Anemia, Sickle Cell

Anemia, Sickle Cell

Definition: A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.

Hemic and Lymphatic Diseases > Hematologic Diseases > Hemoglobinopathies > Anemia, Sickle Cell

Articles related to this term...

• Clinical And Hematological Considerations On A Case Of Microdrepanocytic Disease.

  La Clinica pediatrica

  [More Like This]

• Fat Embolization Associated With Sickle Cell Crisis.

  The Southern medical journal

  [More Like This]

• Sickle Cell Anaemia In An African Child From Nyasaland.

  The Central African journal of medicine

  [More Like This]

• 4 Cases Of A Hemopathic Syndrome Observed In A Group Of Greek Families Characterized By A Hemoglobin With A Greater Electrophoretic Velocity Than Hemoglobin A (Possibly The So-Called Hemoglobin H) & By A Perceptible Ovalocytosis.

  Haematologica

  [More Like This]

• A Study Of Cardiopulmonary Alterations In Patients With Sickle Cell Disease And Its Variants.

  The Journal of clinical investigation

  [More Like This]

• A Study Of The Relationship Between Sickling And Hookworms.

  East African medical journal

  [More Like This]

• Abnormal Hemoglobins In Relation To Diseases.

  Rendiconti - Istituto superiore di sanità

  [More Like This]

• Abnormal Human Haemoglobins. I. The Comparison Of Normal Human And Sickle-Cell Haemoglobins By Fingerprinting.

  Biochimica et biophysica acta

  [More Like This]

• Abnormal Human Haemoglobins. Ii. The Chymotryptic Digestion Of The Trypsin-Resistant Core Of Haemoglobins A And S.

  Biochimica et biophysica acta

  [More Like This]

• Anatomicoclinical Study Of A Case Of Microdrepanocytic Anemia.

  Acta haematologica

  [More Like This]

• Cases From The Medical Grand Rounds, Massachusetts General Hospital; Case 412.

  American practitioner and digest of treatment

  [More Like This]

• Gene Mutations In Human Haemoglobin: The Chemical Difference Between Normal And Sickle Cell Haemoglobin.

  Nature

  [More Like This]

• Gross Hematuria In Sickle-Cell Trait; A Report Of Eight Cases.

  A.M.A. archives of internal medicine

  [More Like This]

• Hb.S-Thalassaemia Disease In India.

  Journal of the Indian Medical Association

  [More Like This]

• Hemoglobin S-C Disease.

  Clinical proceedings - Children's Hospital of the District of Columbia

  [More Like This]

• Hemophilia C & S In A 13-Year-Old Child.

  Pédiatrie

  [More Like This]

• Hereditary Persistence Of Foetal Haemoglobin Production, And Its Interaction With The Sickle-Cell Trait.

  British journal of haematology

  [More Like This]

• Inherited Chronic Hemolytic Anemia: Interaction Of Hemoglobin S With Thalassemia: Case Reports.

  Indian journal of medical sciences

  [More Like This]

• Malignant Melanoma Of The Ciliary Body.

  American journal of ophthalmology

  [More Like This]

• New Research On Drepanocytosis In Madagascar.

  Bulletin de la Société de pathologie exotique et de ses filiales

  [More Like This]