Results 251 to 260 of about 140,652 (287)

The Thalassemias

New England Journal of Medicine, 1976
S H, Orkin, D G, Nathan
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PATHOPHYSIOLOGY OF THALASSEMIA

Annals of the New York Academy of Sciences, 1980
The clinical manifestations in homozygous thalassemia may be attributed to the defect in hemoglobin synthesis (Figure 16). It is best typified by beta thalassemia, where excess alpha chains accumulate to form intracytoplasmic erythrocytic inclusions. This leads to anemia, bone marrow hyperplasia, osteoporosis, hemosiderosis, and organ failure.
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Thalassemia

New England Journal of Medicine, 1972
Daniel Deykin, Christine Balko, David G. Nathan   +2 more
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Thalassemia

Annals of Ophthalmology, 2006
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Thalassemia in China

Annals of the New York Academy of Sciences, 1985
T Y, Yang, X Y, Yang, W C, Ch'en, S L, Qi, Y J, Jin, W J, Gan, Q, Qu   +6 more
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The Thalassemias

2012
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Thalassemia

Hematology/Oncology Clinics of North America, 2018
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Clinical Classification, Screening and Diagnosis for Thalassemia

Hematology/Oncology Clinics of North America, 2018
Chayamon Takpradit, Supachai Ekwattanakit   +1 more
exaly  

Thalassemia trait or thalassemia intermedia

American Journal of Hematology, 2001
openaire   +2 more sources

How I treat thalassemia Free

Blood, 2011
Patricia J Giardina, Eliezer A Rachmilewitz   +1 more
exaly