Sengers RC - Search Results

1

A survey of natural protein intake in Dutch phenylketonuria patients: insight into estimation or measurement of dietary intake.

van Rijn M, Jansma J, Brinksma A, Bakker HD, Boers GH, Carbasius-Weber E, Douwes AC, van den Herberg A, Ter Horst NM, de Klerk JB, de Koning TJ, van den Ploeg L, Rubio-Gozalbo ME, Sels JP, Sengers RC, de Valk HW, Termeulen H, Zweers H, van Spronsen FJ. van Rijn M, et al. Among authors: sengers rc. J Am Diet Assoc. 2008 Oct;108(10):1704-7. doi: 10.1016/j.jada.2008.07.008. J Am Diet Assoc. 2008. PMID: 18926138

2

Does impaired growth of PKU patients correlate with the strictness of dietary treatment? National Dutch PKU Steering Committee.

van Spronsen FJ, Verkerk PH, van Houten M, Smit GP, van der Meer SB, Bakker HD, Sengers RC. van Spronsen FJ, et al. Among authors: sengers rc. Acta Paediatr. 1997 Aug;86(8):816-8. doi: 10.1111/j.1651-2227.1997.tb08603.x. Acta Paediatr. 1997. PMID: 9307159

3

Predictors of mean phenylalanine levels during the first five years of life in patients with phenylketonuria who were treated early. Dutch National PKU Steering Committee.

Verkerk PH, van Spronsen FJ, van Houten M, Smit GP, Sengers RC. Verkerk PH, et al. Among authors: sengers rc. Acta Paediatr Suppl. 1994 Dec;407:70-2. doi: 10.1111/j.1651-2227.1994.tb13456.x. Acta Paediatr Suppl. 1994. PMID: 7766963

4

Impaired prenatal and postnatal growth in Dutch patients with phenylketonuria. The National PKU Steering Committee.

Verkerk PH, van Spronsen FJ, Smit GP, Sengers RC. Verkerk PH, et al. Among authors: sengers rc. Arch Dis Child. 1994 Aug;71(2):114-8. doi: 10.1136/adc.71.2.114. Arch Dis Child. 1994. PMID: 7944529 Free PMC article.

5

Systemic infantile complex I deficiency with fatal outcome in two brothers.

Rubio-Gozalbo ME, Ruitenbeek W, Wendel U, Sengers RC, Trijbels JM, Smeitink JA. Rubio-Gozalbo ME, et al. Among authors: sengers rc. Neuropediatrics. 1998 Feb;29(1):43-5. doi: 10.1055/s-2007-973533. Neuropediatrics. 1998. PMID: 9553949

6

Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations.

Rubio-Gozalbo ME, Dijkman KP, van den Heuvel LP, Sengers RC, Wendel U, Smeitink JA. Rubio-Gozalbo ME, et al. Among authors: sengers rc. Hum Mutat. 2000;15(6):522-32. doi: 10.1002/1098-1004(200006)15:6<522::AID-HUMU4>3.0.CO;2-Y. Hum Mutat. 2000. PMID: 10862082

7

Lipid peroxidation in homocysteinaemia.

Blom HJ, Engelen DP, Boers GH, Stadhouders AM, Sengers RC, de Abreu R, TePoele-Pothoff MT, Trijbels JM. Blom HJ, et al. Among authors: sengers rc. J Inherit Metab Dis. 1992;15(3):419-22. doi: 10.1007/BF02435993. J Inherit Metab Dis. 1992. PMID: 1405484 No abstract available.

8

Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV.

Rubio-Gozalbo ME, Ruitenbeek W, Bentlage HA, Schägger H, Sengers RC, Trijbels JM, ter Laak HJ, Mariman EC, Bakker MM, de Jager J, Smeitink JA. Rubio-Gozalbo ME, et al. Among authors: sengers rc. Eur J Pediatr. 1997 Dec;156(12):931-4. doi: 10.1007/s004310050745. Eur J Pediatr. 1997. PMID: 9453375

9

A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathy.

Rubio-Gozalbo ME, Sengers RC, Trijbels JM, Doesburg WH, Janssen AJ, Verbeek AL, Smeitink JA. Rubio-Gozalbo ME, et al. Among authors: sengers rc. Neuropediatrics. 2000 Jun;31(3):114-21. doi: 10.1055/s-2000-7491. Neuropediatrics. 2000. PMID: 10963097

10

Spinal muscular atrophy-like picture, cardiomyopathy, and cytochrome c oxidase deficiency.

Rubio-Gozalbo ME, Smeitink JA, Ruitenbeek W, Ter Laak H, Mullaart RA, Schuelke M, Mariman EC, Sengers RC, Gabreëls FJ. Rubio-Gozalbo ME, et al. Among authors: sengers rc. Neurology. 1999 Jan 15;52(2):383-6. doi: 10.1212/wnl.52.2.383. Neurology. 1999. PMID: 9932961

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