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B. T. Poll-The

Veröffentlichungen von B. T. Poll-The zu Poll-The, B. T.. ->
weitere Veröffentlichungen von B. T. Poll-The:
Pseudomonoventricle Due to a Malformation of the Septum Pellucidum (1985)
Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders (1999)
Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders (1999)
Plasmacytoid Dendritic Cells and Interferon-alpha in Aicardi-Goutières Syndrome (2007)
Pontocerebellar Hypoplasia Associated with Respiratory-Chain Defects (1999)
Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency (2000)
Pontocerebellar Hypoplasia Associated with Respiratory-Chain Defects (1999)
Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency (2000)
Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders (1999)
Metabolic pigmentary retinopathies: Diagnosis and therapeutic attempts (1992)
Alterations of hepatic peroxisomes in tyrosinaemia type I: Return to fetal type? (1998)
Clinical approach to inherited peroxisomal disorders (1995)
Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiency (1994)
Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiency (1994)
Medium-chain triglyceride loading has no diagnostic power in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (1996)
Veröffentlichungen zu Poll-The, B. T..
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1
Poll-The, B. T.. Pseudomonoventricle Due to a Malformation of the Septum Pellucidum
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 16, No. 01 (2. 1985), p. 39-42
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1985
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2
de Koning, T. J.. Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 30, No. 01 (2. 1999), p. 1-4
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1999
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3
de Koning, T. J.. Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 30, No. 01 (2. 1999), p. 1-4
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1999
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4
Heteren, J. T. van. Plasmacytoid Dendritic Cells and Interferon-alpha in Aicardi-Goutières Syndrome
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 38, No. 06 (12. 2007), p. 269-275
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2007
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5
de Koning, T. J.. Pontocerebellar Hypoplasia Associated with Respiratory-Chain Defects
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 30, No. 02 (4. 1999), p. 93-95
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1999
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6
de Koning, T. J.. Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 31, No. 06 (12. 2000), p. 287-292
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2000
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7
de Koning, T. J.. Pontocerebellar Hypoplasia Associated with Respiratory-Chain Defects
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 30, No. 02 (4. 1999), p. 93-95
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1999
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8
de Koning, T. J.. Hypomyelination and Reversible White Matter Attenuation in 3-Phosphoglycerate Dehydrogenase Deficiency
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 31, No. 06 (12. 2000), p. 287-292
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2000
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9
de Koning, T. J.., Poll-The, B. T.., ... Continuing Education in Neurometabolic Disorders - Serine Deficiency Disorders
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 30, No. 01 (1999), p. 1-4
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1999
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10
Poll-The, B. T., Villemeur, T. Billette, ... Metabolic pigmentary retinopathies: Diagnosis and therapeutic attempts
in: European journal of pediatrics , ISSN 1432-1076, Vol. 151 (1. 1992), p. 2-11
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1992
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11
Kerckaert, I., De Koning, T. J., ... Alterations of hepatic peroxisomes in tyrosinaemia type I: Return to fetal type?
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (3. 1998), p. 186-190
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1998
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12
Poggi-Travert, F., Fournier, B., ... Clinical approach to inherited peroxisomal disorders
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 18 (1. 1995), p. 1-18
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1995
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13
Beekman, R. P., Hofstee, N., ... Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiency
in: European journal of pediatrics , ISSN 1432-1076, Vol. 153 (4. 1994), p. 264-266
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1994
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14
Beekman, R. P., Hofstee, N., ... Rett syndrome in a patient with medium chain acyl-CoA dehydrogenase deficiency
in: European journal of pediatrics , ISSN 1432-1076, Vol. 153 (4. 1994), p. 264-266
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1994
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15
Costa, C. G., Tavares de Almeida, I., ... Medium-chain triglyceride loading has no diagnostic power in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 19 (3. 1996), p. 376-377
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1996
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16
Fournier, B., Smeitink, J. A. M., ... Peroxisomal disorders: A review
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 17 (4. 1994), p. 470-486
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1994
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17
Çoker, M., Klerk, J. B. C., ... Plasma total odd-chain fatty acids in the monitoring of disorders of propionate, methylmalonate and biotin metabolism
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 19 (6. 1996), p. 743-751
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1996
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18
Brink, H. J., Poll-The, B. T., ... Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: Evidence for a Distinct peroxisomal pristanyl-CoA oxidase
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 14 (5. 1991), p. 681-684
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1991
Summary The concentration of pristanic acid was measured in plasma from a patient with an isolated peroxisomal very long chain fatty acid (VLCFA) acyl-CoA oxidase deficiency, a defect in peroxisomalβ-oxidation resulting in accumulation of VLCFA in plasma and tissues. Although peroxisomes are... mehr
Copyright: Copyright 1991 SSIEM and Kluwer Academic Publishers mehr
beteiligte Personen: Brink, H. J. , Poll-The, B. T. , Saudubray, J. M. , Wanders, R. J. A. , Jakobs, C.
Erschienen: 1991.
Serie: Springer Online Journal Archives 1860-2000 [Dig. Serial]
Schlagwörter:
URL: http://dx.doi.org/10.1007/BF01799934
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19
Brink, H. J., Heuvel, C. M. M., ... Peroxisomal disorders: Concentrations of metabolites in cerebrospinal fluid compared with plasma
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 16 (3. 1993), p. 587-590
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1993
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20
Jakobs, C., Kneer, J., ... In vivo stable isotope studies in three patients affected with mitochondrial fatty acid oxidation disorders: Limited diagnostic use of 1-13C fatty acid breath test using bolus...
in: European journal of pediatrics , ISSN 1432-1076, Vol. 156 (1. 1997), p. S78
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1997