✦ LIBER ✦

Homozygous Hereditary Elliptocytosis as the Cause of Haemolytic Anemia in Infancy

✍ Scribed by Nielsen, J. A. ;Strunk, K. W.

Book ID: 114788000
Publisher: Wiley (Blackwell Publishing)
Year: 2009
Weight: 538 KB
Volume: 5
Category: Article
ISSN: 0036-553X
DOI: 10.1111/j.1600-0609.1968.tb00869.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Enzyme deficiencies as the cause of here

Enzyme deficiencies as the cause of hereditary nonspherocytic hemolytic anemia

✍ A. Casado; Ma Casado; Ma R De la Torre; Ma E Lopéz-Fernandez; D. Carrascosa 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 96 KB

BLOOD TRANSFUSION FOR HAEMOLYTIC DISEASE

BLOOD TRANSFUSION FOR HAEMOLYTIC DISEASE AS A CAUSE OF LEUKOCYTOSIS IN THE FETUS

✍ JEROME YANKOWITZ; CARL P. WEINER 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 301 KB 👁 2 views

We evaluated the effect of fetal intravascular transfusion (IVT) of leukocyte-poor red blood cells to correct fetal anaemia due to haemolytic disease on the fetal leukocyte count in 153 patients. Initial, mid-transfusion, and closing haematological studies were obtained when possible. The effect on

Serological identification of Escherichi

Serological identification of Escherichia coli 0157 as cause of haemolytic uraemic syndrome in Netherlands

✍ Chart, Henrik; Rowe, Bernard; Kar, N.Vd; Monnens, L.A.H 📂 Article 📅 1991 🏛 The Lancet 🌐 English ⚖ 169 KB

Serotonin Deficiency in Infancy as One C

Serotonin Deficiency in Infancy as One Cause of a Mental Defect in Phenylketonuria

✍ Woolley, D. W.; Van Der Hoeven, Th. 📂 Article 📅 1964 🏛 American Association for the Advancement of Scienc 🌐 English ⚖ 961 KB

Gene deletion as the cause of α thalassa

Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)

✍ TAYLOR, J. M.; DOZY, ANDREE; KAN, Y. W.; VARMUS, H. E.; LIE-INJO, L. E.; GANESAN 📂 Article 📅 1974 🏛 Nature Publishing Group 🌐 English ⚖ 238 KB

Mutations in the sterol 27-hydoxylase ge

Mutations in the sterol 27-hydoxylase gene (CYP27A) cause hepatitis of infancy as well as cerebrotendinous xanthomatosis

✍ P. T. Clayton; A. Verrips; E. Sistermans; A. Mann; G. Mieli-Vergani; R. Wevers 📂 Article 📅 2002 🏛 Springer 🌐 English ⚖ 109 KB