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K te Velde

Showing results (1-10 of 14) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|June 26, 1982
[Porphyria]K te Velde
Nederlands Tijdschrift Voor Geneeskunde|May 12, 1984
[Hereditary coproporphyria in 2 Dutch families]K te Velde, K H Noordhoek
Nederlands Tijdschrift Voor Geneeskunde|November 9, 1985
[A patient with acute porphyria]K te Velde, J H Wilson
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|May 1, 1995
Evaluation of a first-line spectrophotometric screening test for increased faecal porphyrin concentrationF M Zuijderhoudt, J Dorresteijn-de Bok, K te Velde
The Netherlands Journal of Medicine|January 1, 1986
Acute intermittent porphyria in The Netherlands. Heterogeneity of the enzyme porphobilinogen deaminaseJ H Wilson, F W De Rooy, K Te Velde
Annals of Clinical Biochemistry|March 1, 1995
Evaluation of a first-line spectrophotometric screening test for increased urine porphyrin excretionF M Zuijderhoudt, J Dorresteijn-de Bok, K Te Velde
Nederlands Tijdschrift Voor Geneeskunde|December 23, 1989
[A family study of the initial Dutch patients with porphyria]K te Velde, K H Noordhoek, J H Wilson, et al.
American Journal of Human Genetics|September 1, 1992
High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyriaX F Gu, F de Rooij, G Voortman, et al.
Human Genetics|January 1, 1994
Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresisX F Gu, F de Rooij, G Voortman, et al.
Human Genetics|March 1, 1993
High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Nederlands Tijdschrift Voor Geneeskunde|June 26, 1982
[Porphyria]K te Velde
Nederlands Tijdschrift Voor Geneeskunde|May 12, 1984
[Hereditary coproporphyria in 2 Dutch families]K te Velde, K H Noordhoek
Nederlands Tijdschrift Voor Geneeskunde|November 9, 1985
[A patient with acute porphyria]K te Velde, J H Wilson
European Journal of Clinical Chemistry and Clinical Biochemistry : Journal of the Forum of European Clinical Chemistry Societies|May 1, 1995
Evaluation of a first-line spectrophotometric screening test for increased faecal porphyrin concentrationF M Zuijderhoudt, J Dorresteijn-de Bok, K te Velde
The Netherlands Journal of Medicine|January 1, 1986
Acute intermittent porphyria in The Netherlands. Heterogeneity of the enzyme porphobilinogen deaminaseJ H Wilson, F W De Rooy, K Te Velde
Annals of Clinical Biochemistry|March 1, 1995
Evaluation of a first-line spectrophotometric screening test for increased urine porphyrin excretionF M Zuijderhoudt, J Dorresteijn-de Bok, K Te Velde
Nederlands Tijdschrift Voor Geneeskunde|December 23, 1989
[A family study of the initial Dutch patients with porphyria]K te Velde, K H Noordhoek, J H Wilson, et al.
American Journal of Human Genetics|September 1, 1992
High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyriaX F Gu, F de Rooij, G Voortman, et al.
Human Genetics|January 1, 1994
Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresisX F Gu, F de Rooij, G Voortman, et al.
Human Genetics|March 1, 1993
High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyriaX F Gu, F de Rooij, J S Lee, et al.
Pageof 2