Interaction between hereditary spherocytosis and the beta-thalassemia trait: A case report

Interaction between hereditary spherocytosis and the beta-thalassemia trait: A case report

Show other versions (1)

Bibliographic Details
Main Authors:	Sunita Sharma, Sonal Jain Malhotra, Richa Chauhan
Format:	Article
Language:	English
Published:	Galenos Publishing House 2011-05-01
Series:	Turkish Journal of Hematology
Online Access:	https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-04706

Similar Items

Interaction between hereditary spherocytosis and the beta-thalassemia trait: A case report
by: Sunita Sharma, et al.
Published: (2011-06-01)

Hereditary Spherocytosis in Pregnancy-A Case Report
by: Neethu Mathew, et al.
Published: (2022-08-01)

Hereditary spherocytosis and allied disorders
by: Roberta Russo, et al.
Published: (2019-06-01)

Hemolytic Crisis as the Initial Presentation of Hereditary Spherocytosis Induced by Parvovirus B19 and Herpes Virus Infection in a Patient with the Thalassemia Trait: A Case Report
by: Meriç Kaymak Cihan, et al.
Published: (2012-12-01)

Extramedullary paraspinal hematopoiesis in hereditary spherocytosis
by: Gogia P, et al.
Published: (2008-01-01)

Complications of Evans' syndrome in an infant with hereditary spherocytosis: a case report
by: Kuwana Masataka, et al.
Published: (2009-09-01)

Genotype-degree of hemolysis correlation in hereditary spherocytosis
by: Yimeng Shi, et al.
Published: (2023-06-01)

Hereditary spherocytosis in an 18-month-old boy with pancytopenia: A case report
by: Borhan Moradveisi, et al.
Published: (2013-02-01)

Hypoplastic crisis in hereditary spherocytosis associated with Kawasaki disease
by: Hirokazu Kobushi, et al.
Published: (2023-03-01)

Current diagnostic approach and screening methods for hereditary spherocytosis
by: Paola Bianchi
Published: (2013-03-01)

Human parvovirus infection and aplastic crisis in hereditary spherocytosis
by: A Gogia, et al.
Published: (2011-01-01)

A rare case of hereditary spherocytosis treated with allogenic HSCT
by: Juhi Mehrotra, et al.
Published: (2022-01-01)

Severe hereditary spherocytosis presenting with non-immune fetal hydrops
by: Snehal Mallakmir, et al.
Published: (2023-01-01)

P1527: NEXT GENERATION SEQUENCING IN HEREDITARY SPHEROCYTOSIS DIAGNOSIS
by: A. García Feria, et al.
Published: (2022-06-01)

P1499: GENETIC FACTORS OF IRON OVERLOAD IN HEREDITARY SPHEROCYTOSIS
by: Lucie Donaty, et al.
Published: (2023-08-01)

Reticulocyte Antioxidant Enzymes mRNA Levels versus Reticulocyte Maturity Indices in Hereditary Spherocytosis, β-Thalassemia and Sickle Cell Disease
by: Daniela Melo, et al.
Published: (2024-02-01)

Intractable Diarrhea from Cytomegalovirus Colitis in a Case with Hereditary Spherocytosis
by: Murat Ozkale, et al.
Published: (2015-09-01)

P1536: ERYTHROCYTES’ OXIDATIVE STRESS AND ANTIOXIDANT RESPONSE IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND Β-THALASSEMIA MINOR – A SMALL NUMBER CASE STUDY
by: D. Melo, et al.
Published: (2022-06-01)

Retracted: Study on Management of Blood Transfusion Therapy in Patients with Hereditary Spherocytosis
by: Applied Bionics and Biomechanics
Published: (2023-01-01)

S273: EVIDENCE OF NONINFERIORITY OF MITAPIVAT VERSUS SPLENECTOMY IN MURINE HEREDITARY SPHEROCYTOSIS
by: A. Matte’, et al.
Published: (2022-06-01)

P1480: CLINICAL AND GENETIC STUDY OF HEREDITARY SPHEROCYTOSIS IN THE SPANISH POPULATION.
by: Lucia Castilla, et al.
Published: (2023-08-01)

Red cell abnormalities in a kindred with an uncommon form of hereditary spherocytosis.
by: G Olim, et al.
Published: (1985-05-01)

A de novo ANK1 mutation in a childhood hereditary spherocytosis: a case report
by: Yafeng Wang, et al.
Published: (2023-05-01)

The Complexity of Genotype-Phenotype Correlations in Hereditary Spherocytosis: A Cohort of 95 Patients
by: Annelies van Vuren, et al.
Published: (2019-08-01)

Determination of osmotic resistance of erythrocytes using flow cytometry in patients with hereditary spherocytosis
by: E. F. Mitsura, et al.
Published: (2020-07-01)

Perioperative Concerns in a Parturient with Hereditary Spherocytosis for Lower Segment Cesarean Section
by: Amit Kumar, et al.
Published: (2022-11-01)

Case report: Genetic analysis of a novel intronic inversion variant in the SPTB gene associated with hereditary spherocytosis
by: Bixin Xi, et al.
Published: (2023-12-01)

Anti-E Minor Blood Group Incompatibility and Hereditary Spherocytosis Associated Severe Hyperbilirubinemia: Neonatal Case Report
by: Sema TANRIVERDİ, et al.
Published: (2022-04-01)

Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report
by: Na Wang, et al.
Published: (2023-12-01)

Two cases of vitamin B12 deficiency in patients with beta-thalassemia trait: lessons in diagnosis
by: Kriti Chauhan, et al.
Published: (2023-12-01)

Use of Red Cell Indices for Screening of Hereditary Spherocytosis in Neonates: A Report of Two Cases Confirmed by Exome Sequencing
by: Vinay Batthula, et al.
Published: (2023-11-01)

Laparoscopic concomitant cholecystectomy and splenectomy for true left-sided gall bladder with hereditary spherocytosis
by: Vineeth Bhargav Saraf, et al.
Published: (2024-01-01)

Metabolic Fingerprint in Hereditary Spherocytosis Correlates With Red Blood Cell Characteristics and Clinical Severity
by: Birgit van Dooijeweert, et al.
Published: (2021-07-01)

Mitapivat reprograms the RBC metabolome and improves anemia in a mouse model of hereditary spherocytosis
by: Alessandro Matte, et al.
Published: (2023-10-01)

Laparoscopic splenectomy with the final splenic pedicle transection for hereditary spherocytosis: A video vignette
by: Qiang Sun, et al.
Published: (2023-06-01)

Identification of a novel ANK1 mutation in hereditary spherocytosis co‐existing with BWS
by: Qinghua Zhang, et al.
Published: (2022-04-01)

Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin
by: Sneha Waghela, et al.
Published: (2023-03-01)

Hemoglobin Interlaken in combination with beta thalassemia trait
by: Mara J. Ojeda, et al.
Published: (2013-01-01)

A Search for Beta Thalassemia Trait in India
by: Veda Parthasarathy
Published: (2012-12-01)

Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis
by: Fei Xie, et al.
Published: (2021-04-01)