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| 1 | Compensating for central nervous system dysmyelination:females with a proteolipid protein gene duplication and sustained clinical improvement显示文摘 | Inoue K Tanaka H Scaglia F | 2001 | Ann Neurol2001，50，6： | 1 |
| 2 | Recurrent reciprocal l q21,1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities显示文摘 | Brunetti-Pierri N Berg JS Scaglia F | 2008 | Nat Genet2008，40，12： | 1 |
| 3 | GM1 gangliosidosis : review of clinical,molecular,and therapeutic aspects 显示文摘 | Brunetti-Pierri N Scaglia F | 2008 | Mol Genet Metab2008，94，4： | 1 |
| 4 | Effect of alternative pathway therapy on branched chain amino acid metabolism in urea cycle dis- order patients显示文摘 | Scaglia F Carter S O'Brine WE | 2004 | Mol Genet Metab2004，8110，： | 1 |
| 5 | New insights in nutritional management and amino acid supplementation in urea cycle disorders 显示文摘 | Scaglia F | 2010 | Mol Genet Metab2010，1001，： | 1 |
| 6 | An index for quantifying theaerobic reactivity of municipal solid wastes and derivedwaste products 显示文摘 | B SCAGLIA F ADANI | 2008 | Science of The Total Environment2008，394，1： | 1 |
| 7 | GM 1 gangliosidosis: review of clinical, molecular,and therapeutic aspects 显示文摘 | Brunetti-Pierri N Scaglia F | 2008 | Mol Genet Metab2008，94，4： | 1 |
| 8 | Primary and secondary alterations of neonatal carnitine metabolism 显示文摘 | SCAGLIA F LONGO N | 1999 | Seminars in perinatology1999，23，2： | 1 |
| 9 | Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism 显示文摘 | Scaglia F Brunetti N Kleppe S | 2004 | J Nutr2004，134，10： | 1 |
| 10 | Clinical, Biochemical, and Molecular Spectrum of Hyperargininemia due to Arginase I deficiency 显示文摘 | Scaglia F Lee B | 2006 | Am J Med Genet Part C2006，142，2： | 1 |
| 11 | Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism显示文摘 | Scaglia F Brunetti-Pierri N Kleppe S | 2004 | J Nutr2004，134，10： | 1 |
| 12 | Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males 显示文摘 | Del Gaudio D Fang P Scaglia F | 2006 | Genet Med2006，8，12： | 1 |
| 13 | GM-1 gangliosidosis: review of clinical, molecular, and therapeutic aspects 显示文摘 | Brunetti-Pierri N Scaglia F | 2008 | Mol Genet Metab2008，94，4： | 1 |
| 14 | Effects of biodrying process on municipal solid waste properties显示文摘 | Tambone F Scaglia B Scotti S | 2011 | Bioresource Technol2011，102，16： | 1 |
| 15 | Current molecular diagnostic algorithm for mitochondrial disorders显示文摘 | Wong LJ Scaglia F Graham BH | | 0，，： | 1 |
| 16 | Effects of biodryingprocess on municipal solid waste properties 显示文摘 | Tambone F Scaglia B Scotti S etal | 2011 | Bioresource Technology2011，102，： | 1 |
| 17 | Apoptosis contributes to the involution of Bell mess in the post partum rat pancreas显示文摘 | Scaglia L Smith F E Bonner-Weir | 1995 | Endocrinology1995，136，： | 1 |
| 18 | Predominant cerebellar volume loss as a neuroradiologic feature of pediatric respiratory chain defects显示文摘 | Wong LJ Vladutiu GD | 2005 | Am J Neuroradiol2005，26，： | 1 |
| 19 | Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options显示文摘 | E1-Hattab AW Scaglia F | 2013 | Neurotherapeutics2013，10，2： | 1 |
| 20 | Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options 显示文摘 | E1-Hattab AW Scaglia F | 2013 | Neurotherapeutics2013，10，： | 1 |
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