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| 1 | Microsatellite polymorphism in the human heme oxygenase-1 gene promoter and its application in association studies with Alzheimer and Parkinson disease显示文摘 | Teiko Kimpara A. Takeda Koichi Watanabe Yasuto Itoyama Shuntaro Ikawa Minro Watanabe Hiroyuki Arai Hidetada Sasaki Susumu Higuchi Naoshi Okita Sadao Takase Hiroshi Saito Kazuhiro Takahashi Shigeki Shibahara | 1997 | Human Genetics1997，，1： | 1 |
| 2 | Im- provement in the mechanical strength of magnetostrictive (Fe-Ga-A1)-X-C (X : Zr, Nb and Mo) alloys by carbide precipitation显示文摘 | Toshiya Takahashi Teiko Okazaki Yasubumi Furuya | 2009 | Scripta Mater2009，61，： | 1 |
| 3 | Early postoperative retinal thickness changes and complications after vitrectomy for diabetic macular edema显示文摘 | Teiko Yamamoto Koichiro Hitani Itsuro Tsukahara Shuichi Yamamoto Ryo Kawasaki Hidetoshi Yamashita Shinobu Takeuchi | 2003 | American Journal of Ophthalmology2003，，1： | 1 |
| 4 | Vitrectomy for diabetic macular edema: the role of posterior vitreous detachment and epimacular membrane显示文摘 | Teiko Yamamoto Naoko Akabane Shinobu Takeuchi | 2001 | American Journal of Ophthalmology2001，，3： | 1 |
| 5 | Development of New Magnetostrictive Materials in Heusler Type CoNiGa System显示文摘 | MitsutakaSato Teiko Okazaki Yasubumi Furuya | 2002 | 日本金属学会志2002，66，： | 1 |
| 6 | Networks of neurons,networks of genes:an integrated view of memory consolidation显示文摘 | Teiko Miyashita Stepan Kubik Gail Lewandowski | 2008 | Neurobiol Learn Mem2008，89，3： | 1 |
| 7 | Morphological and functional analyses of diabetic macular edema by optical coherence tomography and multifocal electroretinograms显示文摘 | Shuichi Yamamoto Teiko Yamamoto Masanori Hayashi Shinobu Takeuchi | 2001 | Graefe’s Archive for Clinical and Experimental Ophthalmology2001，，2： | 1 |
| 8 | Characterization of magnetostrictive F e-Ga-based alloys fabricated by rapid solidification 显示文摘 | TOSHlYA T KENJI H TEIKO 0 YASUBUMI F TAKESHI K CHIHIRO S | 2009 | Scripta Materialia2009，60，10： | 1 |
| 9 | Morphological and functional analyses of diabetic macular edema by optical coherence tomography and multifocal electroretinograms显示文摘 | Shuichi Yamamoto Teiko Yamamoto Masanori Hayashi Shinobu Takeuchi | 2001 | Graefe’s Archive for Clinical and Experimental Ophthalmology2001，，2： | 1 |
| 10 | Angioimmunoblastic T-cell lymphoma accompanied by pure red cell aplasia:A case report显示文摘BACKGROUND Angioimmunoblastic T-cell lymphoma(AITL)is a peripheral T-cell lymphoma,which is a rare subtype of lymphoma.Patients with AITL often have skin lesions,which are observed in 50%of all cases;the chief complaint of this patient was palpable purpura.AITL often complicates autoimmune or hematological disorders;however,among these,pure red cell aplasia(PRCA)is a very rare complication of AITL.We herein report a case of AITL with PRCA.CASE SUMMARY A 77-year-old Japanese man presented to our hospital with complaints of loss of appetite for 2 mo and a 10-d history of palpable purpura.On physical examination,the patient was afebrile but had bilateral multiple palpable purpuric lesions over the lower extremities,lower abdomen,and part of the upper extremities.Moreover,lymphadenopathy of the bilateral inguinal,cervical,and supraclavicular nodes was noted.Laboratory and imaging studies and skin biopsy were conducted but were inconclusive.Based on inguinal lymph node excisional biopsy,we diagnosed the patient with AITL.Subsequently,the patient developed progressive normocytic normochromic anemia that necessitated almost daily blood transfusion.The clinical presentations and results of bone marrow assessment were consistent with those of PRCA,which is associated with AITL.Chemotherapy was initiated but was not effective.The patient refused further chemotherapy and opted to continue receiving best supportive care.CONCLUSION PRCA is an extremely rare complication of AITL.As the pathophysiology remains unclear,further research is warranted. | Teiko Kawahigashi Izumi Kitagawa Eri Tanaka | 2020 | World Journal of Clinical Oncology2020，11，6： | 0 |
| 11 | Intravascular lymphoma with hypopituitarism: A case report显示文摘BACKGROUND Intravascular lymphoma(IVL)is a rare subtype of lymphoma involving the growth of lymphoma cells within the vessel lumina without lymphadenopathy.Because of various modes of presentation and its rarity,IVL is often diagnosed postmortem.Herein,we report a case of intravascular B-cell lymphoma with hypopituitarism,an extremely rare complication,that was successfully treated with chemotherapy.CASE SUMMARY An 80-year-old Japanese woman presented with a 7-mo history of a tingling sensation in the lower limbs.She also presented with various other symptoms such as pancytopenia,high fever daily,and unconsciousness with hypoglycemia.Although the doctor who previously treated her diagnosed hypoglycemia as being due to hypopituitarism,the cause of the other symptoms remained uncertain despite a 7-mo evaluation period.We performed bone marrow aspiration to evaluate pancytopenia and found that she had hemophagocytic lymphohistiocytosis(HLH).On the basis of a random skin biopsy for assessing the cause of HLH,she was diagnosed with intravascular B-cell lymphoma.HLH and hypopituitarism were considered secondary to IVL.All her clinical findings matched the presentations of IVL.She was immediately treated with chemotherapy and achieved complete response.She was relapse free two years after treatment.CONCLUSION IVL should be included in the differential diagnosis of hypopituitarism,which although life-threatening,is treatable through prompt diagnosis and appropriate chemotherapy. | Teiko Kawahigashi Shinichi Teshima Eri Tanaka | 2020 | World Journal of Clinical Oncology2020，11，8： | 0 |
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