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  • Mojgan Babanejad; Masoud Motasaddi Zarandy; Nooshin Nikzat; Niloofar Bazazzadegan; S. Arzhangi; Marzieh Mohseni; K. Kahrizi; Hossein Najmabadi (scopusPubMed, 2019-11-01)
    © 2019 Elsevier B.V. Mutations in the GJB2 gene encoding connexin 26 (Cx26) cause autosomal recessive and rarely dominant nonsyndromic sensorineural hearing loss as well as asyndromic hearing impairment with skin problems. ...
  • Babanejad,M; Zarandy,MM; Nikzat,N; Bazazzadegan,N; Arzhangi,S; Mohseni,M; Kahrizi,K; Najmabadi,H (International Journal of Pediatric Otorhinolaryngologyscopusisi, 2019-11-01)
    © 2019 Elsevier B.V. Mutations in the GJB2 gene encoding connexin 26 (Cx26) cause autosomal recessive and rarely dominant nonsyndromic sensorineural hearing loss as well as asyndromic hearing impairment with skin problems. ...
  • Babanejad,M; Zarandy,MM; Nikzat,N; Bazazzadegan,N; Arzhangi,S; Mohseni,M; Kahrizi,K; Najmabadi,H (International journal of pediatric otorhinolaryngologypubmed, 2019-8-17)
    Mutations in the GJB2 gene encoding connexin 26 (Cx26) cause autosomal recessive and rarely dominant nonsyndromic sensorineural hearing loss as well as asyndromic hearing impairment with skin problems. A dominant GJB2 ...
  • Nazary-Moghadam, S; Salavati, M; Esteki, A; Akhbari, B; Keyhani, S; Zeinalzadeh, A (Science Directpubmed, 2019-01)
    BACKGROUND: Several investigations have studied gait variability of individuals with anterior cruciate ligament (ACL) deficiency; however, the effect of dual-tasking on the gait variability of these individuals remained ...
  • Nazary-Moghadam,S; Salavati,M; Esteki,A; Akhbari,B; Keyhani,S; Zeinalzadeh,A (Kneescopusisi, 2019-01-01)
    © 2018 Elsevier B.V. Background: Several investigations have studied gait variability of individuals with anterior cruciate ligament (ACL) deficiency; however, the effect of dual-tasking on the gait variability of these ...
  • Nazary-Moghadam,S; Salavati,M; Esteki,A; Akhbari,B; Keyhani,S; Zeinalzadeh,A (The Kneepubmed, 2018-11-27)
    Several investigations have studied gait variability of individuals with anterior cruciate ligament (ACL) deficiency; however, the effect of dual-tasking on the gait variability of these individuals remained unclear. The ...
  • Hao Hu; Kimia Kahrizi; Luciana Musante; Zohreh Fattahi; Ralf Herwig; Masoumeh Hosseini; Cornelia Oppitz; Seyedeh Sedigheh Abedini; Vanessa Suckow; Farzaneh Larti; Maryam Beheshtian; Bettina Lipkowitz; Tara Akhtarkhavari; Sepideh Mehvari; Sabine Otto; Marzieh Mohseni; Sanaz Arzhangi; Payman Jamali; Faezeh Mojahedi; Maryam Taghdiri; Elaheh Papari; Mohammad Javad Soltani Banavandi; Saeide Akbari; Seyed Hassan Tonekaboni; Hossein Dehghani; Mohammad Reza Ebrahimpour; Ingrid Bader; Behzad Davarnia; Monika Cohen; Hossein Khodaei; Beate Albrecht; Sarah Azimi; Birgit Zirn; Milad Bastami; Dagmar Wieczorek; Gholamreza Bahrami; Krystyna Keleman; Leila Nouri Vahid; Andreas Tzschach; Jutta Gärtner; Gabriele Gillessen-Kaesbach; Jamileh Rezazadeh Varaghchi; Bernd Timmermann; Fatemeh Pourfatemi; Aria Jankhah; Wei Chen; Pooneh Nikuei; Vera M. Kalscheuer; Morteza Oladnabi; Thomas F. Wienker; Hans Hilger Ropers; Hossein Najmabadi (scopusISIscopus, 2019-07-01)
    © 2017, Macmillan Publishers Limited, part of Springer Nature. Autosomal recessive (AR) gene defects are the leading genetic cause of intellectual disability (ID) in countries with frequent parental consanguinity, which ...
  • Hu,H; Kahrizi,K; Musante,L; Fattahi,Z; Herwig,R; Hosseini,M; Oppitz,C; Abedini,SS; Suckow,V; Larti,F; Beheshtian,M; Lipkowitz,B; Akhtarkhavari,T; Mehvari,S; Otto,S; Mohseni,M; Arzhangi,S; Jamali,P; Mojahedi,F; Taghdiri,M; Papari,E; Soltani Banavandi,MJ; Akbari,S; Tonekaboni,SH; Dehghani,H; Ebrahimpour,MR; Bader,I; Davarnia,B; Cohen,M; Khodaei,H; Albrecht,B; Azimi,S; Zirn,B; Bastami,M; Wieczorek,D; Bahrami,G; Keleman,K; Vahid,LN; Tzschach,A; Gärtner,J; Gillessen-Kaesbach,G; Varaghchi,JR; Timmermann,B; Pourfatemi,F; Jankhah,A; Chen,W; Nikuei,P; Kalscheuer,VM; Oladnabi,M; Wienker,TF; Ropers,HH; Najmabadi,H (Molecular Psychiatryscopuspubmedisi, 2019-07-01)
    © 2017, Macmillan Publishers Limited, part of Springer Nature. Autosomal recessive (AR) gene defects are the leading genetic cause of intellectual disability (ID) in countries with frequent parental consanguinity, which ...
  • Hu, H; Kahrizi, K; Musante, L; Fattahi, z (ISIScopus, 2018-07)
    Autosomal recessive (AR) gene defects are the leading genetic cause of intellectual disability (ID) in countries with frequent parental consanguinity, which account for about 1/7th of the world population. Yet, compared ...
  • Arabfard,M; Ohadi,M; Rezaei Tabar,V; Delbari,A; Kavousi,K (BMC Genomicsscopuspubmedisi, 2019-11-09)
    Background: Machine learning can effectively nominate novel genes for various research purposes in the laboratory. On a genome-wide scale, we implemented multiple databases and algorithms to predict and prioritize the human ...
  • James,SL; Theadom,A; Ellenbogen,RG; Bannick,MS; Mountjoy-Venning,WC; Lucchesi,LR; Abbasi,N; Abdulkader,R; Abraha,HN; Adsuar,JC; Afarideh,M; Agrawal,S; Ahmadi,A; Ahmed,MB; Aichour,AN; Aichour,I; Aichour,MTE; Akinyemi,RO; Akseer,N; Alahdab,F; Alebel,A; Alghnam,SA; Ali,BA; Alsharif,U; Altirkawi,K; Andrei,CL; Anjomshoa,M; Ansari,H; Ansha,MG; Antonio,CAT; Appiah,SCY; Ariani,F; Asefa,NG; Asgedom,SW; Atique,S; Awasthi,A; Quintanilla,BPA; Ayuk,TB; Azzopardi,PS; Badali,H; Badawi,A; Balalla,S; Banstola,A; Barker-Collo,SL; Barnighausen,TW; Bedi,N; Behzadifar,M; Behzadifar,M; Bekele,BB; Belachew,AB; Belay,YA; Bennett,DA; Bensenor,IM; Berhane,A; Beuran,M; Bhalla,A; Bhaumik,S; Bhutta,ZA; Biadgo,B; Biffino,M; Bijani,A; Bililign,N; Birungi,C; Boufous,S; Brazinova,A; Brown,AW; Car,M; Cardenas,R; Carrero,JJ; Carvalho,F; Castaneda-Orjuela,CA; Catala-Lopez,F; Chaiah,Y; Champs,AP; Chang,JC; Choi,JYJ; Christopher,DJ; Cooper,C; Crowe,CS; Dandona,L; Dandona,R; Daryani,A; Davitoiu,DV; Degefa,MG; Demoz,GT; Deribe,K; Djalalinia,S; Do,HP; Doku,DT; Drake,TM; Dubey,M; Dubljanin,E; El-Khatib,Z; Eskandarieh,S; Esteghamati,A; Esteghamati,S; Faro,A; Farzadfar,F; Farzaei,MH; Fereshtehnejad,SM; Fernandes,E; Feyissa,GT; Filip,I; Fischer,F; Fukumoto,T; Ganji,M; Gankpe,FG; Gebre,AK; Gebrehiwot,TT; Gezae,KE; Gopalkrishna,G; Goulart,AC; Haagsma,JA; Haj-Mirzaian,A; Haj-Mirzaian,A; Hamadeh,RR; Hamidi,S; Haro,JM; Hassankhani,H; Hassen,HY; Havmoeller,R; Hawley,C; Hay,SI; Hegazy,MI; Hendrie,D; Henok,A; Hibstu,DT; Hoffman,HJ; Hole,MK; Rad,EH; Hosseini,SM; Hostiuc,S; Hu,G; Hussen,MA; Ilesanmi,OS; Irvani,SN; Jakovljevic,M; Jayaraman,S; Jha,RP; Jonas,JB; Jones,KM; Shushtari,ZJ; Jozwiak,JJ; Jurisson,M; Kabir,A; Kahsay,A; Kahssay,M; Kalani,R; Karch,A; Kasaeian,A; Kassa,GM; Kassa,TD; Kassa,ZY; Kengne,AP; Khader,YS; Khafaie,MA; Khalid,N; Khalil,I; Khan,EA; Khan,MS; Khang,YH; Khazaie,H; Khoja,AT; Khubchandani,J; Kiadaliri,AA; Kim,D; Kim,YE; Kisa,A; Koyanagi,A; Krohn,KJ; Defo,BK; Bicer,BK; Kumar,GA; Kumar,M; Lalloo,R; Lami,FH; Lansingh,VC; Laryea,DO; Latifi,A; Leshargie,CT; Levi,M; Li,SS; Liben,ML; Lotufo,PA; Lunevicius,R; Mahotra,NB; Majdan,M; Majeed,A; Malekzadeh,R; Manda,AL; Mansournia,MA; Massenburg,BB; Mate,KKV; Mehndiratta,MM; Mehta,V; Meles,H; Melese,A; Memiah,PTN; Mendoza,W; Mengistu,G; Meretoja,A; Meretoja,TJ; Mestrovic,T; Miazgowski,T; Miller,TR; Mini,GK; Mirica,A; Mirrakhimov,EM; Moazen,B; Mohammadi,M; Mokdad,AH; Molokhia,M; Monasta,L; Mondello,S; Moosazadeh,M; Moradi,G; Moradi,M; Moradi-Lakeh,M; Moradinazar,M; Morrison,SD; Moschos,MM; Mousavi,SM; Murthy,S; Musa,KI; Mustafa,G; Naghavi,M; Naik,G; Najafi,F; Nangia,V; Nascimento,BR; Negoi,I; Nguyen,TH; Nichols,E; Ningrum,DNA; Nirayo,YL; Nyasulu,PS; Ofori-Asenso,R; Ogbo,FA; Oh,IH; Okoro,A; Olagunju,AT; Olagunju,TO; Olivares,PR; Otstavnov,SS; Owolabi,MO; Mahesh,PA; Pakhale,S; Pandey,AR; Pesudovs,K; Pinilla-Monsalve,GD; Polinder,S; Poustchi,H; Prakash,S; Qorbani,M; Radfar,A; Rafay,A; Rafiei,A; Rahimi-Movaghar,A; Rahimi-Movaghar,V; Rahman,M; Rahman,MA; Rai,RK; Rajati,F; Ram,U; Rawaf,DL; Rawaf,S; Reiner,RC; Reis,C; Renzaho,AMN; Resnikoff,S; Rezaei,S; Rezaeian,S; Roever,L; Ronfani,L; Roshandel,G; Roy,N; Ruhago,GM; Saddik,B; Safari,H; Safiri,S; Sahraian,MA; Salamati,P; Saldanha,RD; Samy,AM; Sanabria,J; Santos,JV; Milicevic,MMMS; Sartorius,B; Satpathy,M; Schneider,IJC; Schwebel,DC; Sepanlou,SG; Shabaninejad,H; Shaikh,MAA; Shams-Beyranvand,M; Sharif,M; Sharif-Alhoseini,M; Islam,SMS; She,J; Sheikh,A; Shen,JB; Sheth,KN; Shibuya,K; Shiferaw,MS; Shigematsu,M; Shiri,R; Shiue,I; Shoman,H; Siabani,S; Siddiqi,TJ; Silva,JP; Silveira,DGA; Sinha,DN; Smith,M; Soares,AM; Sobhani,S; Soofi,M; Soriano,JB; Soyiri,IN; Stein,DJ; Stokes,MA; Sufiyan,MB; Sunguya,BF; Sunshine,JE; Sykes,BL; Szoeke,CEI; Tabares-Seisdedos,R; Ao,BJT; Tehrani-Banihashemi,A; Tekle,MG; Temsah,MH; Temsah,O; Topor-Madry,R; Tortajada-Girbes,M; Tran,BX; Tran,KB; Car,LT; Ukwaja,KN; Ullah,I; Usman,MS; Uthman,OA; Valdez,PR; Vasankari,TJ; Venketasubramanian,N; Violante,FS; Wagnew,FS; Waheed,Y; Wang,YP; Weldegwergs,KG; Werdecker,A; Wijeratne,T; Winkler,AS; Wyper,GMA; Yano,Y; Yaseri,M; Yasin,YJ; Ye,PP; Yimer,EM; Yip,P; Yisma,E; Yonemoto,N; Yoon,SJ; Yost,MG; Younis,MZ; Yousefifard,M; Yu,CH; Zaidi,Z; BinZaman,S; Zamani,M; Zenebe,ZM; Zodpey,S; Feigin,VL; Vos,T; Murray,CJL (ELSEVIER SCIENCE INCisi, 2019-18-1)
    Background Traumatic brain injury (TBI) and spinal cord injury (SCI) are increasingly recognised as global health priorities in view of the preventability of most injuries and the complex and expensive medical care they ...
  • GBD 2016 Traumatic Brain Injury and Spinal Cord Injury Collaborators.; Collaborators (374) Abstract (PMCpubmedscopus, 2019)
    BACKGROUND: Traumatic brain injury (TBI) and spinal cord injury (SCI) are increasingly recognised as global health priorities in view of the preventability of most injuries and the complex and expensive medical care they ...
  • Frank,TD; Carter,A; Jahagirdar,D; Biehl,MH; Douwes-Schultz,D; Larson,SL; Arora,M; Dwyer-Lindgren,L; Steuben,KM; Abbastabar,H; Abu-Raddad,LJ; Abyu,DM; Adabi,M; Adebayo,OM; Adekanmbi,V; Adetokunboh,OO; Ahmadi,A; Ahmadi,K; Ahmadian,E; Ahmadpour,E; Ahmed,MB; Akal,CG; Alahdab,F; Alam,N; Albertson,SB; Alemnew,BTT; Alene,KA; Alipour,V; Alvis-Guzman,N; Amini,S; Anbari,Z; Anber,NH; Anjomshoa,M; Antonio,CAT; Arabloo,J; Aremu,O; Areri,HA; Asfaw,ET; Ashagre,AF; Asmelash,D; Asrat,AA; Avokpaho,EFGA; Awasthi,A; Awoke,N; Ayanore,MA; Azari,S; Badawi,A; Bagherzadeh,M; Banach,M; Barac,A; Barnighausen,TW; Basu,S; Bedi,N; Behzadifar,M; Bekele,BB; Belay,SA; Belay,YB; Belayneh,YMM; Berhane,A; Bhat,AG; Bhattacharyya,K; Biadgo,B; Bijani,A; BinSayeed,MS; Bitew,H; Blinov,A; Bogale,KA; Bojia,HA; Nagaraja,SBNB; Butt,ZA; Cahuana-Hurtado,L; Rincon,JCC; Carvalho,F; Chattu,VK; Christopher,DJ; Chu,DT; Crider,R; Dahiru,T; Dandona,L; Dandona,R; Daryani,A; dasNeves,J; DeNeve,JW; Degenhardt,L; Demeke,FM; Demis,ABB; Demissie,DB; Demoz,GT; Deribe,K; DesJarlais,D; Dhungana,GP; Diaz,D; Djalalinia,S; Do,HP; Doan,LP; Duber,H; Dubey,M; Dubljanin,E; Duken,EE; Adema,BD; Effiong,A; Eftekhari,A; Zaki,ME; El-Jaafary,SI; El-Khatib,Z; Elsharkawy,A; Endries,AY; Eskandarieh,S; Eyawo,O; Farzadfar,F; Fatima,B; Fentahun,N; Fernandes,E; Filip,I; Fischer,F; Folayan,MO; Foroutan,M; Fukumoto,T; Fullman,N; Garcia-Basteiro,AL; Gayesa,RT; Gebremedhin,KB; Gebremeskel,GG; Gebreyohannes,KK; Gedefaw,GA; Gelaw,BK; Gesesew,HA; Geta,B; Gezae,KE; Ghadiri,K; Ghashghaee,A; Ginindza,TTG; Gugnani,HC; Guimares,RA; Haile,MT; Hailu,GB; Haj-Mirzaian,A; Haj-Mirzaian,A; Hamidi,S; Handanagic,S; Handiso,DW; Hanfore,LK; Hasanzadeh,A; Hassankhani,H; Hassen,HY; Hay,SI; Henok,A; Hoang,CL; Hosgood,HD; Hosseinzadeh,M; Hsairi,M; Ibitoye,SE; Idrisov,B; Ikuta,KS; Ilesanmi,OS; Irvani,SSN; Iwu,CJ; Jacobsen,KH; James,SL; Jenabi,E; Jha,RP; Jonas,JB; Shushtari,ZJ; Kabir,A; Kabir,Z; Kadel,R; Kasaeian,A; Kassa,B; Kassa,GM; Kassa,TD; Kayode,GA; Kebede,MM; Kefale,AT; Kengne,AP; Khader,YS; Khafaie,MA; Khalid,N; Khan,EA; Khan,G; Khan,J; Khang,YH; Khatab,K; Khazaei,S; Khoja,AT; Kiadaliri,AA; Kim,YJ; Kisa,A; Kisa,S; Kochhar,S; Komaki,H; Koul,PA; Koyanagi,A; Defo,BK; Kumar,GA; Kumar,M; Kuupiel,D; Lal,DK; Lee,JJH; Lenjebo,TL; Leshargie,CT; Macarayan,ERK; Maddison,ER; AbdElRazek,HM; Magis-Rodriguez,C; Mahasha,PW; Majdan,M; Majeed,A; Malekzadeh,R; Manafi,N; Mapoma,CC; Martins-Melo,FR; Masaka,A; Mayenga,ENL; Mehta,V; Meles,GG; Meles,HG; Melese,A; Melku,M; Memiah,PTN; Memish,ZA; Mena,AT; Mendoza,W; Mengistu,DT; Mengistu,G; Meretoja,TJ; Mestrovic,T; Miller,TR; Moazen,B; Mohajer,B; Mohamadi-Bolbanabad,A; Mohammad,KA; Mohammad,Y; Darwesh,AM; Mezerji,NMG; Mohammadi,M; Mohammadibakhsh,R; Mohammadoo-Khorasani,M; Mohammed,JA; Mohammed,S; Mohebi,F; Mokdad,AH; Moodley,Y; Moossavi,M; Moradi,G; Moradi-Lakeh,M; Moschos,MM; Mossie,TB; Mousavi,SM; Muchie,KF; Muluneh,AG; Muriithi,MK; Mustafa,G; Muthupandian,S; Nagarajan,AJ; Naik,G; Najafi,F; Nazari,J; Ndwandwe,DE; Nguyen,CT; Nguyen,HLT; Nguyen,SH; Nguyen,TH; Ningrum,DNA; Nixon,MR; Nnaji,CA; Noroozi,M; Noubiap,JJ; Shiadeh,MN; Obsa,MS; Odame,EA; Ofori-Asenso,R; Ogbo,FA; Okoro,A; Oladimeji,O; Olagunju,AT; Olagunju,TO; Olum,S; Asante,KO; Oren,E; Otstavnov,SS; Mahesh,PA; Padubidri,JR; Pakhale,S; Pakpour,AH; Patel,SK; Paulos,K; Pepito,VCF; Peprah,EK; Piroozi,B; Pourshams,A; Qorbani,M; Rabiee,M; Rabiee,N; Radfar,A; Rafay,A; Rafiei,A; Rahim,F; Rahimi-Movaghar,A; Rahimi-Movaghar,V; Rahman,SU; Ranabhat,CL; Rawaf,S; Reis,C; Renjith,V; Reta,MA; Rezai,MS; Gonazlez,CMR; Roro,EEMM; Rostami,A; Rubino,S; Moghaddam,SS; Safari,S; Sagar,R; Sahraian,MA; Salem,MRR; Salimi,Y; Salomon,JA; Sambala,EZ; Samy,AM; Sartorius,B; Satpathy,M; Sawhney,M; Sayyah,M; Schutte,AE; Sepanlou,SG; Seyedmousavi,S; Shabaninejad,H; Shaheen,AA; Shaikh,MA; Shallo,SA; Shamsizadeh,M; Sharifi,H; Shibuya,K; Shin,JI; Shirkoohi,R; Silva,DAS; Silveira,DGA; Singh,JA; Sisay,MMM; Sisay,M; Sisay,S; Smith,AE; Sokhan,A; Somayaji,R; Soshnikov,S; Stein,DJ; Sufiyan,MB; Sunguya,BF; Sykes,BL; Tadesse,BT; Tadesse,DB; Tamirat,KS; Taveira,N; Tekelemedhin,SW; Temesgen,HD; Tesfay,FH; Teshale,MY; Thapa,S; Tlaye,KG; Topp,SM; Tovani-Palone,MR; Tran,BX; Tran,KB; Ullah,I; Unnikrishnan,B; Uthman,OA; Veisani,Y; Vladimirov,SK; Wada,FW; Waheed,Y; Weldegwergs,KG; Weldesamuel,GTT; Westerman,R; Wijeratne,T; Wolde,HF; Wondafrash,DZ; Wonde,TE; Wondmagegn,BY; Yeshanew,AG; Yilma,MT; Yimer,EM; Yonemoto,N; Yotebieng,M; Youm,Y; Yu,CH; Zaidi,Z; Zarghi,A; Zenebe,ZM; Zewale,TA; Ziapour,A; Zodpey,S; Naghavi,M; Vollset,SE; Wang,HD; Lim,SS; Kyu,HH; Murray,CJL (ELSEVIER INCisi, 2019-6-12)
    Background Understanding the patterns of HIV/AIDS epidemics is crucial to tracking and monitoring the progress of prevention and control efforts in countries. We provide a comprehensive assessment of the levels and trends ...
  • Hossein, M; Fattahi, Z; Abedini, S; Najmabadi, H; Kahrizi, K (2019)
    Intellectual disability (ID), a genetically and clinically heterogeneous disorder, affects 1%-3% of the general population and is a major health problem, especially in developing countries and in populations with a high ...
  • Hosseini,M; Fattahi,Z; Abedini,SS; Hu,H; Ropers,HH; Kalscheuer,VM; Najmabadi,H; Kahrizi,K (American Journal of Medical Genetics, Part Ascopuspubmedisi, 2019-01-01)
    © 2018 Wiley Periodicals, Inc. Intellectual disability (ID), a genetically and clinically heterogeneous disorder, affects 1%–3% of the general population and is a major health problem, especially in developing countries ...
  • Hosseini, M; Fattahi, Z; Abedini, SS; Hu, H; Ropers, HH (wiiley, 2019-01)
    Intellectual disability (ID), a genetically and clinically heterogeneous disorder, affects 1%-3% of the general population and is a major health problem, especially in developing countries and in populations with a high ...
  • Hatamizadeh, Maryam (2019-03)
    Aim The aim of the present study was to assess the implications of Iran's recent health care reforms on nurses’ experience of moral distress, their perceptions of the respect for patient rights and the relationship of ...

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