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

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

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

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

Myeloperoxidase Deficiency: The Secret Under the Flag of Unstained Cell

Autor Patıroğlu, Türkan, Eke Güngör, Hatice, Belohradsky, Julie Sawalle, Ünal, Ekrem, Klein, Christoph
Vydáno 2013

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

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

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

Autor Ozcan, Alper, Unal, Ekrem, Karakukcu, Musa, Coskun, Abdulhakim, Ozdemir, Mehmet Akif, Patiroglu, Turkan
Vydáno 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

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

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

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

Evaluation of childhood solid pseudopapillary tumors of the pancreas

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

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

Autor Berber, Uğur, Özdemir, Mehmet Akif, Unal, Ekrem, Taheri, Serpil, Yildiz, Serkan, Bayramov, Keziban Korkmaz, Güler, Yunus, Per, Hüseyin
Vydáno 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

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

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

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

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

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

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

Autor 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
Vydáno v Mol Cell Proteomics (2019)

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

Autor 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
Vydáno 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...

Autor 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
Vydáno v Turk J Haematol (2016)

Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO Mutation

Autor 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.
Vydáno v Cell (2017)

Hematologically important mutations: Leukocyte Adhesion Deficiency (first update)

Autor 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
Vydáno v Blood Cells Mol Dis (2011)

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

Autor 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
Vydáno v Nat Commun (2020)

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

Autor 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
Vydáno v Nat Commun (2020)

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

Autor 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
Vydáno v Turk J Haematol (2020)