This page includes who's who, literature, achievements at conferences, workshops etc., theme-related sites and newspaper articles concerning hemophilia.
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■Table of Contents
◇Literature (Various Writings)
◇Achievements at Conferences, Workshops etc.
■Literature (Various Writings)
September 30, 2014 The History of Hemophiliacs in Japan: Hospitality of Otherness/Participation in Society/Protest Movements
，Seikatsu Shoin, 304p. ISBN-10: 4865000305 ISBN-13: 978-4-86500-030-6 3000 yen＋tax [amazon]
August 1, 2013 "Collaboration with the World and Anxiety of Aging: Issues the Voluntary Association for Hemophilia Faces"
◆OMURA Kayoko August 1, 2013 "Social Underlying Problems with the Development of Medical Treatment for Hemophilia Seen in Experiences of Patients with Hemophilia", Gendai Shiso
March 10, 2012 "Generation of Activities by People with Hemophilia that Connect with the Society: With Emphasis on Formation of Young Hemophiliac Club", pp.62-84 AMADA Josuke
, MURAKAMI Kiyoshi
& YAMAMOTO Takanori
(Eds.) March 10, 2012 Disputed Point of Differences: Understanding the Modern Discrimination
, Harvestsha, x+299p. ISBN-10:4863390343 ISBN-13: 9784863390348 2835 [amazon]
March 25, 2011 "Patients' Movements and Development of Systems of Patients with Hemophilia in 1970s: Obtaining Pubic Funds and the Course to Official Approval of Self-injection", AMADA Josuke
, KITAMURA Kentaro
& HOTTA Yoshitaro
(Eds.) Governing Aging: Policies and History of Aging
Seikatsu Shoin, ISBN-10: 4903690733 ISBN-13: 9784903690735 3150 [amazon]
November 20, 2010 "From a Pamphlet to Young Hemophiliac Club: Movements toward Activities Conducted by Individuals with Hemophilia Themselves", pp.114-140 YAMAMOTO Takanori
& TAKAHASHI Shinichi (Eds.) Dynamics of "Differences": Practical Challenges of Research and Methodology on Minority
, Report Issued by Research Center for Ars Vivendi of Ritsumeikan University, Vol.14, 408p. ISSN 1882-6539 ※
December 4, 2009 "Look at "Pain": A Pattern of Issues over Patients with Hemophilia", pp.113-142 SAKURAI Hiroko
& HOTTA Yoshitaro
(Eds.) Ethics of Birth: Choice toward "Living"
，Report Issued by Research Center Ars Vivendi of Ritsumeikan University, Vol.10, 194p. ISSN 1882-6539
◆ONO O, SUZUKI Y, YOSHIKAWA K, WADA I, DOI Y, TAKANO M, WADA Y, FUKUSHIMA K; Planning Committee, Japanese Nurse Group for Research of Hemophilia Care 2009 "Assessment of Hemophilia Treatment Practice Pattern in Japan", Hemophilia
◆KELLEY Laurie June 12, 2007 "Taking Japan to the Next Level"
March 31, 2007 "The History of Hemophiliacs in Japan: Until 1983" [Abstract]
(The Doctoral Dissertation)
March 31, 2007 "The Shinsei na gimu
Issue from the Perspective of Hemophiliacs"
Core Ethics 3
March 31, 2006 "System and Technology of Blood Use: Hemophiliacs and Coagulation Factor Products in Postwar Japan"
Core Ethics 2
March 31, 2006 "The Establishment of the "Japan Hemophilia Fraternal Association" and its Successful Effort to Acquire Public Health Coverage for Mediacal Treatment"
Core Ethics 2
March 31, 2005 "The Sabita Honoo
Problem and its Contemporary Significance"
Core Ethics 1
◆FUKUTAKE K. 2000 "Current Status of Hemophilia Patients and Recombinant Coagulation Factor Concentrates in Japan", Semin Thromb Hemost
◆RESTA Robert G. "Genetic Counseling: Coping with the Human Impact of Genetic Disease"
■Achievements at Conferences, Workshops etc.
◆SANO Ryusuke, KITAMURA Kentaro
, ABE Shinji & ONISHI Akahito May 12, 2014 "The History of Hemophilia Community in Japan", World Federation of Hemophilia 2014 World Congress in Melbourne
September 27, 2009 "Formation of 'National Network of Hemophilia Association'", The 6th Annual Convention of Japan Society of Disability Studies
, Suzaku Campus, Ritsumeikan University
November 17, 2007 "Movements by Patients of National Hemophilia Organization"
The 80th Annual Convention ofthe Japan Sociological Society, Kanto Gakuin University
◆Ars Vivendi E-mail Magazine No.103 (August 15, 2013)
◆Chronology: The History of Disabled People (and Their Movement) in Japan
◆『Cross Heart』 (Japanese)
◆Discourses on Prenatal Diagnosis
◆List of Hemophilia Organizations
◆National Hemophilia Network of Japan (Japanese)
◆World Federation of Hemophilia
◆October 18, 2014 "Suicidal cells and the immortal cells of Henrietta Lacks" （The Japan Times
◆May 18, 2011 "Last plaintiff in HIV-tainted blood scandal settles" （The Japan Times
◆April 29, 2005 "Abe, central figure in HIV-tainted blood products scandal, dies" （The Japan Times
◆May 14, 2004 "Hospitals tied to HCV fiasco to be mostly named before ’05" （The Japan Times
◆February 11, 2004 "Abe’s trial over AIDS death set to be halted" （The Japan Times
◆November 30, 2002 "Prosecutors want acquittal of HIV expert overturned" （The Japan Times
◆July 26, 2002 "Law enacted to ensure safety of nation’s blood products" （The Japan Times
◆April 26, 2001 "Hemophiliac with HIV receives liver transplant" （The Japan Times
◆March 31, 2001 "‘Not guilty’ is not innocent" （The Japan Times
◆March 30, 2001 "Bar president says citizens should be involved in trials" （The Japan Times
◆March 17, 2001 "School sued for betraying hemophiliac" （The Japan Times
◆February 24, 2000 "Green Cross chiefs receive prison terms for HIV scandal" （The Japan Times
◆September 30, 1999 "Green Cross execs face bars over HIV scandal" （The Japan Times
◆March 24, 1997 "Green Cross execs plead guilty in blood products debacle" （The Japan Times
◆March 5, 1997 "Abe trial begins next week" （The Japan Times
◆March 4, 1997 "Abe pleads not guilty as HIV trial gets under way" （The Japan Times
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