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Sule Unal

Showing results (81-90 of 105) with videos related to

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Leukemia Research|October 15, 2025
Infectious complications in pediatric acute lymphoblastic leukemia treatment: A comparison of ALL-IC BFM 2009 vs. modified St. Jude total XV in a single-center retrospective cohort studyDilara Unal, Fatma Gumruk, Selin Aytac, et al.
The Turkish Journal of Pediatrics|March 25, 2011
Hematological consequences of pandemic influenza H1N1 infection: a single center experienceSule Unal, Müge Gökçe, Selin Aytaç-Elmas, et al.
Blood Advances|January 3, 2023
Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutationsImmacolata Andolfo, Vittoria Monaco, Flora Cozzolino, et al.
Shock (Augusta, Ga.)|October 30, 2015
THE GLYCOCALYX AND TRAUMA: A REVIEWAndreia Z Chignalia, Feliz Yetimakman, Sarah C Christiaans, et al.
American Journal of Hematology|February 4, 2018
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemiasRoberta Russo, Immacolata Andolfo, Francesco Manna, et al.
Journal of Pediatric Hematology/Oncology|December 17, 2016
Predictors of Suboptimal Follow-up in Pediatric Cancer SurvivorsLeana May, David D Schwartz, Ernest Frugé, et al.
European Journal of Medical Genetics|October 31, 2017
Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experienceLydie Da Costa, Marie-Françoise O'Donohue, Birgit van Dooijeweert, et al.
Journal of Clinical Medicine|January 22, 2021
Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic DiagnosisBarbara Preisler, Behnaz Pezeshkpoor, Atanas Banchev, et al.
American Journal of Hematology|April 26, 2024
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patientsRoberta Marra, Antonella Nostroso, Barbara Eleni Rosato, et al.
Pediatric Blood & Cancer|July 18, 2015
Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense MutationsBianca Tesi, Samuel C C Chiang, Dalia El-Ghoneimy, et al.
Pageof 11

Showing results (81-90 of 105) with videos related to

Sort By:
Pageof 11
Leukemia Research|October 15, 2025
Infectious complications in pediatric acute lymphoblastic leukemia treatment: A comparison of ALL-IC BFM 2009 vs. modified St. Jude total XV in a single-center retrospective cohort studyDilara Unal, Fatma Gumruk, Selin Aytac, et al.
The Turkish Journal of Pediatrics|March 25, 2011
Hematological consequences of pandemic influenza H1N1 infection: a single center experienceSule Unal, Müge Gökçe, Selin Aytaç-Elmas, et al.
Blood Advances|January 3, 2023
Proteome alterations in erythrocytes with PIEZO1 gain-of-function mutationsImmacolata Andolfo, Vittoria Monaco, Flora Cozzolino, et al.
Shock (Augusta, Ga.)|October 30, 2015
THE GLYCOCALYX AND TRAUMA: A REVIEWAndreia Z Chignalia, Feliz Yetimakman, Sarah C Christiaans, et al.
American Journal of Hematology|February 4, 2018
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemiasRoberta Russo, Immacolata Andolfo, Francesco Manna, et al.
Journal of Pediatric Hematology/Oncology|December 17, 2016
Predictors of Suboptimal Follow-up in Pediatric Cancer SurvivorsLeana May, David D Schwartz, Ernest Frugé, et al.
European Journal of Medical Genetics|October 31, 2017
Molecular approaches to diagnose Diamond-Blackfan anemia: The EuroDBA experienceLydie Da Costa, Marie-Françoise O'Donohue, Birgit van Dooijeweert, et al.
Journal of Clinical Medicine|January 22, 2021
Familial Multiple Coagulation Factor Deficiencies (FMCFDs) in a Large Cohort of Patients-A Single-Center Experience in Genetic DiagnosisBarbara Preisler, Behnaz Pezeshkpoor, Atanas Banchev, et al.
American Journal of Hematology|April 26, 2024
Unveiling the genetic landscape of suspected congenital dyserythropoietic anemia type I: A retrospective cohort study of 36 patientsRoberta Marra, Antonella Nostroso, Barbara Eleni Rosato, et al.
Pediatric Blood & Cancer|July 18, 2015
Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense MutationsBianca Tesi, Samuel C C Chiang, Dalia El-Ghoneimy, et al.
Pageof 11