G Schrakamp
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Explore the profile of G Schrakamp including associated specialties, affiliations and a list of published articles.
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23
Citations
286
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Recent Articles
1.
van den Bosch H, Schrakamp G, Hardeman D, Zomer A, Wanders R, Schutgens R
Biochimie
. 1993 Jan;
75(3-4):183-9.
PMID: 8507680
This paper deals with the discovery of plasmalogen deficiency in the cerebro-hepato-renal (Zellweger) syndrome and discusses how this has led to the development of postnatal and prenatal diagnostic procedures for...
2.
Schutgens R, Schrakamp G, Wanders R, Heymans H, Tager J, van den Bosch H
J Inherit Metab Dis
. 1989 Jan;
12 Suppl 1:118-34.
PMID: 2509803
Peroxisomes play an essential role in human cellular metabolism. Peroxisomal disorders, a group of genetic diseases caused by peroxisomal dysfunction, can be classified into three groups: (1) disorders of peroxisome...
3.
Wanders R, Heymans H, Schutgens R, Poll-The B, Saudubray J, Tager J, et al.
J Neurol Sci
. 1988 Apr;
84(2-3):147-55.
PMID: 2454298
The infantile and classical forms of Refsum's disease are generally considered to belong to the newly recognized group of peroxisomal disorders. In this study we carried out a detailed investigation...
4.
Schrakamp G, Schalkwijk C, Schutgens R, Wanders R, Tager J, van den Bosch H
J Lipid Res
. 1988 Mar;
29(3):325-34.
PMID: 3379344
In recent years a growing number of inherited diseases have been recognized to originate from an impairment in one or more peroxisomal functions. Since it is well established that the...
5.
van den Bosch H, Schalkwijk C, Schrakamp G, Wanders R, Schutgens R, Schram A, et al.
Prog Clin Biol Res
. 1988 Jan;
282:139-50.
PMID: 3071794
The Zellweger syndrome is a rare inborn error of metabolism characterized by the absence of morphologically distinguishable peroxisomes. As a consequence tissues and cells from Zellweger patients contain severely reduced...
6.
Wanders R, Schutgens R, Schrakamp G, Tager J, van den Bosch H, Moser A, et al.
J Neurol Sci
. 1987 Feb;
77(2-3):331-40.
PMID: 3819771
Neonatal adrenoleukodystrophy belongs to the newly recognized group of inherited diseases, the peroxisomal disorders. Based on the reported similarities between neonatal adrenoleukodystrophy and the cerebro-hepato-renal (Zellweger) syndrome, we have studied...
7.
Genetic diseases caused by peroxisomal dysfunction. New findings in clinical and biochemical studies
Schutgens R, Wanders R, Nijenhuis A, van den Hoek C, Heymans H, Schrakamp G, et al.
Enzyme
. 1987 Jan;
38(1-4):161-76.
PMID: 3440444
Peroxisomes play an essential role in human cellular metabolism. Peroxisomal disorders, a group of genetic diseases caused by peroxisomal dysfunction, can be classified in three groups namely a group of...
8.
Schutgens R, Wanders R, Heymans H, Schram A, Tager J, Schrakamp G, et al.
J Inherit Metab Dis
. 1987 Jan;
10 Suppl 1:33-45.
PMID: 3119940
In patients with cerebro-hepato-renal (Zellweger) syndrome, the absence of peroxisomes results in an impairment of metabolic processes in which peroxisomes are normally involved. These include the catabolism of very long...
9.
Wanders R, van Roermund C, De Vries C, van den Bosch H, Schrakamp G, Tager J, et al.
Clin Chim Acta
. 1986 Aug;
159(1):1-10.
PMID: 2944672
The presence of a beta-oxidation system in peroxisomes has been well documented. Rather than a duplicate of the mitochondrial beta-oxidation system, peroxisomes seem specially equipped to initiate the oxidation of...
10.
Wanders R, Schutgens R, Schrakamp G, van den Bosch H, Tager J, Schram A, et al.
Eur J Pediatr
. 1986 Aug;
145(3):172-5.
PMID: 2429839
In recent years a number of biochemical abnormalities have been described in patients with the infantile form of Refsum disease, including the accumulation of very long chain fatty acids, trihydroxycoprostanoic...