Works matching AU Bademci, G.

Results: 9

Extremely delayed renal cell carcinoma metastasis mimicking convexity meningioma.

Published in:

Neurocirugía, 2008, v. 19, n. 6, p. 562, doi. 10.4321/S1130-14732008000600008

By:

Bademci, G.;
Bozdogan, O.;
Berdan, F.;
Evliyaoglu, C.

Publication type:

Article

Can facet joint infiltrative analgesia reduce postoperative pain in degenerative lumbar disc surgery?

Published in:

Neurocirugía, 2008, v. 19, n. 1, p. 45, doi. 10.1016/S1130-1473(08)70248-3

By:

Bademci, G.;
Basar, H.;
Sahin, S.;
Ozcakir, S.;
Anbarci, H.;
Evliyaoglu, C.;
Keskil, S.

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

Case report. Tuberculosis of the skull in patient on maintenance haemodialysis.

Published in:

Nephrology Dialysis Transplantation, 1999, v. 14, n. 8, p. 2019, doi. 10.1093/ndt/14.8.2019

By:

Nergizoglu, G;
Duman, N;
Ertürk, S;
Keven, K;
Ates, K;
Akar, H;
Bademci, G;
Berk, Ç;
Erekul, S;
Erbay, B;
Karatan, O;
Ertug, AE

Publication type:

Article

Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss.

Published in:

Scientific Reports, 2016, p. 31622, doi. 10.1038/srep31622

By:

Bademci, G.;
Cengiz, F. B.;
Foster II, J.;
Duman, D.;
Sennaroglu, L.;
Diaz-Horta, O.;
Atik, T.;
Kirazli, T.;
Olgun, L.;
Alper, H.;
Menendez, I.;
Loclar, I.;
Sennaroglu, G.;
Tokgoz-Yilmaz, S.;
Guo, S.;
Olgun, Y.;
Mahdieh, N.;
Bonyadi, M.;
Bozan, N.;
Ayral, A.

Publication type:

Article

Exploring the relationship between the severity of oligozoospermia and the frequencies of sperm chromosome aneuploidies.

Published in:

Andrologia, 2012, v. 44, n. 6, p. 416, doi. 10.1111/j.1439-0272.2012.01298.x

By:

Durak Aras, B.;
Aras, I.;
Can, C.;
Toprak, C.;
Dikoglu, E.;
Bademci, G.;
Ozdemir, M.;
Cilingir, O.;
Artan, S.

Publication type:

Article

A novel mutation in the ARS (component B) gene encoding SLURP-1 in a Turkish family with mal de Meleda.

Published in:

British Journal of Dermatology, 2006, v. 155, n. 2, p. 467, doi. 10.1111/j.1365-2133.2006.07288.x

By:

Muslumanoglu, M. H.;
Sarcoglu, N.;
Cilingir, O.;
Basmaci, T.;
Urer, S .;
Sabuncu, I .;
Demir, S .;
Bademci, G.;
Artan, S .

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