Kaplan P - Search Results

1

Reversible metabolic myopathy in biotinidase deficiency: its possible role in causing hypotonia.

Bay CA, Berry GT, Glauser TA, Hayward JC, Wolf B, Sladky JT, Kaplan P. Bay CA, et al. Among authors: kaplan p. J Inherit Metab Dis. 1995;18(6):701-4. doi: 10.1007/BF02436759. J Inherit Metab Dis. 1995. PMID: 8750607

2

Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.

Bergoffen J, Kaplan P, Hale DE, Bennett MJ, Berry GT. Bergoffen J, et al. Among authors: kaplan p. J Inherit Metab Dis. 1993;16(5):851-6. doi: 10.1007/BF00714277. J Inherit Metab Dis. 1993. PMID: 8295400

3

The glutamine paradox in a neonate with propionic acidaemia and severe hyperammonaemia.

Ierardi-Curto L, Kaplan P, Saitta S, Mazur A, Berry GT. Ierardi-Curto L, et al. Among authors: kaplan p. J Inherit Metab Dis. 2000 Feb;23(1):85-6. doi: 10.1023/a:1005659132147. J Inherit Metab Dis. 2000. PMID: 10682312 No abstract available.

4

Ornithine transcarbamylase deficiency and pancreatitis.

Anadiotis G, Ierardi-Curto L, Kaplan PB, Berry GT. Anadiotis G, et al. Among authors: kaplan pb. J Pediatr. 2001 Jan;138(1):123-4. doi: 10.1067/mpd.2001.109792. J Pediatr. 2001. PMID: 11148526

5

MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation.

Jan W, Zimmerman RA, Wang ZJ, Berry GT, Kaplan PB, Kaye EM. Jan W, et al. Neuroradiology. 2003 Jun;45(6):393-9. doi: 10.1007/s00234-003-0955-7. Epub 2003 May 8. Neuroradiology. 2003. PMID: 12736767

6

Mild Brachmann-de Lange syndrome. Delineation of the clinical phenotype, and characteristic behaviors in a six-year-old boy.

Bay C, Mauk J, Radcliffe J, Kaplan P. Bay C, et al. Among authors: kaplan p. Am J Med Genet. 1993 Nov 15;47(7):965-8. doi: 10.1002/ajmg.1320470706. Am J Med Genet. 1993. PMID: 7507294

7

Newborn screening by tandem mass spectrometry for medium-chain Acyl-CoA dehydrogenase deficiency: a cost-effectiveness analysis.

Venditti LN, Venditti CP, Berry GT, Kaplan PB, Kaye EM, Glick H, Stanley CA. Venditti LN, et al. Among authors: kaplan pb. Pediatrics. 2003 Nov;112(5):1005-15. doi: 10.1542/peds.112.5.1005. Pediatrics. 2003. PMID: 14595039

8

Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency.

Kaplan P, Ficicioglu C, Mazur AT, Palmieri MJ, Berry GT. Kaplan P, et al. Mol Genet Metab. 2006 Aug;88(4):322-6. doi: 10.1016/j.ymgme.2006.04.003. Epub 2006 Jun 5. Mol Genet Metab. 2006. PMID: 16750411

9

Branched-chain amino acid-free parenteral nutrition in the treatment of acute metabolic decompensation in patients with maple syrup urine disease.

Berry GT, Heidenreich R, Kaplan P, Levine F, Mazur A, Palmieri MJ, Yudkoff M, Segal S. Berry GT, et al. Among authors: kaplan p. N Engl J Med. 1991 Jan 17;324(3):175-9. doi: 10.1056/NEJM199101173240307. N Engl J Med. 1991. PMID: 1898534 Free article. No abstract available.

10

Intellectual outcome in children with maple syrup urine disease.

Kaplan P, Mazur A, Field M, Berlin JA, Berry GT, Heidenreich R, Yudkoff M, Segal S. Kaplan P, et al. J Pediatr. 1991 Jul;119(1 Pt 1):46-50. doi: 10.1016/s0022-3476(05)81037-6. J Pediatr. 1991. PMID: 2066858 Free article.

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