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Aquaculture carrying capacity of Nile tilapia Oreochromis niloticus and Nile crocodile Crocodylus niloticus in Lake Kariba, Zambia and Zimbabwe

Aquaculture Environment Interactions, 2022-01, Vol.14, p.113-125

2022

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Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update

Human mutation, 1999, Vol.13 (1), p.44-53

1999

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Tissue-Specific Splicing Mutation in Acute Intermittent Porphyria

Proceedings of the National Academy of Sciences - PNAS, 1989-01, Vol.86 (2), p.661-664

1989

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Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry: Recurrent mutation p.R59W in variegate porphyria

British journal of dermatology (1951), 2012-02, Vol.166 (2), p.261-265

2012

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Jaundice in non-cirrhotic primary biliary cirrhosis: the premature ductopenic variant

Gut, 2001-08, Vol.49 (2), p.276-281

2001

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Porphyria

Nederlands tijdschrift voor geneeskunde, 1982-06, Vol.126 (26), p.1161

te Velde, K

1982

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Acute intermittent porphyria in The Netherlands. Heterogeneity of the enzyme porphobilinogen deaminase

Netherlands journal of medicine, 1986, Vol.29 (11), p.393

1986

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Optimum start and building mass

Bâtiment international, Building research & practice, 1986-09, Vol.14 (5), p.306-310

te Velde, K.

1986

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Detection of Latent Pernicious Anaemia

BMJ, 1966-09, Vol.2 (5516), p.764-765

1966

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A patient with acute porphyria

Nederlands tijdschrift voor geneeskunde, 1985-11, Vol.129 (45), p.2174

1985

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Evaluation of a first-line spectrophotometric screening test for increased faecal porphyrin concentration

European journal of clinical chemistry and clinical biochemistry, 1995-05, Vol.33 (5), p.285

1995

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Evaluation and clinical application of the Enterotest for the determination of human biliary porphyrin composition

European journal of clinical chemistry and clinical biochemistry, 1995-07, Vol.33 (7), p.453

1995

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Efficacy and safety of pravastatin in Dutch patients with hypercholesteremia and additional coronary risk factors

Atherosclerosis, 1995-06, Vol.115, p.S128-S128

1995

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Evaluation of a First-Line Spectrophotometric Screening Test for Increased Urine Porphyrin Excretion

Annals of clinical biochemistry, 1995-03, Vol.32 (2), p.186-189

1995

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Comparison of the Efficacy and Safety of Trandolapril and Captopril for 16 Weeks in Mild-to-Moderate Essential Hypertension

Journal of cardiovascular pharmacology, 1994, Vol.23 Suppl 4, p.S73-76

1994

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54.2: Technology for the Hopping Electron Cathode

SID International Symposium Digest of technical papers, 2002-05, Vol.33 (1), p.1396-1399

2002

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High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyria

Human genetics, 1993-03, Vol.91 (2), p.128-130

1993

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Hereditary coproporphyria in 2 Dutch families

Nederlands tijdschrift voor geneeskunde, 1984-05, Vol.128 (19), p.892

1984

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High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyria

American journal of human genetics, 1992-09, Vol.51 (3), p.660-665

1992

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Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresis

Human genetics, 1994, Vol.93 (1), p.47-52

1994

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A family study of the initial Dutch patients with porphyria

Nederlands tijdschrift voor geneeskunde, 1989-12, Vol.133 (51), p.2547

1989

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Diagnosis and Treatment of Acute Intermittent Porphyria

Scandinavian journal of gastroenterology, 1989, Vol.24 (S171), p.32-37

1989

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Porphyria cutanea tarda

Nederlands tijdschrift voor geneeskunde, 1976-05, Vol.120 (22), p.952

1976

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Evaluation of a first-line spectrophotometric screening test for increased uring porphyrin excretion

Annals of clinical biochemistry, 1995, Vol.32, p.186-189

1995

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Primary acquired hypogammaglobulinemia, myasthenia, and thymoma

Annals of internal medicine, 1966-09, Vol.65 (3), p.554

1966

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Aquaculture carrying capacity of Nile tilapia Oreochromis niloticus and Nile crocodile Crocodylus niloticus in Lake Kariba, Zambia and Zimbabwe

Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update

Tissue-Specific Splicing Mutation in Acute Intermittent Porphyria

Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry: Recurrent mutation p.R59W in variegate porphyria

Jaundice in non-cirrhotic primary biliary cirrhosis: the premature ductopenic variant

Porphyria

Acute intermittent porphyria in The Netherlands. Heterogeneity of the enzyme porphobilinogen deaminase

Optimum start and building mass

Detection of Latent Pernicious Anaemia

A patient with acute porphyria

Evaluation of a first-line spectrophotometric screening test for increased faecal porphyrin concentration

Evaluation and clinical application of the Enterotest for the determination of human biliary porphyrin composition

Efficacy and safety of pravastatin in Dutch patients with hypercholesteremia and additional coronary risk factors

Evaluation of a First-Line Spectrophotometric Screening Test for Increased Urine Porphyrin Excretion

Comparison of the Efficacy and Safety of Trandolapril and Captopril for 16 Weeks in Mild-to-Moderate Essential Hypertension

54.2: Technology for the Hopping Electron Cathode

High prevalence of a point mutation in the porphobilinogen deaminase gene in Dutch patients with acute intermittent porphyria

Hereditary coproporphyria in 2 Dutch families

High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyria

Detection of eleven mutations causing acute intermittent porphyria using denaturing gradient gel electrophoresis

A family study of the initial Dutch patients with porphyria

Diagnosis and Treatment of Acute Intermittent Porphyria

Porphyria cutanea tarda

Evaluation of a first-line spectrophotometric screening test for increased uring porphyrin excretion

Primary acquired hypogammaglobulinemia, myasthenia, and thymoma

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