¥Ç¥ë¥Þ¥É¥í¡¼¥à Dermadrome The summary for this Japanese page contains characters that cannot be correctly displayed in this language/character set. http://akimichi.homeunix.net/~emile/aki/medical/dermatology/node24.html
Contents The summary for this Japanese page contains characters that cannot be correctly displayed in this language/character set. http://xakimich.hp.infoseek.co.jp/dermatology/node1.html
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English Journal-EG Mochizuki Y, Yoshihashi H, Oishi M, Takasu T, Nozawa K, Uchiyama T, Sawada S CrowFukasesyndrome a case associated with vasospastic angina Acta Neurologica http://133.43.84.139/English Journal-EG.html
Extractions: Case History and Clinical Findings: Examinations: The following pathologically laboratory results were found: erythrocyte sedimentation rale (ESR) 35/55 mm n. W., C-reactive protein (CRP) up to 39 mg/l, leucocytes up to 13.5/nl, LH and FHS were elevated corresponding to hypergonadotropic hypogonadism, renal failure with at the beginning a selective glomerular proteinuria, as well as a monoclonal IgG-gammopathy. The bone marrow aspiration as well as the bone marrow biopsy revealed neither plasmocytoma nor a malignant systemic disease. The ultrasound examination showed enlarged liver, spleen, and kidneys. Treatment and Follow-up: After excluding a connective tissue disease and an infection and with the missing proof of a malignant tumor treatment was started with parenteral methylprednisolon 500 mg on 3 consecutive days under the hypothesis of classic panarteriitis nodosa, even when multiple biopsies were negative. Under the treatment, the elevated inflammatory parameters and renal failure improved, but deteriorated quickly after discontinuation of the corticosteroid medication. The second kidney biopsy showed a chronic scaring glomerulopathy of the hemolytic uremic syndrome type. In the follow-up the renal insufficiency was improved by corticosteroids. With the manifestation of a bilateral sensory polyneuropathy in January 1994, the diagnosis of a POEMS syndrome was most likely.
A14:Neurology - School Of Medicine sarcoidosis. J Neurol 247 544549, 2000. KOIKE Haruki, SOBUE Gen Crow-Fukasesyndrome. Neuropathology 20, Suppl. S69-S72, 2000. KURU http://www.med.nagoya-u.ac.jp/medlib/achieve/2000/a14.html
Extractions: CARRILLO Maria Christina, MINAMI Chiyoko, KITANI Kenichi, MARUYAMA Wakako, OHASHI K., YAMAMOTO T., NAOI Makoto, KANAI Setsuko, YOUDIM Moussa: Enhancing effect of rasagiline on superoxide dismutase and catalase activities in the dopaminergic system in the rat. Life Sci 67: 577-585, 2000. HISHIKAWA Nozomi, HASHIZUME Yoshio, HIRAYAMA Masaaki, IMAMURA Kazuhiro, WASHIMI Yukihiko, KOIKE Yasuo, MABUCHI Chiyuki, YOSHIDA Mari, SOBUE Gen: Brainstem-type Lewy body disease presenting with progressive autonomic failure and lethargy. Clin Auton Res 10: 139-143, 2000. INUKAI Akira, DOYU Manabu, KATO Takashi, LIANG Yideng, KURU Satoshi, YAMAMOTO Masahiko, KOBAYASHI Yasushi, SOBUE Gen: Reduced expression of DMAHP/SIX5 gene in myotonic dystrophy muscle. Muscle Nerve 23: 1421-1426, 2000. INUKAI Akira, KURU Satoshi, LIANG Yideng, TAKANO Akemi, KOBAYASHI Yasushi, SAKAI Motoko, DOYU Manabu, SOBUE Gen: Expression of HLA-DR and its enhancing molecules in muscle fibers in polymyositis. Muscle Nerve 23: 385-392, 2000. ISHIGAKI Shinsuke, NIWA Jun-ichi, YOSHIHARA Tsuyoshi, MITSUMA Norimasa, DOYU Manabu, SOBUE Gen: Two novel genes, human neugrin and mouse m-neugrin, are upregulated with neuronal differentiation in neuroblastoma cells. Biochem Biophys Res Commun 279: 526-533, 2000.
Arch Neurol -- Page Not Found a role in the therapy of patients with unresectable brain tumors 20 and the CrowFukasesyndrome, and possibly as well in patients with diabetic retinopathy. http://archneur.ama-assn.org/issues/v59n5/ffull/ned10016.html
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