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Academic Journal

Updates on clinical and laboratory aspects of hereditary dyserythropoietic anemias.

Subjects: CONGENITAL hemolytic anemia; HIGH throughput screening (Drug development); GENOME-wide association studies

  • Source: International Journal of Laboratory Hematology; Aug2024, Vol. 46 Issue 4, p595-605, 11p

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Academic Journal

Southeast Asian ovalocytosis detected in a critical patient with COVID‐19 pneumonia.

Subjects: CLINICAL pathology; COVID-19; GENETIC mutation

  • Source: International Journal of Laboratory Hematology. Oct2022, Vol. 44 Issue 5, pe215-e218. 4p.

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Academic Journal

Posterior reversible encephalopathy syndrome in a child, following splenectomy under combined general and spinal anaesthesia.

Subjects: SPLENECTOMY; GENERAL anesthesia; LORAZEPAM

  • Source: Anaesthesia Reports; Jul-Dec2023, Vol. 11 Issue 2, p1-4, 4p

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Academic Journal

Hereditary spherocytosis without pronounced spherocytes on the peripheral blood smear.

Subjects: BLOOD testing; HYPERBILIRUBINEMIA; NEONATAL jaundice

  • Source: International Journal of Laboratory Hematology. Feb2023, Vol. 45 Issue 1, p6-8. 3p.

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Academic Journal

A novel SPTB frameshift deletion causing hereditary spherocytosis identified by next‐generation sequencing in a Chinese family.

Subjects: GENETIC mutation; SEQUENCE analysis; GENETIC variation

  • Source: International Journal of Laboratory Hematology. Dec2021, Vol. 43 Issue 6, pe294-e297. 4p.

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Academic Journal

Quantitative measurement of red cell surface protein expression reveals new biomarkers for hereditary spherocytosis.

Subjects: *CONGENITAL hemolytic anemia; *ACADEMIC medical centers; *ERYTHROCYTESNETHERLANDS

  • Source: International Journal of Laboratory Hematology. Aug2018, Vol. 40 Issue 4, pe74-e77. 4p.

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Academic Journal

Detection of Southern Asian Ovalocytosis with Sysmex XN‐10: A complement to the decision tree previously described.

Subjects: LABORATORY equipment & supplies; AUTOMATION equipment; DECISION treesSOUTH Asia

  • Source: International Journal of Laboratory Hematology. Apr2022, Vol. 44 Issue 2, pe84-e86. 3p.

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Academic Journal

Novel PLKR mutations in four families with pyruvate kinase deficiency.

Subjects: FAMILIES; GENES; GENETIC mutation

  • Source: International Journal of Laboratory Hematology. Apr2020, Vol. 42 Issue 2, pe84-e87. 4p.

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Academic Journal

Evaluation of a hereditary spherocytosis screening algorithm by automated blood count using reticulocytes and erythrocytic parameters on the Sysmex XN‐series.

Subjects: ERYTHROCYTES; ALGORITHMS; BLOOD cell countBELGIUM

  • Source: International Journal of Laboratory Hematology. Apr2020, Vol. 42 Issue 2, pe88-e91. 4p.

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Academic Journal

Coinheritance of hereditary ellyptocytosis, pyruvate kinase, and glucose‐6‐phosphate dehidrogenase mutations. A rare anemia diagnostic paradigm.

Subjects: ERYTHROCYTES; ALLELES; BLOOD testing

  • Source: International Journal of Laboratory Hematology. Apr2020, Vol. 42 Issue 2, pe55-e58. 4p.

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  • 1-10 of  147 results for ""CONGENITAL hemolytic anemia""