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Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. 1991
C Dionisi Vici, and
A B Burlina, and
E Bertini, and
C Bachmann, and
M R Mazziotta, and
F Zacchello, and
G Sabetta, and
D E Hale
Department of Metabolism, Bambino Gesù Children's Hospital, Rome, Italy.
Related Publications
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Neuromuscular disorders : NMD,
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December 2007,
Revista espanola de cardiologia,
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M R Mazziotta, and
F Zacchello, and
G Sabetta, and
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International journal of cardiology,
C Dionisi Vici, and
A B Burlina, and
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M R Mazziotta, and
F Zacchello, and
G Sabetta, and
D E Hale
February 1993,
Lancet (London, England),
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A B Burlina, and
E Bertini, and
C Bachmann, and
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F Zacchello, and
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December 1997,
The Journal of pediatrics,
C Dionisi Vici, and
A B Burlina, and
E Bertini, and
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F Zacchello, and
G Sabetta, and
D E Hale
June 1997,
American journal of ophthalmology,
C Dionisi Vici, and
A B Burlina, and
E Bertini, and
C Bachmann, and
M R Mazziotta, and
F Zacchello, and
G Sabetta, and
D E Hale
February 1999,
Neurology,
C Dionisi Vici, and
A B Burlina, and
E Bertini, and
C Bachmann, and
M R Mazziotta, and
F Zacchello, and
G Sabetta, and
D E Hale
January 2017,
Retinal cases & brief reports,
C Dionisi Vici, and
A B Burlina, and
E Bertini, and
C Bachmann, and
M R Mazziotta, and
F Zacchello, and
G Sabetta, and
D E Hale
January 2012,
Ophthalmic research,
C Dionisi Vici, and
A B Burlina, and
E Bertini, and
C Bachmann, and
M R Mazziotta, and
F Zacchello, and
G Sabetta, and
D E Hale
March 1998,
American journal of obstetrics and gynecology,
