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11,115 Possible Causes for De, Trichlorobacter, Wever, al, ET

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  • Bartonella Henselae

    Caso clínico: Presentamos el caso de un varón de 24 meses de edad remitido a nuestro centro por un cuadro de fiebre de larga evolución asociado a dolor abdominal recurrente[actapediatrica.com] Regnery RL, et al.[lgcstandards-atcc.org] For such pathogens, there is obviously still a need to identify antigens to establish a reliable, fast and high-throughput assay (Dupon et al. ).[ncbi.nlm.nih.gov] We report the first molecularly confirmed case of B. henselae infection in an AIDS patient in state of Rio de Janeiro, Brazil.[ncbi.nlm.nih.gov] .: 49-761-2036529 Fax: 49-761-2036562 DE 2. University Children's Hospital, Freiburg, Germany DE[link.springer.com]

    Missing: Trichlorobacter Wever
  • Pneumonia

    This retrospective study was conducted on trauma patients with VAP, who received de-escalation therapy (de-escalation group) or non-de-escalation therapy (non-de-escalation[ncbi.nlm.nih.gov] Tomashefski, Jr. []; et al. (2008). Dail and Hammar's pulmonary pathology (3rd ed.). New York: Springer. p. 228. ISBN 978-0-387-98395-0 .[en.wikipedia.org] Acute fibrinous and organizing pneumonia (AFOP) is a new histopathological pattern of acute lung injury first described by Beasley et al. in 2002.[ncbi.nlm.nih.gov] ., et al. (August 24, 2018). Medscape: Community-acquired pneumonia (CAP). Available online at . Accessed on September 8, 2018. Mosenifar, Z., et al. (July 24, 2018).[labtestsonline.org] All the guidelines supported the antibiotic de-escalation strategy, whereas the majority of the guidelines (5 of 6) recommended that empirical antibiotic therapy should be[ncbi.nlm.nih.gov]

    Missing: Trichlorobacter Wever
  • GLUT1 Deficiency Syndrome

    Using whole-genome sequencing, we identified a de novo 5'-UTR variant in SLC2A1, generating a novel translation initiation codon, severely compromising SLC2A1 function.[ncbi.nlm.nih.gov] PMID: 16712556 Ramm-Pettersen, A, et al.[invitae.com] . ; Wevers, R.A. ; Veltman, J.A. ; Kamsteeg, E.J.[repository.ubn.ru.nl] Heterozygous mutations in the GLUT1/SLC2A1 gene, occurring de novo or inherited as an autosomal dominant trait, result in cerebral energy failure and a clinical condition[ncbi.nlm.nih.gov] Leen WG, Wevers RA, Kamsteeg EJ, Scheffer H, Verbeek MM, Willemsen MA. Cerebrospinal fluid analysis in the workup of GLUT1 deficiency syndrome: a systematic review.[ghr.nlm.nih.gov]

    Missing: Trichlorobacter
  • De Barsy Moens Diercks Syndrome

    Prognosis - De Barsy syndrome Not supplied. Treatment - De Barsy syndrome Not supplied. Resources - De Barsy syndrome Not supplied.[checkorphan.org] Bicknell LS, Pitt J, Aftimos S, et al.[rarediseases.org] Retrieved 2011-08-14 . a b Morava, Éva; Guillard, Maïlys; Lefeber, Dirk J; Wevers, Ron A (2009). "Autosomal recessive cutis laxa syndrome revisited" .[en.wikipedia.org] Elŝutite 2011-08-14 . a b Moravo, Éva; Guillard, Maïlys; Lefeber, Dirk J; Wevers, Ron A (2009). " Aŭtosoma recesiva cutis laxa sindromo revizitita " .[epo.wikitrans.net] ) Who gets De Barsy Syndrome?[dovemed.com]

    Missing: Trichlorobacter
  • Influenza

    Clínicas da Faculdade de Medicina da Universidade de São Paulo while the 2014 and 2015 studies were conducted at CRIE.[ncbi.nlm.nih.gov] In Brazil, the first laboratory confirmed case of FluA/H1N1/09pdm was in July 2009 (Pires Neto et al. 2013).[ncbi.nlm.nih.gov] Indeed, from the data presented in the paper by de Boer et al. it can be inferred that replacing QIV for TIV would mean a 25-29% budget increase for seasonal influenza vaccination[ncbi.nlm.nih.gov] Hill G, Cihlar T, Oo C, et al.[emedicine.medscape.com] Enfermedades Respiratorias, Clínica de Investigación en Enfermedades Infecciosas, Mexico, D.[influenzareport.com]

    Missing: Trichlorobacter Wever
  • Mucopolysaccharidosis 6

    -acumulare de sulfatid in substanta alba Boala Krabe Deficit enzimatic: galactocerebrosid ß-galactosidaza Date clinice si de laborator: - autosomal recesiv - debut la 3-6[preferatele.com] Galsulfasa (Naglazyme ) per al tractament de la mucopolisacaridosi VI. Barcelona: Agència d’Avaluació de Tecnologia i Recerca Mèdiques; 2010.[scientiasalut.gencat.cat] Poorthuis BJ, Wevers RA, Kleijer WJ, et al. The frequency of lysosomal storage diseases in The Netherlands. Hum Genet . 1999 Jul-Aug. 105(1-2):151-6. [Medline] .[emedicine.medscape.com] […] del Cauca, Popayán, Colombia 2 Fundación Pública Galega de Medicina Xenómica, Hospital de Santiago de Compostela, Spain 3 Instituto de Medicina Legal, Facultad de Medicina[scitechnol.com] Arlt et al., (1994) J Biol Chem 269:9638-9643. Villani et al., (2010) Genet Test Mol Biomarkers 14:113-120. Garrido et al., (2007) Mol Genet Metab 92:122-130.[genedx.com]

    Missing: Trichlorobacter
  • Sjogren-Larsson Syndrome

    Ben Hamouda Service de radiologie de l’institut national de neurologie, rue Jébal Lakhdhar La Rabta Bab Saâdoun, 1007 Tunis, Tunisie N.[em-consulte.com] Sillén A, Anton-Lamprecht I, Braun-Quentin C, et al. (1998). "Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjögren–Larsson syndrome".[en.wikipedia.org] . ; Wevers, R.A. ; Roeleveld, N. ; Willemsen, M.A.A.P.[repository.ubn.ru.nl] Wevers Ronald J. A. Wanders Hans R. Waterham Michèl A. A. P.[link.springer.com] [1] Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller AB, Narwal R, et al.[degruyter.com]

    Missing: Trichlorobacter
  • Thrombocytosis

    , trombocitemia (trastorno) , trombocitemia (hallazgo) , Recuento de trombocitos aumentado , aumento de plaquetas , incremento de plaquetas , trombocitosis (trastorno) ,[fpnotebook.com] Beutler E, Coller BS, Lichtman MA, et al., eds. New York: McGraw-Hill, 2001, pp. 1541-1549. 2 . Alexandrakis A, MG, Passam FH, Perisinakis K, et al.[antimicrobe.org] JA; Kurtz, LE; Katz, S Arterial embolism caused by large mobile aortic thrombus in the absence of atherosclerosis, associated with iron deficiency anemia Bukharovich, IF; Wever-Pinzon[deepdyve.com] Eyster ME, Saletan SL, Rabellino EM, et al: Familial essential thrombocythemia. Am J Med 80:497, 1986. 39.[medtextfree.wordpress.com] Bukharovich IF, Wever-Pinzon O, Shah A, Todd G, Chaudhry FA, Sherrid MV.[springermedizin.at]

    Missing: Trichlorobacter
  • Xanthomatosis

    Richard Knisely Winkelmann Vista de fragmentos - 1960 Pathology of the connective tissue diseases Dugald Lindsay Gardner Vista de fragmentos - 1965 Todos los resultados de[books.google.es] , Waterreus et al 1987 , Berginer et al 1994 , Dotti et al 1994 , De Stefano et al 2001 ].[leukodystrophyresourceresearch.org] Clayton PT, Verrips A, Sistermans E, Mann A, Mieli-Vergani G, Wevers R.[jdrntruhs.org] Comentarios de usuarios - Escribir una reseña No hemos encontrado ninguna reseña en los sitios habituales.[books.google.es] ., 1975 ; Swartz et al ., 1982 ; Kuriyama et al ., 1991 ; Restuccia et al ., 1992 ; Dotti et al ., 1994 ).[brain.oxfordjournals.org]

    Missing: Trichlorobacter
  • Insect Bite

    Planes de salud de Kaiser Permanente en el país: Kaiser Foundation Health Plan, Inc., en el Norte y Sur de California y Hawái • Kaiser Foundation Health Plan de Colorado •[healthy.kaiserpermanente.org] Campbell RL, et al. Anaphylaxis: Emergency treatment. . Accessed Jan. 9, 2018. .[mayoclinic.org] ., Varga, E. et al. Allergen Immunotherapy for Insect Venom Allergy: A Systematic Review and Meta-Analysis . Allergy . 2017. 72(3):342-365.[verywellhealth.com] ET The Ache: Insect bites can put an itchy and painful dent in summer fun.[wsj.com] ¿Esa roncha es de urticaria o de un picadura de insecto? ' insect bite ' aparece también en las siguientes entradas: Spanish:[wordreference.com]

    Missing: Trichlorobacter Wever