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Pediatric Pathology|July 1, 1991
Diagnosis of unsuspected fetal metabolic storage disease by routine placental examinationD J Roberts, M G Ampola, J M LageThe New England Journal of Medicine|August 14, 1975
Prenatal therapy of a patient with vitamin-B12-responsive methylmalonic acidemiaM G Ampola, M J Mahoney, E Nakamura, et al.Pediatric Neurology|March 1, 1989
Intermittent dystonia in Hartnup diseaseB T Darras, M G Ampola, W H Dietz, et al.Journal of Child Neurology|August 1, 1997
Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature reviewA N Prasad, J C Breen, M G Ampola, et al.Pediatric Research|March 1, 1984
Congenital expression of prolidase defect in prolidase deficiencyE R Naughten, S P Proctor, H L Levy, et al.American Journal of Human Genetics|May 1, 1983
The prognosis of hyperlysinemia: an interim reportJ Dancis, J Hutzler, M G Ampola, et al.The Journal of Pediatrics|March 1, 1987
New England Maternal PKU Project: prospective study of untreated and treated pregnancies and their outcomesF J Rohr, L B Doherty, S E Waisbren, et al.Pageof 1