Zobrazeno 1 - 10
of 1 634
pro vyhledávání: '"Ritika R"'
Autor:
Daniel Romero-Alvarez, Manuel Calvopiña, Emily Cisneros-Vásquez, Daniel Garzon-Chavez, Alaine K. Warren, Lauren S. Bennett, Ritika R. Janapati, Carlos Bastidas-Caldes, Melanie Cabezas-Moreno, Jacobus H. de Waard, Daniela Silva-Martinod, Roxane Schaub, Mary Jackson, A. Townsend Peterson, Charlotte Avanzi
Publikováno v:
Emerging Infectious Diseases, Vol 30, Iss 12, Pp 2629-2632 (2024)
We found Mycobacterium leprae, the most common etiologic agent of Hansen disease or leprosy, in tissues from 9 (18.75%) of 48 nine-banded armadillos (Dasypus novemcinctus) collected across continental Ecuador. Finding evidence of a wildlife reservoir
Externí odkaz:
https://doaj.org/article/252a071a8bcf4c76a98f525bf77a8641
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 18 (2024)
Disease-associated microglia (DAM) are a subset of microglia that appear at various stages of central nervous system neurodegenerative diseases. DAM were identified using single-cell RNA sequencing within Alzheimer’s Disease (AD) where they were ch
Externí odkaz:
https://doaj.org/article/a433b68608b048c4a8ad198264e9c6ba
Autor:
Amy Mann, Arameh Aghababaie, Jennifer Kalitsi, Daniel Martins, Yannis Paloyelis, Ritika R. Kapoor
Publikováno v:
Molecular Autism, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Background Septo-optic dysplasia (SOD) is a rare condition diagnosed in children with two or more of the following: hypopituitarism, midline brain abnormalities, and optic nerve hypoplasia. Children with SOD experience varied visual impairme
Externí odkaz:
https://doaj.org/article/c12e3ec64c6f4a1792fbe765a0b2d1ca
Autor:
Pankaj Agrawal, Sally Newbold, Ayisha Al Busaidi, Ritika R Kapoor, Nick Thomas, Simon JB Aylwin, Charles R Buchanan, Ved Bhushan Arya
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 27, Iss 4, Pp 320-324 (2022)
Pituitary apoplexy typically presents with acute headache, vomiting, visual disturbance, and confusion. Herein, we report a rare presentation of ischemic stroke due to pituitary apoplexy. A 16.5-year-old male presented with reduced Glasgow Coma Scale
Externí odkaz:
https://doaj.org/article/05bedfee044c402e985317309df508d9
Autor:
Hüseyin Anil Korkmaz, Ritika R Kapoor, Jennifer Kalitsi, Simon JB Aylwin, Charles R Buchanan, Ved Bhushan Arya
Publikováno v:
International Journal of Endocrinology, Vol 2022 (2022)
Introduction. Paediatric cohorts of central diabetes insipidus (CDI) have shown varying prevalence for different causes of CDI. The objective of this study was to determine the causes of CDI and long-term outcome in children and adolescents from a Te
Externí odkaz:
https://doaj.org/article/330eaf96cd3a4ea7977d2bb243df405b
Publikováno v:
Frontiers in Psychiatry, Vol 12 (2021)
The concept of “acquired autism” refers to the hypothesis that amongst the massive heterogeneity that encompasses autism spectrum disorder (ASD) there may be several phenotypes that are neither syndromic nor innate. Strong and consistent evidence
Externí odkaz:
https://doaj.org/article/ddc25efa7c5147c9951699b8f79765f6
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-4 (2019)
Diazoxide is the first-line treatment for patients with hyperinsulinaemic hypoglycaemia (HH). Approximately 50% of patients with HH are diazoxide resistant. However, marked diazoxide sensitivity resulting in severe hyperglycaemia is extremely uncom
Externí odkaz:
https://doaj.org/article/7d9b332bb89c4cbca06c5d7fee711aa6
Autor:
Daphne Yau, Thomas W Laver, Antonia Dastamani, Senthil Senniappan, Jayne A L Houghton, Guftar Shaikh, Tim Cheetham, Talat Mushtaq, Ritika R Kapoor, Tabitha Randell, Sian Ellard, Pratik Shah, Indraneel Banerjee, Sarah E Flanagan
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0228417 (2020)
Congenital hyperinsulinism (CHI) is a significant cause of hypoglycaemia in neonates and infants with the potential for permanent neurologic injury. Accurate calculations of the incidence of rare diseases such as CHI are important as they inform heal
Externí odkaz:
https://doaj.org/article/bcf7bd9b0a414b47a5a19639403cea32
Autor:
Mann, Amy, Kalitsi, Jennifer, Jani, Khushali, Martins, Daniel, Kapoor, Ritika R, Paloyelis, Yannis
Publikováno v:
In Frontiers in Neuroendocrinology January 2025 76
Publikováno v:
Frontiers in Endocrinology, Vol 2 (2011)
BackgroundLoss of function mutations in the genes encoding the pancreatic β-cell ATP-sensitive potassium (KATP) channel are identified in approximately 80% of patients with diazoxide-unresponsive hyperinsulinaemic-hypoglycaemia (HH). For a small num
Externí odkaz:
https://doaj.org/article/3158ae4c327d4754867c5dcbf2dbfa18