Ketel AG - Search Results

1

Quantitative aspects of the parenchyma-stroma relationship in experimentally induced cholestasis.

Aronson DC, de Haan J, James J, Bosch KS, Ketel AG, Houtkooper JM, Heijmans HS. Aronson DC, et al. Among authors: ketel ag. Liver. 1988 Apr;8(2):116-26. doi: 10.1111/j.1600-0676.1988.tb00978.x. Liver. 1988. PMID: 3367710

2

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): respiratory-chain abnormalities in cultured fibroblasts.

Barth PG, Van den Bogert C, Bolhuis PA, Scholte HR, van Gennip AH, Schutgens RB, Ketel AG. Barth PG, et al. Among authors: ketel ag. J Inherit Metab Dis. 1996;19(2):157-60. doi: 10.1007/BF01799418. J Inherit Metab Dis. 1996. PMID: 8739954 Free article. No abstract available.

3

Clinical and biochemical observations on a child with a deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase.

Ketel A, Ket JL, Schutgens RB, Duran M, Wadman SK. Ketel A, et al. J Inherit Metab Dis. 1980;3(3):89-90. doi: 10.1007/BF02312535. J Inherit Metab Dis. 1980. PMID: 6158624 No abstract available.

4

3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency: postnatal management following prenatal diagnosis by analysis of maternal urine.

Duran M, Schutgens RB, Ketel A, Heymans H, Bertssen MW, Ketting D, Wadman SK. Duran M, et al. J Pediatr. 1979 Dec;95(6):1004-7. doi: 10.1016/s0022-3476(79)80297-8. J Pediatr. 1979. PMID: 91680 No abstract available.

5

Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase.

Schutgens RB, Heymans H, Ketel A, Veder HA, Duran M, Ketting D, Wadman SK. Schutgens RB, et al. J Pediatr. 1979 Jan;94(1):89-91. doi: 10.1016/s0022-3476(79)80364-9. J Pediatr. 1979. PMID: 758433 No abstract available.

6

Exercise-induced asthma and cardiovascular fitness in asthmatic children.

Thio BJ, Nagelkerke AF, Ketel AG, van Keeken BL, Dankert-Roelse JE. Thio BJ, et al. Among authors: ketel ag. Thorax. 1996 Feb;51(2):207-9. doi: 10.1136/thx.51.2.207. Thorax. 1996. PMID: 8711660 Free PMC article.

7

Complex medical history of a patient with a compound heterozygous mutation in C1QC.

Lubbers R, Beaart-van de Voorde LJJ, van Leeuwen K, de Boer M, Gelderman KA, van den Berg MJ, Ketel AG, Simon A, de Ree J, Huizinga TWJ, Steup-Beekman GM, Trouw LA. Lubbers R, et al. Among authors: ketel ag. Lupus. 2019 Sep;28(10):1255-1260. doi: 10.1177/0961203319865029. Epub 2019 Jul 29. Lupus. 2019. PMID: 31357913 Free PMC article.

8

Marked variability in clinical presentation and outcome of patients with C1q immunodeficiency.

van Schaarenburg RA, Schejbel L, Truedsson L, Topaloglu R, Al-Mayouf SM, Riordan A, Simon A, Kallel-Sellami M, Arkwright PD, Åhlin A, Hagelberg S, Nielsen S, Shayesteh A, Morales A, Tam S, Genel F, Berg S, Ketel AG, Merlijn van den Berg J, Kuijpers TW, Olsson RF, Huizinga TW, Lankester AC, Trouw LA. van Schaarenburg RA, et al. Among authors: ketel ag. J Autoimmun. 2015 Aug;62:39-44. doi: 10.1016/j.jaut.2015.06.002. Epub 2015 Jun 26. J Autoimmun. 2015. PMID: 26119135

9

The diagnostic work up of growth failure in secondary health care; an evaluation of consensus guidelines.

Grote FK, Oostdijk W, De Muinck Keizer-Schrama SM, van Dommelen P, van Buuren S, Dekker FW, Ketel AG, Moll HA, Wit JM. Grote FK, et al. Among authors: ketel ag. BMC Pediatr. 2008 May 13;8:21. doi: 10.1186/1471-2431-8-21. BMC Pediatr. 2008. PMID: 18477383 Free PMC article.

10

[Coma in a child after treatment with the 'magic salve' lidocaine-prilocaine cream].

Wieringa JW, Ketel AG, van Houten MA. Wieringa JW, et al. Among authors: ketel ag. Ned Tijdschr Geneeskd. 2006 Aug 19;150(33):1805-7. Ned Tijdschr Geneeskd. 2006. PMID: 16967588 Dutch.

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