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Academic Journal

Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemia.

  • Authors : Fournier CM; INSERM U409, Faculté de Médecine Xavier Bichat, Paris, France.; Nicolas G

Subjects: Erythrocytes, Abnormal* ; Mutation* ; RNA Splicing*

  • Source: Blood [Blood] 1997 Jun 15; Vol. 89 (12), pp. 4584-90.Publisher: Elsevier Country of Publication: United States NLM ID: 7603509 Publication Model: Print Cited Medium: Print ISSN: 0006-4971 (Print)

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Academic Journal

Evaluation of ICSH schistocyte measurement guidelines in France.

  • Authors : Lesesve JF; Service d'Hématologie Biologique, University Hospital, Nancy, France; Sciences Academy, Nancy, France.

Subjects: Anemia, Hemolytic/Anemia, Hemolytic/Anemia, Hemolytic/*diagnosis ; Erythrocytes, Abnormal/Erythrocytes, Abnormal/Erythrocytes, Abnormal/*pathology ; Practice Guidelines as Topic/Practice Guidelines as Topic/Practice Guidelines as Topic/*standards

  • Source: International journal of laboratory hematology [Int J Lab Hematol] 2013 Dec; Vol. 35 (6), pp. 601-7. Date of Electronic Publication: 2013 Apr 22.Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 101300213 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Incidence of hereditary spherocytosis in a population of jaundiced neonates.

  • Authors : Saada V; Laboratoire d'Hématologie, d'Immunologie et de Cytogénétique, Hôpital de Bicêtre, APHP, and Faculté de Médecine Paris-Sud, Le Kremlin Bicêtre, France.; Cynober T

Subjects: Jaundice, Neonatal/Jaundice, Neonatal/Jaundice, Neonatal/*epidemiology ; Spherocytosis, Hereditary/Spherocytosis, Hereditary/Spherocytosis, Hereditary/*epidemiology; Case-Control Studies

  • Source: Pediatric hematology and oncology [Pediatr Hematol Oncol] 2006 Jul-Aug; Vol. 23 (5), pp. 387-97.Publisher: Informa Healthcare Country of Publication: England NLM ID: 8700164 Publication Model: Print Cited Medium: Internet ISSN: 1521-0669

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Academic Journal

Hb Gerland [alpha55(E4)Val-->Ala (alpha2)]: a new neutral alpha chain variant involving the alpha2 gene.

  • Authors : Lacan P; Molecular Pathology Unit, Department of Biochemistry, Edouard Herriot Hospital, Lyon, France.; Aubry M

Subjects: Hemoglobins, Abnormal/Hemoglobins, Abnormal/Hemoglobins, Abnormal/*genetics ; alpha-Thalassemia/alpha-Thalassemia/alpha-Thalassemia/*genetics; Adult

  • Source: Hemoglobin [Hemoglobin] 2001 Nov; Vol. 25 (4), pp. 417-20.Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print Cited Medium: Print ISSN: 0363-0269

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Academic Journal

[Results of hemograms of a series of top-level cyclists: an example of a factor of biological variability].

Subjects: Blood Cell Count* ; Hematologic Tests*; Bicycling/Bicycling/Bicycling/*physiology

  • Source: Annales de biologie clinique [Ann Biol Clin (Paris)] 2000 Jul-Aug; Vol. 58 (4), pp. 467-71.Publisher: John Libbey Eurotext Country of Publication: France NLM ID: 2984690R Publication Model: Print Cited Medium:

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Academic Journal

[Frequency of thalassemia in the South-East of France].

Subjects: Thalassemia/Thalassemia/Thalassemia/*epidemiology; Anemia, Hypochromic/Anemia, Hypochromic/Anemia, Hypochromic/diagnosis ; Chromatography, DEAE-Cellulose

  • Source: Nouvelle revue francaise d'hematologie [Nouv Rev Fr Hematol (1978)] 1976; Vol. 16 (3), pp. 329-36.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7909092 Publication Model: Print Cited Medium: Print NLM ISO Abbreviation:

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  • 1-7 of  7 results for ""Erythrocytes, Abnormal""