Zobrazeno 1 - 6
of 6
pro vyhledávání: '"P G, Stalboerger"'
Autor:
Tyler J. Rolland, Timothy E. Peterson, Ramandeep Takhter, Skylar A. Rizzo, Soulmaz Boroumand, Ao Shi, Tyra A. Witt, Mary Nagel, Cassandra K. Kisby, Sungjo Park, Lois A. Rowe, Christopher R. Paradise, Laura R. E. Becher, Brooke D. Paradise, Paul G. Stalboerger, Emanuel C. Trabuco, Atta Behfar
Publikováno v:
npj Regenerative Medicine, Vol 7, Iss 1, Pp 1-17 (2022)
Abstract Urinary incontinence afflicts up to 40% of adult women in the United States. Stress urinary incontinence (SUI) accounts for approximately one-third of these cases, precipitating ~200,000 surgical procedures annually. Continence is maintained
Externí odkaz:
https://doaj.org/article/f302f092892549b692c321282915b005
Autor:
Tyler J. Rolland, Timothy E. Peterson, Raman Deep Singh, Skylar A. Rizzo, Soulmaz Boroumand, Ao Shi, Tyra A. Witt, Mary Nagel, Cassandra K. Kisby, Sungjo Park, Lois A. Rowe, Christopher R. Paradise, Laura R. E. Becher, Brooke D. Paradise, Paul G. Stalboerger, Emanuel C. Trabuco, Atta Behfar
Publikováno v:
npj Regenerative Medicine, Vol 7, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/cfa46d27f5aa475783881ef28822d402
Autor:
R B Jenkins, E Pras, S B Raff, George P. Chrousos, Constantine Tsigos, P G Stalboerger, J A Carney, Constantine S. Mitsiadis, Constantine A. Stratakis
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 81:3607-3614
Carney complex (CC) is a familial multiple neoplasia and lentiginosis syndrome, transmitted in an autosomal dominant manner. It is the only familial form of cardiac and skin myxomas known and includes endocrine neoplasms causing Cushing's syndrome [p
Publikováno v:
Transplantation Journal. 94:780
Autor:
G W, Dewald, C R, Schad, E R, Christensen, M E, Law, A R, Zinsmeister, P G, Stalboerger, S M, Jalal, R C, Ash, R B, Jenkins
Publikováno v:
Bone marrow transplantation. 12(2)
We investigated the efficacy of fluorescence-labelled chromosome probes (CEP-X/Y) for the X and Y chromosomes to study patients who have had opposite sex BMT. These probes hybridize to the centromere region of the X chromosome and nearly the entire l
Autor:
R B, Jenkins, M M, Le Beau, W J, Kraker, T J, Borell, P G, Stalboerger, E M, Davis, L, Penland, A, Fernald, R, Espinosa, D J, Schaid
Publikováno v:
Blood. 79(12)
Trisomy 8 is a common anomaly in bone marrow (BM) cells of patients with myeloproliferative disorders (MPD), myelodysplastic syndromes (MDS), or acute nonlymphocytic leukemia (ANLL). We studied the efficacy of fluorescence in situ hybridization (FISH