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121. Objective To evaluate the safety measures for children with severe aplastic anemia, treated by the combination of human immunoglobulin and cyclosporin A.

122. Results The most common clinical symptoms were menorrhagia, anemia, pain and sterility.

123. Objective To evaluate the clinical implications of IgG subclass in autoimmune hemolytic anemia ( AIHA ).

124. Objective: To explore the clinical therapeutic method with simple, easy and less side effect for the infant with Mediterranean anemia.

125. Patients with primary myelofibrosis feel fatigued, and they sometimes take an anemia drug to stimulate growth of oxygen-carrying red blood cells.

126. In doing so, they paved the way for the early detection of genetic diseases such as sickle-cell anemia, and for new scientific leaps such as animal cloning.

127. Objective : To analyze the clinical features and treatment outcomes of autoirnmune hemolytic anemia ( AIHA ).

128. The most common cause for a hypochromic microcytic anemia is iron deficiency.

129. The patients involved did not suffered from anemia, liver and renal function disfunction, heart and cerebrovascular disease, diabetes and TB.

130. Inherited deficiency of pyruvate kinase, a key glycolytic enzyme, causes ATP deficiency, which leads to reduced RBC life span and hemolytic anemia.

131. Pernicious anemia: Slow - developing disease in which vitamin B 12 deficiency impairs red - Blood - cell production.

132. Results:8 cases were positive by screening and the positive rate was 0.16%. 3 cases were pregnant women, 3 cases were Mediterranean anemia and 2 cases were blood disease.

133. The main clinical features included longterm fever, anepithymia, weight loss , pain upper quadrant, splenomegalia, and anemia.

134. Examples of so-called SNP diseases are sickle-cell anemia and Huntington's disease, where a single variant or mutation has a dramatic effect.

135. Objective To explore the changes of immature reticulocyte fraction (IRF) in renal anemia.

136. Objective : To improve recognization of treatment to autoimmune hemolytic anemia.

137. The prevalence of anemia which ever reported was only 1.18 % among IUD users.

138. You only get malaria protection. It's only when you inherit the mutation from both parents that you get sickle-cell anemia.

139. Thus, leukemic patients are prone to anemia, thrombocytopenia, and granulocytopenia and all of the complications that ensue(sentencedict.com), particularly complications of bleeding and infection.

140. Paying more attention to environmental and social changes would be helpful to prevent aplastic anemia.

141. Methods: The clinical data of 42 in patients with senile megaloblastic anemia was analyzed.

142. Signicant signs of HAN poisoning include hemolytic anemia, methemoglobinemia, splenomegaly,(Sentencedict) erythrocyte destruction and Heinz body formation.

143. Sickle-cell anemia is a blood disease that causes the cell to form a characteristic sickle-shape.

144. The study was aimed to explore clinical result of cyclosporin A (CsA) and androgens for treatment of myelodysplastic syndrome (MDS) with refractory anemia.

145. He had juvenile diabetes, anemia, a skin infection, and so many other complications that Hill can't even recall them all.

146. The clinical research part of this project aims to observe the clinical effect of tortoise plastron as an enrichment of kidney on aplastic anemia which falls into the category of deficiency of Yin.

147. Aplastic anemia , a disease of the bone marrow, is a rare disorder in the United States.

148. Chemical factors were the most common reason for secondary aplastic anemia.

149. These medicines, called biologics or biologicals, are typically injected and treat a range of conditions including anemia, rheumatoid arthritis, hepatitis and cancer.

150. Hemolytic anemia, enlargement of the spleen, and pathologic changes in the liver, kidneys, and heart muscle may occur as secondary effects of methemoglobinemia , which is reversible.