Most Cited & Viewed
Most Cited & Viewed Papers
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Cardiovascular Complications in β-Thalassemia: Getting to the Heart of It
by
Nathalie Akiki, Mohammad H. Hodroj, Rayan Bou-Fakhredin, Kamal Matli and Ali T. Taher
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The Outcomes of Patients with Haemoglobin Disorders in Cyprus: A Joined Report of the Thalassaemia International Federation and the Nicosia and Paphos Thalassaemia Centres (State Health Services Organisation)
by
Michael Angastiniotis, Soteroula Christou, Annita Kolnakou, Evangelia Pangalou, Irene Savvidou, Dimitrios Farmakis and Androulla Eleftheriou
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The Effect of COVID-19 on Hemoglobinopathy Patients’ Daily Lives While Quarantined: Four Greek Hospitals’ Experiences
by
Sophia Delicou, Aikaterini Xydaki, Konstantinos Manganas, Emmanouil Koullias, Loukia Evliati, Chryssoula Kalkana, Michael D. Diamantidis, Achilles Manafas, Marianna Katsatou, Leonidas Roumpatis and Theodoros Aforozis
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Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
by
Angela Vitrano, Khaled M. Musallam, Antonella Meloni, Sebastiano Addario Pollina, Mehran Karimi, Amal El-Beshlawy, Mahmoud Hajipour, Vito Di Marco, Saqib Hussain Ansari, Aldo Filosa, Paolo Ricchi, Adriana Ceci, Shahina Daar, Efthymia Vlachaki, Sylvia Titi Singer, Zaki A. Naserullah, Alessia Pepe, Salvatore Scondotto, Gabriella Dardanoni, Fedele Bonifazi, Vijay G. Sankaran, Elliott Vichinsky, Ali T. Taher, Aurelio Maggio and International Working Group on Thalassemia (IWG-THAL)add
Show full author list
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Hemoglobin Disorders in Europe: A Systematic Effort of Identifying and Addressing Unmet Needs and Challenges by the Thalassemia International Federation
by
Michael Angastiniotis, Lily Cannon, Eleni Antoniou, Angelo Loris Brunetta, George Constantinou, Eva Maria Knoll, Dimitris Loukopoulos, Anton Skafi and Androulla Eleftheriou
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Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment
by
Duantida Songdej and Suthat Fucharoen
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CRISPR Gene Therapy: A Promising One-Time Therapeutic Approach for Transfusion-Dependent β-Thalassemia—CRISPR-Cas9 Gene Editing for β-Thalassemia
by
Udani Gamage, Kesari Warnakulasuriya, Sonali Hansika and Gayathri N. Silva
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Infection and Potential Challenge of Childhood Mortality in Sickle Cell Disease: A Comprehensive Review of the Literature from a Global Perspective
by
Tarun Sahu, Babita Pande, Henu Kumar Verma, L V K S Bhaskar, Meenakshi Sinha, Ramanjan Sinha and Pasupuleti Visweswara Rao
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Hb Mazandaran (α1) α51 Gly > Cys(CE9), c.154 GGC > TGC: A Novel Haemoglobin Variant of α1-Globin Gene
by
Hossein Jalali, Mohammad Reza Mahdavi, Mahan Mahdavi and Adeleh Abbasi
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Infection and Potential Challenge of Childhood Mortality in Sickle Cell Disease: A Comprehensive Review of the Literature from a Global Perspective
by
Tarun Sahu, Babita Pande, Henu Kumar Verma, L V K S Bhaskar, Meenakshi Sinha, Ramanjan Sinha and Pasupuleti Visweswara Rao
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Spectrum of Thalassemia and Hemoglobinopathy Using Capillary Zone Electrophoresis: A Facility-Based Single Centred Study at icddr,b in Bangladesh
by
Anamul Hasan, Jigishu Ahmed, Bikash Chandra Chanda, Maisha Aniqua, Raisa Akther, Palash Kanti Dhar, Kazi Afrin Binta Hasan, Abdur Rouf Siddique, Md. Zahidul Islam, Sharmine Zaman Urmee and Dinesh Mondal
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Infection and Potential Challenge of Childhood Mortality in Sickle Cell Disease: A Comprehensive Review of the Literature from a Global Perspective
by
Tarun Sahu, Babita Pande, Henu Kumar Verma, L V K S Bhaskar, Meenakshi Sinha, Ramanjan Sinha and Pasupuleti Visweswara Rao
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What Is the Relevance of Murburn Concept in Thalassemia and Respiratory Diseases?
by
Kelath Murali Manoj
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Understanding the Intricacies of Iron Overload Associated with β-Thalassemia: A Comprehensive Review
by
Subhangi Basu, Motiur Rahaman, Tuphan Kanti Dolai, Praphulla Chandra Shukla and Nishant Chakravorty
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Association between Glomerular Filtration Rate and β-Thalassemia Major: A Systematic Review and Meta-Analysis
by
Shahad Saif Khandker, Nurani Jannat, Deepannita Sarkar, Alif Hasan Pranto, Ismoth Ara Hoque, Jemema Zaman, Md. Nizam Uddin and Ehsan Suez
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The Benign Clone Causing Aplastic Anaemia
by
Shaun R. McCann and Andrea Piccin
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Molecular Epidemiology of HCV Infection among Multi-Transfused β-Thalassemia Patients in Eastern India: A Six-Year Observation
by
Supradip Dutta, Aritra Biswas, Sagnik Bakshi, Promisree Choudhury, Raina Das, Shreyasi Nath, Prosanto Chowdhury, Maitreyee Bhattacharyya, Sharmistha Chakraborty, Shanta Dutta and Provash Chandra Sadhukhan
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HbAdrian (α1:c.251del, p.Leu84Argfs*19)—A Novel Pathogenic Variant in the α1-Globin Gene Associated with Microcytosis from the North of Iran
by
Hossein Jalali, Hossein Karami, Mahan Mahdavi and Mohammad Reza Mahdavi
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Association of Bone Disorder and Gene Polymorphism of PPAR-γ Pro12 Ala in Egyptian Children with β-Thalassemia
by
Ahmed M. Abdel Hamied, Heba Mostafa Ahmed, Dina H. Eldahshan, Dalia S. Morgan, Abdel Meged A. Abdel Meged, Marwa O. Elgendy, Mohamed S. Imam, Turki A. H. Alotaibi, Majed M. S. Alotaibi, Manal T. N. Alotaibi, Sarah S. S. Alshalan and Sara O. Elgendy
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Amlodipine Therapy in β-Thalassemia Patients: A Systematic Review and Meta-Analysis on Ferritin Levels and Liver MRI T2*
by
Aily Aliasgharian, Hossein Karami, Mohammad Zahedi, Reza Jahanshahi, Hossein Bakhtiari-Dovvombaygi, Amirreza Nasirzadeh, Mohammad Naderisorki, Mehrnoush Kosaryan, Ebrahim Salehifar, Mobin Ghazaiean, Saeid Bitaraf and Hadi Darvishi-Khezri
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Amlodipine Therapy in β-Thalassemia Patients: A Systematic Review and Meta-Analysis on Ferritin Levels and Liver MRI T2*
by
Aily Aliasgharian, Hossein Karami, Mohammad Zahedi, Reza Jahanshahi, Hossein Bakhtiari-Dovvombaygi, Amirreza Nasirzadeh, Mohammad Naderisorki, Mehrnoush Kosaryan, Ebrahim Salehifar, Mobin Ghazaiean, Saeid Bitaraf and Hadi Darvishi-Khezri
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A Case Report of Hyperhemolytic Syndrome in Sickle Cell Disease, with a Special Focus on Avoiding the Use of Transfusions
by
Omar Obajed Al-Ali, György Pfliegler, Ferenc Magyari, Fanni Borics, László Imre Pinczés, Árpád Illés and Boglárka Brúgós
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Challenges of Iron Chelation in Thalassemic Children
by
Alkistis Adramerina and Marina Economou
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Causes of Hospitalizations in Pediatric Patients with Thalassemia under the National Health Coverage Scheme in Thailand
by
Pimlak Charoenkwan, Patcharee Komvilaisak, Kaewjai Thepsuthummarat, Panya Seksarn and Kitti Torcharus
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β Thalassemia Mutation Flow in Indonesia: A Migration Perspective
by
Lantip Rujito, Ziske Maritska and Abdul Salam Sofro
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Unveiling Extramedullary Hematopoiesis: A Case Report Highlighting the Causes, Symptoms, and Management Strategies
by
Konstantinos Manganas, Aikaterini Xydaki, Angeliki Kotsiafti, Olympia Papakonstantinou and Sophia Delicou
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Psychological Burden among Pediatric Thalassemia Major Patients in Indonesia: A Review
by
Teny Tjitra Sari, Ludi Dhyani Rahmartani, Angga Wirahmadi, Nathasha Brigitta Selene, Stephen Diah Iskandar and Pustika Amalia Wahidiyat
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CRISPR Gene Therapy: A Promising One-Time Therapeutic Approach for Transfusion-Dependent β-Thalassemia—CRISPR-Cas9 Gene Editing for β-Thalassemia
by
Udani Gamage, Kesari Warnakulasuriya, Sonali Hansika and Gayathri N. Silva
|
|
Hemoglobin Disorders in Europe: A Systematic Effort of Identifying and Addressing Unmet Needs and Challenges by the Thalassemia International Federation
by
Michael Angastiniotis, Lily Cannon, Eleni Antoniou, Angelo Loris Brunetta, George Constantinou, Eva Maria Knoll, Dimitris Loukopoulos, Anton Skafi and Androulla Eleftheriou
|
|
Cardiovascular Complications in β-Thalassemia: Getting to the Heart of It
by
Nathalie Akiki, Mohammad H. Hodroj, Rayan Bou-Fakhredin, Kamal Matli and Ali T. Taher
|
|
Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment
by
Duantida Songdej and Suthat Fucharoen
|
|
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
by
Angela Vitrano, Khaled M. Musallam, Antonella Meloni, Sebastiano Addario Pollina, Mehran Karimi, Amal El-Beshlawy, Mahmoud Hajipour, Vito Di Marco, Saqib Hussain Ansari, Aldo Filosa, Paolo Ricchi, Adriana Ceci, Shahina Daar, Efthymia Vlachaki, Sylvia Titi Singer, Zaki A. Naserullah, Alessia Pepe, Salvatore Scondotto, Gabriella Dardanoni, Fedele Bonifazi, Vijay G. Sankaran, Elliott Vichinsky, Ali T. Taher, Aurelio Maggio and International Working Group on Thalassemia (IWG-THAL)add
Show full author list
remove
Hide full author list
|
|
Going Back to Fundamentals: Three Marriageable Actions for Thalassemia and Carrier Population Management
by
Sehjeong Kim, Hamda AlDhaheri and So-Yeun Kim
|
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Redesigning New Policy Options for Thalassemia Prevention in Sri Lanka
by
Nadeeja Amarasinghe, Amila Amarasena, Anoj Thabrew, Prabhath Werawatte, Anuja Premawardhena, Farnaz Malik, Mohamed Abusayeed and Champika Wickramasinghe
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Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?
by
Tsz Yuen Au, Shamiram Benjamin and Oskar Wojciech Wiśniewski
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Highlights on the Luspatercept Treatment in Thalassemia
by
Yesim Aydinok
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Spectrum of Thalassemia and Hemoglobinopathy Using Capillary Zone Electrophoresis: A Facility-Based Single Centred Study at icddr,b in Bangladesh
by
Anamul Hasan, Jigishu Ahmed, Bikash Chandra Chanda, Maisha Aniqua, Raisa Akther, Palash Kanti Dhar, Kazi Afrin Binta Hasan, Abdur Rouf Siddique, Md. Zahidul Islam, Sharmine Zaman Urmee and Dinesh Mondal
|
Downloads | Article |
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Spectrum of Thalassemia and Hemoglobinopathy Using Capillary Zone Electrophoresis: A Facility-Based Single Centred Study at icddr,b in Bangladesh
by
Anamul Hasan, Jigishu Ahmed, Bikash Chandra Chanda, Maisha Aniqua, Raisa Akther, Palash Kanti Dhar, Kazi Afrin Binta Hasan, Abdur Rouf Siddique, Md. Zahidul Islam, Sharmine Zaman Urmee and Dinesh Mondal
|
|
Understanding the Intricacies of Iron Overload Associated with β-Thalassemia: A Comprehensive Review
by
Subhangi Basu, Motiur Rahaman, Tuphan Kanti Dolai, Praphulla Chandra Shukla and Nishant Chakravorty
|
|
Infection and Potential Challenge of Childhood Mortality in Sickle Cell Disease: A Comprehensive Review of the Literature from a Global Perspective
by
Tarun Sahu, Babita Pande, Henu Kumar Verma, L V K S Bhaskar, Meenakshi Sinha, Ramanjan Sinha and Pasupuleti Visweswara Rao
|
|
Association between Glomerular Filtration Rate and β-Thalassemia Major: A Systematic Review and Meta-Analysis
by
Shahad Saif Khandker, Nurani Jannat, Deepannita Sarkar, Alif Hasan Pranto, Ismoth Ara Hoque, Jemema Zaman, Md. Nizam Uddin and Ehsan Suez
|
|
The Benign Clone Causing Aplastic Anaemia
by
Shaun R. McCann and Andrea Piccin
|
|
Association of Bone Disorder and Gene Polymorphism of PPAR-γ Pro12 Ala in Egyptian Children with β-Thalassemia
by
Ahmed M. Abdel Hamied, Heba Mostafa Ahmed, Dina H. Eldahshan, Dalia S. Morgan, Abdel Meged A. Abdel Meged, Marwa O. Elgendy, Mohamed S. Imam, Turki A. H. Alotaibi, Majed M. S. Alotaibi, Manal T. N. Alotaibi, Sarah S. S. Alshalan and Sara O. Elgendy
|
|
Molecular Epidemiology of HCV Infection among Multi-Transfused β-Thalassemia Patients in Eastern India: A Six-Year Observation
by
Supradip Dutta, Aritra Biswas, Sagnik Bakshi, Promisree Choudhury, Raina Das, Shreyasi Nath, Prosanto Chowdhury, Maitreyee Bhattacharyya, Sharmistha Chakraborty, Shanta Dutta and Provash Chandra Sadhukhan
|
|
Amlodipine Therapy in β-Thalassemia Patients: A Systematic Review and Meta-Analysis on Ferritin Levels and Liver MRI T2*
by
Aily Aliasgharian, Hossein Karami, Mohammad Zahedi, Reza Jahanshahi, Hossein Bakhtiari-Dovvombaygi, Amirreza Nasirzadeh, Mohammad Naderisorki, Mehrnoush Kosaryan, Ebrahim Salehifar, Mobin Ghazaiean, Saeid Bitaraf and Hadi Darvishi-Khezri
|
|
What Is the Relevance of Murburn Concept in Thalassemia and Respiratory Diseases?
by
Kelath Murali Manoj
|
|
HbAdrian (α1:c.251del, p.Leu84Argfs*19)—A Novel Pathogenic Variant in the α1-Globin Gene Associated with Microcytosis from the North of Iran
by
Hossein Jalali, Hossein Karami, Mahan Mahdavi and Mohammad Reza Mahdavi
|
Downloads | Article |
---|---|
Amlodipine Therapy in β-Thalassemia Patients: A Systematic Review and Meta-Analysis on Ferritin Levels and Liver MRI T2*
by
Aily Aliasgharian, Hossein Karami, Mohammad Zahedi, Reza Jahanshahi, Hossein Bakhtiari-Dovvombaygi, Amirreza Nasirzadeh, Mohammad Naderisorki, Mehrnoush Kosaryan, Ebrahim Salehifar, Mobin Ghazaiean, Saeid Bitaraf and Hadi Darvishi-Khezri
|
|
Challenges of Iron Chelation in Thalassemic Children
by
Alkistis Adramerina and Marina Economou
|
|
β Thalassemia Mutation Flow in Indonesia: A Migration Perspective
by
Lantip Rujito, Ziske Maritska and Abdul Salam Sofro
|
|
A Case Report of Hyperhemolytic Syndrome in Sickle Cell Disease, with a Special Focus on Avoiding the Use of Transfusions
by
Omar Obajed Al-Ali, György Pfliegler, Ferenc Magyari, Fanni Borics, László Imre Pinczés, Árpád Illés and Boglárka Brúgós
|
|
Causes of Hospitalizations in Pediatric Patients with Thalassemia under the National Health Coverage Scheme in Thailand
by
Pimlak Charoenkwan, Patcharee Komvilaisak, Kaewjai Thepsuthummarat, Panya Seksarn and Kitti Torcharus
|
|
Unveiling Extramedullary Hematopoiesis: A Case Report Highlighting the Causes, Symptoms, and Management Strategies
by
Konstantinos Manganas, Aikaterini Xydaki, Angeliki Kotsiafti, Olympia Papakonstantinou and Sophia Delicou
|
|
Psychological Burden among Pediatric Thalassemia Major Patients in Indonesia: A Review
by
Teny Tjitra Sari, Ludi Dhyani Rahmartani, Angga Wirahmadi, Nathasha Brigitta Selene, Stephen Diah Iskandar and Pustika Amalia Wahidiyat
|
Downloads | Article |
---|---|
CRISPR Gene Therapy: A Promising One-Time Therapeutic Approach for Transfusion-Dependent β-Thalassemia—CRISPR-Cas9 Gene Editing for β-Thalassemia
by
Udani Gamage, Kesari Warnakulasuriya, Sonali Hansika and Gayathri N. Silva
|
|
Hemoglobin Disorders in Europe: A Systematic Effort of Identifying and Addressing Unmet Needs and Challenges by the Thalassemia International Federation
by
Michael Angastiniotis, Lily Cannon, Eleni Antoniou, Angelo Loris Brunetta, George Constantinou, Eva Maria Knoll, Dimitris Loukopoulos, Anton Skafi and Androulla Eleftheriou
|
|
Cardiovascular Complications in β-Thalassemia: Getting to the Heart of It
by
Nathalie Akiki, Mohammad H. Hodroj, Rayan Bou-Fakhredin, Kamal Matli and Ali T. Taher
|
|
Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment
by
Duantida Songdej and Suthat Fucharoen
|
|
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity
by
Angela Vitrano, Khaled M. Musallam, Antonella Meloni, Sebastiano Addario Pollina, Mehran Karimi, Amal El-Beshlawy, Mahmoud Hajipour, Vito Di Marco, Saqib Hussain Ansari, Aldo Filosa, Paolo Ricchi, Adriana Ceci, Shahina Daar, Efthymia Vlachaki, Sylvia Titi Singer, Zaki A. Naserullah, Alessia Pepe, Salvatore Scondotto, Gabriella Dardanoni, Fedele Bonifazi, Vijay G. Sankaran, Elliott Vichinsky, Ali T. Taher, Aurelio Maggio and International Working Group on Thalassemia (IWG-THAL)add
Show full author list
remove
Hide full author list
|
|
Going Back to Fundamentals: Three Marriageable Actions for Thalassemia and Carrier Population Management
by
Sehjeong Kim, Hamda AlDhaheri and So-Yeun Kim
|
|
Redesigning New Policy Options for Thalassemia Prevention in Sri Lanka
by
Nadeeja Amarasinghe, Amila Amarasena, Anoj Thabrew, Prabhath Werawatte, Anuja Premawardhena, Farnaz Malik, Mohamed Abusayeed and Champika Wickramasinghe
|
|
Is the Role of Hepcidin and Erythroferrone in the Pathogenesis of Beta Thalassemia the Key to Developing Novel Treatment Strategies?
by
Tsz Yuen Au, Shamiram Benjamin and Oskar Wojciech Wiśniewski
|
|
Highlights on the Luspatercept Treatment in Thalassemia
by
Yesim Aydinok
|
|
Spectrum of Thalassemia and Hemoglobinopathy Using Capillary Zone Electrophoresis: A Facility-Based Single Centred Study at icddr,b in Bangladesh
by
Anamul Hasan, Jigishu Ahmed, Bikash Chandra Chanda, Maisha Aniqua, Raisa Akther, Palash Kanti Dhar, Kazi Afrin Binta Hasan, Abdur Rouf Siddique, Md. Zahidul Islam, Sharmine Zaman Urmee and Dinesh Mondal
|