-
1
-
-
0015236227
-
Special pattern of widespread neuroblastoma with a favourable prognosis
-
G.J. D'Angio, A.E. Evans, and C.E. Koop Special pattern of widespread neuroblastoma with a favourable prognosis Lancet 1 1971 1046 1049
-
(1971)
Lancet
, vol.1
, pp. 1046-1049
-
-
D'Angio, G.J.1
Evans, A.E.2
Koop, C.E.3
-
2
-
-
0033565296
-
Terminology and morphologic criteria of neuroblastic tumors: Recommendations by the International Neuroblastoma Pathology Committee
-
H. Shimada, I.M. Ambros, L.P. Dehner, J. Hata, V.V. Joshi, and B. Roald Terminology and morphologic criteria of neuroblastic tumors: recommendations by the International Neuroblastoma Pathology Committee Cancer 86 1999 349 363
-
(1999)
Cancer
, vol.86
, pp. 349-363
-
-
Shimada, H.1
Ambros, I.M.2
Dehner, L.P.3
Hata, J.4
Joshi, V.V.5
Roald, B.6
-
3
-
-
0024423140
-
Familial occurrence of neuroblastoma, von Recklinghausen's neurofibromatosis, Hirschsprung's agangliosis and jaw-winking syndrome
-
N. Clausen, P. Andersson, and N. Tommerup Familial occurrence of neuroblastoma, von Recklinghausen's neurofibromatosis, Hirschsprung's agangliosis and jaw-winking syndrome Acta Paediatr. Scand. 78 1989 736 741
-
(1989)
Acta Paediatr. Scand.
, vol.78
, pp. 736-741
-
-
Clausen, N.1
Andersson, P.2
Tommerup, N.3
-
4
-
-
0036136634
-
Congenital central hypoventilation syndrome associated with Hirschsprung's disease and neuroblastoma: Case of multiple neurocristopathies
-
T. Rohrer, D. Trachsel, G. Engelcke, and J. Hammer Congenital central hypoventilation syndrome associated with Hirschsprung's disease and neuroblastoma: case of multiple neurocristopathies Pediatr. Pulmonol. 33 2002 71 76
-
(2002)
Pediatr. Pulmonol.
, vol.33
, pp. 71-76
-
-
Rohrer, T.1
Trachsel, D.2
Engelcke, G.3
Hammer, J.4
-
5
-
-
0021261878
-
Amplification of N-MYC in untreated human neuroblastomas correlates with advanced disease stage
-
G.M. Brodeur, R.C. Seeger, M. Schwab, H.E. Varmus, and J.M. Bishop Amplification of N-MYC in untreated human neuroblastomas correlates with advanced disease stage Science 224 1984 1121 1124
-
(1984)
Science
, vol.224
, pp. 1121-1124
-
-
Brodeur, G.M.1
Seeger, R.C.2
Schwab, M.3
Varmus, H.E.4
Bishop, J.M.5
-
6
-
-
0029049717
-
A region of consistent deletion in neuroblastoma within human chromosome 1 p36.2-36.3
-
P.S. White, J.M. Maris, C. Beltinger, E. Sulman, H.N. Marshall, and M. Fujimori A region of consistent deletion in neuroblastoma within human chromosome 1 p36.2-36.3 Proc. Natl Acad. Sci. USA 92 1995 5520 5524
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 5520-5524
-
-
White, P.S.1
Maris, J.M.2
Beltinger, C.3
Sulman, E.4
Marshall, H.N.5
Fujimori, M.6
-
7
-
-
0033600283
-
Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma
-
N. Bown, S. Cotterill, M. Lastowska, S. O'Neill, A.D. Pearson, and D. Plantaz Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma N. Engl. J. Med. 340 1999 1954 1961
-
(1999)
N. Engl. J. Med.
, vol.340
, pp. 1954-1961
-
-
Bown, N.1
Cotterill, S.2
Lastowska, M.3
O'Neill, S.4
Pearson, A.D.5
Plantaz, D.6
-
8
-
-
0037366067
-
Neuroblastoma: Biological insights into a clinical enigma
-
G.M. Brodeur Neuroblastoma: biological insights into a clinical enigma Nat. Rev. Cancer 3 2003 203 216
-
(2003)
Nat. Rev. Cancer
, vol.3
, pp. 203-216
-
-
Brodeur, G.M.1
-
9
-
-
0015402175
-
Mutation and cancer: Neuroblastoma and pheochromocytoma
-
A.G. Knudson, and L.C. Strong Mutation and cancer: neuroblastoma and pheochromocytoma Am. J. Hum. Genet. 24 1972 514 532
-
(1972)
Am. J. Hum. Genet.
, vol.24
, pp. 514-532
-
-
Knudson, A.G.1
Strong, L.C.2
-
10
-
-
12144291333
-
Germline mutations of the Paired-Like Homeobox 2B (PHOX2B) gene in neuroblastoma
-
D. Trochet, F. Bourdeaut, I. Janoueix-Lerosey, A. Deville, L. De Pontual, and G. Schleiermacher Germline mutations of the Paired-Like Homeobox 2B (PHOX2B) gene in neuroblastoma Am. J. Hum. Genet. 74 2004 761 764
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 761-764
-
-
Trochet, D.1
Bourdeaut, F.2
Janoueix-Lerosey, I.3
Deville, A.4
De Pontual, L.5
Schleiermacher, G.6
-
11
-
-
4544265599
-
Germline PHOX2B mutation in hereditary neuroblastoma
-
Y.P. Mosse, M. Laudenslager, D. Khazi, A.J. Carlisle, C.L. Winter, E. Rappaport, and J.M. Maris Germline PHOX2B mutation in hereditary neuroblastoma Am. J. Hum. Genet. 75 2004 727 730
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 727-730
-
-
Mosse, Y.P.1
Laudenslager, M.2
Khazi, D.3
Carlisle, A.J.4
Winter, C.L.5
Rappaport, E.6
Maris, J.M.7
-
12
-
-
8944253286
-
Familial predisposition to neuroblastoma does not map to chromosome band 1p36
-
J.M. Maris, S.M. Kyemba, T.R. Rebbeck, P.S. White, E.P. Sulman, and S.J. Jensen Familial predisposition to neuroblastoma does not map to chromosome band 1p36 Cancer Res. 56 1996 3421 3425
-
(1996)
Cancer Res.
, vol.56
, pp. 3421-3425
-
-
Maris, J.M.1
Kyemba, S.M.2
Rebbeck, T.R.3
White, P.S.4
Sulman, E.P.5
Jensen, S.J.6
-
13
-
-
0035197483
-
Exclusion of candidate genes and chromosomal regions in familial neuroblastoma
-
G.P. Tonini, C. McConville, R. Cusano, S.A. Rees, M. Dagnino, and L. Longo Exclusion of candidate genes and chromosomal regions in familial neuroblastoma Int. J. Mol. Med. 7 2001 85 89
-
(2001)
Int. J. Mol. Med.
, vol.7
, pp. 85-89
-
-
Tonini, G.P.1
McConville, C.2
Cusano, R.3
Rees, S.A.4
Dagnino, M.5
Longo, L.6
-
14
-
-
0037112452
-
Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13
-
J.M. Maris, M.J. Weiss, Y. Mosse, G. Hii, C. Guo, and P.S. White Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13 Cancer Res. 62 2002 6651 6658
-
(2002)
Cancer Res.
, vol.62
, pp. 6651-6658
-
-
Maris, J.M.1
Weiss, M.J.2
Mosse, Y.3
Hii, G.4
Guo, C.5
White, P.S.6
-
15
-
-
18444376143
-
Linkage analysis in families with recurrent neuroblastoma
-
P. Perri, L. Longo, C. McConville, R. Cusano, S.A. Rees, and M. Seri Linkage analysis in families with recurrent neuroblastoma Ann. NY Acad. Sci. 963 2002 74 84
-
(2002)
Ann. NY Acad. Sci.
, vol.963
, pp. 74-84
-
-
Perri, P.1
Longo, L.2
McConville, C.3
Cusano, R.4
Rees, S.A.5
Seri, M.6
-
16
-
-
0037191925
-
Weak linkage at 4p16 to predisposition for human neuroblastoma
-
P. Perri, L. Longo, R. Cusano, C.M. McConville, S.A. Rees, and M. Devoto Weak linkage at 4p16 to predisposition for human neuroblastoma Oncogene 21 2002 8356 8360
-
(2002)
Oncogene
, vol.21
, pp. 8356-8360
-
-
Perri, P.1
Longo, L.2
Cusano, R.3
McConville, C.M.4
Rees, S.A.5
Devoto, M.6
-
17
-
-
0033609337
-
The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives
-
A. Pattyn, X. Morin, H. Cremer, C. Goridis, and J.F. Brunet The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives Nature 399 1999 366 370
-
(1999)
Nature
, vol.399
, pp. 366-370
-
-
Pattyn, A.1
Morin, X.2
Cremer, H.3
Goridis, C.4
Brunet, J.F.5
-
18
-
-
19944426569
-
The Phox2B homeobox gene is mutated in sporadic neuroblastomas
-
V. van Limpt, A. Schramm, A. van Lakeman, P. Sluis, A. Chan, M. van Noesel, F. Baas, H. Caron, A. Egger, R. Versteeg, The Phox2B homeobox gene is mutated in sporadic neuroblastomas, Oncogene 23 (57) (2004) 9280-9288.
-
(2004)
Oncogene
, vol.23
, Issue.57
, pp. 9280-9288
-
-
Van Limpt, V.1
Schramm, A.2
Van Lakeman, A.3
Sluis, P.4
Chan, A.5
Van Noesel, M.6
Baas, F.7
Caron, H.8
Egger, A.9
Versteeg, R.10
-
19
-
-
18344381314
-
PHOX2B mutations and genetic predisposition to neuroblastoma
-
P. Perri, T. Bachetti, L. Longo, I. Matera, M. Seri, G.P. Tonini, I. Ceccherini, PHOX2B mutations and genetic predisposition to neuroblastoma, Oncogene 24 (18) (2005) 3050-3053.
-
(2005)
Oncogene
, vol.24
, Issue.18
, pp. 3050-3053
-
-
Perri, P.1
Bachetti, T.2
Longo, L.3
Matera, I.4
Seri, M.5
Tonini, G.P.6
Ceccherini, I.7
-
20
-
-
0037767913
-
Familial neuroblastoma: A complex heritable disease
-
G.P. Tonini, L. Longo, S. Coco, and P. Perri Familial neuroblastoma: a complex heritable disease Cancer Lett. 197 2003 41 45
-
(2003)
Cancer Lett.
, vol.197
, pp. 41-45
-
-
Tonini, G.P.1
Longo, L.2
Coco, S.3
Perri, P.4
-
21
-
-
0034602646
-
A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus
-
S. Bolk, A. Pelet, R.M. Hofstra, M. Angrist, R. Salomon, and D. Croaker A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus Proc. Natl Acad. Sci. USA 97 2000 268 273
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 268-273
-
-
Bolk, S.1
Pelet, A.2
Hofstra, R.M.3
Angrist, M.4
Salomon, R.5
Croaker, D.6
-
22
-
-
18544365991
-
Segregation at three loci explains familial and population risk in Hirschsprung disease
-
S. Bolk Gabriel, R. Salomon, A. Pelet, M. Angrist, J. Amiel, and M. Fornage Segregation at three loci explains familial and population risk in Hirschsprung disease Nat. Genet. 31 2002 89 93
-
(2002)
Nat. Genet.
, vol.31
, pp. 89-93
-
-
Bolk Gabriel, S.1
Salomon, R.2
Pelet, A.3
Angrist, M.4
Amiel, J.5
Fornage, M.6
-
23
-
-
1842579395
-
The oligogenic properties of Bardet-Biedl syndrome
-
N. Katsanis The oligogenic properties of Bardet-Biedl syndrome Hum. Mol. Genet. 13 Spec. No. 1 2004 R65 R71
-
(2004)
Hum. Mol. Genet.
, vol.131
-
-
Katsanis, N.1
-
24
-
-
0037389246
-
Genetic modifiers in human development and malformation syndromes, including chaperone proteins, Hum
-
A. Slavotinek, and L.G. Biesecker Genetic modifiers in human development and malformation syndromes, including chaperone proteins, Hum Mol. Genet. 12 Spec. No. 1 2003 45 50
-
(2003)
Mol. Genet.
, vol.121
, pp. 45-50
-
-
Slavotinek, A.1
Biesecker, L.G.2
-
25
-
-
0036844229
-
Multiple hits during early embryonic development: Digenic diseases and holoprosencephaly
-
J.E. Ming, and M. Muenke Multiple hits during early embryonic development: digenic diseases and holoprosencephaly Am. J. Hum. Genet. 71 2002 1017 1032
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1017-1032
-
-
Ming, J.E.1
Muenke, M.2
|