262 results on '"Willén, Helena"'
Search Results
52. Comparison of Chromosomal Patterns with Clinical Features in 165 Lipomas: A Report of the CHAMP Study Group
53. Fine needle aspiration in the diagnosis of bone tumors
54. Tumor necrosis and prognosis in osteosarcoma
55. Duplication of chromosome segment 12q15-24 is associated with atypical lipomatous tumors. A report of the CHAMP collaborative study group
56. Urokinase-plasminogen-activator levels and prognosis in 69 soft-tissue sarcomas
57. Cytogenetic studies on fine-needle aspiration samples from osteosarcoma and Ewing's sarcoma
58. 19p + marker chromosome correlates with relapse in malignant fibrous histiocytoma
59. Trisomy 20 is a primary chromosome aberration in desmoid tumors
60. Cytogenetic findings in malignant peripheral nerve sheath tumors
61. Expression of proliferating cell nuclear antigen (PCNA) and Ki-67 in soft tissue sarcoma. Is prognostic significance histotype-specific?
62. Prognosis following locally recurrent soft‐tissue sarcoma. A staging system based on primary and recurrent tumour characteristics
63. Cytogenetic intratumor heterogeneity in soft tissue tumors
64. Proliferating cell nuclear antigen (PCNA) in high-grade malignant fibrous histiocytoma: Prognostic value in 48 patients
65. MDM2 gene amplification correlates with ring chromosomes in soft tissue tumors
66. Clonal chromosome aberrations in three sacral chordomas
67. Cytogenetic aberrations in 188 benign and borderline adipose tissue tumors
68. Loss of chromosome band 8q24 in sporadic osteocartilaginous exostoses
69. Liposarcoma: A population-based epidemiologic and prognostic study of features of 43 patients, including tumor DNA content
70. Aberrations of chromosome segment 12q13–15 characterize a subgroup of hemangiopericytomas
71. Chromosome aberrations in tenosynovial giant cell tumors and nontumorous synovial tissue
72. Comparative cytogenetic and dna flow cytometric analysis of 150 bone and soft-tissue tumors
73. Rearrangement of band q13 on both chromosomes 12 in a periosteal chondroma
74. Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11)
75. Soft tissue leiomyosarcoma. A population-based epidemiologic and prognostic study of 48 patients, including cellular dna content
76. Supernumerary ring chromosomes in five bone and soft tissue tumors of low or borderline malignancy
77. Cartilage Regeneration After Proximal Tibial Osteotomy for Medial Gonarthrosis
78. Chromosome aberrations in 35 primary ovarian carcinomas
79. Re-evaluation of histological diagnosesof malignant mesothelioma byimmunohistochemistry.
80. Chromosomal abnormalities in giant cell tumors of bone
81. Chromosome analysis of 96 uterine leiomyomas
82. Bilateral ovarian carcinoma: Cytogenetic evidence of unicentric origin
83. Malignant fibrous histiocytoma of soft tissue. A population-based epidemiologic and prognostic study of 137 patients
84. Malignant fibrous histiocytomas with a 19p+ marker chromosome have increased relapse rate
85. Parallel karyotypic evolution and tumor progression in uterine leiomyoma
86. Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas
87. Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2
88. Trisomy 12 is a consistent chromosomal aberration in benign ovarian tumors
89. Trisomy 12 in uterine leiomyomas
90. Trisomy 5 and loss of the Y chromosome as the sole cytogenetic anomalies in a cavernous hemangioma/angiosarcoma
91. Chromosomal rearrangements in chondromatous tumors
92. Chromosome rearrangements in two uterine sarcomas
93. Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.
94. Propagation of a poorly differentiated human pulmonary adenocarcinoma in nude athymic rats.
95. Necrotizing sialometaplasia of the lip simulating squamous cell carcinoma.
96. A case of Ewing's sarcoma diagnosed by fine needle aspiration: Light microscopy, electron microscopy and chromosomal analysis.
97. Complex karyotypic anomalies in a bizarre leiomyoma of the uterus.
98. Consistent occurrence of a 19p+ marker chromosome and loss of 11p material in ovarian seropapillary cystadenocarcinomas.
99. Characteristic karyotypic anomalies identify subtypes of malignant fibrous histiocytoma.
100. Localized Primary Amyloidosis of the Ureter.
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