Zobrazeno 1 - 10
of 694
pro vyhledávání: '"Usha, G"'
Autor:
Yuvashri, R., Thendral, Era Dravida, Jonathan, D. Reuben, Fathima, A. Anish, Laavanya, K., Usha, G.
Publikováno v:
In Chemical Physics Impact December 2024 9
Publikováno v:
In Journal of Molecular Structure 15 July 2024 1308
Autor:
Fathima, A. Anish, Kumaravel, Varuna, Jonathan, D. Reuben, Sadasivam, Senthil Kumar, Yuvashri, R., Usha, G.
Publikováno v:
In Chemical Physics Impact June 2024 8
Publikováno v:
In Journal of Molecular Structure 5 January 2024 1295 Part 2
Autor:
Timothy A. Howell, Louis S. Matza, Usha G. Mallya, Anthony P. Goldstone, W. Scott Butsch, Ethan Lazarus
Publikováno v:
Obesity Science & Practice, Vol 9, Iss 4, Pp 376-382 (2023)
Abstract Objective Rare genetic diseases of obesity typically present with hyperphagia, a pathologic desire to consume food. Cost‐utility models assessing the value of treatments for these rare diseases will require health state utilities represent
Externí odkaz:
https://doaj.org/article/b889b1a8691641c289ab324c2b56ef3a
Autor:
Elizabeth Forsythe, Usha G. Mallya, Min Yang, Caroline Huber, Mary Lynn Cala, Alexandra Greatsinger, Ella Hagopian, Jeremy Pomeroy, Andrea M. Haqq
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-12 (2023)
Abstract Background Bardet-Biedl syndrome (BBS) is a rare, genetically heterogeneous obesity syndrome associated with hyperphagia. Given the early onset of BBS symptoms in childhood and multifaceted complications, this study aimed to quantify the car
Externí odkaz:
https://doaj.org/article/13858c5d51db43c5b28162d8281e35cc
Autor:
Elizabeth Forsythe, Usha G. Mallya, Min Yang, Caroline Huber, Mary Lynn Cala, Alexandra Greatsinger, Ella Hagopian, Jeremy Pomeroy, Andrea M. Haqq
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Signs and symptoms of Bardet–Biedl syndrome (BBS) occur during early childhood, progress over time, and place substantial, multifaceted burden on patients and their caregivers. Hyperphagia may be a contributing factor to early-o
Externí odkaz:
https://doaj.org/article/b0b9f9b20aad497f8d8c3b210f153398
Autor:
Jonathan, D. Reuben, DravidaThendral, Era., Krishna Priya, M., Angeline Shirmila, D., Anish Fathima, A, Yuvashri, R, Usha, G.
Publikováno v:
In Journal of Molecular Structure 15 November 2023 1292
Publikováno v:
In Journal of Molecular Structure 15 July 2023 1284
Autor:
Elizabeth Forsythe, Robert M. Haws, Jesús Argente, Philip Beales, Gabriel Á. Martos-Moreno, Hélène Dollfus, Costel Chirila, Ari Gnanasakthy, Brieana C. Buckley, Usha G. Mallya, Karine Clément, Andrea M. Haqq
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Bardet–Biedl syndrome is a rare genetic disease associated with hyperphagia and early-onset, severe obesity. There is limited evidence on how hyperphagia and obesity affect health-related quality of life in patients with Bardet
Externí odkaz:
https://doaj.org/article/95baf4bee81746aaaf9b8a040bb3a09a