cystine and CADASILM

cystine has been researched along with CADASILM in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Callaerts-Vegh, Z; Carmeliet, P; Collen, D; D'Hooge, R; Dewerchin, M; Lupu, F; Moons, L; Nuyens, D; Silasi-Mansat, R; Souffreau, J; Van Nuffelen, A; Wallays, G	1
Cacchiò, G; Cavallaro, T; Fabrizi, GM; Ragno, M; Scarcella, M; Silvaggio, F; Taioli, F; Trojano, L	1

Other Studies

2 other study(ies) available for cystine and CADASILM

Article	Year
Notch3 Arg170Cys knock-in mice display pathologic and clinical features of the neurovascular disorder cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Arteriosclerosis, thrombosis, and vascular biology, 2011, Volume: 31, Issue:12 Topics: Animals; Arginine; Brain; CADASIL; Capillaries; Cystine; Disease Models, Animal; Fertility; Gene Knock-In Techniques; Mice; Motor Activity; Muscle, Smooth, Vascular; Mutation; Receptor, Notch3; Receptors, Notch	2011
Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2007, Volume: 28, Issue:4 Topics: Aged; CADASIL; Cystine; Exons; Family Health; Female; Glycine; Humans; Italy; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Receptor, Notch3; Receptors, Notch	2007

Article

Year

Notch3 Arg170Cys knock-in mice display pathologic and clinical features of the neurovascular disorder cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Arteriosclerosis, thrombosis, and vascular biology, 2011, Volume: 31, Issue:12

Topics: Animals; Arginine; Brain; CADASIL; Capillaries; Cystine; Disease Models, Animal; Fertility; Gene Knock-In Techniques; Mice; Motor Activity; Muscle, Smooth, Vascular; Mutation; Receptor, Notch3; Receptors, Notch

2011

Clinical presentation of CADASIL in an Italian patient with a rare Gly528Cys exon 10 NOTCH3 gene mutation.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2007, Volume: 28, Issue:4

Topics: Aged; CADASIL; Cystine; Exons; Family Health; Female; Glycine; Humans; Italy; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Receptor, Notch3; Receptors, Notch

2007