-
1
-
-
0035807348
-
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
-
Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM (2001) Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 413:488-494
-
(2001)
Nature
, vol.413
, pp. 488-494
-
-
Levy, G.G.1
Nichols, W.C.2
Lian, E.C.3
Foroud, T.4
Mcclintick, J.N.5
McGee, B.M.6
Yang, A.Y.7
Siemieniak, D.R.8
Stark, K.R.9
Gruppo, R.10
Sarode, R.11
Shurin, S.B.12
Chandrasekaran, V.13
Stabler, S.P.14
Sabio, H.15
Bouhassira, E.E.16
Upshaw Jr., J.D.17
Ginsburg, D.18
Tsai, H.M.19
-
2
-
-
0037015057
-
Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity
-
Kokame K, Matsumoto M, Soejima K, Yagi H, Ishizashi H, Funato M, Tamai H, Konno M, Kamide K, Kawano Y, Miyata T, Fujimura Y (2002) Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci USA 99:11902-11907
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 11902-11907
-
-
Kokame, K.1
Matsumoto, M.2
Soejima, K.3
Yagi, H.4
Ishizashi, H.5
Funato, M.6
Tamai, H.7
Konno, M.8
Kamide, K.9
Kawano, Y.10
Miyata, T.11
Fujimura, Y.12
-
3
-
-
0032522952
-
Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
-
Furlan M, Robles R, Solenthaler M, Lammle B (1998) Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura. Blood 91:839-2846
-
(1998)
Blood
, vol.91
, pp. 839-2846
-
-
Furlan, M.1
Robles, R.2
Solenthaler, M.3
Lammle, B.4
-
4
-
-
0032569840
-
Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
-
Tsai HM, Lian EC (1998) Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 339:1585-1594
-
(1998)
N Engl J Med
, vol.339
, pp. 1585-1594
-
-
Tsai, H.M.1
Lian, E.C.2
-
5
-
-
0030663259
-
Moyamoya disease and syndrome
-
Hoffman HJ (1997) Moyamoya disease and syndrome. Clin Neurol Neurosurg 99(Suppl 2):S39-S44
-
(1997)
Clin Neurol Neurosurg
, vol.99
, Issue.SUPPL. 2
-
-
Hoffman, H.J.1
-
6
-
-
0036224556
-
Moyamoya disease: A review
-
Gosalakkal JA (2002) Moyamoya disease: A review. Neurol India 50:6-10
-
(2002)
Neurol India
, vol.50
, pp. 6-10
-
-
Gosalakkal, J.A.1
-
7
-
-
0028229877
-
Moyamoya disease associated with thrombotic thrombocytopenic purpura (TTP)
-
Hiyama H, Kusano R, Muragaki Y, Miura N (1994) Moyamoya disease associated with thrombotic thrombocytopenic purpura (TTP). No Shinkei Geka 22:567-572
-
(1994)
No Shinkei Geka
, vol.22
, pp. 567-572
-
-
Hiyama, H.1
Kusano, R.2
Muragaki, Y.3
Miura, N.4
-
8
-
-
0032918258
-
Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura
-
Furlan M, Robles R, Morselli B, Sandoz P, Lämmle B (1999) Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura. Thromb Haemost 81:8-13
-
(1999)
Thromb Haemost
, vol.81
, pp. 8-13
-
-
Furlan, M.1
Robles, R.2
Morselli, B.3
Sandoz, P.4
Lämmle, B.5
-
9
-
-
0035408661
-
Upshaw-Schulman syndrome revisited: A concept of congenital thrombotic thrombocytopenic purpura
-
Kinoshita S, Yoshioka A, Park YD, Ishizashi H, Konno M, Funato M, Matsui T, Titani K, Yagi H, Matsumoto M, Fujimura Y (2001) Upshaw-Schulman syndrome revisited: A concept of congenital thrombotic thrombocytopenic purpura. Int J Hematol 74:101-108
-
(2001)
Int J Hematol
, vol.74
, pp. 101-108
-
-
Kinoshita, S.1
Yoshioka, A.2
Park, Y.D.3
Ishizashi, H.4
Konno, M.5
Funato, M.6
Matsui, T.7
Titani, K.8
Yagi, H.9
Matsumoto, M.10
Fujimura, Y.11
-
10
-
-
10744226155
-
Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome
-
Matsumoto M, Kokame K, Soejima K, Miura M, Hayashi S, Fujii Y, Iwai A, Ito E, Tsuji Y, Takeda-Shitaka M, Iwadate M, Umeyama H, Yagi H, Ishizashi H, Banno F, Nakagaki T, Miyata T, Fujimura Y (2004) Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome. Blood 103:1305-1310
-
(2004)
Blood
, vol.103
, pp. 1305-1310
-
-
Matsumoto, M.1
Kokame, K.2
Soejima, K.3
Miura, M.4
Hayashi, S.5
Fujii, Y.6
Iwai, A.7
Ito, E.8
Tsuji, Y.9
Takeda-Shitaka, M.10
Iwadate, M.11
Umeyama, H.12
Yagi, H.13
Ishizashi, H.14
Banno, F.15
Nakagaki, T.16
Miyata, T.17
Fujimura, Y.18
-
11
-
-
4644271599
-
Identification of novel mutations in ADAMTS13 in an adult patient with congenital thrombotic thrombocytopenic purpura
-
Research Project on Genetics of Thrombosis
-
Uchida T, Wada H, Mizutani M, Iwashita M, Ishihara H, Shibano T, Suzuki M, Matsubara Y, Soejima K, Matsumoto M, Fujimura Y, Ikeda Y, Murata M, Research Project on Genetics of Thrombosis (2004) Identification of novel mutations in ADAMTS13 in an adult patient with congenital thrombotic thrombocytopenic purpura. Blood 104:2081-2083
-
(2004)
Blood
, vol.104
, pp. 2081-2083
-
-
Uchida, T.1
Wada, H.2
Mizutani, M.3
Iwashita, M.4
Ishihara, H.5
Shibano, T.6
Suzuki, M.7
Matsubara, Y.8
Soejima, K.9
Matsumoto, M.10
Fujimura, Y.11
Ikeda, Y.12
Murata, M.13
-
12
-
-
0027190974
-
The CUB domain. A widespread module in developmentally regulated proteins
-
Bork P, Beckmann G (1993) The CUB domain. A widespread module in developmentally regulated proteins. J Mol Biol 231:539-545
-
(1993)
J Mol Biol
, vol.231
, pp. 539-545
-
-
Bork, P.1
Beckmann, G.2
-
13
-
-
0942287728
-
Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13
-
Pimanda JE, Maekawa A, Wind T, Paxton J, Chesterman CN, Hogg PJ (2004) Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13. Blood 103:627-629
-
(2004)
Blood
, vol.103
, pp. 627-629
-
-
Pimanda, J.E.1
Maekawa, A.2
Wind, T.3
Paxton, J.4
Chesterman, C.N.5
Hogg, P.J.6
-
14
-
-
33749367421
-
Apical sorting of ADAMTS13 in vascular endothelial cells and Madin-Darby canine kidney cells depends on the CUB domains and their association with lipid rafts
-
Shang D, Zheng XW, Niiya M, Zheng XL (2006) Apical sorting of ADAMTS13 in vascular endothelial cells and Madin-Darby canine kidney cells depends on the CUB domains and their association with lipid rafts. Blood 108:2207-2215
-
(2006)
Blood
, vol.108
, pp. 2207-2215
-
-
Shang, D.1
Zheng, X.W.2
Niiya, M.3
Zheng, X.L.4
-
15
-
-
34548834974
-
The cooperative activity between the carboxyl-terminal TSP1 repeats and the CUB domains of ADAMTS13 is crucial for recognition of von Willebrand factor under flow
-
Zhang P, Pan W, Rux AH, Sachais BS, Zheng XL (2007) The cooperative activity between the carboxyl-terminal TSP1 repeats and the CUB domains of ADAMTS13 is crucial for recognition of von Willebrand factor under flow. Blood 110:1887-1894
-
(2007)
Blood
, vol.110
, pp. 1887-1894
-
-
Zhang, P.1
Pan, W.2
Rux, A.H.3
Sachais, B.S.4
Zheng, X.L.5
-
16
-
-
0030715614
-
Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis (Moyamoya' disease) of the Ministry of Healthand Welfare, Japan
-
Members of the Research Committee on spontaneous Occlusion of the Circle of Willis (Moyamoya disease) of Ministry and Welfare, Japan
-
Fukui M, Members of the Research Committee on spontaneous Occlusion of the Circle of Willis (Moyamoya disease) of Ministry and Welfare, Japan (1997) Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis (Moyamoya' disease) of the Ministry of Healthand Welfare, Japan. Clin Neurol Neurosurg 99:S238-S240
-
(1997)
Clin Neurol Neurosurg
, vol.99
-
-
Fukui, M.1
-
17
-
-
0029829803
-
Is unilateral Moyamoya disease different from moyamoya disease
-
Houkin K, Abe H, Yoshimoto T, Takahashi A (1996) Is unilateral Moyamoya disease different from moyamoya disease. J Neurosurg 85:772-776
-
(1996)
J Neurosurg
, vol.85
, pp. 772-776
-
-
Houkin, K.1
Abe, H.2
Yoshimoto, T.3
Takahashi, A.4
-
18
-
-
0344625384
-
A clinical comparison of definite moyamoya disease between South Korea and Japan
-
Ikezaki K, Han DH, Kawano T, Kinukawa N, Fukui M (1997) A clinical comparison of definite moyamoya disease between South Korea and Japan. Stroke 28:2513-2517
-
(1997)
Stroke
, vol.28
, pp. 2513-2517
-
-
Ikezaki, K.1
Han, D.H.2
Kawano, T.3
Kinukawa, N.4
Fukui, M.5
|