207,667 research outputs found
Edward I. Hashimoto: interview on April 25, 1984; May 2, 1984; and May 11, 1984
No full textTranscript (typescript, 89 pages) of three interviews with Edward I. Hashimoto, a Japanese-American living in Utah in 1984. Mr. Hashimoto (b. 1911) tells about his genealogy and the life of his parents and other family members in Japan. He details his father\u27s immigrant experiences including working for the railroad, surviving an ambush by cowboys, and arranging immigration of Japanese laborers for mining and farming companies. He reminisces about his own childhood in Salt Lake City\u27s "Japan Town," discusses prostitution and syphllis, discrimination, getting his medical degree from Harvard, and practicing in Salt Lake City. Other topics covered include Japanese folk medicine, civilian life in World War II, and teaching anatomy at the University of Uta
A short proof of a theorem of M. Hashimoto
No full textAbstractRecently M. Hashimoto announced that the resolutions of determinantal ideals depend on the characteristic of the base field. The purpose of this note is to give a short proof of this result. One should stress that even though the method we use is different from Hashimoto's, his result provided us with the clue where the additional relation exists
Paralomis jamsteci TAKEDA & HASHIMOTO 1990
No full text<i>PARALOMIS JAMSTECI</i> TAKEDA & HASHIMOTO, 1990 <p> <i>Type locality</i>: North Pacific Ocean, Okinawa Trough, hydrothermal vents of the Minami-Ensei Knoll; 28°23.4′N, 127°38.4′E; 710 m.</p> <p> <i>Known range</i>: Known only from the type locality (above).</p> <p> <i>Material</i>: North Pacific Ocean, Okinawa Trough, Minami-Ensei Knoll, 28°23.4′N, 127°38.4′E; 710 m; <i>Shinkai 2000</i> dive 428; 26 July 1989; NSMT-Cr 10172 [holotype female (ovigerous)], NSMT-Cr 10173 (paratype, 1 male), USNM and MNHN (2 ovigerous females) (Takeda & Hashimoto, 1990; also see Hashimoto <i>et al.</i>, 1990, 1995; Hashimoto, 1997, in Desbruyeres & Segonzac, 1997).</p> <p> <i>Remarks</i>: <i>Paralomis jamsteci</i> was described as living among beds of mytilid mussels near vent openings (Takeda & Hashimoto, 1990; Hashimoto <i>et al</i>., 1995). Hashimoto (1997, in Desbruyeres & Segonzac, 1997: 199) described the ecology of the species as ‘crawling around bacterial mats close to hydrothermal vents’ with vent temperatures reaching 269 °C. Hashimoto <i>et al.</i> (1995) also mentioned two other unidentified species of <i>Paralomis</i> living at the Minami-Ensei vent fields (Hashimoto <i>et al.</i>, 1995; Chevaldonné & Olu, 1996). To date the species is known only from that site and from the specimens noted above. See Chevaldonné & Olu (1996: 289) for reports of this species feeding on vesicomyid and mytilid bivalves.</p>Published as part of <i>Martin, Joel W. & Haney, Todd A., 2005, Decapod crustaceans from hydrothermal vents and cold seeps: a review through 2005, pp. 445-522 in Zoological Journal of the Linnean Society 145 (4)</i> on page 485, DOI: 10.1111/j.1096-3642.2005.00178.x, <a href="http://zenodo.org/record/5434828">http://zenodo.org/record/5434828</a>
Hashimoto-Enzephalopathie – steroid-sensitive Enzephalopathie
No full textZusammenfassungDie Hashimoto-Enzephalopathie ist eine gut behandelbare, steroid-sensitive Enzephalopathie, die sich durch eine Assoziation mit einer Autoimmun-Thyreoiditis (Hashimoto-Thyreoiditis) auszeichnet. Bis jetzt wurden ca. 110 Fallbeschreibungen der Hashimoto-Enzephalopathie in allen Altersgruppen berichtet. Unklarheit besteht über die zugrunde liegenden pathogenetischen Mechanismen. Es können zwei charakteristische Verläufe mit im Vordergrund stehenden neurologischen und psychiatrischen Symptomen unterschieden werden: eine schleichend progrediente Variante und eine akute vaskulitische Form. Trotz unterschiedlicher klinischer Präsentation findet sich generell ein gutes Ansprechen auf eine immunsuppressive Therapie. Bei konsequenter Behandlung ist von einer guten Prognose auszugehen. Im Rahmen des aktuellen Überblicks gehen wir unter anderem auf die zur Zeit diskutierten Ätiologiemodelle, die diagnostischen Standards und die empfohlenen Therapieschemata ein. Differenzialdiagnostische und differenzialtherapeutische Konsequenzen werden diskutiert.</jats:p
Flow Dynamics in Model Aneurysms Associated with Simulated Vasospasm
No full textFlow Dynamics in Model Aneurysms Associated with Simulated Vasospasm. Takuo Hashimoto, M.D., George M. Austin, M.D. N.D., 23 pg
A Difficult Decision-Hashimoto's Thyroiditis or Subacute Thyroiditis? [Zor Bir Karar - Hashimoto Tiroiditi mi Yoksa Subakut Tiroidit mi?]
No full textSubacute thyroiditis generally presents with pain in the thyroid region, fever, thyrotoxicosis and elevated markers of acute inflammation. On the other hand, Hashimoto's thyroiditis is most frequently diagnosed in the hypothyroid phase with positive antithyroid autoantibodies. Here, we describe the case of a patient who presented with clinical features of subacute thyroiditis but laboratory and pathological features compatible with Hashimoto's thyroiditis. The patient was finally diagnosed with painful Hashimoto's thyroiditis
Aspectos ultrasonográficos da tireóide na doença de hashimoto.
No full textTrabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Clínica Médica, Curso de Medicina, Florianópolis, 200
Coexistence of sarcoidosis and Hashimoto thyroiditis
No full textSarcoidosis is a chronic, inflammatory disease with unknown cause characterized by non-caseating granuloma formations. It can present with bilateral hilar lymphadenopathy, skin lesions, eye involvement and locomotor system findings. Hashimoto thyroiditis is an organ-specific autoimmune disease characterized by increased autoantibody synthesis. Sarcoidosis can involve different endocrine glands. Thyroid gland involvement may lead to increased thyroid function disorders and autoantibodies. Herein, we report an 80-year-old female patient with sarcoidosis and Hashimoto coexistence
RAGE polymorphisms and oxidative stress levels in Hashimoto's thyroiditis
No full textBackground: Polymorphisms of the receptor for advanced glycation end products (RAGE) gene have been studied in various autoimmune disorders, but not in Hashimoto's thyroiditis. Also, increased oxidative stress has been described in patients with Hashimoto's thyroiditis. The aim of this study was to investigate the possible role of two common RAGE polymorphisms (−429T>C, −374T>A) in Hashimoto's thyroiditis; in parallel, we studied oxidative stress levels. Materials and methods: A total of 300 consecutive euthyroid women were examined and classified into three groups: Hashimoto's thyroiditis with treatment (n = 96), Hashimoto's thyroiditis without treatment (n = 109) and controls (n = 95). For a rough evaluation of oxidative stress, total lipid peroxide levels in serum were measured. The −429T>C AluI and −374T>A MfeI polymorphisms of RAGE were studied in genomic DNA. Results: Significant association of the RAGE system with Hashimoto's thyroiditis was found only with regard to the prevalence of the −429T>C, but not with −374T>A polymorphism. The levels of oxidative stress were significantly elevated in Hashimoto's thyroiditis patients under treatment. Further analysis demonstrated that an oxidative stress cut-off value of 590 μmol/L is associated with an increased risk of progression of Hashimoto's thyroiditis from euthyroidism to hypothyroidism; this risk is further increased in carriers of the RAGE −429T>C polymorphism. Conclusions: Our findings indicate that both examined risk factors may be implicated in the occurrence of Hashimoto's thyroiditis, but this covers only a fraction of the pathophysiology of the disease. © 2017 Stichting European Society for Clinical Investigation Journal Foundatio
Melkersson-Rosenthal syndrome in a patient with Hashimoto disease
No full textIntroduction: Melkersson-Rosenthal syndrome (MRS) is a rare neurologic disease of unknown etiology. It is characterized by a triad of symptoms: relapsing peripheral facial paralysis; orofacial edema and fissured tongue. The pathological findings are varied but often characterized by the presence of noncaseating granuloma. There are few cases of MRS coexistent with Hashimoto disease in the literature. Purpose: To present a case of MRS coexistent with Hashimoto disease. Case presentation: We report a case of a 32-year-old woman with coexisting MRS and autoimmune thyroiditis, Hashimoto disease. Fissured tongue and recurrent cheilitis of the upper lip were observed. In her medical history, she had facial nerve palsy. Histopathological examination of the upper lips mucose membrane revealed the presence of granulomas confirming the diagnosis. Conclusions: Cooperation between clinicians and histopathologists is vital in diagnosing MRS. The presence of the anti-TPO antibodies in the case reported here could suggest a correlation between immunological alteration characteristics of autoimmune thyroiditis and MRS
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