-
1
-
-
0000865130
-
Moyamoya disease: Diagnosis, treatment and recent achievement
-
Barnett HJ, Mohr JP, Stein BM, Yatsu FM (eds): New York, Livingstone
-
Yonekawa Y, Goto Y, Ogata N: Moyamoya disease: Diagnosis, treatment and recent achievement; in Barnett HJ, Mohr JP, Stein BM, Yatsu FM (eds): Stroke: Pathophysiology, Diagnosis and Management. New York, Livingstone, 1992, pp 721-747.
-
(1992)
Stroke: Pathophysiology, Diagnosis and Management
, pp. 721-747
-
-
Yonekawa, Y.1
Goto, Y.2
Ogata, N.3
-
2
-
-
0032960708
-
Moyamoya disease: Status 1998
-
Yonekawa Y, Taub E: Moyamoya disease: Status 1998. Neurologist 1999;5:13-23.
-
(1999)
Neurologist
, vol.5
, pp. 13-23
-
-
Yonekawa, Y.1
Taub, E.2
-
3
-
-
0030716214
-
Moyamoya disease in Europe, past and present status
-
Yonekawa Y, Ogata N, Kaku Y, Taub E, Imhof HG: Moyamoya disease in Europe, past and present status. Clin Neurol Neurosurg 1997; 99(suppl 2):58-60.
-
(1997)
Clin Neurol Neurosurg
, vol.99
, Issue.2 SUPPL.
, pp. 58-60
-
-
Yonekawa, Y.1
Ogata, N.2
Kaku, Y.3
Taub, E.4
Imhof, H.G.5
-
4
-
-
0038809824
-
Moyamoya disease
-
Barnett HJ, Bogousslavsky J, Meldrum H (eds): Philadelphia, Lippincott, Williams & Wilkins
-
Yonekawa Y, Khan N: Moyamoya disease; in Barnett HJ, Bogousslavsky J, Meldrum H (eds): Ischemic Stroke: Advances in Neurology. Philadelphia, Lippincott, Williams & Wilkins, 2003, vol 92, pp 113-118.
-
(2003)
Ischemic Stroke: Advances in Neurology
, vol.92
, pp. 113-118
-
-
Yonekawa, Y.1
Khan, N.2
-
5
-
-
0026719393
-
Worldwide distribution of moyamoya disease
-
Tokyo
-
Goto Y, Yonekawa Y: Worldwide distribution of moyamoya disease. Neurol Med Chir (Tokyo) 1992;32:883-886.
-
(1992)
Neurol Med Chir
, vol.32
, pp. 883-886
-
-
Goto, Y.1
Yonekawa, Y.2
-
6
-
-
0033105525
-
Ocular malformations, moyamoya disease and midline cranial defects: A distinct syndrome
-
Bakri SJ, Siker D, Masaryk T, Luciano MG, Traboulsi EI: Ocular malformations, moyamoya disease and midline cranial defects: A distinct syndrome. Am J Ophthalmol 1999;127:356-357.
-
(1999)
Am J Ophthalmol
, vol.127
, pp. 356-357
-
-
Bakri, S.J.1
Siker, D.2
Masaryk, T.3
Luciano, M.G.4
Traboulsi, E.I.5
-
8
-
-
0036107865
-
Cardio-facio-cutaneous syndrome and moyamoya syndrome
-
Ishiguro Y, Kubota T, Takenaka J, Maruyama K, Okumura A, Negoro T, Watanabe K: Cardio-facio-cutaneous syndrome and moyamoya syndrome. Brain Dev 2002;24:245-249.
-
(2002)
Brain Dev
, vol.24
, pp. 245-249
-
-
Ishiguro, Y.1
Kubota, T.2
Takenaka, J.3
Maruyama, K.4
Okumura, A.5
Negoro, T.6
Watanabe, K.7
-
9
-
-
0031965006
-
Moyamoya syndrome associated with congenital heart disease
-
Lutterman J, Scott M, Nass R, Geva T: Moyamoya syndrome associated with congenital heart disease. Pediatrics 1998;101:57-60.
-
(1998)
Pediatrics
, vol.101
, pp. 57-60
-
-
Lutterman, J.1
Scott, M.2
Nass, R.3
Geva, T.4
-
10
-
-
0031914310
-
Morning glory disc anomaly and moyamoya vessels
-
Massaro M, Thorarensen O, Liu GT, Maguire AM, Zimmerman RA, Brodsky MC: Morning glory disc anomaly and moyamoya vessels. Arch Ophthalmol 1998;116:253-254.
-
(1998)
Arch Ophthalmol
, vol.116
, pp. 253-254
-
-
Massaro, M.1
Thorarensen, O.2
Liu, G.T.3
Maguire, A.M.4
Zimmerman, R.A.5
Brodsky, M.C.6
-
12
-
-
0022003152
-
Cerebral arterial dolichoectasia associated with moyamoya vessels
-
Yamada K, Hayakawa T, Ushio Y, Mitomo M: Cerebral arterial dolichoectasia associated with moyamoya vessels. Surg Neurol 1985;23:19-24.
-
(1985)
Surg Neurol
, vol.23
, pp. 19-24
-
-
Yamada, K.1
Hayakawa, T.2
Ushio, Y.3
Mitomo, M.4
-
13
-
-
0022922661
-
Surgically treated cerebral arterial ectasia with so-called moyamoya vessels
-
Hanakita J, Miyake H, Nagayasu S, Nishi S, Suzuki T: Surgically treated cerebral arterial ectasia with so-called moyamoya vessels. Neurosurgery 1986;19:271-273.
-
(1986)
Neurosurgery
, vol.19
, pp. 271-273
-
-
Hanakita, J.1
Miyake, H.2
Nagayasu, S.3
Nishi, S.4
Suzuki, T.5
-
15
-
-
0033858921
-
Morning glory disk anomaly, choroidal coloboma and congenital constrictive malformations of the internal carotid arteries (moyamoya disease)
-
Krishnan C, Roy A, Traboulsi E: Morning glory disk anomaly, choroidal coloboma and congenital constrictive malformations of the internal carotid arteries (moyamoya disease). Ophthalmic Genet 2000;21:21-24.
-
(2000)
Ophthalmic Genet
, vol.21
, pp. 21-24
-
-
Krishnan, C.1
Roy, A.2
Traboulsi, E.3
-
16
-
-
0027223043
-
Congenital aplasia of the iris sphincter and dilator muscles
-
Buys Y, Buncic JR, Enzenauer RW, Mednick E, O'Keefe M: Congenital aplasia of the iris sphincter and dilator muscles. Can J Ophthalmol 1993;28:72-75.
-
(1993)
Can J Ophthalmol
, vol.28
, pp. 72-75
-
-
Buys, Y.1
Buncic, J.R.2
Enzenauer, R.W.3
Mednick, E.4
O'Keefe, M.5
-
18
-
-
0027383729
-
Gillespie syndrome reported as bilateral congenital mydriasis
-
Quaerrell O: Gillespie syndrome reported as bilateral congenital mydriasis. Br J Ophthalmol 1993;77:827-828.
-
(1993)
Br J Ophthalmol
, vol.77
, pp. 827-828
-
-
Quaerrell, O.1
-
20
-
-
0032722616
-
Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent
-
Ades LC, Davies R, Haan EA, Holman KJ, Watson KC, Sreetharan D, Cao SN, Milewicz DM, Bateman JF, Chiodo AA, Eccles M, McNoe L, Harbord M: Aortic dissection, patent ductus arteriosus, iris hypoplasia and brachytelephalangy in a male adolescent. Clin Dysmorphol 1999;8:269-276.
-
(1999)
Clin Dysmorphol
, vol.8
, pp. 269-276
-
-
Ades, L.C.1
Davies, R.2
Haan, E.A.3
Holman, K.J.4
Watson, K.C.5
Sreetharan, D.6
Cao, S.N.7
Milewicz, D.M.8
Bateman, J.F.9
Chiodo, A.A.10
Eccles, M.11
McNoe, L.12
Harbord, M.13
-
21
-
-
0036546933
-
Clinicopathologic reports, case reports and small case series: Congenital mydriasis, failure of accommodation and patent ductus arteriosus
-
Graf MH, Jungherr A: Clinicopathologic reports, case reports and small case series: Congenital mydriasis, failure of accommodation and patent ductus arteriosus. Arch Ophthalmol 2002;120:509-510.
-
(2002)
Arch Ophthalmol
, vol.120
, pp. 509-510
-
-
Graf, M.H.1
Jungherr, A.2
-
22
-
-
0033071406
-
Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26
-
Ikeda H, Sasaki T, Yoshimoto T, Fukui M, Arinami T: Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet 1999;64:533-537.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 533-537
-
-
Ikeda, H.1
Sasaki, T.2
Yoshimoto, T.3
Fukui, M.4
Arinami, T.5
-
23
-
-
0034128146
-
Linkage analysis of moyamoya disease on chromosome 6
-
Inoue TK, Ikezaki K, Sasazuki T, Matsushima T, Fukui M: Linkage analysis of moyamoya disease on chromosome 6. J Child Neurol 2000;15:179-182.
-
(2000)
J Child Neurol
, vol.15
, pp. 179-182
-
-
Inoue, T.K.1
Ikezaki, K.2
Sasazuki, T.3
Matsushima, T.4
Fukui, M.5
-
24
-
-
0006954274
-
Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25
-
Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M: Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke 2000;31:930-935.
-
(2000)
Stroke
, vol.31
, pp. 930-935
-
-
Yamauchi, T.1
Tada, M.2
Houkin, K.3
Tanaka, T.4
Nakamura, Y.5
Kuroda, S.6
Abe, H.7
Inoue, T.8
Ikezaki, K.9
Matsushima, T.10
Fukui, M.11
|