-
1
-
-
0037465833
-
Facial hemangioma and cerebral corticovascular dysplasia: A syndrome associated with epilepsy
-
Aeby A, Guerrini R, David P, Rodesh G, Raybaud C, Van Bogaert P. 2003. Facial hemangioma and cerebral corticovascular dysplasia: A syndrome associated with epilepsy. Neurology 60:1030-1032.
-
(2003)
Neurology
, vol.60
, pp. 1030-1032
-
-
Aeby, A.1
Guerrini, R.2
David, P.3
Rodesh, G.4
Raybaud, C.5
Van Bogaert, P.6
-
2
-
-
1842688674
-
PHACES syndrome: A review of eight previously unreported cases with late aterial occlusions
-
Bhattacharya JJ, Luo CB, Alvarez H, Rodesch G, Pongpeck S, Lasjaunias PL. 2004. PHACES syndrome: A review of eight previously unreported cases with late aterial occlusions. Neuroradiology 46:227-233.
-
(2004)
Neuroradiology
, vol.46
, pp. 227-233
-
-
Bhattacharya, J.J.1
Luo, C.B.2
Alvarez, H.3
Rodesch, G.4
Pongpeck, S.5
Lasjaunias, P.L.6
-
3
-
-
0021751450
-
An unusual case of Sturge-Weber syndrome
-
Billson VR, Gillam GL. 1984. An unusual case of Sturge-Weber syndrome. Pathology 16:462-465.
-
(1984)
Pathology
, vol.16
, pp. 462-465
-
-
Billson, V.R.1
Gillam, G.L.2
-
4
-
-
0030762078
-
Hox D3 induces an angiogenic phenotype in endothelial cells
-
Boudreau N, Andrews C, Srebrow A, Ravanpay A, Cheresh DA. 1997. Hox D3 induces an angiogenic phenotype in endothelial cells. J Cell Biol 139:257-264.
-
(1997)
J Cell Biol
, vol.139
, pp. 257-264
-
-
Boudreau, N.1
Andrews, C.2
Srebrow, A.3
Ravanpay, A.4
Cheresh, D.A.5
-
5
-
-
0031866315
-
Cerebral vasculopathy and neurologic sequelae in infants with cervicofacial hemangioma: Report of eight patients
-
Burrows PE, Robertson RL, Mulliken JB, Beardsley DS, Chaloupka JC, Ezekowitz RAB, Scott RM. 1998. Cerebral vasculopathy and neurologic sequelae in infants with cervicofacial hemangioma: Report of eight patients. Radiology 207:601-607.
-
(1998)
Radiology
, vol.207
, pp. 601-607
-
-
Burrows, P.E.1
Robertson, R.L.2
Mulliken, J.B.3
Beardsley, D.S.4
Chaloupka, J.C.5
Rab, E.6
Scott, R.M.7
-
6
-
-
0032544399
-
An enhancer element in the Eph A2 (Eck) gene sufficient for rhombomere-specific expression is activated by Hox A1 and Hox B1 homeobox proteins
-
Chen F, Ruley HE. 1998. An enhancer element in the Eph A2 (Eck) gene sufficient for rhombomere-specific expression is activated by Hox A1 and Hox B1 homeobox proteins. J Biol Chem 273:24670-24675.
-
(1998)
J Biol Chem
, vol.273
, pp. 24670-24675
-
-
Chen, F.1
Ruley, H.E.2
-
7
-
-
0032914717
-
Aneurysm of the ascending aorta in a neonate
-
Chien HYC, Sung T-C. 1999. Aneurysm of the ascending aorta in a neonate. Acta Paediatr Sin 40:121-123.
-
(1999)
Acta Paediatr Sin
, vol.40
, pp. 121-123
-
-
Chien, H.Y.C.1
Sung, T.-C.2
-
8
-
-
0036900838
-
Hemangiomas of infancy: Clinical characteristics, morphologic subtypes, and their relationship to race, ethnicity, and sex
-
Chiller KG, Passaro D, Frieden IJ. 2002. Hemangiomas of infancy: Clinical characteristics, morphologic subtypes, and their relationship to race, ethnicity, and sex. Arch Dermatol 138:1567-1576.
-
(2002)
Arch Dermatol
, vol.138
, pp. 1567-1576
-
-
Chiller, K.G.1
Passaro, D.2
Frieden, I.J.3
-
9
-
-
0000351336
-
Canadian paediatric ischemic stroke registry: Analysis of children with arterial ischemic stroke
-
deVeber G, The Canadian Pediatric Ischemic Stroke Study Group. 2000. Canadian paediatric ischemic stroke registry: Analysis of children with arterial ischemic stroke [abstract]. Ann Neurol 48:526.
-
(2000)
Ann Neurol
, vol.48
, pp. 526
-
-
DeVeber, G.1
-
10
-
-
0347361458
-
Arterial ischemic strokes in infants and children: An overview of current approaches
-
deVeber G. 2003. Arterial ischemic strokes in infants and children: An overview of current approaches. Semin Thromb Hemost 29:567-573.
-
(2003)
Semin Thromb Hemost
, vol.29
, pp. 567-573
-
-
DeVeber, G.1
-
11
-
-
33645029208
-
Early stroke and cerebral vasculopathy in children with facial hemangiomas and PHACE association
-
Drolet BA, Dohil B, Golomb MR, Wells R, Murowski L, Tamburro J, Sty J, Friedlander SF. 2006. Early stroke and cerebral vasculopathy in children with facial hemangiomas and PHACE association. Pediatrics 117:959-964.
-
(2006)
Pediatrics
, vol.117
, pp. 959-964
-
-
Drolet, B.A.1
Dohil, B.2
Golomb, M.R.3
Wells, R.4
Murowski, L.5
Tamburro, J.6
Sty, J.7
Friedlander, S.F.8
-
12
-
-
3042820393
-
Death from cerebrovascular infarction in a patient with PHACES syndrome
-
Espunes SP, Santos-Juanes J, Villanueva AM, Torre AC, Galan CR, Sanchez del Rio J. 2004. Death from cerebrovascular infarction in a patient with PHACES syndrome. J Am Acad Dermatol 51:142-143.
-
(2004)
J Am Acad Dermatol
, vol.51
, pp. 142-143
-
-
Espunes, S.P.1
Santos-Juanes, J.2
Villanueva, A.M.3
Torre, A.C.4
Galan, C.R.5
Sanchez Del Rio, J.6
-
13
-
-
0031922119
-
The ephrins and Eph receptors in neural development
-
Flanagan JG, Vanderhaeghen P. 1998. The ephrins and Eph receptors in neural development. Annu Rev Neurosci 21:309-345.
-
(1998)
Annu Rev Neurosci
, vol.21
, pp. 309-345
-
-
Flanagan, J.G.1
Vanderhaeghen, P.2
-
14
-
-
0029939078
-
PHACE syndrome: The association of posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities
-
Frieden IJ, Reese V, Cohen D. 1996. PHACE syndrome: The association of posterior fossa brain malformations, hemangiomas, arterial anomalies, coarctation of the aorta and cardiac defects, and eye abnormalities. Arch Dermatol 132:307-311.
-
(1996)
Arch Dermatol
, vol.132
, pp. 307-311
-
-
Frieden, I.J.1
Reese, V.2
Cohen, D.3
-
15
-
-
33646085476
-
Hypopituitarism in PHACES Association
-
in press
-
Goddard DS, Liang MG, Chamlin SL, Svoren BM, Spack NP, Mulliken JB. 2006. Hypopituitarism in PHACES Association. Pediatr Dermatol (in press).
-
(2006)
Pediatr Dermatol
-
-
Goddard, D.S.1
Liang, M.G.2
Chamlin, S.L.3
Svoren, B.M.4
Spack, N.P.5
Mulliken, J.B.6
-
16
-
-
0028339983
-
The thyroid transcription factor-1 gene is a candidate target for regulation by Hox proteins
-
Guazzi S, Lonigro R, Pintonello L, Boncinelli E, DiLauro R, Mavillo F. 1994. The thyroid transcription factor-1 gene is a candidate target for regulation by Hox proteins. Eur Mol Biol Organ J 13:3339-3347.
-
(1994)
Eur Mol Biol Organ J
, vol.13
, pp. 3339-3347
-
-
Guazzi, S.1
Lonigro, R.2
Pintonello, L.3
Boncinelli, E.4
Dilauro, R.5
Mavillo, F.6
-
17
-
-
33646081004
-
Prospective study of infantile hemangiomas: Clinical characteristics predicting complications and treatment
-
in press
-
Haggstrom AN, Drolet BA, Baselga E, Chamlin S, Esterly NB, Garzon M, Horii KA, Lucky A, Mancini A, Metry D, Newell B, Nopper A, Frieden IJ. 2006. Prospective study of infantile hemangiomas: Clinical characteristics predicting complications and treatment. Pediatrics (in press).
-
(2006)
Pediatrics
-
-
Haggstrom, A.N.1
Drolet, B.A.2
Baselga, E.3
Chamlin, S.4
Esterly, N.B.5
Garzon, M.6
Horii, K.A.7
Lucky, A.8
Mancini, A.9
Metry, D.10
Newell, B.11
Nopper, A.12
Frieden, I.J.13
-
18
-
-
33645032584
-
Patterns of infantile hemangiomas: New clues to hemangioma pathogenesis and embryonic facial development
-
Haggstrom AN, Lammer EJ, Schneider RA, Marcucio R, Frieden IJ. 2006. Patterns of infantile hemangiomas: New clues to hemangioma pathogenesis and embryonic facial development. Pediatrics 117:698-703.
-
(2006)
Pediatrics
, vol.117
, pp. 698-703
-
-
Haggstrom, A.N.1
Lammer, E.J.2
Schneider, R.A.3
Marcucio, R.4
Frieden, I.J.5
-
19
-
-
0033016108
-
Eph receptors and ephrins: Effectors of morphogenesis
-
Holder N, Klein R. 1999. Eph receptors and ephrins: Effectors of morphogenesis. Development 126:2033-2044.
-
(1999)
Development
, vol.126
, pp. 2033-2044
-
-
Holder, N.1
Klein, R.2
-
20
-
-
0034691665
-
Severe hypothyroidism caused by type 3 iodothyronine deiodinase in infantile hemangiomas
-
Huang SA, Tu HM, Harney JW, Venihaki M, Butte AJ, Kozakewich HP, Fishman SJ, Larsen PR. 2000. Severe hypothyroidism caused by type 3 iodothyronine deiodinase in infantile hemangiomas. N Engl J Med 343:185-189.
-
(2000)
N Engl J Med
, vol.343
, pp. 185-189
-
-
Huang, S.A.1
Tu, H.M.2
Harney, J.W.3
Venihaki, M.4
Butte, A.J.5
Kozakewich, H.P.6
Fishman, S.J.7
Larsen, P.R.8
-
21
-
-
0036605276
-
Complete overlap of PHACE syndrome and sternal malformation-vascular dysplasia association
-
James PA, McGaughran J. 2002. Complete overlap of PHACE syndrome and sternal malformation-vascular dysplasia association. Am J Med Genet 110:78-84.
-
(2002)
Am J Med Genet
, vol.110
, pp. 78-84
-
-
James, P.A.1
McGaughran, J.2
-
22
-
-
3042818824
-
Risk factors for arterial ischemic stroke in childhood
-
Kirkham FJ, Hogan AM. 2004. Risk factors for arterial ischemic stroke in childhood. CNS Spectr 9:451-464.
-
(2004)
CNS Spectr
, vol.9
, pp. 451-464
-
-
Kirkham, F.J.1
Hogan, A.M.2
-
23
-
-
0033777040
-
Basal meningoencephalocele, anomaly of optic disc and panhypopituitarism in association with moyamoya disease
-
Komiyama M, Yasui T, Sakamoto H, Fujita K, Sato T, Ota M, Sugita M. 2000. Basal meningoencephalocele, anomaly of optic disc and panhypopituitarism in association with moyamoya disease. Pediatr Neurosurg 33:100-104.
-
(2000)
Pediatr Neurosurg
, vol.33
, pp. 100-104
-
-
Komiyama, M.1
Yasui, T.2
Sakamoto, H.3
Fujita, K.4
Sato, T.5
Ota, M.6
Sugita, M.7
-
25
-
-
0142168040
-
Cervico-cerebrovascular anomalies in children with PHACE syndrome
-
Luo CB, Lasjaunias P, Teng MMH, Chang FC, Lirng JF, Chang CY. 2003. Cervico-cerebrovascular anomalies in children with PHACE syndrome. J Formos Med Assoc 102:379-386.
-
(2003)
J Formos Med Assoc
, vol.102
, pp. 379-386
-
-
Luo, C.B.1
Lasjaunias, P.2
Teng, M.M.H.3
Chang, F.C.4
Lirng, J.F.5
Chang, C.Y.6
-
27
-
-
2442717851
-
Association of solitary, segmental hemangiomas of the skin and visceral hemangiomatosis
-
Metry DW, Hawrot A, Altman C, Frieden IJ. 2004. Association of solitary, segmental hemangiomas of the skin and visceral hemangiomatosis. Arch Dermatol 140:591-596.
-
(2004)
Arch Dermatol
, vol.140
, pp. 591-596
-
-
Metry, D.W.1
Hawrot, A.2
Altman, C.3
Frieden, I.J.4
-
28
-
-
0034707595
-
Homeobox B3 promotes capillary morphogenesis and angiogenesis
-
Myers C, Charboneau A, Boudreau N. 2000. Homeobox B3 promotes capillary morphogenesis and angiogenesis. J Cell Biol 148:343-351.
-
(2000)
J Cell Biol
, vol.148
, pp. 343-351
-
-
Myers, C.1
Charboneau, A.2
Boudreau, N.3
-
29
-
-
0042866003
-
Arterial ischemic stroke in neonates, infants, and children: An overview of underlying conditions, imaging methods, and treatment modalities
-
Nowak-Gottl U, Gunther G, Kurnik K, Strater R, Kirkham F. 2003. Arterial ischemic stroke in neonates, infants, and children: An overview of underlying conditions, imaging methods, and treatment modalities. Semin Thromb Hemost 29:405-414.
-
(2003)
Semin Thromb Hemost
, vol.29
, pp. 405-414
-
-
Nowak-Gottl, U.1
Gunther, G.2
Kurnik, K.3
Strater, R.4
Kirkham, F.5
-
30
-
-
0028670234
-
Balanced translocation (t 2q;10p) and ocular anomalies. A possible HOX gene defect
-
Nucci P, Manitto MP, Faiella A, Boncinelli E, Brancato R. 1994. Balanced translocation (t 2q;10p) and ocular anomalies. A possible HOX gene defect. Ophthalmic Genet 15:129-131.
-
(1994)
Ophthalmic Genet
, vol.15
, pp. 129-131
-
-
Nucci, P.1
Manitto, M.P.2
Faiella, A.3
Boncinelli, E.4
Brancato, R.5
-
31
-
-
0020322650
-
CNS anomalies and the midline as a 'developmental field'
-
Opitz JM, Gilbert EF. 1982. CNS anomalies and the midline as a 'developmental field.' Am J Med Genet 12:443-455.
-
(1982)
Am J Med Genet
, vol.12
, pp. 443-455
-
-
Opitz, J.M.1
Gilbert, E.F.2
-
32
-
-
0028790532
-
Facial haemangioma, agenesis of the internal carotid artery and dysplasia of the cerebral cortex: Case report
-
Pascual-Castroviejo I, Viano J, Pascual-Pascual SI, Martinez V. 1995. Facial haemangioma, agenesis of the internal carotid artery and dysplasia of the cerebral cortex: Case report. Neuroradiology 37:692-695.
-
(1995)
Neuroradiology
, vol.37
, pp. 692-695
-
-
Pascual-Castroviejo, I.1
Viano, J.2
Pascual-Pascual, S.I.3
Martinez, V.4
-
34
-
-
0027267613
-
Sternal cleft associated with vascular anomalies and micrognathia
-
Pasic M, Carrel T, Tonz M, Niederhauser U, Von Segesser LK. Turina MI. 1993. Sternal cleft associated with vascular anomalies and micrognathia. Ann Thorac Surg 56:165-168.
-
(1993)
Ann Thorac Surg
, vol.56
, pp. 165-168
-
-
Pasic, M.1
Carrel, T.2
Tonz, M.3
Niederhauser, U.4
Von Turina Mi, S.L.K.5
-
35
-
-
1242320250
-
Morning glory syndrome associated with posterior pituitary - Ectopia and hypopituitarism
-
Pierre-Filho PP, Limeira-Soares PH, Marcondes AM. 2004. Morning glory syndrome associated with posterior pituitary - ectopia and hypopituitarism. Acta Ophthalmol Scand 82:89-92.
-
(2004)
Acta Ophthalmol Scand
, vol.82
, pp. 89-92
-
-
Pierre-Filho, P.P.1
Limeira-Soares, P.H.2
Marcondes, A.M.3
-
37
-
-
0034737051
-
Giant congenital aortic aneurysm with cleft sternum, supraumbilical raphe and hemangiomatosis: Report and review
-
Raas-Rothschild A, Nir A, Gillis R, Rein AJJT. 2000. Giant congenital aortic aneurysm with cleft sternum, supraumbilical raphe and hemangiomatosis: Report and review. Am J Med Genet 90:243-245.
-
(2000)
Am J Med Genet
, vol.90
, pp. 243-245
-
-
Raas-Rothschild, A.1
Nir, A.2
Gillis, R.3
Rein, A.J.J.T.4
-
38
-
-
0027189536
-
Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cervical verebra and defects in the closure of the sternal rudiments
-
Ramirez-Solis R, Zheng H, Whiting J, Krumlauf R, Bradley A. 1993. Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cervical verebra and defects in the closure of the sternal rudiments. Cell 73:279-294.
-
(1993)
Cell
, vol.73
, pp. 279-294
-
-
Ramirez-Solis, R.1
Zheng, H.2
Whiting, J.3
Krumlauf, R.4
Bradley, A.5
-
39
-
-
0027447096
-
The association of facial hemangiomas with Dandy-Walker and other posterior fossa malformations
-
Reese V, Frieden IJ, Paller AS, Esterly NB, Ferriero D, Levy ML, Lucky AW, Gellis SE, Siegfried EC. 1993. The association of facial hemangiomas with Dandy-Walker and other posterior fossa malformations. J Pediatr 122:379-384.
-
(1993)
J Pediatr
, vol.122
, pp. 379-384
-
-
Reese, V.1
Frieden, I.J.2
Paller, A.S.3
Esterly, N.B.4
Ferriero, D.5
Levy, M.L.6
Lucky, A.W.7
Gellis, S.E.8
Siegfried, E.C.9
-
40
-
-
0035187824
-
Posterior fossa and arterial abnormalities in patients with facial capillary hemangioma: Presumed incomplete phenotypic expression of PHACES syndrome
-
Rossi A, Bava GL, Biancheri R, Tortori-Donati P. 2001. Posterior fossa and arterial abnormalities in patients with facial capillary hemangioma: Presumed incomplete phenotypic expression of PHACES syndrome. Neuroradiology 43:934-940.
-
(2001)
Neuroradiology
, vol.43
, pp. 934-940
-
-
Rossi, A.1
Bava, G.L.2
Biancheri, R.3
Tortori-Donati, P.4
-
41
-
-
0023108252
-
Aneurysm of the ascending aorta associated with sternal cleft, cutaneous hemangioma, and occlusion of the right innominate artery in a neonate
-
Schicken LS, Brenner JI, Baker KR, Ringel RE, Pacifico A. 1987. Aneurysm of the ascending aorta associated with sternal cleft, cutaneous hemangioma, and occlusion of the right innominate artery in a neonate. Am Heart J 113:202-204.
-
(1987)
Am Heart J
, vol.113
, pp. 202-204
-
-
Schicken, L.S.1
Brenner, J.I.2
Baker, K.R.3
Ringel, R.E.4
Pacifico, A.5
-
42
-
-
0019929398
-
Coarctation of the aorta with congenital hemangioma of the face and neck and aneurysm or dilatation of a subclavian or innominate artery. A new syndrome?
-
Schneeweiss A, Blieden LC, Shem-Tov A, Motro M, Feigel A, Neufeld HN. 1982. Coarctation of the aorta with congenital hemangioma of the face and neck and aneurysm or dilatation of a subclavian or innominate artery. A new syndrome? Chest 82:186-187.
-
(1982)
Chest
, vol.82
, pp. 186-187
-
-
Schneeweiss, A.1
Blieden, L.C.2
Shem-Tov, A.3
Motro, M.4
Feigel, A.5
Neufeld, H.N.6
-
43
-
-
0036644143
-
Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: Possible PHACE syndrome
-
Slavotinek AM, Dubovsky E, Dietz HC, Lacbawan F. 2002. Report of a child with aortic aneurysm, orofacial clefting, hemangioma, upper sternal defect, and marfanoid features: Possible PHACE syndrome. Am J Med Genet 110:283-288.
-
(2002)
Am J Med Genet
, vol.110
, pp. 283-288
-
-
Slavotinek, A.M.1
Dubovsky, E.2
Dietz, H.C.3
Lacbawan, F.4
-
45
-
-
0031894510
-
Genetic interactions between Hox A1 and Hox B1 reveal new roles in regulation of early hindbrain patterning
-
Studer M, Gavalas A, Marshall H, Ariza-McNaughton L, Rijili FM, Chambon P, Krumlauf R. 1998. Genetic interactions between Hox A1 and Hox B1 reveal new roles in regulation of early hindbrain patterning. Development 125:1025-1036.
-
(1998)
Development
, vol.125
, pp. 1025-1036
-
-
Studer, M.1
Gavalas, A.2
Marshall, H.3
Ariza-McNaughton, L.4
Rijili, F.M.5
Chambon, P.6
Krumlauf, R.7
-
46
-
-
0035165103
-
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia
-
Thomas PQ, Dattani MT, Brickman JM, McNay D, Warne G, Zacharin M, Cameron F, Hurst J, Woods K, Dunger D, Stanhope R, Forrest S, Robinson IC, Beddington RS. 2001. Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia. Hum Mol Genet 10:39-45.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 39-45
-
-
Thomas, P.Q.1
Dattani, M.T.2
Brickman, J.M.3
McNay, D.4
Warne, G.5
Zacharin, M.6
Cameron, F.7
Hurst, J.8
Woods, K.9
Dunger, D.10
Stanhope, R.11
Forrest, S.12
Robinson, I.C.13
Beddington, R.S.14
-
47
-
-
0036190989
-
Endocrinopathies associated with midline cerebral and cranial malformations
-
Traggiai C, Stanhope R. 2002. Endocrinopathies associated with midline cerebral and cranial malformations. J Pediatr 140:252-255.
-
(2002)
J Pediatr
, vol.140
, pp. 252-255
-
-
Traggiai, C.1
Stanhope, R.2
-
48
-
-
0041807969
-
The nonrandom distribution of facial hemangiomas
-
Waner M, North PE, Scherer KA, Frieden IJ, Waner A, Mihm MC Jr. 2003. The nonrandom distribution of facial hemangiomas. Arch Dermatol 139:869-875.
-
(2003)
Arch Dermatol
, vol.139
, pp. 869-875
-
-
Waner, M.1
North, P.E.2
Scherer, K.A.3
Frieden, I.J.4
Waner, A.5
Mihm Jr., M.C.6
-
49
-
-
0033195244
-
Unusual malformation of the aortic arch in a patient with a large facial hemangioma
-
Zeevi B, Berant M. 1999. Unusual malformation of the aortic arch in a patient with a large facial hemangioma. Cardiol Young 9:539-540.
-
(1999)
Cardiol Young
, vol.9
, pp. 539-540
-
-
Zeevi, B.1
Berant, M.2
|