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Results of search for 'su:"Refsum Disease"', page 24 of 33
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Authors
Avigan, J
Eldjarn, L
Gibberd, F B
Jakobs, C
Laudat, P
Moser, H W
Poll-The, B T
Poulos, A
Refsum, S
Saudubray, J M
Schutgens, R B
Sharp, P
Sidey, M C
Skjeldal, O H
Steinberg, D
Stokke, O
Suzuki, Y
Try, K
Wanders, R J
Wanders, Ronald J A
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Topics
Adolescent
Adult
Animals
Child
Fatty Acids
Female
Humans
Infant
Male
Microbodies
Middle Aged
Phytanic Acid
Refsum Disease
blood
complications
diagnosis
enzymology
genetics
metabolism
pathology
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Results
461.
Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.
[electronic resource]
by
Brul, S
Westerveld, A
Strijland, A
Wanders, R J
Schram, A W
Heymans, H S
Schutgens, R B
van den Bosch, H
Tager, J M
Producer:
19880803
In:
The Journal of clinical investigation
vol. 81
Online resources:
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462.
[Polyneuropathy: neuropathies due to metabolic deficiencies].
[electronic resource]
by
Takeuchi, H
Tarui, S
Producer:
19830214
In:
Nihon rinsho. Japanese journal of clinical medicine
vol. 40
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463.
Bile acids and conjugates identified in metabolic disorders by fast atom bombardment and tandem mass spectrometry.
[electronic resource]
by
Libert, R
Hermans, D
Draye, J P
Van Hoof, F
Sokal, E
de Hoffmann, E
Producer:
19920218
In:
Clinical chemistry
vol. 37
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464.
Plasma polyenoic very-long-chain fatty acids in peroxisomal disease: biochemical discrimination of Zellweger's syndrome from other phenotypes.
[electronic resource]
by
Poulos, A
Sharp, P
Johnson, D
Producer:
19890209
In:
Neurology
vol. 39
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465.
Pathological changes in intramuscular nerves.
[electronic resource]
by
Coers, C
Producer:
19730130
In:
Neurology India
vol. 20
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466.
Identification of fatty aldehyde dehydrogenase in the breakdown of phytol to phytanic acid.
[electronic resource]
by
van den Brink, Daan M
van Miert, Joram N I
Dacremont, Georges
Rontani, Jean-François
Jansen, Gerbert A
Wanders, Ronald J A
Producer:
20041124
In:
Molecular genetics and metabolism
vol. 82
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467.
Peroxisomal disorders. A review of a recently recognized group of clinical entities.
[electronic resource]
by
Talwar, D
Swaiman, K F
Producer:
19871112
In:
Clinical pediatrics
vol. 26
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468.
Neonatal adrenoleukodystrophy.
[electronic resource]
by
Aubourg, P
Scotto, J
Rocchiccioli, F
Feldmann-Pautrat, D
Robain, O
Producer:
19860425
In:
Journal of neurology, neurosurgery, and psychiatry
vol. 49
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469.
[Chromatographic procedures for plasma lipids analysis].
[electronic resource]
by
Müller, M
Novak, A
Producer:
19780426
In:
Das Medizinische Laboratorium
vol. 31
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470.
Rud syndrome: congenital ichthyosis, hypogonadism, mental retardation, retinitis pigmentosa and hypertrophic polyneuropathy.
[electronic resource]
by
Larbrisseau, A
Carpenter, S
Producer:
19821216
In:
Neuropediatrics
vol. 13
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471.
[Refsum's disease].
[electronic resource]
by
Rougier, J
Producer:
19710209
In:
Archives d'ophtalmologie et revue generale d'ophtalmologie
vol. 30
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472.
Hereditary and acquired polyneuropathies. Electrophysiologic aspects.
[electronic resource]
by
Miller, R G
Producer:
19851115
In:
Neurologic clinics
vol. 3
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473.
Neurological associations of pigmentary retinopathy.
[electronic resource]
by
McDonald, W I
Producer:
19730912
In:
Transactions of the ophthalmological societies of the United Kingdom
vol. 92
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474.
Infantile refsum disease with enamel defects: a case report.
[electronic resource]
by
Tran, Dorothy
Greenhill, William
Wilson, Stephen
Producer:
20111108
In:
Pediatric dentistry
vol. 33
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475.
Permanent pacemaker implantation in infants, children, and adolescents. Long-term follow-up.
[electronic resource]
by
Benrey, J
Gillette, P C
Nasrallah, A T
Hallman, G L
Producer:
19760401
In:
Circulation
vol. 53
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476.
Heredopathia atactica polyneuritiformis (Refsum's diseases). An audiological examination of two patients.
[electronic resource]
by
Bergsmark, J
Djupesland, G
Producer:
19690104
In:
European neurology
vol. 1
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477.
[Human peroxisome-deficient disorders and pathogenic gene].
[electronic resource]
by
Fujiki, Y
Producer:
19950711
In:
Rinsho shinkeigaku = Clinical neurology
vol. 34
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478.
[Presence of crystalline inclusions in Schwann cells in several peripheral neuropathies].
[electronic resource]
by
Lyon, G
Evrard, P
Producer:
19710106
In:
Comptes rendus hebdomadaires des seances de l'Academie des sciences. Serie D: Sciences naturelles
vol. 271
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479.
Nutritional and metabolic aspects of heredopathia atactica polyneuritiformis (Refsum's syndrome).
[electronic resource]
by
Lenk, W
Producer:
19740928
In:
Nutrition and metabolism
vol. 16
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480.
Refsum's disease: characterization of the enzyme defect in cell culture.
[electronic resource]
by
Herndon, J H
Steinberg, D
Uhlendorf, B W
Fales, H M
Producer:
19690705
In:
The Journal of clinical investigation
vol. 48
Online resources:
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