Zobrazeno 1 - 10
of 191
pro vyhledávání: '"Mark J. Pettenati"'
Autor:
Guillermo Galdon, Nima Pourhabibi Zarandi, Nicholas A. Deebel, Sue Zhang, Olivia Cornett, Dmitry Lyalin, Mark J. Pettenati, YanHe Lue, Christina Wang, Ronald Swerdloff, Thomas D. Shupe, Colin Bishop, Kimberly Stogner, Stanley J. Kogan, Stuart Howards, Anthony Atala, Hooman Sadri-Ardekani
Publikováno v:
Bioengineering, Vol 11, Iss 7, p 677 (2024)
Increasing survival rates of children following cancer treatment have resulted in a significant population of adult survivors with the common side effect of infertility. Additionally, the availability of genetic testing has identified Klinefelter syn
Externí odkaz:
https://doaj.org/article/0d499f5a34b345c688140e6641678963
Autor:
Guillermo Galdon, Nicholas A. Deebel, Nima Pourhabibi Zarandi, Darren Teramoto, YanHe Lue, Christina Wang, Ronald Swerdloff, Mark J. Pettenati, William G. Kearns, Stuart Howards, Stanley Kogan, Anthony Atala, Hooman Sadri-Ardekani
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Klinefelter Syndrome (KS) is characterized by a masculine phenotype, supernumerary sex chromosomes (47, XXY), and impaired fertility due to loss of spermatogonial stem cells (SSCs). Early testicular cryopreservation could be an option for future fert
Externí odkaz:
https://doaj.org/article/dca5682826f54e5e814853440325de06
Autor:
Guillermo Galdon, Nicholas A. Deebel, Nima Pourhabibi Zarandi, Mark J. Pettenati, Stanley Kogan, Christina Wang, Ronald S. Swerdloff, Anthony Atala, Yanhe Lue, Hooman Sadri-Ardekani
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 1, p 173 (2021)
Klinefelter syndrome (KS) is characterized by a masculine phenotype, supernumerary sex chromosomes (usually XXY), and spermatogonial stem cell (SSC) loss in their early life. Affecting 1 out of every 650 males born, KS is the most common genetic caus
Externí odkaz:
https://doaj.org/article/41f4a11e3d8b44e2a488ec102c850444
Publikováno v:
Case Reports in Hematology, Vol 2020 (2020)
Mantle cell lymphoma is a non-Hodgkin lymphoproliferative neoplasm with several clinical and morphologic variants linked, primarily, through genetic derangement of the cyclin D1 locus. Aberrant phenotypes have been described, though prognostic data i
Externí odkaz:
https://doaj.org/article/0433750184f146b19b6a6eaa7eade9b0
Autor:
Seema Naik, Kristy Tayapongsak, Katherine Robbins, Cyrus Koresh Manavi, Mark J. Pettenati, David D. Grier
Publikováno v:
Case Reports in Oncology, Vol 6, Iss 1, Pp 6-14 (2013)
Posttransplant lymphoproliferative disorders (PTLD) are a rare, but serious complication following transplantation. Late-onset PTLD are often associated with more monoclonal lesions and consequently have a worse prognosis. There are only isolated cas
Externí odkaz:
https://doaj.org/article/83502968bd794a2f96a8a9c861d3655f
Autor:
Amudha Palanisamy, Paul Persad, Patrick P. Koty, Laurie L. Douglas, Robert J. Stratta, Jeffrey Rogers, Amber M. Reeves-Daniel, Giuseppe Orlando, Alan C. Farney, Michael W. Beaty, Mark J. Pettenati, Samy S. Iskandar, David D. Grier, Scott A. Kaczmorski, William H. Doares, Michael D. Gautreaux, Barry I. Freedman, Bayard L. Powell
Publikováno v:
Case Reports in Nephrology, Vol 2015 (2015)
We report the rare occurrence of donor-derived myeloid sarcoma in two kidney transplant patients who received organs from a single deceased donor. There was no evidence of preexisting hematologic malignancy in the donor at the time of organ recovery.
Externí odkaz:
https://doaj.org/article/61f5b3f777b749dcb2e9e5ad4a7d1a43
Autor:
Guillermo Galdon, Nicholas A. Deebel, Nima Pourhabibi Zarandi, Mark J. Pettenati, Stanley Kogan, Christina Wang, Ronald S. Swerdloff, Anthony Atala, Yanhe Lue, Hooman Sadri-Ardekani
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 173, p 173 (2022)
International journal of molecular sciences, vol 23, iss 1
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 173
International Journal of Molecular Sciences
International journal of molecular sciences, vol 23, iss 1
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 173
International Journal of Molecular Sciences
Klinefelter syndrome (KS) is characterized by a masculine phenotype, supernumerary sex chromosomes (usually XXY), and spermatogonial stem cell (SSC) loss in their early life. Affecting 1 out of every 650 males born, KS is the most common genetic caus
Autor:
William T Harrison, Elena M Fenu, Mark Giffen, Stacey S O'Neill, Mark J. Pettenati, Giovanni Insuasti-Beltran
Publikováno v:
The American journal of forensic medicine and pathology. 42(2)
Acute myeloid leukemia can rarely cause sudden, unexpected death in children. Presentation may be non-specific and death may occur in children with no prior medical history. Herein we present the case of a previously healthy 2-year and 2 month-old Wh
Publikováno v:
Journal of Urology. 203
INTRODUCTION AND OBJECTIVE:Around 1% of general population of men suffer from azoospermia who divided into two categories: Obstructive (OA) and non-obstructive azoospermia (NOA). The most precise s...
Autor:
Angela G Niehaus, Paula Moore, Mark J. Pettenati, Nancy S Rosenthal, Robert K McCall, Bayard L. Powell
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.