-
1
-
-
0003212441
-
Neurofibroma. Tumors of the peripheral nervous system
-
third series, fascicle 24. Washington, DC, Armed Forces Institute of Pathology
-
Scheithauer BW, Woodruff JM, Erlandson RA (eds): Neurofibroma. Tumors of the peripheral nervous system. Atlas of Tumor Pathology, third series, fascicle 24. Washington, DC, Armed Forces Institute of Pathology 1999, pp 177-218
-
(1999)
Atlas of Tumor Pathology
, pp. 177-218
-
-
Scheithauer, B.W.1
Woodruff, J.M.2
Erlandson, R.A.3
-
2
-
-
0034582121
-
What are the CD34+ cells in benign peripheral nerve sheath tumors? Double immunostaining study of CD34 and S-100 protein
-
Khalifa MA, Montgomery EA, Ismiil N, Azumi N: What are the CD34+ cells in benign peripheral nerve sheath tumors? Double immunostaining study of CD34 and S-100 protein. Am J Clin Pathol 2000, 114: 123-126
-
(2000)
Am J Clin Pathol
, vol.114
, pp. 123-126
-
-
Khalifa, M.A.1
Montgomery, E.A.2
Ismiil, N.3
Azumi, N.4
-
3
-
-
0034006709
-
Pigmented (melanotic) neurofibroma: A clinicopathologic and immunohistochemical analysis of 19 lesions from 17 patients
-
Fetsch JF, Michal M, Miettinen M: Pigmented (melanotic) neurofibroma: a clinicopathologic and immunohistochemical analysis of 19 lesions from 17 patients. Am J Surg Pathol 2000, 24:331-343
-
(2000)
Am J Surg Pathol
, vol.24
, pp. 331-343
-
-
Fetsch, J.F.1
Michal, M.2
Miettinen, M.3
-
4
-
-
0024957180
-
Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: Loss of heterozygosity for chromosome 17
-
Skuse GR, Kosciolek BA, Rowley PT: Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17. Genes Chromosomes Cancer 1989, 1:36-41
-
(1989)
Genes Chromosomes Cancer
, vol.1
, pp. 36-41
-
-
Skuse, G.R.1
Kosciolek, B.A.2
Rowley, P.T.3
-
5
-
-
0027468594
-
Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
-
Legius E, Marchuk DA, Collins FS, Glover TW: Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis. Nat Genet 1993, 3:122-126
-
(1993)
Nat Genet
, vol.3
, pp. 122-126
-
-
Legius, E.1
Marchuk, D.A.2
Collins, F.S.3
Glover, T.W.4
-
6
-
-
0027159475
-
Genetic alterations in a malignant schwannoma from a patient with neurofibromatosis (NF1)
-
Lothe RA, Saeter G, Danielsen HE, Stenwig AE, Høyheim B, O'Connell P, Børresen A-L: Genetic alterations in a malignant schwannoma from a patient with neurofibromatosis (NF1). Path Res Pract 1993, 189: 465-471
-
(1993)
Path Res Pract
, vol.189
, pp. 465-471
-
-
Lothe, R.A.1
Saeter, G.2
Danielsen, H.E.3
Stenwig, A.E.4
Høyheim, B.5
O'Connell, P.6
Børresen, A.-L.7
-
7
-
-
0028819644
-
Alterations at chromosome 17 loci in peripheral nerve sheath tumors
-
Lothe RA, Slettan A, Saeter G, Brøgger A Børresen A-L, Nesland JM: Alterations at chromosome 17 loci in peripheral nerve sheath tumors. J Neuropathol Exp Neurol 1995, 54:65-73
-
(1995)
J Neuropathol Exp Neurol
, vol.54
, pp. 65-73
-
-
Lothe, R.A.1
Slettan, A.2
Saeter, G.3
Brøgger, A.4
Børresen, A.-L.5
Nesland, J.M.6
-
8
-
-
0029160585
-
Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene
-
Colman SD, Williams CA, Wallace RW: Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene. Nat Genet 1995, 11:90-92
-
(1995)
Nat Genet
, vol.11
, pp. 90-92
-
-
Colman, S.D.1
Williams, C.A.2
Wallace, R.W.3
-
9
-
-
0031578233
-
Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene
-
Däschner K, Assum G, Eisenbarth I, Krone W, Hoffmeyer S, Wortmann S, Heymer B, Keher-Sawatzki H: Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene. Biochem Biophys Res Commun 1997, 234:346-350
-
(1997)
Biochem Biophys Res Commun
, vol.234
, pp. 346-350
-
-
Däschner, K.1
Assum, G.2
Eisenbarth, I.3
Krone, W.4
Hoffmeyer, S.5
Wortmann, S.6
Heymer, B.7
Keher-Sawatzki, H.8
-
10
-
-
0030850675
-
Confirmation of a double-hit model for the NF1 gene in benign neurofibromas
-
Serra E, Puig S, Otero D, Gaona A, Kruyer H, Ars E, Estivill X, Lázaro C: Confirmation of a double-hit model for the NF1 gene in benign neurofibromas. Am J Hum Genet 1997, 61:512-519
-
(1997)
Am J Hum Genet
, vol.61
, pp. 512-519
-
-
Serra, E.1
Puig, S.2
Otero, D.3
Gaona, A.4
Kruyer, H.5
Ars, E.6
Estivill, X.7
Lázaro, C.8
-
11
-
-
0032856294
-
Allelic loss of the NF1 gene in NF1-associated plexiform neurofibromas
-
Kluwe L, Friedrich RE, Mautner VF: Allelic loss of the NF1 gene in NF1-associated plexiform neurofibromas. Cancer Genet Cytogenet 1999, 113:65-69
-
(1999)
Cancer Genet Cytogenet
, vol.113
, pp. 65-69
-
-
Kluwe, L.1
Friedrich, R.E.2
Mautner, V.F.3
-
12
-
-
0033922008
-
Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1
-
Rasmussen SA, Overman J, Thomson SAM, Colman SD, Abernathy CR, Trimpert RE, Moose R, Virdi G, Roux K, Bauer M, Rojiani AM, Maria BL, Muir D, Wallace MR: Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1. Genes Chromosomes Cancer 2000, 28:425-431
-
(2000)
Genes Chromosomes Cancer
, vol.28
, pp. 425-431
-
-
Rasmussen, S.A.1
Overman, J.2
Thomson, S.A.M.3
Colman, S.D.4
Abernathy, C.R.5
Trimpert, R.E.6
Moose, R.7
Virdi, G.8
Roux, K.9
Bauer, M.10
Rojiani, A.M.11
Maria, B.L.12
Muir, D.13
Wallace, M.R.14
-
13
-
-
0031739872
-
Perineurial malignant peripheral nerve sheath tumor (MPNST): A clinicopathologic, immunohistochemical, and ultrastructural study of seven cases
-
Hirose T, Scheithauer BW, Sano T: Perineurial malignant peripheral nerve sheath tumor (MPNST): a clinicopathologic, immunohistochemical, and ultrastructural study of seven cases. Am J Surg Pathol 1998, 22:1368-1378
-
(1998)
Am J Surg Pathol
, vol.22
, pp. 1368-1378
-
-
Hirose, T.1
Scheithauer, B.W.2
Sano, T.3
-
14
-
-
0033986253
-
Culture of cytogenetically abnormal Schwann cells from benign and malignant NF1 tumors
-
Wallace MR, Rasmussen SA, Lim IT, Bray BA, Zori RT, Muir D: Culture of cytogenetically abnormal Schwann cells from benign and malignant NF1 tumors. Genes Chromosomes Cancer 2000, 27:117-123
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 117-123
-
-
Wallace, M.R.1
Rasmussen, S.A.2
Lim, I.T.3
Bray, B.A.4
Zori, R.T.5
Muir, D.6
-
15
-
-
0034639937
-
Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1
-
Rutkowski JL, Wu K, Gutmann DH, Boyer PJ, Legius E: Genetic and cellular defects contributing to benign tumor formation in neurofibromatosis type 1. Hum Mol Genet 2000, 9:1059-1066
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1059-1066
-
-
Rutkowski, J.L.1
Wu, K.2
Gutmann, D.H.3
Boyer, P.J.4
Legius, E.5
-
16
-
-
0030957310
-
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2
-
Gutmann DH, Aylsworth A, Carey JC, Korf B, Marks J, Pyeritz RE, Rubenstein A, Viskochil D: The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. J Am Med Assoc 1997, 278:51-57
-
(1997)
J Am Med Assoc
, vol.278
, pp. 51-57
-
-
Gutmann, D.H.1
Aylsworth, A.2
Carey, J.C.3
Korf, B.4
Marks, J.5
Pyeritz, R.E.6
Rubenstein, A.7
Viskochil, D.8
-
17
-
-
0035126321
-
PS6K amplification characterizes a small subset of anaplastic meningiomas
-
Cai DX, James CD, Scheithauer BW, Couch FJ, Perry A: PS6K amplification characterizes a small subset of anaplastic meningiomas. Am J Clin Pathol 2001, 115:213-218
-
(2001)
Am J Clin Pathol
, vol.115
, pp. 213-218
-
-
Cai, D.X.1
James, C.D.2
Scheithauer, B.W.3
Couch, F.J.4
Perry, A.5
-
18
-
-
0029994338
-
Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissue
-
Rao UNM, Surti U, Hoffner L, Yaw K: Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissue. Cancer Genet Cytogenet 1996, 88:17-25
-
(1996)
Cancer Genet Cytogenet
, vol.88
, pp. 17-25
-
-
Rao, U.N.M.1
Surti, U.2
Hoffner, L.3
Yaw, K.4
-
19
-
-
0029081452
-
Absence of mutation at the GAP-related domain of the neurofibromatosis type 1 gene in sporadic neurofibrosarcomas and other bone and soft tissue sarcomas
-
Gómez L, Barr os C, Kreicbergs A, Zetterberg A, Pestaña A, Castresana JS: Absence of mutation at the GAP-related domain of the neurofibromatosis type 1 gene in sporadic neurofibrosarcomas and other bone and soft tissue sarcomas. Cancer Genet Cytogenet 1995, 81:173-174
-
(1995)
Cancer Genet Cytogenet
, vol.81
, pp. 173-174
-
-
Gómez, L.1
Barr Os, C.2
Kreicbergs, A.3
Zetterberg, A.4
Pestaña, A.5
Castresana, J.S.6
|