Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Sydney M. Brown"'
Autor:
Cheney, C. R.
Publikováno v:
Medium Ævum, 1965 Jan 01. 34(2), 142-143.
Externí odkaz:
https://www.jstor.org/stable/43631211
Autor:
Kenney, John F.
Publikováno v:
The Catholic Historical Review, 1966 Apr 01. 52(1), 110-112.
Externí odkaz:
https://www.jstor.org/stable/25017765
Autor:
Little, Lester K.
Publikováno v:
Church History, 1966 Sep 01. 35(3), 367-368.
Externí odkaz:
https://www.jstor.org/stable/3162327
Autor:
Iris R. Hartley, Rachel I. Gafni, Kelly L. Roszko, Sydney M. Brown, Luis F. de Castro, Amanda Saikali, Carlos R. Ferreira, William A. Gahl, Karel Pacak, Jenny E. Blau, Alison M. Boyce, Isidro B. Salusky, Michael T. Collins, Pablo Florenzano
Publikováno v:
Journal of Bone and Mineral Research. 37:2174-2185
Fibroblast growth factor-23 (FGF23) measurement is a critical tool in the evaluation of patients with disordered phosphate homeostasis. Available laboratory reference ranges for blood FGF23 were developed using samples from normophosphatemic individu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9684916a97dfa1bdddba217675c4fa43
https://doi.org/10.1002/jbmr.4702
https://doi.org/10.1002/jbmr.4702
Autor:
null Iris R Hartley, null Rachel I Gafni, null Kelly L Roszko, null Sydney M Brown, null Luis F de Castro, null Amanda Saikali, null Carlos R Ferreira, null William A Gahl, null Karel Pacak, null Jenny E. Blau, null Alison M Boyce, null Isidro B Salusky, null Michael T Collins, null P Florenzano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e617895fd77348bf0ae88e2793143ef5
https://doi.org/10.1002/jbmr.4702/v2/response1
https://doi.org/10.1002/jbmr.4702/v2/response1
Autor:
Thanh Huynh, Ying Pang, Karel Pacak, Sydney M Brown, Michael T. Collins, Kelly L Roszko, Zhengping Zhuang
Publikováno v:
Journal of Bone and Mineral Research. 36:315-321
Fibroblast growth factor 23 (FGF23) is a key phosphate- and vitamin D-regulating hormone. FGF23 circulates as an intact 251 amino acid protein or N- and C-terminal degradation products. Hormone activity resides in the intact molecule, but it has been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce3f1d6394dec9f987c03d95eb48ec5a
https://doi.org/10.1002/jbmr.4195
https://doi.org/10.1002/jbmr.4195
Autor:
J. W. Gray
Publikováno v:
The Journal of Ecclesiastical History. 16:234-235
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40fdc9710cfc192bdeaf9929fb7ace02
https://doi.org/10.1017/s0022046900054142
https://doi.org/10.1017/s0022046900054142
Autor:
Harvey Kushner, Pablo Florenzano, Kristen S. Pan, Sydney M Brown, Alison M. Boyce, Michael T. Collins, Lori C. Guthrie, Luis F de Castro, Scott M. Paul
Publikováno v:
Journal of Bone and Mineral Research. 34:653-660
Fibrous dysplasia (FD) is a mosaic disease in which bone is replaced with fibro-osseous tissue. Lesions expand during childhood, reaching final burden by age 15 years. In vitro data suggest that disease activity decreases in adulthood; however, there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::857eb7adac7818179e5d84bec679b9cc
https://doi.org/10.1002/jbmr.3649
https://doi.org/10.1002/jbmr.3649
Autor:
Michael T. Collins, Galina Nesterova, Sydney M Brown, Carlos Ferreira, Sri Harsha Tella, Adom Whitaker, Renata C. Pereira, William A. Gahl, Luis F de Castro, Pablo Florenzano, Dorothy I. Bulas, Isidro B. Salusky, Mary Scott Roberts, Rachel I Gafni
Publikováno v:
Journal of Bone and Mineral Research. 33:1870-1880
Nephropathic cystinosis is a rare lysosomal storage disorder. Patients present in the first year of life with renal Fanconi syndrome that evolves to progressive chronic kidney disease (CKD). Despite the multiple risk factors for bone disease, the fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f4a8e05b5f08ba4d7389db6b7a256c1
https://doi.org/10.1002/jbmr.3522
https://doi.org/10.1002/jbmr.3522
Autor:
Pablo, Florenzano, Carlos, Ferreira, Galina, Nesterova, Mary Scott, Roberts, Sri Harsha, Tella, Luis Fernandez, de Castro, Sydney M, Brown, Adom, Whitaker, Renata C, Pereira, Dorothy, Bulas, Rachel I, Gafni, Isidro B, Salusky, William A, Gahl, Michael T, Collins
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 33(10)
Nephropathic cystinosis is a rare lysosomal storage disorder. Patients present in the first year of life with renal Fanconi syndrome that evolves to progressive chronic kidney disease (CKD). Despite the multiple risk factors for bone disease, the fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd99303bc943487ccf358b12c72da198
https://pubmed.ncbi.nlm.nih.gov/29905968
https://pubmed.ncbi.nlm.nih.gov/29905968