✦ LIBER ✦

Body Composition in Homozygous β-Thalassemia

✍ Scribed by J. KALEF-EZRA; A. ZIBIS; N. CHALIASSOS; I. HATZIKONSTANTINOU; A. KARANTANAS

Book ID: 111396450
Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 155 KB
Volume: 904
Category: Article
ISSN: 0890-6564
DOI: 10.1111/j.1749-6632.2000.tb06527.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Amenorrhea in β-Homozygous Thalassemia M

Amenorrhea in β-Homozygous Thalassemia Major

✍ GEORGE TOLIS; ARTEMIS PAPANDREOU; IOANNIS KARYDIS 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 399 KB

Pulmonary function abnormalities in homo

Pulmonary function abnormalities in homozygous β-thalassemia

✍ Reed W. Hoyt; Nina Scarpa; Robert W. Wilmott; Alan Cohen; Elias Schwartz 📂 Article 📅 1986 🏛 Elsevier Science 🌐 English ⚖ 299 KB

α-Globin loci in homozygous β-thalassemi

α-Globin loci in homozygous β-thalassemia intermedia

✍ P. Triadou; C. Lapoumeroulie; R. Girot; D. Labie 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 279 KB

Homozygous beta-thalassemia intermediate (TI) differs from thalassemia major (TM) in being less severe clinically. Associated alpha-thalassemia could account for the TI phenotype by reducing the alpha/non-alpha chain imbalance. We have analyzed the alpha loci of 9 TI and 11 TM patients by restrictio

Insulin resistance and hyperinsulinemia

Insulin resistance and hyperinsulinemia in homozygous β-thalassemia

✍ Paolo Cavallo-Perin; Giovanni Pacini; Franco Cerutti; Anna Bessone; Carmen Condo 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 581 KB

Survival in Medically Treated Patients w

Survival in Medically Treated Patients with Homozygous β-Thalassemia

✍ Olivieri, Nancy F.; Nathan, David G.; MacMillan, James H.; Wayne, Alan S.; Liu, 📂 Article 📅 1994 🏛 Massachusetts Medical Society 🌐 English ⚖ 894 KB

Different severity of homozygous β-thala

Different severity of homozygous β-thalassemia among siblings

✍ P. Winichagoon; S. Fucharoen; V. Thonglairoam; P. Wasi 📂 Article 📅 1987 🏛 Springer 🌐 English ⚖ 172 KB

Different degrees of severity of anemia are presented in three siblings with homozygous beta-thalassemia. II-1, the most severely affected one, is splenectomized and needs frequent blood transfusion, while II-4 has mild anemia and never receives transfusion. II-3 has moderate anemia and mild jaundic