Scurvy: A rare cause of arthritis in a child with neurologic disorder

od Küçükaydın, Zeynep, Dursun, İsmail, Daldaban, Burcu, Özcan, Alper, Ünal, Ekrem
izdano v Eur J Rheumatol (2018)

Long-Term Patient-Customized Therapy for a Pathogenic EPO Mutation

od Ejaz, Ayesha, Ozcan, Alper, Unal, Ekrem, Karakukcu, Musa, Sankaran, Vijay G.
izdano v Med (N Y) (2020)

Myeloperoxidase Deficiency: The Secret Under the Flag of Unstained Cell

od Patıroğlu, Türkan, Eke Güngör, Hatice, Belohradsky, Julie Sawalle, Ünal, Ekrem, Klein, Christoph
Izdano 2013

Diagnostic and prognostic significance of glypican 5 and glypican 6 gene expression levels in gastric adenocarcinoma

od DINCCELIK-ASLAN, MELIKE, GUMUS-AKAY, GUVEM, ELHAN, ATILLA HALIL, UNAL, EKREM, TUKUN, AJLAN
izdano v Mol Clin Oncol (2015)

Vena cava superior syndrome in the children with mediastinal tumors: Single-center experience

od Ozcan, Alper, Unal, Ekrem, Karakukcu, Musa, Coskun, Abdulhakim, Ozdemir, Mehmet Akif, Patiroglu, Turkan
izdano v North Clin Istanb (2020)

Web-based survey of resources for treatment and long-term follow-up for children with brain tumors in developing countries

od QADDOUMI, Ibrahim, UNAL, Ekrem, DIEZ, Blanca, KEBUDI, Rejin, QUINTANA, Yuri, BOUFFET, Eric, CHANTADA, Guillermo
Izdano 2011

Effectiveness of Ankaferd BloodStopper in Prophylaxis and Treatment of Oral Mucositis in Childhood Cancers Evaluated with Plasma Citrulline Levels

od Patıroğlu, Türkan, Erdoğ Şahin, Nagihan, Ünal, Ekrem, Kendirci, Mustafa, Karakükcü, Musa, Özdemir, Mehmet Akif
izdano v Turk J Haematol (2018)

Evaluation of childhood solid pseudopapillary tumors of the pancreas

od Ozcan, Alper, Arslanoglu, Ceyda, Unal, Ekrem, Patiroglu, Turkan, Ozdemir, Mehmet Akif, Deniz, Kemal, Ozcan, Serdal Sadet, Karakukcu, Musa
izdano v North Clin Istanb (2018)

Genetic Polymorphism of VKORC1-1639 in Children With Intracranial Hemorrhage Due to Vitamin K Deficiency

od Berber, Uğur, Özdemir, Mehmet Akif, Unal, Ekrem, Taheri, Serpil, Yildiz, Serkan, Bayramov, Keziban Korkmaz, Güler, Yunus, Per, Hüseyin
izdano v Clin Appl Thromb Hemost (2018)

X-linked severe combined immunodeficiency due to a novel mutation complicated with hemophagocytic lymphohistiocytosis and presented with invagination: A case report

od Patiroglu, Turkan, Haluk Akar, H., van den Burg, Mirjam, Unal, Ekrem, Akyildiz, Basak N., Tekerek, Nazan U., Yilmaz, Ebru
Izdano 2014

Assessment of Patients with von Willebrand Disease with ISTH/BAT and PBQ Scores

od Belen Apak, Fatma Burcu, Ümit, Elif Gülsüm, Zengin, Yağmur, Sezgin Evim, Melike, Ünal, Ekrem, Özbaş, Hasan Mücahit, Acıpayam, Can
izdano v Turk J Haematol (2020)

Twenty children with non-Wilms renal tumors from a reference center in Central Anatolia, Turkey

od ÜNAL*, Ekrem, YILMAZ, Ebru, ÖZCAN, Alper, IŞIK, Bilgen, KARAKÜKCÜ, Musa, TURAN, Cuneyt, AKGÜN, Hülya, ÖZTÜRK, Figen, COŞKUN, Abdulhakim, ÖZDEMIR, Mehmet Akif, PATIROĞLU, Türkan
izdano v Turk J Med Sci (2020)

Proteome Analysis of Human Neutrophil Granulocytes From Patients With Monogenic Disease Using Data-independent Acquisition

od Grabowski, Piotr, Hesse, Sebastian, Hollizeck, Sebastian, Rohlfs, Meino, Behrends, Uta, Sherkat, Roya, Tamary, Hannah, Ünal, Ekrem, Somech, Raz, Patıroğlu, Türkan, Canzar, Stefan, van der Werff Ten Bosch, Jutte, Klein, Christoph, Rappsilber, Juri
izdano v Mol Cell Proteomics (2019)

Common Variable Immune Deficiency, Autoimmune Hemolytic Anemia and Pancytopenia associated with a Defect in IKAROS

od YILMAZ, Ebru, KUEHN, Hye Sun, ODAKIR, Eda, NIEMELA, Julie E., OZCAN, Alper, EKEN, Ahmet, ROHLFS, Meino, CANSEVER, Murat, GOK, Veysel, AYDIN, Firdevs, KARAKUKCU, Musa, HAUCK, Fabian, KLEIN, Christoph, UNAL, Ekrem, ROSENZWEIG, Sergio D., PATIROGLU, Turkan
izdano v J Pediatr Hematol Oncol (2021)

Prognostic Factors and a New Prognostic Index Model for Children and Adolescents with Hodgkin’s Lymphoma Who Underwent Autologous Hematopoietic Stem Cell Transplantation: A Multice...

od Kesik, Vural, Ataş, Erman, Karakükcü, Musa, Aksoylar, Serap, Erbey, Fatih, Taçyıldız, Nurdan, Küpesiz, Alphan, Öniz, Haldun, Ünal, Ekrem, Kansoy, Savaş, Öztürk, Gülyüz, Elli, Murat, Kaya, Zühre, Ünal, Emel, Hazar, Volkan, Yılmaz Bengoa, Şebnem, Karasu, Gülsün, Atay, Didem, Dağdemir, Ayhan, Ören, Hale, Koçak, Ülker, Yeşilipek, M. Akif
izdano v Turk J Haematol (2016)

Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation

od Kim, Ah Ram, Ulirsch, Jacob C., Wilmes, Stephan, Unal, Ekrem, Moraga, Ignacio, Karakukcu, Musa, Yuan, Daniel, Kazerounian, Shideh, Abdulhay, Nour J., King, David S., Gupta, Namrata, Gabriel, Stacey B., Lander, Eric S., Patiroglu, Turkan, Ozcan, Alper, Ozdemir, Mehmet Akif, Garcia, K. Christopher, Piehler, Jacob, Gazda, Hanna T., Klein, Daryl E., Sankaran, Vijay G.
izdano v Cell (2017)

Hematologically important mutations: Leukocyte Adhesion Deficiency (first update)

od van de Vijver, Edith, Maddalena, Anne, Sanal, Özden, Holland, Steven M., Uzel, Gulbu, Madkaikar, Manisha, de Boer, Martin, van Leeuwen, Karin, Köker, M. Yavuz, Parvaneh, Nima, Fischer, Alain, Law, S.K. Alex, Klein, Nigel, Tezcan, F. Ilhan, Unal, Ekrem, Patiroglu, Turkan, Belohradsky, Bernd, Schwartz, Klaus, Somech, Raz, Kuijpers, Taco W., Roos, Dirk
izdano v Blood Cells Mol Dis (2011)

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

od Łyszkiewicz, Marcin, Ziętara, Natalia, Frey, Laura, Pannicke, Ulrich, Stern, Marcel, Liu, Yanshan, Fan, Yanxin, Puchałka, Jacek, Hollizeck, Sebastian, Somekh, Ido, Rohlfs, Meino, Yilmaz, Tuğba, Ünal, Ekrem, Karakukcu, Musa, Patiroğlu, Türkan, Kellerer, Christina, Karasu, Ebru, Sykora, Karl-Walter, Lev, Atar, Simon, Amos, Somech, Raz, Roesler, Joachim, Hoenig, Manfred, Keppler, Oliver T., Schwarz, Klaus, Klein, Christoph
izdano v Nat Commun (2020)

Author Correction: Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

od Łyszkiewicz, Marcin, Ziętara, Natalia, Frey, Laura, Pannicke, Ulrich, Stern, Marcel, Liu, Yanshan, Fan, Yanxin, Puchałka, Jacek, Hollizeck, Sebastian, Somekh, Ido, Rohlfs, Meino, Yilmaz, Tuğba, Ünal, Ekrem, Karakukcu, Musa, Patiroğlu, Türkan, Kellerer, Christina, Karasu, Ebru, Sykora, Karl-Walter, Lev, Atar, Simon, Amos, Somech, Raz, Roesler, Joachim, Hoenig, Manfred, Keppler, Oliver T., Schwarz, Klaus, Klein, Christoph
izdano v Nat Commun (2020)

Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations

od Atik, Tahir, Işık, Esra, Onay, Hüseyin, Akgün, Bilçağ, Shamsali, Moharram, Kavaklo, Kaan, Evim, Melike, Tüysüz, Gülen, Özbek, Namık Yaşar, Şahin, Fahri, Salcıoğlu, Zafer, Albayrak, Canan, Oymak, Yeşim, Ünal, Ekrem, Belen, Fatma Burcu, Yılmaz Keskin, Ebru, Balkan, Can, Baytan, Birol, Küpesiz, Alphan, Culha, Vildan, Tahtakesen Güçer, Tuba Nur, Güneş, Adalet Meral, Özkınay, Ferda
izdano v Turk J Haematol (2020)