Hepatitis B Vaccine-Associated Atypical Hemolytic Uremic Syndrome

por Avcı, Zekai, Bayram, Cengiz, Malbora, Barış
Publicado 2013

Pseudo Chediak-Higashi Anomaly

por Avcı, Zekai, Malbora, Barış, Özbek, Namık
Publicado 2013

Successful Treatment of Refractory Diamond-Blackfan Anemia Using Metoclopramide and Prednisolone

por Malbora, Barış, Avcı, Zekai, Özbek, Namık
Publicado 2012

Hemophagocytic Lymphohistiocytosis and Pelger-Huët Anomaly Associated with Colchicine Intoxication

por Malbora, Baris, Polat, Emine, Akyuz, Sare Gulfem
Publicado 2014

Severe Adenovirus Infection Associated with Hemophagocytic Lymphohistiocytosis

por Hoşnut, Ferda Özbay, Özçay, Figen, Malbora, Barış, Hızlı, Şamil, Özbek, Namık
Publicado 2014

Effects of Zinc Sulfate Supplementation in Treatment of Iron Defi ciency Anemia

por Gülsan, Meltem, Malbora, Barış, Avcı, Zekai, Bayraktar, Nilüfer, Bozkaya, İkbal, Özbek, Namik
Publicado 2013

Ophthalmologic Findings in Children with Leukemia: A Single-Center Study

por Orhan, Betül, Malbora, Barış, Akça Bayar, Sezin, Avcı, Zekai, Alioğlu, Bülent, Özbek, Namık
Publicado 2016

Lack of Early Inflammation Signs of Acute Compartment Syndrome in an Immunodeficient Patient

por Belen, Burcu, Çakıcı, Özlem, Uzakgider, Melikşah, Öniz, Haldun, Türker, Meral, Atabay, Berna, Malbora, Barış, Karapınar, Levent
Publicado 2017

Early Postnatal Hemorrhagic Shock Due to Intraabdominal Hemorrhage in a Newborn with Severe Hemophilia A

por Erol, Sara, Aydın, Banu, Dilli, Dilek, Malbora, Barış, Beken, Serdar, Çınar, Hasibe Gökçe, Zenciroğlu, Ayşegül, Okumuş, Nurullah
Publicado 2014

Hemoglobin H Disease in Turkey: Experience from Eight Centers

por Ünal, Selma, Oktay, Gönül, Acıpayam, Can, İlhan, Gül, Gali, Edip, Celkan, Tiraje, Bay, Ali, Malbora, Barış, Akar, Nejat, Oymak, Yeşim, Toptaş, Tayfur
Publicado 2016

Intracranial Bleeding in a Female Hemophilia Patient: Molecular Analysis of the Factor 8 Gene and Determination of a Novel Mutation

por Tatlı Güneş, Burçak, Önder Siviş, Zühal, Ataseven, Eda, Malbora, Barış, Türker, Meral, Belen, Fatma Burcu, Atabay, Berna, Atik, Tahir, Işık, Esra, Özkınay, Ferda
Publicado 2018

A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family

por Guipponi, Michel, Masclaux, Frédéric, Sloan-Béna, Frédérique, Di Sanza, Corinne, Özbek, Namik, Peyvandi, Flora, Menegatti, Marzia, Casini, Alessandro, Malbora, Baris, Neerman-Arbez, Marguerite
Publicado 2021

cDNA sequencing increases the molecular diagnostic yield in Chediak-Higashi syndrome

por Kuptanon, Chulaluk, Morimoto, Marie, Nicoli, Elena-Raluca, Stephen, Joshi, Yarnell, David S., Dorward, Heidi, Owen, William, Parikh, Suhag, Ozbek, Namik Yasar, Malbora, Baris, Ciccone, Carla, Gunay-Aygun, Meral, Gahl, William A., Introne, Wendy J., Malicdan, May Christine V.
Publicado 2023

Outcomes of Eltrombopag Treatment and Development of Iron Deficiency in Children with Immune Thrombocytopenia in Turkey

por Koca Yozgat, Ayça, Leblebisatan, Göksel, Akbayram, Sinan, Çınar Özel, Simge, Karakaş, Zeynep, Erduran, Erol, Yılmaz, Şebnem, Koçak, Ülker, Ünal, Şule, Özdemir, Gül Nihal, Albayrak, Meryem, Zengin, Emine, Oymak, Yeşim, Bör, Özcan, Çakmaklı, Hasan Fatih, Söker, Murat, Gürlek Gökçebay, Dilek, Tokgöz, Hüseyin, Malbora, Barış, Karaman, Serap, Celkan, Tiraje, Şaşmaz, İlgen, Yaralı, Neşe, Ören, Hale, Ünüvar, Ayşegül, Özbek, Namık Yaşar
Publicado 2020

Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients

por Garavelli, Livia, Ivanovski, Ivan, Caraffi, Stefano Giuseppe, Santodirocco, Daniela, Pollazzon, Marzia, Cordelli, Duccio Maria, Abdalla, Ebtesam, Accorsi, Patrizia, Adam, Margaret P., Baldo, Chiara, Bayat, Allan, Belligni, Elga, Bonvicini, Federico, Breckpot, Jeroen, Callewaert, Bert, Cocchi, Guido, Cuturilo, Goran, Devriendt, Koenraad, Dinulos, Mary Beth, Djuric, Olivera, Epifanio, Roberta, Faravelli, Francesca, Formisano, Debora, Giordano, Lucio, Grasso, Marina, Grønborg, Sabine, Iodice, Alessandro, Iughetti, Lorenzo, Lacombe, Didier, Maggi, Massimo, Malbora, Baris, Mammi, Isabella, Moutton, Sebastien, Møller, Rikke, Muschke, Petra, Napoli, Manuela, Pantaleoni, Chiara, Pascarella, Rosario, Pellicciari, Alessandro, Poch-Olive, Maria Luisa, Raviglione, Federico, Rivieri, Francesca, Russo, Carmela, Savasta, Salvatore, Scarano, Gioacchino, Selicorni, Angelo, Silengo, Margherita, Sorge, Giovanni, Tarani, Luigi, Tone, Luis Gonzaga, Toutain, Annick, Trimouille, Aurelien, Valera, Elvis Terci, Vergano, Samantha Schrier, Zanotta, Nicoletta, Zollino, Marcella, Dobyns, William B, Paciorkowski, Alex R
Publicado 2017

Mowat-Wilson syndrome: growth charts

por Ivanovski, Ivan, Djuric, Olivera, Broccoli, Serena, Caraffi, Stefano Giuseppe, Accorsi, Patrizia, Adam, Margaret P., Avela, Kristina, Badura-Stronka, Magdalena, Bayat, Allan, Clayton-Smith, Jill, Cocco, Isabella, Cordelli, Duccio Maria, Cuturilo, Goran, Di Pisa, Veronica, Dupont Garcia, Juliette, Gastaldi, Roberto, Giordano, Lucio, Guala, Andrea, Hoei-Hansen, Christina, Inaba, Mie, Iodice, Alessandro, Nielsen, Jens Erik Klint, Kuburovic, Vladimir, Lazalde-Medina, Brissia, Malbora, Baris, Mizuno, Seiji, Moldovan, Oana, Møller, Rikke S., Muschke, Petra, Otelli, Valeria, Pantaleoni, Chiara, Piscopo, Carmelo, Poch-Olive, Maria Luisa, Prpic, Igor, Marín Reina, Purificación, Raviglione, Federico, Ricci, Emilia, Scarano, Emanuela, Simonte, Graziella, Smigiel, Robert, Tanteles, George, Tarani, Luigi, Trimouille, Aurelien, Valera, Elvis Terci, Schrier Vergano, Samantha, Writzl, Karin, Callewaert, Bert, Savasta, Salvatore, Street, Maria Elisabeth, Iughetti, Lorenzo, Bernasconi, Sergio, Giorgi Rossi, Paolo, Garavelli, Livia
Publicado 2020