Incidence, treatment method and recurrence rate in giant cell granulomas: Retrospective study von Ari, Ilgin, Adiloglu, Selen, Aktas, Alper, Yasan, Göknur Topaloglu, Usman, Ecem, Aksoy, Sena

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Evaluation of clinical signs and magnetic resonance imaging findings in patients with temporomandibular disorders von Topaloglu Yasan, Goknur, Adiloglu, Selen, Tuz, Hakan H., Sahar, Dilek

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Retrospective evaluation of pathologic fractures in medication related osteonecrosis of the jaw von Topaloglu Yasan, Goknur, Adiloglu, Selen, Koseoglu, Osman Taha

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The effect of drug holiday before tooth extraction on the development of medication-related osteonecrosis of the jaw in cancer patients receiving intravenous bisphosphonates von Çiğdem Karaca, Göknur Topaloğlu-Yasan, Selen Adiloğlu, Ecem Usman

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The effect of chronic dental inflammation on development of stage 0 medication-related osteonecrosis of the jaw von Topaloglu, Goknur, Koseoglu, Osman Taha, Karaca, Cigdem, Kosemehmetoglu, Kemal

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Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families von Kolkiran, Abdulkerim, Şimşek-Kiper, Pelin Özlem, Topaloğlu Yasan, Göknur, Karaosmanoğlu, Beren, Taşkıran, Ekim, Utine, Gülen Eda, Tüz, Hakan H., Boduroğlu, Koray

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The effect of drug holiday before tooth extraction on the development of medication-related osteonecrosis of the jaw in cancer patients receiving intravenous bisphosphonates von Karaca, Çiğdem, Topaloğlu-Yasan, Göknur, Adiloğlu, Selen, Usman, Ecem

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Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defects von Haliloglu, Goknur, Becker, Kerstin, Temucin, Cagri, Talim, Beril, Küçükşahin, Nalan, Pergande, Matthias, Motameny, Susanne, Nürnberg, Peter, Aydingoz, Ustun, Topaloglu, Haluk, Cirak, Sebahattin

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Evidence-based guideline summary: Evaluation, diagnosis, and management of congenital muscular dystrophy: Report of the Guideline Development Subcommittee of the American Academy o... von Haliloglu, Goknur, Topaloglu, Haluk

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Clinical features, muscle biopsy scores, myositis specific antibody profiles and outcome in juvenile dermatomyositis von Sag, Erdal, Demir, Selcan, Bilginer, Yelda, Talim, Beril, Haliloglu, Goknur, Topaloglu, Haluk, Ozen, Seza

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Inflammatory milieu of muscle biopsies in juvenile dermatomyositis von Sag, Erdal, Kale, Gulsev, Haliloglu, Goknur, Bilginer, Yelda, Akcoren, Zuhal, Orhan, Diclehan, Gucer, Safak, Topaloglu, Haluk, Ozen, Seza, Talim, Beril

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Diagnosis of Duchenne muscular dystrophy in Italy in the last decade: Critical issues and areas for improvements von Haliloglu, Goknur, Karaduman, Ayşe, Topaloglu, Haluk

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Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency von Yıldız, Yılmaz, Talim, Beril, Haliloglu, Goknur, Topaloglu, Haluk, Akçören, Zuhal, Dursun, Ali, Sivri, Hatice Serap, Coşkun, Turgay, Tokatlı, Ayşegül

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Clinical characteristics of megaconial congenital muscular dystrophy due to choline kinase beta gene defects in a series of 15 patients von Haliloglu, Goknur, Talim, Beril, Sel, Cigdem Genc, Topaloglu, Haluk

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The genomic and clinical landscape of fetal akinesia von Pergande, Matthias, Motameny, Susanne, Özdemir, Özkan, Kreutzer, Mona, Wang, Haicui, Daimagüler, Hülya-Sevcan, Becker, Kerstin, Karakaya, Mert, Ehrhardt, Harald, Elcioglu, Nursel, Ostojic, Slavica, Chao, Cho-Ming, Kawalia, Amit, Duman, Özgür, Koy, Anne, Hahn, Andreas, Reimann, Jens, Schoner, Katharina, Schänzer, Anne, Westhoff, Jens H., Schwaibold, Eva Maria Christina, Cossee, Mireille, Imbert-Bouteille, Marion, von Pein, Harald, Haliloglu, Göknur, Topaloglu, Haluk, Altmüller, Janine, Nürnberg, Peter, Thiele, Holger, Heller, Raoul, Cirak, Sebahattin

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Congenital mirror movements in a patient with alpha-dystroglycanopathy due to a novel POMK mutation von Ardicli, Didem, Gocmen, Rahsan, Talim, Beril, Sprute, Rosanne, Haliloglu, Goknur, Cirak, Sebahattin, Topaloglu, Haluk

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Evaluation and follow-up of patients diagnosed with hypophysitis: a cohort study von Hacioglu, Aysa, Karaca, Zuleyha, Uysal, Serhat, Ozkaya, Hande Mefkure, Kadioglu, Pınar, Selcukbiricik, Ozlem Soyluk, Gul, Nurdan, Yarman, Sema, Koksalan, Damla, Selek, Alev, Canturk, Zeynep, Cetinarslan, Berrin, Corapcioglu, Demet, Sahin, Mustafa, Sah Unal, Fatma Tugce, Babayeva, Afruz, Akturk, Mujde, Ciftci, Sema, Piskinpasa, Hamide, Dokmetas, Hatice Sebile, Dokmetas, Meric, Sahin, Onur, Eraydın, Ayten, Fenkci, Semin, Ozturk, Sadettin, Akarsu, Ersin, Omma, Tulay, Erkan, Buruc, Burhan, Sebnem, Pehlivan Koroglu, Esma, Saygili, Fusun, Kilic Kan, Elif, Atmaca, Aysegul, Elbuken, Gulsah, Alphan Uc, Ziynet, Gorar, Suheyla, Hekimsoy, Zeliha, Pekkolay, Zafer, Bostan, Hayri, Bayram, Fahri, Yorulmaz, Goknur, Sener, Selcuk Yusuf, Turan, Kubra, Celik, Ozlem, Dogruel, Hakan, Ertorer, Eda, Turhan Iyidir, Ozlem, Topaloglu, Omercan, Cansu, Guven Baris, Unluhizarci, Kursad, Kelestimur, Fahrettin

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Erratum to ‘Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency’ [Pediatric Neurology 99 (2019) 69–75] von Yıldız, Yılmaz, Talim, Beril, Haliloglu, Goknur, Topaloglu, Haluk, Akçören, Zuhal, Dursun, Ali, Sivri, Hatice Serap, Coşkun, Turgay, Tokatlı, Ayşegül

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Early-onset chronic axonal neuropathy, strokes, and hemolysis: Inherited CD59 deficiency von Haliloglu, Goknur, Maluenda, Jérome, Sayinbatur, Bahattin, Aumont, Cedric, Temucin, Cagri, Tavil, Betul, Cetin, Mualla, Oguz, Kader K, Gut, Ivo, Picard, Veronique, Melki, Judith, Topaloglu, Haluk

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Selenoprotein N‐related myopathy: a retrospective natural history study to guide clinical trials von Silwal, Arpana, Sarkozy, Anna, Scoto, Mariacristina, Ridout, Deborah, Schmidt, Anne, Laverty, Aidan, Henriques, Matilde, D'Argenzio, Luigi, Main, Marion, Mein, Rachael, Manzur, Adnan Y, Abel, Francois, Al‐Ghamdi, Fouad, Genetti, Casie A, Ardicli, Didem, Haliloglu, Goknur, Topaloglu, Haluk, Beggs, Alan H, Muntoni, Francesco

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