Monnens L - Search Results

1

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

Poll-The BT, Saudubray JM, Ogier HA, Odièvre M, Scotto JM, Monnens L, Govaerts LC, Roels F, Cornelis A, Schutgens RB, et al. Poll-The BT, et al. Among authors: monnens l. Eur J Pediatr. 1987 Sep;146(5):477-83. doi: 10.1007/BF00441598. Eur J Pediatr. 1987. PMID: 2445576

2

Disturbed adrenocortical function in cerebro-hepato-renal syndrome of Zellweger.

Govaerts L, Monnens L, Melis T, Trijbels F. Govaerts L, et al. Among authors: monnens l. Eur J Pediatr. 1984 Nov;143(1):10-2. doi: 10.1007/BF00442740. Eur J Pediatr. 1984. PMID: 6096149

3

Cerebro-hepato-renal syndrome of Zellweger: clinical symptoms and relevant laboratory findings in 16 patients.

Govaerts L, Monnens L, Tegelaers W, Trijbels F, van Raay-Selten A. Govaerts L, et al. Among authors: monnens l. Eur J Pediatr. 1982 Oct;139(2):125-8. doi: 10.1007/BF00441495. Eur J Pediatr. 1982. PMID: 7151832

4

Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.

Wanders RJ, van Roermund CW, Westra R, Schutgens RB, van der Ende MA, Tager JM, Monnens LA, Baadenhuysen H, Govaerts L, Przyrembel H, et al. Wanders RJ, et al. Among authors: monnens la. Clin Chim Acta. 1987 Jun 15;165(2-3):311-9. doi: 10.1016/0009-8981(87)90176-8. Clin Chim Acta. 1987. PMID: 3652453

5

[Peroxisomes--in search of their function in man].

Monnens L, Trijbels F, Govaerts L. Monnens L, et al. Tijdschr Kindergeneeskd. 1985 Aug;53(4):129-36. Tijdschr Kindergeneeskd. 1985. PMID: 3909510 Review. Dutch.

6

Disturbed very long chain (C24-C26) fatty acid pattern in fibroblasts of patients with Zellweger's syndrome.

Govaerts L, Bakkeren J, Monnens L, Maas J, Trijbels F, Kleijer W. Govaerts L, et al. Among authors: monnens l. J Inherit Metab Dis. 1985;8(1):5-8. doi: 10.1007/BF01805473. J Inherit Metab Dis. 1985. PMID: 3921760

7

Urinary polyamine and metabolite excretion by children with Zellweger's syndrome.

Govaerts LC, van den Berg GA, Theeuwes A, Muskiet FA, Monnens LA. Govaerts LC, et al. Among authors: monnens la. Clin Chim Acta. 1990 Nov 15;192(1):61-7. doi: 10.1016/0009-8981(90)90272-t. Clin Chim Acta. 1990. PMID: 2261698

8

Biochemical studies in the liver and muscle of patients with Zellweger syndrome.

Trijbels JM, Berden JA, Monnens LA, Willems JL, Janssen AJ, Schutgens RB, van den Broek-Van Essen M. Trijbels JM, et al. Among authors: monnens la. Pediatr Res. 1983 Jun;17(6):514-7. doi: 10.1203/00006450-198306000-00018. Pediatr Res. 1983. PMID: 6877906

9

[A child with Zellweger's cerebrohepatorenal syndrome].

Govaerts L, Corstiaensen J, Bakkeren J, Trujbels F, Monnens L. Govaerts L, et al. Among authors: monnens l. Tijdschr Kindergeneeskd. 1983 Apr;51(2):65-7. Tijdschr Kindergeneeskd. 1983. PMID: 6879587 Dutch.

10

Further analysis of the disturbed adrenocortical function in the cerebro-hepato-renal syndrome of Zellweger.

Govaerts L, Sippell WG, Monnens L. Govaerts L, et al. Among authors: monnens l. J Inherit Metab Dis. 1989;12(4):423-8. doi: 10.1007/BF01802037. J Inherit Metab Dis. 1989. PMID: 2560099

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