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Argininemia: a treatable genetic cause of progressive spastic diplegia simulating cerebral palsy: case reports and literature review.
Prasad AN, Breen JC, Ampola MG, Rosman NP. Prasad AN, et al. Among authors: ampola mg. J Child Neurol. 1997 Aug;12(5):301-9. doi: 10.1177/088307389701200502. J Child Neurol. 1997. PMID: 9378897 Review.
Transient neonatal hyperglycinemia.
Schiffmann R, Kaye EM, Willis JK 3rd, Africk D, Ampola M. Schiffmann R, et al. Ann Neurol. 1989 Feb;25(2):201-3. doi: 10.1002/ana.410250218. Ann Neurol. 1989. PMID: 2919871
Abnormal cholesterol metabolism in the Smith-Lemli-Opitz syndrome: report of clinical and biochemical findings in four patients and treatment in one patient.
Irons M, Elias ER, Tint GS, Salen G, Frieden R, Buie TM, Ampola M. Irons M, et al. Am J Med Genet. 1994 May 1;50(4):347-52. doi: 10.1002/ajmg.1320500409. Am J Med Genet. 1994. PMID: 8209913
Intermittent dystonia in Hartnup disease.
Darras BT, Ampola MG, Dietz WH, Gilmore HE. Darras BT, et al. Among authors: ampola mg. Pediatr Neurol. 1989 Mar-Apr;5(2):118-20. doi: 10.1016/0887-8994(89)90038-6. Pediatr Neurol. 1989. PMID: 2712944
New England Consortium: a model for medical evaluation of expanded newborn screening with tandem mass spectrometry.
Albers S, Waisbren SE, Ampola MG, Brewster TG, Burke LW, Demmer LA, Filiano J, Greenstein RM, Ingham CL, Korson MS, Marsden D, Schwartz RC, Seashore MR, Shih VE, Levy HL. Albers S, et al. Among authors: ampola mg. J Inherit Metab Dis. 2001 Apr;24(2):303-4. doi: 10.1023/a:1010391623104. J Inherit Metab Dis. 2001. PMID: 11405349 No abstract available.
Newborn screening compared to clinical identification of biochemical genetic disorders.
Waisbren SE, Read CY, Ampola M, Brewster TG, Demmer L, Greenstein R, Ingham CL, Korson M, Msall M, Pueschel S, Seashore M, Shih VE, Levy HL; New England Consortium of Metabolic Programs. Waisbren SE, et al. J Inherit Metab Dis. 2002 Nov;25(7):599-600. doi: 10.1023/a:1022003726224. J Inherit Metab Dis. 2002. PMID: 12638945
The prognosis of hyperlysinemia: an interim report.
Dancis J, Hutzler J, Ampola MG, Shih VE, van Gelderen HH, Kirby LT, Woody NC. Dancis J, et al. Among authors: ampola mg. Am J Hum Genet. 1983 May;35(3):438-42. Am J Hum Genet. 1983. PMID: 6407303 Free PMC article.
Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
Waisbren SE, Albers S, Amato S, Ampola M, Brewster TG, Demmer L, Eaton RB, Greenstein R, Korson M, Larson C, Marsden D, Msall M, Naylor EW, Pueschel S, Seashore M, Shih VE, Levy HL. Waisbren SE, et al. JAMA. 2003 Nov 19;290(19):2564-72. doi: 10.1001/jama.290.19.2564. JAMA. 2003. PMID: 14625333
Determination of phenylalanine and tyrosine in dried blood specimens by ion-exchange chromatography using the Hitachi L-8800 analyzer.
Allard P, Cowell LD, Zytkovicz TH, Korson MS, Ampola MG. Allard P, et al. Among authors: ampola mg. Clin Biochem. 2004 Oct;37(10):857-62. doi: 10.1016/j.clinbiochem.2004.06.004. Clin Biochem. 2004. PMID: 15369715
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