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1Academic Journal
المؤلفون: Weinsheimer, Shantel, Nelson, Jeffrey, Abla, Adib A, Ko, Nerissa U, Tsang, Cynthia, Okoye, Obiora, Zabramski, Joseph M, Akers, Amy, Zafar, Atif, Mabray, Marc C, Hart, Blaine L, Morrison, Leslie, McCulloch, Charles E, Kim, Helen, Brain Vascular Malformation Consortium Cerebral Cavernous Malformation Investigator Group *
المصدر: Journal of the American Heart Association. 12(3)
مصطلحات موضوعية: Brain Vascular Malformation Consortium Cerebral Cavernous Malformation Investigator Group *, Humans, Hemangioma, Cavernous, Central Nervous System, Intracranial Hemorrhages, Cerebral Hemorrhage, Central Nervous System Vascular Malformations, Risk Factors, cerebral cavernous malformation, familial, hemorrhage, risk factor, Stroke, Clinical Research, Brain Disorders, Neurosciences, Rare Diseases, Aetiology, 2.1 Biological and endogenous factors, Cardiorespiratory Medicine and Haematology
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/1m7870fk
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2Academic Journal
المؤلفون: Cardinell, Jillian L, Ramjist, Joel M, Chen, Chaoliang, Shi, Weisong, Nguyen, Nhu Q, Yeretsian, Tiffany, Choi, Matthew, Chen, David, Clark, Dewi S, Curtis, Anne, Kim, Helen, Faughnan, Marie E, Yang, Victor XD
المصدر: Scientific Reports. 12(1)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Engineering, Biomedical Engineering, Bioengineering, Rare Diseases, Hematology, Biomedical Imaging, 4.2 Evaluation of markers and technologies, Detection, screening and diagnosis, Angiography, Clinical Trials as Topic, Fractals, Humans, Image Interpretation, Computer-Assisted, Microcirculation, Neovascularization, Pathologic, Pattern Recognition, Automated, Pilot Projects, Predictive Value of Tests, Regional Blood Flow, Skin, Telangiectasia, Hereditary Hemorrhagic, Tomography, Optical Coherence, Brain Vascular Malformation Consortium HHT Investigator Group
وصف الملف: application/pdf
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3Academic Journal
المؤلفون: Thompson, KP, Nelson, J, Kim, H, Pawlikowska, L, Marchuk, DA, Lawton, MT, Faughnan, Marie E
المصدر: Orphanet Journal of Rare Diseases. 16(1)
مصطلحات موضوعية: Digestive Diseases, Rare Diseases, Hematology, Good Health and Well Being, Activin Receptors, Type II, Arteriovenous Fistula, Endoglin, Humans, Prospective Studies, Retrospective Studies, Telangiectasia, Hereditary Hemorrhagic, Hereditary hemorrhagic telangiectasia, Vascular malformation, Arteriovenous malformation, Telangiectasia, Predictors of mortality, Brain Vascular Malformation Consortium HHT Investigator Group, Other Medical and Health Sciences, Genetics & Heredity
وصف الملف: application/pdf
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4Academic Journal
المؤلفون: Thompson, KP, Nelson, J, Kim, H, Weinsheimer, SM, Marchuk, DA, Lawton, MT, Krings, T, Faughnan, ME
المصدر: Orphanet Journal of Rare Diseases. 16(1)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Clinical Sciences, Clinical Research, Genetics, Neurosciences, Rare Diseases, Brain Disorders, Hematology, Activin Receptors, Type II, Arteriovenous Fistula, Central Nervous System Vascular Malformations, Endoglin, Humans, Intracranial Arteriovenous Malformations, Prospective Studies, Telangiectasia, Hereditary Hemorrhagic, Brain Vascular Malformation Consortium HHT Investigator Group, Other Medical and Health Sciences, Genetics & Heredity, Clinical sciences
وصف الملف: application/pdf
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5Academic Journal
المؤلفون: Kilian, Alexandra, Latino, Giuseppe A, White, Andrew J, Clark, Dewi, Chakinala, Murali M, Ratjen, Felix, McDonald, Jamie, Whitehead, Kevin, Gossage, James R, Lin, Doris, Henderson, Katharine, Pollak, Jeffrey, McWilliams, Justin P, Kim, Helen, Lawton, Michael T, Faughnan, Marie E, the Brain Vascular Malformation Consortium HHT Investigator Group
المصدر: Journal of clinical medicine. 9(9)
مصطلحات موضوعية: the Brain Vascular Malformation Consortium HHT Investigator Group, ACVRL1, ENG, Hereditary hemorrhagic telangiectasia, SMAD4, arteriovenous malformation, genotype–phenotype correlation, pediatrics, genotype-phenotype correlation, Clinical Sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/1c81h48r
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6Academic Journal
المؤلفون: Meybodi, Ali Tayebi, Kim, Helen, Nelson, Jeffrey, Hetts, Steven W, Krings, Timo, terBrugge, Karel G, Faughnan, Marie E, Lawton, Michael T, Brain Vascular Malformation Consortium HHTInvestigator Group
المصدر: Neurosurgery. 82(1)
مصطلحات موضوعية: Brain Vascular Malformation Consortium HHTInvestigator Group, Brain, Humans, Intracranial Arteriovenous Malformations, Central Nervous System Vascular Malformations, Telangiectasia, Hereditary Hemorrhagic, Treatment Outcome, Retrospective Studies, Databases, Factual, Adolescent, Adult, Aged, Middle Aged, Child, Child, Preschool, Infant, Female, Male, Young Adult, AVM grading, Arteriovenous malformation, Brain vascular malformation consortium, Embolization, Hereditary hemorrhagic telangiectasia, Microsurgical resection, Radiosurgery, Rendu-Osler-Weber disease, Neurosciences, Pediatric, Clinical Research, Brain Disorders, Rare Diseases, Congenital Structural Anomalies, Clinical Sciences, Neurology & Neurosurgery
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/4hr4f52f
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7Academic Journal
المؤلفون: Pawlikowska, Ludmila, Nelson, Jeffrey, Guo, Diana E, McCulloch, Charles E, Lawton, Michael T, Kim, Helen, Faughnan, Marie E, Brain Vascular Malformation Consortium HHT Investigator Group
المصدر: Molecular genetics & genomic medicine. 6(3)
مصطلحات موضوعية: Brain Vascular Malformation Consortium HHT Investigator Group, Liver, Lung, Brain, Humans, Intracranial Arteriovenous Malformations, Intracranial Hemorrhages, Central Nervous System Vascular Malformations, Telangiectasia, Hereditary Hemorrhagic, Transforming Growth Factor beta, Genotype, Phenotype, Mutation, Adult, Aged, Middle Aged, Female, Male, Vascular Malformations, Genetic Association Studies, arteriovenous malformation, genetic modifiers, hereditary hemorrhagic telangiectasia, intracerebral hemorrhage, vascular malformation, Rare Diseases, Stroke, Congenital Structural Anomalies, Pediatric, Genetics, Neurosciences, Aetiology, 2.1 Biological and endogenous factors, Medicinal and Biomolecular Chemistry, Clinical Sciences
وصف الملف: application/pdf
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8Academic Journal
المؤلفون: Pawlikowska, Ludmila, Nelson, Jeffrey, Guo, Diana E, McCulloch, Charles E, Lawton, Michael T, Young, William L, Kim, Helen, Faughnan, Marie E, Brain Vascular Malformation Consortium HHT Investigator Group
المصدر: American journal of medical genetics. Part A. 167(6)
مصطلحات موضوعية: Brain Vascular Malformation Consortium HHT Investigator Group, Liver, Brain, Humans, Telangiectasia, Hereditary Hemorrhagic, Activin Receptors, Type II, Receptors, Cell Surface, Antigens, CD, Logistic Models, Gene Expression, Heterozygote, Phenotype, Mutation, Polymorphism, Single Nucleotide, Adult, Aged, Middle Aged, Female, Male, Vascular Malformations, Endoglin, arteriovenous malformation, genetic modifier, hereditary hemorrhagic telangiectasia, phenotype, vascular malformation, Genetics, Hematology, Clinical Research, Rare Diseases, Stem Cell Research, Stem Cell Research - Nonembryonic - Non-Human, Pediatric, Aetiology, 2.1 Biological and endogenous factors, Clinical Sciences
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/4155b3k8
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9Academic Journal
المؤلفون: Krings, T, Kim, H, Power, S, Nelson, J, Faughnan, ME, Young, WL, terBrugge, KG, Brain Vascular Malformation Consortium HHT Investigator Group
المصدر: AJNR. American journal of neuroradiology. 36(5)
مصطلحات موضوعية: Brain Vascular Malformation Consortium HHT Investigator Group, Humans, Intracranial Arteriovenous Malformations, Telangiectasia, Hereditary Hemorrhagic, Radiography, Adult, Middle Aged, Female, Male, Genetic Association Studies, Genetics, Congenital Structural Anomalies, Pediatric, Neurosciences, Rare Diseases, Clinical Sciences, Nuclear Medicine & Medical Imaging
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/1m62c70x
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10Academic Journal
المؤلفون: Kim, Helen, Nelson, Jeffrey, Krings, Timo, terBrugge, Karel G, McCulloch, Charles E, Lawton, Michael T, Young, William L, Faughnan, Marie E, Brain Vascular Malformation Consortium HHT Investigator Group
المصدر: Stroke. 46(5)
مصطلحات موضوعية: Brain Vascular Malformation Consortium HHT Investigator Group, Humans, Intracranial Arteriovenous Malformations, Intracranial Hemorrhages, Aneurysm, Ruptured, Telangiectasia, Hereditary Hemorrhagic, Recurrence, Survival Analysis, Retrospective Studies, Cohort Studies, Socioeconomic Factors, Adolescent, Adult, Aged, Middle Aged, Child, Child, Preschool, Infant, Infant, Newborn, Female, Male, Young Adult, arteriovenous malformations, cerebral hemorrhage, natural history, telangiectasia, hereditary hemorrhagic, Neurosciences, Prevention, Rare Diseases, Stroke, Brain Disorders, Pediatric, Congenital Structural Anomalies, Cardiorespiratory Medicine and Haematology, Clinical Sciences, Neurology & Neurosurgery
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/6w48f3xp
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11Academic Journal
المؤلفون: Choquet, Hélène, Pawlikowska, Ludmila, Nelson, Jeffrey, McCulloch, Charles E, Akers, Amy, Baca, Beth, Khan, Yasir, Hart, Blaine, Morrison, Leslie, Kim, Helen, Brain Vascular Malformation Consortium (BVMC) Study
المصدر: Cerebrovascular diseases (Basel, Switzerland). 38(6)
مصطلحات موضوعية: Brain Vascular Malformation Consortium (BVMC) Study, Brain, Humans, Hemangioma, Cavernous, Central Nervous System, Cerebral Hemorrhage, Inflammation, Microtubule-Associated Proteins, Receptors, Interleukin-6, Receptors, Transforming Growth Factor beta, Proto-Oncogene Proteins, Interleukin-4, Magnetic Resonance Imaging, Severity of Illness Index, Genes, MHC Class II, Polymorphism, Genetic, Adolescent, Adult, Aged, Aged, 80 and over, Middle Aged, Child, Female, Male, Scavenger Receptors, Class A, Toll-Like Receptor 4, Young Adult, KRIT1 Protein, Lipopolysaccharide Receptors, Receptor, Transforming Growth Factor-beta Type II, Hispanic or Latino, Protein Serine-Threonine Kinases, Rare Diseases, Neurosciences, Brain Disorders, Clinical Research, Genetics, 2.1 Biological and endogenous factors, Aetiology, Cerebral cavernous malformation, CCM1 disease severity, Intracerebral hemorrhage, Brain lesion count, Inflammation and immune response modifier genes, Clinical Sciences, Neurology & Neurosurgery
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/02v4g1n5
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12
المؤلفون: Helen Kim, Marie E. Faughnan, K. P. Thompson, Michael T. Lawton, Douglas A. Marchuk, Jeffrey Nelson, Ludmilla Pawlikowska
المصدر: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Orphanet journal of rare diseases, vol 16, iss 1
Orphanet Journal of Rare Diseasesمصطلحات موضوعية: medicine.medical_specialty, Anemia, Activin Receptors, Activin Receptors, Type II, Population, lcsh:Medicine, Vascular malformation, Type II, Arteriovenous malformation, Rare Diseases, Internal medicine, medicine, otorhinolaryngologic diseases, Humans, Pharmacology (medical), Prospective Studies, Hereditary Hemorrhagic, education, Telangiectasia, Brain Vascular Malformation Consortium HHT Investigator Group, Genetics (clinical), Retrospective Studies, Genetics & Heredity, education.field_of_study, Other Medical and Health Sciences, Proportional hazards model, business.industry, Research, lcsh:R, Endoglin, ACVRL1, Hematology, General Medicine, medicine.disease, Predictors of mortality, Good Health and Well Being, Hereditary hemorrhagic telangiectasia, Arteriovenous Fistula, Life expectancy, Telangiectasia, Hereditary Hemorrhagic, medicine.symptom, Digestive Diseases, business
وصف الملف: application/pdf