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Haematologica|July 1, 1990
Preliminary experience with the differential pH technique for glucose-6-phosphate dehydrogenase (G6PD) measurement in whole blood: application to an area with high prevalence of thalassaemia and G6PD deficiencyA Mosca, M Paderi, A Sanna, et al.Current Opinion in Ophthalmology|August 21, 2023
Linezolid optic neuropathyH Victoria Miller, Angela A Cao, Collin M McClelland, et al.Plant Disease|March 12, 2019
QTLs for Resistance to Fusarium Ear Rot in a Multiparent Advanced Generation Intercross (MAGIC) Maize PopulationA Butrón, R Santiago, A Cao, et al.European Journal of Nuclear Medicine|January 1, 1982
An analytical approach to single photon emission computed tomography with the attenuation effectF P Soussaline, A Cao, G Le Coq, et al.The Journal of Biological Chemistry|October 25, 1984
Initiation codon mutation as a cause of alpha thalassemiaM Pirastu, G Saglio, J C Chang, et al.International Journal of Spine Surgery|May 28, 2019
Postoperative Complications Following Orthopedic Spine Surgery: Is There a Difference Between Men and Women?Jessica H Heyer, N A Cao, Richard L Amdur, et al.Gait & Posture|December 20, 2019
Causes of out-toeing gait in children with cerebral palsyLisa A Cao, Susan A Rethlefsen, Tishya A L Wren, et al.European Journal of Pediatrics|March 21, 1998
Early and severe neurological features in a Wilson disease patient compound heterozygous for two frameshift mutationsA Angius, V Dessi, M Lovicu, et al.Human Genetics|September 1, 1990
Molecular bases for cystic fibrosis in the Sardinian populationG B Leoni, C Rosatelli, R Sardu, et al.Haematologica|March 26, 1999
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemiaR Galanello, M D Cipollina, C Dessì, et al.Pageof 37