Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sanjeev Kothare"'
Publikováno v:
Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine. 18(11)
Central hypoventilation is a rare cause of respiratory failure that has been associated with multiple underlying disorders, including congenital central hypoventilation syndrome, obesity hypoventilation syndrome, and several neuromuscular conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6dc96b632e26203e5ea2edf4e571d579
https://pubmed.ncbi.nlm.nih.gov/35912694
https://pubmed.ncbi.nlm.nih.gov/35912694
Publikováno v:
Journal of Clinical Sleep Medicine. 18:2695-2698
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1aacfd4efe6f99b865859757251df0a
https://doi.org/10.5664/jcsm.10148
https://doi.org/10.5664/jcsm.10148
Autor:
Annie H. Roliz, Sanjeev Kothare
Publikováno v:
Current Neurology and Neuroscience Reports. 22:551-563
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5174ce2e69eaf1c99e7988adada8a08
https://doi.org/10.1007/s11910-022-01219-1
https://doi.org/10.1007/s11910-022-01219-1
Autor:
Stephanie Enner, Yash D. Shah, Aaqil Ali, Jane E. Cerise, Justin Esposito, Lorry Rubin, Anupama Subramony, Sanjeev Kothare
Publikováno v:
Journal of Child Neurology. 37:426-433
Background: Acute neurological complications from COVID-19 have been reported in both pediatric and adult populations. Chronic symptoms after recovery have been reported in adults and can include neuropsychiatric and sleep symptoms. Persistent sympto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51b12685bd442c7af825515b84ba1c68
https://doi.org/10.1177/08830738221075924
https://doi.org/10.1177/08830738221075924
Autor:
Victoria Cheung BA, Sara Wertenteil, Susan Sasson, Suzanne Vento RN, Sanjeev Kothare MD, Howard Trachtman MD
Publikováno v:
Global Pediatric Health, Vol 2 (2015)
Background . Restless legs syndrome (RLS) is a sleep disorder characterized by an urge to move or the presence of unpleasant sensations in the extremities. The prevalence of RLS is higher in children and adults with chronic kidney disease and in adul
Externí odkaz:
https://doaj.org/article/375025a00cb4428082e05d8e79f61c16
Publikováno v:
Child's Nervous System. 38:693-693
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4945868180e18c21d6082dca9a4cec18
https://doi.org/10.1007/s00381-022-05475-x
https://doi.org/10.1007/s00381-022-05475-x
Publikováno v:
International Journal of Human Genetics. 2:49-53
The present study reports the correlation of maternal age and chromosomal aberration found in 160 Down syndrome cases. The clinical diagnosis of Down Syndrome was evaluated with reference to cytogenetic profiles and maternal age,which revealed that 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a39d303445b7ba2d0e81eda05e344d3f
https://doi.org/10.1080/09723757.2002.11885784
https://doi.org/10.1080/09723757.2002.11885784
Autor:
Heather, Olson, Yiping, Shen, Jennifer, Avallone, Beth R, Sheidley, Rebecca, Pinsky, Ann M, Bergin, Gerard T, Berry, Frank H, Duffy, Yaman, Eksioglu, David J, Harris, Fuki M, Hisama, Eugenia, Ho, Mira, Irons, Christina M, Jacobsen, Philip, James, Sanjeev, Kothare, Omar, Khwaja, Jonathan, Lipton, Tobias, Loddenkemper, Jennifer, Markowitz, Kiran, Maski, J Thomas, Megerian, Edward, Neilan, Peter C, Raffalli, Michael, Robbins, Amy, Roberts, Eugene, Roe, Caitlin, Rollins, Mustafa, Sahin, Dean, Sarco, Alison, Schonwald, Sharon E, Smith, Janet, Soul, Joan M, Stoler, Masanori, Takeoka, Wen-Han, Tan, Alcy R, Torres, Peter, Tsai, David K, Urion, Laura, Weissman, Robert, Wolff, Bai-Lin, Wu, David T, Miller, Annapurna, Poduri
Publikováno v:
Annals of neurology. 75(6)
To evaluate the role of copy number abnormalities detectable using chromosomal microarray (CMA) testing in patients with epilepsy at a tertiary care center.We identified patients with International Classification of Diseases, ninth revision (ICD-9) c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e152bd64618ddddafc31e79ce94e7dc0
https://pubmed.ncbi.nlm.nih.gov/25112510
https://pubmed.ncbi.nlm.nih.gov/25112510
Autor:
Annapurna, Poduri, Erin L, Heinzen, Vida, Chitsazzadeh, Francesco Massimo, Lasorsa, P Christina, Elhosary, Christopher M, LaCoursiere, Emilie, Martin, Christopher J, Yuskaitis, Robert Sean, Hill, Kutay Deniz, Atabay, Brenda, Barry, Jennifer N, Partlow, Fahad A, Bashiri, Radwan M, Zeidan, Salah A, Elmalik, Mohammad M U, Kabiraj, Sanjeev, Kothare, Tommy, Stödberg, Amy, McTague, Manju A, Kurian, Ingrid E, Scheffer, A James, Barkovich, Ferdinando, Palmieri, Mustafa A, Salih, Christopher A, Walsh
Publikováno v:
Annals of neurology, vol 74, iss 6
ObjectiveTo identify a genetic cause for migrating partial seizures in infancy (MPSI).MethodsWe characterized a consanguineous pedigree with MPSI and obtained DNA from affected and unaffected family members. We analyzed single nucleotide polymorphism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f41271935478b87260842545488f12f8
https://escholarship.org/uc/item/9wx1d0z8
https://escholarship.org/uc/item/9wx1d0z8
Autor:
Morse, Anne Marie, Sanjeev, Kothare
Publikováno v:
Medical Sciences; Mar2018, Vol. 6 Issue 1, p16, 10p