-
1
-
-
0002725175
-
Hypogenesis of bilateral internal carotid arteries
-
Takeuchi K, Shimizu K: Hypogenesis of bilateral internal carotid arteries. No To Shinkei 1957; 9: 37-43.
-
(1957)
No To Shinkei
, vol.9
, pp. 37-43
-
-
Takeuchi, K.1
Shimizu, K.2
-
2
-
-
0026658049
-
A case of turners syndrome associated with moyamoya disease in Japanese
-
Ajimi Y, Uchida K, Kawase T, Toya S: A case of Turner's syndrome associated with moyamoya disease (in Japanese). No Shinkei Geka 1992; 20: 1021-1024.
-
(1992)
No Shinkei Geka
, vol.20
, pp. 1021-1024
-
-
Ajimi, Y.1
Uchida, K.2
Kawase, T.3
Toya, S.4
-
3
-
-
0026045759
-
On the association of moyamoya disease with downs syndrome
-
pt 4)
-
Berg JM, Armstrong D: On the association of moyamoya disease with Down's syndrome. J Ment Defic Res 1991; 35(pt 4):398-403.
-
(1991)
J. Ment. Defic. Res.
, vol.35
, pp. 398-403
-
-
Berg, J.M.1
Armstrong, D.2
-
4
-
-
0027528791
-
An autopsied case of Williams syndrome complicated by moyamoya disease
-
Kawai M, Nishikawa T, Tanaka M, Ando A, Kasajima T, Higa T, Tanikawa T, Kagawa M, Momma K: An autopsied case of Williams syndrome complicated by moyamoya disease. Acta Paediatr Jpn 1993; 35: 63-67. (Pubitemid 23107267)
-
(1993)
Acta Paediatrica Japonica (Overseas Edition)
, vol.35
, Issue.1
, pp. 63-67
-
-
Kawai, M.1
Nishikawa, T.2
Tanaka, M.3
Ando, A.4
Kasajima, T.5
Higa, T.6
Tanikawa, T.7
Kagawa, M.8
Momma, K.9
-
5
-
-
0024370647
-
Alagille syndrome associated with Moyamoya disease
-
Rachmel A, Zeharia A, Neuman-Levin M, Weitz R, Shamir R, Dinari G: Alagille syndrome associated with moyamoya disease. Am J Med Genet 1989; 33: 89-91. (Pubitemid 19171120)
-
(1989)
American Journal of Medical Genetics
, vol.33
, Issue.1
, pp. 89-91
-
-
Rachmel, A.1
Zeharia, A.2
Neuman-Levin, M.3
Weitz, R.4
Shamir, R.5
Dinari, G.6
-
6
-
-
0026694404
-
Neurofibromatosis cerebral vasculopathy in an infant: Clinical neuroradiographic and neuropathologic studies
-
Woody RC, Perrot LJ, Beck SA: Neurofibromatosis cerebral vasculopathy in an infant: clinical, neuroradiographic, and neuropathologic studies. Pediatr Pathol 1992; 12: 613-619.
-
(1992)
Pediatr Pathol.
, vol.12
, pp. 613-619
-
-
Woody, R.C.1
Perrot, L.J.2
Beck, S.A.3
-
7
-
-
0042320658
-
Microcephalic osteodysplastic primordial short stature type II with cafe-au-lait spots and moyamoya disease [2]
-
Nishimura G, Hasegawa T, Fujino M, Hori N, Tomita Y: Microcephalic osteodysplastic primordial short stature type II with cafeau- lait spots and moyamoya disease (letter). Am J Med Genet A 2003; 117A:299-301. (Pubitemid 37063998)
-
(2003)
American Journal of Medical Genetics
, vol.117 A
, Issue.3
, pp. 299-301
-
-
Nishimura, G.1
Hasegawa, T.2
Fujino, M.3
Hori, N.4
Tomita, Y.5
-
8
-
-
0031810368
-
Multiple intracranial aneurysms in a patient with Seckel syndrome
-
DOI 10.1007/s003810050181
-
D'Angelo VA, Ceddia A, Zelante L, Florio FP: Multiple intracranial aneurysms in a patient with Seckel syndrome. Childs Nerv Syst 1998; 14: 82-84. (Pubitemid 28269429)
-
(1998)
Child's Nervous System
, vol.14
, Issue.1-2
, pp. 82-84
-
-
D'Angelo, V.A.1
Ceddia, A.M.P.2
Zelante, L.3
Florio, F.P.4
-
9
-
-
0346958253
-
Malignant hypertension and cerebral haemorrhage in Seckel syndrome
-
DOI 10.1007/s00431-003-1310-z
-
di Bartolomeo RD, Polidori G, Piastra M, Viola L, Zampino G, Chiaretti A: Malignant hypertension and cerebral haemorrhage in Seckel syndrome. Eur J Pediatr 2003; 162: 860-862. (Pubitemid 37523837)
-
(2003)
European Journal of Pediatrics
, vol.162
, Issue.12
, pp. 860-862
-
-
Di Bartolomeo, R.1
Polidori, G.2
Piastra, M.3
Viola, L.4
Zampino, G.5
Chiaretti, A.6
-
10
-
-
9344239397
-
Seckel syndrome with polyarteritis nodosa
-
Kutlu R, Alkan A, Kutlu O, Yakinci C: Seckel syndrome with polyarteritis nodosa. Indian Pediatr 2004; 41: 1158-1161. (Pubitemid 39557087)
-
(2004)
Indian Pediatrics
, vol.41
, Issue.11
, pp. 1158-1161
-
-
Kutlu, R.1
Alkan, A.2
Kutlu, O.3
Yakinci, C.4
-
11
-
-
0032981383
-
Severe hypertensive sequelae in a child with Seckel syndrome (bird-like dwarfism)
-
DOI 10.1007/s004670050623
-
Sorof JM, Dow-Smith C, Moore PJ: Severe hypertensive sequelae in a child with Seckel syndrome (bird-like dwarfism). Pediatr Nephrol 1999; 13: 343-346. (Pubitemid 29243742)
-
(1999)
Pediatric Nephrology
, vol.13
, Issue.4
, pp. 343-346
-
-
Sorof, J.M.1
Dow-Smith, C.2
Moore, P.J.3
-
12
-
-
4344631651
-
Majewski osteodysplastic primordial dwarfism type II (MOPD II): Natural history and clinical findings
-
Hall JG, Flora C, Scott CI Jr, Pauli RM, Tanaka KI: Majewski osteodysplastic primordial dwarfism type II (MOPD II): natural history and clinical findings. Am J Med Genet A 2004; 130A:55-72. (Pubitemid 39121562)
-
(2004)
American Journal of Medical Genetics
, vol.130 A
, Issue.1
, pp. 55-72
-
-
Hall, J.G.1
Flora, C.2
Scott Jr., C.I.3
Pauli, R.M.4
Tanaka, K.I.5
-
13
-
-
28444440611
-
Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke: Clinical report and review of cerebral vascular anomalies
-
DOI 10.1002/ajmg.a.31009
-
Brancati F, Castori M, Mingarelli R, Dallapiccola B: Majewski osteodysplastic primordial dwarfism type II (MOPD II) complicated by stroke: clinical report and review of cerebral vascular anomalies. Am J Med Genet A 2005; 139: 212-215. (Pubitemid 41740592)
-
(2005)
American Journal of Medical Genetics
, vol.139 A
, Issue.3
, pp. 212-215
-
-
Brancati, F.1
Castori, M.2
Mingarelli, R.3
Dallapiccola, B.4
-
14
-
-
3042767201
-
Microcephalic osteodysplastic primordial dwarfism type II: A child with café au lait lesions, cutis marmorata, and Moyamoya disease [3]
-
Kannu P, Kelly P, Aftimos S: Microcephalic osteodysplastic primordial dwarfism type II: a child with café au lait lesions, cutis marmorata, and moyamoya disease. Am J Med Genet A 2004; 128A:98-100. (Pubitemid 38856828)
-
(2004)
American Journal of Medical Genetics
, vol.128 A
, Issue.1
, pp. 98-100
-
-
Kannu, P.1
Aftimos, S.2
Kelly, P.3
-
15
-
-
14644396144
-
Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type II
-
DOI 10.1016/j.braindev.2004.06.007
-
Ozawa H, Takayama C, Nishida A, Nagai T, Nishimura G, Higurashi M: Pachygyria in a girl with microcephalic osteodysplastic primordial short stature type II. Brain Dev 2005; 27: 237-240. (Pubitemid 40312037)
-
(2005)
Brain and Development
, vol.27
, Issue.3 SPEC. ISS.
, pp. 237-240
-
-
Ozawa, H.1
Takayama, C.2
Nishida, A.3
Nagai, T.4
Nishimura, G.5
Higurashi, M.6
-
16
-
-
2442430342
-
Microcephalic osteodysplastic primordial short stature type II with café-au-lait spots and moyamoya disease: Another patient [3]
-
Young ID, Barrow M, Hall CM: Microcephalic osteodysplastic primordial short stature type II with café-au-lait spots and moyamoya disease: another patient. Am J Med Genet A 2004; 127A:218-220. (Pubitemid 38649970)
-
(2004)
American Journal of Medical Genetics
, vol.127 A
, Issue.2
, pp. 218-220
-
-
Young, I.D.1
Barrow, M.2
Hall, C.M.3
-
17
-
-
0029743815
-
Early development of intimal thickening in superficial temporal arteries in patients with moyamoya disease
-
Aoyagi M, Fukai N, Yamamoto M, Nakagawa K, Matsushima Y, Yamamoto K: Early development of intimal thickening in superficial temporal arteries in patients with moyamoya disease. Stroke 1996; 27: 1750-1754. (Pubitemid 26332498)
-
(1996)
Stroke
, vol.27
, Issue.10
, pp. 1750-1754
-
-
Aoyagi, M.1
Fukai, N.2
Yamamoto, M.3
Nakagawa, K.4
Matsushima, Y.5
Yamamoto, K.6
-
18
-
-
38949087294
-
Mutations in the pericentrin (PCNT) gene cause primordial dwarfism
-
DOI 10.1126/science.1151174
-
Rauch A, Thiel CT, Schindler D, Wick U, Crow YJ, Ekici AB, van Essen AJ, Goecke TO, Al-Gazali L, Chrzanowska KH, Zweier C, Brunner HG, Becker K, Curry CJ, Dallapiccola B, Devriendt K, Dörfler A, Kinning E, Megarbane A, Meinecke P, Semple RK, Spranger S, Toutain A, Trembath RC, Voss E, Wilson L, Hennekam R, de Zegher F, Dörr HG, Reis A: Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Science 2008; 319: 816-819. (Pubitemid 351225872)
-
(2008)
Science
, vol.319
, Issue.5864
, pp. 816-819
-
-
Rauch, A.1
Thiel, C.T.2
Schindler, D.3
Wick, U.4
Crow, Y.J.5
Ekici, A.B.6
Van Essen, A.J.7
Goecke, T.O.8
Al-Gazali, L.9
Chrzanowska, K.H.10
Zweier, C.11
Brunner, H.G.12
Becker, K.13
Curry, C.J.14
Dallapiccola, B.15
Devriendt, K.16
Dorfler, A.17
Kinning, E.18
Megarbane, A.19
Meinecke, P.20
Semple, R.K.21
Spranger, S.22
Toutain, A.23
Trembath, R.C.24
Voss, E.25
Wilson, L.26
Hennekam, R.27
De Zegher, F.28
Dorr, H.-G.29
Reis, A.30
more..
-
19
-
-
33744791440
-
Re: Majewski osteoplastic primordial dwarfism type II MOPD II complicated by stroke
-
Hall JG: Re: Majewski osteoplastic primordial dwarfism type II (MOPD II) complicated by stroke. Am J Med Genet A 2006; 140: 1356.
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 1356
-
-
Hall, J.G.1
-
20
-
-
0031671047
-
Microcephalic osteodysplastic primordial dwarfism type II: Report of three cases and review
-
DOI 10.1002/(SICI)1096-8628(19981102)80:1<25::AID-AJMG5>3.0.CO;2-0
-
Majewski F, Goecke TO: Microcephalic osteodysplastic primordial dwarfism type II: report of three cases and review. Am J Med Genet 1998; 80: 25-31. (Pubitemid 28476106)
-
(1998)
American Journal of Medical Genetics
, vol.80
, Issue.1
, pp. 25-31
-
-
Majewski, F.1
Goecke, T.O.2
-
21
-
-
2942717080
-
Prevalence of stenoocclusive lesions in the renal and abdominal arteries in moyamoya disease
-
Togao O, Mihara F, Yoshiura T, Tanaka A, Kuwabara Y, Morioka T, Matsushima T, Sasaki T, Honda H: Prevalence of stenoocclusive lesions in the renal and abdominal arteries in moyamoya disease. AJR Am J Roentgenol 2004; 183: 119-122. (Pubitemid 38789023)
-
(2004)
American Journal of Roentgenology
, vol.183
, Issue.1
, pp. 119-122
-
-
Togao, O.1
Mihara, F.2
Yoshiura, T.3
Tanaka, A.4
Kuwabara, Y.5
Morioka, T.6
Matsushima, T.7
Sasaki, T.8
Honda, H.9
-
22
-
-
0029800129
-
Task force report on high blood pressure in children and adolescents: A working group report from the national high blood pressure education program
-
National High Blood Pressure Education Program Working Group on Hypertension Control in Children and Adolescents: Update on the 1987 pt 1
-
National High Blood Pressure Education Program Working Group on Hypertension Control in Children and Adolescents: Update on the 1987 Task Force Report on High Blood Pressure in Children and Adolescents: a working group report from the National High Blood Pressure Education Program. Pediatrics 1996; 98(pt 1):649-658.
-
(1996)
Pediatrics
, Issue.98
, pp. 649-658
-
-
-
23
-
-
0030716216
-
Cerebral hemodynamics and metabolism in Moyamoya disease - A positron emission tomography study
-
PII S0303846797000619
-
Kuwabara Y, Ichiya Y, Sasaki M, Yoshida T, Masuda K, Ikezaki K, Matsushima T, Fukui M: Cerebral hemodynamics and metabolism in moyamoya disease: a positron emission tomography study. Clin Neurol Neurosurg 1997; 99(suppl 2):S74-S78. (Pubitemid 27489069)
-
(1997)
Clinical Neurology and Neurosurgery
, vol.99
, Issue.SUPPL. 2
-
-
Kuwabara, Y.1
Ichiya, Y.2
Sasaki, M.3
Yoshida, T.4
Masuda, K.5
Ikezaki, K.6
Matsushima, T.7
Fukui, M.8
-
24
-
-
0030894935
-
Haemodynamic ischaemia in paediatric moyamoya disease associated with renovascular hypertension
-
DOI 10.1007/BF01844761
-
Takagi Y, Hashimoto N, Goto Y: Haemodynamic ischemia in paediatric moyamoya disease associated with renovascular hypertension. Acta Neurochir (Wien) 1997; 139: 257-258. (Pubitemid 27144071)
-
(1997)
Acta Neurochirurgica
, vol.139
, Issue.3
, pp. 257-258
-
-
Takagi, Y.1
Hashimoto, N.2
Goto, Y.3
-
25
-
-
0023491931
-
Malignant primary cardiac tumors. The Cleveland Clinic experience, 1956 to 1986
-
Bear PA, Moodie DS: Malignant primary cardiac tumors: the Cleveland Clinic experience, 1956 to 1986. Chest 1987; 92: 860-862. (Pubitemid 18008620)
-
(1987)
Chest
, vol.92
, Issue.5
, pp. 860-862
-
-
Bear, P.A.1
Moodie, D.S.2
-
26
-
-
41949097475
-
Moyamoya disease in pediatric patients: Outcomes of neurosurgical interventions
-
Veeravagu A, Guzman R, Patil CG, Hou LC, Lee M, Steinberg GK: Moyamoya disease in pediatric patients: outcomes of neurosurgical interventions. Neurosurg Focus 2008; 24:E16.
-
(2008)
Neurosurg. Focus.
, vol.24
-
-
Veeravagu, A.1
Guzman, R.2
Patil, C.G.3
Hou, L.C.4
Lee, M.5
Steinberg, G.K.6
|