| scholarly article | Q13442814 |
| P2093 | author name string | Cheryl M Coffin | |
| Scott C Borinstein | |||
| Jessica L Davis | |||
| P2860 | cites work | The controversial nosology of benign nerve sheath tumors: neurofilament protein staining demonstrates intratumoral axons in many sporadic schwannomas | Q47759251 |
| Childhood neurofibromatosis: risk factors for malignant disease | Q48354822 | ||
| Aggressive fibromatosis (desmoid tumor) is a monoclonal disorder. | Q50962782 | ||
| Rhabdomyosarcoma, osteosarcoma, and adrenocortical carcinoma in a child with a germline p53 mutation. | Q51610150 | ||
| Desmoid tumors -- a characterization of patients seen at Mayo Clinic 1976-1999. | Q51802398 | ||
| Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutations. | Q53132716 | ||
| Association between benign and malignant peripheral nerve sheath tumors in NF1. | Q53576233 | ||
| Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma. | Q54434638 | ||
| Gardner fibroma: a clinicopathologic and immunohistochemical analysis of 45 patients with 57 fibromas. | Q54446074 | ||
| Extending the phenotypes associated with DICER1 mutations. | Q54564111 | ||
| High incidence of malformation syndromes in a series of 1,073 children with cancer. | Q55040281 | ||
| Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid syndrome) and atypical teratoid/rhabdoid tumor. | Q55208704 | ||
| Familial Adenomatous Polyposis | Q56486183 | ||
| Congenital Disseminated Malignant Rhabdoid Tumor and Cerebellar Tumor Mimicking Medulloblastoma in Monozygotic Twins | Q56866397 | ||
| Frequent hSNF5/INI1 Germline Mutations in Patients with Rhabdoid Tumor | Q57266605 | ||
| Germline and somaticNF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs) | Q57266693 | ||
| Increasing the specificity of diagnostic criteria for schwannomatosis | Q57266735 | ||
| The epidemiology of sarcoma | Q21195878 | ||
| Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers | Q24534231 | ||
| Malignant peripheral nerve sheath tumours in neurofibromatosis 1 | Q24679356 | ||
| Germline mutation of INI1/SMARCB1 in familial schwannomatosis | Q24682982 | ||
| Update on desmoid tumors | Q27002396 | ||
| Germline INI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor | Q28140066 | ||
| Simultaneous presentation of atypical teratoid/rhabdoid tumor in siblings | Q28142250 | ||
| Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene | Q28181722 | ||
| Diagnostic criteria for schwannomatosis | Q28256490 | ||
| Germline mutations in HRAS proto-oncogene cause Costello syndrome | Q28272971 | ||
| Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer | Q28277002 | ||
| Human homolog of patched, a candidate gene for the basal cell nevus syndrome | Q28281033 | ||
| The neurofibromatosis type 1 gene encodes a protein related to GAP | Q28301160 | ||
| Germline and somatic NF1 mutations in sporadic and NF1-associated malignant peripheral nerve sheath tumours | Q28306740 | ||
| Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases. | Q30489944 | ||
| Clinical and genetic aspects of neurofibromatosis 1. | Q33520192 | ||
| Congenital disseminated malignant rhabdoid tumor: a distinct clinicopathologic entity demonstrating abnormalities of chromosome 22q11. | Q33541515 | ||
| Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome | Q33645991 | ||
| Rhabdomyosarcoma in a patient with cardio-facio-cutaneous syndrome | Q33877333 | ||
| Elevated risk for MPNST in NF1 microdeletion patients | Q33904745 | ||
| Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk | Q33905119 | ||
| Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome. | Q34112667 | ||
| Five additional Costello syndrome patients with rhabdomyosarcoma: proposal for a tumor screening protocol | Q34115295 | ||
| Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma | Q34207682 | ||
| Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome? | Q34232464 | ||
| Neurofibromatosis type 1 and childhood cancer | Q34357450 | ||
| Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation | Q34363853 | ||
| Association of childhood rhabdomyosarcoma with neurofibromatosis type I and birth defects | Q34371040 | ||
| Desmoid tumours in familial adenomatous polyposis | Q34378300 | ||
| Neurofibromatosis 1 and neurofibromatosis 2: a twenty first century perspective. | Q34577777 | ||
| Specific mutations in the beta-catenin gene (CTNNB1) correlate with local recurrence in sporadic desmoid tumors. | Q34597947 | ||
| The desmoid syndrome. New aspects in the cause, pathogenesis and treatment of the desmoid tumor | Q34694666 | ||
| A syndrome of various cutaneous pigmented lesions, myxoid neurofibromata and atrial myxoma: the NAME syndrome | Q34718468 | ||
| The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. | Q34741372 | ||
| Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes. | Q34907470 | ||
| Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors | Q34915348 | ||
| Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome | Q34964076 | ||
| DICER1 mutations in familial pleuropulmonary blastoma | Q34992567 | ||
| Genetic predisposition and screening in pediatric cancer | Q35064135 | ||
| Susceptible stages in Schwann cells for NF1-associated plexiform neurofibroma development | Q35133489 | ||
| Concordant rhabdoid tumor of the kidney in a set of identical twins with discordant outcomes | Q35148736 | ||
| Molecular analysis of the rhabdoid predisposition syndrome in a child: a novel germline hSNF5/INI1 mutation and absence of c-myc amplification | Q35189235 | ||
| Confirmation of a double-hit model for the NF1 gene in benign neurofibromas | Q35249470 | ||
| Malignant peripheral nerve sheath tumour arising within neurofibroma. An immunohistochemical analysis in the comparison between benign and malignant components | Q35399426 | ||
| Desmoid tumour in familial adenomatous polyposis. A review of literature | Q35566038 | ||
| Trisomies 8 and 20 characterize a subgroup of benign fibrous lesions arising in both soft tissue and bone | Q35786273 | ||
| Sensitive detection of deletions of one or more exons in the neurofibromatosis type 2 (NF2) gene by multiplexed gene dosage polymerase chain reaction | Q35789823 | ||
| The neurofibromatosis type 2 gene is mutated in perineurial cell tumors: a molecular genetic study of eight cases. | Q35842044 | ||
| Inherited cancer in children: practical/ethical problems and challenges | Q35935505 | ||
| Hereditary cancer predisposition syndromes | Q36002146 | ||
| Second primary neoplasms in patients with retinoblastoma | Q36027090 | ||
| Rhabdomyosarcoma associated with familial adenomatous polyposis | Q36446282 | ||
| Hereditary cancer predisposition in children: genetic basis and clinical implications | Q36461758 | ||
| Plexiform neurofibroma genesis: questions of Nf1 gene dose and hyperactive mast cells | Q36517090 | ||
| Guidelines for the diagnosis and management of individuals with neurofibromatosis 1 | Q36653938 | ||
| Li-Fraumeni syndrome: report of a clinical research workshop and creation of a research consortium | Q36672536 | ||
| Pleuropulmonary blastoma: a marker for familial disease | Q36799690 | ||
| Clinical relevance of molecular genetics to paediatric sarcomas | Q36806186 | ||
| Immunohistochemistry for beta-catenin in the differential diagnosis of spindle cell lesions: analysis of a series and review of the literature. | Q36915487 | ||
| Pediatric nonrhabdomyosarcoma soft tissue sarcomas | Q37202480 | ||
| Neurofibromatosis type 1 revisited | Q37360771 | ||
| Inherited cancer syndromes in children and young adults | Q37698940 | ||
| Neonatal Gardner fibroma: a sentinel presentation of severe familial adenomatous polyposis | Q37808062 | ||
| Malignant peripheral nerve sheath tumors (MPNST): the Mayo Clinic experience | Q37921212 | ||
| INI1-deficient tumors: diagnostic features and molecular genetics | Q37936128 | ||
| Pathology of peripheral nerve sheath tumors: diagnostic overview and update on selected diagnostic problems | Q37983396 | ||
| Some general considerations about the clinicopathologic aspects of soft tissue tumors in children and adolescents | Q37989189 | ||
| Neurogenic tumors of soft tissue | Q37993923 | ||
| Myogenic tumors in children and adolescents | Q37993928 | ||
| Soft tissue tumors of uncertain origin | Q37993931 | ||
| High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor | Q38301206 | ||
| Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas | Q38340286 | ||
| Malignant peripheral nerve sheath tumor: a comparison of grade, immunophenotype, and cell cycle/growth activation marker expression in sporadic and neurofibromatosis 1-related lesions | Q38450838 | ||
| Neurofibromatosis and associated neuroectodermal tumors: a congenital neurocristopathy | Q39503112 | ||
| Malignant peripheral nerve sheath tumors. A clinicopathologic study of 120 cases | Q39587986 | ||
| Congenital anomalies associated with rhabdomyosarcoma: an autopsy study of 115 cases. A report from the Intergroup Rhabdomyosarcoma Study Committee (representing the Children's Cancer Study Group, the Pediatric Oncology Group, the United Kingdom Chi | Q39627641 | ||
| Malignant schwannoma associated with von Recklinghausen's neurofibromatosis | Q39891722 | ||
| Desmoid tumors and mesenteric fibromatosis in Gardner's syndrome: report of kindred 109. | Q39895302 | ||
| Immunohistochemical detection of EGFR, fibrillin-2, P-cadherin and AP2beta as biomarkers for rhabdomyosarcoma diagnostics | Q39976938 | ||
| Von Recklinghausen neurofibromatosis | Q40262766 | ||
| Neoplasms in proteus syndrome | Q40465565 | ||
| Glandular peripheral nerve sheath tumors | Q40786425 | ||
| Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene | Q41667422 | ||
| Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site | Q41920930 | ||
| Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma | Q41925944 | ||
| Rhabdomyosarcomas and radiation hypersensitivity in a mouse model of Gorlin syndrome | Q42455110 | ||
| Further evidence of the increased risk for malignant peripheral nerve sheath tumour from a Scottish cohort of patients with neurofibromatosis type 1 | Q42727043 | ||
| Rhabdoid tumor of the kidney is a component of the rhabdoid predisposition syndrome | Q43997399 | ||
| Hereditary retinoblastoma, lipoma, and second primary cancers | Q44731716 | ||
| Prevalence and spectrum of germline mutations of the p53 gene among patients with sarcoma | Q44949974 | ||
| Cancer in the families of children with soft tissue sarcoma | Q44993844 | ||
| Neurofibroma and cellular neurofibroma with atypia: a report of 14 tumors | Q46081821 | ||
| Value of PET in the assessment of patients with neurofibromatosis type 1. | Q46989265 | ||
| Excess of neuromuscular spindles in a fetus with Costello syndrome: a clinicopathological report. | Q47261130 | ||
| Familial sarcoma: challenging pedigrees | Q47416952 | ||
| Non-linkage of familial rhabdoid tumors to SMARCB1 implies a second locus for the rhabdoid tumor predisposition syndrome | Q47586739 | ||
| Congenital and childhood plexiform (multinodular) cellular schwannoma: a troublesome mimic of malignant peripheral nerve sheath tumor | Q47607067 | ||
| Abdominal desmoid in familial adenomatous polyposis presenting as a pancreatic cystic lesion | Q47615946 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 68-87 | |
| P577 | publication date | 2013-11-18 | |
| P1433 | published in | Histopathology | Q1524040 |
| P1476 | title | Syndrome-associated soft tissue tumours | |
| P478 | volume | 64 |
| Q42416908 | Alveolar Rhabdomyosarcoma in a 69-Year-Old Woman Receiving Glucagon-Like Peptide-2 Therapy |
| Q49191676 | Common lesions in a rare entity - Gardner's syndrome |
| Q51047347 | Congenital Disseminated Extrarenal Malignant Rhabdoid Tumor. |
| Q42279595 | From Gardner fibroma diagnosis to constitutional APC mutation detection: a one-way street. |
| Q36142754 | Probing for a deeper understanding of rhabdomyosarcoma: insights from complementary model systems. |
| Q38893082 | Sarcomas Associated With Genetic Cancer Predisposition Syndromes: A Review |
| Q51807102 | Soft Tissue Perineurioma in a Child With Neurofibromatosis Type 1: A Case Report and Review of the Literature. |
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