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SP-0547 Connecting the patient into the clinical trial: the role of an RTT

Radiotherapy and oncology, 2023-05, Vol.182, p.S429-S430

Losekoot, N.

2023

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Simple and selective method for the determination of various tyrosine kinase inhibitors used in the clinical setting by liquid chromatography tandem mass spectrometry

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2010-05, Vol.878 (15), p.1059-1068

2010

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Thymidine phosphorylase in cancer cells stimulates human endothelial cell migration and invasion by the secretion of angiogenic factors

British journal of cancer, 2011-03, Vol.104 (7), p.1185-1192

2011

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The effect of allopurinol and low-dose thiopurine combination therapy on the activity of three pivotal thiopurine metabolizing enzymes: Results from a prospective pharmacological study

Journal of Crohn's and colitis, 2013-11, Vol.7 (10), p.812-819

2013

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“The only thing I know is that I know nothing”: 5-fluorouracil in human milk

Annals of oncology, 2012-02, Vol.23 (2), p.543-544

2012

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Induction of Resistance to the Lipophilic Cytarabine Prodrug Elacytarabine (CP-4055) in CEM Leukemic Cells

Nucleosides, nucleotides & nucleic acids, 2010-06, Vol.29 (4-6), p.394-399

2010

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In vitro activity and mechanism of action of a duplex and multidrug of ethynylcytidine and 5-fluorodeoxyuridine

Nucleic Acids Symposium Series, 2008, Vol.52 (1), p.651-651

2008

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"The only thing I know is that I know nothing": 5-fluorouracil in human milk

Annals of oncology : official journal of the European Society for Medical Oncology, 2012, Vol.23 (2), p.543-544

2012

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IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management

The journal of clinical endocrinology and metabolism, 2016-04, Vol.101 (4), p.1627-1636

2016

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Proteomics of Urinary Vesicles Links Plakins and Complement to Polycystic Kidney Disease

Journal of the American Society of Nephrology, 2016-10, Vol.27 (10), p.3079-3092

2016

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Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant

Molecular and cellular endocrinology, 2023-01, Vol.559, p.111799-111799, Article 111799

2023

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Reduced penetrance alleles for Huntington’s disease: a multi-centre direct observational study

Journal of medical genetics, 2007-03, Vol.44 (3), p.e68-e68

2007

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Splice Site Mutations in GH1 Detected in Previously (Genetically) Undiagnosed Families with Congenital Isolated Growth Hormone Deficiency Type II

Hormone research in paediatrics, 2013-01, Vol.80 (6), p.390-396

2013

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Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders

Journal of medical genetics, 1997-05, Vol.34 (5), p.382-390

1997

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Predicting adaptation to presymptomatic DNA testing for late onset disorders : Who will experience distress?

Journal of medical genetics, 1998-09, Vol.35 (9), p.745-754

1998

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Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer

Anticancer research, 1992-09, Vol.12 (5), p.1731

1992

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Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene

Journal of medical genetics, 1991-04, Vol.28 (4), p.252-255

1991

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Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India

Human genetics, 1988-10, Vol.80 (2), p.157-160

1988

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Multiple recombination events are responsible for the heterogeneity of α+‐thalassemia haplotypes among the forest tribes of Andhra Pradesh, India

Annals of human genetics, 1991-01, Vol.55 (1), p.43-50

1991

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Phenotypic characterization of individuals with 30-40 CAG repeat in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

American journal of human genetics, 1996, Vol.59 (1), p.16-22

1996

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Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders: Comparing questionnaire results with in-depth interviews

American journal of medical genetics, 1998-01, Vol.75 (1), p.62-74

1998

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The surgical approach to the idiopathic hypertrophic subaortic stenosis via the left atrium

Journal of cardiovascular surgery, 1967-07, Vol.8 (4), p.284

1967

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Prevalence and molecular heterogeneity of alpha+ thalassemia in two tribal populations from Andhra Pradesh, India

Human genetics, 1988, Vol.80 (2), p.157-160

1988

Volltextzugriff (PDF)

Anomalous left coronary artery arising from the pulmonary artery. A report on two cases with successful surgical therapy

British Heart Journal, 1966-09, Vol.28 (5), p.646-653

1966

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Hyperbaric oxygen in the palliative surgical treatment of heart defects with cyanosis (results in 58 patients)

Nederlands tijdschrift voor geneeskunde, 1971-12, Vol.115 (49), p.2050

1971

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SP-0547 Connecting the patient into the clinical trial: the role of an RTT

Simple and selective method for the determination of various tyrosine kinase inhibitors used in the clinical setting by liquid chromatography tandem mass spectrometry

Thymidine phosphorylase in cancer cells stimulates human endothelial cell migration and invasion by the secretion of angiogenic factors

The effect of allopurinol and low-dose thiopurine combination therapy on the activity of three pivotal thiopurine metabolizing enzymes: Results from a prospective pharmacological study

“The only thing I know is that I know nothing”: 5-fluorouracil in human milk

Induction of Resistance to the Lipophilic Cytarabine Prodrug Elacytarabine (CP-4055) in CEM Leukemic Cells

In vitro activity and mechanism of action of a duplex and multidrug of ethynylcytidine and 5-fluorodeoxyuridine

"The only thing I know is that I know nothing": 5-fluorouracil in human milk

IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management

Proteomics of Urinary Vesicles Links Plakins and Complement to Polycystic Kidney Disease

Atypical STAT5B deficiency, severe short stature and mild immunodeficiency associated with a novel homozygous STAT5B Variant

Reduced penetrance alleles for Huntington’s disease: a multi-centre direct observational study

Splice Site Mutations in GH1 Detected in Previously (Genetically) Undiagnosed Families with Congenital Isolated Growth Hormone Deficiency Type II

Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders

Predicting adaptation to presymptomatic DNA testing for late onset disorders : Who will experience distress?

Detection of K-ras mutations by denaturing gradient gel electrophoresis (DGGE): a study on pancreatic cancer

Homozygous beta+ thalassaemia owing to a mutation in the cleavage-polyadenylation sequence of the human beta globin gene

Prevalence and molecular heterogeneity of alfa+ thalassemia in two tribal populations from Andhra Pradesh, India

Multiple recombination events are responsible for the heterogeneity of α+‐thalassemia haplotypes among the forest tribes of Andhra Pradesh, India

Phenotypic characterization of individuals with 30-40 CAG repeat in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

Distress in individuals facing predictive DNA testing for autosomal dominant late-onset disorders: Comparing questionnaire results with in-depth interviews

The surgical approach to the idiopathic hypertrophic subaortic stenosis via the left atrium

Prevalence and molecular heterogeneity of alpha+ thalassemia in two tribal populations from Andhra Pradesh, India

Anomalous left coronary artery arising from the pulmonary artery. A report on two cases with successful surgical therapy

Hyperbaric oxygen in the palliative surgical treatment of heart defects with cyanosis (results in 58 patients)

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