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Armagan Incesulu

Research Profile

Geographic Areas

Turkey

Disorders

Procedures

Physiology

Chemicals & Drugs

Concepts & Ideas

Living Beings

Homozygote

Devices

Cochlear Implants

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Publications

TOP 3
Murat Erdogan; Armagan Incesulu; Ercan Kaya; Hamdi Cakli; Cemal Cingi; M Kezban Gürbüz; Erkan Ozudogru; Erdal Seren; Cem Kecik
Evaluation of nasal airway alterations associated with septorhinoplasty by both objective and subjective methods.
Leman Birdane; Melek Kezban Gurbuz; Armagan Incesulu; Demet Ozbabalik
Sacculocolic reflex in patients with dementia: is it possible to use it for early diagnosis?
F Basak Cengiz; Duygu Duman; Asli Sirmaci; Suna Tokgöz-Yilmaz; Seyra Erbek; Hatice Oztürkmen-Akay; Armagan Incesulu; Yvonne Jemimah Edwards; Hilal Ozdag; Xue Zhong Liu; Mustafa Tekin
Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.

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All Publications

2013: Murat Erdogan; Armagan Incesulu; Ercan Kaya; Hamdi Cakli; Cemal Cingi; M Kezban Gürbüz; Erkan Ozudogru; Erdal Seren; Cem Kecik
Evaluation of nasal airway alterations associated with septorhinoplasty by both objective and subjective methods.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2013;270(1):99-106.
2012: Leman Birdane; Melek Kezban Gurbuz; Armagan Incesulu; Demet Ozbabalik
Sacculocolic reflex in patients with dementia: is it possible to use it for early diagnosis?
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2012;33(1):17-21.
2010: F Basak Cengiz; Duygu Duman; Asli Sirmaci; Suna Tokgöz-Yilmaz; Seyra Erbek; Hatice Oztürkmen-Akay; Armagan Incesulu; Yvonne Jemimah Edwards; Hilal Ozdag; Xue Zhong Liu; Mustafa Tekin
Recurrent and private MYO15A mutations are associated with deafness in the Turkish population.
Genetic testing and molecular biomarkers 2010;14(4):543-50.
2009: A Sirmaci; H Oztürkmen-Akay; Seyra Erbek; Armagan Incesulu; D Duman; S Taşir-Yilmaz; H Ozdağ; Mustafa Tekin
A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia.
Clinical genetics 2009;75(6):562-7.
2009: Asli Sirmaci; Duygu Duman; Hatice Oztürkmen-Akay; Seyra Erbek; Armagan Incesulu; Burcu Oztürk-Hişmi; Z Serap Arici; E Berrin Yüksel-Konuk; Seda Taşir-Yilmaz; Suna Tokgöz-Yilmaz; Filiz Basak Cengiz; Idil Aslan; Müzeyyen Yildirim; Aylin Hasanefendioğlu-Bayrak; Abdullah Ayçiçek; Ismail Yilmaz; Suat Fitoz; Fazilet Altin; Hilal Ozdağ; Mustafa Tekin
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.
International journal of pediatric otorhinolaryngology 2009;73(5):699-705.
2008: Armagan Incesulu; Baki Adapinar; Cem Kecik
Cochlear implantation in cases with incomplete partition type III (X-linked anomaly).
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2008;265(11):1425-30.
2008: Zuleyha Yildiz; Arzu Ulu; Armagan Incesulu; Yalcin Ozkaptan; Nejat Akar
The importance of thrombotic risk factors in the development of idiopathic sudden hearing loss.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2008;14(3):356-9.
2008: Mustafa Tekin; H Oztürkmen Akay; Suat Fitoz; S Birnbaum; Filiz Basak Cengiz; L Sennaroğlu; Armagan Incesulu; E B Yüksel Konuk; A Hasanefendioğlu Bayrak; S Sentürk; I Cebeci; G E Utine; E Tunçbilek; W E Nance; D Duman
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.
Clinical genetics 2008;73(6):554-65.
2007: Suat Fitoz; Levent Sennaroğlu; Armagan Incesulu; Filiz Basak Cengiz; Yasemin Koç; Mustafa Tekin
SLC26A4 mutations are associated with a specific inner ear malformation.
International journal of pediatric otorhinolaryngology 2007;71(3):479-86.
2007: Yaprak E Cirçir; Armagan Incesulu; Mustafa Tekin
[Screening of the mitochondrial 12S rRNA (MTRNR1) gene in probands with sensorineural hearing loss].
Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat 2007;17(2):75-80.
2007: Armagan Incesulu; Rudolf Häusler
Advantages and risks of various sealing procedures of the oval window: vein graft, adipose tissue, gelfoam, merogel.
Advances in oto-rhino-laryngology 2007;65():206-9.
2006: Burcu Oztürk Hişmi; Suna Tokgöz Yilmaz; Armagan Incesulu; Mustafa Tekin
Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypes.
International journal of pediatric otorhinolaryngology 2006;70(10):1687-94.
2006: Mustafa Tekin; Suat Fitoz; Serap Arici; Ergun Cetinkaya; Armagan Incesulu
Niikawa-Kuroki (Kabuki) syndrome with congenital sensorineural deafness: evidence for a wide spectrum of inner ear abnormalities.
International journal of pediatric otorhinolaryngology 2006;70(5):885-9.
2005: Mustafa Tekin; Duygu Akcayoz; Armagan Incesulu
A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathy.
American journal of medical genetics. Part A 2005;138(1):6-10.
2005: Sinan Kocaturk; Sumru Yardimci; Altan Yildirim; Armagan Incesulu
Preventive therapy for postoperative purulent otorrhea after ventilation tube insertion.
American journal of otolaryngology 2005;26(2):123-7.
2005: S T Arican; Armagan Incesulu; B Inceoglu; Mustafa Tekin
Alterations in the GJB3 and CLDN14 genes in families with nonsyndromic sensorineural hearing loss.
Genetic counseling (Geneva, Switzerland) 2005;16(3):309-11.
2004: Armagan Incesulu; Sinan Kocaturk; Mesut Vural
Cochlear implantation in chronic otitis media.
The Journal of laryngology and otology 2004;118(1):3-7.
2003: Sinan Kocatürk; Selma Kurukahvecioğlu; Armagan Incesulu; Unsal Erkam
[A case of laryngeal chondroradionecrosis].
Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat 2003;11(1):29-32.
2003: Armagan Incesulu; Mesut Vural; Unsal Erkam
Children with cochlear implants: parental perspective.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2003;24(4):605-11.
2003: Mustafa Tekin; Türker Duman; Gönül Boğoçlu; Armagan Incesulu; Elif Comak; Inci Ozgur Ilhan; Nejat Akar
Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: roles of parental consanguinity and assortative mating.
Human mutation 2003;21(5):552-3.
2003: Sinan Kocatürk; Tayfur Demiray; Armagan Incesulu; Ebru Kandirali; Unsal Erkam; Ali Mert
[Comparison of adenoid and tonsil core cultures in chronic adenotonsillitis].
Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat 2003;10(3):105-9.
2003: Armagan Incesulu; Sinan Kocatürk; Bahri Keyik; Esin Cakmakçi; Unsal Erkam; Baki Hekimoğlu
[A comparison between findings of high resolution computed tomography and magnetic resonance imaging in the preoperative assessment of cochlear implant patients].
Kulak burun boğaz ihtisas dergisi : KBB = Journal of ear, nose, and throat 2003;10(3):98-104.
2003: Mustafa Tekin; Türker Duman; G Boğoçlu; Armagan Incesulu; Elif Comak; Suat Fitoz; E Yilmaz; Inci Ozgur Ilhan; Nejat Akar
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.
European journal of pediatrics 2003;162(3):154-8.
2003: Mustafa Tekin; Türker Duman; G Boğoçlu; Armagan Incesulu; Sükrü Cin; Nejat Akar
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene.
Genetic counseling (Geneva, Switzerland) 2003;14(4):379-86.
2002: Armagan Incesulu; Mesut Vural; Unsal Erkam; Sinan Kocaturk
Cochlear implantation in children with inner ear malformations: report of two cases.
International journal of pediatric otorhinolaryngology 2002;65(2):171-9.