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O.P van Diggelen

Veröffentlichungen von O.P van Diggelen zu van Diggelen, O.P. ->
weitere Veröffentlichungen von O.P van Diggelen:
Glycogen storage disease type III with diagnosis complicated by gluten-sensitive enteropathy (1998)
Association products of native and derived ribosomal subunits of E. coli and their stability during centrifugation (1971)
Pitfalls in the Diagnosis of Multiple Sulfatase Deficiency (2001)
Late-Onset Globoid Cell Leucodystrophy (Krabbe's Disease) (1985)
Pitfalls in the Diagnosis of Multiple Sulfatase Deficiency (2001)
Debranching enzyme in fibroblasts, amniotic fluid cells and chorionic villi: pre- and postnatal diagnosis of glycogenosis type III (1985)
Intergenic complementation after fusion of fibroblasts from different patients with β-galactosidase deficiency (1979)
Endogenous HPRT activity in a cryptic strain of mycoplasma and its effect on cellular resistance to selective media in infected cell lines (1977)
Pitfalls in the Diagnosis of Multiple Sulfatase Deficiency (2001)
Enhanced proteolytic degradation of normal β-galactosidase in the lysosomal storage disease with combined β-galactosidase and neuraminidase deficiency (1982)
Niemann-Pick Disease Type A and B are Clinically but also Enzymatically Heterogeneous: Pitfall in the Laboratory Diagnosis of Sphingomyelinase Deficiency Associated with the Mutation Q292 K (2003)
Niemann-Pick Disease Type A and B are Clinically but also Enzymatically Heterogeneous: Pitfall in the Laboratory Diagnosis of Sphingomyelinase Deficiency Associated with the Mutation Q292 K (2003)
Niemann-Pick Disease Type A and B are Clinically but also Enzymatically Heterogeneous: Pitfall in the Laboratory Diagnosis of Sphingomyelinase Deficiency Associated with the Mutation Q292 K (2003)
Prenatal diagnosis of Niemann-Pick disease type C (1992)
Characteristics of maltase activity in amniotic fluid (1985)
Veröffentlichungen zu van Diggelen, O.P.
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1
Artan, R., van Diggelen, O. P., ... Glycogen storage disease type III with diagnosis complicated by gluten-sensitive enteropathy
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (4. 1998), p. 437-438
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1998
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2
van Diggelen, O.P., Oostrom, H., ... Association products of native and derived ribosomal subunits of E. coli and their stability during centrifugation
in: FEBS Letters, in: FEBS Letters . - Amsterdam : Elsevier, ISSN 0014-5793, ZDB-ID 1460391-3 Vol. 19, No. 2 (1971), p. 115-120
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1971
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3
Mancini, Grazia M. S.. Pitfalls in the Diagnosis of Multiple Sulfatase Deficiency
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 32, No. 01 (2. 2001), p. 38-40
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2001
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4
Loonen, M. C. B.. Late-Onset Globoid Cell Leucodystrophy (Krabbe's Disease)
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 16, No. 03 (8. 1985), p. 137-142
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1985
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5
Mancini, Grazia M. S.. Pitfalls in the Diagnosis of Multiple Sulfatase Deficiency
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 32, No. 01 (2. 2001), p. 38-40
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2001
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6
van Diggelen, O.P., Janse, H.C., ... Debranching enzyme in fibroblasts, amniotic fluid cells and chorionic villi: pre- and postnatal diagnosis of glycogenosis type III
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 149, No. 2-3 (1985), p. 129-134
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1985
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7
Hoeksema, H.L., Van Diggelen, O.P., ... Intergenic complementation after fusion of fibroblasts from different patients with β-galactosidase deficiency
in: BBA - Enzymology, in: BBA - Enzymology . - Amsterdam : Elsevier, ISSN 0005-2744, ZDB-ID 2209533-0 Vol. 566, No. 1 (1979), p. 72-79
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1979
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8
van Diggelen, O.P., Phillips, D.M., ... Endogenous HPRT activity in a cryptic strain of mycoplasma and its effect on cellular resistance to selective media in infected cell lines
in: Experimental Cell Research, in: Experimental Cell Research . - Amsterdam : Elsevier, ISSN 0014-4827, ZDB-ID 1466780-0 Vol. 106, No. 1 (1977), p. 191-203
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1977
Copyright: Copyright (c) 2005 Elsevier (USA) mehr
beteiligte Personen: van Diggelen, O.P. , Phillips, D.M. , Shin, S.-I.
Erschienen: 1977.
Serie: ScienceDirect Elsevier journal backfiles [Dig. Serial]
Schlagwörter:
URL: http://dx.doi.org/10.1016/0014-4827(77)90256-7
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9
Mancini, Grazia M. S.., van Diggelen, O. P.., ... Pitfalls in the Diagnosis of Multiple Sulfatase Deficiency
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 32, No. 01 (2001), p. 38-40
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2001
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10
Van Diggelen, O.P., Hoogeveen, A.T., ... Enhanced proteolytic degradation of normal β-galactosidase in the lysosomal storage disease with combined β-galactosidase and neuraminidase deficiency
in: Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular, in: Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular . - Amsterdam : Elsevier, ISSN 0167-4838, ZDB-ID 2209539-1 Vol. 703, No. 1 (1982), p. 69-76
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1982
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11
Backes, J.., Bauer, P.., ... Niemann-Pick Disease Type A and B are Clinically but also Enzymatically Heterogeneous: Pitfall in the Laboratory Diagnosis of Sphingomyelinase Deficiency Associated with the...
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 34, No. 06 (12. 2003), p. 301-306
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2003
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12
Backes, J.., Bauer, P.., ... Niemann-Pick Disease Type A and B are Clinically but also Enzymatically Heterogeneous: Pitfall in the Laboratory Diagnosis of Sphingomyelinase Deficiency Associated with the...
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 34, No. 06 (12. 2003), p. 301-306
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2003
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13
Harzer, K.., Rolfs, A.., ... Niemann-Pick Disease Type A and B are Clinically but also Enzymatically Heterogeneous: Pitfall in the Laboratory Diagnosis of Sphingomyelinase Deficiency Associated with the...
in: Neuropediatrics. - Stuttgart [u.a.] : Thieme, ISSN 1439-1899, Vol. 34, No. 06 (2003), p. 301-306
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2003
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14
de Winter, J.M., Janse, H.C., ... Prenatal diagnosis of Niemann-Pick disease type C
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 208, No. 3 (1992), p. 173-181
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1992
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15
Claass, A.H.W., van Diggelen, O.P., ... Characteristics of maltase activity in amniotic fluid
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 145, No. 3 (1985), p. 275-281
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1985
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16
Phillips, S.G., Phillips, D.M., ... Spontaneous cell hybridization of somatic cells present in sperm suspensions
in: Experimental Cell Research, in: Experimental Cell Research . - Amsterdam : Elsevier, ISSN 0014-4827, ZDB-ID 1466780-0 Vol. 98, No. 2 (1976), p. 429-443
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1976
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17
Verheijen, F.W., Janse, H.C., ... Two genetically different MU-NANA neuraminidases in human leucocytes
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 117, No. 2 (1983), p. 470-478
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1983
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18
Hu, P., Reuser, A.J.J., ... Biosynthesis of human α-N-acetylgalactosaminidase: Defective phosphorylation and maturation in infantile α-NAGA deficiency
in: Biochemical and Biophysical Research Communications, in: Biochemical and Biophysical Research Communications . - Amsterdam : Elsevier, ISSN 0006-291X, ZDB-ID 1461396-7 Vol. 175, No. 3 (1991), p. 1097-1103
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1991
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19
Kleijer, W. J., Keulemans, J. L. M., ... Prevalent mutations in the GALC gene of patients with Krabbe disease of Dutch and other European origin
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 20 (4. 1997), p. 587-594
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1997
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20
Weber, B., van de Kamp, J. J. P., ... Identification of a common mutation (R245H) in Sanfilippo A patients from the Netherlands
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (4. 1998), p. 416-422
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ähnliche Vorschläge
1998