المؤلفون: Kinsi Oberoi, Alam S. Grewal, Leema Reddy Peddareddygari

المصدر: Case Reports in Neurology, Vol 12, Iss 2, Pp 255-259 (2020)

مصطلحات موضوعية: myelin protein zero gene, duplication mutation, nonprogressive demyelinating neuropathy, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.karger.com/Article/FullText/509266; https://doaj.org/toc/1662-680X

URL الوصول: https://doaj.org/article/78118e3cd9b84f7c98b13f274be961e9

المؤلفون: Garth E. Ringheim, Matthew Wampole, Kinsi Oberoi

المصدر: Frontiers in Immunology, Vol 12 (2021)

مصطلحات موضوعية: Bruton’s tyrosine kinase (BTK), B cell, autoimmune disease, rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, Immunologic diseases. Allergy, RC581-607

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fimmu.2021.662223/full; https://doaj.org/toc/1664-3224

URL الوصول: https://doaj.org/article/1d974e25811a42f398673ada2e8ac130

المؤلفون: Leema Reddy Peddareddygari, Kinsi Oberoi, Raji P. Grewal

المصدر: Case Reports in Neurology, Vol 10, Iss 3, Pp 272-278 (2018)

مصطلحات موضوعية: Digenic inheritance, Double heterozygous variants, CAPN3 gene, DES gene, Limb girdle muscular dystrophy, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.karger.com/Article/FullText/492664; https://doaj.org/toc/1662-680X

URL الوصول: https://doaj.org/article/db3ee622a67d4d3b984b0e07aa652faf

المؤلفون: Leema Reddy Peddareddygari, Kinsi Oberoi, Raji P. Grewal

المصدر: Case Reports in Neurology, Vol 10, Iss 1, Pp 38-44 (2018)

مصطلحات موضوعية: Charcot-Marie-Tooth disease type 4C, SH3TC2 gene, Novel variants, Asian Indian, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.karger.com/Article/FullText/486589; https://doaj.org/toc/1662-680X

URL الوصول: https://doaj.org/article/9b59ed9284e54701a7dffc40316da8f6

المؤلفون: Kinsi Oberoi, Kabir S. Grewal, Leema Reddy Peddareddygari

المصدر: Journal of Community Hospital Internal Medicine Perspectives, Vol 10, Iss 4, Pp 369-370 (2020)

مصطلحات موضوعية: spastic paraplegia type 4, recurrent urinary tract infection, neurological disorders, spast gene, Internal medicine, RC31-1245

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2000-9666

URL الوصول: https://doaj.org/article/7820a312b1764487af3a73be11d7995d

المؤلفون: Leema Reddy Peddareddygari, Kinsi Oberoi, Jaasrini Reddy Vellore, Raji P. Grewal

المصدر: Case Reports in Neurology, Vol 8, Iss 2, Pp 120-126 (2016)

مصطلحات موضوعية: Charcot-Marie-Tooth disease type 2B, Phenotype variability, Digeneic effect, RAB7A/LRSAM1 gene interactions, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: http://www.karger.com/Article/FullText/446872; https://doaj.org/toc/1662-680X

URL الوصول: https://doaj.org/article/59033e0e72ba49b0bfac0c1bfa98b9c0

المؤلفون: Leema Reddy Peddareddygari, Kinsi Oberoi, Raji P. Grewal

المصدر: Case Reports in Neurological Medicine, Vol 2014 (2014)

مصطلحات موضوعية: Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2090-6668; https://doaj.org/toc/2090-6676

URL الوصول: https://doaj.org/article/e3ad8b8342724defb90e6d57fe3f9706

المؤلفون: Leema Reddy Peddareddygari, Kinsi Oberoi, Raji P Grewal

المصدر: Cureus.

مصطلحات موضوعية: General Engineering

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::70d0e27bfd05a898a6ba3172a7a4e7fa
https://doi.org/10.7759/cureus.30550

المؤلفون: Leema Reddy Peddareddygari, Kinsi Oberoi, Raji P. Grewal

المصدر: Journal of Neurology Research. 9:60-64

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::84a2ff830a477d494d483f3c82300747
https://doi.org/10.14740/jnr547

المؤلفون: Raji P. Grewal, Leema Reddy Peddareddygari, Leroy R. Sharer, Kinsi Oberoi

المصدر: Journal of Clinical Neuromuscular Disease. 20:214-216

مصطلحات موضوعية: Male, 0301 basic medicine, Pathology, medicine.medical_specialty, Weakness, Proximal muscle weakness, 030105 genetics & heredity, Inflammatory myopathy, 03 medical and health sciences, 0302 clinical medicine, Muscular Diseases, Genotype, medicine, Humans, Myopathy, Exome sequencing, RYR1, Muscle biopsy, medicine.diagnostic_test, Electromyography, business.industry, Ryanodine Receptor Calcium Release Channel, General Medicine, Middle Aged, medicine.disease, Neurology, Mutation, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b13ce2d8d8fbf6fd7b3699bef59df79
https://doi.org/10.1097/cnd.0000000000000237

المؤلفون: Garth E. Ringheim (7547299), Matthew Wampole (11639998), Kinsi Oberoi (11640001)

مصطلحات موضوعية: Immunology, Applied Immunology (incl. Antibody Engineering, Xenotransplantation and T-cell Therapies), Autoimmunity, Cellular Immunology, Humoural Immunology and Immunochemistry, Immunogenetics (incl. Genetic Immunology), Innate Immunity, Transplantation Immunology, Tumour Immunology, Immunology not elsewhere classified, Genetic Immunology, Animal Immunology, Veterinary Immunology, Bruton’s tyrosine kinase (BTK), B cell, autoimmune disease, rheumatoid arthritis, systemic lupus erythematosus, multiple sclerosis, pemphigus vulgaris, Sjogren’s syndrome

Relation: https://figshare.com/articles/dataset/Table_2_Bruton_s_Tyrosine_Kinase_BTK_Inhibitors_and_Autoimmune_Diseases_Making_Sense_of_BTK_Inhibitor_Specificity_Profiles_and_Recent_Clinical_Trial_Successes_and_Failures_xlsx/16922338

الاتاحة: https://doi.org/10.3389/fimmu.2021.662223.s002

المؤلفون: Raji P. Grewal, Leema Reddy Peddareddygari, Kinsi Oberoi

المصدر: Case Reports in Neurology
Case Reports in Neurology, Vol 10, Iss 1, Pp 38-44 (2018)

مصطلحات موضوعية: 0301 basic medicine, Pes cavus, Sciatic Neuropathy, Charcot-Marie-Tooth disease type 4C, Population, SH3TC2 gene, Case Report, Compound heterozygosity, medicine.disease_cause, lcsh:RC346-429, 03 medical and health sciences, 0302 clinical medicine, Asian Indian, SH3TC2, medicine, education, lcsh:Neurology. Diseases of the nervous system, Genetic testing, Genetics, education.field_of_study, Mutation, medicine.diagnostic_test, business.industry, medicine.disease, 030104 developmental biology, Neurology (clinical), Novel variants, Haploinsufficiency, business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58210fcd1b8d39e920c14ce52105f62d
http://europepmc.org/articles/PMC5836280

المؤلفون: Leema Reddy Peddareddygari, Ada Baisre-de Leon, Raji P. Grewal, Kinsi Oberoi

المصدر: Journal of clinical neuromuscular disease. 19(4)

مصطلحات موضوعية: 0301 basic medicine, Male, Weakness, Anoctamins, Compound heterozygosity, 03 medical and health sciences, Exon, 0302 clinical medicine, medicine, Humans, Genetic Testing, Muscular dystrophy, Myopathy, Creatine Kinase, Genetics, Muscle biopsy, medicine.diagnostic_test, business.industry, General Medicine, Middle Aged, medicine.disease, Magnetic Resonance Imaging, 030104 developmental biology, Neurology, Muscular Dystrophies, Limb-Girdle, Mutation (genetic algorithm), Mutation, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery, Limb-girdle muscular dystrophy

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f19f75ffa89ecbdbd5505106fb59d9e5
https://pubmed.ncbi.nlm.nih.gov/29794579