2007

Post MC, Budts WIHL, Westermann CJJ
Cardiac and Pulmonary Right-to-left shunts.
Migraine Disorders Research Trends, chapter 13, 2007 Nova Science Publishers, Inc.

Van Tuyl SA, Letteboer TG, Rogge-Wolf C, Kuipers EJ, Snijder RJ, Westermann CJJ, Stolk MF
Assessment of intestinal vascular malformations in patients with hereditary hemorrhagic teleangiectasia and anemia. Eur J Gastroent Hepat 2007; 19:153-158.   

2006

Post MC, Thijs V, Schoonewille WJ, Budts W, Snijder RJ, Plokker Th. Westermann CJJ.
Embolization of pulmonary arteriovenous malformations and decrease in prevalence of migraine. Neurology 2006;66:202-5.

Letteboer TGW, Mager JJ, Snijder RJ, Koeleman BPC, Lindhout D, Ploos van Amster JK, Westermann CJJ.
Genotype-phenotype relationship in Hereditary Hemorrhagic Telangiectasis.
J Med Gen 2006;43:371-377

Driesche S van der, Feyen A, Thorikay M, Lux A, Westermann CJJ, Dikje P ten, Mummery CL, Lebrin F.
Functional analysis of ∆ 32bpIns11bp mutation in endoglin. Submitted

Driesche S van der, Laake LW van, Post S, Feijen A, Jansen MA, Driessens MH, Mager JJ, Snijder RJ, Westermann CJJ, Doevendans PA, Echteld CJA, Dijke P ten, Arthur MH, Goumans MJ, Lebrin F, Mummery CL.
Defective blood derived endothelial cell mediated vascular repair contributes to the etiology of hereditary hemorrhagic telangiectasia.
Submitted.

Gallione CJ, Richards JA, Letteboer TGW, Wushlow D, Prigoda NL, Leedan TP,. Ganguly A, Castells A, Ploos van Amstel JK, Westermann CJJ, Pyerits RE, Marchuk DA.
SMAD4 Mutations Found in Unselected HHT Patients.
J Med Genet 2006; 43:793-797.

Letteboer TGW, Mager JJ, Snijder RJ, Lindhout D, Ploos van Amstel JK, Zanen P, Westermann JJ.
Localisation and age distribution of telangiectases in Hereditary Hemorrhagic Telangiectasia. Submitted.

Letteboer TGW, Kuit RM, Disch FJM, Mager JJ, Snijder RJ, Lindhout D, Ploos van Amstel JK, Zanen P, Westermann CJJ.
Epistaxis, onset and frequency in HHT-1 and HHT-2. Submitted.

Tuyl SAC van, Tenthof van Noorden J, Letteboer TGW, Kuipers EJ, Snijder RJ, Westermann CJJ, Stolk MFJ.
Assessment of intestinal vascular malformations in patients with hereditary hemorrhagic telangiectasia and anaemia.
Submitted.

2005

Letteboer TGW,Mager JJ,Snijder RJ,Koeleman BPC,Lindhout D,Ploos van Amstel JK,Westermann CJJ
Genotype-phenotype relationship in Hereditary Hemorrhagic Telangiectasia,
J Med Gen; 2005: in press.

Letteboer TGW, Zewald RA, Kamping EJ, Haas G de, Mager JJ, Snijder RJ, Lindhout D, Hennekam FAM, Westermann CJJ, Ploos van Amstel JK
Hereditary hemorrhagic telangiectasia: ENG and ALK-1 mutations in Dutch patients
Hum.Genet. 2005; 116:8-16

Post MC, Westermann CJJ et al.
A pulmonary right-to-left shunt in patients with HHT is associated with an increased prevalence of migraine. Chest 2005; 128:2485-2489.

2004

Gallione CJ, Repetto GM, Legius E, Rustgi AK, Schelley SL, Tejpar S, Mitchell G, Drovin E, Westermann CJJ, Marchuk DA.
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4)
Lancet 2004; 363:852-59

2003

Westermann CJJ, Rosina AF, Vries V de, Coteau PA de
The prevalence and manifestations of HHT in the Afro-Caribbean population of the Netherlands Antilles: A family screening Am
J Med Gen 2003; 116A:324-8

Westermann CJJ
De ziekte van Rendu-Osler-Weber: diagnose, genotype-fenotype
Ned Tijdschr Geneeskd 2003; 147:442

Mager JJ
Pulmonale arterioveneuze malformaites: diagnose, complicaties, behandelng
Ned Tijdschr Geneeskd 2003; 147:442-3

Driesche S van der, Mummery CL, Westermann CJJ
Hereditary hemorrhagic telangiectasia: an update on transforming growth factor β signaling in vasculogenesis and angiogenesis.
Cardiovasc. Research 2003; 58:20-31

Westermann CJJ, Rosina AF, Vries V de, Mager JJ
Hoge prevalentie van de ziekte van Rendu-Osler-Weber in de Afro-Caribische bevolking van de Nederlandse Antillen
Ned Tijdschr Geneeskd 2003; 147:1595-1600

2002

Mager JJ, Zanen P, Verzijlbergen F, Westermann CJJ, Haitjema T, Herk G van, Lammers JWJ
Quantification of right-to-left shunt with 99mTC-labelled albumin macroaggregates and 100% oxygen in patients with hereditary haemorrhagic tlangiectasia
Cinical Science 2002; 102:127-134

Willemse RB, Westermann CJJ, Van der Top WP
Cerebrovasculaire malformaties bij hereditaire hemorrhagische teleangiectasie:en
Ned Tijdschr Neurologie 2002; 6:472-6

Koppen S. Korver CRW, Dalinghaus M, Westermann CJJ
Neonatal pulmonary arteriovenous malformation in hereditary haemorrhagic telangiectasia
Arch Dis Child Fetal Neonatal Ed 2002; 87:F226-227

Mager JJ
Clinical aspects of hereditary haemorrhagic telangiectasia
Proefschrift 2002, Utrecht

2001

Mager JJ, Overtoom TThC, Mauser HW, Westermann CJJ
Early cerebral infarction after embolotherapy of a pulmonary arteriovenous malformation
JVIR 2001; 12:122-3

Mager JJ, Schutgens REG, Haas FJLM, Westermann CJJ
The early course of D-dimer concentration following pulmonary artery embolisation
Thromb Haemost 2001; 86:1578-9

2000

Gallione CJ, Scheessele EA, Reinhardt D, Duits AJ, Berg JN, Westermann CJJ, Marchuk DA
Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effect.
Hum Gent 2000: 107:40-4

Mager JJ, Westermann CJJ
Value of capillary microscopy in the diagnosis of Hereditary Hemorrhagic Telangiectasia
Arch Dermatol 2000; 136:732-4

Shovin CL, Guttmacher AE, Buscarini E, Faughnan M, Hyland RH, Westermann CJJ, Kjeldsen AD, Plauchu H.
Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber Syndrome)
Am J Med Genet 2000; 91:66-7

Willemse RB, Mager JJ, Westermann CJJ, Overtoom TThC, Mauser H, Wolbers JG
Bleeding risk of cerebrovascular malformations in hereditary hemorrhagic talangiectasia.
J Neurosurg 2000; 92:779-84

1999

Mager JJ, Mauser HW, Westermann CJJ
Intracraniële arterioveneuze malformatie bij zwangere vrouwen
Ned Tijdschr Geneeskd 1999; 143:1116

1998

Gallione CJ, Klaus DJ, Yeh EY, Stenzel TT, Xue Y, Anthony KB, McAllister KA, Baldwin MA, Berg JN, Lux A, Smith JD, Vary CP, Craigen WJ, Westermann CJJ, Warner ML, Miller YE, Jackson EC, Guttmacher AE, Marchuk DA.
Mutation and expression analysis of the endoglin gene in hereditary hemorrhagic telangiectasia reveals null alleles
Hum Mutat. 1998; 11:286-294

1996

Haitjema Tj, Balder W, Disch FJM, Westermann CJJ
Epistaxis in hereditary haemorrhagic telangiectasia
Rhinology 1996; 34:176-8

Haitjema Tj, Westermann CJJ, Overtoom TTjC, Timmer R, Disch FJM, Mauser HW, Lammers j-WJ
Hereditary hemorrhagic tlangiectasia (Osler-Weber-Rendu disease). New insights in pathogenesis, complications, and treatment
Arch Intern Med 1996; 156:714-9

Haitjema Tj, Berg JM ten, Overtoom TTjC, Ernst JMPG, Westermann CJJ
Unusual complications after embolization of a pulmonary arteriovenous malformation.
Chest 1996; 109:1401-4

Haitjema Tj, Snippenburg R van, Disch FJM, Overtoom TTjC, Westermann CJJ
Recidiverende epistaxis: soms de ziekte van Rendu-Osler-Weber.
Ned Tijdschr Geneeskd 1996; 140:2157-60

Haitjema Tj, Westermann CJJ, Overtoom TTjC
Letter to the editor
Arch Intern Med 1996; 156:2628

1995

Haitjema Tj
Hereditary hemorrhagic telangiectasia
Proefschrift 1995, Utrecht

Haitjema Tj, Disch F, Overtoom TTjC, Westermann CJJ, Lammers J-WJ
Screening family members of patients with hereditary hemorrhagic teleangiectasia
Am J Med 1995; 99:519-524

Haitjema Tj, Overtoom TTjC, Westermann CJJ, Lammers J-WJ
Embolization of pulmonary arteriovenous malformations – results and follow-up in 32 patients
Thorax 1995; 50:719-723

Haitjema Tj, Westermann CJJ
Is aanvullend onderzoek altijd een aanvulling bij vermoeden van paradoxe embolie?
Ned T Geneeskd 1995; 139:1105

1994

McAllister KA, Grogg KM, Johnson DW, Gallione CJ, Baldwin MA, Jackson CE, Helmbold EA, Markel DS, McKinnon WC, Murrell J, McCormick MK, Perical-Vance MA, Heutink P, Oostra BA, Haitjema Tj, Westermann CJJ, Porteous ME, Guttmacher AE, Letarte M, Marchuk DA
Endoglin, a TGF-β binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia tyype 1.
Nature Genetics 1994; 8:345-51

Westermann CJJ
Hereditary Hemorrhagic Telangiectasia in people of African descent
Bulletin HHT Foundation 1994; 11

Heutink P, Haitjema T, Breedveld GJ, Janssen B, Sandkuyl LA, Bontekoe CJM, Westermann CJJ, Oostra BA
Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence of locus heterogeneity
J Med Genet 1994; 31: 933-6

1993

Haitjema Tj, Westermann CJJ, Overtoom TTjC
Embolisation of pulmonary arteriovenous malformations
Chest 1993; 103:191S

Berg JWM ter, Dippel DWJ, Habbema JDF, Westermann CJJ, Tulleken CAF, Willemse J
Unruptured intracranial arteriovenous malformations with hereditary haemorrhagic telangiectasia
Acta Neurochir 1993; 121:34-42