Zobrazeno 1 - 10
of 71
pro vyhledávání: '"E. Overwater"'
Publikováno v:
Cardiogenetics, Vol 11, Iss 3, Pp 129-131 (2021)
A spontaneous coronary artery dissection as the sole presenting feature of vascular Ehlers-Danlos syndrome is an uncommon finding. We present a 33-year-old woman with sudden onset chest pain caused by a spontaneous coronary artery dissection. Genetic
Externí odkaz:
https://doaj.org/article/9bc33baf535b4d279838b5b1337a1e3a
Akademický článek
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Publikováno v:
Cardiogenetics, Vol 11, Iss 14, Pp 129-131 (2021)
Cardiogenetics, 11(3), 129-131. PAGEPRESS PUBL
Bos, J, Overwater, E, Dirksen, M T, Simsek, S, Demirdas, S & Houweling, A C 2021, ' Spontaneous Coronary Artery Dissection as Presenting Feature of Vascular Ehlers-Danlos Syndrome ', Cardiogenetics, vol. 11, no. 3, pp. 129-131 . https://doi.org/10.3390/cardiogenetics11030014
Cardiogenetics, 11(3), 129-131
Cardiogenetics, 11(3), 129-131. PAGEPRESS PUBL
Bos, J, Overwater, E, Dirksen, M T, Simsek, S, Demirdas, S & Houweling, A C 2021, ' Spontaneous Coronary Artery Dissection as Presenting Feature of Vascular Ehlers-Danlos Syndrome ', Cardiogenetics, vol. 11, no. 3, pp. 129-131 . https://doi.org/10.3390/cardiogenetics11030014
Cardiogenetics, 11(3), 129-131
A spontaneous coronary artery dissection as the sole presenting feature of vascular Ehlers-Danlos syndrome is an uncommon finding. We present a 33-year-old woman with sudden onset chest pain caused by a spontaneous coronary artery dissection. Genetic
Autor:
Kees P.J. Braun, Marie-Claire Y. de Wit, Floor E. Jansen, Hanna M. Hulshof, Iris E. Overwater, Juliette Brenner
Publikováno v:
European Journal of Paediatric Neurology, 25, 113-119. W.B. Saunders
Background Tuberous sclerosis complex (TSC) is a highly variable condition and its clinical features cannot reliably be predicted from the genotype. Counselling of parents of a child with TSC is challenging because of the variability of the condition
Publikováno v:
Therapeutics and Clinical Risk Management. 15:951-955
Up to 90% of patients with tuberous sclerosis complex (TSC) have epilepsy, and in over half of patients seizure control cannot be achieved by regular antiepileptic drugs. The underlying problem is mTOR hyperactivation due to loss of function of the T
Publikováno v:
Therapeutics and Clinical Risk Management
Up to 90% of patients with tuberous sclerosis complex (TSC) have epilepsy, and in over half of patients seizure control cannot be achieved by regular antiepileptic drugs. The underlying problem is mTOR hyperactivation due to loss of function of the T
Autor:
Henriëtte A. Moll, Thijs van der Vaart, Marie-Claire Y. de Wit, Leontine W. ten Hoopen, Floor E. Jansen, André B. Rietman, Iris E. Overwater, Dimitris Rizopoulos, Sabine E. Mous, Karen Bindels-de Heus, Ype Elgersma
Publikováno v:
Neurology, 93(2), E200-E209. Lippincott Williams & Wilkins
ObjectiveTo investigate whether mammalian target of rapamycin inhibitor everolimus can improve intellectual disability, autism, and other neuropsychological deficits in children with tuberous sclerosis complex (TSC).MethodsIn this 12-month, randomize
Autor:
Alessandra Maugeri, Arjan C. Houweling, Clémence Vanlerberghe, A.C. Brehin, M. J. H. Baars, Nadine Hanna, E Overwater, Laurent Gouya, J. P. van Tintelen, Geneviève Baujat, Els Voorhoeve, Marion Gérard, Luisa Marsili, Pauline Arnaud
Publikováno v:
European Heart Journal. 40
Background Mutations in TGFB3 cause Loeys-Dietz syndrome-5 (LDS5), an autosomal dominantly inherited connective tissue disorder. LDS5 is characterized by aortic aneurysms and dissections associated with systemic features mainly involving the ocular a
Interdependence of clinical factors predicting cognition in children with tuberous sclerosis complex
Autor:
Hester F. Lingsma, A.m. Van Den Ouweland, Barbara J. H. Verhaar, M. C. Y. de Wit, Iris E. Overwater, H. A. Moll, L. W. (Leontine) ten Hoopen, Mark Nellist, G. C. B. Bindels de Heus, Ype Elgersma
Publikováno v:
Journal of neurology, 264(1), 161-167. D. Steinkopff-Verlag
Journal of Neurology
Journal of Neurology, 264(1), 161-167. D. Steinkopff-Verlag
Journal of Neurology
Journal of Neurology, 264(1), 161-167. D. Steinkopff-Verlag
Cognitive development in patients with tuberous sclerosis complex is highly variable. Predictors in the infant years would be valuable to counsel parents and to support development. The aim of this study was to confirm factors that have been reported