Author/Creator: Lodi, R - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Lodi, R

1. "Agrypnia excitata" in a case of sporadic Creutzfeldt–Jakob disease VV2. Issue 2 (16th January 2009)

Authors:: La Morgia, C; Parchi, P; Capellari, S; Lodi, R; Tonon, C; Rinaldi, R; Mondini, S; Cirignotta, F
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 80:Issue 2(2009)
Page Start:: 244
Record Type:: Journal Article
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2. Brain and muscle energy metabolism studied in vivo by 31P-magnetic resonance spectroscopy in NARP syndrome. Issue 12 (December 1994)

Authors:: Lodi, R; Montagna, P; Iotti, S; Zaniol, P; Barboni, P; Puddu, P; Barbiroli, B
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 57:Issue 12(1994)
Page Start:: 1492
Record Type:: Journal Article
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3. Brain and skeletal muscle bioenergetic failure in familial hypobetalipoproteinaemia. Issue 6 (June 1997)

Authors:: Lodi, R; Rinaldi, R; Gaddi, A; Iotti, S; D'Alessandro, R; Scoz, N; Battino, M; Carelli, V; Azzimondi, G; Zaniol, P; Barbiroli, B
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 62:Issue 6(1997)
Page Start:: 574
Record Type:: Journal Article
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4. Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathy. Issue 6 (1st June 2002)

Authors:: Lodi, R; Carelli, V; Cortelli, P; Iotti, S; Valentino, M L; Barboni, P; Pallotti, F; Montagna, P; Barbiroli, B
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 72:Issue 6(2002)
Page Start:: 805
Record Type:: Journal Article
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5. Simultaneous penetrating wounds of the myocardium and aorta caused by firearms: surgical treatment. Issue 6 (December 1979)

Authors:: Lodi, R; Bondioli, A; Domenichini, G; Mazzetti, C; Morandi, U; Bonati, L; Byrnes, J J
Journal:: Thorax
Issue:: Volume 34:Issue 6(1979)
Page Start:: 819
Record Type:: Journal Article
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6. The 13042G→A/ND5 mutation in mtDNA is pathogenic and can be associated also with a prevalent ocular phenotype. Issue 7 (30th June 2006)

Authors:: Valentino, M L; Barboni, P; Rengo, C; Achilli, A; Torroni, A; Lodi, R; Tonon, C; Barbiroli, B; Fortuna, F; Montagna, P; Baruzzi, A; Carelli, V
Journal:: Journal of medical genetics
Issue:: Volume 43:Issue 7(2006)
Page Start:: e38
Record Type:: Journal Article
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