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European Journal of Neurology
|
May 16, 2000
Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms
J Aasly, O P van Diggelen, A M Boer, et al.
Genitourinary Medicine
|
April 1, 1987
Factors that inhibit adherence of Treponema pallidum (Nichols strain) to a human fibroblastic cell line: development in serum of patients with syphilis
J J van der Sluis, J A Koehorst, A M Boer
Journal of Inherited Metabolic Disease
|
January 1, 1993
A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease type D (MPS IIID)
W He, Voznyi YaV, A M Boer, et al.
The British Journal of Venereal Diseases
|
October 1, 1980
Autolymphocytotoxins in syphilis
N J de Jong, J A Koehorst, J J van der Sluis, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 2, 2008
[Summary of the practice guideline 'Thyroid disorders' (first revision) from the Dutch College of General Practitioners]
J van Lieshout, P Wessels, E van Rijswijk, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease C (MPS III C)
Voznyi YaV, E A Karpova, T V Dudukina, et al.
Molecular Genetics and Metabolism
|
October 16, 2010
Hemoglobin precipitation greatly improves 4-methylumbelliferone-based diagnostic assays for lysosomal storage diseases in dried blood spots
L F Oemardien, A M Boer, G J G Ruijter, et al.
JIMD Reports
|
November 26, 2013
Newborn screening for hunter disease: a small-scale feasibility study
G J G Ruijter, D A Goudriaan, A M Boer, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Elevated plasma chitotriosidase activity in various lysosomal storage disorders
Y Guo, W He, A M Boer, et al.
Clinical Genetics
|
November 1, 1996
Asymptomatic and late-onset ornithine transcarbamylase (OTC) deficiency in males of a five-generation family, caused by an A208T mutation
O P van Diggelen, J Zaremba, W He, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
European Journal of Neurology
|
May 16, 2000
Phosphoglycerate kinase deficiency in two brothers with McArdle-like clinical symptoms
J Aasly, O P van Diggelen, A M Boer, et al.
Genitourinary Medicine
|
April 1, 1987
Factors that inhibit adherence of Treponema pallidum (Nichols strain) to a human fibroblastic cell line: development in serum of patients with syphilis
J J van der Sluis, J A Koehorst, A M Boer
Journal of Inherited Metabolic Disease
|
January 1, 1993
A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease type D (MPS IIID)
W He, Voznyi YaV, A M Boer, et al.
The British Journal of Venereal Diseases
|
October 1, 1980
Autolymphocytotoxins in syphilis
N J de Jong, J A Koehorst, J J van der Sluis, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
February 2, 2008
[Summary of the practice guideline 'Thyroid disorders' (first revision) from the Dutch College of General Practitioners]
J van Lieshout, P Wessels, E van Rijswijk, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1993
A fluorimetric enzyme assay for the diagnosis of Sanfilippo disease C (MPS III C)
Voznyi YaV, E A Karpova, T V Dudukina, et al.
Molecular Genetics and Metabolism
|
October 16, 2010
Hemoglobin precipitation greatly improves 4-methylumbelliferone-based diagnostic assays for lysosomal storage diseases in dried blood spots
L F Oemardien, A M Boer, G J G Ruijter, et al.
JIMD Reports
|
November 26, 2013
Newborn screening for hunter disease: a small-scale feasibility study
G J G Ruijter, D A Goudriaan, A M Boer, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1995
Elevated plasma chitotriosidase activity in various lysosomal storage disorders
Y Guo, W He, A M Boer, et al.
Clinical Genetics
|
November 1, 1996
Asymptomatic and late-onset ornithine transcarbamylase (OTC) deficiency in males of a five-generation family, caused by an A208T mutation
O P van Diggelen, J Zaremba, W He, et al.
Page
of 1