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Published in Journal of medical genetics (01.10.2009)
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Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
Stover, E H, Borthwick, K J, Bavalia, C, Eady, N, Fritz, D M, Rungroj, N, Giersch, A B S, Morton, C C, Axon, P R, Akil, I, Al-Sabban, E A, Baguley, D M, Bianca, S, Bakkaloglu, A, Bircan, Z, Chauveau, D, Clermont, M-J, Guala, A, Hulton, S A, Kroes, H, Li Volti, G, Mir, S, Mocan, H, Nayir, A, Ozen, S, Rodriguez Soriano, J, Sanjad, S A, Tasic, V, Taylor, C M, Topaloglu, R, Smith, A N, Karet, F E
Published in Journal of medical genetics (01.11.2002)
Published in Journal of medical genetics (01.11.2002)
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Mutations in the Chloride-Bicarbonate Exchanger Gene AE1 Cause Autosomal Dominant but not Autosomal Recessive Distal Renal Tubular Acidosis
Karet, F. E., Gainza, F. J., Gyory, A. Z., Unwin, R. J., Wrong, O., Tanner, M. J. A., Nayir, A., Alpay, H., Santos, F., Hulton, S. A., Bakkaloglu, A., Ozen, S., Cunningham, M. J., Di Pietro, A., Walker, W. G., Lifton, R. P.
Published in Proceedings of the National Academy of Sciences - PNAS (26.05.1998)
Published in Proceedings of the National Academy of Sciences - PNAS (26.05.1998)
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What Has Changed in Pediatric Kidney Transplantation in Turkey? Experience of an Evolving Center
Arpali, E, Kocak, B, Karatas, C, Kanmaz, T, Nayir, A, Kalayoğlu, M
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Published in Transplantation proceedings (01.04.2013)
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Methods of Improving Superconductive Fault Current Limiting Devices in Power Engineering
Hashimov, A. M., Nayir, Ahmet, Kazimov, S. A., Bondyakov, A. S., Hasanova, S. I.
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Published in Elektronika ir elektrotechnika (01.01.2013)
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Frequency of renal malformations in turner syndrome: analysis of 82 Turkish children
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Published in Pediatric nephrology (Berlin, West) (01.10.2000)
Published in Pediatric nephrology (Berlin, West) (01.10.2000)
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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome
Sadowski, Carolin E, Lovric, Svjetlana, Ashraf, Shazia, Pabst, Werner L, Gee, Heon Yung, Kohl, Stefan, Engelmann, Susanne, Vega-Warner, Virginia, Fang, Humphrey, Halbritter, Jan, Somers, Michael J, Tan, Weizhen, Shril, Shirlee, Fessi, Inès, Lifton, Richard P, Bockenhauer, Detlef, El-Desoky, Sherif, Kari, Jameela A, Zenker, Martin, Kemper, Markus J, Mueller, Dominik, Fathy, Hanan M, Soliman, Neveen A, Hildebrandt, Friedhelm
Published in Journal of the American Society of Nephrology (01.06.2015)
Published in Journal of the American Society of Nephrology (01.06.2015)
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Isolated cerebellar involvement in a case of posterior reversible leukoencephalopathy
Soysal, D.D., Caliskan, M., Aydin, K., Nayir, A., Karaböcüoglu, M., Çitak, A., Uzel, N.
Published in Clinical radiology (01.11.2006)
Published in Clinical radiology (01.11.2006)
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Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
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Published in Journal of medical genetics (01.02.2011)
Published in Journal of medical genetics (01.02.2011)
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Hemostatic problems and thromboembolic complications in nephrotic children
CITAK, A, EMRE, S, SIRIN, A, BILGE, I, NAYIR, A
Published in Pediatric nephrology (Berlin, West) (01.02.2000)
Published in Pediatric nephrology (Berlin, West) (01.02.2000)
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Haemoperfusion in Amanita phalloides poisoning
Aji, D Y, Calişkan, S, Nayir, A, Mat, A, Can, B, Yaşar, Z, Ozşahin, H, Cullu, F, Sever, L
Published in Journal of tropical pediatrics (1980) (01.12.1995)
Published in Journal of tropical pediatrics (1980) (01.12.1995)
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The gene mutated in juvenile nephronophthisis type 4 encodes a novel protein that interacts with nephrocystin
Salomon, Rémi, Bacq, Delphine, Landthaler, Gilbert, Gribouval, Olivier, Silbermann, Flora, Antignac, Corinne, Milford, David, Mollet, Géraldine, Nayir, Ahmet, Rizzoni, Gianfranco, Saunier, Sophie
Published in Nature genetics (01.10.2002)
Published in Nature genetics (01.10.2002)
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Mutations in ATP6N1B , encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing
Karet, Fiona E, Smith, Annabel N, Skaug, Jennifer, Choate, Keith A, Nayir, Ahmet, Bakkaloglu, Aysin, Ozen, Seza, Hulton, Sally A, Sanjad, Sami A, Al-Sabban, Essam A, Lifton, Richard P, Scherer, Stephen W
Published in Nature genetics (01.09.2000)
Published in Nature genetics (01.09.2000)
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Mutations in the gene encoding B1 subunit of H + -ATPase cause renal tubular acidosis with sensorineural deafness
Lifton, Richard P, Karet, Fiona E, Finberg, Karin E, Nelson, Raoul D, Nayir, Ahmet, Mocan, Hilal, Sanjad, Sami A, Rodriguez-Soriano, Juan, Santos, Fernando, Cremers, Cor W.R.J, Pietro, Antonio Di, Hoffbrand, Barry I, Winiarski, Jacek, Bakkaloglu, Aysin, Ozen, Seza, Dusunsel, Ruhan, Goodyer, Paul, Hulton, Sally A, Wu, Doris K, Skvorak, Anne B, Morton, Cynthia C, Cunningham, Michael J, Jha, Vivekanand
Published in Nature genetics (01.01.1999)
Published in Nature genetics (01.01.1999)
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Follow-up results of synthetic vascular grafts in children undergoing hemodialysis
Nayir, A, Sönmez, Y, Sirin, A, Emre, S, Aydoğan, U
Published in Turkish journal of pediatrics (01.07.1995)
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Published in Turkish journal of pediatrics (01.07.1995)
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