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1. Full Text Soft tissue angiofibroma: Clinicopathologic, immunohistochemical and molecular analysis of 14 cases
by Bekers, E.M and Groenen, P.J.T.A and Verdijk, M.A.J and Raaijmakers-van Geloof, W.L and Roepman, P and Vink, R and Gilhuijs, N.D and Gorp, J.M. van and Bovee, J.V and Creytens, D.H and Flanagan, A.M and Suurmeijer, A.J and Mentzel, T and Arbajian, E and Flucke, U.E and The genetics of soft tissue tumors and Lund University and Division of Clinical Genetics and Avdelningen för klinisk genetik and Lunds universitet and Genetiska avvikelser i mjukdelstumörer
Genes, Chromosomes & Cancer, ISSN 1045-2257, 2017, Volume 56, Issue 10, pp. 750 - 757
Soft tissue angiofibroma is rare and has characteristic histomorphological and genetic features. For diagnostic purposes, there are no specific antibodies... 
CELLULAR ANGIOFIBROMA | FUSION | NEOPLASM | ONCOLOGY | TRANSLOCATIONS | GENES | GENETICS & HEREDITY | IN-SITU HYBRIDIZATION | TRANSCRIPTIONAL COACTIVATOR | RADIATION | Antigens, CD34 - metabolism | Basic Helix-Loop-Helix Transcription Factors - genetics | Genes, abl - genetics | Humans | Middle Aged | Repressor Proteins - genetics | Male | Nuclear Receptor Coactivator 2 - metabolism | STAT6 Transcription Factor - genetics | STAT6 Transcription Factor - metabolism | Guanine Nucleotide-Releasing Factor 2 - genetics | Angiofibroma - genetics | Angiofibroma - pathology | Adolescent | Soft Tissue Neoplasms - pathology | Adult | Female | Aged | Oncogene Fusion - genetics | Antigens, CD34 - genetics | Child | Nuclear Receptor Coactivator 2 - genetics | Soft Tissue Neoplasms - genetics | Immunohistochemistry | Viral antibodies | RNA sequencing | Antibodies | RNA | Analysis | CD34 antigen | Transcription | Cell fusion | Gene expression | Males | Ribonucleic acid--RNA | Desmin | Neoplasms | Gene sequencing | Polymerase chain reaction | Stat6 protein | Diagnostic systems | Lesions | Fusion protein | Females | Extremities | Tumors | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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2. Full Text Novel EWSR1-SMAD3 Gene Fusions in a Group of Acral Fibroblastic Spindle Cell Neoplasms
by Kao, Y.C and Flucke, U.E and Eijkelenboom, A and Zhang, L and Sung, Y.S and Suurmeijer, A.J and Antonescu, C.R
American Journal of Surgical Pathology, ISSN 0147-5185, 2018, Volume 42, Issue 4, pp. 522 - 528
Benign/low-grade fibroblastic tumors encompass a broad spectrum of tumors with different morphologies and molecular genetic abnormalities. However, despite... 
spindle cell tumor | fibroblastic tumor | SMAD3 | ERG | EWSR1 | acral | FIBROSIS | SURGERY | SMADS | PHOSPHATURIC MESENCHYMAL TUMORS | PATHOLOGY | RECURRENT | MUTATIONS | TRANSCRIPTION FACTOR | EXPRESSION | Immunohistochemistry | Transcriptional Regulator ERG - analysis | Humans | Middle Aged | Skin Neoplasms - chemistry | Infant | Male | Neoplasms, Fibrous Tissue - pathology | Smad3 Protein - genetics | Neoplasms, Fibrous Tissue - genetics | Neoplasms, Fibrous Tissue - surgery | Neoplasms, Fibrous Tissue - chemistry | Female | Skin Neoplasms - surgery | Fibroblasts - chemistry | Skin Neoplasms - pathology | Genetic Predisposition to Disease | Biomarkers, Tumor - analysis | RNA-Binding Protein EWS - genetics | Gene Fusion | In Situ Hybridization, Fluorescence | Fibroblasts - pathology | Phenotype | Skin Neoplasms - genetics | Biomarkers, Tumor - genetics | Connective tissue tumors | Development and progression | Care and treatment | Genetic aspects | Health aspects | Gene fusion
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3. Full Text Adherence to Guidelines for Adult (Non-GIST) Soft Tissue Sarcoma in the Netherlands: A Plea for Dedicated Sarcoma Centers
by Hoekstra, H.J and Haas, R.L.M and Verhoef, C and Suurmeijer, A.J and Rijswijk, C.S.P. van and Bongers, B.G.H and Graaf, W.T.A. van der and Ho, V.K
Annals of Surgical Oncology, ISSN 1068-9265, 2017, Volume 24, Issue 11, pp. 3279 - 3288
INTRODUCTION: Optimal management of soft tissue sarcoma (STS) remains a challenge. A nationwide survey assessed the quality of STS care in the Netherlands,... 
CLINICAL-PRACTICE GUIDELINES | REFERRAL PATTERNS | SURVIVAL | AUDIT | SURGERY | DIAGNOSIS | MANAGEMENT | METASTASIS | ONCOLOGY | CONFORMITY | REGION | Prognosis | Follow-Up Studies | Humans | Middle Aged | Male | Sarcoma - therapy | Netherlands | Guideline Adherence | Aged, 80 and over | Adult | Female | Registries | Surveys and Questionnaires | Aged | Sarcoma - epidemiology | Practice Guidelines as Topic | Sarcoma | Analysis | Hospitals | Bone and Soft Tissue Sarcomas
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4. Full Text Epithelioid Hemangioendothelioma: clinicopathologic, immunhistochemical, and molecular genetic analysis of 39 cases
by Flucke, Uta and Vogels, Rob J. C and de Saint Aubain Somerhausen, Nicolas and Creytens, David H and Riedl, Robert G and van Gorp, Joost M and Milne, Anya N and Huysentruyt, Clement J and Verdijk, Marian A. J and van Asseldonk, Monique M and Suurmeijer, Albert J. H and Bras, Johannes and Palmedo, Gabriele and Groenen, Patricia J. T. A and Mentzel, Thomas
Diagnostic pathology, ISSN 1746-1596, 2014, Volume 9, Issue 1, pp. 131 - 131
Epithelioid hemangioendothelioma is a malignant, often indolent vascular tumor which occurs at various anatomic sites. Based on a reciprocal translocation t... 
Vascular tumors | Liver | Lung | Epithelioid hemangioendothelioma | Skin | Soft tissue | Bone | FUSION | TISSUE | EXTRASKELETAL MYXOID CHONDROSARCOMA | SOFT PART SARCOMA | PATHOLOGY | PSEUDOMYOGENIC HEMANGIOENDOTHELIOMA | MYOEPITHELIAL TUMORS | MORPHOLOGIC SPECTRUM | EWSR1 GENE | TRANSCRIPTION FACTOR | Immunohistochemistry | Biomarkers, Tumor - analysis | Humans | Middle Aged | In Situ Hybridization, Fluorescence | Male | Reverse Transcriptase Polymerase Chain Reaction | Hemangioendothelioma, Epithelioid - pathology | Young Adult | Hemangioendothelioma, Epithelioid - genetics | Adolescent | Aged, 80 and over | Adult | Female | Aged | Child | Analysis | Studies | Polymerase chain reaction | Pathology | Keratin | Hospitals | Genes | Metastasis | Cytoplasm
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5. Full Text Radiofrequency ablation in the treatment of atypical cartilaginous tumours in the long bones: lessons learned from our experience
by Dierselhuis, E.F and Overbosch, J and Kwee, T.C and Suurmeijer, A.J and Ploegmakers, J.J.W and Stevens, M and Jutte, P.C
Skeletal Radiology, ISSN 0364-2348, 2019, Volume 48, Issue 6, pp. 881 - 887
BACKGROUND: Surgery is the cornerstone of treatment of symptomatic cartilaginous neoplasms. We previously studied the application of radiofrequency ablation of... 
Atypical cartilaginous tumours | Pathology | Low-grade chondrosarcoma | Medicine & Public Health | Orthopedics | Minimally invasive | Radiofrequency ablation | Nuclear Medicine | Imaging / Radiology | MANAGEMENT | PHENOL | PREVALENCE | LESIONS | INTRALESIONAL CURETTAGE | ADJUVANT | THERAPY | I CHONDROSARCOMA | ENCHONDROMAS | ORTHOPEDICS | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Prospective Studies | Bone Neoplasms - diagnostic imaging | Humans | Middle Aged | Male | Neoplasms, Connective Tissue - surgery | Bone Neoplasms - surgery | Neoplasms, Connective Tissue - diagnostic imaging | Magnetic Resonance Imaging | Contrast Media | Radiofrequency Ablation | Adult | Female | Aged | Postoperative Complications - diagnostic imaging | Neoplasm, Residual - diagnostic imaging | Radio frequency | Curettage | Magnetic resonance imaging | Surgery | Gadolinium | Needles | Bones | Patients | Ablation | Catheters | Neoplasms | Tumors | Scientific
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6. Full Text Solitary fibrous tumor - clinicopathologic, immunohistochemical and molecular analysis of 28 cases
by Vogels, Rob J. C and Vlenterie, Myrella and Versleijen-Jonkers, Yvonne M. H and Ruijter, Emiel and Bekers, Elise M and Verdijk, Marian A. J and Link, Monique M and Bonenkamp, Johannes J and van der Graaf, Winette T. A and Slootweg, Pieter J and Suurmeijer, Albert J. H and Groenen, Patricia J. T. A and Flucke, Uta
Diagnostic Molecular Pathology, ISSN 1746-1596, 11/2014, Volume 9, Issue 1, pp. 224 - 224
Background: Solitary fibrous tumor is a mesenchymal tumor of fibroblastic type, which can affect any region of body. Recently, a recurrent gene fusion... 
DIAGNOSIS | NAB2-STAT6 fusion | ANGIOFIBROMA | Solitary fibrous tumor | STAT6 immunohistochemistry | EGR1 immunohistochemistry | FEATURES | GENE | RT-PCR | Soft tissue | STAT6 | Hemangiopericytoma | SPECTRUM | RISK-ASSESSMENT | EXPRESSION | NCOA2 | PATHOLOGY | Immunohistochemistry | Predictive Value of Tests | Solitary Fibrous Tumors - chemistry | Humans | Middle Aged | Male | STAT6 Transcription Factor - genetics | Young Adult | Time Factors | Aged, 80 and over | Adult | Female | Solitary Fibrous Tumors - genetics | Biomarkers, Tumor - analysis | Solitary Fibrous Tumors - mortality | Repressor Proteins - genetics | Gene Fusion | Treatment Outcome | STAT6 Transcription Factor - analysis | Early Growth Response Protein 1 - analysis | Reverse Transcriptase Polymerase Chain Reaction | Solitary Fibrous Tumors - pathology | Aged | Biomarkers, Tumor - genetics | Solitary Fibrous Tumors - diagnosis | Solitary Fibrous Tumors - therapy | Deregulation | Netherlands | Analysis | Genetic transcription | Research | Tumors | Proteins | Polymerase chain reaction | Pathology | Genes | Risk assessment | Protein expression | Radiation therapy | Metastasis | Patients
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7. Myoepithelial Tumors of Bone
by Song, Wangzhao and Flucke, Uta and Suurmeijer, Albert J.H
Surgical Pathology Clinics, ISSN 1875-9181, 09/2017, Volume 10, Issue 3, pp. 657 - 674
Myoepithelial tumors (METs) of bone (BMETs) are a rare but distinct tumor entity. METs that are cytologically benign are termed myoepitheliomas; METs with... 
Immunohistochemistry | Pathology | EWSR1 | FUS | Myoepithelioma | Myoepithelial carcinoma | Bone | Fusion gene | Calcium-Binding Proteins - metabolism | rab GTP-Binding Proteins - metabolism | Myoepithelioma - metabolism | Diagnosis, Differential | Humans | RNA-Binding Protein EWS - genetics | Glial Fibrillary Acidic Protein - metabolism | Bone Neoplasms - pathology | Myoepithelioma - pathology | Myoepithelioma - genetics | Bone Neoplasms - metabolism | Keratins - metabolism | Gene Rearrangement | Biomarkers, Tumor - metabolism | Bone Neoplasms - genetics | Microfilament Proteins - metabolism
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8. Full Text High Resolution Systematic Digital Histological Quantification of Cardiac Fibrosis and Adipose Tissue in Phospholamban p.Arg14del Mutation Associated Cardiomyopathy
by Gho, Johannes M. I. H and van Es, Rene and Stathonikos, Nikolas and Harakalova, Magdalena and te Rijdt, Wouter P and Suurmeijer, Albert J. H and van der Heijden, Jeroen F and de Jonge, Nicolaas and Chamuleau, Steven A. J and de Weger, Roel A and Asselbergs, Folkert W and Vink, Aryan
PLoS ONE, ISSN 1932-6203, 04/2014, Volume 9, Issue 4, p. e94820
Myocardial fibrosis can lead to heart failure and act as a substrate for cardiac arrhythmias. In dilated cardiomyopathy diffuse interstitial reactive fibrosis... 
CRITERIA | THERAPY | MYOCARDIAL FIBROSIS | CARDIOVASCULAR MAGNETIC-RESONANCE | BIOPSY | DILATED CARDIOMYOPATHY | LETHAL | RIGHT-VENTRICULAR CARDIOMYOPATHY/DYSPLASIA | MULTIDISCIPLINARY SCIENCES | Cardiomyopathy, Dilated - genetics | Cardiomyopathy, Dilated - pathology | Genetic Predisposition to Disease | Calcium-Binding Proteins | Cardiomyopathy, Dilated - complications | Humans | Middle Aged | Adipose Tissue - pathology | Male | Myocardium - pathology | Mutation - genetics | Arrhythmias, Cardiac - pathology | Phenotype | Image Processing, Computer-Assisted | Fibrosis | Arrhythmias, Cardiac - complications | Arrhythmias, Cardiac - genetics | Adipose tissues | Complications and side effects | Gene mutations | Cardiomyopathy | Physiological aspects | Genetic aspects | Research | Heart diseases | Health aspects | Risk factors | Heart failure | Heart | Animal models | High resolution | Nuclear magnetic resonance--NMR | Heart attacks | Adipose tissue | Cardiomyocytes | Phospholamban | Adipocytes | Patients | Substrates | Connective tissues | Pathology | Dilated cardiomyopathy | Biopsy | Myocardium | Extracellular matrix | Mutation | Ventricle | Cardiology | Nuclear magnetic resonance | NMR
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9. Full Text A single digital droplet PCR assay to detect multiple KIT exon 11 mutations in tumor and plasma from patients with gastrointestinal stromal tumors
by Boonstra, P.A and Elst, A. Ter and Tibbesma, M and Bosman, L.J and Mathijssen, R and Atrafi, F and Coevorden, F. van and Steeghs, N and Farag, S and Gelderblom, H and Graaf, W.T.A. van der and Desar, I.M.E and Maier, J and Overbosch, J and Suurmeijer, A.J and Gietema, J and Schuuring, E and Reyners, A.K
Oncotarget, ISSN 1949-2553, 2018, Volume 9, pp. 13870 - 13883
Background: Gastrointestinal stromal tumors (GISTs) are characterized by oncogenic KIT mutations that cluster in two exon 11 hotspots. The aim of this study... 
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10. Full Text The Amount of Autophagy-Related Cardiomyocyte Cell Death Is Associated With the Type of Pathogenic Mutation in Genetic Dilated Cardiomyopathy
by van der Klooster, Z.J and Sepehrkhouy, S and Harakalova, M and Goldschmeding, R and de Jonge, N and Suurmeijer, A.J and de Weger, R.A and Asselbergs, F.W and Vink, A
Journal of Heart and Lung Transplantation, ISSN 1053-2498, 2015, Volume 34, Issue 4, pp. S38 - S39
Surgery | Cell death | Genetic aspects
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11. Full Text Assessment of a new scoring system for predicting non-sentinel node positivity in sentinel node-positive melanoma patients
by Wevers, K.P and Murali, R and Bastiaannet, E and Scolyer, R.A and Suurmeijer, A.J and Thompson, J.F and Hoekstra, H.J
European Journal of Surgical Oncology, ISSN 0748-7983, 2012, Volume 39, Issue 2, pp. 179 - 184
Abstract Background When completion lymph node dissection (CLND) is performed in sentinel node (SN)-positive melanoma patients, a positive non-sentinel node... 
Hematology, Oncology and Palliative Medicine | Surgery | Completion lymph node dissection | Sentinel node | Non-sentinel node | Melanoma | Predictors | SURVIVAL | INVOLVEMENT | METASTASES | BIOPSY | FOLLOW-UP | NONSENTINEL LYMPH-NODES | FEATURES | LYMPHADENECTOMY | PRIMARY CUTANEOUS MELANOMA | DISEASE | SURGERY | ONCOLOGY | Lymph Node Excision | Lymphatic Metastasis - diagnosis | Skin Neoplasms - pathology | Multivariate Analysis | Predictive Value of Tests | Lymph Nodes - pathology | Lymph Nodes - surgery | Neoplasm Invasiveness | Humans | Middle Aged | Risk Factors | Male | Melanoma - pathology | Netherlands | Adult | Female | Aged | Retrospective Studies | Sentinel Lymph Node Biopsy | Melanoma - surgery | Skin Neoplasms - surgery | Medicine, Experimental | Medical research | Analysis
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12. Full Text NR4A3 rearrangement reliably distinguishes between the clinicopathologically overlapping entities myoepithelial carcinoma of soft tissue and cellular extraskeletal myxoid chondrosarcoma
by Flucke, U.E and Tops, B.B.J and Verdijk, M.A.J and Cleef, P.J. van and Zwam, P.H. van and Slootweg, P.J and Bovee, J.V and Riedl, R.G and Creytens, D.H and Suurmeijer, A.J.H and Mentzel, T
Virchows Archiv, ISSN 0945-6317, 2012, Volume 460, Issue 6, pp. 621 - 628
Myoepithelial carcinoma of soft tissue (MEC) and cellular extraskeletal myxoid chondrosarcoma (cEMC) share striking similarities. In this paper, we compare ten... 
EWSR1 rearrangement | Myoepithelial carcinoma of soft tissue | Soft tissue tumours | Extraskeletal myxoid chondrosarcoma | NR4A3 rearrangement | FUSION GENE | PATHOLOGY | MOLECULAR ANALYSIS | REAPPRAISAL | TEC | EWSR1 | PARACHORDOMA | BONE | MIXED TUMORS | Calmodulin-Binding Proteins - genetics | Immunohistochemistry | RNA-Binding Proteins - genetics | Humans | Middle Aged | In Situ Hybridization, Fluorescence | Male | DNA-Binding Proteins - genetics | Myoepithelioma - pathology | Myoepithelioma - genetics | Keratins - biosynthesis | Receptors, Thyroid Hormone - genetics | Receptors, Steroid - genetics | Gene Rearrangement | Soft Tissue Neoplasms - pathology | Chondrosarcoma - genetics | Chondrosarcoma - pathology | Adult | Female | Aged | Soft Tissue Neoplasms - genetics | RNA-Binding Protein EWS | Carcinoma | Actin | Metastasis | Muscle proteins | Intermediate filament proteins | Cancer | Tumors | Original
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13. Full Text Bone sarcoma incidence in the Netherlands
by Goedhart, Louren M and Ho, Vincent K.Y and Dijkstra, P.D.S and Schreuder, Hendrik W.B and Schaap, Gerard R and Ploegmakers, Joris J.W and van der Geest, Ingrid C.M and van de Sande, Michiel A.J and Bramer, Jos A and Suurmeijer, Albert J.H and Jutte, Paul C
Cancer Epidemiology, ISSN 1877-7821, 06/2019, Volume 60, pp. 31 - 38
Chondrosarcoma, osteosarcoma and Ewing sarcoma form the majority of malignant primary tumours of bone. High-grade bone sarcomas require intensive treatment due... 
Chondrosarcoma | Ewing sarcoma | Sarcoma | Osteosarcoma | Survival | Incidence | EWINGS-SARCOMA | SINGLE INSTITUTION | PROGNOSTIC-FACTORS | EUROPE | PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH | ONCOLOGY | EXTREMITY | SURVEILLANCE | HIGH-GRADE OSTEOSARCOMA | EPIDEMIOLOGY | Migration | Bone tumors | Ewing's sarcoma | Confidence intervals | Biomedical materials | Classification | Population | Bones | Biocompatibility | Trends | Localization | Age | Statistical analysis | Invasiveness | Hazards | Regression analysis | Patients | Bone cancer | Chemotherapy | Biopsy | Medical prognosis | Bone | Tumors
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14. Full Text Myxoid liposarcoma of the foot: a study of 8 cases
by Bekers, Elise M and Song, Wangzhao and Suurmeijer, Albert J.H and Bonenkamp, Johannes J and van der Geest, Ingrid C and Braam, Petra M and Ploegmakers, Marieke J.M and Desar, Ingrid M.E and Tops, Bastiaan B.J and van Gorp, Joost M and Creytens, David H and Mentzel, Thomas and Flucke, Uta
Annals of Diagnostic Pathology, ISSN 1092-9134, 12/2016, Volume 25, pp. 37 - 41
Myxoid liposarcoma is the only translocation-associated liposarcoma subtype. It classically originates in the deep soft tissues of the thigh. At distal sites... 
Ankle | Myxoid liposarcoma | EWSR1 rearrangement | FUS rearrangement | Acral site | Foot | FUSION | PROGNOSTIC-FACTORS | NEOPLASM | MRI | PATTERNS | LIPOMA | PATHOLOGY | FEATURES | ROUND-CELL LIPOSARCOMA | PRIMARY EXTREMITY LIPOSARCOMA | LIPOBLASTOMA | Prognosis | Translocation, Genetic - physiology | Thigh - pathology | Humans | Middle Aged | Liposarcoma, Myxoid - pathology | Male | Neoplasm Recurrence, Local - diagnosis | Sarcoma - pathology | Neoplasm Recurrence, Local - pathology | Liposarcoma, Myxoid - diagnosis | Adult | Female | Aged | Sarcoma - diagnosis | Foot - pathology
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15. Full Text The feasibility of optical coherence tomography guided thrombus aspiration in patients with non-ST-elevation myocardial infarction after initial conservative therapy – A pilot study
by Wieringa, Wouter G and Lexis, Chris P.H and Diercks, Gilles F.H and Lipsic, Erik and Tan, Eng-Shiong and Schurer, Remco A.J and van der Werf, Hindrik W and van den Heuvel, Ad F.M and Suurmeijer, Albert J.H and Zijlstra, Felix and de Smet, Bart J.G.L and Pundziute, Gabija
International Journal of Cardiology, ISSN 0167-5273, 10/2013, Volume 168, Issue 5, pp. 4981 - 4982
Cardiovascular | Thrombus aspiration | Optical coherence tomography | Non-STEMI | Coronary artery disease | PERCUTANEOUS CORONARY INTERVENTION | PROGNOSTIC VALUE | CARDIAC & CARDIOVASCULAR SYSTEMS | Prospective Studies | Tomography, Optical Coherence | Humans | Risk Factors | Male | Treatment Outcome | Feasibility Studies | Coronary Thrombosis - therapy | Myocardial Infarction - therapy | Pilot Projects | Thrombectomy - methods | Electrocardiography | Female | Aged | Care and treatment | Thrombosis | Heart attack | Blood clot
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16. Full Text Insulin-like growth factors and insulin-like growth factor-binding proteins in relation to disease status and incidence of hypoglycaemia in patients with a gastrointestinal stromal tumour
by Rikhof, B and Doorn, J. van and Suurmeijer, A.J.H and Rautenberg, M.W and Groenen, P.J.T.A and Verdijk, M.A.J and Jager, P.L and Jong, S. de and Gietema, J.A and Graaf, W.T.A. van der
Annals of Oncology, ISSN 0923-7534, 2009, Volume 20, Issue 9, pp. 1582 - 1588
OBJECTIVE: Patients with a gastrointestinal stromal tumour (GIST) suffering from non-islet cell tumour-induced hypoglycaemia (NICTH), being associated with... 
Non-islet cell tumour-induced hypoglycaemia | Imatinib | IGFBP-2 | Gastrointestinal stromal tumour | IGF-II | ISLET CELL TUMOR | FACTOR-II | gastrointestinal stromal tumour | BLOOD-GLUCOSE | imatinib | SERUM | CANCER | ONCOLOGY | non-islet cell tumour-induced hypoglycaemia | EMISSION-TOMOGRAPHY | EXPRESSION | CARCINOMA | IMATINIB MESYLATE | Hypoglycemia - epidemiology | Biomarkers, Tumor - analysis | Cyst Fluid - chemistry | Humans | Middle Aged | Insulin-Like Growth Factor Binding Proteins - blood | Male | Incidence | Young Adult | Hypoglycemia - etiology | Gastrointestinal Stromal Tumors - blood | Gastrointestinal Stromal Tumors - pathology | Aged, 80 and over | Adult | Female | Gastrointestinal Stromal Tumors - complications | Aged | Hypoglycemia - blood | Cyst Fluid - metabolism | Somatomedins - analysis
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17. Full Text Response: The value of sentinel lymph node biopsy in the management of head and neck melanoma
by Doting, M.H.E and de Vries, M and Plukker, J.T and Jager, P.L and Post, W.J and Suurmeijer, A.J and Hoekstra, H.J
Journal of Surgical Oncology, ISSN 0022-4790, 05/2007, Volume 95, Issue 6, pp. 523 - 523
SURGERY | RISK | SELECTIVE LYMPHADENECTOMY | ONCOLOGY | INCREASE
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