Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Daniel S Krauth"'
Publikováno v:
Medical Mycology Case Reports, Vol 33, Iss , Pp 14-17 (2021)
Invasive osteoarticular infections (IOI) due to Scedosporium spp. are rare in the immune competent patient, but have been associated with direct inoculation from antecedent trauma. Here we describe a case of IOI due to Scedosporium dehoogii in a prev
Externí odkaz:
https://doaj.org/article/71828dc9aa0642a5b92531a7ba034085
Autor:
Daniel S Krauth
Publikováno v:
Military Medicine. 187:186-188
Amidst a constrained supply of novel therapeutics for the outpatient treatment of mild-to-moderate COVID-19, clinicians face new challenges, especially among those practicing at overseas military treatment facilities. Although prescribers may be unfa
Publikováno v:
Military Medicine
We describe a patient with subclinical coccidioidomycosis who experienced rapid disease dissemination shortly after SARS-CoV-2 infection, suggesting host immune response dysregulation to coccidioidomycosis by SARS-CoV-2. We hypothesize that disrupted
Publikováno v:
Clinical Case Reports
Key Clinical Message Central nervous system (CNS) tuberculosis should be considered in patients from endemic nations with worsening neurological symptoms. If imaging reveals possible CNS tuberculomas, potentially life‐threatening lesions should be
Autor:
Yang C. Fann, Stephen P. Daiger, Kari Branham, Linn Gieser, Magnus Abrahamson, Shomi S. Bhattacharya, Radu Cojocaru, James S. Friedman, Sara J. Bowne, Joseph W. Ray, Noor M. Ghiasvand, Kory R. Johnson, Christina Chakarova, Lotta Gränse, David G. Birch, Gonçalo R. Abecasis, Dianna K. Hughbanks-Wheaton, Naushin Waseem, Matthew Brooks, Lori S. Sullivan, Edward H. Trager, Daniel S. Krauth, Debra K. Breuer, Harald H H Göring, Andrew R. Webster, Vesna Ponjavic, Ritu Khanna, Sten Andréasson, Therése Hugosson, John R. Heckenlively, Anand Swaroop
Publikováno v:
The American Journal of Human Genetics. 84(6):792-800
Retinitis pigmentosa (RP) refers to a genetically heterogeneous group of progressive neurodegenerative diseases that result in dysfunction and/or death of rod and cone photoreceptors in the retina. So far, 18 genes have been identified for autosomal-
Autor:
Daniel S. Krauth, Cécilia Maubaret, Kecia L. Feathers, Chunqiao Liu, R.E. Hurd, George E. Thomas, Robert K. Koenekoop, Irma Lopez, Maria M Campos, Matthew Brooks, John R. Heckenlively, Andrew R. Webster, Naushin Waseem, Hirva Bakeri, Ignacio R. Rodriguez, Manessa Shaw, Bo Chang, Anand Swaroop, James S. Friedman, Shomi S. Bhattacharya, Kari Branham, Debra A. Thompson
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 107(35)
Retinal degenerative diseases, such as retinitis pigmentosa and Leber congenital amaurosis, are a leading cause of untreatable blindness with substantive impact on the quality of life of affected individuals and their families. Mouse mutants with ret