Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Cindy Scurlock"'
Autor:
Sara Mansoorshahi, Cindy Scurlock, Scientific Advisory Board of the Turner Syndrome Society of the United States Research Registry, Siddharth K Prakash
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-5 (2024)
Abstract Background Many different clinical specialists provide care to patients with Turner syndrome (TS), who have highly variable clinical manifestations. Therefore, a national TS registry is essential to inform a cohesive approach to healthcare a
Externí odkaz:
https://doaj.org/article/efd8180ba7d144ccb6588d0f8dfe8e3d
Autor:
Michael Silberbach, Alan C. Braverman, Siddharth K. Prakash, Jolien W. Roos-Hesselink, Emilio Quezada, Cindy Scurlock
Publikováno v:
International Journal of Cardiology. 377:44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a47b47b2f29793f985ea56cfab00362b
https://doi.org/10.1016/j.ijcard.2023.01.075
https://doi.org/10.1016/j.ijcard.2023.01.075
Autor:
Vaneeta Bamba, Lynne L. Levitsky, Ashley W. Wong, Greysha Rivera-Cruz, Cindy Scurlock, Angela E. Lin
Publikováno v:
J Assist Reprod Genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9eff0edcef384ab1be3747b6e9c554a3
https://doi.org/10.1007/s10815-022-02457-5
https://doi.org/10.1007/s10815-022-02457-5
Autor:
Benjamin C Bugajski, Teresa Scerbak, David E. Sandberg, Kathleen L. Dooley Maley, Dianne Singer, Cindy Scurlock, Michael Silberbach, Sally J. Eder, Denise D. Culin, Achamyeleh Gebremariam
Publikováno v:
American journal of medical genetics. Part C, Seminars in medical genetics. 181(1)
Despite major discoveries, traditional biomedical research has not always addressed topics perceived as priorities by patients and their families. Patient-centered care is predicated on research taking such priorities into account. The present study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7440fbee6510a322d54140930614225c
https://pubmed.ncbi.nlm.nih.gov/30767373
https://pubmed.ncbi.nlm.nih.gov/30767373
Autor:
Nunilo Rubio, Avni Shah, Paul Kruszka, Soniely Lugo‐Ruiz, Cheryl L. Maslen, Vaneeta Bamba, Shanlee M Davis, Michelle Rivera-Davila, Michael Silberbach, Gary A. Lorigan, Melissa Crenshaw, Karen Rubin, Rebecca C. Knickmeyer, Siddharth K. Prakash, Aaron T. Dorfman, Cindy Scurlock
Publikováno v:
Am J Med Genet C Semin Med Genet
To address knowledge gaps about Turner syndrome (TS) associated disease mechanisms, the Turner Syndrome Society of the United States created the Turner Syndrome Research Registry (TSRR), a patient-powered registry for girls and women with TS. More th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d22f4dc6118f964a6f0b75fe73313d4
https://pubmed.ncbi.nlm.nih.gov/30758128
https://pubmed.ncbi.nlm.nih.gov/30758128
Autor:
Siddharth K, Prakash, Melissa L, Crenshaw, Philippe F, Backeljauw, Michael, Silberbach, Cindy, Scurlock, Denise D, Culin, Kelly C, Ranallo, Angela E, Lin
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 21(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d210c9159f7a5d2dcba6613cc58ab9b6
https://pubmed.ncbi.nlm.nih.gov/30573795
https://pubmed.ncbi.nlm.nih.gov/30573795
Autor:
Angela E. Lin, Denise D. Culin, Kelly C. Ranallo, Cindy Scurlock, Philippe F. Backeljauw, Melissa Crenshaw, Siddharth K. Prakash, Michael Silberbach
Publikováno v:
Genetics in Medicine. 21:1882-1883
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c60fd946147f055945e9f56998cd7be
https://doi.org/10.1038/s41436-018-0411-z
https://doi.org/10.1038/s41436-018-0411-z
Autor:
Steven D. Chernausek, Cheryl L. Maslen, Joan Foodim, Victoria L. Pemberton, David C. Page, David S. Hong, Philippe Backeljauw, Siddharth K. Prakash, Nelly Mauras, Laura P. Fasciano, Allan L. Reiss, Scott Hawley, Rebecca C. Knickmeyer, Barbara M. Lippe, Joseph T. Cernich, Michael Silberbach, Gary A. Lorigan, David A. Cole, Carolyn A. Bondy, Cindy Scurlock, Angela E. Lin, Kelly C. Ranallo, David E. Sandberg, Paul Kruszka, Charmian A. Quigley
Publikováno v:
PMC
American journal of medical genetics. Part A, vol 167A, iss 9
American journal of medical genetics. Part A, vol 167A, iss 9
Turner syndrome, a congenital condition that affects ∼1/2,500 births, results from absence or structural alteration of the second sex chromosome. There has been substantial effort by numerous clinical and genetic research groups to delineate the cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05f28f143fe19fdbaad6d3fb90c37623
https://orcid.org/0000-0001-9920-3411
https://orcid.org/0000-0001-9920-3411
