Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kavya Rao"'
Autor:
Rajendra Singh Jain, Deepak Jain, Sourabh Murarka, Arvind Vyas, Bhawna Sharma, Trilochan Srivastava, Kamlesh Kumar, Yavnika Jain, Kavya Rao, Jitesh Agrawal, Shankar Tejwani
Publikováno v:
Annals of Indian Academy of Neurology, Vol 25, Iss 2, Pp 246-255 (2022)
Background: More and more cases of myelin oligodendrocyte glycoprotein (MOG) antibody are being diagnosed with the availability of laboratory tests helping us to know the differing patterns from AQP-4 antibody disease and we need to understand the na
Externí odkaz:
https://doaj.org/article/099209fc383b42fcbcc401c06a4aef17
Autor:
Mariana Lopez Martinolich, Hope Northrup, Pedro Mancias, Paul Hillman, Kavya Rao, Kate Mowrey
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 3, Pp n/a-n/a (2022)
Abstract Background Nance‐Horan syndrome (NHS) is a rare X‐linked genetic disorder characterized by ophthalmologic and dental anomalies as well as dysmorphic facies. The clinical phenotype in males includes congenital cataracts, vision loss, micr
Externí odkaz:
https://doaj.org/article/b07e123e7afe44eba40fab20502b987b
Publikováno v:
BioEssays. 45
Autor:
Janelle, Wagner, Sonal, Bhatia, B Oyinkan, Marquis, Imelda, Vetter, Christopher W, Beatty, Rebecca, Garcia, Charuta, Joshi, Gogi, Kumar, Kavya, Rao, Nilika, Singhal, Karen, Skjei
Publikováno v:
Journal of Clinical Psychology in Medical Settings.
Epilepsy affects 1% of youth and is associated with neurocognitive and psychosocial comorbidities, increased risk of mortality, and poor health-related outcomes. Health disparities in children and youth with epilepsy (CYE) have been understudied. A S
Autor:
Mariana Lopez Martinolich, Hope Northrup, Pedro Mancias, Paul Hillman, Kavya Rao, Kate Mowrey
Publikováno v:
Molecular geneticsgenomic medicine. 10(3)
Nance-Horan syndrome (NHS) is a rare X-linked genetic disorder characterized by ophthalmologic and dental anomalies as well as dysmorphic facies. The clinical phenotype in males includes congenital cataracts, vision loss, microcornea, nystagmus, micr
Autor:
RajendraSingh Jain, Deepak Jain, Sourabh Murarka, Arvind Vyas, Bhawna Sharma, Trilochan Srivastava, Kamlesh Kumar, Yavnika Jain, Kavya Rao, Jitesh Agrawal, Shankar Tejwani
Publikováno v:
Annals of Indian Academy of Neurology. 25(2)
More and more cases of myelin oligodendrocyte glycoprotein (MOG) antibody are being diagnosed with the availability of laboratory tests helping us to know the differing patterns from AQP-4 antibody disease and we need to understand the natural course
Autor:
Kim Williams, Dinabel Peralta-Reich, Rebecca Fisk, Kavita Kasat, Tung Ming Leung, Aaron Potash, Victoria Reichman, Marty Ellington, Luisa Gonzalez-Ballesteros, Guillaume Stoffels, Kavya Rao, Ana Degoy
Publikováno v:
Pediatric Quality & Safety
Introduction: Neonatologists have long struggled with identifying and treating early-onset sepsis (EOS) without overexposing newborns to unnecessary antibiotics. Methods: In January 2016, we instituted an EOS protocol based mainly on the 2012 AAP gui
Publikováno v:
Child Neurology Open, Vol 6 (2019)
Child Neurology Open
Child Neurology Open
The authors describe a 12-year-old girl with an atypical presentation of Bartonella encephalitis. She presented with fever and altered mental status and developed flaccid paralysis of her left upper extremity a day later. An electroencephalogram show
Autor:
Kavya Rao, Jeya T. Nadarajah, Janet Raboud, DeSheng Su, Sharon Walmsley, Mona Loutfy, Micaela Collins
Publikováno v:
Clinical Infectious Diseases. 55:1568-1574
Background. Human immunodeficiency virus (HIV)–related facial lipoatrophy is a devastating adverse effect of antiretroviral therapy. At this time, the most viable treatment option is cosmetic surgery with synthetic fillers. Bio-Alcamid has many adv