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scopus: 6602190341

Cnossen, M.H.

(Marjon Cnossen)


children stroke factor study disease complication mutation risk factors prothrombotic coagulation factors screening perinatal stroke prothrombotic perinatal hbh disease outcome patient child group coagulation netherland neonate table disorder disability thrombosis hemoglobin symptom sample result signi analysis deletion problem a-thalassemie codon nf 1 patients laboratory parent onset health ischemic stroke follow-up carrier proband rotterdam impairment erasmus mc childhood ischemic paediatric mthfr mother infarction prevalence neurofibromatosi presentation erasmu level month questionnaire genotype infant neurofibroma glioma classi fication leiden sinovenous thrombosis ficant number blood globin neurol value incidence pathway motor a-thalassaemia hb h disease pathway glioma percentage




8 Most Recent Publications

Relationship between neonatal screening results by HPLC and the number of a-thalassaemia gene mutations; Consequences for the cut-off value (Article)
Bouva, M.J. Sollaino, C. Perseu, L. Galanello, R. Giordano, P.C. Harteveld, C.L. Cnossen, M.H. Schielen, P.C.J.I. Elvers, L.H. Peters, M.
2011-12-01
Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb rotterdam): Two novel α2 gene mutations associated with mild α-Thalassemia found in the same family after newborn screening (Article)
Giordano, P.C. Cnossen, M.H. Harteveld, C.L. Joosten, A.M.S. Jansen, C.A.M. Hakvoort, T.E. Bakker-Verweij, M. Arkesteijn, S.J.G. Delft, P. van Waye, J.S. Bouva, M.J.
2010-08-01
Paediatric arterial ischaemic stroke: Functional outcome and risk factors (Article)
Cnossen, M.H. Aarsen, F.K. Akker, S.L.J. van den Danen, R. Appel, I.M. Steyerberg, E.W. Catsman-Berrevoets, C.E.
2010-04-01
Etiology and treatment of perinatal stroke; a role for prothrombotic coagulation factors? (Article)
Cnossen, M.H. Ommen, C.H. van Appel, I.M.
2009-10-01
'Getting involved with the wrong one': Diagnostics of thalassemia (Article)
Segers, H. Scharnhorst, V. Busari, J.O.O. Cnossen, M.H.
2009-08-01
A prospective 10 year follow up study of patients with neurofibromatosis type 1 (Article)
Cnossen, M.H. Goede-Bolder, A. de Broek, K.M. van den Waasdorp, C.M. Oranje, A.P. Stroink, H. Simonsz, H.J. Ouweland, A.M.W. van den Halley, D.J.J. Niermeijer, M.F.
1998-01-01
Neurofibromatosis Type I: a clinical and molecular genetic study (Doctoral Thesis)
Cnossen, M.H.
1997-12-17
Endocrinologic disorders and optic pathway gliomas in children with neurofibromatosis type 1 (Article)
Cnossen, M.H. Stam, E.N. Cooiman, L.C.M.G. Simonsz, H.J. Stroink, H. Oranje, A.P. Halley, D. Goede-Bolder, A. de Niermeijer, M.F. Muinck Keizer-Schrama, S.M.P.F. de
1997-10-01