Cargando…

Sickle cell-β thalassemia with concomitant hemophilia A: a rare presentation

Detalles Bibliográficos
Autores principales:	Dhiman, Pratibha, Chaudhary, Rahul, Sudha, Krishna
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2015
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4705056/ https://www.ncbi.nlm.nih.gov/pubmed/26770958 http://dx.doi.org/10.5045/br.2015.50.4.264

Ejemplares similares

HB E/β°Thalassemia can present with normal phenotype
por: Pal, Ranabir, et al.
Publicado: (2010)

Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia
por: Hançer, Veysel Sabri, et al.
Publicado: (2020)

Serum Lipids in Turkish Patients with β-Thalassemia Major and β-Thalassemia Minor
por: Işık Balcı, Yasemin, et al.
Publicado: (2016)

Microfilaria concomitant with metastatic deposits of adenocarcinoma in lymph node fine needle aspiration cytology: A chance finding
por: Kolte, Sachin S, et al.
Publicado: (2010)

Microcytic Anemia: An Insidious Presentation of Sickle Cell Beta+ Thalassemia, a Rare Sickle Cell Variant
por: Shankar, Malavika, et al.
Publicado: (2022)

Delta beta thalassemia: a rare hemoglobin variant
por: Mansoori, Huma, et al.
Publicado: (2016)

Reticulocytes indices in β thalassemia trait individuals
por: Wagner, Sandrine Comparsi, et al.
Publicado: (2011)

Low HbA2 Level in β-Thalassemia Trait
por: ÖZSOYLU, Şinasi
Publicado: (2013)

A rare case of Huntington's disease presenting with treatment-resistant psychosis
por: Singhai, Kartik, et al.
Publicado: (2019)

An Unusual Presentation of Hairy Cell Leukemia
por: Gajendra, Smeeta, et al.
Publicado: (2019)

Sleeve Gastrectomy in a Severe Hemophilia A Patient: One of the Very Rare Cases
por: Davulcu, Eren Arslan, et al.
Publicado: (2020)

Acquired Hemophilia
por: Özsoylu, Şinasi
Publicado: (2014)

Graham-Little-Piccardi-Lassueur Syndrome With Concomitant Mucocutaneous Lichen Planus: Rare Presentation in a Man
por: Dhiman, Avita, et al.
Publicado: (2022)

Anesthetic management of a patient with sickle β(+) thalassemia
por: Bharati, Saswata, et al.
Publicado: (2011)

Sex-specific transcriptional profiles identified in β-thalassemia patients
por: Nanou, Aikaterini, et al.
Publicado: (2021)

Echocardiografic abnormalities in patients with sickle cell/β-thalassemia do not depend on the β-thalassemia phenotype
por: Benites, Bruno Deltreggia, et al.
Publicado: (2019)

Hematological malignancies complicating β-thalassemia syndromes: a single center experience
por: Alavi, Samin, et al.
Publicado: (2013)

MRI Evaluation of Liver Iron Concentration in Patients with β-Thalassemia Major
por: Karimi, M, et al.
Publicado: (2010)

Silymarin therapy and improvement of cardiac outcome in patients with β-thalassemia major
por: Khezri, Hadi Darvishi, et al.
Publicado: (2016)

Pain in β-thalassemia major patients: an important yet neglected issue
por: Zeydi, Amir Emami, et al.
Publicado: (2018)

HBB-deficient Macaca fascicularis monkey presents with human β-thalassemia
por: Huang, Yan, et al.
Publicado: (2019)

Did the Proband Have Thalassemia Intermedia or Severe Thalassemia Trait?
por: Özsoylu, Şinasi
Publicado: (2012)

β-Thalassemia Mutation At Codon 37 (Tgg>>Tga) Detected In A Turkish Family
por: Güleç, Derya, et al.
Publicado: (2013)

Tricuspid-valve regurgitant jet velocity as a risk factor for death in β-thalassemia
por: Derchi, Giorgio, et al.
Publicado: (2022)

Neonatal Hemophilia: A Rare Presentation
por: Ferreira, Nuno, et al.
Publicado: (2015)

Formulas for the Detection β-Thalassemia Carriers Are Affected by Changes in Red Cell Parameters
por: Aslan, Deniz
Publicado: (2018)

Is the HIV Seroprevalence among Iraqi Patients with β-thalassemia Major Underestimated or not Prevalent?
por: Al-Mendalawi, Mahmood Dhahir
Publicado: (2021)

Responses of β-thalassemia and compound heterozygote of Sickle/βthalassemia of BCL11A Gene Polymorphism in Pakistani Patients
por: Soomro, Nayab, et al.
Publicado: (2023)

ß-thalassemia and alkaptonuria
por: Yasri, Sora, et al.
Publicado: (2014)

Alloimmunization in Thalassemia Patients
por: Joob, Beuy, et al.
Publicado: (2019)

Iron overload assessment in β Thalassemia Major – is T2* Magnetic Resonance Imaging the answer?
por: Ali, Natasha
Publicado: (2017)

Survival and causes of death in 2,033 patients with non-transfusion-dependent β-thalassemia
por: Musallam, Khaled M., et al.
Publicado: (2021)

RE: Six-year outcome of the national premarital screening and genetic counseling program for sickle cell disease and β-thalassemia in Saudi Arabia
por: Al-Mendalawi, Mahmood Dhahir
Publicado: (2011)

Quality of Life in Hemophilia Complicated by Inhibitors
por: Bastani, P, et al.
Publicado: (2012)

Co-Existence of Hereditary Pyrimidine 5’-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation
por: Agapidou, A., et al.
Publicado: (2012)

A Rare Concomitance of Two Blaschkoid Pigmentary Disorders: A Juggle of Pigmentary Mosaicism
por: Daroach, Manju, et al.
Publicado: (2019)

Rare Presentation of β-Thalassemia Intermedia With a Phenotype of Dilated Cardiomyopathy
por: Nakaya, Yuichiro, et al.
Publicado: (2023)

Prevalence of glucose dysregulation (GD) in patients with β-thalassemias in different countries: A preliminary ICET-A survey
por: de Sanctis, Vincenzo, et al.
Publicado: (2021)

A rare case of spontaneous bilateral extradural hematoma in a sickle cell disease child
por: Patra, Sunil K., et al.
Publicado: (2012)

Mutational spectrum of thalassemias in India
por: Panigrahi, Inusha, et al.
Publicado: (2007)

Cannot write session to /tmp/vufind_sessions/sess_s5hj7ann3lsj4aa4plv698aqsr