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22. Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias. Shefer Averbuch N; Steinberg-Shemer O; Dgany O; Krasnov T; Noy-Lotan S; Yacobovich J; Kuperman AA; Kattamis A; Ben Barak A; Roth-Jelinek B; Chubar E; Shabad E; Dufort G; Ellis M; Wolach O; Pazgal I; Abu Quider A; Miskin H; Tamary H Eur J Haematol; 2018 Sep; 101(3):297-304. PubMed ID: 29786897 [TBL] [Abstract][Full Text] [Related]
23. A novel PIEZO1 mutation in a patient with dehydrated hereditary stomatocytosis: a case report and a brief review of literature. Zama D; Giulietti G; Muratore E; Andolfo I; Russo R; Iolascon A; Pession A Ital J Pediatr; 2020 Jul; 46(1):102. PubMed ID: 32703298 [TBL] [Abstract][Full Text] [Related]
24. [In the differential diagnosis of hemolytic anemias]. Blum KU Dtsch Med J; 1967 Feb; 18(3):66-70. PubMed ID: 5594502 [No Abstract] [Full Text] [Related]
25. Inborn errors of metabolism in red cells of congenital hemolytic anemias. PRANKERD TA Am J Med; 1957 May; 22(5):724-9. PubMed ID: 13410962 [No Abstract] [Full Text] [Related]
26. An overview of immune hemolytic anemias. Domen RE Cleve Clin J Med; 1998 Feb; 65(2):89-99. PubMed ID: 9509700 [TBL] [Abstract][Full Text] [Related]
27. THE METABOLISM OF ERYTHROCYTES, AND ITS RELATION TO HEMOLYTIC ANEMIAS IN THE NEWBORN. OSKI FA Pediatr Clin North Am; 1965 Aug; 12():687-712. PubMed ID: 14312833 [No Abstract] [Full Text] [Related]
28. Targeted Next Generation Sequencing (NGS) to Diagnose Hereditary Hemolytic Anemias. Bharadwaj R; Raman T; Thangadorai R; Munirathnam D Int J Hematol Oncol Stem Cell Res; 2020 Jul; 14(3):177-180. PubMed ID: 33024524 [TBL] [Abstract][Full Text] [Related]
29. [Infukoll exchange sedimentation in the framework of diagnosis of hemolytic anemias]. Riechers F; Brandstädter W Dtsch Gesundheitsw; 1968 Jan; 23(2):65-71. PubMed ID: 5697697 [No Abstract] [Full Text] [Related]
30. [Diagnosis of congenital hemolytic anemia by comprehensive gene analysis: significance and limitations]. Kanno H; Ogura H Rinsho Ketsueki; 2021; 62(5):472-479. PubMed ID: 34248124 [TBL] [Abstract][Full Text] [Related]
32. Targeted next-generation sequencing identified novel mutations associated with hereditary anemias in Brazil. Svidnicki MCCM; Zanetta GK; Congrains-Castillo A; Costa FF; Saad STO Ann Hematol; 2020 May; 99(5):955-962. PubMed ID: 32266426 [TBL] [Abstract][Full Text] [Related]
33. Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients. Zaninoni A; Fermo E; Vercellati C; Consonni D; Marcello AP; Zanella A; Cortelezzi A; Barcellini W; Bianchi P Front Physiol; 2018; 9():451. PubMed ID: 29755372 [TBL] [Abstract][Full Text] [Related]
34. Hereditary hemolytic anemias in Greece. HOREMIS K; ZANOS L Bull World Med Assoc; 1953 Jan; 5(1):28. PubMed ID: 13029560 [No Abstract] [Full Text] [Related]
35. [Radioactive iron and chromium study of erythropoiesis and destruction of red corpuscles in congenital hemolytic anemias]. MALAMOS B; GYFTAKI S; KESSE M Rev Med Moyen Orient; 1962; 19():19-30. PubMed ID: 14468798 [No Abstract] [Full Text] [Related]