Mucopolysaccharidosis: Otolaryngologic findings, obstructive sleep apnea and accumulation of glucosaminoglycans in lymphatic tissue of the upper airway by Gönüldaş, Burhanettin, Yılmaz, Taner, Sivri, H. Serap, Güçer, K. Şafak, Kılınç, Kamer, Genç, G. Aydan, Kılıç, Mustafa, Coşkun, Turgay

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Response to Early Coenzyme Q10 Supplementation Is not Sustained in CoQ10 Deficiency Caused by CoQ2 Mutation by Eroglu, Fehime K., Ozaltin, Fatih, Gönç, Nazlı, Nalçacıoğlu, Hülya, Özçakar, Z. Birsin, Yalnızoğlu, Dilek, Güçer, Şafak, Orhan, Diclehan, Eminoğlu, Fatma Tuba, Göçmen, Rahşan, Alikaşifoğlu, Ayfer, Topaloğlu, Rezan, Düzova, Ali

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Erratum to ‘Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation’ [Pediatric Neurology 88 (2018) 71–74] by Eroglu, Fehime K., Ozaltin, Fatih, Gönç, Nazli, Nalçacıoğlu, Hülya, Özçakar, Z. Birsin, Yalnızoğlu, Dilek, Güçer, Şafak, Orhan, Diclehan, Eminoğlu, Fatma Tuba, Göçmen, Rahşan, Alikaşifoğlu, Ayfer, Topaloğlu, Rezan, Düzova, Ali

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Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency by Olsen, Rikke K.J., Koňaříková, Eliška, Giancaspero, Teresa A., Mosegaard, Signe, Boczonadi, Veronika, Mataković, Lavinija, Veauville-Merllié, Alice, Terrile, Caterina, Schwarzmayr, Thomas, Haack, Tobias B., Auranen, Mari, Leone, Piero, Galluccio, Michele, Imbard, Apolline, Gutierrez-Rios, Purificacion, Palmfeldt, Johan, Graf, Elisabeth, Vianey-Saban, Christine, Oppenheim, Marcus, Schiff, Manuel, Pichard, Samia, Rigal, Odile, Pyle, Angela, Chinnery, Patrick F., Konstantopoulou, Vassiliki, Möslinger, Dorothea, Feichtinger, René G., Talim, Beril, Topaloglu, Haluk, Coskun, Turgay, Gucer, Safak, Botta, Annalisa, Pegoraro, Elena, Malena, Adriana, Vergani, Lodovica, Mazzà, Daniela, Zollino, Marcella, Ghezzi, Daniele, Acquaviva, Cecile, Tyni, Tiina, Boneh, Avihu, Meitinger, Thomas, Strom, Tim M., Gregersen, Niels, Mayr, Johannes A., Horvath, Rita, Barile, Maria, Prokisch, Holger

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Erratum to 'Response to early coenzyme Q10 supplementation is not sustained in CoQ10 deficiency caused by CoQ2 mutation' PNU 88C (2018) 71-74 by Eroglu, Fehime K, Ozaltin, Fatih, Gönç, Nazli, Nalçacıoğlu, Hülya, Özçakar, Z Birsin, Yalnızoğlu, Dilek, Güçer, Şafak, Orhan, Diclehan, Eminoğlu, Fatma Tuba, Göçmen, Rahşan, Alikaşifoğlu, Ayfer, Topaloğlu, Rezan, Düzova, Ali

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ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS by Korkmaz, Emine, Lipska-Ziętkiewicz, Beata S, Boyer, Olivia, Gribouval, Olivier, Fourrage, Cecile, Tabatabaei, Mansoureh, Schnaidt, Sven, Gucer, Safak, Kaymaz, Figen, Arici, Mustafa, Dinckan, Ayhan, Mir, Sevgi, Bayazit, Aysun K, Emre, Sevinc, Balat, Ayse, Rees, Lesley, Shroff, Rukshana, Bergmann, Carsten, Mourani, Chebl, Antignac, Corinne, Ozaltin, Fatih, Schaefer, Franz

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MEFV gene mutations in familial Mediterranean fever phenotype II patients with renal amyloidosis in childhood: a retrospective clinicopathological and molecular study by Balci, Banu, Tinaztepe, Keriman, Yilmaz, Engin, Guçer, Şafak, Ozen, Seza, Topaloğlu, Rezan, Beşbaş, Nesrin, Ozguç, Meral, Bakkaloğlu, Ayşin

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Successful renal transplantation in a child with ANCA-associated microscopic polyangiitis by BESBAS, Nesrin, OZALTIN, Fatih, TINAZTEPE, Keriman, GÜCER, Safak, OZEN, Seza, BAKKALOGLU, Mehmet, BAKKALOGLU, Aysin

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Hepatitis-B virus associated nephropathies: a clinicopathological study in 14 children by OZDAMAR, Sukru O, GUCER, Safak, TINAZTEPE, Keriman

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