Pubblicazioni dott.ssa Federica Invernizzi 26. Baruffini E, Horvath R ...
Pubblicazioni dott.ssa Federica Invernizzi 26. Baruffini E, Horvath R ...
Pubblicazioni dott.ssa Federica Invernizzi 26. Baruffini E, Horvath R ...
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galactocerebrosidase gene in neural progenitor cells. Neuroreport. 1998<br />
Dec 1;9(17):3823-7.<br />
03. Wataya K, Akanuma J, Cavadini P, Aoki Y, Kure S, <strong>Invernizzi</strong> F,<br />
Yoshida I, Kira J, Taroni F, Matsubara Y, Narisawa K. Two CPT2<br />
mutations in three Japanese patients with carnitine palmitoyltransferase II<br />
deficiency: functional analysis and association with polymorphic<br />
haplotypes and two clinical phenotypes. Hum Mutat. 1998;11(5):377-86.<br />
02. Ribes A, Riudor E, Garavaglia B, Martinez G, Arranz A, <strong>Invernizzi</strong> F,<br />
Briones P, Lamantea E, Sentis M, Barcelo A, Roig M. Mild or absent<br />
clinical signs in twin sisters with short-chain acyl-CoA dehydrogenase<br />
deficiency. Eur J Pediatr. 1998 Apr;157(4):317-20.<br />
01. Minetti C, Garavaglia B, Bado M, <strong>Invernizzi</strong> F, Bruno C, Rimoldi M,<br />
Pons R, Taroni F, Cordone G. Very-long-chain acyl-coenzyme A<br />
dehydrogenase deficiency in a child with recurrent myoglobinuria.<br />
Neuromuscul Disord. 1998 Feb;8(1):3-6.<br />
Milano, 26-04-2010 dr.<strong>ssa</strong> <strong>Federica</strong> <strong>Invernizzi</strong><br />
<strong>Pubblicazioni</strong> F. <strong>Invernizzi</strong> Pagina 4 di 4
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