Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency - 07/10/17
Doi : 10.1016/S0022-3476(05)80039-3
Carlo Dionisi Vici, MD a, b, c, d, Alberto B. Burlina, MD a, b, c, d, Enrico Bertini, MD a, b, c, d, Claude Bachmann, MD a, b, c, d, Mercedes R.M. Mazziotta, MD a, b, c, d, ⁎, F. Zacchello, MD a, b, c, d, Gaetano Sabetta, MD a, b, c, d, Daniel E. Hale, MD a, b, c, d
a Department of Metabolism, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy
b Department of Pediatrics, University of Padua, Padua, Italy
c Department of Clinical Chemistry, Centre Hospitalier Universitaire Vaudois, University of Lausanne, Lausanne, Switzerland
d Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania USA
*Reprint requests: Daniel E. Hale, MD, Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia, 34th Street at Civic Center Boulevard, Philadelphia, PA 19104.
© 1991
Publié par Elsevier Masson SAS.
Vol 118 - N° 5
P. 744-746 - mai 1991 Retour au numéro
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