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HDL associates with insulin resistance and beta-cell dysfunction in South Asian families at risk of type 2 diabetes

Journal of diabetes and its complications, 2021-10, Vol.35 (10), p.107993, Article 107993

2021

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Afamelanotide for Erythropoietic Protoporphyria

The New England journal of medicine, 2015-07, Vol.373 (1), p.48-59

2015

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Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands

Cellular and molecular biology (Noisy-le-Grand, France), 2009-07, Vol.55 (2), p.64

2009

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STRAD in Peutz-Jeghers syndrome and sporadic cancers

Journal of clinical pathology, 2005-10, Vol.58 (10), p.1091-1095

2005

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LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Journal of medical genetics, 2006-05, Vol.43 (5), p.e18-e18

2006

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Acrylate yellow filters in operating lights protect against photosensitization tissue damage

British journal of surgery, 2000-02, Vol.87 (2), p.231-235

2000

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Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

British journal of cancer, 2005-03, Vol.92 (6), p.1126-1129

2005

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Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome

British journal of cancer, 2005-03, Vol.92 (6), p.1126-1129

2005

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Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRAD , and MO25 , in Peutz-Jeghers syndrome

British journal of cancer, 2005-03, Vol.92 (6), p.1126-1129

2005

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Genotype/phenotype correlation in patients with Erythropoietic Protoporphyria

Biochemical Society transactions, 2002-06, Vol.30 (3), p.A72-A72

2002

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Residual activity of human porphobilinogen deaminase with R167Q or R167W mutations: an explanation for survival of homozygous and compound heterozygous acute intermittent porphyrics

Cellular and molecular biology (Noisy-le-Grand, France), 2002-12, Vol.48 (8), p.861

2002

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Two course illuminating scheme improves aminolevulinic acid photodynamic therapy in cell cultures

Cellular and molecular biology (Noisy-le-Grand, France), 2002-12, Vol.48 (8), p.903

2002

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From gene to disease; 'frame shift'-mutation in the CARD15-gene and Crohn's disease

Nederlands tijdschrift voor geneeskunde, 2002-12, Vol.146 (52), p.2539

2002

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Two different point G to a mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria

The Journal of clinical investigation, 1990-11, Vol.86 (5), p.1511-1516

1990

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Peutz-Jeghers syndrome: 78-year follow-up of the original family

The Lancet (British edition), 1999-04, Vol.10, p.1211-1215

1999

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An Escherichia coli Mutant with an Altered Elongation Factor Tu

Proceedings of the National Academy of Sciences - PNAS, 1974-02, Vol.71 (2), p.460-463

1974

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Primary Bile Acid Malabsorption: A Pathophysiologic and Clinical Entity?

Scandinavian journal of gastroenterology, 1992, Vol.27 (S194), p.66-70

1992

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Taming microwave plasma to beat thermodynamics in CO2 dissociation

Faraday discussions, 2015-01, Vol.183, p.233-248

2015

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Na+-dependent bile acid transport in the ileum: The balance between diarrhea and constipation

Gastroenterology (New York, N.Y. 1943), 1990-01, Vol.98 (1), p.25-32

1990

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How does hip osteoarthritis differ from knee osteoarthritis?

Osteoarthritis and cartilage, 2022-01, Vol.30 (1), p.32-41

2022

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Functional Outcomes and Urological Complications after Genital Gender Affirming Surgery with Urethral Lengthening in Transgender Men

The Journal of urology, 2020-07, Vol.204 (1), p.104-109

2020

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The pan phosphoinositide 3-kinase/mammalian target of rapamycin inhibitor SAR245409 (voxtalisib/XL765) blocks survival, adhesion and proliferation of primary chronic lymphocytic leukemia cells

Leukemia, 2016-02, Vol.30 (2), p.337-345

2016

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Genetic and environmental factors driving congenital solitary functioning kidney

Nephrology, dialysis, transplantation, 2024-02, Vol.39 (3), p.463-472

2024

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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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HDL associates with insulin resistance and beta-cell dysfunction in South Asian families at risk of type 2 diabetes

Afamelanotide for Erythropoietic Protoporphyria

Evidence for an ancestral founder of the common R116W mutation in the hydroxymethylbilane synthase gene in acute intermittent porphyria in The Netherlands

STRAD in Peutz-Jeghers syndrome and sporadic cancers

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

Acrylate yellow filters in operating lights protect against photosensitization tissue damage

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRAD , and MO25 , in Peutz-Jeghers syndrome

Genotype/phenotype correlation in patients with Erythropoietic Protoporphyria

Residual activity of human porphobilinogen deaminase with R167Q or R167W mutations: an explanation for survival of homozygous and compound heterozygous acute intermittent porphyrics

Two course illuminating scheme improves aminolevulinic acid photodynamic therapy in cell cultures

From gene to disease; 'frame shift'-mutation in the CARD15-gene and Crohn's disease

Two different point G to a mutations in exon 10 of the porphobilinogen deaminase gene are responsible for acute intermittent porphyria

Peutz-Jeghers syndrome: 78-year follow-up of the original family

An Escherichia coli Mutant with an Altered Elongation Factor Tu

Primary Bile Acid Malabsorption: A Pathophysiologic and Clinical Entity?

Taming microwave plasma to beat thermodynamics in CO2 dissociation

Oil-Based or Water-Based Contrast for Hysterosalpingography in Infertile Women

Na+-dependent bile acid transport in the ileum: The balance between diarrhea and constipation

How does hip osteoarthritis differ from knee osteoarthritis?

Functional Outcomes and Urological Complications after Genital Gender Affirming Surgery with Urethral Lengthening in Transgender Men

The pan phosphoinositide 3-kinase/mammalian target of rapamycin inhibitor SAR245409 (voxtalisib/XL765) blocks survival, adhesion and proliferation of primary chronic lymphocytic leukemia cells

Genetic and environmental factors driving congenital solitary functioning kidney

Diagnosis and Treatment of Acute Intermittent Porphyria

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