E. Leter

发表

Definition of a moving gross target volume for stereotactic radiation therapy of stented coronary arteries.

Patrick W Serruys, Peter C Levendag, Stéphane G Carlier, 2002, International journal of radiation oncology, biology, physics.

Coronary stent traversed volume during the cardiac cycle defined as a target for high-precision radiotherapy by using biplane angiograms.

P. Serruys, C. Slager, P. Levendag, 2002, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort

M. Blok, C. V. van Asperen, A. V. D. van den Ouweland, 2019, Familial Cancer.

Four-dimensional imaging of thoracic target volumes in conformal radiotherapy

E. Leter, 2005 .

A de novoFLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation

Q. Waisfisz, P. Postmus, E. Thunnissen, 2012, Familial Cancer.

Renal cancer and pneumothorax risk in Birt–Hogg–Dubé syndrome; an analysis of 115 FLCN mutation carriers from 35 BHD families

E. Bongers, P. Postmus, R. Oldenburg, 2011, British Journal of Cancer.

Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families.

P. Postmus, F. Menko, T. V. van Os, 2008, The Journal of investigative dermatology.

Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort study.

Julie O. Culver, L. Kiemeney, M. Kloor, 2011, The Lancet. Oncology.

New mutations and an updated database for the patched‐1 (PTCH1) gene

A. Paulussen, P. Steijlen, K. Mosterd, 2018, Molecular genetics & genomic medicine.

Risk Factors for Hemoptysis in Idiopathic and Hereditary Pulmonary Arterial Hypertension

B. Boerrigter, H. Bogaard, A. Boonstra, 2013, PloS one.

TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension

E. Bongers, L. Hoefsloot, R. Hofstra, 2013, Journal of Medical Genetics.

Severely reduced diffusion capacity in idiopathic pulmonary arterial hypertension: patient characteristics and treatment responses

N. Westerhof, E. Nossent, H. Bogaard, 2013, European Respiratory Journal.

Evaluation of yield and experiences of age‐related molecular investigation for heritable and nonheritable causes of mismatch repair deficient colorectal cancer to identify Lynch syndrome

I. Nagtegaal, M. Ligtenberg, N. Hoogerbrugge, 2020, International journal of cancer.

Familial multiple discoid fibromas: a look-alike of Birt-Hogg-Dubé syndrome not linked to the FLCN locus.

Q. Waisfisz, J. V. van Waesberghe, P. Postmus, 2012, Journal of the American Academy of Dermatology.

TBX 4 mutations ( small patella syndrome ) are associated with childhood-onset pulmonary arterial hypertension

E. Bongers, L. Hoefsloot, R. Hofstra, 2013 .

Genotype-phenotype associations in a large PTEN Hamartoma Tumor Syndrome (PHTS) patient cohort.

J. Schuurs-Hoeijmakers, M. Genuardi, T. Kleefstra, 2022, European journal of medical genetics.

Genetic counselling for pulmonary arterial hypertension: a matter of variable variability

J. Gille, A. Boonstra, A. Vonk Noordegraaf, 2011, Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation.

A de novoFLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation

Q. Waisfisz, P. Postmus, E. Thunnissen, 2013, Familial Cancer.

Counseling young women with early breast cancer on fertility preservation

E. Leter, J. Derhaag, I. Vriens, 2019, Journal of Assisted Reproduction and Genetics.

Clinical Aspects of SDHA-Related Pheochromocytoma and Paraganglioma: A Nationwide Study

W. Dinjens, R. Oldenburg, C. Tops, 2018, The Journal of clinical endocrinology and metabolism.

Universal Tumor DNA BRCA1/2 Testing of Ovarian Cancer: Prescreening PARPi Treatment and Genetic Predisposition

M. C. Vos, I. Nagtegaal, L. Kooreman, 2019, Journal of the National Cancer Institute.

Lack of genotype-phenotype correlation in basal cell nevus syndrome: a Dutch multicenter retrospective cohort study.

A. Wagner, P. Steijlen, K. Mosterd, 2020, Journal of the American Academy of Dermatology.

TP53 germline mutation testing in early-onset breast cancer: findings from a nationwide cohort

M. Blok, C. V. van Asperen, A. V. D. van den Ouweland, 2019, Familial Cancer.

Postzygotic mosaicism in basal cell naevus syndrome

A. Paulussen, M. Geel, P. Steijlen, 2017, The British journal of dermatology.

Four-dimensional multislice computed tomography for determination of respiratory lung tumor motion in conformal radiotherapy.

Thomas Flohr, Peter C Levendag, Filippo Cademartiri, 2005, International journal of radiation oncology, biology, physics.

Dosimetric comparison between high-precision external beam radiotherapy and endovascular brachytherapy for coronary artery in-stent restenosis.

P. Serruys, P. Levendag, P. Nowak, 2002, International journal of radiation oncology, biology, physics.

Cancer risks by sex and variant type in PTEN Hamartoma Tumor Syndrome.

J. Schuurs-Hoeijmakers, C. Houdayer, S. Aretz, 2022, Journal of the National Cancer Institute.

Comparison of different methods to define a target volume for external beam radiation therapy of restenotic coronary arteries.

P. Levendag, P. Nowak, P. Serruys, 2001, Cardiovascular radiation medicine.