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From diagnosis to personalized medicine: comprehensive approaches for patient care (Roche Diagnostics) Yasuhito Tanaka (Chairperson) Professor,Director Department of Virology & Liver Unit, Crinical Laboratory Nagoya City University Graduate School of Medical Sciences (Speakers) Reinhard Bertele (Roche Diagnostics K.K.) Chris Newhouse (Roche Diagnostics K.K.) Shigehisa Nagahashi (Roche Diagnostics K.K.) The field of diagnostics is evolving from simply providing tools for disease diagnosis, to also providing tools for personalized medicine. Roche has an industry leading portfolio, which utilizes many technologies to support disease diagnosis, monitoring, and therapy guidance as well as treatment options. We would like share with you some insight into some of the new tools we have developed for physicians to manage patient care in the areas of infectious diseases and oncology and which are currently in focus in the medical community. This seminar will cover recent advances in the fields of Immunochemistry, Nucleic Acid Testing, and Automated Tissue Diagnostics. Roche has developed a comprehensive panel of immunoassays, coupled with nucleic acid tests which cover a wide variety of applications such as screening, diagnosis of acute and chronic infection and therapy monitoring. In addition, in the field of oncology, there are many new tools which analyze the disease status within tissue samples. All of these examples bring us step-by-step closer to having truly personalized medicines. Many of the above tools come together as part of Roche’s leading efforts in the development of diagnostic tests along with innovative drugs to realize the dream of personalized healthcare. Roche continues to improve our tests and to expand the portfolio for different clinical settings, maintaining our global leadership. Roche continues to invest in many exciting activities on our continuous path to innovate healthcare. - 30 -
Scientific Innovation Seminar (Abbott Diagnostics) 1. Meeting the Challenge of HIV Diversity and Application of Metagenomic-Based Technologies for Virus Discovery John R Hackett, Jr., Ph.D. Abbott Laboratories, 100 Abbott Park Road, D-09GN, Bldg. AP20, Abbott Park, IL 60064-3500 USA 2. PLEX-ID Technology as a Single Tool for the Detection and Typing of Microbiological Infections in Immuno-Compromised Patients Jérôme Le Goff 1 , Linda Feghoul 1 , Jean Menotti 1 , Jean Luc Donay 1 , Séverine Mercier-Delarue 1 , Jean Louis Pons 1 , Marcus Picard-Maureau² and François Simon 1 1- Université Paris-Diderot, Hôpital Saint-Louis, Paris, France 2- Abbott Ibis Biosciences, 65205 Wiesbaden, Germany - 31 -
Page 1 and 2: Program / Abstract Book
Page 3 and 4: Welcome Dear Friends and Colleagues
Page 5 and 6: ASCPaLM 2012 Executive Committee Pr
Page 7 and 8: Sponsors and supporters Abbott Japa
Page 9 and 10: Approximate Flight Times to Japan F
Page 11 and 12: The Kyoto City Subway system is eas
Page 13 and 14: Scientific Program Information Spea
Page 15 and 16: Event Hall is located by the confer
Page 17 and 18: Keynote Lecture (Chaired by Mitsuru
Page 19 and 20: FO 1 CLINICAL PATHOLOGY SCOPE IN CA
Page 21 and 22: FO 3 SUSTAINED EXPRESSION OF A NEUR
Page 23 and 24: FO 5 INDIAN STUDY OF LIVER FUNCTION
Page 25 and 26: Advanced Technical Seminar Sekisui
Page 27 and 28: Measurement of Albuminuria (Siemens
Page 29 and 30: The current status of the diagnosis
Page 31 and 32: Establishment of Reference Interval
Page 33: Innovative Lipid Biomarkers (Denka
Page 37 and 38: PLEX-ID Technology as a Single Tool
Page 39 and 40: POSTER SESSION 1. Clinical Chemistr
Page 41 and 42: Naoko Yamaguchi, Tomohiro Takeda, C
Page 43 and 44: in Type 2 Diabetes Mellitus First D
Page 45 and 46: No. 36. Identification of autoantib
Page 47 and 48: Okamura 1) , Masahumi Takata 2) , M
Page 49 and 50: Hunsuk Suh 1 MD, PhD, Jonghee Shin
Page 51 and 52: Department of Pathology, Kansai Med
Page 53 and 54: No. 80. Introduction of HCV Quantif
Page 55 and 56: No. 91. Genome-wide association ana
Page 57 and 58: Abstracts - 53 -
Page 59 and 60: No. 2 (PC2) Soluble FcγRIIIa Mφ l
Page 61 and 62: No. 4 (PC 4) Detection of hereditar
Page 63 and 64: No. 6 (PC 6) Analysis of cholestery
Page 65 and 66: No. 8 (PC 8) Development of the enz
Page 67 and 68: No. 10 (PC 10) Direct analysis of c
Page 69 and 70: No. 12 (PC 12) Reference value for
Page 71 and 72: No. 14 (PC 14) Detection of autoant
Page 73 and 74: No. 16 (PC 16) Temporal changes in
Page 75 and 76: No. 18 (PC 18) IODINE STATUS AMONG
Page 77 and 78: No. 20 (PC 20) Plasma free Fatty Ac
Page 79 and 80: No. 22 (PE 1) Two-Step Biochemical
Page 81 and 82: No. 24 (PE 3) Adiponectin HMW Level
Page 83 and 84: No. 26 (PE 5) Analysis of von Wille
Page 85 and 86:
No. 28 (PI 2) Diagnostic value of A
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No. 30 (PI 4) Evaluation of Hepatri
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No. 32 (PI 6) Discrepancy between s
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No. 34 (PI 8) Inhibition of the NF-
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No. 36 (PH 2) Identification of aut
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No. 38 (PH 4) Contribution of uncon
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No. 40 (PH 6) Red Blood Cells absor
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No. 42 (PH 8) Great impact of the b
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No. 44 (PH 10) Relation between VKO
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No. 46 (PH 12) Suspect of malaria i
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No. 48 (PH 14) Intravascular large
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No. 50 (PH 16) Calculation of Measu
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No. 52 (PM 1) High seroprevalence o
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No. 54 (PM 3) Epidemiological and m
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No. 56 (PM 5) Tuberculosis screenin
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No. 58 (PM 7) Mycobacterium Kyorine
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No. 60 (PM 9) Sensitive, one, two-d
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No. 62 (PM 11) Simultaneous inhibit
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No. 64 (PM 13) Measurement of Proca
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No. 66 (PF 1) Comparison of four po
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No. 68 (PP 1) The expressions of O
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No. 70 (PP 3) Poorly differentiated
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No. 72 (PP 5) The morphological cha
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No. 74 (PP 7) Neuropathological fin
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No. 76 (PMB 2) Diagnostic strategie
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No. 78 (PMB 4) Study of essential o
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No. 80 (PMB 6) Introduction of HCV
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No. 82 (PMB 8) Analysis of Fas exon
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No. 84 (PMB 10) A rapid and automat
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No. 86 (PMB 12) Increased expressio
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No 88 (PO 2) Assessment of early ma
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No. 90 (PO 4) The role of Rb2/p130
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No. 92 (PO 6) Molecular analysis of
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No. 94 (PO 8) The genealogical stud
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No. 96 (P0 10) Regulatory and pro-i
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No. 98 (PO 12) Chaotic Nature of My
Page 157 and 158:
[Memo] - 153 -
Page 159 and 160:
- 155 -
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