-
1Academic Journal
المؤلفون: Magalí Fernández, María Laura Casaux, Martín Fraga, Rafael Vignoli, Inés Bado, Pablo Zunino, Ana Umpiérrez
المصدر: Microorganisms; Volume 11; Issue 7; Pages: 1704
مصطلحات موضوعية: Shiga toxin-producing E. coli, dairy calf, mortality, MDR STEC
جغرافية الموضوع: agris
وصف الملف: application/pdf
Relation: Gut Microbiota; https://dx.doi.org/10.3390/microorganisms11071704
-
2
المؤلفون: Francis O. Walker, Juliette Harris, Holly Delgado, David Simon, Paul J. Tuite, Jayaraman Rao, Kelly E. Lyons, Tilak Mendis, Bala V. Manyam, Joanna Hamman, Deborah Fontaine, Terry Reed, William C. Nichols, Sharon Evans, Joanne Wojcieszek, Peggy Gray, Anette Nieves, Carson Reider, P. Michael Conneally, W.R. Wayne Martin, Kathy Davis, Christine Hunter, Daniel D. Truong, John M. Bertoni, Hubert H. Fernandez, Joseph H. Friedman, Nathan Pankratz, Margaret C. Lannon, Kenneth Marek, Maryan DeAngelis, Mark Stacy, Debra Berry, Mariann DiMinno, Robyn Schacherer, Becky Dunlop, Michel Panisset, Carmen Serrano Ramos, Alice Rudolph, Tatiana Foroud, Theresa A. Zesiewicz, David Grimes, An Tran, Joan Werner, Jean Hall, Sandra Roque, Magali Fernandez, Joseph Jankovic, Michael J. Aminoff, Rachel Saunders Pullman, Maureen A. Leehey, Cliff Shults, Deborah Judd, William C. Koller, Mark Forrest Gordon, Cheryl Halter, Ali H. Rajput, Pam Andrews, Stephen G. Reich, Theresa Derian, Alex Rajput, Stephanie Thomas, Galit Kleimer-Fisman, Susan Mendick, Robert A. Hauser, Danna Jennings, Paul Gordon, Stewart A. Factor, Peter A. LeWitt, Un Jung Kang, Karyn Boyar, Ronald F. Pfeiffer, Robert L. Rodnitzky, Jean P. Hubble, Jeannine Petit, Mayank Pathak, Julie H. Carter, Maureen Cook, William J. Weiner, Rajesh Pahwa, Christopher F. O'Brien, Karen Marder, Joan Young, Judith Dobson, Richard Camicioli, Lawrence Elmer, Jo Belden, Julie So, Theresa Shirley, Anthony E. Lang, Roger Kurlan, Kelli Williamson, Brenda Pfeiffer, Victoria Hunt, Sean K. Uniacke, Clifford W. Shults, Karen Blindauer, Lauren Seeberger, Brian Wulbrecht, Carolyn Peterson
المصدر: Movement Disorders. 19:649-655
مصطلحات موضوعية: Adult, Heterozygote, Parkinson's disease, Adolescent, Locus (genetics), Disease, Biology, Loss of heterozygosity, Central nervous system disease, Exon, Degenerative disease, Nuclear Receptor Subfamily 4, Group A, Member 2, medicine, Humans, Point Mutation, Genetic Predisposition to Disease, Aged, Aged, 80 and over, Genetics, Polymorphism, Genetic, Homozygote, Parkinson Disease, Middle Aged, medicine.disease, Introns, DNA-Binding Proteins, Neurology, Immunology, Cohort, DNA Transposable Elements, Neurology (clinical), Transcription Factors
-
3
المؤلفون: Thomas D. Bird, Hillary Lipe, Wendy H Raskind, John Wolff, Mark Matsushita, Magali Fernandez
المصدر: Neurology. 57:106-110
مصطلحات موضوعية: Adult, Genetic Markers, Male, Candidate gene, Adolescent, Genetic Linkage, Movement, Locus (genetics), Biology, Benign hereditary chorea, Chorea, Genetic linkage, medicine, Humans, Coding region, GTP Cyclohydrolase, Aged, Genes, Dominant, Chromosomes, Human, Pair 14, Recombination, Genetic, Genetics, Middle Aged, Pedigree, Genetic marker, Mutation, Female, Neurology (clinical), Lod Score, medicine.symptom, BCH code
-
4
المؤلفون: Hillary Lipe, Mark Matsushita, Thomas D. Bird, Wendy H. Raskind, John Wolff, Magali Fernandez, Eric C. Yuen, William D. Graf
المصدر: Annals of Neurology. 49:486-492
مصطلحات موضوعية: Episodic ataxia, Genetics, Choreoathetosis, Chorea, Locus (genetics), Paroxysmal dyskinesia, medicine.disease, Benign hereditary chorea, Neurology, Dyskinesia, medicine, Neurology (clinical), Myokymia, medicine.symptom, Psychology
-
5
المصدر: Blood. 93:2208-2216
مصطلحات موضوعية: Immunology, Intron, Promoter, Cell Biology, Hematology, Biology, Biochemistry, Molecular biology, Viral vector, hemic and lymphatic diseases, Gene expression, Expression cassette, Enhancer, Gene, Locus control region
-
6
المؤلفون: Karen Williams, Carolyn Peterson, S. Narayan, Margaret F. Turk, Julie H. Carter, C. Schell, Carlos Singer, Chad W. Christine, Paul J. Tuite, Robyn Schacherer, J. Whetteckey, S. Phipps, Diane K. Marek, William C. Nichols, John M. Bertoni, A. H. Rajput, Kenneth Marek, An Tran, P. Ryan, J. Hevezi, Joan Werner, Kelvin L. Chou, S. Chouinard, James Sutton, Margaret C. Lannon, T. Ajax, Joan Young, Deborah Judd, L. Zelaya, David Grimes, Magali Fernandez, Theresa A. Zesiewicz, Mark Stacy, Peggy Gray, Debra Berry, Michael J. Aminoff, C. Horn, C. Costan-Toth, J. Mannetter, Patricia Simpson, Susan Rolandelli, Tatiana Foroud, T. Tra, S. Wilson, Judith Dobson, Nestor Galvez-Jimenez, Donna Schwieterman, Shirley Uy, K. Price, J. Wojcieszek, Anette Nieves, Paul Atchison, Susan Bennett, L. Klassen, A. Podichetty, Vincent Calabrese, Becky Dunlop, D. Kamp, Holly Delgado, Sandra Roque, Maureen A. Leehey, Richard Camicioli, Julie So, Jayaraman Rao, Kelly E. Lyons, Kapil D. Sethi, A. Wang, Lynn Marlor, David Oakes, S. Culver, Juan Sanchez-Ramos, L. Woodward, J. Danielson, Jeannine Petit, Joann Belden, E. Licari, M. Meacham, Deborah Fontaine, Sharon Evans, C. Stone, S. Morehouse, Christopher F. O'Brien, G. Podskalny, J. Fraser, Anthony E. Lang, W.R. Wayne Martin, Carmen Serrano, H. Poiffaut, Stewart A. Factor, Joanne Wojcieszek, S. Belber, L. Davis, C. Allen, J. Hall, Judy Richman, Joseph Jankovic, Carson Reider, Stephen G. Reich, Stephanie Thomas, Kathy Davis, Richard B. Dewey, Karen Marder, T. Demarcaida, A. Kaczmarek, Lauren Seeberger, C. Halter, Mary Lou Klimek, Donald S. Higgins, Miodrag Velickovic, Joanna Hamann, Eric Siemers, E. Ohmann, C. Dingmann, Galit Kleiner-Fisman, Shari Niswonger, Theresa Derian, Maryan DeAngelis, Aileen Shinaman, Tilak Mendis, M. Rundle, Susan Mendick, L. Giffin, Karen Blindauer, Paul Gordon, Andrew Feigin, L. Shulman, Maureen Cook, Brian Wulbrecht, Rajesh Pahwa, T. Foroud, Un Jung Kang, Arthur Watts, Oksana Suchowersky, C. Joubert, J. Vo, Mandar Jog, M. Panisset, Roberta Winnick, Ronald F. Pfeiffer, Barbara Shannon, Jean P. Hubble, Clifford W. Shults, T. Gales, Tanya Simuni, M. Wolff, Hubert H. Fernandez, Pam Andrews, Karyn Boyar, Brad A. Racette, Vicki Hunt, Christine Hunter, Daniel D. Truong, L. Good, Robert L. Rodnitzky, P. Rodriguez, Sandra K. Kostyk, T. Shirley, Cheryl Halter, Peter A LeWitt, W. Weiner, Ryan J. Uitti, Lisa Scollins, Marc L. Gordon, J. Carpenter, Alice Rudolph, Lewis Sudarsky, Robert A. Hauser, Cliff Shults, Bala V. Manyam, Francis O. Walker, Juliette Harris, Marguerite Wieler, K. Dustin, Kelli Williamson, Brenda Pfeiffer, William C. Koller, Frederick J. Marshall, V. Hagen, A. Campbell, B. Hutchinson, L. Elmer, Anja Rudolph, K. Haas, Tori Ross, Rachel Saunders-Pullman, Nathan Pankratz, E. Aiken, Mariann DiMinno, Peggy Roberge, Arif Dalvi, B. Hayward, Mayank Pathak, David Simon, Michael W. Pauciulo, Holly A. Shill, M. Marotta-Kollarus, K. Ligon, Alok Sahay, Joseph H. Friedman, Neal Hermanowicz, E. Julian-Baros, Irenita Gardiner, N. Luong, Danna Jennings, R. Kurlan, P. M. Conneally
المصدر: Movement Disorders. 22:254-256
مصطلحات موضوعية: Adult, Male, Parkinson's disease, Adolescent, Genotype, Arginine, Guanine, Protein Serine-Threonine Kinases, Biology, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, medicine.disease_cause, Diagnosis, Differential, chemistry.chemical_compound, Degenerative disease, medicine, Humans, Point Mutation, Aged, Aged, 80 and over, Genetics, Mutation, Substitution (logic), Adenine Nucleotide Translocator 1, Genetic Variation, Parkinson Disease, Middle Aged, medicine.disease, LRRK2, nervous system diseases, Amino Acid Substitution, Neurology, chemistry, Female, Neurology (clinical), Carrier Proteins
-
7
المؤلفون: Karen Blindauer, Lauren Seeberger, Brian Wulbrecht, Joan Young, Victoria Hunt, Judith Dobson, Lisa Byder, Clifford W. Shults, Deborah Fontaine, William C. Nichols, P. Michael Conneally, Carolyn Peterson, Julie H. Carter, Hubert H. Fernandez, Margaret C. Lannon, William C. Koller, Joanne Wojcieszek, Lawrence Elmer, Jayaraman Rao, Mark Stacy, Jo Belden, Bala V. Manyam, Julie So, Theresa Shirley, Stephen G. Reich, Stephanie Thomas, John M. Bertoni, Peggy Gray, Marguerite Wieler, Anette Nieves, Rachel Saunders Pullman, Mayank Pathak, Kenneth Marek, Debra Berry, Holly Delgado, Christopher F. O'Brien, Anthony E. Lang, Karen Marder, Ali H. Rajput, Eric Siemers, Cheryl Halter, Michel Panisset, Galit Kleimer-Fisman, Kelly E. Lyons, Robyn Schacherer, Richard Camicioli, Tatiana Foroud, Alex Rajput, Carson Reider, Kathy Davis, Robert A. Hauser, Theresa A. Zesiewicz, Deborah Judd, Susan Mendick, Maryan De Angelis, Sandra Roque, Alice Rudolph, Becky Dunlop, An Tran, Maureen Cook, Christine Hunter, Daniel D. Truong, Stewart A. Factor, Michael J. Aminoff, David Oakes, Sharon Evans, Paul J. Tuite, Jean Hall, David Grimes, W.R. Wayne Martin, Magali Fernandez, Joanna Hamman, Francis O. Walker, Pam Andrews, Karyn Boyar, Juliette Harris, Tilak Mendis, Nathan Pankratz, Mariann DiMinno, Robert L. Rodnitzky, Rajesh Pahwa, Peter A. LeWitt, Jeannine Petit, William J. Weiner, Un Jung Kang, Joseph Jankovic, Ronald F. Pfeiffer, Aileen Shinaman, Jean P. Hubble, Mark Forrest Gordon, Danna Jennings, Joseph H. Friedman, Carmen Serrano Ramos, Roger Kurlan, Kelli Williamson, Brenda Pfeiffer, Frederick J. Marshall
المصدر: Movement disorders : official journal of the Movement Disorder Society. 21(1)
مصطلحات موضوعية: Apolipoprotein E, Adult, Lewy Body Disease, Male, Risk, medicine.medical_specialty, Pathology, Parkinson's disease, Adolescent, Genotype, Apolipoprotein E4, Statistics as Topic, Disease, Neuropsychological Tests, Apolipoproteins E, Alzheimer Disease, Internal medicine, mental disorders, medicine, Dementia, Humans, Allele, Risk factor, Alleles, Aged, Aged, 80 and over, Neurologic Examination, business.industry, Genetic Carrier Screening, Homozygote, Parkinson Disease, Middle Aged, medicine.disease, Survival Analysis, Neurology, lipids (amino acids, peptides, and proteins), Female, Neurology (clinical), Alzheimer's disease, Age of onset, business, Mental Status Schedule
-
8
المؤلفون: Carolyn Peterson, Peggy Gray, Anette Nieves, Julie H. Carter, Lauren Seeberger, William C. Nichols, John M. Bertoni, Anja Rudolph, Francis O. Walker, Juliette Harris, L. Liu, Un Jung Kang, P. M. Conneally, Kenneth Marek, Alex Rajput, Shirley Uy, Michael Panisset, Becky Dunlop, Margaret C. Lannon, Stephen G. Reich, Frederick J. Marshall, Kelly E. Lyons, Stephanie Thomas, Karen Bindauer, Ronald F. Pfeiffer, Maryan DeAngelis, David Oakes, William J. Weiner, Jean P. Hubble, Joseph H. Friedman, Deborah Fontaine, Victoria Hunt, Karyn Boyer, Richard Camicioli, Julie So, Theresa Shirley, Christopher F. O'Brien, Carmen Serrano Ramos, Sean K. Uniacke, Lawrence I. Golbe, Eric Siemers, Roger Kurlan, Kelli Williamson, Cheryl Halter, Brenda Pfeiffer, Karen Marder, Jean Hall, Clifford W. Shults, Peter A. LeWitt, Lisa Scollins, Judith Dobson, Robert L. Rodnitzky, Lawrence Elmer, Hubert H. Fernandez, Jeannine Petit, Tatiana Foroud, Susan Mendick, Deborah Judd, Joseph Jankovic, Paul Gordon, Anhoa Tran, Rajesh Pahwa, Aileen Shinaman, Sandra Roque, Paul J. Tuite, David Simon, Joanna Hamann, Danna Jennings, Christine Hunter, Daniel D. Truong, Holly Delgado, Theresa A. Zesiewicz, Pamela Andrews, Michael J. Aminoff, Mark Stacy, Debra Berry, Sharon Evans, W.R. Wayne Martin, Robert A. Hauser, Nathan Pankratz, Mariann DiMinno, William C. Koller, Bala V. Manyam, Marguerite Wieler, Carson Reider, Kathy Davis, Mayank Pathak, Patricia Simpson, Mark Forrest Gordon, David Grimes, Magali Fernandez, Joann Belden, Joanne Wojcieszek, Robyn Schacherer, Tilak Mendis, Rachel Saunders Pullman, Ali H. Rajput, Juan Sanchez-Ramos, Stewart A. Factor
المصدر: Scopus-Elsevier
مصطلحات موضوعية: Genetics, Mutation, Heterozygote, Ubiquitin-Protein Ligases, Parkinson Disease, Biology, Middle Aged, medicine.disease_cause, Genetic determinism, Parkin, nervous system diseases, Loss of heterozygosity, Genotype, North America, medicine, Humans, Neurology (clinical), Genetic Testing, Allele, Age of onset, Age of Onset, Exome sequencing, Aged
-
9
المؤلفون: Charis Eng, Lauri A. Aaltonen, Magali Fernandez, Maija Ht Kiuru
المصدر: Nature reviews. Cancer. 3(3)
مصطلحات موضوعية: Heterozygote, Free Radicals, General Mathematics, Citric Acid Cycle, Neovascularization, Physiologic, Apoptosis, Disease, Pheochromocytoma, Biology, Fumarate Hydratase, Paraganglioma, Mitochondrial Encephalomyopathies, Multienzyme Complexes, Neoplastic Syndromes, Hereditary, Leiomyomatosis, medicine, Humans, Gene, Carcinoma, Renal Cell, Mitochondrial enzymes, chemistry.chemical_classification, Genetics, Applied Mathematics, Succinate dehydrogenase, Electron Transport Complex II, Homozygote, Cancer, medicine.disease, Kidney Neoplasms, Mitochondria, Succinate Dehydrogenase, Protein Subunits, Enzyme, Tumour development, chemistry, Fumarase, Mutation, biology.protein, Energy Metabolism, Oxidoreductases, Forecasting
-
10
المؤلفون: Zoran Brkanac, Hillary Lipe, Laura Bylenok, Magali Fernandez, John Wolff, David Nochlin, Wendy H. Raskind, Thomas D. Bird, Mark Matsushita
المصدر: Archives of neurology. 59(8)
مصطلحات موضوعية: Adult, Male, Spinocerebellar Ataxia Type 1, Adolescent, Genetic Linkage, Locus (genetics), Biology, Centimorgan, Arts and Humanities (miscellaneous), Autosomal dominant cerebellar ataxia, Genetic linkage, medicine, Humans, Spinocerebellar Ataxias, Child, Genes, Dominant, Genetics, Cerebellar ataxia, Chromosome Mapping, Middle Aged, medicine.disease, Penetrance, Pedigree, Spinocerebellar ataxia, Female, Neurology (clinical), medicine.symptom, Chromosomes, Human, Pair 19
-
11
المؤلفون: John Wolff, Mark Matsushita, Hilary Lipe, Thomas D. Bird, Wendy H. Raskind, Zoran Brkanac, Magali Fernandez
المصدر: American journal of medical genetics. 114(4)
مصطلحات موضوعية: Adult, Pathology, medicine.medical_specialty, Ataxia, Sensory axonal neuropathy, Adolescent, Cerebellar Ataxia, Molecular Sequence Data, Neurological disorder, Sensory ataxia, medicine, Humans, Child, Genetics (clinical), Aged, Genes, Dominant, Cerebellar ataxia, business.industry, Brain, Chromosome Mapping, Sensory loss, Middle Aged, medicine.disease, Magnetic Resonance Imaging, Pedigree, Muscular Atrophy, Peripheral neuropathy, Spinocerebellar ataxia, medicine.symptom, Lod Score, business, Chromosomes, Human, Pair 7
-
12
المؤلفون: Donna Russo, Cindy Bos, Charis Eng, Kristin A. Waite, Mary Ella M Pierpont, Ellen T. Matloff, Robert Pilarski, Lois A. Greenberg, Magali Fernandez, Gerald L. Feldman, Xiao Ping Zhou, Annette R. Patterson, Heather Hampel, Majed Dasouki, Najah T. Nassif, Jennifer Ivanovich
المصدر: The American Journal of Human Genetics. (2):404-411
مصطلحات موضوعية: Male, medicine.disease_cause, Polymerase Chain Reaction, Germline, Exon, Phosphatidylinositol 3-Kinases, 0302 clinical medicine, Bannayan–Riley–Ruvalcaba syndrome, Genetics(clinical), Promoter Regions, Genetic, Genetics (clinical), Sequence Deletion, Genetics & Heredity, 0303 health sciences, Mutation, biology, Cowden syndrome, Syndrome, Exons, Protein-Serine-Threonine Kinases, 3. Good health, 030220 oncology & carcinogenesis, Uterine Neoplasms, Female, Genotype, Breast Neoplasms, Protein Serine-Threonine Kinases, 03 medical and health sciences, Germline mutation, Report, Proto-Oncogene Proteins, medicine, Genetics, PTEN, Humans, Thyroid Neoplasms, PI3K/AKT/mTOR pathway, Germ-Line Mutation, 030304 developmental biology, Polymorphism, Genetic, Base Sequence, Tumor Suppressor Proteins, PTEN Phosphohydrolase, DNA, medicine.disease, Molecular biology, Phosphoric Monoester Hydrolases, Case-Control Studies, Cancer research, biology.protein, Hamartoma Syndrome, Multiple, Proto-Oncogene Proteins c-akt
وصف الملف: application/pdf
-
13
المؤلفون: Juan Sanchez-Ramos, Paul J. Tuite, Stewart A. Factor, Mark Forrest Gordon, Sharon Evans, W.R. Wayne Martin, Michel Panisset, Patricia Simpson, Joann Belden, Deborah Fontaine, Joanne Wojcieszek, William C. Nichols, P. Michael Conneally, Margaret C. Lannon, Rachel Saunders Pullman, Anhoa Tran, Mark Stacy, Debra Berry, Un Jung Kang, Hubert H. Fernandez, Peggy Gray, Anette Nieves, Joanna Hamann, Ali H. Rajput, Tatiana Foroud, Shirley Uy, Ronald F. Pfeiffer, Jean P. Hubble, Maryan DeAngelis, Mayank Pathak, Sandra Roque, David Simon, Danna Jennings, William J. Weiner, Karyn Boyar, Holly Delgado, Lawrence I. Golbe, Alice Rudolph, Kelly E. Lyons, Tilak Mendis, Joseph H. Friedman, Joseph Jankovic, Carmen Serrano Ramos, Robert L. Rodnitzky, Rajesh Pahwa, Aileen Shinaman, Susan Mendick, Jean Hall, Paul Gordon, Judith Dobson, Nathan Pankratz, Becky Dunlop, Mariann DiMinno, Cliff Shults, Pamela Andrews, Robert A. Hauser, Peter A. LeWitt, Julie So, David Oakes, Theresa Shirley, Carson Reider, Bala V. Manyam, Kathy Davis, Francis O. Walker, Jeannine Petit, Marguerite Wieler, Juliette Harris, Stephen G. Reich, Stephanie Thomas, Christine Hunter, Daniel D. Truong, Eric Siemers, William C. Koller, Julie H. Carter, Theresa A. Zesiewicz, Michael J. Aminoff, David Grimes, Magali Fernandez, Richard Camicioli, Robyn Schacherer, Joan Werner, Christopher F. O'Brien, Karen Marder, Lawrence Elmer, Victoria Hunt, Sean K. Uniacke, Cheryl Halter, Roger Kurlan, Kelli Williamson, Alex Rajput, Brenda Pfeiffer, Lisa Scollins, John M. Bertoni, Kenneth Marek, Karen Blindauer, Lauren Seeberger, Carolyn Peterson, Frederick J. Marshall, Deborah Judd
المصدر: The American Journal of Human Genetics. (4):1053-1057
مصطلحات موضوعية: Genetic Markers, Male, Ubiquitin-Protein Ligases, Pedigree chart, Biology, Genetic determinism, Ligases, 03 medical and health sciences, 0302 clinical medicine, Degenerative disease, Report, medicine, Genetics, Humans, Family, Genetics(clinical), Family history, Genetics (clinical), 030304 developmental biology, Linkage (software), 0303 health sciences, Chromosome, Chromosome Mapping, Parkinson Disease, medicine.disease, Genetic marker, Chromosomes, Human, Pair 2, Female, Alzheimer's disease, Lod Score, 030217 neurology & neurosurgery
-
14
المؤلفون: Zoran Brkanac, Wendy H. Raskind, Thomas D. Bird, Mark Matsushita, Hillary Lipe, Magali Fernandez, Christophe L. M. J. Verlinde, John Wolff, David Nochlin, Patrick J. Cimino, Xiao Jian Tan, Dong Hui Chen, Laura Bylenok
المصدر: The American Journal of Human Genetics. (4):839-849
مصطلحات موضوعية: Male, Models, Molecular, Ataxia, Protein Conformation, Molecular Sequence Data, Mutation, Missense, Ataxin 1, 03 medical and health sciences, 0302 clinical medicine, Reference Values, Genetics, medicine, Humans, Spinocerebellar Ataxias, Missense mutation, Genetics(clinical), Amino Acid Sequence, Conserved Sequence, Protein Kinase C, Genetics (clinical), Genes, Dominant, 030304 developmental biology, 0303 health sciences, Polymorphism, Genetic, Sequence Homology, Amino Acid, biology, Cerebellar ataxia, Articles, medicine.disease, PRKCG Gene, Pedigree, Isoenzymes, Ataxin, biology.protein, Spinocerebellar ataxia, Female, medicine.symptom, Trinucleotide repeat expansion, Sequence Alignment, 030217 neurology & neurosurgery
-
15
المؤلفون: Elena M. Martinez, Magali Fernandez
المصدر: Hispania. 72:968
مصطلحات موضوعية: Linguistics and Language, Education