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leukocyte vs leucocyte

Both 'leukocyte' and 'leucocyte' are correct spellings of the term referring to a type of white blood cell. The spelling 'leukocyte' is more commonly used in American English, while 'leucocyte' is more common in British English. Both spellings are widely accepted and understood in the medical field.

Last updated: March 24, 2024 • 864 views

leukocyte

This is a correct spelling of the term referring to a type of white blood cell.

The term 'leukocyte' is commonly used in American English to refer to a type of white blood cell.
  • The BAL fluid may be analysed for total and differential leukocyte counts, total protein, and lactate dehydrogenase.
  • Leukocyte and histamine levels are normal.
  • If leukocyte counts exceed 50 x 109/ l after the expected nadir, filgrastim should be discontinued immediately.
  • It reduces leukocyte infiltration into the inflamed tissue.
  • Decreased serum estradiol and progesterone concentrations have been lon reported in women treated with human leukocyte interferon.
  • Decreased serum estradiol and progesterone concentrations have been reported in women treated with human leukocyte interferon.
  • Positive dipstick for leukocyte esterase and/or nitrate
  • Preclinical data from conventional studies of repeated dose toxicity revealed the expected pharmacological effects including increases in leukocyte count, myeloid hyperplasia in bone marrow, extramedullary haematopoiesis and splenic enlargement.
  • Those are the only people who are a match for Nesbit's blood type and human leukocyte antigen.
  • However, during the period of administration of filgrastim for PBPC mobilisation, it should be discontinued or its dose should be reduced if the leukocyte counts rise to > 70 x 109/ l.
  • Decreased serum estradiol and progesterone concentrations have been reported in women treated with human leukocyte interferon. na
  • It is recommended that chemotherapy not be added to treatment with steroids since there is no experience with administration of both steroids and chemotherapy during treatment of the leukocyte activation syndrome due to TRISENOX.
  • Leukocyte and histamine levels are normal.
  • Leukocyte Activation Syndrome (APL Differentiation Syndrome):
  • pharmacological effects including increases in leukocyte count, myeloid hyperplasia in bone marrow, od
  • International Units are determined by comparison of the activity of the recombinant interferon alfa-2b with the activity of the international reference preparation of human leukocyte interferon established by the World Health Organisation.
  • recombinant interferon alfa-2b with the activity of the international reference preparation of human leukocyte interferon established by the World Health Organisation. na
  • Cetuximab has not been studied in patients presenting with one or more of the following laboratory parameters: haemoglobin < 9 g/ dl leukocyte count < 3000/ mm³ absolute neutrophil count < 1500/ mm³ platelet count < 100000/ mm³
  • This is a human leukocyte workup.
  • If leukocyte counts exceed 50 x 109/ l after the expected nadir, filgrastim should be discontinued immediately.

Alternatives:

  • white blood cell
  • white cell
  • WBC
  • granulocyte
  • lymphocyte

leucocyte

This is a correct spelling of the term referring to a type of white blood cell.

The term 'leucocyte' is more commonly used in British English to refer to a type of white blood cell.
  • Patients receiving gemcitabine should be monitored prior to each dose for platelet, leucocyte and granulocyte counts.
  • Dose-limiting adverse reactions are reductions in thrombocyte, leucocyte and granulocyte counts (see section 4.2).
  • A closer monitoring of the leucocyte cystine levels is recommended in these patients.
  • Dose adjustment is not normally required; however, leucocyte cystine levels should be monitored.
  • The following haematological examinations should be made at the end of the test period: haematocrit, haemoglobin concentration, erythrocyte count, total and differential leucocyte count, platelet count and a measure of blood clotting time/potential.
  • haematology, including at least haematocrit, haemoglobin concentration, erythrocyte count, total and differential leucocyte count and a measure of clotting potential;
  • The following haematological examinations should be made at the end of the test period: haematocrit, haemoglobin concentrations, erythrocyte count, reticulocytes, total and differential leucocyte count, platelet count and a measure of blood clotting time/potential.
  • The goal of therapy is to keep leucocyte cystine levels below 1 nmol hemicystine/ mg protein.
  • Nephropathic cystinosis must have been diagnosed by both clinical signs and biochemical investigations (leucocyte cystine measurements).
  • The dose should be raised if there is adequate tolerance and the leucocyte cystine level remains > 1 nmol hemicystine/ mg protein.
  • Her leucocyte level is getting lower and lower
  • The leucocyte cystine level reaches its minimum (mean (± sd) value:
  • - When your or your child's disorder has been confirmed by leucocyte cystine measurements, the
  • The decrease in leucocyte cystine levels is correlated to the cysteamine plasma concentration over the six hours following the administration of CYSTAGON.

Alternatives:

  • white blood cell
  • white cell
  • WBC
  • granulocyte
  • lymphocyte

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