Works by Tekin, M.

Results: 70

Predicting miscarriage using systemic immune‐inflammation index.

Published in:

Journal of Obstetrics & Gynaecology Research, 2022, v. 48, n. 3, p. 587, doi. 10.1111/jog.15156

By:

Turgut, Ezgi;
Yildirim, Muradiye;
Sakcak, Bedri;
Ayhan, Sule G.;
Tekin, Ozlem M.;
Sahin, Dilek

Publication type:

Article

First Study in Men Evaluating a Surgical Robotic Tool Providing Autonomous Inner Ear Access for Cochlear Implantation.

Published in:

Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.804507

By:

Topsakal, Vedat;
Heuninck, Emilie;
Matulic, Marco;
Tekin, Ahmet M.;
Mertens, Griet;
Van Rompaey, Vincent;
Galeazzi, Pablo;
Zoka-Assadi, Masoud;
van de Heyning, Paul

Publication type:

Article

A Bibliometric Analysis of Publications on Tinnitus: A Study Based on Web of Science Data From 1980 to 2020.

Published in:

Journal of International Advanced Otology, 2023, v. 19, n. 2, p. 121, doi. 10.5152/iao.2023.22082

By:

Yaz, Furkan;
Büttner, Michael;
Tekin, Ahmet M.;
Bahşi, İlhan;
Topsakal, Vedat

Publication type:

Article

Global Research on Hereditary Hearing Impairment Over the Last 40 Years: A Bibliometric Study.

Published in:

Journal of International Advanced Otology, 2021, v. 17, n. 6, p. 482, doi. 10.5152/iao.2021.21276

By:

Tekin, Ahmet M.;
Bahşi, İlhan;
Bayazit, Yıldırım A.;
Topsakal, Vedat

Publication type:

Article

Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss.

Published in:

Journal of the European Academy of Dermatology & Venereology, 2022, v. 36, n. 9, p. 1606, doi. 10.1111/jdv.18207

By:

Vona, B.;
Schwartzbaum, D.A.;
Rodriguez, A.A.;
Lewis, S.S.;
Toosi, M.B.;
Radhakrishnan, P.;
Bozan, N.;
Akın, R.;
Doosti, M.;
Manju, R.;
Duman, D.;
Sineni, C.J.;
Nampoothiri, S.;
Karimiani, E.G.;
Houlden, H.;
Bademci, G.;
Tekin, M.;
Girisha, K.M.;
Maroofian, R.;
Douzgou, S.

Publication type:

Article

What is the Diagnostic Role of Adenoid Hypertrophy and Adult-Onset Otitis Media with Effusion in Clinically Asymptomatic Nasopharyngeal Carcinoma?

Published in:

West Indian Medical Journal, 2024, v. 71, n. 1, p. 19, doi. 10.7727/wimj.2017.098

By:

Ozdamar, O. I.;
Acar, G. O.;
Tekin, M.

Publication type:

Article

Effects of spinal anesthesia and laryngeal mask anesthesia on mood states during hemorrhoidectomy.

Published in:

2007

By:

Kisli E;
Agargun MY;
Tekin M;
Selvi Y;
Karaayvaz M;
Kisli, Erol;
Agargun, M Yucel;
Tekin, Murat;
Selvi, Yavuz;
Karaayvaz, Muammer

Publication type:

journal article

A rare ANOS1 variant in siblings with Kallmann syndrome identified by whole exome sequencing.

Published in:

Andrology, 2018, v. 6, n. 1, p. 53, doi. 10.1111/andr.12432

By:

Lopategui, D. M.;
Griswold, A. J.;
Arora, H.;
Clavijo, R. I.;
Tekin, M.;
Ramasamy, R.

Publication type:

Article

Variants in <italic>CIB2</italic> cause DFNB48 and not USH1J.

Published in:

Clinical Genetics, 2018, v. 93, n. 4, p. 812, doi. 10.1111/cge.13170

By:

Booth, K. T.;
Kahrizi, K.;
Babanejad, M.;
Daghagh, H.;
Bademci, G.;
Arzhangi, S.;
Zareabdollahi, D.;
Duman, D.;
El‐amraoui, A.;
Tekin, M.;
Najmabadi, H.;
Azaiez, H.;
Smith, R. J.

Publication type:

Article

A Mayan founder mutation is a common cause of deafness in Guatemala.

Published in:

Clinical Genetics, 2016, v. 89, n. 4, p. 461, doi. 10.1111/cge.12676

By:

Carranza, C.;
Menendez, I.;
Herrera, M.;
Castellanos, P.;
Amado, C.;
Maldonado, F.;
Rosales, L.;
Escobar, N.;
Guerra, M.;
Alvarez, D.;
Foster, J.;
Guo, S.;
Blanton, S.H.;
Bademci, G.;
Tekin, M.

Publication type:

Article

A homozygous SIX6 mutation is associated with optic disc anomalies and macular atrophy and reduces retinal ganglion cell differentiation.

Published in:

Clinical Genetics, 2015, v. 87, n. 2, p. 192, doi. 10.1111/cge.12374

By:

Yariz, K.O.;
Sakalar, Y.B.;
Jin, X.;
Hertz, J.;
Sener, E.F.;
Akay, H.;
Özbek, M.N.;
Farooq, A.;
Goldberg, J.;
Tekin, M.

Publication type:

Article

Comprehensive genetic testing can save lives in hereditary hearing loss.

Published in:

Clinical Genetics, 2015, v. 87, n. 2, p. 190, doi. 10.1111/cge.12376

By:

Tekin, D.;
Tutar, E.;
Ozturkmen Akay, H.;
Blanton, S.;
Foster, J.;
Tekin, M.

Publication type:

Article

Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction.

Published in:

Clinical Genetics, 2014, v. 86, n. 6, p. 589, doi. 10.1111/cge.12321

By:

Foster, J.;
Kapoor, S.;
Diaz‐Horta, O.;
Singh, A.;
Abad, C.;
Rastogi, A.;
Moharana, R.;
Tekeli, O.;
Walz, K.;
Tekin, M.

Publication type:

Article

Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290.

Published in:

Clinical Genetics, 2014, v. 86, n. 4, p. 387, doi. 10.1111/cge.12296

By:

Ghaffari, S.R.;
Rafati, M.;
Ghaffari, G.;
Morra, M.;
Tekin, M.

Publication type:

Article

A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss.

Published in:

Clinical Genetics, 2012, v. 81, n. 3, p. 289, doi. 10.1111/j.1399-0004.2011.01654.x

By:

Yariz, KO;
Walsh, T;
Akay, H;
Duman, D;
Akkaynak, AC;
King, M-C;
Tekin, M

Publication type:

Article

Are blood pressure values compatible with medication adherence in hypertensive patients?

Published in:

Nigerian Journal of Clinical Practice, 2016, v. 19, n. 4, p. 460, doi. 10.4103/1119-3077.180060

By:

Uludag, A.;
Sahin, E. M.;
Agaoglu, H.;
Gungor, S.;
Ertekin, Y. H.;
Tekin, M.

Publication type:

Article

Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients.

Published in:

QJM: An International Journal of Medicine, 2000, v. 93, n. 10, p. 681

By:

Yalçinkaya, F.;
Tekİn, M.;
Çakar, N.;
Akar, E.;
Akar, N.;
Tümer, N.

Publication type:

Article

Development and comparative analysis of a pure fuel cell configuration for a light commercial vehicle.

Published in:

International Journal of Environmental Science & Technology (IJEST), 2023, v. 20, n. 6, p. 6197, doi. 10.1007/s13762-022-04629-3

By:

Tekin, M.;
Karamangil, M. İ.

Publication type:

Article

Evaluation of the academic productivity of the top 100 worldwide physicians in the field of otorhinolaryngology and head and neck surgery using the Google Scholar h-index as the bibliometrics ranking system.

Published in:

Journal of Laryngology & Otology, 2018, v. 132, n. 12, p. 1097, doi. 10.1017/S0022215118002190

By:

Kalcioglu, M T;
Ileri, Y;
Ozdamar, O I;
Yilmaz, U;
Tekin, M

Publication type:

Article

A comparative study of protein and free amino acid contents in some important ancient wheat lines.

Published in:

Quality Assurance & Safety of Crops & Foods, 2019, v. 11, n. 2, p. 191, doi. 10.3920/QAS2018.1382

By:

Akar, T.;
Cengiz, M. F.;
Tekin, M.

Publication type:

Article

Evaluation of a Less Invasive Cochlear Implant Surgery in OPA1 Mutations Provoking Deafblindness.

Published in:

Genes, 2023, v. 14, n. 3, p. 627, doi. 10.3390/genes14030627

By:

Tekin, Ahmet M.;
Baelen, Hermine;
Heuninck, Emilie;
Bayazıt, Yıldırım A.;
Mertens, Griet;
Rompaey, Vincent van;
Heyning, Paul van de;
Topsakal, Vedat

Publication type:

Article

A New Pathogenic Variant in POU3F4 Causing Deafness Due to an Incomplete Partition of the Cochlea Paved the Way for Innovative Surgery.

Published in:

Genes, 2021, v. 12, n. 5, p. 613, doi. 10.3390/genes12050613

By:

Tekin, Ahmet M.;
Matulic, Marco;
Wuyts, Wim;
Assadi, Masoud Zoka;
Mertens, Griet;
Rompaey, Vincent van;
Li, Yongxin;
Heyning, Paul van de;
Topsakal, Vedat;
Ophoff, Roel;
Schrauwen, Isabelle

Publication type:

Article

Percutaneous Management of Ulcerative Glandular Hypervascularization after Virag-I Operation.

Published in:

Urologia Internationalis, 2001, v. 66, n. 1, p. 38, doi. 10.1159/000056562

By:

Peskircioglu, Levent;
Tekin, M. Ilteris;
Boyvat, Fatih;
Özkardes, Hakan

Publication type:

Article

Clinical observations. Familial Mediterranean fever - renal involvement by diseases other than amyloid.

Published in:

Nephrology Dialysis Transplantation, 1999, v. 14, n. 2, p. 475, doi. 10.1093/ndt/14.2.475

By:

Tekin, M;
Yalçinkaya, F;
Tümer, N;
Çakar, N;
Koçak, H;
Özkaya, N;
Gençgönül, H

Publication type:

Article

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome.

Published in:

2008

By:

Ergür AT;
Öcur G;
Berberoglu M;
Tekin M;
Kiliç BG;
Aycan Z;
Kutlu A;
Adiyaman P;
Siklar Z;
Akar N;
Sahin A;
Akçayöz D

Publication type:

Journal Article

A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia.

Published in:

Clinical Genetics, 2009, v. 75, n. 6, p. 562, doi. 10.1111/j.1399-0004.2009.01183.x

By:

Sırmac, A.;
Öztürkmen-Akay, H.;
Erbek, S.;
İncesulu, A.;
Duman, D.;
Taşır-Yılmaz, S;
Özda, H.;
Tekin, M.

Publication type:

Article

Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia.

Published in:

Clinical Genetics, 2008, v. 73, n. 6, p. 554, doi. 10.1111/j.1399-0004.2008.01004.x

By:

Tekin, M.;
Akay, H. Öztürkmen;
Fitoz, S.;
Birnbaum, S.;
Cengiz, F. B.;
Sennaroğlu, L.;
İncesulu, A.;
Konuk, E. B. Yüksel;
Bayrak, A. Hasanefendioğlu;
Şentürk, S.;
Cebeci, İ;
Ütine, G. E.;
Tunçbilek, E.;
Nance, W. E.;
Duman, D.

Publication type:

Article

Evidence for single origins of 35delG and delE120 mutations in theGJB2gene in Anatolia.

Published in:

Clinical Genetics, 2005, v. 67, n. 1, p. 31, doi. 10.1111/j.1399-0004.2004.00334.x

By:

Tekin, M.;
Bo&gcaron;oclu, G;
Arican, S. T.;
Orman, M. N.;
Tastan, H.;
Elsayed, S.;
Akar, N.

Publication type:

Article

Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.

Published in:

Clinical Genetics, 2003, v. 64, n. 4, p. 371, doi. 10.1034/j.1399-0004.2003.00144.x

By:

Tekin, M;
Akçayöz, D;
Çomak, E;
Boğoçlu, G;
Duman, T;
Fitoz, S;
İlhan, İ;
Akar, N

Publication type:

Article

657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.

Published in:

Clinical Genetics, 2002, v. 62, n. 1, p. 84, doi. 10.1034/j.1399-0004.2002.620112.x

By:

Tekin, M;
Doğu, F;
Taçyıldız, N;
Akar, E;
İkincioğullari, A;
Oğur, G;
Yavuz, G;
Babacan, E;
Akar, N

Publication type:

Article

Waardenburg syndrome type 3 (Klein–Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?

Published in:

Clinical Genetics, 2001, v. 60, n. 4, p. 301, doi. 10.1034/j.1399-0004.2001.600408.x

By:

Tekin, M;
Bodurtha, JN;
Nance, WE;
Pandya, A

Publication type:

Article

W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness.

Published in:

Clinical Genetics, 2001, v. 59, n. 4, p. 269, doi. 10.1034/j.1399-0004.2001.590409.x

By:

Tekin, M.;
Amos, K. S.;
Xia, X. J.;
Oelrich, M. K.;
Liu, X. Z.;
Nance, W. E.;
Pandya, A.

Publication type:

Article

Experimental analysis of the volumetric and thermal efficiency performance of a novel direct piezo-acting CVVT mechanism.

Published in:

International Journal of Green Energy, 2024, v. 21, n. 5, p. 948, doi. 10.1080/15435075.2023.2226265

By:

Sürmen, A.;
Karamangil, M.I;
Avcı, A;
Dirim, B.;
Işıklı, F.;
Tekin, M.;
Türköz, N.

Publication type:

Article

A New Pathogenic Variant in the TRIOBP Associated with Profound Deafness Is Remediable with Cochlear Implantation.

Published in:

2021

By:

Tekin, Ahmet M.;
de Ceulaer, Geert;
Govaerts, Paul;
Bayazit, Yıldırım;
Wuyts, Wim;
Van de Heyning, Paul;
Topsakal, Vedat

Publication type:

journal article

Possibility of an Information System on Plants of South-West Asia with Particular Reference to the Turkish Plants Data Service (TUBIVES).

Published in:

Turkish Journal of Botany, 2004, v. 28, n. 1/2, p. 119

By:

Babaç, M. Tekin

Publication type:

Article

Protective effect of glucagon-like peptide-2 in experimental corrosive esophagitis.

Published in:

Diseases of the Esophagus, 2015, v. 28, n. 3, p. 258, doi. 10.1111/dote.12195

By:

Tekin, M.;
Topaloğlu, N.;
Küçük, A.;
Deniz, M.;
Yıldırım, Ş.;
Erdem, H.

Publication type:

Article

Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey.

Published in:

2003

By:

Tekin, M.;
Duman, T.;
Boğoçlu, G.;
İncesulu, A.;
Çomak, E.;
Fitoz, S.;
Yilmaz, E.;
İlhan, İ.;
Akar, N.;
Boğoçlu, G;
Incesulu, A;
Comak, E;
Ilhan, I;
İncesulu, A;
Yılmaz, E;
İlhan, I

Publication type:

journal article

A 17-month-old with extreme prenatal-onset growth delay. Microcephalic osteodysplastic primordial dwarfism type II.

Published in:

2000

By:

Tekin, Mustafa;
Ng, Janice;
Bodurtha, Joann;
Tekin, M;
Ng, J;
Bodurtha, J

Publication type:

journal article

Tulipa koyuncui Eker & Babaç sp. nov. (Liliaceae) from east Anatolia, Turkey.

Published in:

Nordic Journal of Botany, 2010, v. 28, n. 3, p. 324, doi. 10.1111/j.1756-1051.2009.00591.x

By:

Eker, İsmail;
Babaç, M. Tekin

Publication type:

Article

Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis.

Published in:

2000

By:

Tekin, M;
Yalçınkaya, F;
Tümer, N;
Akar, N;
Mısırlıoğlu, M;
Çakar, N;
Yalçinkaya, F;
Tümer, N;
Misirlioğlu, M;
Cakar, N

Publication type:

journal article

TRIPLE ORAL ANTIDIABETIC OR METFORMIN-BASAL INSULIN COMBINATION: TESTING TWO DIFFERENT APPROACHES OF CONSENSUS ALGORITHM IN ADJUSTING ANTIDIABETIC THERAPY. AN OPEN-LABEL, RANDOMIZED STUDY.

Published in:

Acta Endocrinologica (1841-0987), 2012, v. 8, n. 4, p. 587, doi. 10.4183/aeb.2012.587

By:

Mesci, B.;
Oguz, A.;
Coksert Kilic, D.;
Celik, S.;
Sahin, G.;
Tekin, M.;
Sariisik, A.;
Koroglu, G.;
Takir, M.;
Sagun, G.;
Tamer, G.

Publication type:

Article

REFINED CARBOHYDRATE RESTRICTED DIET VERSUS CONVENTIONAL DIABETIC DIET IN TYPE 2 DIABETIC PATIENTS TREATED BY INSULIN.

Published in:

Acta Endocrinologica (1841-0987), 2010, v. 6, n. 2, p. 203, doi. 10.4183/aeb.2010.203

By:

Mesci, B.;
Celik, S.;
Kilic, D. Coksert;
Tekin, M.;
Oguz, A.

Publication type:

Article

Ureteroscopic Treatment of Proximal Ureter Stones with the Aid of an Antegrade Occlusion Balloon Catheter.

Published in:

Acta Radiologica, 2006, v. 47, n. 1, p. 103, doi. 10.1080/02841850500335028

By:

Dİrİm, A.;
Tekİn, M. I.;
Aytekİn, C.;
Peskİrcİoglu, L.;
Boyvat, F.;
Ozkardes, H.

Publication type:

Article

More than 40 years of cochlear implant research: A bibliometric analysis.

Published in:

Cochlear Implants International: An Interdisciplinary Journal, 2024, v. 25, n. 3, p. 222, doi. 10.1080/14670100.2024.2330793

By:

Abari, Jaouad;
Tekin, Ahmet M.;
Bahşi, Ilhan;
Topsakal, Vedat

Publication type:

Article

Evaluation of Surface Properties of Four Tooth-Colored Restorative Materials.

Published in:

Acta Physica Polonica: A, 2015, v. 128, n. 2B, p. B-310, doi. 10.12693/APhysPolA.128.B-310

By:

ARSLANOGLU, Z.;
ALTAN, H.;
SAHIN, O.;
TEKIN, M. G.;
ADIGÜZEL, M.

Publication type:

Article

The Effect of the Grain Parameters on the Characterization of Polycrystalline CuS Films.

Published in:

Arabian Journal for Science & Engineering (Springer Science & Business Media B.V. ), 2013, v. 38, n. 7, p. 1895, doi. 10.1007/s13369-012-0392-1

By:

Bedir, M.;
Öztaş, M.;
Tekin, M.

Publication type:

Article

Protracted arthritis of familial Mediterranean fever (an unusual complication).

Published in:

British Journal of Rheumatology, 1997, v. 36, n. 11, p. 1228

By:

YalÃ§inkaya, F;
Tekin, M;
TÃ¼mer, N;
Ozkaya, N

Publication type:

Article

The Effect of p.Arg25Cys Alteration in NKX2-5 on Conotruncal Heart Anomalies: Mutation or Polymorphism?

Published in:

Pediatric Cardiology, 2008, v. 29, n. 1, p. 126, doi. 10.1007/s00246-007-9058-2

By:

Akçaboy, M. İ.;
Cengiz, F. B.;
İnceoğlu, B.;
Uçar, T.;
Atalay, S.;
Tutar, E.;
Tekin, M.

Publication type:

Article

Bilateral Coronary Artery Dilatation and Supravalvular Pulmonary Stenosis in a Child with Noonan Syndrome.

Published in:

Pediatric Cardiology, 2005, v. 26, n. 6, p. 848, doi. 10.1007/s00246-005-0935-2

By:

Uçar, T.;
Atalay, S.;
Tekin, M.;
Tutar, E.

Publication type:

Article

Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation.

Published in:

British Journal of Dermatology, 2011, v. 165, n. 4, p. 917, doi. 10.1111/j.1365-2133.2011.10455.x

By:

Erken, H.;
Yariz, K.O.;
Duman, D.;
Kaya, C.T.;
Sayin, T.;
Heper, A.O.;
Tekin, M.

Publication type:

Article