Search Results - Mahmut Coker

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  1. 1
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    False Positive Diagnosis of Lysosomal Storage Disease Based on Dried Blood Spot Sample; Leucocyte Number of a Challenging Factor by Eser Yıldırım Sözmen, Meral Dondurmacı, Sema Kalkan Uçar, Mahmut Çoker

    Published 2018
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  2. 2
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    A Patient with MSUD: Acute Management with Sodium Phenylacetate/Sodium Benzoate and Sodium Phenylbutyrate by Melis Köse, Ebru Canda, Mehtap Kagnici, Sema Kalkan Uçar, Mahmut Çoker

    Published 2017
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  3. 3
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    Clinical Features of 29 Patients with Hereditary Tyrosinemia I in Western Turkey by Havva Yazıcı, Esra Er, Ebru Canda, Sara Habif, Sema Kalkan Uçar, Mahmut Çoker

    Published 2018
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  4. 4
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    Clinical Presentation and Follow Up of Patients with Mucopolysaccharidosis Type IVA (Morquio A Disease): Single Center Experience by Ebru Canda, Havva Yazıcı, Esra Er, Cenk Eraslan, Sema Kalkan Uçar, Mahmut Çoker

    Published 2018
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  5. 5
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    Impact of the COVID-19 Pandemic on Inherited Metabolic Diseases: Evaluation of Enzyme Replacement Treatment Adherence with Telemedicine by Merve Yoldaş Çelik, Ebru Canda, Havva Yazıcı, Fehime Erdem, Sema Kalkan Uçar, Mahmut Çöker

    Published 2022
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  6. 6
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    Fabry disease: An overlooked diagnosis in adult cardiac patients by Meral Kayıkçıoğlu, Evrim Şimşek, Sema Kalkan Uçar, Selen Bayraktaroğlu, Hüseyin Onay, Eser Sözmen, Mahmut Çoker

    Published 2017
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  7. 7
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    An Evalution of the Demographic and Clinical Characterictics of Patients with GM2 Gangliosidosis by Esra Er, Ebru Canda, Havva Yazıcı, Cenk Eraslan, Eser Sözmen, Sema Kalkan Uçar, Mahmut Çoker

    Published 2018
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  8. 8
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    Clinical, Biochemical and Molecular Characteristics of Fifteen Patients with Mucopolysaccharidosis Type II in Western Turkey by Havva Yazıcı, Ebru Canda, Esra Er, Sema Kalkan Uçar, Hüseyin Onay, Ferda Özkınay, Mahmut Çoker

    Published 2018
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  9. 9
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    Expert opinion on patient journey, diagnosis and clinical monitoring in acid sphingomyelinase deficiency in Turkey: a pediatric metabolic disease specialist's perspective by Nur Arslan, Mahmut Coker, Gulden Fatma Gokcay, Ertugrul Kiykim, Halise Neslihan Onenli Mungan, Fatih Ezgu

    Published 2023
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  10. 10
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    Tyrosinemia Type I and Reversible Neurogenic Crisis After a One-Month Interruption of Nitisinone by Havva Yazıcı, Ebru Canda, Esra Er, Mehmet Arda Kılınç, Sema Kalkan Uçar, Bülent Karapınar, Mahmut Çoker

    Published 2018
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  11. 11
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    Initial and Final Status of the Patients with Niemann Pick A and B: Ege University Experience by Ebru Canda, Havva Yazıcı, Esra Er, Sema Kalkan Uçar, Hüseyin Onay, Eser Sözmen, Ferda Özkınay, Mahmut Çoker

    Published 2018
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  12. 12
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    Evaluation of Cardiovascular Involvement and Cytokine Levels in Patients with Mucopolysaccharidosis by Ebru Canda, Melis Köse, Mehtap Kağnıcı, Meral Dondurmacı, Sema Kalkan Uçar, Eser Sözmen, Reşit Ertürk Levent, Mahmut Çöker

    Published 2019
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  13. 13
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    A Mortal Complication in a Case with Mucopolysaccharidosis type I Following Hematopoietic Stem Cell Transplantation: Pulmonary Haemorrhage by Havva Yazıcı, Ebru Canda, Esra Er, Baris Malbora, Burcu Ozturk Hismi, Huseyin Onay, Serap Aksoylar, Sema Kalkan Uçar, Ferda Ozkinay, Mahmut Çoker

    Published 2021
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  14. 14
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    Nephrotic syndrome in a patient with Glycogen Storage Disease Type IXb. by Merve Yoldas Celik, Havva Yazıcı, Fehime Erdem, Ebru Canda, Banu Sarsik Kumbaraci, Ipek Kaplan Bulut, Sema Kalkan Ucar, Süleyman Caner Kabasakal, Mahmut Çoker

    Published 2022
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  15. 15
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    Mild Aromatic L-Amino Acid Decarboxylase Deficiency Causing Hypoketotic Hypoglycemia in a 4-year-old Girl by Merve Yoldaş Çelik, Ebru Canda, Havva Yazıcı, Fehime Erdem, Ayşe Yüksel Yanbolu, Ayça Aykut, Asude Durmaz, Ahmet Anık, Sema Kalkan Uçar, Mahmut Çoker

    Published 2024
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  16. 16
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    Clinical, Neuroimaging, and Genetic Features of the Patients with L-2-Hydroxyglutaric Aciduria by Ebru Canda, Melis Köse, Havva Yazıcı, Esra Er, Cenk Eraslan, Ferda Özkınay, Mahmut Çoker, Sema Kalkan Uçar, Sara Habif, Emin Karaca, Hüseyin Onay

    Published 2018
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  17. 17
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    Glutaric Aciduria Type I Diagnosis Case with Normal Glutaryl Carnitine and Urine Organic Acid Analysis by Ebru Canda, Havva Yazıcı, Esra Er, Cenk Eraslan, Yasemin Atik Altınok, Hepsen Mine Serin, Sara Habif, Gül Serdaroğlu, Sema Kalkan Uçar, Hüseyin Onay, Ferda Özkınay, Mahmut Çoker

    Published 2018
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