pour Jafari | K Ghatreh Samani | K Safa Chaleshtori | M Kasiri | M Shahrani | GR Mobini | M Mansouri | D Modarresinia | M Jafari
Prevalence of neonatal hearing impairment in province capitals

Author(s): M Firouzbakht | H Eftekhar Ardebili | F Majlesi | A Rahimi | M Esmailzadeh
Electrophysiological changes on brainstem auditory evoked potentials in hypothyroid patients

Author(s): M. Chandrasekhar*, V. Kowsalya and B. Vijayalakshmi
Double Cochlea in a Member of Familial Ossicular Chain Absence (Five Cases)

Author(s): Jalal Jalalshokouhi | Aliakbar Ameri | Mansour Fatehi | Taghi Khorsandi
Diagnosis Deafness in a Child

Author(s): Robabeh Taghavi
Neurofibromatosis Type II

Author(s): Masomeh Rozbehani | Akram Kasiri Ghahi
COCHLEAR IMPLANTATION IN IRAN

Author(s): M.H. Khalessi | S. Abdi | M.T. Khorsandi
SUPPRESSION OF TINNITUS IN PATIENTS UNDERGOING COCHLEAR IMPLANTATION

Author(s): M. T. Khorsandi | H. Borghei |  S. Abdi
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS: REPORT OF A CASE AND LITERATURE REVIEW

Author(s): P. Mansouri. | M. R. Mortazavi Z. Saraii Naragki
Oral Communication Development in Severe to Profound Hearing Impaired Children After Receiving Aural Habilitation

Author(s): Daneshmandan Naeimeh | Borghei Pedram | Yazdany Nasrin | Soleimani Farin | Vameghi Roshanak
Waardenburg Syndrome Type I – A Concise Diagnostic Study

Author(s): Daksha Dixit* | Sureshbhai P. Rathod | Shilpa M. Bhimalli | Sheetal V. Pattanshetti | Veereshkumar S. Shirol | Tulsibhai C. Singel
The impact of hearing loss on the quality of life in adults

Author(s): Tatović Milica | Babac Snežana | Đerić Dragoslava | Aničić Ružica | Ivanković Zoran
Long-term outcome in relationship to neonatal transfusion volume in extremely premature infants: a comparative cohort study

Author(s): von Lindern Jeannette | Khodabux Chantal | Hack Karien | van Haastert Ingrid | Koopman-Esseboom Corine | van Zwieten Paul | Brand Anneke | Walther Frans
Pontine tegmental cap dysplasia: developmental and cognitive outcome in three adolescent patients

Author(s): Briguglio Marilena | Pinelli Lorenzo | Giordano Lucio | Ferraris Alessandro | Germanò Eva | Micheletti Serena | Severino Mariasavina | Bernardini Laura | Loddo Sara | Tortorella Gaetano | Ormitti Francesca | Gasparotti Roberto | Rossi Andrea | Valente Enza
Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

Author(s): Bonnet Crystel | Grati M'hamed | Marlin Sandrine | Levilliers Jacqueline | Hardelin Jean-Pierre | Parodi Marine | Niasme-Grare Magali | Zelenika Diana | Délépine Marc | Feldmann Delphine | Jonard Laurence | El-Amraoui Aziz | Weil Dominique | Delobel Bruno | Vincent Christophe | Dollfus Hélène | Eliot Marie-Madeleine | David Albert | Calais Catherine | Vigneron Jacqueline | Montaut-Verient Bettina | Bonneau Dominique | Dubin Jacques | Thauvin Christel | Duvillard Alain | Francannet Christine | Mom Thierry | Lacombe Didier | Duriez Françoise | Drouin-Garraud Valérie | Thuillier-Obstoy Marie-Françoise | Sigaudy Sabine | Frances Anne-Marie | Collignon Patrick | Challe Georges | Couderc Rémy | Lathrop Mark | Sahel José-Alain | Weissenbach Jean | Petit Christine | Denoyelle Françoise
A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population

Author(s): Imtiaz Faiqa | Taibah Khalid | Ramzan Khushnooda | Bin-Khamis Ghada | Kennedy Shelley | Al-Mubarak Bashayer | Trabzuni Daniah | Allam Rabab | Al-Mostafa Abeer | Sogaty Sameera | Al-Shaikh Abdulmoneem | Bamukhayyar Saeed | Meyer Brian | Al-Owain Mohammed
Correlation Between the Audiologic Findings and Tinnitus Disorder

Author(s): Mondelli, Maria Fernanda Capoani Garcia | Rocha, Alice Borges da
Postural Evaluation of Vertebral Column in Children and Teenagers with Hearing Loss

Author(s): Melo, Renato de Souza | Silva, Polyanna Waleska Amorim da | Silva, Lícia Vasconcelos Carvalho da | Toscano, Carla Fabiana da Silva
Profile of Iranian GJB2 Mutations in Young Population with Novel Mutation

Author(s): Masoumeh Falah | Massoud Houshmand | Susan Akbaroghli | Saeid Mahmodian | Yaser Ghavami | Mohammad Farhadi
STEREOLOGICAL ANALYSIS OF THE COCHLEAR NUCLEI OF MONKEY (MACACA FASCICULARIS) AFTER DEAFFERENTATION

Author(s): Ana M Insausti | Ricardo Insausti | Luis M Cruz-Orive | Manuel Manrique
Reliability of standardized assessment for adults who are deafblind

Author(s): Dawn M. Guthrie, PhD | Robyn Pitman, MA | Paul Stolee, PhD | Graham Strong, OD, MSc | Jeff Poss, PhD | Erin Y. Tjam, PhD | Lindsay Bowman, MPH | Melody Ashworth, MSc | John P. Hirdes, PhD
Gênero e surdez / Gender and deafness

Author(s): Madalena Klein | Daniele de Paula Formozo
Epidemiology of prelingual sensorineural hearing impairment at a children’s center in Bogotá, Colombia between 1997 and 2008

Author(s): Claudia Talero-Gutiérrez | Liliana Romero | Irma Carvajalino | Milciades Ibáñez
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