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Bollettino Della Societa Italiana Di Biologia Sperimentale|February 28, 1984
[Nutritional habits of homozygote beta-thalassemic subjects]P Pranzetti, L Manca, G Cuccuru, et al.British Journal of Haematology|May 1, 1991
Diminished A gamma T fetal globin levels in Sardinian haplotype II beta 0-thalassaemia patients are associated with a four base pair deletion in the A gamma T promoterL Manca, E Cocco, D Gallisai, et al.Hemoglobin|January 1, 1988
Abnormal gamma-globin gene arrangements in SardiniansL Manca, B Masala, M Orzalesi, et al.The Cochrane Database of Systematic Reviews|October 21, 2006
Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron diseaseS E Langmore, E J Kasarskis, M L Manca, et al.The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Clinical and biochemical features of muscle dysfunction in subclinical hypothyroidismF Monzani, N Caraccio, G Siciliano, et al.Hemoglobin|March 18, 2000
A new, electrophoretically silent, fetal hemoglobin variant: Hb F-Calabria [Ggamma118(GH1)Phe-->Leu]L Manca, L Cherchi, M C De Rosa, et al.Neuromuscular Disorders : NMD|March 11, 2000
Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathiesG Siciliano, M L Manca, M Renna, et al.Clinical Genetics|August 31, 1999
Epidemiology of dystrophinopathies in North-West Tuscany: a molecular genetics-based revisitationG Siciliano, A Tessa, M Renna, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathiesG Siciliano, M Mancuso, L Pasquali, et al.Biochemical Genetics|October 1, 1991
Electrophoretic and chromatographic evidence for allelic polymorphisms in the river buffalo alpha-globin gene complexA Di Luccia, L Iannibelli, P Ferranti, et al.Pageof 10