Vergani L - Search Results

1

Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitro.

Vergani L, Angelini C. Vergani L, et al. Neuromuscul Disord. 1999 Jul;9(5):320-2. doi: 10.1016/s0960-8966(98)00131-x. Neuromuscul Disord. 1999. PMID: 10407853

2

L-carnitine uptake in differentiating human cultured muscle.

Martinuzzi A, Vergani L, Rosa M, Angelini C. Martinuzzi A, et al. Among authors: vergani l. Biochim Biophys Acta. 1991 Nov 12;1095(3):217-22. doi: 10.1016/0167-4889(91)90102-4. Biochim Biophys Acta. 1991. PMID: 1958696

3

Liver fatty acid-binding protein in two cases of human lipid storage.

Vergani L, Fanin M, Martinuzzi A, Galassi A, Appi A, Carrozzo R, Rosa M, Angelini C. Vergani L, et al. Mol Cell Biochem. 1990 Oct 15-Nov 8;98(1-2):225-30. doi: 10.1007/BF00231388. Mol Cell Biochem. 1990. PMID: 2266963

4

Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient.

Gianazza E, Vergani L, Wait R, Brizio C, Brambilla D, Begum S, Giancaspero TA, Conserva F, Eberini I, Bufano D, Angelini C, Pegoraro E, Tramontano A, Barile M. Gianazza E, et al. Among authors: vergani l. Electrophoresis. 2006 Mar;27(5-6):1182-98. doi: 10.1002/elps.200500687. Electrophoresis. 2006. PMID: 16470778

5

Fatal lipid storage with abnormal mitochondria in an infant.

Angelini C, Battistella PA, Laverda A, Pierobon-Bormioli S, Salviati G, Vergani L. Angelini C, et al. Among authors: vergani l. Acta Neuropathol Suppl. 1981;7:221-5. doi: 10.1007/978-3-642-81553-9_66. Acta Neuropathol Suppl. 1981. PMID: 6939240

6

Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathies.

Vergani L, Barile M, Angelini C, Burlina AB, Nijtmans L, Freda MP, Brizio C, Zerbetto E, Dabbeni-Sala F. Vergani L, et al. Brain. 1999 Dec;122 ( Pt 12):2401-11. doi: 10.1093/brain/122.12.2401. Brain. 1999. PMID: 10581232

7

Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells.

Loro E, Rinaldi F, Malena A, Masiero E, Novelli G, Angelini C, Romeo V, Sandri M, Botta A, Vergani L. Loro E, et al. Among authors: vergani l. Cell Death Differ. 2010 Aug;17(8):1315-24. doi: 10.1038/cdd.2010.33. Epub 2010 Apr 30. Cell Death Differ. 2010. PMID: 20431600

8

Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidation.

Angelini C, Vergani L, Martinuzzi A. Angelini C, et al. Among authors: vergani l. Crit Rev Clin Lab Sci. 1992;29(3-4):217-42. doi: 10.3109/10408369209114601. Crit Rev Clin Lab Sci. 1992. PMID: 1489518 Review.

9

[Myopathies caused by defects of lipid and carbohydrate metabolism].

Angelini C, Martinuzzi A, Micaglio G, Vergani L. Angelini C, et al. Among authors: vergani l. Riv Neurol. 1988 Jan-Feb;58(1):15-25. Riv Neurol. 1988. PMID: 3047844 Review. Italian. No abstract available.

10

Clinical varieties of carnitine and carnitine palmitoyltransferase deficiency.

Angelini C, Trevisan C, Isaya G, Pegolo G, Vergani L. Angelini C, et al. Among authors: vergani l. Clin Biochem. 1987 Feb;20(1):1-7. doi: 10.1016/s0009-9120(87)80090-5. Clin Biochem. 1987. PMID: 3552320 Review.

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