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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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ähnliche Vorschläge
2000
White matter abnormalities are a feature of many inborn errors of metabolism and magnetic resonance imaging (MRI) of the brain has become an important tool in the diagnostic workup of these disorders. Recently, patients were reported with a potentially treatable disorder of serine biosynthesis.... mehr
1. Verfasser: de Koning, T. J..
beteiligte Personen: Jaeken, J., , Pineda, M., , Poll-The, B. T.. , Van Maldergem, L.. , van der Knaap, M. S..
Erschienen: Stuttgart ; New York : Georg Thieme Verlag, 2000.
Schlagwörter:
URL: http://dx.doi.org/10.1055/s-2000-12944
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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
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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