Zobrazeno 1 - 10
of 24
pro vyhledávání: '"G M TERWINDT"'
Publikováno v:
The Journal of Headache and Pain, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Background Migraine is a disabling neurological disorder whose diagnosis is based on clinical criteria. A shortcoming of these criteria is that they do not fully capture the underlying neurobiological factors and sex-specific complications i
Externí odkaz:
https://doaj.org/article/784d84eea6e142718552a05153e32f7a
Autor:
S. Voigt, E. A. Koemans, I. Rasing, E. S. van Etten, G. M. Terwindt, F. Baas, K. Kaushik, A. C. G. M. van Es, M. A. van Buchem, M. J. P. van Osch, M. A. A. van Walderveen, C. J. M. Klijn, M. M. Verbeek, L. van der Weerd, M. J. H. Wermer
Publikováno v:
Trials, Vol 24, Iss 1, Pp 1-6 (2023)
Abstract Background Cerebral amyloid angiopathy (CAA) is a disease caused by the accumulation of the amyloid-beta protein and is a major cause of intracerebral hemorrhage (ICH) and vascular dementia in the elderly. The presence of the amyloid-beta pr
Externí odkaz:
https://doaj.org/article/aea914d44b86478b88e22d6bbf1175f2
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 161
Migraine is often regarded as a debilitating headache disorder without long-term consequences. However, migraine is an important risk factor for cardiovascular disease, especially in young women who suffer from migraine with aura. This increased risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::364d1a2371f9886f9b5c93f79b9ab83e
https://pubmed.ncbi.nlm.nih.gov/28247836
https://pubmed.ncbi.nlm.nih.gov/28247836
Publikováno v:
Cephalalgia : an international journal of headache. 28(2)
A possible relation between migraine and epilepsy has been a matter of debate for many decades. Clinical, epidemiological and therapeutic similarities may be coincidental and are no proof of a common aetiological background. However, a genetically de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::63e16470014547ba16959513d1ec9a7c
https://pubmed.ncbi.nlm.nih.gov/18197881
https://pubmed.ncbi.nlm.nih.gov/18197881
Autor:
A H Stam, M D Ferrari, J. Haan, K R J Vanmolkot, H.B. Ginjaar, A.M.J.M. van den Maagdenberg, W. S. Frankhuizen, E E Kors, Rune R. Frants, E Leshinsky-Silver, R Gilad, G M Terwindt, H P H Kremer, Jutta Gärtner, J. Brown
Publikováno v:
Clinical Genetics, 74, 5, pp. 481-5
Clinical Genetics, 74, 481-5
Clinical Genetics, 74, 481-5
Contains fulltext : 70291.pdf (Publisher’s version ) (Closed access) Of the 18 missense mutations in the CACNA1A gene, which are associated with familial hemiplegic migraine type 1 (FHM1), only mutations S218L, R583Q and T666M were identified in mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65166defbaa02853de53f305d9c08e05
https://hdl.handle.net/2066/70291
https://hdl.handle.net/2066/70291
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 151(37)
New epidemiological studies suggest a relationship between migraine (especially migraine with aura) and cardiovascular disease. However, the absolute risk of cardiovascular disease for migraine patients is still low even though the relative risk is 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1dcf3a12d1e6f949becbfbee53b18205
https://pubmed.ncbi.nlm.nih.gov/17929710
https://pubmed.ncbi.nlm.nih.gov/17929710
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 150(19)
The relationship between patent foramen ovale (PFO) and migraine is controversial. A common genetic background seems possible, but there is no evidence for a causal relationship. Despite the lack of evidence, PFO closure is recommended in many countr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b6e59785e8b064ef792a0befcd9ffcc
https://pubmed.ncbi.nlm.nih.gov/16733978
https://pubmed.ncbi.nlm.nih.gov/16733978
Autor:
A M J M, van den Maagdenberg, E E, Kors, E R, Brunt, W, van Paesschen, J, Pascual, D, Ravine, S, Keeling, K R J, Vanmolkot, F L M G, Vermeulen, G M, Terwindt, J, Haan, R R, Frants, M D, Ferrari
Publikováno v:
Journal of neurology. 249(11)
We analysed the CACNA1A gene, located on chromosome 19p13, in three unrelated families and one sporadic case with episodic ataxia type 2 (EA-2). In two of the families and the sporadic patient, novel truncating mutations, which disrupt the reading fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c633e16bab25943f8e9ecc0f71d5f1e5
https://pubmed.ncbi.nlm.nih.gov/12420090
https://pubmed.ncbi.nlm.nih.gov/12420090
Publikováno v:
European journal of human genetics : EJHG. 6(4)
Clinical and genetic heterogeneity as well as influence of environmental factors have hampered identification of the genetic factors which are involved in episodic diseases such as migraine, episodic ataxia and epilepsy. The study of rare, but clearl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b143925397dfea6191bf08190aa598e6
https://pubmed.ncbi.nlm.nih.gov/9781035
https://pubmed.ncbi.nlm.nih.gov/9781035
Publikováno v:
Histology and histopathology. 13(3)
Neurotransmitter release, neuronal excitation, and a whole variety of other neuronal functions are controlled by the intra/extra cellular Ca2+ gradient. The major pathway for entry of Ca2+ into the excitable cells is mediated by voltage-gated Ca2+ ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0e0a6f0886d76419fac3f4038f32014e
https://pubmed.ncbi.nlm.nih.gov/9690139
https://pubmed.ncbi.nlm.nih.gov/9690139