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Results of search for 'au:"GIESBERTS, M A"', page 1 of 2
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Authors
AALBERS, J G
Aronson, D C
BORG, W A
Bartsocas, C
Blom, W
Giesberts, M A
Hooghwinkel, G J
Liem, K O
Mooy, P D
Przyrembel, H
Riedstra, J W
Scholte, H R
Teijema, H L
Versprille, A
van Gelderen, H H
van Gemund, J J
van Nie, C J
van Pelt, J F
van de Kamp, J J
von Figura, K
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Adolescent
Adult
Animals
Biopsy
Child
Child, Preschool
Female
Glucuronidase
Glycosaminoglycans
Humans
Infant
Leukocytes
Male
Middle Aged
Mucopolysaccharidoses
Mucopolysaccharidosis III
blood
genetics
metabolism
urine
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Your search returned 22 results.
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1.
Deficiency of lysosomal enzymes in storage diseases.
[electronic resource]
by
Den Tandt, W R
Giesberts, M A
Producer:
19730906
In:
Biochemical medicine
vol. 7
Online resources:
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2.
[The significance of urinary hydroxyproline excretion in children].
[electronic resource]
by
van Gemund, J J
Vio, P M
Giesberts, M A
Producer:
19680916
In:
Maandschrift voor kindergeneeskunde
vol. 35
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3.
Hypoketosis as a cause of symptoms in childhood hypoglycemia.
[electronic resource]
by
Teijema, H L
van Gelderen, H H
Giesberts, M A
Producer:
19801120
In:
European journal of pediatrics
vol. 134
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4.
[The excretion of N-acetyl-beta-D-glucosaminidase in the urine of children with urinary tract diseases].
[electronic resource]
by
Zandvliet, E E
Giesberts, M A
van Gelderen, H H
Producer:
19840419
In:
Tijdschrift voor kindergeneeskunde
vol. 51
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5.
A semi-quantitative micromethod for the determination of free glycosaminoglycans in serum. Results from studies on serum of healthy children of various age and patients affected by mucopolysaccharidosis.
[electronic resource]
by
Melet, J
Hooghwinkel, G J
Giesberts, M A
van Gelderen, H H
Producer:
19810317
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 108
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6.
D-Lactic acidosis in a boy with short bowel syndrome.
[electronic resource]
by
Schoorel, E P
Giesberts, M A
Blom, W
van Gelderen, H H
Producer:
19810116
In:
Archives of disease in childhood
vol. 55
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7.
Deficiency of 4-methyl umbelliferyl-beta-galactosidase activity in the liver of seven patients with Hurler's disease.
[electronic resource]
by
van Gemund, J J
Giesberts, M A
Gorsira, M C
Willighagen, R G
Producer:
19690626
In:
Maandschrift voor kindergeneeskunde
vol. 36
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8.
Electron microscopy of intestinal suction-biopsy specimens as an aid in the diagnosis of mucopolysaccharidoses and other lysosomal storage diseases.
[electronic resource]
by
Van Gemund, J J
Daems, W T
Vio, P A
Giesberts, M A
Producer:
19720503
In:
Maandschrift voor kindergeneeskunde
vol. 39
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9.
Genetic heterogeneity and clinical variability in the Sanfilippo syndrome (types A, B, and C).
[electronic resource]
by
van de Kamp, J J
Niermeijer, M F
von Figura, K
Giesberts, M A
Producer:
19820212
In:
Clinical genetics
vol. 20
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10.
Dicarboxylic aminoaciduria: an inborn error of glutamate and aspartate transport with metabolic implications, in combination with a hyperprolinemia.
[electronic resource]
by
Teijema, H L
van Gelderen, H H
Giesberts, M A
Laurent de Angulo, M S
Producer:
19740322
In:
Metabolism: clinical and experimental
vol. 23
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11.
Morquio-B disease, spondyloepiphyseal dysplasia associated with acid beta-galactosidase deficiency. Report of three cases in one family.
[electronic resource]
by
van Gemund, J J
Giesberts, M A
Eerdmans, R F
Blom, W
Kleijer, W J
Producer:
19830909
In:
Human genetics
vol. 64
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12.
Effects of atrial pressure on the rate of neonatal pig hearts.
[electronic resource]
by
Versprille, A
van Nie, C J
Riedstra, J W
Giesberts, M A
Bruins, C L
Producer:
19700228
In:
Pflugers Archiv : European journal of physiology
vol. 314
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13.
Functional behaviour of the foramen ovale in the newborn piglet.
[electronic resource]
by
van Nie, C J
Versprille, A
Giesberts, M A
Riedstra, J W
Beneken, J E
Rohmer, J
Producer:
19700228
In:
Pflugers Archiv : European journal of physiology
vol. 314
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14.
Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin.
[electronic resource]
by
Mooy, P D
Przyrembel, H
Giesberts, M A
Scholte, H R
Blom, W
van Gelderen, H H
Producer:
19850307
In:
European journal of pediatrics
vol. 143
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15.
Effects of a high-protein diet in acid maltase deficiency.
[electronic resource]
by
Padberg, G W
Wintzen, A R
Giesberts, M A
Sterk, P J
Molenaar, A J
Hermans, J
Producer:
19890629
In:
Journal of the neurological sciences
vol. 90
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16.
Sanfilippo B disease in two related sibships. Biochemical studies in patients, parents and sibs.
[electronic resource]
by
Liem, K O
Giesberts, M A
van de Kamp, J J
van Pelt, J F
Hooghwinkel, G J
Producer:
19770125
In:
Clinical genetics
vol. 10
Online resources:
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17.
Effective D-penicillamine treatment of an early diagnosed patient with Wilson's disease.
[electronic resource]
by
van Wouwe, J P
van Weel-Sipman, M H
Giesberts, M A
Ruiter, D J
van Gelderen, H H
Producer:
19850221
In:
European journal of pediatrics
vol. 143
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18.
Sanfilippo type C disease: clinical findings in four patients with a new variant of mucopolysaccharidosis III.
[electronic resource]
by
Bartsocas, C
Gröbe, H
van de Kamp, J J
von Figura, K
Kresse, H
Klein, U
Giesberts, M A
Producer:
19790716
In:
European journal of pediatrics
vol. 130
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19.
Glutaric aciduria type II: multiple defects in isolated muscle mitochondria and deficient beta-oxidation in fibroblasts.
[electronic resource]
by
Mooy, P D
Giesberts, M A
van Gelderen, H H
Scholte, H R
Luyt-Houwen, I E
Przyrembel, H
Blom, W
Producer:
19841119
In:
Journal of inherited metabolic disease
vol. 7 Suppl 2
Online resources:
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20.
Clinical variability in Sanfilippo B disease: a report on six patients in two related sibships.
[electronic resource]
by
van de Kamp, J J
van Pelt, J F
Liem, K O
Giesberts, M A
Niepoth, L T
Staalman, C R
Producer:
19770125
In:
Clinical genetics
vol. 10
Online resources:
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