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1دورية أكاديمية
المؤلفون: Rukmani Lekhraj, Shirin Lalezari, Jennifer T. Aguilan, Jiyue Qin, Simone Sidoli, Wenzhu Mowrey, Seema Gollamudi, Parviz Lalezari
المصدر: Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
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2دورية أكاديمية
المؤلفون: Seema Gollamudi, Rukmani Lekhraj, Shirin Lalezari, Parviz Lalezari
المصدر: Alzheimer’s & Dementia: Translational Research & Clinical Interventions, Vol 6, Iss 1, Pp n/a-n/a (2020)
مصطلحات موضوعية: brain, C1GALT1/T‐synthase, COSMC/C1GALT1C1, late‐onset Alzheimer's disease, mutations, Neurology. Diseases of the nervous system, RC346-429, Geriatrics, RC952-954.6
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2352-8737
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3دورية أكاديمية
المؤلفون: Seema Gollamudi, Ashu Johri, Noel Y Calingasan, Lichuan Yang, Olivier Elemento, M Flint Beal
المصدر: PLoS ONE, Vol 7, Iss 5, p e36191 (2012)
وصف الملف: electronic resource
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المؤلفون: Rukmani Lekhraj, Shirin Lalezari, Jennifer T. Aguilan, Jiyue Qin, Simone Sidoli, Wenzhu Mowrey, Seema Gollamudi, Parviz Lalezari
المصدر: Scientific reports. 12(1)
مصطلحات موضوعية: Multidisciplinary, Immunoglobulin M, Alzheimer Disease, Immunoglobulin G, Brain, Humans, Frontal Lobe
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المؤلفون: Parviz Lalezari, Rukmani Lekhraj, Shirin Lalezari, Seema Gollamudi
المصدر: Alzheimer’s & Dementia: Translational Research & Clinical Interventions, Vol 6, Iss 1, Pp n/a-n/a (2020)
Alzheimer's & Dementia : Translational Research & Clinical Interventionsمصطلحات موضوعية: 0301 basic medicine, brain, Tn antigen, Disease, Biology, 03 medical and health sciences, 0302 clinical medicine, late‐onset Alzheimer's disease, Coding region, RC346-429, Research Articles, chemistry.chemical_classification, C1GALT1/T‐synthase, RC952-954.6, Promoter, mutations, Molecular biology, Blot, Psychiatry and Mental health, 030104 developmental biology, chemistry, Geriatrics, T SYNTHASE, COSMC/C1GALT1C1, Neurology (clinical), Neurology. Diseases of the nervous system, Glycoprotein, 030217 neurology & neurosurgery, Research Article
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المؤلفون: David E. Riley, Seema Gollamudi, Gurutz Linazasoro, João Guimarães, William B. Dobyns, Deborah Raymond, Susan B. Bressman, C. J. M. Frijns, Bret C. Haake, Laurie J. Ozelius, Allison Brashear, Michel Borg, Rachel Saunders-Pullman, Jacek Zaremba, Christine Klein, Alexander Münchau, Andrew Green, Patricia de Carvalho Aguiar, David Webb, Marina A. J. Tijssen
المساهمون: ANS - Amsterdam Neuroscience, Neurology
المصدر: Brain, 130(Part 3), 828-835. Oxford University Press
مصطلحات موضوعية: Adult, Heterozygote, medicine.medical_specialty, Adolescent, Genotype, Limb dystonia, Biology, Parkinsonian Disorders, ATP1A2, Internal medicine, ATP1A3, Tremor, medicine, Humans, Age of Onset, Child, Familial hemiplegic migraine, Family Health, Dystonia, Movement Disorders, Alternating hemiplegia of childhood, Parkinsonism, Extremities, Middle Aged, medicine.disease, nervous system diseases, Phenotype, Endocrinology, Child, Preschool, Mutation, Female, Neurology (clinical), Sodium-Potassium-Exchanging ATPase, Age of onset
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d0ae61302e30b311ff0a4c0ea44661f
https://doi.org/10.1093/brain/awl340 -
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مصطلحات موضوعية: Genetic Markers, Male, medicine.medical_specialty, Pediatrics, Genotype, DNA Mutational Analysis, Neurological disorder, Gene mutation, Parkinsonian Disorders, ATP1A3, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Age of Onset, Child, Clinical/Scientific Notes, Dystonia, business.industry, Parkinsonism, Alternating hemiplegia of childhood, Brain, medicine.disease, nervous system diseases, Endocrinology, Amino Acid Substitution, Dystonic Disorders, Positron-Emission Tomography, Acute Disease, Mutation, Disease Progression, Muscle Hypotonia, Neurology (clinical), Age of onset, Sodium-Potassium-Exchanging ATPase, business, Deglutition Disorders, Dystonic disorder
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c35aa2574c3d8e2f8e56b8a69887f20
https://europepmc.org/articles/PMC2833268/ -
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المؤلفون: Laurie J. Ozelius, Beom S. Jeon, Jiyoung Kim, Jee Young Lee, Seema Gollamudi
المصدر: Movement Disorders. 22:1808-1809
مصطلحات موضوعية: Adult, Male, Threonine, medicine.medical_specialty, Pediatrics, Neurological disorder, Biology, Gene mutation, Methionine, Parkinsonian Disorders, Internal medicine, ATP1A3, medicine, Humans, Genetic testing, Dystonia, Korea, medicine.diagnostic_test, Parkinsonism, Point mutation, medicine.disease, nervous system diseases, Endocrinology, Neurology, Dystonic Disorders, Mutation, Mutation (genetic algorithm), Neurology (clinical), Sodium-Potassium-Exchanging ATPase
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المؤلفون: Noel Y. Calingasan, Lichuan Yang, M. Flint Beal, Seema Gollamudi, Olivier Elemento, Ashu Johri
المصدر: PLoS ONE, Vol 7, Iss 5, p e36191 (2012)
PLoS ONEمصطلحات موضوعية: Male, lcsh:Medicine, Peroxisome proliferator-activated receptor, Transcriptomes, Transcriptome, Mice, 0302 clinical medicine, Mesencephalon, Molecular Cell Biology, Gene Regulatory Networks, Genome Sequencing, lcsh:Science, Receptor, Oligonucleotide Array Sequence Analysis, chemistry.chemical_classification, 0303 health sciences, Multidisciplinary, Reverse Transcriptase Polymerase Chain Reaction, Wnt signaling pathway, Parkinson Disease, Genomics, 3. Good health, Pyridazines, Neurology, Maneb, Medicine, Peroxisome proliferator-activated receptor delta, Signal transduction, Research Article, Signal Transduction, Paraquat, Biology, Signaling Pathways, 03 medical and health sciences, Genome Analysis Tools, Genetics, Animals, Humans, Gene Networks, Parkinson Disease, Secondary, Pesticides, 030304 developmental biology, G protein-coupled receptor, Gene Expression Profiling, lcsh:R, Erythropoietin-producing hepatocellular (Eph) receptor, Computational Biology, Molecular biology, Corpus Striatum, Mice, Inbred C57BL, chemistry, Cancer research, lcsh:Q, Gene Function, Molecular Neuroscience, Genome Expression Analysis, 030217 neurology & neurosurgery, Neuroscience
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10دورية أكاديميةThe phenotypic spectrum of rapid-onset dystonia–parkinsonism (RDP) and mutations in the ATP1A3 gene.
المؤلفون: Allison Brashear, William B. Dobyns, Patricia de Carvalho Aguiar, Michel Borg, C. J. M. Frijns, Seema Gollamudi, Andrew Green, João Guimaraes, Bret C. Haake, Christine Klein, Gurutz Linazasoro, Alexander Münchau, Deborah Raymond, David Riley, Rachel Saunders-Pullman, Marina A. J. Tijssen, David Webb, Jacek Zaremba, Susan B. Bressman, Laurie J. Ozelius
المصدر: Brain: A Journal of Neurology; Mar2007, Vol. 130 Issue 3, p828-835, 8p
مصطلحات موضوعية: DYSTONIA, EXTRAPYRAMIDAL disorders, MUSCLE diseases, PARKINSON'S disease