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Siccibacter turicensis; Slackia exigua; Sneathia sanguinegens; Solobacterium moorei; Sphingobacterium spiritivorum
(Fung M, Zompi S, Seng H, . Plasma cell-free DNA next-generation sequencing to diagnose and monitor infections in allogeneic hematopoietic stem cell transplant patients. Open Forum Infect Dis. 2018;5(12):ofy301. doi:10.1093/ofid/ofy30130581881)
Fung M, Zompi S, Seng H, . Plasma cell-free DNA next-generation sequencing to diagnose and monitor infections in allogeneic hematopoietic stem cell transplant patients. Open Forum Infect Dis. 2018;5(12):ofy301. doi:10.1093/ofid/ofy30130581881Fung M, Zompi S, Seng H, . Plasma cell-free DNA next-generation sequencing to diagnose and monitor infections in allogeneic hematopoietic stem cell transplant patients. Open Forum Infect Dis. 2018;5(12):ofy301. doi:10.1093/ofid/ofy30130581881, Fung M, Zompi S, Seng H, . Plasma cell-free DNA next-generation sequencing to diagnose and monitor infections in allogeneic hematopoietic stem cell transplant patients. Open Forum Infect Dis. 2018;5(12):ofy301. doi:10.1093/ofid/ofy30130581881
Paecilomyces hepiali; Paracoccidioides brasiliensis; Paracoccidioides lutzii; Penicillium antarcticum; Penicillium brasilianum; Penicillium capsulatum; Penicillium carneum; Penicillium coprophilum
(Gafter-Gvili A, Fraser A, Paul M, . Antibiotic prophylaxis for bacterial infections in afebrile neutropenic patients following chemotherapy. Cochrane Database Syst Rev. 2012;1:CD004386. doi:10.1002/14651858.CD004386.pub322258955)
Gafter-Gvili A, Fraser A, Paul M, . Antibiotic prophylaxis for bacterial infections in afebrile neutropenic patients following chemotherapy. Cochrane Database Syst Rev. 2012;1:CD004386. doi:10.1002/14651858.CD004386.pub322258955Gafter-Gvili A, Fraser A, Paul M, . Antibiotic prophylaxis for bacterial infections in afebrile neutropenic patients following chemotherapy. Cochrane Database Syst Rev. 2012;1:CD004386. doi:10.1002/14651858.CD004386.pub322258955, Gafter-Gvili A, Fraser A, Paul M, . Antibiotic prophylaxis for bacterial infections in afebrile neutropenic patients following chemotherapy. Cochrane Database Syst Rev. 2012;1:CD004386. doi:10.1002/14651858.CD004386.pub322258955
Granulibacter bethesdensis; Granulicatella adiacens; Granulicatella elegans; Grimontia hollisae; Haemophilus aegyptius; Haemophilus ducreyi; Haemophilus haemolyticus
Bloodstream infection event (central line-associated bloodstream infection and non-central line associated bloodstream infection)
Schizophyllum commune; Sporopachydermia quercuum; Sporothrix brasiliensis; Sporothrix globosa; Sporothrix insectorum; Sporothrix pallida; Sporothrix schenckii; Stachybotrys chartarum
Colletotrichum falcatum; Colletotrichum fioriniae; Colletotrichum gloeosporioides
Nocardia cummidelens; Nocardia cyriacigeorgica; Nocardia dassonvillei; Nocardia elegans
Lactobacillus acidophilus; Lactobacillus casei; Lactobacillus crispatus; Lactobacillus fermentum; Lactobacillus gasseri; Lactobacillus iners; Lactobacillus jensenii
Torque teno virus 6; Torque teno virus 7; Torque teno virus 8; Trichodysplasia spinulosa-associated polyomavirus
Legionella quinlivanii; Legionella sainthelensi; Legionella shakespearei; Legionella steelei
Leptotrichia goodfellowii; Leptotrichia shahii; Leptotrichia wadei; Leuconostoc citreum
Corynebacterium tuscaniense; Corynebacterium ulcerans; Corynebacterium urealyticum; Corynebacterium ureicelerivorans; Corynebacterium xerosis; Coxiella burnetii; Cupriavidus gilardii
Janibacter indicus; Jonesia denitrificans; Kerstersia gyiorum; Kingella denitrificans; Kingella kingae
M. Christensen, M. Heyman, M. Möttönen, B. Zeller, G. Jonmundsson, H. Hasle (2005)
Treatment‐related death in childhood acute lymphoblastic leukaemia in the Nordic countries: 1992–2001British Journal of Haematology, 131
Christensen (2005)
Treatment-related death in childhood acute lymphoblastic leukaemia in the Nordic countries: 1992-2001.Br J Haematol, 131
Research Brief Report Evaluation of mcfDNA-seq to Predict Bloodstream Infection in Pediatric Patients With Cancer
Mycoplasma fermentans; Mycoplasma genitalium; Mycoplasma hominis
Mucor indicus; Mucor irregularis; Mucor velutinosus; Myceliophthora thermophila
Alphapapillomavirus 10; Alphapapillomavirus 11
(Cheung YT, Eskind A, Inaba H, . Association of bacteremic sepsis with long-term neurocognitive dysfunction in pediatric patients with acute lymphoblastic leukemia. JAMA Pediatr. 2018;172(11):1092-1095. doi:10.1001/jamapediatrics.2018.250030264151)
Cheung YT, Eskind A, Inaba H, . Association of bacteremic sepsis with long-term neurocognitive dysfunction in pediatric patients with acute lymphoblastic leukemia. JAMA Pediatr. 2018;172(11):1092-1095. doi:10.1001/jamapediatrics.2018.250030264151Cheung YT, Eskind A, Inaba H, . Association of bacteremic sepsis with long-term neurocognitive dysfunction in pediatric patients with acute lymphoblastic leukemia. JAMA Pediatr. 2018;172(11):1092-1095. doi:10.1001/jamapediatrics.2018.250030264151, Cheung YT, Eskind A, Inaba H, . Association of bacteremic sepsis with long-term neurocognitive dysfunction in pediatric patients with acute lymphoblastic leukemia. JAMA Pediatr. 2018;172(11):1092-1095. doi:10.1001/jamapediatrics.2018.250030264151
Eikenella corrodens; Elizabethkingia anophelis; Elizabethkingia meningoseptica
T. Blauwkamp, Simone Thair, Michael Rosen, L. Blair, M. Lindner, I. Vilfan, T. Kawli, F. Christians, S. Venkatasubrahmanyam, Gregory Wall, Anita Cheung, Zoë Rogers, G. Meshulam-Simon, L. Huijse, S. Balakrishnan, J. Quinn, D. Hollemon, David Hong, M. Vaughn, Mickey Kertesz, S. Bercovici, J. Wilber, Samuel Yang (2019)
Analytical and clinical validation of a microbial cell-free DNA sequencing test for infectious diseaseNature Microbiology, 4
Phellinus noxius; Phialophora attae; Phoma herbarum; Phycomyces blakesleeanus; Pichia anomala; Pneumocystis carinii; Pneumocystis jirovecii; Pneumocystis murina
Penicillium vulpinum; Phaeoacremonium minimum; Phanerochaete carnosa
Alternaria alternata; Alternaria arborescens; Alternaria brassicicola; Anncaliia algerae
Malassezia nana; Malassezia obtusa; Malassezia pachydermatis; Malassezia slooffiae
(2020)
Delftia acidovoransDefinitions
Scedosporium apiospermum; Scedosporium aurantiacum; Scedosporium boydii
H. Inaba, H. Inaba, Deqing Pei, J. Wolf, S. Howard, S. Howard, R. Hayden, M. Go, Olga Varechtchouk, T. Hahn, Jassada Buaboonnam, M. Metzger, M. Metzger, J. Rubnitz, J. Rubnitz, Raul Ribeiro, R. Ribeiro, J. Sandlund, J. Sandlund, S. Jeha, S. Jeha, C. Cheng, W. Evans, W. Evans, M. Relling, M. Relling, C. Pui, C. Pui (2016)
Infection-related complications during treatment for childhood acute lymphoblastic leukemiaAnnals of Oncology, 28
Porcine circovirus 1; Porcine circovirus 2; Primate bocaparvovirus 1; Pseudocowpox virus
Apophysomyces trapeziformis; Apophysomyces variabilis; Aspergillus aculeatus
Enterococcus gallinarum; Enterococcus gilvus; Enterococcus haemoperoxidus; Enterococcus hirae; Enterococcus italicus; Enterococcus malodoratus; Enterococcus mundtii
(Adler A, Yaniv I, Solter E, . Catheter-associated bloodstream infections in pediatric hematology-oncology patients: factors associated with catheter removal and recurrence. J Pediatr Hematol Oncol. 2006;28(1):23-28.16394888)
Adler A, Yaniv I, Solter E, . Catheter-associated bloodstream infections in pediatric hematology-oncology patients: factors associated with catheter removal and recurrence. J Pediatr Hematol Oncol. 2006;28(1):23-28.16394888Adler A, Yaniv I, Solter E, . Catheter-associated bloodstream infections in pediatric hematology-oncology patients: factors associated with catheter removal and recurrence. J Pediatr Hematol Oncol. 2006;28(1):23-28.16394888, Adler A, Yaniv I, Solter E, . Catheter-associated bloodstream infections in pediatric hematology-oncology patients: factors associated with catheter removal and recurrence. J Pediatr Hematol Oncol. 2006;28(1):23-28.16394888
Alphapapillomavirus 9
Haemophilus parainfluenzae; Haemophilus paraphrohaemolyticus; Haemophilus quentini; Haemophilus sputorum; Hafnia alvei; Hafnia paralvei
P. Ramanan, J. Barreto, D. Osmon, P. Tosh (2014)
Rothia Bacteremia: a 10-Year Experience at Mayo Clinic, Rochester, MinnesotaJournal of Clinical Microbiology, 52
Dysgonomonas capnocytophagoides; Dysgonomonas gadei; Dysgonomonas hofstadii
Trichoderma virens; Trichophyton; Trichophyton benhamiae; Trichosporon asahii
Stenotrophomonas acidaminiphila; Stenotrophomonas maltophilia; Streptobacillus moniliformis; Streptococcus agalactiae; Streptococcus anginosus
Koichi Yamada, Hiroki Namikawa, H. Fujimoto, K. Nakaie, Etsuko Takizawa, Yasuyo Okada, Akiko Fujita, H. Kawaguchi, Yasutaka Nakamura, Junko Abe, Y. Kaneko, H. Kakeya (2017)
Clinical Characteristics of Methicillin-resistant Coagulase-negative Staphylococcal Bacteremia in a Tertiary HospitalInternal Medicine, 56
Stemphylium lycopersici; Syncephalastrum monosporum; Syncephalastrum racemosum
(Ivy MI, Thoendel MJ, Jeraldo PR, . Direct detection and identification of prosthetic joint infection pathogens in synovial fluid by metagenomic shotgun sequencing. J Clin Microbiol. 2018;56(9):e00402-18. doi:10.1128/JCM.00402-1829848568)
Ivy MI, Thoendel MJ, Jeraldo PR, . Direct detection and identification of prosthetic joint infection pathogens in synovial fluid by metagenomic shotgun sequencing. J Clin Microbiol. 2018;56(9):e00402-18. doi:10.1128/JCM.00402-1829848568Ivy MI, Thoendel MJ, Jeraldo PR, . Direct detection and identification of prosthetic joint infection pathogens in synovial fluid by metagenomic shotgun sequencing. J Clin Microbiol. 2018;56(9):e00402-18. doi:10.1128/JCM.00402-1829848568, Ivy MI, Thoendel MJ, Jeraldo PR, . Direct detection and identification of prosthetic joint infection pathogens in synovial fluid by metagenomic shotgun sequencing. J Clin Microbiol. 2018;56(9):e00402-18. doi:10.1128/JCM.00402-1829848568
Lomentospora prolificans; Macrophomina phaseolina; Madurella mycetomatis; Malassezia caprae; Malassezia cuniculi; Malassezia dermatis; Malassezia equina; Malassezia furfur; Malassezia globosa
(Flygare S, Simmon K, Miller C, . Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profiling. Genome Biol. 2016;17(1):111. doi:10.1186/s13059-016-0969-127224977)
Flygare S, Simmon K, Miller C, . Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profiling. Genome Biol. 2016;17(1):111. doi:10.1186/s13059-016-0969-127224977Flygare S, Simmon K, Miller C, . Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profiling. Genome Biol. 2016;17(1):111. doi:10.1186/s13059-016-0969-127224977, Flygare S, Simmon K, Miller C, . Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profiling. Genome Biol. 2016;17(1):111. doi:10.1186/s13059-016-0969-127224977
Morgan Ivy, Matthew Thoendel, P. Jeraldo, K. Greenwood-Quaintance, A. Hanssen, M. Abdel, N. Chia, J. Yao, A. Tande, J. Mandrekar, Robin Patel (2018)
Direct Detection and Identification of Prosthetic Joint Infection Pathogens in Synovial Fluid by Metagenomic Shotgun SequencingJournal of Clinical Microbiology, 56
Staphylococcus epidermidis; Staphylococcus equorum; Staphylococcus gallinarum
Legionella wadsworthii; Legionella waltersii; Leifsonia aquatica; Leminorella grimontii
Aspergillus luchuensis; Aspergillus nidulans; Aspergillus niger; Aspergillus nomius
(Christensen MS, Heyman M, Möttönen M, Zeller B, Jonmundsson G, Hasle H; Nordic Society of Paediatric Haematology and Oncology (NOPHO). Treatment-related death in childhood acute lymphoblastic leukaemia in the Nordic countries: 1992-2001. Br J Haematol. 2005;131(1):50-58. doi:10.1111/j.1365-2141.2005.05736.x16173962)
Christensen MS, Heyman M, Möttönen M, Zeller B, Jonmundsson G, Hasle H; Nordic Society of Paediatric Haematology and Oncology (NOPHO). Treatment-related death in childhood acute lymphoblastic leukaemia in the Nordic countries: 1992-2001. Br J Haematol. 2005;131(1):50-58. doi:10.1111/j.1365-2141.2005.05736.x16173962Christensen MS, Heyman M, Möttönen M, Zeller B, Jonmundsson G, Hasle H; Nordic Society of Paediatric Haematology and Oncology (NOPHO). Treatment-related death in childhood acute lymphoblastic leukaemia in the Nordic countries: 1992-2001. Br J Haematol. 2005;131(1):50-58. doi:10.1111/j.1365-2141.2005.05736.x16173962, Christensen MS, Heyman M, Möttönen M, Zeller B, Jonmundsson G, Hasle H; Nordic Society of Paediatric Haematology and Oncology (NOPHO). Treatment-related death in childhood acute lymphoblastic leukaemia in the Nordic countries: 1992-2001. Br J Haematol. 2005;131(1):50-58. doi:10.1111/j.1365-2141.2005.05736.x16173962
A. Gafter-Gvili, Abigail Fraser, M. Paul, M. Wetering, L. Kremer, L. Leibovici (2005)
Antibiotic prophylaxis for bacterial infections in afebrile neutropenic patients following chemotherapy.The Cochrane database of systematic reviews, 4
(Simon R. Optimal two-stage designs for phase II clinical trials. Control Clin Trials. 1989;10(1):1-10. doi:10.1016/0197-2456(89)90015-92702835)
Simon R. Optimal two-stage designs for phase II clinical trials. Control Clin Trials. 1989;10(1):1-10. doi:10.1016/0197-2456(89)90015-92702835Simon R. Optimal two-stage designs for phase II clinical trials. Control Clin Trials. 1989;10(1):1-10. doi:10.1016/0197-2456(89)90015-92702835, Simon R. Optimal two-stage designs for phase II clinical trials. Control Clin Trials. 1989;10(1):1-10. doi:10.1016/0197-2456(89)90015-92702835
A. Gaur, D. Bundy, E. Werner, J. Hord, Marlene Miller, L. Tang, J. Lawlor, A. Billett (2017)
A Prospective, Holistic, Multicenter Approach to Tracking and Understanding Bloodstream Infections in Pediatric Hematology-Oncology PatientsInfection Control & Hospital Epidemiology, 38
Capronia semi-immersa; Ceratocystis adiposa; Ceratocystis albifundus; Ceratocystis eucalypticola; Ceratocystis fimbriata; Ceratocystis manginecans; Ceratocystis platani; Cercospora fijiensis
Streptococcus suis; Streptococcus thermophilus; Streptococcus tigurinus; Streptococcus uberis; Streptococcus vestibularis; Streptomyces cattleya; Streptomyces somaliensis
Kluyveromyces lactis; Lachancea kluyveri; Lachancea lanzarotensis; Lachancea thermotolerans
Edwardsiella hoshinae; Edwardsiella tarda; Eggerthella lenta; Ehrlichia canis; Ehrlichia chaffeensis
Morganella morganii; Morococcus cerebrosus; Mycobacterium abscessus
Candida succiphila; Candida tanzawaensis; Candida tenuis; Candida tropicalis; Candida utilis
Mycobacterium iranicum; Mycobacterium kansasii; Mycobacterium koreense
Vaccinia virus; Varicella-zoster virus (VZV); Variola virus; WU Polyomavirus; Yaba monkey tumor virus
Mycobacterium thermoresistibile; Mycobacterium triplex; Mycobacterium tuberculosis complex; Mycobacterium tusciae; Mycobacterium vaccae; Mycobacterium wolinskyi; Mycobacterium xenopi
(Centers for Disease Control and Prevention. Bloodstream infection event (central line-associated bloodstream infection and non-central line associated bloodstream infection). http://www.cdc.gov/nhsn/PDFs/pscManual/4PSC_CLABScurrent.pdf. Accessed February 4, 2019.)
Centers for Disease Control and Prevention. Bloodstream infection event (central line-associated bloodstream infection and non-central line associated bloodstream infection). http://www.cdc.gov/nhsn/PDFs/pscManual/4PSC_CLABScurrent.pdf. Accessed February 4, 2019.Centers for Disease Control and Prevention. Bloodstream infection event (central line-associated bloodstream infection and non-central line associated bloodstream infection). http://www.cdc.gov/nhsn/PDFs/pscManual/4PSC_CLABScurrent.pdf. Accessed February 4, 2019., Centers for Disease Control and Prevention. Bloodstream infection event (central line-associated bloodstream infection and non-central line associated bloodstream infection). http://www.cdc.gov/nhsn/PDFs/pscManual/4PSC_CLABScurrent.pdf. Accessed February 4, 2019.
Y. Cheung, Aaron Eskind, H. Inaba, M. Hudson, C. Pui, K. Krull, J. Wolf (2018)
Association of Bacteremic Sepsis With Long-term Neurocognitive Dysfunction in Pediatric Patients With Acute Lymphoblastic LeukemiaJAMA Pediatrics, 172
B. Goldstein, B. Giroir, A. Randolph (2005)
International pediatric sepsis consensus conference: Definitions for sepsis and organ dysfunction in pediatrics*Pediatric Critical Care Medicine, 6
Staphylococcus pasteuri; Staphylococcus pettenkoferi; Staphylococcus pseudintermedius; Staphylococcus saprophyticus; Staphylococcus schleiferi; Staphylococcus sciuri; Staphylococcus simiae
Gemella morbillorum; Gemella sanguinis; Gordonia bronchialis; Gordonia rubripertincta
Lactobacillus sakei; Lactobacillus ultunensis; Lactococcus garvieae; Laribacter hongkongensis; Leclercia adecarboxylata; Legionella anisa
(Finch ER, Janke LJ, Smith CA, . Bloodstream infections exacerbate incidence and severity of symptomatic glucocorticoid-induced osteonecrosis. Pediatr Blood Cancer. 2019;66(6):e27669. doi:10.1002/pbc.2766930758124)
Finch ER, Janke LJ, Smith CA, . Bloodstream infections exacerbate incidence and severity of symptomatic glucocorticoid-induced osteonecrosis. Pediatr Blood Cancer. 2019;66(6):e27669. doi:10.1002/pbc.2766930758124Finch ER, Janke LJ, Smith CA, . Bloodstream infections exacerbate incidence and severity of symptomatic glucocorticoid-induced osteonecrosis. Pediatr Blood Cancer. 2019;66(6):e27669. doi:10.1002/pbc.2766930758124, Finch ER, Janke LJ, Smith CA, . Bloodstream infections exacerbate incidence and severity of symptomatic glucocorticoid-induced osteonecrosis. Pediatr Blood Cancer. 2019;66(6):e27669. doi:10.1002/pbc.2766930758124
Penicillium digitatum; Penicillium expansum; Penicillium flavigenum; Penicillium freii
Escherichia coli; Escherichia fergusonii; Escherichia hermannii; Escherichia vulneris
(Inaba H, Pei D, Wolf J, . Infection-related complications during treatment for childhood acute lymphoblastic leukemia. Ann Oncol. 2017;28(2):386-392.28426102)
Inaba H, Pei D, Wolf J, . Infection-related complications during treatment for childhood acute lymphoblastic leukemia. Ann Oncol. 2017;28(2):386-392.28426102Inaba H, Pei D, Wolf J, . Infection-related complications during treatment for childhood acute lymphoblastic leukemia. Ann Oncol. 2017;28(2):386-392.28426102, Inaba H, Pei D, Wolf J, . Infection-related complications during treatment for childhood acute lymphoblastic leukemia. Ann Oncol. 2017;28(2):386-392.28426102
(Wolf J, Tang L, Flynn PM, . Levofloxacin prophylaxis during induction therapy for pediatric acute lymphoblastic leukemia. Clin Infect Dis. 2017;65(11):1790-1798. doi:10.1093/cid/cix64429020310)
Wolf J, Tang L, Flynn PM, . Levofloxacin prophylaxis during induction therapy for pediatric acute lymphoblastic leukemia. Clin Infect Dis. 2017;65(11):1790-1798. doi:10.1093/cid/cix64429020310Wolf J, Tang L, Flynn PM, . Levofloxacin prophylaxis during induction therapy for pediatric acute lymphoblastic leukemia. Clin Infect Dis. 2017;65(11):1790-1798. doi:10.1093/cid/cix64429020310, Wolf J, Tang L, Flynn PM, . Levofloxacin prophylaxis during induction therapy for pediatric acute lymphoblastic leukemia. Clin Infect Dis. 2017;65(11):1790-1798. doi:10.1093/cid/cix64429020310
Legionella longbeachae; Legionella maceachernii; Legionella massiliensis; Legionella micdadei; Legionella moravica; Legionella norrlandica; Legionella oakridgensis
(Gaur AH, Bundy DG, Werner EJ, ; Children’s Hospital Association Childhood Cancer & Blood Disorders Network (CCBDN). A prospective, holistic, multicenter approach to tracking and understanding bloodstream infections in pediatric hematology-oncology patients. Infect Control Hosp Epidemiol. 2017;38(6):690-696. doi:10.1017/ice.2017.5728399945)
Gaur AH, Bundy DG, Werner EJ, ; Children’s Hospital Association Childhood Cancer & Blood Disorders Network (CCBDN). A prospective, holistic, multicenter approach to tracking and understanding bloodstream infections in pediatric hematology-oncology patients. Infect Control Hosp Epidemiol. 2017;38(6):690-696. doi:10.1017/ice.2017.5728399945Gaur AH, Bundy DG, Werner EJ, ; Children’s Hospital Association Childhood Cancer & Blood Disorders Network (CCBDN). A prospective, holistic, multicenter approach to tracking and understanding bloodstream infections in pediatric hematology-oncology patients. Infect Control Hosp Epidemiol. 2017;38(6):690-696. doi:10.1017/ice.2017.5728399945, Gaur AH, Bundy DG, Werner EJ, ; Children’s Hospital Association Childhood Cancer & Blood Disorders Network (CCBDN). A prospective, holistic, multicenter approach to tracking and understanding bloodstream infections in pediatric hematology-oncology patients. Infect Control Hosp Epidemiol. 2017;38(6):690-696. doi:10.1017/ice.2017.5728399945
Proteus vulgaris; Providencia alcalifaciens; Providencia rettgeri; Providencia stuartii
Malassezia yamatoensis; Memnoniella echinata; Metarhizium acridum; Metarhizium album; Metarhizium anisopliae; Metarhizium brunneum; Metarhizium guizhouense; Metarhizium majus
Rickettsia slovaca; Rickettsia typhi; Riemerella anatipestifer
Shewanella algae; Shewanella putrefaciens; Shigella boydii; Shigella dysenteriae; Shigella flexneri
Listeria monocytogenes; Listeria seeligeri; Listeria welshimeri; Mannheimia haemolytica; Megasphaera micronuciformis; Microbacterium foliorum; Microbacterium maritypicum
Metarhizium robertsii; Metschnikowia bicuspidata; Metschnikowia fructicola; Microsporum canis; Microsporum gypseum; Mortierella alpina; Mortierella elongata; Mortierella verticillata; Mucor ambiguus
Empedobacter falsenii
Talaromyces atroroseus; Talaromyces cellulolyticus; Talaromyces leycettanus; Talaromyces stipitatus; Talaromyces wortmannii; Thermoascus crustaceus; Thermomyces lanuginosus
Human polyomavirus 6; Human polyomavirus 7; JC polyomavirus; Kaposi sarcoma-associated herpesvirus; KI polyomavirus; Merkel cell polyomavirus; Molluscum contagiosum virus; Monkeypox virus
Trypanosoma cruzi; Wuchereria bancrofti Viruses Adeno-associated dependoparvovirus A; Adeno-associated dependoparvovirus B
Paraburkholderia fungorum; Paracoccus sanguinis; Paracoccus yeei; Parvimonas micra
E. Dinleyici, Z. Yargic, Ozcan Bor, A. Kiremitçi, G. Durmaz (2010)
Tigecycline treatment of multi‐drug‐resistant Corynebacterium jeikeium infection in a child with relapsing and refractory acute lymphoblastic leukemiaPediatric Blood & Cancer, 55
(Blauwkamp TA, Thair S, Rosen MJ, . Analytical and clinical validation of a microbial cell-free DNA sequencing test for infectious disease. Nat Microbiol. 2019;4(4):663-674. doi:10.1038/s41564-018-0349-630742071)
Blauwkamp TA, Thair S, Rosen MJ, . Analytical and clinical validation of a microbial cell-free DNA sequencing test for infectious disease. Nat Microbiol. 2019;4(4):663-674. doi:10.1038/s41564-018-0349-630742071Blauwkamp TA, Thair S, Rosen MJ, . Analytical and clinical validation of a microbial cell-free DNA sequencing test for infectious disease. Nat Microbiol. 2019;4(4):663-674. doi:10.1038/s41564-018-0349-630742071, Blauwkamp TA, Thair S, Rosen MJ, . Analytical and clinical validation of a microbial cell-free DNA sequencing test for infectious disease. Nat Microbiol. 2019;4(4):663-674. doi:10.1038/s41564-018-0349-630742071
J. Wolf, Li Tang, P. Flynn, C. Pui, A. Gaur, Yilun Sun, H. Inaba, Tracy Stewart, R. Hayden, H. Hakim, S. Jeha (2017)
Levofloxacin Prophylaxis During Induction Therapy for Pediatric Acute Lymphoblastic LeukemiaClinical Infectious Diseases, 65
Aureobasidium melanogenum; Aureobasidium namibiae; Aureobasidium pullulans
(Goldstein B, Giroir B, Randolph A; International Consensus Conference on Pediatric Sepsis. International pediatric sepsis consensus conference: definitions for sepsis and organ dysfunction in pediatrics. Pediatr Crit Care Med. 2005;6(1):2-8. doi:10.1097/01.PCC.0000149131.72248.E615636651)
Goldstein B, Giroir B, Randolph A; International Consensus Conference on Pediatric Sepsis. International pediatric sepsis consensus conference: definitions for sepsis and organ dysfunction in pediatrics. Pediatr Crit Care Med. 2005;6(1):2-8. doi:10.1097/01.PCC.0000149131.72248.E615636651Goldstein B, Giroir B, Randolph A; International Consensus Conference on Pediatric Sepsis. International pediatric sepsis consensus conference: definitions for sepsis and organ dysfunction in pediatrics. Pediatr Crit Care Med. 2005;6(1):2-8. doi:10.1097/01.PCC.0000149131.72248.E615636651, Goldstein B, Giroir B, Randolph A; International Consensus Conference on Pediatric Sepsis. International pediatric sepsis consensus conference: definitions for sepsis and organ dysfunction in pediatrics. Pediatr Crit Care Med. 2005;6(1):2-8. doi:10.1097/01.PCC.0000149131.72248.E615636651
E. Wilson (1927)
Probable Inference, the Law of Succession, and Statistical InferenceJournal of the American Statistical Association, 22
M. Fung, S. Zompi, H. Seng, D. Hollemon, Adama Parham, David Hong, S. Bercovici, E. Dolan, Kathy Lien, J. Teraoka, A. Logan, P. Chin-Hong (2018)
Plasma Cell–Free DNA Next-Generation Sequencing to Diagnose and Monitor Infections in Allogeneic Hematopoietic Stem Cell Transplant PatientsOpen Forum Infectious Diseases, 5
Candida haemulonis; Candida homilentoma; Candida intermedia; Candida ipomoeae; Candida kefyr; Candida kipukae; Candida krusei; Candida lusitaniae; Candida nivariensis; Candida orthopsilosis
Toxocara canis; Toxoplasma gondii; Trichinella; Trichomonas vaginalis; Trichuris trichiura
Pyrenochaeta lycopersici; Pyrenochaeta mackinnonii; Ramichloridium mackenziei
Leptosphaeria maculans; Lichtheimia corymbifera; Lichtheimia ramosa
Candida pseudohaemulonii; Candida psychrophila; Candida sojae; Candida sorbophila
Emily Finch, L. Janke, Colton Smith, Seth Karol, Deqing Pei, Cheng Cheng, S. Kaste, H. Inaba, C. Pui, J. Wolf, M. Relling (2019)
Bloodstream infections exacerbate incidence and severity of symptomatic glucocorticoid‐induced osteonecrosisPediatric Blood & Cancer, 66
Nocardia farcinica; Nocardia flavorosea; Nocardia fusca; Nocardia gamkensis; Nocardia grenadensis; Nocardia harenae; Nocardia higoensis; Nocardia ignorata; Nocardia inohanensis
Herpes B virus; Herpes simplex virus type 1 (HSV-1)
Leuconostoc mesenteroides; Leuconostoc pseudomesenteroides; Listeria grayi; Listeria innocua
K. Bae, J. Shin, Seongkoo Kim, S. Han, Jae Lee, Dong‐Gun Lee, N. Chung, B. Cho, D. Jeong, J. Kang (2018)
Enterococcal bacteremia in febrile neutropenic children and adolescents with underlying malignancies, and clinical impact of vancomycin resistanceInfection, 47
Paenibacillus alvei; Pandoraea apista
Enterococcus cecorum; Enterococcus columbae; Enterococcus dispar; Enterococcus durans
Fusobacterium ulcerans; Fusobacterium varium; Gardnerella vaginalis; Gemella bergeri
Trachipleistophora hominis; Trichoderma asperellum; Trichoderma atroviride; Trichoderma gamsii; Trichoderma hamatum; Trichoderma harzianum; Trichoderma longibrachiatum; Trichoderma parareesei
Ochrobactrum oryzae; Odoribacter splanchnicus; Oerskovia turbata; Oligella ureolytica; Oligella urethralis; Olsenella uli; Oribacterium sinus; Orientia tsutsugamushi
Steven Flygare, K. Simmon, Chase Miller, Yi Qiao, Brett Kennedy, Tonya Sera, E. Graf, K. Tardif, A. Kapusta, Shawn Rynearson, C. Stockmann, Krista Queen, S. Tong, K. Voelkerding, A. Blaschke, C. Byington, Seemalata Jain, A. Pavia, K. Ampofo, K. Eilbeck, Gabor Marth, M. Yandell, R. Schlaberg (2016)
Taxonomer: an interactive metagenomics analysis portal for universal pathogen detection and host mRNA expression profilingGenome Biology, 17
Encephalitozoon cuniculi; Encephalitozoon hellem; Encephalitozoon intestinalis
A. Adler, I. Yaniv, E. Solter, E. Freud, Z. Samra, J. Stein, S. Fisher, I. Levy (2006)
Catheter-Associated Bloodstream Infections in Pediatric Hematology-Oncology Patients: Factors Associated With Catheter Removal and RecurrenceJournal of Pediatric Hematology/Oncology, 28
R. Simon (1989)
Optimal two-stage designs for phase II clinical trials.Controlled clinical trials, 10 1
Mycobacterium asiaticum
Eubacterium nodatum; Facklamia hominis; Facklamia sourekii; Filifactor alocis; Finegoldia magna; Francisella hispaniensis; Francisella noatunensis; Francisella philomiragia
This pilot cohort study estimates sensitivity and specificity of plasma microbial cell-free DNA sequencing for its ability to predict bloodstream infection in patients at high risk of life-threatening infection.
JAMA Oncology – American Medical Association
Published: Apr 19, 2020
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