Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Elizabeth Petri Henske"'
Publikováno v:
European Respiratory Review, Vol 26, Iss 143 (2017)
Lymphangioleiomyomatosis (LAM) is a destructive cystic lung disease. Mammalian target of rapamycin (mTOR) inhibitors are the primary treatment for LAM but it is unknown whether these immunosuppressing medications increase the risk for or the severity
Externí odkaz:
https://doaj.org/article/b0411d1c02f046c59b210b9eeccd05e0
Autor:
Darcy A. Krueger, Hope Northrup, Steven Roberds, Katie Smith, Julian Sampson, Bruce Korf, David J. Kwiatkowski, David Mowat, Mark Nellist, Sue Povey, Petrus de Vries, Anna Byars, David Dunn, Kevin Ess, Dena Hook, Anna Jansen, Bryan King, Mustafa Sahin, Vicky Whittemore, Elizabeth Thiele, E. Martina Bebin, Harry T. Chugani, Peter Crino, Paolo Curatolo, Greg Holmes, Rima Nabbout, Finbar O'Callaghan, James Wheless, Joyce Wu, Thomas N. Darling, Edward W. Cowen, Elizabeth Gosnell, Adelaide Hebert, Greg Mlynarczyk, Keyomaurs Soltani, Joyce Teng, Mari Wataya-Kaneda, Patricia M. Witman, Chris Kingswood, John Bissler, Klemens Budde, John Hulbert, Lisa Guay-Woodford, Matthias Sauter, Bernard Zonneberg, Sergiusz Jóźwiak, Ute Bartels, Moncef Berhouma, David Neal Franz, Mary Kay Koenig, E. Steve Roach, Jonathan Roth, Henry Wang, Howard Weiner, Francis X. McCormack, Khalid Almoosa, Alan Brody, Charles Burger, Vincent Cottin, Geraldine Finlay, Jennifer Glass, Elizabeth Petri Henske, Simon Johnson, Robert Kotloff, David Lynch, Joel Moss, Karen Smith, Jay Rhu, Angelo Taveira Da Silva, Lisa R. Young, Timothy Knilans, Robert Hinton, Ashwin Prakash, Robb Romp, Arun D. Singh, Ashish DebRoy, Pei-Lung Chen, Steven Sparagana, Michael D. Frost
Publikováno v:
Pediatric Neurology. 49(4):255-265
BackgroundTuberous sclerosis complex is a genetic disorder affecting every organ system, but disease manifestations vary significantly among affected individuals. The diverse and varied presentations and progression can be life-threatening with signi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::723d739eb435e0358d14b153600d4269
Autor:
Hope Northrup, Darcy A. Krueger, Steven Roberds, Katie Smith, Julian Sampson, Bruce Korf, David J. Kwiatkowski, David Mowat, Mark Nellist, Sue Povey, Petrus de Vries, Anna Byars, David Dunn, Kevin Ess, Dena Hook, Anna Jansen, Bryan King, Mustafa Sahin, Vicky Whittemore, Elizabeth Thiele, E. Martina Bebin, Harry T. Chugani, Peter Crino, Paolo Curatolo, Greg Holmes, Rima Nabbout, Finbar O'Callaghan, James Wheless, Joyce Wu, Thomas N. Darling, Edward W. Cowen, Elizabeth Gosnell, Adelaide Hebert, Greg Mlynarczyk, Keyomaurs Soltani, Joyce Teng, Mari Wataya-Kaneda, Patricia M. Witman, Chris Kingswood, John Bissler, Klemens Budde, John Hulbert, Lisa Guay-Woodford, Matthias Sauter, Bernard Zonneberg, Sergiusz Jóźwiak, Ute Bartels, Moncef Berhouma, David Neal Franz, Mary Kay Koenig, E. Steve Roach, Jonathan Roth, Henry Wang, Howard Weiner, Francis X. McCormack, Khalid Almoosa, Alan Brody, Charles Burger, Vincent Cottin, Geraldine Finlay, Jennifer Glass, Elizabeth Petri Henske, Simon Johnson, Robert Kotloff, David Lynch, Joel Moss, Karen Smith, Jay Rhu, Angelo Taveira Da Silva, Lisa R. Young, Timothy Knilans, Robert Hinton, Ashwin Prakash, Robb Romp, Arun D. Singh, Ashish DebRoy, Pei-Lung Chen, Steven Sparagana, Michael D. Frost
Publikováno v:
Pediatric Neurology. 49:243-254
BACKGROUND: Tuberous sclerosis complex is highly variable in clinical presentation and findings. Disease manifestations continue to develop over the lifetime of an affected individual. Accurate diagnosis is fundamental to implementation of appropriat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12a26d4c528c59947541c14b538c321a
https://doi.org/10.1016/j.pediatrneurol.2013.08.001
https://doi.org/10.1016/j.pediatrneurol.2013.08.001
Autor:
Bernd W. Scheithauer, Stephen J. Dreyer, Keita Fujikawa, Lisa L. Wessner, Jay Bernstein, Tahseen Al-Saleem, Johannes Bjornsson, Elizabeth Petri Henske, E. Steven Roach, Kathleen Patterson
Publikováno v:
Cancer. 83:2208-2216
BACKGROUND The tuberous sclerosis complex (TSC) is an autosomal dominant disorder characterized by seizures, mental retardation, and benign tumors of the brain, heart, skin, and kidney. Malignant tumors also can occur in patients with tuberous sclero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa71690ed2eefc2d4c0ecdd3b6abf399
https://doi.org/10.1002/(sici)1097-0142(19981115)83:10<2208::aid-cncr21>3.0.co
https://doi.org/10.1002/(sici)1097-0142(19981115)83:10<2208::aid-cncr21>3.0.co
Publikováno v:
Methods in molecular medicine. 126
Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome characterized by seizures, mental retardation, and benign tumors of many organs, including the brain, kidneys, skin, retina, and heart. TSC is caused by mutations in the TSC1 and TSC2 tumo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5ebd6b3aa77db08b0f405d5e4a098f68
https://pubmed.ncbi.nlm.nih.gov/16930013
https://pubmed.ncbi.nlm.nih.gov/16930013
Autor:
Elizabeth Petri Henske
Publikováno v:
Oncology Times. 23:36-37
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abf83fced7b0244b8d1b57929622e2dc
https://doi.org/10.1097/01.cot.0000313794.86490.a2
https://doi.org/10.1097/01.cot.0000313794.86490.a2
Autor:
Elizabeth Petri Henske
Publikováno v:
Genes, Chromosomes & Cancer; Dec2003, Vol. 38 Issue 4, p376, 6p