Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Joy, Desai"'
Autor:
Zabeen K. Mahuwala, Dhruvkumar M Patel, Mukundkumar V Patel, Joy Desai, Harsh D Patel, Jayanti K Gurumukhani, Maitri M Patel
Publikováno v:
The Open Neurology Journal. 15:31-36
Background: Posterior reversible encephalopathy syndrome (PRES) is clinicoradiological disease entity characterized by headache, seizures, altered sensorium and corticalvisual loss with characteristic MRI features of subcortical white matter hyperint
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::134e158fe98a7ad4d4b3077aa2aa80be
https://doi.org/10.2174/1874205x02115010031
https://doi.org/10.2174/1874205x02115010031
Autor:
R, Srinivasa, Sanjib, Sinha, Satishchandra, Parthasarthy, Sudhir, Kothari, Rahul, Baviskar, Sita, Jayalakshmi, Bhawana, Sharma, Ravindra K, Garg, Joy, Desai, Nandan, Yardi, Meenakshi Sundaram, Salvadeeswaran, Sangeeta, Ravat, Mohan, Das, Roop, Gursahani, Swaroop, Suresh, Alok, Rasal, Sami, Elmoufti
Publikováno v:
Neurology India. 68(6)
Nearly one-third of patients don't achieve seizure control with existing antiepileptic drugs. Brivaracetam (BRV) is a new member of the racetam class of drug, designed to selectively target SV2A, with binding affinity 15- to 30-fold greater than that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0779bb27268161693e08f8e6ce94dabb
https://pubmed.ncbi.nlm.nih.gov/33342876
https://pubmed.ncbi.nlm.nih.gov/33342876
Autor:
Henry Houlden, Joshua Hersheson, Prochi F. Madon, Yo-Tsen Liu, Reema Paudel, Conceição Bettencourt, Noshir Wadia, Sarah Wiethoff, Joy Desai
Publikováno v:
Cerebellum (London, England)
Autosomal-recessive cerebellar ataxias (ARCA) are clinically and genetically heterogeneous conditions primarily affecting the cerebellum. Mutations in the PNPLA6 gene have been identified as the cause of hereditary spastic paraplegia and complex form
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d6b9b21f777b65b17fcd473241426f2
https://doi.org/10.1007/s12311-016-0769-x
https://doi.org/10.1007/s12311-016-0769-x
Autor:
Joy Desai
Publikováno v:
Practice Pearls in Neurology: Series 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2e6de6cebd4348f418822a2f3537885
https://doi.org/10.5005/jp/books/14148_10
https://doi.org/10.5005/jp/books/14148_10
Publikováno v:
Journal of the International Association of Physicians in AIDS Care. 5:157-160
Neurologic dysfunction complicating HIV infection may occur in up to 70% of AIDS patients. The advent of highly active antiretroviral therapy has reduced central nervous system opportunistic infections. Immune reconstitutions after highly active anti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55b0f6beeb47b3b890138d351586d999
https://doi.org/10.1177/1545109706294853
https://doi.org/10.1177/1545109706294853
Publikováno v:
Movement Disorders. 15:313-317
We describe three patients who developed a rapidly evolving posttraumatic akinetic-rigid syndrome (ARS), the clinical manifestations of which were similar to Parkinson's disease, including response to levodopa. Despite initial imaging studies showing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::857bb1b309f156eb7ad7da354b902fec
https://doi.org/10.1002/1531-8257(200003)15:2<313::aid-mds1017>3.0.co
https://doi.org/10.1002/1531-8257(200003)15:2<313::aid-mds1017>3.0.co
Autor:
Michael Swash, Joy Desai
Publikováno v:
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders. 1:105-112
The classification and nomenclature of motor neuron disease, whether sporadic or familial, is confused. For example, both the sporadic and familial motor neuron diseases are phenotypically heterogeneous and, in familial ALS, phenotypic heterogeneity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26696cb2d4e5e3147b9f7f491537533e
https://doi.org/10.1080/14660820050515403
https://doi.org/10.1080/14660820050515403
Publikováno v:
Journal of the Neurological Sciences. 170:5-10
Primary lateral sclerosis (PLS) is a rare degenerative disorder of the upper motor neuron. Its nosological status and relationship to other motor neuron syndromes, especially amyotrophic lateral sclerosis (ALS), is uncertain. Diagnostic criteria have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a8efe038ea755163ac41ce08de9979b
https://doi.org/10.1016/s0022-510x(99)00184-7
https://doi.org/10.1016/s0022-510x(99)00184-7
Autor:
Joy Desai
Publikováno v:
Epilepsia. 49:47-49
In the treatment of seizures and epilepsy associated with central nervous system (CNS) infections, drug-drug interactions may significantly and unexpectedly impact outcome not only of epilepsy but also of the infectious disorders in both emergent and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::918161b2078005210a8ec7bc91d7ef1a
https://doi.org/10.1111/j.1528-1167.2008.01756.x
https://doi.org/10.1111/j.1528-1167.2008.01756.x
Publikováno v:
Brain. 121:2341-2355
Clinical revaluation and genetic analysis of six Indian pedigrees, segregating autosomal dominant cerebellar ataxia, slow saccades and peripheral neuropathy, has been undertaken, and expansion at the spinocerebellar ataxia 2 (SCA2) locus was confirme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1d5ffa5214e918339b50cf562127906
https://doi.org/10.1093/brain/121.12.2341
https://doi.org/10.1093/brain/121.12.2341