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1. Full Text Part I: Spinal-cord neoplasms—intradural neoplasms
by Traul, David E, MD and Shaffrey, Mark E, MD and Schiff, David, Dr
Lancet Oncology, The, ISSN 1470-2045, 2007, Volume 8, Issue 1, pp. 35 - 45
Summary Intradural spinal-cord tumours are an uncommon but important consideration in the differential diagnosis of patients with back pain, radicular pain,... 
Hematology, Oncology and Palliative Medicine | FILUM TERMINALE | PROGNOSTIC-FACTORS | ONCOLOGY | INTRAMEDULLARY SUBEPENDYMOMA | POSTOPERATIVE RADIOTHERAPY | FOLLOW-UP | EPENDYMOMAS | OF-THE-LITERATURE | CAUDA-EQUINA | SURGICAL-TREATMENT | TUMORS | Spinal Cord Neoplasms - pathology | Humans | Spinal Cord Neoplasms - classification | Tumors | Pain | Reviews | sensorimotor system | Neurons | Parenchyma | Adjuvants | Differential diagnosis | Glial cells | sphincter | Metastases
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2. Full Text Clinical Outcomes and Late Endocrine, Neurocognitive, and Visual Profiles of Proton Radiation for Pediatric Low-Grade Gliomas
by Greenberger, Benjamin A., AB and Pulsifer, Margaret B., PhD and Ebb, David H., MD and MacDonald, Shannon M., MD and Jones, Robin M., MD and Butler, William E., MD and Huang, Mary S., MD and Marcus, Karen J., MD and Oberg, Jennifer A., ED and Tarbell, Nancy J., MD and Yock, Torunn I., MD
International Journal of Radiation Oncology, Biology, Physics, ISSN 0360-3016, 2014, Volume 89, Issue 5, pp. 1060 - 1068
Purpose/Objective(s) Primary low-grade gliomas are common brain tumors of childhood, many of which require radiation therapy (RT) as definitive treatment.... 
Radiology | Hematology, Oncology and Palliative Medicine | MOYAMOYA SYNDROME | THERAPY | ONCOLOGY | CONFORMAL RADIOTHERAPY | ASTROCYTOMAS | STEREOTACTIC RADIOTHERAPY | HYPOTHALAMIC GLIOMAS | CHILDHOOD | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | OPTIC PATHWAY GLIOMA | BRAIN-TUMORS | CHILDREN | Organs at Risk - radiation effects | Age Factors | Humans | Proton Therapy - adverse effects | Brain Neoplasms - pathology | Child, Preschool | Brain Neoplasms - complications | Glioma - radiotherapy | Glioma - complications | Young Adult | Pituitary Gland - radiation effects | Neoplasm Grading | Glioma - pathology | Retrospective Studies | Spinal Cord Neoplasms - radiotherapy | Brain Neoplasms - mortality | Brain Neoplasms - radiotherapy | Child | Cognition - radiation effects | Optic Chiasm | Radiotherapy Dosage | Glioma - mortality | Treatment Outcome | Intelligence - radiation effects | Brain Neoplasms - drug therapy | Spinal Cord Neoplasms - drug therapy | Spinal Cord Neoplasms - complications | Disease-Free Survival | Spinal Cord Neoplasms - mortality | Adolescent | Hippocampus - radiation effects | Radiotherapy, Conformal - adverse effects | Spinal Cord Neoplasms - pathology | Proton Therapy - methods | Temporal Lobe - radiation effects | Glioma - drug therapy | Radiotherapy, Conformal - methods | Sects | Pediatrics | Medical colleges | Gliomas | Patient outcomes | Radiation | Children | Health aspects | Chemotherapy | Brain tumors | Radiotherapy | Cancer | GLIOMAS | HIPPOCAMPUS | PATIENTS | SPINAL CORD | INJURIES | RADIOLOGY AND NUCLEAR MEDICINE | PEDIATRICS | PROTON BEAMS | RADIATION DOSES | RADIOTHERAPY | CHEMOTHERAPY | HYPOTHALAMUS
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3. Full Text Changing incidence and improved survival of gliomas
by Ho, Vincent K.Y and Reijneveld, Jaap C and Enting, Roelien H and Bienfait, Henri P and Robe, Pierre and Baumert, Brigitta G and Visser, Otto and Dutch Soc Neuro-Oncology LWNO and Dutch Society for Neuro-Oncology (LWNO)
European Journal of Cancer, ISSN 0959-8049, 2014, Volume 50, Issue 13, pp. 2309 - 2318
Abstract Background Tumours of the central nervous system (CNS) represent a relatively rare but serious health burden. This study provides insight into the... 
Hematology, Oncology and Palliative Medicine | Glioma | Glioblastoma | Central nervous system | Oligoastrocytoma | Survival | Astrocytoma | Ependymoma | Oligodendroglioma | Incidence | TRENDS | CANCER | LOW-GRADE GLIOMAS | BRAIN-TUMORS | ADJUVANT TEMOZOLOMIDE | PHASE-3 TRIAL | MALIGNANT GLIOMAS | CENTRAL-NERVOUS-SYSTEM | RADIOTHERAPY | ONCOLOGY | Glioma - mortality | Astrocytoma - epidemiology | Humans | Middle Aged | Netherlands - epidemiology | Brain Neoplasms - pathology | Male | Survival Rate | Glioma - epidemiology | Glioblastoma - epidemiology | Astrocytoma - pathology | Spinal Cord Neoplasms - mortality | Glioblastoma - pathology | Glioma - pathology | Female | Spinal Cord Neoplasms - pathology | Aged | Brain Neoplasms - mortality | Glioblastoma - mortality | Astrocytoma - mortality | Brain Neoplasms - epidemiology | Spinal Cord Neoplasms - epidemiology | Gliomas
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4. Full Text High frequency of H3F3A (K27M) mutations characterizes pediatric and adult high-grade gliomas of the spinal cord
by Gessi, M and Gielen, GH and Dreschmann, V and Waha, A and Pietsch, T
ACTA NEUROPATHOLOGICA, ISSN 0001-6322, 09/2015, Volume 130, Issue 3, pp. 435 - 437
GLIOBLASTOMA | HISTONE H3.3 | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | Spinal Cord - metabolism | Humans | Middle Aged | Brain Neoplasms - pathology | Brain Neoplasms - genetics | Child, Preschool | Infant | Spinal Cord Neoplasms - metabolism | Brain Neoplasms - metabolism | Glioma - metabolism | Glioma - genetics | Young Adult | Histones - genetics | Neoplasm Grading | Spinal Cord - pathology | Glioma - pathology | Adolescent | Biomarkers, Tumor - metabolism | Adult | Spinal Cord Neoplasms - pathology | Mutation | Spinal Cord Neoplasms - genetics | Child | Infant, Newborn
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5. Full Text Statistical Report of Central Nervous System Tumors Histologically Diagnosed in the Sichuan Province of China from 2008 to 2013: A West China Glioma Center Report
by Wang, Xiang and Chen, Jin-xiu and Zhou, Qiao and Liu, Yan-hui and Mao, Qing and You, Chao and Chen, Ni and Xiong, Li and Duan, Jie and Liu, Liang
Annals of Surgical Oncology, ISSN 1068-9265, 12/2016, Volume 23, Issue S5, pp. 946 - 953
Sichuan is a province in the west of China with a population of 81.4 million. This is the first statistical report of central nervous system (CNS) tumors... 
Oncology | Medicine & Public Health | Surgical Oncology | Surgery | SURGERY | ONCOLOGY | EPIDEMIOLOGY | Adenoma - ethnology | Tibet - ethnology | Age Factors | Adenoma - epidemiology | Humans | Middle Aged | Spinal Cord Neoplasms - secondary | Brain Neoplasms - pathology | Child, Preschool | Infant | Male | Incidence | Young Adult | Brain Neoplasms - secondary | Meningioma - epidemiology | Nerve Sheath Neoplasms - pathology | Adult | Female | Meningioma - ethnology | Child | Glioblastoma - ethnology | Infant, Newborn | Spinal Cord Neoplasms - ethnology | Pituitary Neoplasms - epidemiology | Nerve Sheath Neoplasms - epidemiology | Pituitary Neoplasms - pathology | China - epidemiology | Glioblastoma - epidemiology | Meningioma - pathology | Glioblastoma - pathology | Adolescent | Sex Factors | Adenoma - pathology | Brain - pathology | Spinal Cord Neoplasms - pathology | Nerve Sheath Neoplasms - ethnology | Brain Neoplasms - epidemiology | Brain Neoplasms - ethnology | Spinal Cord Neoplasms - epidemiology | Gliomas | Analysis | Brain tumors | Central nervous system | Cancer
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6. Full Text Ependymoma
by Reni, Michele and Gatta, Gemma and Mazza, Elena and Vecht, Charles
Critical Reviews in Oncology and Hematology, ISSN 1040-8428, 2007, Volume 63, Issue 1, pp. 81 - 89
Abstract Ependymomas are rare tumours of neuroectodermal origin classified as myxopapillary ependymoma and subependymoma (grade I), ependymoma (grade II) and... 
Hematology, Oncology and Palliative Medicine | Ependymomas | Treatment | Prognosis | treatment | MOLECULAR-GENETIC ANALYSIS | PROGNOSTIC-FACTORS | POSTERIOR-FOSSA EPENDYMOMAS | SPINAL-CORD EPENDYMOMAS | MALIGNANT BRAIN-TUMORS | CHOROID-PLEXUS TUMORS | prognosis | ependymomas | RADIATION-THERAPY | ONCOLOGY | NERVOUS-SYSTEM TUMORS | CHILDRENS CANCER GROUP | HEMATOLOGY | INTRACRANIAL EPENDYMOMA | Ependymoma - etiology | Age Distribution | Brain Neoplasms - etiology | Humans | Brain Neoplasms - pathology | Male | Spinal Cord Neoplasms - metabolism | Glial Fibrillary Acidic Protein - metabolism | Brain Neoplasms - metabolism | Brain Neoplasms - surgery | Incidence | Infratentorial Neoplasms - metabolism | Ependymoma - diagnosis | Infratentorial Neoplasms - epidemiology | Infratentorial Neoplasms - etiology | Spinal Cord Neoplasms - surgery | Ependymoma - pathology | Female | Spinal Cord Neoplasms - radiotherapy | Brain Neoplasms - radiotherapy | Ependymoma - epidemiology | Infratentorial Neoplasms - radiotherapy | Brain Neoplasms - diagnosis | Risk Factors | Neoplasm Recurrence, Local | Spinal Cord Neoplasms - etiology | Infratentorial Neoplasms - pathology | Ependymoma - metabolism | Ependymoma - surgery | Sex Factors | Spinal Cord Neoplasms - diagnosis | Survival Analysis | Infratentorial Neoplasms - surgery | Spinal Cord Neoplasms - pathology | Neoplasm Staging | Ependymoma - radiotherapy | Infratentorial Neoplasms - diagnosis | Brain Neoplasms - epidemiology | Spinal Cord Neoplasms - epidemiology | Chemotherapy | Cancer | Tumors
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7. Full Text Co‐occurrence of histone H3 K27M and BRAF V600E mutations in paediatric midline grade I ganglioglioma
by Pagès, Mélanie and Beccaria, Kevin and Boddaert, Nathalie and Saffroy, Raphaël and Besnard, Aurore and Castel, David and Fina, Frédéric and Barets, Doriane and Barret, Emilie and Lacroix, Ludovic and Bielle, Franck and Andreiuolo, Felipe and Tauziède‐Espariat, Arnault and Figarella‐Branger, Dominique and Puget, Stéphanie and Grill, Jacques and Chrétien, Fabrice and Varlet, Pascale
Brain Pathology, ISSN 1015-6305, 01/2018, Volume 28, Issue 1, pp. 103 - 111
Ganglioglioma (GG) is a grade I tumor characterized by alterations in the MAPK pathway, including BRAF V600E mutation. Recently, diffuse midline glioma with an... 
BRAF V600E | ganglioglioma | midline | H3 K27M | TUMOR RECURRENCE | INTRINSIC PONTINE GLIOMA | H3F3A | SUBGROUPS | PATHOLOGY | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | POSTERIOR-FOSSA | MOLECULAR CLASSIFICATION | BRAF(V600E) MUTATION | PILOCYTIC ASTROCYTOMA | GENETIC ALTERATIONS | Proteins | Pediatrics | Genetic aspects | Gene mutations | Gliomas | Brain tumors | Brain | Brain cancer | MAP kinase | Patients | Neuronal-glial interactions | Glioma | Quality | Fatalities | Mutation | Diagnosis | Histone H3 | Tumors | Life Sciences | Human health and pathology | Neurons and Cognition | Neurobiology | Genetics | Human genetics | Cancer
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8. Full Text Surgery for spinal cord ependymomas: Outcome and prognostic factors
by Boström, Azize and Von Lehe, Marec and Hartmann, Wolfgang and Pietsch, Torsten and Feuss, Mareike and Boström, Jan P and Schramm, Johannes and Simon, Matthias
Neurosurgery, ISSN 0148-396X, 02/2011, Volume 68, Issue 2, pp. 302 - 309
BACKGROUND: Spinal cord tumors account for 5% to 10% of all primary central nervous system tumors. The most common intramedullary neoplasms are ependymomas,... 
Microsurgery | Myxopapillary ependymoma | McCormick grade | Spinal ependymoma | SURGERY | MANAGEMENT | MYXOPAPILLARY EPENDYMOMAS | POSTOPERATIVE RADIOTHERAPY | ADULTS | RADIATION | CLINICAL NEUROLOGY | PREDICTORS | SURGICAL RESECTION | RETROSPECTIVE ANALYSIS | Prognosis | Humans | Middle Aged | Kaplan-Meier Estimate | Male | Treatment Outcome | Recovery of Function | Young Adult | Disease-Free Survival | Spinal Cord Neoplasms - mortality | Ependymoma - surgery | Ependymoma - mortality | Adolescent | Aged, 80 and over | Spinal Cord Neoplasms - surgery | Adult | Ependymoma - pathology | Female | Spinal Cord Neoplasms - pathology | Aged | Child | Spinal cord | Patients | Medical prognosis | Surgery | Tumors
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9. Full Text Prognostic factors and clinical outcomes in patients with leptomeningeal metastasis from solid tumors
by Waki, Fusako and Waki, Fusako and Ando, Masashi and Ando, Masashi and Takashima, Atsuo and Takashima, Atsuo and Yonemori, Kan and Yonemori, Kan and Nokihara, Hiroshi and Nokihara, Hiroshi and Miyake, Mototaka and Miyake, Mototaka and Tateishi, Ukihide and Tateishi, Ukihide and Tsuta, Koji and Tsuta, Koji and Shimada, Yasuhiro and Shimada, Yasuhiro and Fujiwara, Yasuhiro and Fujiwara, Yasuhiro and Tamura, Tomohide and Tamura, Tomohide
Journal of Neuro-Oncology, ISSN 0167-594X, 6/2009, Volume 93, Issue 2, pp. 205 - 212
Background Leptomeningeal metastasis (LM) occurs in 4–15% of patients with solid tumors. Although the clinical outcomes in cancer patients have been improving... 
Intrathecal chemotherapy | Medicine & Public Health | MRI | Prognostic factor | Oncology | Leptomeningeal metastasis | Cancer | DIAGNOSIS | METHOTREXATE | CYTOLOGY | CHEMOTHERAPY | CLINICAL NEUROLOGY | BREAST-CANCER | MENINGEAL CARCINOMATOSIS | ONCOLOGY | DISEASE | CARCINOMATOUS MENINGITIS | NEOPLASTIC MENINGITIS | Prognosis | Lung Neoplasms - mortality | Humans | Middle Aged | Spinal Cord Neoplasms - secondary | Brain Neoplasms - pathology | Lung Neoplasms - pathology | Male | Stomach Neoplasms - pathology | Young Adult | Brain Neoplasms - secondary | Meningeal Neoplasms - drug therapy | Time Factors | Aged, 80 and over | Adult | Female | Retrospective Studies | Brain Neoplasms - mortality | Meningeal Neoplasms - mortality | Neoplasms - drug therapy | Breast Neoplasms - pathology | Neoplasm Metastasis - pathology | Survival Analysis | Breast Neoplasms - mortality | Spinal Cord Neoplasms - pathology | Aged | Meningeal Neoplasms - pathology | Neoplasms - pathology | Stomach Neoplasms - mortality | Meningeal Neoplasms - secondary | Care and treatment | Chemotherapy | Lung cancer | Patient outcomes | Metastasis | Universities and colleges
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10. Full Text The natural history of hemangioblastomas of the central nervous system in patients with von Hippel-Lindau disease
by Wanebo, John E and Lonser, Russell R and Glenn, Gladys M and Oldfield, Edward H
Journal of Neurosurgery, ISSN 0022-3085, 01/2003, Volume 98, Issue 1, pp. 82 - 94
Object. The goals of this study were to define the natural history and growth pattern of hemangioblastomas of the central nervous system (CNS) that are... 
Neoplasm | Hemangioblastoma | Central nervous system | Von Hippel-Lindau disease | SURGERY | von Hippel-Lindau disease | TUMOR-SUPPRESSOR GENE | PHENOTYPE | hemangioblastoma | RADIOSURGERY | CLINICAL-FEATURES | IDENTIFICATION | CLINICAL NEUROLOGY | central nervous system | FAMILIES | GERMLINE MUTATIONS | neoplasm | GROWTH-FACTOR | RECEPTORS | EXPRESSION | Predictive Value of Tests | Follow-Up Studies | Outcome Assessment (Health Care) | Brain Stem Neoplasms - pathology | Hemangioblastoma - etiology | Humans | Cerebellar Neoplasms - etiology | Male | Spinal Cord Neoplasms - physiopathology | von Hippel-Lindau Disease - complications | von Hippel-Lindau Disease - pathology | Brain Stem Neoplasms - physiopathology | Time Factors | Adult | Female | Retrospective Studies | Cerebellar Neoplasms - pathology | Cerebellar Neoplasms - physiopathology | Severity of Illness Index | Supratentorial Neoplasms - etiology | Supratentorial Neoplasms - pathology | Supratentorial Neoplasms - physiopathology | Brain Stem Neoplasms - etiology | Spinal Cord Neoplasms - etiology | von Hippel-Lindau Disease - physiopathology | Hemangioblastoma - physiopathology | Magnetic Resonance Imaging | Hemangioblastoma - pathology | Spinal Cord Neoplasms - pathology
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11. Full Text Primary spinal cord astroblastoma: Case report
by Yamada, Shoko Merrit and Tomita, Yusuke and Shibui, Soichiro and Takahashi, Mikiko and Kawamoto, Masashi and Nobusawa, Sumihito and Hirato, Junko
Journal of Neurosurgery: Spine, ISSN 1547-5654, 06/2018, Volume 28, Issue 6, pp. 642 - 646
Astroblastoma is a rare tumor that is thought to occur exclusively in the cerebrum. To the authors' knowledge, no cases of spinal cord astroblastoma have been... 
Oncology | Astroblastoma | Spinal cord | Temozolomide | Radiation | Bevacizumab | Neoplasms, Neuroepithelial - therapy | Young Adult | Neoplasms, Neuroepithelial - diagnosis | Diagnosis, Differential | Humans | Spinal Cord Neoplasms - diagnosis | Female | Spinal Cord Neoplasms - pathology | Combined Modality Therapy | Neoplasms, Neuroepithelial - pathology | Recovery of Function | Spinal Cord Neoplasms - therapy | temozolomide | SURGERY | astroblastoma | radiation | bevacizumab | spinal cord | oncology | CLINICAL NEUROLOGY | FEATURES
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12. Full Text Rosette-Forming Glioneuronal Tumor of Spinal Cord
by Collin, Adrien and Adle-Biassette, Homa and Lecler, Augustin
World Neurosurgery, ISSN 1878-8750, 11/2018, Volume 119, pp. 242 - 243
Rosette-forming glioneuronal tumor has recently been included in the World Health Organization classification as a low-grade tumor. It usually occurs in young... 
Spinal | Rosette-forming glioneuronal tumor | Tumor | MRI | RGNT | SURGERY | CLINICAL NEUROLOGY | Spinal Cord Neoplasms - diagnostic imaging | Diagnosis, Differential | Glioma - diagnostic imaging | Glioma - pathology | Humans | Spinal Cord Neoplasms - surgery | Adult | Female | Spinal Cord Neoplasms - pathology | Glioma - surgery | Tumors
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13. Full Text Biology and management of ependymomas
by Wu, Jing and Armstrong, Terri S and Gilbert, Mark R
Neuro-Oncology, ISSN 1522-8517, 07/2016, Volume 18, Issue 7, pp. 902 - 913
Ependymomas are rare primary tumors of the central nervous system in children and adults that comprise histologically similar but genetically distinct... 
ependymoma | Collaborative Ependymoma Research Network | rare disease | management | molecular classification | ADULT PATIENTS | PROGNOSTIC-FACTORS | MALIGNANT BRAIN-TUMORS | REFRACTORY EPENDYMOMA | SPINAL MYXOPAPILLARY EPENDYMOMAS | CLINICAL NEUROLOGY | POSTOPERATIVE CHEMOTHERAPY | IMMUNOHISTOCHEMICAL MARKERS | ONCOLOGY | INFRATENTORIAL EPENDYMOMA | CENTRAL-NERVOUS-SYSTEM | INTRACRANIAL EPENDYMOMA | Glioma, Subependymal - pathology | Animals | Humans | Brain Neoplasms - pathology | Spinal Cord Neoplasms - diagnosis | Brain Neoplasms - genetics | Quality of Life | Ependymoma - pathology | Spinal Cord Neoplasms - pathology | Ependymoma - genetics | Glioma, Subependymal - genetics | Disease Models, Animal | Invited Reviews
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14. Full Text Pathology of Spinal Ependymomas: An Institutional Experience Over 25 Years in 134 Patients
by Tarapore, Phiroz E and Modera, Peter and Naujokas, Agne and Oh, Michael C and Amin, Beejal and Tihan, Tarik and Parsa, Andrew T and Ames, Christopher P and Chou, Dean and Mummaneni, Praveen V and Weinstein, Phillip R
Neurosurgery, ISSN 0148-396X, 08/2013, Volume 73, Issue 2, pp. 247 - 255
BACKGROUND:Ependymomas constitute approximately 40% of primary intraspinal tumors. Current World Health Organization (WHO) grading may not correlate with... 
Myxopapillary | Adjuvant radiation | Classic | Spine | Ependymoma | SURVIVAL | SURGERY | STEM-CELLS | MYXOPAPILLARY EPENDYMOMAS | PROGNOSIS | FOLLOW-UP | CORD EPENDYMOMAS | TUMORS | CLINICAL NEUROLOGY | CHILDREN | OUTCOMES | AGE | Prognosis | Humans | Middle Aged | Male | Ependymoma - therapy | Neoplasm Recurrence, Local - pathology | Young Adult | Neurosurgical Procedures | Neoplasm Grading | Ependymoma - mortality | Adult | Ependymoma - pathology | Female | Retrospective Studies | Radiotherapy, Adjuvant | Child | Spinal Cord Neoplasms - therapy | Kaplan-Meier Estimate | Treatment Outcome | Disease-Free Survival | Magnetic Resonance Imaging | Spinal Cord Neoplasms - mortality | Adolescent | Spinal Cord Neoplasms - pathology | Aged | Neoplasm Recurrence, Local - epidemiology
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