Zobrazeno 1 - 10
of 1 254
pro vyhledávání: '"A. K. Desai"'
Publikováno v:
Asian Journal of Medical Sciences, Vol 15, Iss 11, Pp 108-114 (2024)
Background: Chronic obstructive pulmonary disease (COPD) is now one of the top three causes of death worldwide. Despite the availability of various kinds of treatments, there is a paucity of data regarding potential treatment for COPD. Aims and Ob
Externí odkaz:
https://doaj.org/article/16539f4ad4814ca18eda53a92b8250ca
Autor:
Angie H. Fares, Ankit K. Desai, Laura E. Case, Cassie Sharon, Amy Klinepeter, Amelia Kirby, Matthew T. Lisi, Rebecca L. Koch, Priya S. Kishnani
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 41, Iss , Pp 101141- (2024)
Infantile-onset Pompe disease (IOPD) is caused by a deficiency in the enzyme acid alpha-glucosidase (GAA). It is characterized by severe and progressive hypertrophic cardiomyopathy and muscle weakness with death in the first 2 years of life if left u
Externí odkaz:
https://doaj.org/article/6ea6d9796f1448e0a4eef059199db424
Publikováno v:
Journal of Materials and Engineering Structures, Vol 11, Iss 2, Pp 143-154 (2024)
The specific objectives of this experimentation is to investigate the splitting tensile strength of concrete subjected to partial setting with varying proportions of fly ash (20% and 25%) and 1% synthetic polypropylene fibers. The examination encompa
Externí odkaz:
https://doaj.org/article/e79b9409b0544394a84e941d9b4b18a5
Autor:
Olulade Ayodele, Rohan C. Parikh, Elizabeth Esterberg, Mayank Ajmera, Bridgett Goodwin, James Williams, Nirav K. Desai, David A. Katzka
Publikováno v:
Gastro Hep Advances, Vol 3, Iss 5, Pp 659-670 (2024)
Background and Aims: Limited real-world nontertiary care evidence on the patient therapeutic journey and disease burden of eosinophilic esophagitis (EoE) exists. The aim was to collect real-world data on the EoE patient journey across different age g
Externí odkaz:
https://doaj.org/article/08c7ec01ad574d75aed08691639226d9
Autor:
C. Laxuman, Yogesh Dashrath Naik, B. K. Desai, Mallikarjun Kenganal, Bharat Patil, B. S. Reddy, D. H. Patil, Sidramappa Chakurte, P. H. Kuchanur, Shiva Kumar K, Ashok Kumar Gaddi, L. N. Yogesh, Jayaprakash Nidagundi, B. M. Dodamani, Gururaj Sunkad, Mahendar Thudi, Rajeev K. Varshney
Publikováno v:
The Plant Genome, Vol 17, Iss 2, Pp n/a-n/a (2024)
Abstract Fusarium wilt (FW) is the most severe soil‐borne disease of chickpea that causes yield losses up to 100%. To improve FW resistance in JG 11, a high‐yielding variety that became susceptible to FW, we used WR 315 as the donor parent and fo
Externí odkaz:
https://doaj.org/article/aded9662871445778a9fe9a2ee8a1c22
Autor:
Hui-An Chen, Rai-Hseng Hsu, Ching-Ya Fang, Ankit K. Desai, Ni-Chung Lee, Wuh-Liang Hwu, Fuu-Jen Tsai, Priya S. Kishnani, Yin-Hsiu Chien
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionPompe disease, a lysosomal storage disorder, is characterized by acid α-glucosidase (GAA) deficiency and categorized into two main subtypes: infantile-onset Pompe disease (IOPD) and late-onset Pompe disease (LOPD). The primary treatment,
Externí odkaz:
https://doaj.org/article/d580f3c7d33d45768fcfbe1d68b78034
Autor:
Robin M. Pokrzywinski, Bridgett Goodwin, Evan S. Dellon, Ellyn Kodroff, Anne Brooks, Adam Bailey, James Williams, Nirav K. Desai
Publikováno v:
Journal of Patient-Reported Outcomes, Vol 7, Iss 1, Pp 1-14 (2023)
Abstract Background The Dysphagia Symptom Questionnaire (DSQ) is a patient-reported outcome measure that assesses the frequency and severity of dysphagia in patients with eosinophilic esophagitis (EoE); however, it has only been validated for use in
Externí odkaz:
https://doaj.org/article/e3b91581a62d403485c5cdf9b76d5429
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 10, Pp 01-05 (2023)
Introduction: The mushrooming of Fixed-dose Combinations (FDCs) has been observed in the past decade in the Indian market. The majority of these FDCs are irrational and put patient safety at risk. Aim: To evaluate Adverse Drug Reactions (ADRs) du
Externí odkaz:
https://doaj.org/article/dfc95f79cbd7460ca57a7fe08c224f08
Autor:
Ankit K. Desai, Garima Shrivastava, Christina L. Grant, Raymond Y. Wang, Trevor D. Burt, Priya S. Kishnani
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionHigh sustained anti-rhGAA antibody titers (HSAT; ≥12,800) are directly linked to reduced efficacy of enzyme replacement therapy (ERT) and subsequent clinical deterioration in infantile-onset Pompe disease (IOPD). We have previously demo
Externí odkaz:
https://doaj.org/article/feaa2ff9617e4639b0282d4875ed2de3
Autor:
Ankit K. Desai, P. Brian Smith, John S. Yi, Amy S. Rosenberg, Trevor D. Burt, Priya S. Kishnani
Publikováno v:
Frontiers in Immunology, Vol 14 (2024)
IntroductionThe efficacy of enzyme replacement therapy (ERT) with alglucosidase alfa for infantile-onset Pompe disease (IOPD) is limited in some patients due to the development of high and sustained antibody titers (HSAT; ≥12,800).MethodsWe carried
Externí odkaz:
https://doaj.org/article/ec2469dc10d54eddb7249c22c74a9079