van der Meer SB - Search Results

1

Clinical outcome and long-term management of 17 patients with propionic acidaemia.

van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, Depondt E, Rapoport D, Rabier D, Charpentier C, Parvy P, Bardet J, Kamoun P, Saudubray JM. van der Meer SB, et al. Eur J Pediatr. 1996 Mar;155(3):205-10. doi: 10.1007/BF01953939. Eur J Pediatr. 1996. PMID: 8929729

2

Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemia.

van der Meer SB, Poggi F, Spada M, Bonnefont JP, Ogier H, Hubert P, Depondt E, Rapoport D, Rabier D, Charpentier C, et al. van der Meer SB, et al. J Pediatr. 1994 Dec;125(6 Pt 1):903-8. doi: 10.1016/s0022-3476(05)82005-0. J Pediatr. 1994. PMID: 7996362 Clinical Trial.

3

Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: diagnostic failure of protein loading and allopurinol challenge tests.

Spada M, Guardamagna O, Rabier D, van der Meer SB, Parvy P, Bardet J, Ponzone A, Saudubray JM. Spada M, et al. Among authors: van der meer sb. J Pediatr. 1994 Aug;125(2):249-51. doi: 10.1016/s0022-3476(94)70205-5. J Pediatr. 1994. PMID: 8040774

4

Prenatal treatment of a patient with vitamin B12-responsive methylmalonic acidemia.

van der Meer SB, Spaapen LJ, Fowler B, Jakobs C, Kleijer WJ, Wendel U. van der Meer SB, et al. J Pediatr. 1990 Dec;117(6):923-6. doi: 10.1016/s0022-3476(05)80138-6. J Pediatr. 1990. PMID: 2246694 No abstract available.

5

The prevalence of Helicobacter pylori serum antibodies in children with recurrent abdominal pain.

van der Meer SB, Forget PP, Loffeld RJ, Stobberingh E, Kuijten RH, Arends JW. van der Meer SB, et al. Eur J Pediatr. 1992 Nov;151(11):799-801. doi: 10.1007/BF01957927. Eur J Pediatr. 1992. PMID: 1468451

6

Unexplained familial benign methylmalonic aciduria.

Martens DH, Bakker JA, van der Meer SB, Spaapen LJ. Martens DH, et al. Among authors: van der meer sb. Eur J Pediatr. 2002 Apr;161(4):219-20. doi: 10.1007/s00431-002-0930-z. Eur J Pediatr. 2002. PMID: 12014390 No abstract available.

7

Metabolic investigation of a patient with Rett syndrome.

Vles JS, Spaapen LJ, Schrander-Stumpel C, van der Meer S. Vles JS, et al. Eur J Pediatr. 1989 Aug;148(8):786. doi: 10.1007/BF00443113. Eur J Pediatr. 1989. PMID: 2792136 No abstract available.

8

Failure to detect phenylketonuria.

Verkerk PH, van der Meer SB. Verkerk PH, et al. Among authors: van der meer sb. Eur J Pediatr. 1995 Feb;154(2):163. doi: 10.1007/BF01991924. Eur J Pediatr. 1995. PMID: 7720748 No abstract available.

9

Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism.

Wendel U, Baumgartner R, van der Meer SB, Spaapen LJ. Wendel U, et al. Among authors: van der meer sb. Pediatr Res. 1991 Apr;29(4 Pt 1):403-5. doi: 10.1203/00006450-199104000-00015. Pediatr Res. 1991. PMID: 1852536

10

Clinical and biochemical presentation of siblings with COG-7 deficiency, a lethal multiple O- and N-glycosylation disorder.

Spaapen LJ, Bakker JA, van der Meer SB, Sijstermans HJ, Steet RA, Wevers RA, Jaeken J. Spaapen LJ, et al. Among authors: van der meer sb. J Inherit Metab Dis. 2005;28(5):707-14. doi: 10.1007/s10545-005-0015-z. J Inherit Metab Dis. 2005. PMID: 16151902

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