-
1
-
-
12844271083
-
Update on the genetics of stroke and cerebrovascular disease
-
Alberts M.J. and Tournier-Lasserve E. (2005). Update on the genetics of stroke and cerebrovascular disease. Stroke 36, 179-181.
-
(2005)
Stroke
, vol.36
, pp. 179-181
-
-
Alberts, M.J.1
Tournier-Lasserve, E.2
-
2
-
-
0027390357
-
Autosomal dominant leukoencephalopathy and subcortical ischemic stroke
-
Baudrimont M., Dubas F., Joutel A., Tournier-Lasserve E. and Bousser M-G. (1993). Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study. Stroke 24, 122-125.
-
(1993)
A clinicopathological study. Stroke
, vol.24
, pp. 122-125
-
-
Baudrimont, M.1
Dubas, F.2
Joutel, A.3
Tournier-Lasserve, E.4
Bousser, M-G.5
-
3
-
-
57549083804
-
Notch3 is a major regulator of vascular tone in cerebral and tail resistance arteries
-
Belin de Chantemèle E.J., Retailleau K., Pinaud F., Vessières E., Bocquet A., Guihot A.L., Lemaire B., Domenga V., Baufreton C., Loufrani L., Joutel A. and Henrion D. (2008). Notch3 is a major regulator of vascular tone in cerebral and tail resistance arteries. Arterioscler. Thromb. Vasc. Biol. 28, 2216-2224.
-
(2008)
Arterioscler. Thromb. Vasc. Biol.
, vol.28
, pp. 2216-2224
-
-
Belin de Chantemèle, E.J.1
Retailleau, K.2
Pinaud, F.3
Vessières, E.4
Bocquet, A.5
Guihot, A.L.6
Lemaire, B.7
Domenga, V.8
Baufreton, C.9
Loufrani, L.10
Joutel, A.11
Henrion, D.12
-
4
-
-
0029834598
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): A morphological study of a German family
-
Bergmann M., Ebke M., Yuan Y., Brück W., Mugler M. and Schwendemann G. (1996). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a morphological study of a German family. Acta Neuropathol. 92, 341-350.
-
(1996)
Acta Neuropathol.
, vol.92
, pp. 341-350
-
-
Bergmann, M.1
Ebke, M.2
Yuan, Y.3
Brück, W.4
Mugler, M.5
Schwendemann, G.6
-
5
-
-
79956356333
-
Notch3 is essential for regulation of the renal vascular tone
-
Boulos N., Helle F., Dussaule J.C., Placier S., Milliez P., Djudjaj S., Guerrot D., Joutel A., Ronco P., Boffa J.J. and Chatziantoniou C. (2011). Notch3 is essential for regulation of the renal vascular tone. Hypertension 57, 1176-1182.
-
(2011)
Hypertension
, vol.57
, pp. 1176-1182
-
-
Boulos, N.1
Helle, F.2
Dussaule, J.C.3
Placier, S.4
Milliez, P.5
Djudjaj, S.6
Guerrot, D.7
Joutel, A.8
Ronco, P.9
Boffa, J.J.10
Chatziantoniou, C.11
-
6
-
-
67650960613
-
High recurrence of the R1006C Notch3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
-
Cappelli A., Ragno M., Cacchiò G., Scarcella M., Staffolani P. and Pianese L. (2009). High recurrence of the R1006C Notch3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Neurosci. Lett. 462, 176-178.
-
(2009)
Neurosci. Lett.
, vol.462
, pp. 176-178
-
-
Cappelli, A.1
Ragno, M.2
Cacchiò, G.3
Scarcella, M.4
Staffolani, P.5
Pianese, L.6
-
7
-
-
0029089247
-
Clinical spectrum of CADASIL: A study of 7 families
-
Chabriat H., Vahedi K., Iba-Zizen M.T., Joutel A., Nibbio A., Nagy T.G., Krebs M.O., Jul J., Dubois B., Ducrocq X., Levasseur M., Mas J.L., Lyon-Caen O., Tournier-Lasserve E. and Bousser M.G. (1995). Clinical spectrum of CADASIL: a study of 7 families. Lancet 346, 934-939.
-
(1995)
Lancet
, vol.346
, pp. 934-939
-
-
Chabriat, H.1
Vahedi, K.2
Iba-Zizen, M.T.3
Joutel, A.4
Nibbio, A.5
Nagy, T.G.6
Krebs, M.O.7
Jul, J.8
Dubois, B.9
Ducrocq, X.10
Levasseur, M.11
Mas, J.L.12
Lyon-Caen, O.13
Tournier-Lasserve, E.14
Bousser, M.G.15
-
8
-
-
1642326305
-
ESH/ESC Hypertension Guidelines Committee. Practice guidelines for primary care physicians: 2003 ESH/ESC hypertension guidelines
-
Cifkova R., Erdine S., Fagard R., Farsang C., Heagerty A.M., Kiowski W., Kjeldsen S., Lüscher T., Mallion J.M., Mancia G., Poulter N., Rahn K.H., Rodicio J.L., Ruilope L.M., van Zwieten P., Waeber B., Williams B. and Zanchetti A. (2003). ESH/ESC Hypertension Guidelines Committee. Practice guidelines for primary care physicians: 2003 ESH/ESC hypertension guidelines. J. Hypertens. 21, 1779-1786.
-
(2003)
J. Hypertens.
, vol.21
, pp. 1779-1786
-
-
Cifkova, R.1
Erdine, S.2
Fagard, R.3
Farsang, C.4
Heagerty, A.M.5
Kiowski, W.6
Kjeldsen, S.7
Lüscher, T.8
Mallion, J.M.9
Mancia, G.10
Poulter, N.11
Rahn, K.H.12
Rodicio, J.L.13
Ruilope, L.M.14
van Zwieten, P.15
Waeber, B.16
Williams, B.17
Zanchetti, A.18
-
9
-
-
84867525461
-
Normal renal anatomy, histology, and development. In: Atlas of nontumor pathology
-
D'Agati V.D., Jennette J.C. and Silva F.G. (eds). ARP Press, Silver Spring. Maryland
-
D'Agati V.D., Jennette J.C. and Silva F.G. (2005). Normal renal anatomy, histology, and development. In: Atlas of nontumor pathology. Non-neoplastic kidney diseases. D'Agati V.D., Jennette J.C. and Silva F.G. (eds). ARP Press, Silver Spring. Maryland. pp 1-18.
-
(2005)
Non-neoplastic kidney diseases
, pp. 1-18
-
-
D'Agati, V.D.1
Jennette, J.C.2
Silva, F.G.3
-
10
-
-
33846185489
-
Genetics of ischaemic stroke
-
Dichgans M. (2007). Genetics of ischaemic stroke. Lancet Neurol. 6, 149-161.
-
(2007)
Lancet Neurol.
, vol.6
, pp. 149-161
-
-
Dichgans, M.1
-
11
-
-
8644219667
-
Notch3 is required for arterial identity and maturation of vascular smooth muscle cells
-
Domenga V., Fardoux P., Lacombe P., Monet M., Maciazek J., Krebs L.T., Klonjkowski B., Berrou E., Mericskay M., Li Z., Tournier-Lasserve E., Gridley T. and Joutel A. (2004). Notch3 is required for arterial identity and maturation of vascular smooth muscle cells. Genes Dev. 18, 2730-2735.
-
(2004)
Genes Dev.
, vol.18
, pp. 2730-2735
-
-
Domenga, V.1
Fardoux, P.2
Lacombe, P.3
Monet, M.4
McIazek, J.5
Krebs, L.T.6
Klonjkowski, B.7
Berrou, E.8
Mericskay, M.9
Li, Z.10
Tournier-Lasserve, E.11
Gridley, T.12
Joutel, A.13
-
12
-
-
47149098061
-
Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Is NOTCH3 mutation the common culprit? Am
-
Guerrot D., Francois A., Boffa J.J., Boulos N., Hanoy M., Legallicier B., Triquenot-Bagan A., Guyant-Marechal L., Laquerriere A., Freguin-Bouilland C., Ronco P. and Godin M. (2008). Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit? Am. J. Kidney Dis. 52, 340-345.
-
(2008)
J. Kidney Dis.
, vol.52
, pp. 340-345
-
-
Guerrot, D.1
Francois, A.2
Boffa, J.J.3
Boulos, N.4
Hanoy, M.5
Legallicier, B.6
Triquenot-Bagan, A.7
Guyant-Marechal, L.8
Laquerriere, A.9
Freguin-Bouilland, C.10
Ronco, P.11
Godin, M.12
-
13
-
-
33747766146
-
Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL
-
Ishiko A., Shimizu A., Nagata E., Takahashi K., Tabira T. and Suzuki N. (2006). Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL. Acta Neuropathol. 112, 333-339.
-
(2006)
Acta Neuropathol.
, vol.112
, pp. 333-339
-
-
Ishiko, A.1
Shimizu, A.2
Nagata, E.3
Takahashi, K.4
Tabira, T.5
Suzuki, N.6
-
14
-
-
78649983227
-
Pathogenesis of CADASIL: Transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature
-
Joutel A. (2011). Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature. Bioessays 33, 73-80.
-
(2011)
Bioessays
, vol.33
, pp. 73-80
-
-
Joutel, A.1
-
15
-
-
16044362074
-
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
-
Joutel A., Corpechot C., Ducros A., Vahedi K., Chabriat H., Mouton P., Alamowitch S., Domenga V., Cécillon M., Maréchal E., Maciazek J., Vayssière C., Cruaud C., Cabanis E.A., Ruchoux M.M., Weissenbach J., Bach J.F., Bousser M.G. and Tournier-Lasserve E. (1996). Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 383, 707-710.
-
(1996)
Nature
, vol.383
, pp. 707-710
-
-
Joutel, A.1
Corpechot, C.2
Ducros, A.3
Vahedi, K.4
Chabriat, H.5
Mouton, P.6
Alamowitch, S.7
Domenga, V.8
Cécillon, M.9
Maréchal, E.10
McIazek, J.11
Vayssière, C.12
Cruaud, C.13
Cabanis, E.A.14
Ruchoux, M.M.15
Weissenbach, J.16
Bach, J.F.17
Bousser, M.G.18
Tournier-Lasserve, E.19
-
16
-
-
0031590602
-
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients
-
Joutel A., Vahedi K., Corpechot C., Troesch A., Chabriat H., Vayssière C., Cruaud C., Maciazek J., Weissenbach J., Bousser M.G., Bach J.F. and Tournier-Lasserve E. (1997). Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients. Lancet 350, 1511-1515.
-
(1997)
Lancet
, vol.350
, pp. 1511-1515
-
-
Joutel, A.1
Vahedi, K.2
Corpechot, C.3
Troesch, A.4
Chabriat, H.5
Vayssière, C.6
Cruaud, C.7
McIazek, J.8
Weissenbach, J.9
Bousser, M.G.10
Bach, J.F.11
Tournier-Lasserve, E.12
-
17
-
-
17644438177
-
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients
-
Joutel A., Andreux F., Gaulis S., Domenga V., Cécillon M., Battail N., Piga N., Chapon F., Godfrain C. and Tournier-Lasserve E. (2000). The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients. J. Clin. Invest. 105, 597-605.
-
(2000)
J. Clin. Invest.
, vol.105
, pp. 597-605
-
-
Joutel, A.1
Andreux, F.2
Gaulis, S.3
Domenga, V.4
Cécillon, M.5
Battail, N.6
Piga, N.7
Chapon, F.8
Godfrain, C.9
Tournier-Lasserve, E.10
-
18
-
-
0035894640
-
Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis
-
Joutel A., Favrole P., Labauge P., Chabriat H., Lescoat C., Andreux F., Domenga V., Cécillon M., Vahedi K., Ducros A., Cave-Riant F., Bousser M.G. and Tournier-Lasserve E. (2001). Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis. Lancet 358, 2049-2051.
-
(2001)
Lancet
, vol.358
, pp. 2049-2051
-
-
Joutel, A.1
Favrole, P.2
Labauge, P.3
Chabriat, H.4
Lescoat, C.5
Andreux, F.6
Domenga, V.7
Cécillon, M.8
Vahedi, K.9
Ducros, A.10
Cave-Riant, F.11
Bousser, M.G.12
Tournier-Lasserve, E.13
-
19
-
-
33947271015
-
Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
-
Kusaba T., Hatta T., Kimura T., Sonomura K., Tanda S., Kishimoto N., Kameyama H., Okigaki M., Mori Y., Ishigami N., Mizuno T., Nakagawa M. and Matsubara H. (2007). Renal involvement in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Clin. Nephrol. 67, 182-187.
-
(2007)
Clin. Nephrol.
, vol.67
, pp. 182-187
-
-
Kusaba, T.1
Hatta, T.2
Kimura, T.3
Sonomura, K.4
Tanda, S.5
Kishimoto, N.6
Kameyama, H.7
Okigaki, M.8
Mori, Y.9
Ishigami, N.10
Mizuno, T.11
Nakagawa, M.12
Matsubara, H.13
-
20
-
-
0032781960
-
Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL
-
Mayer M., Straube A., Bruening R., Uttner J., Pongratz D., Gasser T., Dichgans M. and Muller-Hocker M. (1999). Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL. J. Neurol. 246, 526-532.
-
(1999)
J. Neurol.
, vol.246
, pp. 526-532
-
-
Mayer, M.1
Straube, A.2
Bruening, R.3
Uttner, J.4
Pongratz, D.5
Gasser, T.6
Dichgans, M.7
Muller-Hocker, M.8
-
21
-
-
8744285720
-
Fibrosis and stenosis of the long penetrating cerebral arteries: The cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Miao Q., Paloneva T., Tuominen S., Pöyhönen M., Tuisku S., Viitanen M. and Kalimo H. (2004). Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Brain Pathol. 14, 358-364.
-
(2004)
Brain Pathol.
, vol.14
, pp. 358-364
-
-
Miao, Q.1
Paloneva, T.2
Tuominen, S.3
Pöyhönen, M.4
Tuisku, S.5
Viitanen, M.6
Kalimo, H.7
-
22
-
-
22844446634
-
Spectrum of mutations in biopsy-proven CADASIL: Implications for diagnostic strategies
-
Peters N., Opherk C., Bergmann T., Castro M., Herzog J. and Dichgans M. (2005). Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies. Arch. Neurol. 62, 1091-1094.
-
(2005)
Arch. Neurol.
, vol.62
, pp. 1091-1094
-
-
Peters, N.1
Opherk, C.2
Bergmann, T.3
Castro, M.4
Herzog, J.5
Dichgans, M.6
-
23
-
-
1642317567
-
CADASIL or CADVaSIL
-
Rafalowska J., Fidzianska A., Dziewulska D., Podlecka A., Szpak G.M. and Kwiecinski H. (2004). CADASIL or CADVaSIL? Neuropathology 24, 16-20.
-
(2004)
Neuropathology
, vol.24
, pp. 16-20
-
-
Rafalowska, J.1
Fidzianska, A.2
Dziewulska, D.3
Podlecka, A.4
Szpak, G.M.5
Kwiecinski, H.6
-
24
-
-
33749073835
-
Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene
-
Ragno M., Fabrizi G.M., Cacchiò G., Scarcella M., Sirocchi G., Selvaggio F., Taioli F., Ferrarini M. and Trojano L. (2006). Two novel Italian CADASIL families from Central Italy with mutation CGC-TGC at codon 1006 in the exon 19 Notch3 gene. Neurol. Sci. 27, 252-256.
-
(2006)
Neurol. Sci.
, vol.27
, pp. 252-256
-
-
Ragno, M.1
Fabrizi, G.M.2
Cacchiò, G.3
Scarcella, M.4
Sirocchi, G.5
Selvaggio, F.6
Taioli, F.7
Ferrarini, M.8
Trojano, L.9
-
25
-
-
0019967975
-
The Global Deterioration Scale for assessment of primary degenerative dementia
-
Reisberg B., Ferris S.H., De Leon M.J. and Crook T. (1982). The Global Deterioration Scale for assessment of primary degenerative dementia. Am. J. Psychiatry 139, 1136-1139.
-
(1982)
Am. J. Psychiatry
, vol.139
, pp. 1136-1139
-
-
Reisberg, B.1
Ferris, S.H.2
de Leon, M.J.3
Crook, T.4
-
26
-
-
0031930666
-
Endothelial changes in muscle and skin biopsies in patients CADASIL
-
Ruchoux M.M. and Maurage C.A. (1998). Endothelial changes in muscle and skin biopsies in patients CADASIL. Neuropathol. Appl. Neurobiol. 24, 60-65.
-
(1998)
Neuropathol. Appl. Neurobiol.
, vol.24
, pp. 60-65
-
-
Ruchoux, M.M.1
Maurage, C.A.2
-
27
-
-
0028113875
-
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL
-
Ruchoux M.M., Chabriat H., Bousser M.G., Baudrimont M. and Tournier-Lasserve E. (1994). Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL. Stroke 25, 2291-2292.
-
(1994)
Stroke
, vol.25
, pp. 2291-2292
-
-
Ruchoux, M.M.1
Chabriat, H.2
Bousser, M.G.3
Baudrimont, M.4
Tournier-Lasserve, E.5
-
28
-
-
0029050447
-
Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
-
Ruchoux M.M., Guerouaou D., Vandenhaute B., Pruvo J.P., Vermersch P. and Leys D. (1995). Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Acta Neuropathol. 89, 500-512.
-
(1995)
Acta Neuropathol.
, vol.89
, pp. 500-512
-
-
Ruchoux, M.M.1
Guerouaou, D.2
Vandenhaute, B.3
Pruvo, J.P.4
Vermersch, P.5
Leys, D.6
-
29
-
-
0027339590
-
A semiquantitative rating scale for the assessment of signal hyperintensities on magnetic resonance imaging
-
Scheltens P., Barkhof F., Leys D., Pruvo J.P., Nauta J.J., Vermersch P., Steinling M. and Valk J. (1993). A semiquantitative rating scale for the assessment of signal hyperintensities on magnetic resonance imaging. J. Neurol. Sci. 114, 7-12.
-
(1993)
J. Neurol. Sci.
, vol.114
, pp. 7-12
-
-
Scheltens, P.1
Barkhof, F.2
Leys, D.3
Pruvo, J.P.4
Nauta, J.J.5
Vermersch, P.6
Steinling, M.7
Valk, J.8
-
30
-
-
65249114174
-
Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients
-
Tikka S., Mykkänen K., Ruchoux M.M., Bergholm R., Junna M., Pöyhönen M., Yki-Järvinen H., Joutel A., Viitanen M., Baumann M. and Kalimo H. (2009). Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients. Brain 132, 933-939.
-
(2009)
Brain
, vol.132
, pp. 933-939
-
-
Tikka, S.1
Mykkänen, K.2
Ruchoux, M.M.3
Bergholm, R.4
Junna, M.5
Pöyhönen, M.6
Yki-Järvinen, H.7
Joutel, A.8
Viitanen, M.9
Baumann, M.10
Kalimo, H.11
-
31
-
-
0027479304
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
-
Tournier-Lasserve E., Joutel A., Melki J., Weissenbach J., Lathrop G.M., Chabriat H., Mas J.L., Cabanis E.A., Baudrimont M., Maciazek J., Bach M.A. and Bousser M.G. (1993). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat. Genet. 3, 256-259.
-
(1993)
Nat. Genet.
, vol.3
, pp. 256-259
-
-
Tournier-Lasserve, E.1
Joutel, A.2
Melki, J.3
Weissenbach, J.4
Lathrop, G.M.5
Chabriat, H.6
Mas, J.L.7
Cabanis, E.A.8
Baudrimont, M.9
McIazek, J.10
Bach, M.A.11
Bousser, M.G.12
-
32
-
-
79953887891
-
Notch3 mutations and clinical features in 33 mainland Chinese families with CADASIL
-
Wang Z., Yuan Y., Zhang W., Lv H., Hong D., Chen B., Liu Y., Luan X., Xie S. and Wu S. (2011). Notch3 mutations and clinical features in 33 mainland Chinese families with CADASIL. J. Neurol. Neurosurg. Psychiatry 82, 534-539.
-
(2011)
J. Neurol. Neurosurg. Psychiatry
, vol.82
, pp. 534-539
-
-
Wang, Z.1
Yuan, Y.2
Zhang, W.3
Lv, H.4
Hong, D.5
Chen, B.6
Liu, Y.7
Luan, X.8
Xie, S.9
Wu, S.10
|