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101. Abnormal visual-evoked potentials in leukemic children after cranial radiation.

102. Lymphocyte changes in favism: in vitro evidence of a modifying effect of bilirubin and hemoglobin on T-lymphocyte receptors.

103. Hemoglobin G San José [beta 2 7 (A4) Glu to Gly alpha 2], beta thalassemia, and alpha thalassemia in a Sicilian family.

104. Insulin and growth hormone secretion in a leukaemic girl with hypothalamic syndrome.

107. Some aspects of neurotoxicity associated with central nervous system prophylaxis in childhood leukemia.

108. Susceptibility to infections in beta-thalassemia major.

109. Leukocyte function and characterization of leukocyte glucose-6-phosphate dehydrogenase in Sicilian mutants.

110. Unusual combination of genetic defects in a Sicilian boy: G gamma delta beta thalassemia, G gamma A gamma heterocellular HPFH, beta (0) thalassemia, and albinism.

111. Haemoglobin synthesis in bone marrow of patients with beta O and beta +-thalassaemia.

112. Letter: Visceral leishmaniasis in Italy.

113. Transient increase of fetal haemoglobin in kala-azar.

114. Unusual combination of genetic defects in a Sicilian family: beta-thalassaemia, haemoglobin Lepore Boston-Washington and heterocellular hereditary persistence of fetal haemoglobin.

115. T-lymphocyte subpopulation changes during hemolysis in glucose-6-phosphate dehydrogenase (G6PD)-deficient children.

116. Leukocyte alkaline phosphatase (LAP). A useful marker of zinc status in beta-thalassemic patients.

118. Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S.

119. [Influence of transfusion regime on precocious fusion of the proximal humeral epiphysis in thalassemia major].

120. Population structure of eastern Sicily.

122. Hemoglobinopathies in Italy.

124. Convulsions and intracranial calcifications in a leukemic infant receiving only intrathecal methotrexate as central nervous system prophylaxis.

128. New case of apoprotein C-II deficiency.

132. Prenatal diagnosis of thalassemia: the viewpoint of patients.

133. A new rare variant of the glyoxalase I system of the red cell: GLO-Sicily.

135. Heterogeneity of beta-thalassemia intermedia.

136. Fetal haemoglobin in early malignant osteopetrosis.

139. K cell activity in acute lymphoblastic leukaemia of childhood.

141. A case of multiple neonatal haemangiomatosis with favourable outcome following steroid therapy.

143. Cranial irradiation and platelet monoamine oxidase in ALL.

144. Thalassaemia of intermediate severity resulting from the interaction between alpha- and beta-thalassaemia.

146. Early iron chelation therapy in thalassemia major.

148. Abnormal or absent beta mRNA in betao Ferrara and gene deletion in delta beta thalassaemia.

150. Distribution of enzyme polymorphisms in six Sicilian communes.

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