Alpha Thalassemia Latest Advances

Diagnostic challenges and the importance of genetic testing in α/β-thalassemia: a case report.

Journal: Laboratory medicine

Published: April 12, 2026

Identification of Human Transferrin Receptor as an Entry Co-receptor for Parvovirus B19 Infection of Human Erythroid Progenitor Cells.

Journal: bioRxiv : the preprint server for biology

Published: April 10, 2026

A Case of Hb Quong Sze Co-Inherited Thai Deletion Resulting in Falsely Elevated HbA1c Values.

Journal: Clinical laboratory

Published: April 07, 2026

Placental Expression of CD15 in Fetal Anemia From Hydrops Fetalis.

Journal: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Published: April 01, 2026

A Rare Phenotype of X-linked Myotubular Myopathy: Hydrops Fetalis and Refractory Congenital Chylothorax with Fatal Outcome.

Journal: Zeitschrift fur Geburtshilfe und Neonatologie

Published: March 26, 2026

Beta-arrestin 1/2 are essential for embryonic lymphatic vessel development.

Journal: JCI insight

Published: March 26, 2026

Clinical clues to recognizing hereditary dehydrated stomatocytosis (DHSt) in children.

Journal: Archivos argentinos de pediatria

Published: March 17, 2026

Maternal Mirror Syndrome Associated with Hyperreactio Luteinalis and Non-Immune Fetal Hydrops.

Journal: Zeitschrift fur Geburtshilfe und Neonatologie

Published: March 10, 2026

Progressive non-immune hydrops fetalis associated with RASA1 mutation: prenatal imaging and genomic insights.

Journal: BMJ case reports

Published: February 28, 2026

Severe Aortic Regurgitation with New Congestive Heart Failure Following Fetal Aortic Valvuloplasty - A Case Report.

Journal: Pediatric cardiology

Published: February 08, 2026

Genetic screening and typing study of Thalassemia among ethnic Miao Group in Qianxinan area of China

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: February 06, 2026

Antenatal Diagnosis and Management of Congenital Pulmonary Airway Malformation: A Case Report.

Journal: Cureus

Published: February 02, 2026

Alpha Thalassemia Latest Advances

Find the Latest Research About Alpha Thalassemia

Diagnostic challenges and the importance of genetic testing in α/β-thalassemia: a case report.

Diagnostic challenges and the importance of genetic testing in α/β-thalassemia: a case report.

Identification of Human Transferrin Receptor as an Entry Co-receptor for Parvovirus B19 Infection of Human Erythroid Progenitor Cells.

Identification of Human Transferrin Receptor as an Entry Co-receptor for Parvovirus B19 Infection of Human Erythroid Progenitor Cells.

A Case of Hb Quong Sze Co-Inherited Thai Deletion Resulting in Falsely Elevated HbA1c Values.

A Case of Hb Quong Sze Co-Inherited Thai Deletion Resulting in Falsely Elevated HbA1c Values.

Placental Expression of CD15 in Fetal Anemia From Hydrops Fetalis.

Placental Expression of CD15 in Fetal Anemia From Hydrops Fetalis.

A Rare Phenotype of X-linked Myotubular Myopathy: Hydrops Fetalis and Refractory Congenital Chylothorax with Fatal Outcome.

A Rare Phenotype of X-linked Myotubular Myopathy: Hydrops Fetalis and Refractory Congenital Chylothorax with Fatal Outcome.

Beta-arrestin 1/2 are essential for embryonic lymphatic vessel development.

Beta-arrestin 1/2 are essential for embryonic lymphatic vessel development.

Clinical clues to recognizing hereditary dehydrated stomatocytosis (DHSt) in children.

Clinical clues to recognizing hereditary dehydrated stomatocytosis (DHSt) in children.

Maternal Mirror Syndrome Associated with Hyperreactio Luteinalis and Non-Immune Fetal Hydrops.

Maternal Mirror Syndrome Associated with Hyperreactio Luteinalis and Non-Immune Fetal Hydrops.

Progressive non-immune hydrops fetalis associated with RASA1 mutation: prenatal imaging and genomic insights.

Progressive non-immune hydrops fetalis associated with RASA1 mutation: prenatal imaging and genomic insights.

Severe Aortic Regurgitation with New Congestive Heart Failure Following Fetal Aortic Valvuloplasty - A Case Report.

Severe Aortic Regurgitation with New Congestive Heart Failure Following Fetal Aortic Valvuloplasty - A Case Report.

Genetic screening and typing study of Thalassemia among ethnic Miao Group in Qianxinan area of China

Genetic screening and typing study of Thalassemia among ethnic Miao Group in Qianxinan area of China

Antenatal Diagnosis and Management of Congenital Pulmonary Airway Malformation: A Case Report.

Antenatal Diagnosis and Management of Congenital Pulmonary Airway Malformation: A Case Report.