Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Meenal Mendiratta"'
Autor:
Guohua Zhang, Meenal Mendiratta, Bobby Guillory, Jiaohua Luo, Blaga Belinova, Andres Splenser, Tripti Halder, Jose M. Garcia, Ji An Chen, Yi-Ping Li
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle. 6:132-143
Background Cachexia and muscle atrophy are common consequences of cancer and chemotherapy administration. The novel hormone ghrelin has been proposed as a treatment for this condition. Increases in food intake and direct effects on muscle proteolysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ff39215649839cc7e9abc1afca45bb6
https://doi.org/10.1002/jcsm.12023
https://doi.org/10.1002/jcsm.12023
Autor:
Johanna Viau, Colindres, Marni, Axelrad, Laurence, McCullough, E O'Brian, Smith, Gene O, Huang, Duong D, Tu, Jennifer L, Bercaw-Pratt, Min-Jye, Cheni, Meenal, Mendiratta, Sheila, Gunn, Reid, Sutton, Charles, Macias, Lefkothea P, Karaviti
Publikováno v:
Pediatric endocrinology reviews : PER. 13(3)
45,X/46,XY gonadal dysgenesis is a disorder of sexual differentiation with a wide clinical presentation, ranging from Turner-like females to individuals with genital ambiguity to azoospermic but otherwise normal-appearing males. Hence, patients can b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd9d624c1bfc18ec4d2134513559f18b
https://pubmed.ncbi.nlm.nih.gov/27116846
https://pubmed.ncbi.nlm.nih.gov/27116846
Autor:
Ji-An, Chen, Andres, Splenser, Bobby, Guillory, Jiaohua, Luo, Meenal, Mendiratta, Blaga, Belinova, Tripti, Halder, Guohua, Zhang, Yi-Ping, Li, Jose M, Garcia
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle
Background Cachexia and muscle atrophy are common consequences of cancer and chemotherapy administration. The novel hormone ghrelin has been proposed as a treatment for this condition. Increases in food intake and direct effects on muscle proteolysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::054040f1318b42873efdda9ffcadb923
https://pubmed.ncbi.nlm.nih.gov/26136189
https://pubmed.ncbi.nlm.nih.gov/26136189
Autor:
Yaping Yang, Christine M. Eng, Meenal Mendiratta, Lefkothea P. Karaviti, Alecia Willis, Andrea E. Balazs, Lorraine Potocki
Publikováno v:
International Journal of Pediatric Endocrinology, Vol 2011, Iss 1, p 5 (2011)
International Journal of Pediatric Endocrinology
International Journal of Pediatric Endocrinology
Isolated hypocortisolism due to ACTH deficiency is a rare condition that can be caused by homozygous or compound heterozygous mutations in the gene encoding proopiomelanocortin (POMC). Loss of function mutations of POMC gene typically results in adre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e10c14d9143aa11a12c049c3c296c273
http://www.ijpeonline.com/content/2011/1/5
http://www.ijpeonline.com/content/2011/1/5
Autor:
Mirna X Escalante, Meenal Mendiratta, Jennifer E Dietrich, Nancy A Sokkary, Laurence McCullough, Marni E Axelrad, Vernon R Sutton, Rona Y Sonabend, Shannon L French, Sheila K Gunn, Lefkothea P Karaviti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25af65d6c235bb43edb43de64f47c89f
https://doi.org/10.1210/endo-meetings.2011.part4.p13.p3-732
https://doi.org/10.1210/endo-meetings.2011.part4.p13.p3-732
