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         Crow-fukase Syndrome:     more detail

41. Medicine Arena - Journal Resources
ChiaYu Chu; Chih-Hsin Yang; Hsien-Ching Chiu. Increased Serum Levelof Vascular Endothelial Growth Factor in crow-fukase syndrome, p317.
http://rudolfo.ingentaselect.com/vl=1/cl=7/ini=medarena/nw=1/rpsv/cw/www/tandf/a
Acta Dermato-Venereologica
View all issues Search this title
Volume 81 Number 4 2001 EDITORIAL Anders Vahlquist Microsatellite Instability in Malignant Melanomas Can Autofluorescence Demarcate Basal Cell Carcinoma from Normal Skin? A Comparison with Protoporphyrin IX Fluorescence Renhua Na; Ida-Marie Stender; Hans Christian Wulf Scratch Induction in the Rat by Intradermal Serotonin: a Model for Pruritus J. S. Thomsen; M. B. Petersen; E. Benfeldt; S. B. Jensen; J. Serup Cytokine Profile of Patients with Mycosis Fungoides and the Immunomodulatory Effect of AS101 M. Shohat; E. Hodak; B. Sredni; B. Shohat; D. Sredni; M. David Stereological Quantification of Lymphocytes in Skin Biopsies from Atopic Dermatitis Patients Expression and Function of CD43 and CDw60 on T Cells from Patients with Atopic Dermatitis Increasing Incidence Rates of Squamous Cell Carcinoma of the Skin in Sweden Clinical Scoring of Cutaneous Mastocytosis Rogier Heide; Maritza A. Middelkamp Hup; Paul G. H. Mulder; Arnold P. Oranje Development and Validation of a Questionnaire for Diagnosing Atopic Dermatitis Anne B. Olesen; Karen Bang; Svend Juul; Kristian Thestrup-Pedersen

42. Clinical Nephrology, Vol. 55, 6/01
Monoclonal Ig production can also be observed associated with various symptoms, that,taken together, have been described as the crowfukase syndrome or POEMS
http://www.clinnephrol.com/dustri/31nephrology/31cn0106.htm
Volume 55, No. 6/2001 (June) Contents Originals Glomerular lesions in patients with Churg-Strauss syndrome and the anti-myeloperoxidase antibody
Y. Kikuchi, N. Ikehata, O. Tajima, N. Yoshizawa and S. Miura Cost-benefit analysis and prediction of 24-hour proteinuria from the spot urine protein-creatinine ratio
V.C. Chitalia, J. Kothari, E.J. Wells, J.H. Livesey, R.A. Robson, M. Searle and K.L. Lynn Clinical significance of the fractional excretion of anions in metabolic acidosis
H.Y. Kim, J.S. Han, U.S. Jeon, K.W. Joo, J.-H. Earm, C. Ahn, S. Kim, J.S. Lee and G.-H. Kim L-arginine supplementation in young renal allograft recipients with chronic transplant dysfunction
X.-Z. Zhang, G. Ardissino, L. Ghio, A.S. Tirelli, V. Daccò, D. Colombo, E. Pace, S. Testa and A. Claris-Appiani Erythrocyte nitric oxide metabolism in patients with chronic renal failure
I. Durak, H.S. Öztürk, S. Elgün, M.Y.B. Çimen and S. Yalçin Relationships between homocysteine and related amino acids in chronic hemodialysis patients
S.P. McDonald, M.J. Whiting, G.A. Tallis and J.A.J. Barbara

43. CancerLIT 709420
H; Maruyama A; Oida J; Kawamoto Y; Kouhara N; Oka N; Shirase T; Kitaichi M; AkiguchiI; Shibasaki H TI A patient with crow-fukase syndrome associated with
http://cancerweb.ncl.ac.uk/cancernet/cancerlit/709420.html

44. PHCentral - Medical Issues: Scientific Literature Archive: 07/27/00
Jonosono M; Maruyama Y; Maruyama I; Osame M Title Highly concentrated vascular endothelialgrowth factor in platelets in crowfukase syndrome Journal MUSCLE
http://www.phcentral.org/medical/sci-lit/072700.html
HOME Help Advanced Search Site Map ... About PHC
Current Scientific Literature: Archive 07/27/00 ARCHIVE PAGES Before 7/17/99
Author/s:
Deng Z, Morse JH, Slager SL, Cuervo M, Moore KJ, Venetos G, Kalachikov S, Cayanis E,4 Fischer SG,4 Barst RJ, Hodge SE, Knowles JA
Title: Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein ReceptorII Gene
Journal: AMERICAN JOURNAL OF HUMAN GENETICS ELECTRONIC EDITION (to be published in September 2000 print edition)
Article
Author/s: Albes JM; Eckstein FS; Heinemann MK; Gerhard Ziemer G
Title: Successful weaning of a transplanted heart from biventricular assist device
Journal: ANNALS OF THORACIC SURGERY, Volume 70, Issue pages 277-278 (2000)
Article
Author/s: Black MD; Shukla V; Rao V; Smallhorn JF; Freedom RM
Title: Repair of isolated multiple muscular ventricular septal defects: the septal obliteration technique
Journal: ANNALS OF THORACIC SURGERY, Volume 70, Issue 1, pages 106-110 (2000)

45. Ohtapaper
Saida, K., Kawakami, H., Kidate, N., Ishikawa, K., Ohta. M. Nishitani,H. crowfukase syndrome Muscle Nerve Supple 1 S223 1994.
http://www.kobepharma-u.ac.jp/~cclab/ohta2.htm
  • Localization of the five disulfide bridges in Toxin B from the venom of the Indian cobra ( Naja naja ).
    Biochem.Biophys.Res.Commun., 55:431-438, 1973.
  • Chemical modification of tyrosine residue in "Toxin B" from the venom of the Indian cobra,Naja naja.
    Biochem.Biophys.Res.Commun., 56:981-987,1974.
  • Ohta,M. Hayashi,K.
    Chemical modification of the tryptophan residue in toxin B from the Indian cobra. Biochem.Biophys.Res.Commun., 57:973-979,1974.
  • The primary structure of toxin B from the Indian cobra Naja naja.
    FEBS Lett., 71:161-166,1976.
  • Raman spectrum of Toxin B in relation to structure and toxicity.
    FEBS Lett., 72:291-294,1976.
  • Nakao,K., Nishitani,H., Ohta,M., Suzuki,M.,.and Hayashi,K. Anti-acetylcholine receptor IgG in neonatal myasthenia gravis. New Engl. J. Med., 297:169,1977.
  • ¼’J@—TC’†”öˆê˜aC‘¾“cŒõà†C–ìŒû’åŽqC—с@‹±ŽO@ ƒAƒZƒ`ƒ‹ƒRƒŠƒ“Žó—e‘̍R‘̂ƏdÇ‹Ø–³—͏ǁD@ ˆãŠw‚Ì‚ ‚ä‚݁C 102:335-340,1977.
  • ‘¾“cŒõà†C’†”öˆê˜aC¼’J@—TCò‘òK]C—с@‹±ŽO@ ˆãŠw‚Ì‚ ‚ä‚݁C101:763-766,1977
  • ’†”öˆê˜aC¼’J@—TC‘¾“cŒõà†C—é–؏«•vC‰œ–앐•FC–]ŒŽNOC–kð”ŽŒúC —с@‹±ŽO@ ˆãŠw‚Ì‚ ‚ä‚݁C102:201-203,1977.
  • 46. ?T
    5) crowfukase syndrome (Takatsuki disease, osteosclerotic myeloma, POEMS*).*polyneuropathy, organomgaly, endocrinopathy, M protein, and skin changes.
    http://www.showa.gunma-u.ac.jp/~hmura/mm-diagnosis.htm

    47. Crow-fukase Syndrome (codes) Pep Syndrome (pigmentation, Oedema,
    Name POEMS SYNDROME Synonyms, crowfukase syndrome (codes). pep syndrome(pigmentation, oedema, plasma cell dyscrasia) (codes). polyneuropathy
    http://malattierare.pediatria.unipd.it/pubblicaMR/mr_dx_ing.asp?mr=274

    48. C Information Sites
    CriglerNajjar Syndrome@; Crohn's Disease@; crow-fukase syndrome@; Cryptosporidiosis@;Cubital Tunnel Syndrome@; Cushing's Syndrome@; Cyclic
    http://www.healthorgs.com/ConditionsandDiseases/C/
    HEALTHorgs.com Search The Largest Human Reviewed Health Database on Internet
    (Not sure of spelling? Use first letters and * such as abc* or abcd* or abcde*) Match:.. All Any
    Format: Long Short
    Search Words: Search the Internet
    (Not sure of spelling? Use first letters and * such as abc* or abcd* or abcde*) Match:.. All Any
    Format: Long Short
    Search Words: Top Health Conditions and Diseases : C

    49. Vindex, De Vindplaats Van Het Nederlandse Web
    Craniosynostosis@ Creutzfeldt Jakob Disease@ Cri du Chat Syndrome@ CriglerNajjarSyndrome@ Crohn's Disease@ crow-fukase syndrome@ Cryptosporidiosis@ Cubital
    http://www.vindex.nl/dir/Health/Conditions_and_Diseases/C

    hulp
    contact persoonlijke instellingen voeg uw site toe ...
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    50. S000516c - POEMS Syndrome
    The kidney disease of crowfukase (POEMS) syndrome a clinico-pathological study of four cases.
    http://www.emory.edu/WHSCL/grady/amreport/litsrch99/s000516c.html
    [litsrch99/page_header.html] POEMS Syndrome 5/16/00 (Del Rio) Group: Tuesday Interns RE: A 24 year old African American fe male with undiagnosed fever and renal insufficiency. Question: What is the POEMS syndrome? Neurology. 54(3):772-3, 2000 Feb 8. POEMS syndrome with necrotizing vasculitis: a novel feature of vascular abnormalities. Journal of Cutaneous Pathology. 27(2):87-92, 2000 Feb. Glomeruloid hemangioma in POEMS syndrome shows two different immunophenotypic endothelial cells. American Journal of Dermatopathology. 21(6):567-70, 1999 Dec. POEMS syndrome with xanthomatous cells. Polyneuropathy Organomegaly Endocrinopathy M-protein Skin changes. Nephrology, Dialysis, Transplantation. 14(10):2370-8, 1999 Oct. A spectrum of clinicopathological features of nephropathy associated with POEMS syndrome. Chest. 115(6):1740-2, 1999 Jun. Pulmonary manifestations of POEMS syndrome: case report and literature review. Clinical Infectious Diseases. 28(3):678-9, 1999 Mar. Antibodies to human herpesvirus 8 in POEMS (polyneuropathy, organomegaly, endocrinopathy, M protein, skin: changes) syndrome with multicentric Castleman's disease.

    51. ORPHANET® : Base De Données Sur Les Maladies Rares Et Les Médicaments Orpheli
    Translate this page de Croissance lente des cheveux Cronkhite canada syndrome de Cross syndrome deCrouzon, maladie de crow-fukase, syndrome de Cryoglobulinémie Cryptococcose
    http://www.orpha.net/Pat/FRC.html
    Liste des maladies commençant par C
    Cacchi-Ricci, maladie de

    CACH syndrome

    CADASIL

    Caffey, maladie de
    ...
    Czeizel syndrome de

    52. POEMS
    Translate this page POEMS. Voir également Castleman (tumeur ou maladie de),. En anglais POEMSsyndrome. Synonymes syndrome de crow-fukase, syndrome de Takatsuki.
    http://www.vulgaris-medical.com/textp/poems.html
    POEMS Voir également Castleman (tumeur ou maladie de), En anglais : POEMS syndrome. Synonymes : syndrome de Crow-Fukase, syndrome de Takatsuki. Acronyme (sigle prononcé comme un mot ordinaire, sans l’épeler) de :
    P : Polyneuropathie
    O : Organomégalie
    E : Endocrinopathie
    M : Monoclonale
    S : Anomalie cutanée (en anglais : Skinchanges)
    Syndrome (association de symptômes) rare dont l'origine est inconnue et qui a tout d'abord été décrit au Japon. Il se caractérise par une neuropathie (atteinte du système nerveux) périphérique (à différencier du système nerveux central regroupant le cerveau, le cervelet et la moelle épinière entre autres). Symptômes
    • Hépato splénomégalie : augmentation de volume du foie et de la rate
    • Adénopathie : affection des ganglions
    • Gynécomastie : augmentation des glandes mammaires
    • Impuissance
    • Aménorrhée : absence de règles
    • Hyperpigmentation : augmentation de la coloration cutanée
    • Epaississement de la peau
    Le labo
    Il montre une dysglobulinémie monoclonale. La dysglobulinémie est une maladie rencontrée parfois chez le sujet âgé ou chez certains malades présentant une atteinte du système lymphoïde (rate, thymus, ganglions, organes lymphoïdes), une maladie auto-immune (le malade fabrique des anticorps contre ses propres tissus) ou une cirrhose du foie. Cette pathologie inconnue peut frapper 2 à 3 % de la population de plus de 70 ans. Elle est causée par la présence d'une certaine quantité de protéines anormales dans le sang. Ce sont des anticorps (immunoglobulines) provenant d’une lignée unique, appelés également clones de cellules plasmocytaires. Les plasmocytes sont issus d’une variété de globules blancs fabriqués dans la moelle osseuse.

    53. Liste C
    Translate this page de) Crohn (maladie de) Croissance osseuse (tables de) Crosby (test de) Crosti etGianotti Crouzon (maladie de) crow-fukase (syndrome de) Cruentée Cruralgie
    http://www.vulgaris-medical.com/listc.html
    Recherche dans cette liste Menu document.write('ACCESA UXRUBRIQUES') C
    Cacchi et Ricci (Maladie de)

    Cachectine

    Cachexie

    C réactive protéine (CRP)
    ...
    Cytosquelette

    54. Quest Diagnostics: Clinical Spotlight
    Overproduction of vascular endothelial growth factor/vascular permeabilityfactor is causative in crowfukase (POEMS) syndrome. Muscle Nerve.
    http://www.questdiagnostics.com/hcp/hcp_home_spotlight_latov.html
    Peripheral Neuropathy and Monoclonal Gammopathy Norman Latov, MD, PhD
    Professor of Neurology and Neuroscience
    Weill Medical College of Cornell University
    New York, NY USA Introduction Classification of Monoclonal Gammopathies The monoclonal gammopathies are routinely classified according to immunoglobulin class and associated lymphoproliferative or plasma cell disorder (Table 1). Table 1. Monoclonal Gammopathy Classification IgM monoclonal gammopathies:
    • Nonmalignant IgM monoclonal gammopathy Waldenström’s macroglobulinemia Chronic lymphocytic leukemia B-cell lymphoma
    IgG or IgA monoclonal gammopathies:
    • Nonmalignant IgG or IgA monoclonal gammopathies Multiple myeloma Osteosclerotic myeloma
    Light or heavy chain diseases:
    • Heavy chain myeloma ( g , µ, or a Light chain myeloma (k or l
    In most cases, the monoclonal gammopathies associated with neuropathy are nonmalignant, but 20 to 35% of the IgM monoclonal gammopathies are associated with Waldenström’s macroglobulinemia, and 8 to 17% of the IgA and IgG monoclonal gammopathies are associated with myeloma. The rate of transformation from the nonmalignant to the malignant state is approximately 2% per year. Estimates as to the incidence of neuropathy range from 3-32% in patients with all types of monoclonal gammopathy, 5-50% in IgM monoclonal gammopathies, and 6-25% in IgG and IgA monoclonal gammopathies. Although IgG or IgA monoclonal gammopathies are more frequent than IgM monoclonal gammopathies in the normal population, more patients with neuropathy have IgM than IgG or IgA monoclonal gammopathies. This is consistent with the greater incidence of neuropathy in the IgM monoclonal gammopathies.

    55. Internal Medicine III / School Of Medicine
    MIYAKAWA Koichiro, TORIYAMA Takanobu, KAWAHARA Hirohisa, SHIGEMATSU Hidekazu Thekidney disease of crowfukase (POEMS)syndrome a clinicopathological study of
    http://www.med.nagoya-u.ac.jp/medlib/achieve/1991/b-3.html
    Internal Medicine III / School of Medicine
  • DEL MONTE Monte A., RABBANI Ramin, DIAZ Tarcisio C., LATTIMER Sarah A., NAKAMURA Jiro, BRENNAN Mary C., GREENE Douglas A.: Sorbitol, myo-inositol and rod outer segment phagocytosis in glucose-exposed cultured human retinal pigment epithelial cells: in vitro modeling of the myo-inositol depletion hypothesis of diabetic complications. Diabetes 40: 1335-1345, 1991.
  • FUKATSU Atsushi, MATSUO Seiichi, TAMAI Hirofumi, MATSUDA Tadashi, HIRANO Toshio: Expression of interleukin 6 in normal and diseased human kidney. Lab Invest 65: 61-66, 1991.
  • FUKATSU Atsushi, TAMAI Hirofumi, NISHIKAWA Kazuhiro, MATSUKAWA Wahei, YOSHIDA Futoshi, MATSUO Seiichi, TAKEDA Asami, KODERA Kazuo, MOROZUMI Kunio, ITO Yasuhiko, MIYAKAWA Koichiro, TORIYAMA Takanobu, KAWAHARA Hirohisa, SHIGEMATSU Hidekazu: The kidney disease of Crow-Fukase (POEMS)syndrome: a clinicopathological study of four cases. Clin Nephrol 36: 76-82, 1991.
  • HAMADA Yoji, KITOH Ryuzo, RASKIN Philip: Crucial role of aldose reductase activity and plasma glucose level in sorbitol accumulation in erythrocytes from diabetic patients. Diabetes 40: 1233-1240, 1991.
  • HOTTA Nigishi, KAKUTA Hironobu, KOH Naoki, FUKASAWA Hideo, YASUMA Tetsu, AWAYA Shinobu, SAKAMOTO Nobuo: In vitro retinal and erythrocyte polyol pathway regulation by hormones and an aldose reductase inhibitor. Diabetes Res Clin Pract 14: 29-36, 1991.
  • 56. IgG Lambda Multiple Myeloma And Diffuse Necrobiotic Xanthogranuloma Association:
    Br J Dermatol 1989; 121 1237. 9. Shelley WB, Shelley ED. The skin changesin the crow-fukase (POEMS) syndrome. Arch Dermatol 1987; 123 85-7. 10.
    http://www.john-libbey-eurotext.fr/articles/ejd/7/7/519-21/
    European Journal of Dermatology European Journal of Dermatology. Vol. 7, Issue 7, October - November 1997: 519-21, Clinical Reports IgG lambda multiple myeloma and diffuse necrobiotic xanthogranuloma association: a case report* *Oral Communication presented at the XXXII National Congress of the "Associazione dei Dermatologi Ospedalieri Italiani" (Naples, 20-23 October 1993) Angelo CARABELLI1
    Emanuela CECCA1
    Giovanni CROVETTI2
    Concetto DE FILIPPO2
    Andrea BREZZI3
    Carlo CAMPIGLIA1
    Marco GUIZZARDI1
    Flavio CANDIANI1
    Egidio BERTANI1 1, Department of Dermatology, S. Antonio Abate Hospital, Via Pastori
    2, 21013 Gallarate (VA), Italy.
    Fax: (+39) 331.75.12.45. 2, Department of Immunohaematology, S. Antonio Abate Hospital, Gallarate (VA), Italy. A. Brezzi: Ist Department of Dermatology, University of Milan, Italy. Reprints A. Carabelli. RESUME SUMMARY ARTICLE,

    57. •xŽRˆã‰È–ò‰È‘åŠw —Տ°ŒŸ¸ˆãŠwuÀ‹ÆÑ (2001”N)
    K, Jonosono M, Hashiguchi T, Kawabata M, Osame M, Kitajima I VEGF is causativefor pulmonary hypertension in apatients with crowfukase (POEMS) syndrome.
    http://www.toyama-mpu.ac.jp/hp/clla/gyousekishuu01.html
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    5F Sugiyama S., Ozawa T., Taki H., Maruyama M., Yamashita N., Ohta M., Hirata M., and Kobayashi M. Hereditary angioedema with a de novo mutation of exon8 in the C1 inhibitor gene showing recurrent edema of the hands around the peripheral joints. Arthritis and Rheum. 44; 974-977,2001.
    6FYamada T., Yamada H., Morikawa M., Kato E. H., Kishida T., Ohnaka Y., Nikaido H., Ozawa T., and Fujimoto S. Management of pregnancy with congenital antithrombiin III deficiency: Two case reports and a review of the literature. J. Obstrt. Gynaecol. Res. 27; 189-197, 2001.
    7F ŠÝ•Ó”üKA“‡“cŒ«ˆêAÎ‘q’¼ŒhAìãd•FAÔˆä‘ì–çA¬àV“N•v Carpenter ÇŒóŒQ‚Ì Ç—áD“úŒ`‰ïŽA A
    FKubo T, Kitajima I, Makinodan A, Nirastuka S, Inoue S, Otsuka G, Ohashi S, Ueshima K,Hirasawa Y: Fibrin Monomer would be useful predictor of pulmonary embolism following total hip arthropathy.-preliminary report- J. Orthopaedic Sci 6

    58. 1.
    K, Arisato T, Osame M Overproduction of vascular endothelial growth factor/vascularpermeability factor causative in crowfukase (POEMS) syndrome.Muscle Nerve
    http://www.toyama-mpu.ac.jp/md/clm/rinken.html
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    ‹³Š¯’èˆõ‚ª‚²‚­­‚È‚¢‚±‚Æ‚©‚çAuÀ‚Æ‚µ‚čL”͂Ȉ㗕ª–ì‚Ì‘S‚Ăɐ¸’Ê‚·‚邱‚Ƃ͍¢“ï‚Æ‚ÍŽv‚í‚ê‚邪A‹³Š¯‚̐ê–啪–ì‚ÌŒ¤‹†‚ð[‚ß‚È‚ª‚ç‚àAã‹LÓ–±‚ð‰Ê‚½‚·‚½‚ß‚Ì—LŒø‚ÈŽè’i‚ðlˆÄ‚µ‚Ä‚¢‚­•K—v‚ª‚ ‚é‚à‚̂ƍl‚¦‚éB ‹³ŽöF –k“‡ ŒM •‹³ŽöF ¬•û ‘¥•v •Žèi•a‰@ŒŸ¸•”jF¬‘ò “N•v ‚RDŒ¤‹†‰Û‘è i‚PjŒ¤‹†‰Û‘è FŒŒŠÇV¶ŠÖ˜AŽ¾Š³‚É‚¨‚¯‚é“]ŽÊˆöŽqˆÙí‚ÆŒŒŠÇV¶•a‚ɑ΂·‚éˆâ“`Žqˆã–ò•i‚ÌŠJ”­B ƒADŒ¤‹†‚Ì–Ú“I ƒCDŒ¤‹†‚Ì’B¬“x F ‚Pj¡‚Ü‚Å‚É–¾‚ç‚©‚É‚µ‚½VEGF•a‚Å‚ ‚é•‚Žî‚ÆŒŒŠÇV¶‚ðŽåÇó‚Æ‚·‚éŒ`Ž¿×–EŽîiPOEMSÇŒóŒQj‚Ì•ªŽq•a‘Ô‚ð“]ŽÊˆöŽq‰ðÍ‚©‚ç‰ð–¾‚µA“]ŽÊˆöŽq’²ß‚ð‚ß‚´‚µ‚½V‚µ‚¢Ž¡—–@‚ðŠJ”­‚·‚éB

    59. _ŒoÇŒóŒQII
    4, Postpolio syndrome(?), , 356. 4), Lewis-Sumner?, ?, 492. 5), crow-fukase?, ? , 496.
    http://www.nippon-rinsho.co.jp/backnum/s_mokuji/shinkei_2.html
    _ŒoÇŒóŒQ@II •W‘è ƒgƒbƒvƒI[ƒT[ III m‘ÌŠO˜HŒnŽ¾Š³n AD 1j ‰¡’n@³”V 2j ŽR‘º@ˆÀO 3j 4j 5j X@@G¶ 6j ‹ß“¡@’q‘P ‹ß“¡@’q‘P 1j is«Šjã«–ƒáƒ 2j ¬ŽR@Žå•v 3j ‘å”]”玿Šî’êŠj•Ï«Ç ‘Š”n@–F–¾ 4j ‘ºã@M”V 5j 6j ˆêŽ_‰»’Y‘f’†“Å ƒƒ`ƒ‹ƒAƒ‹ƒR[ƒ‹’†“Å ‹´Œû@‰pŽu 7j ƒˆƒAƒLƒlƒWƒA is«’W‘“‹…•Ï«ÇiHallervorden„ŸSpatz•aadult type of neuroaxonal dystrophy) ’·’JìˆêŽq ’W‘“‹…•Ž¿ƒ‹ƒC‘̈ޏkÇ ’·’JìˆêŽq ‚Ñ‚Ü‚ñ«ƒŒƒr[¬‘Ì•a ¬ã@Œ›Ži BD •‘“¥‰^“®ÇŒóŒQ 1j Huntington•a ‹ààV@ˆê˜Y 2j —Lž™ÔŒŒ‹…•‘“¥•aC‰Æ‘°«‹ØˆÞk«—Lž™ÔŒŒ‹…•‘“¥•a œA£Œ¹“ñ˜Y 3j McLeodÇŒóŒQ ¼àV@³–L 4j —ǐ«ˆâ“`«•‘“¥•a ²“¡@—T“¹ 5j ˜Vl«•‘“¥•a 6j Ž•óŠjÔŠjE’W‘“‹…ƒ‹ƒC‘̈ޏkÇiDRPLA chorea‚ÌŠÓ•ÊŽ¾Š³‚Æ‚µ‚āj 7j Sydenham•‘“¥•a ²“¡@—T“¹ ƒAƒeƒg[ƒ[ –쑺@–FŽq ”­ì«ƒqƒ‡ƒŒƒAEƒAƒeƒg[ƒ[ 1j ”­ì«‰^“®—U”­«ƒqƒ‡ƒŒƒAEƒAƒeƒg[ƒ[ A–؁@@² 2j ”­ì«ƒWƒXƒgƒjƒAEƒqƒ‡ƒŒƒAEƒAƒeƒg[ƒ[ A–؁@@² –«‘½”­«ƒ`ƒbƒNÇiGilles de la TouretteÇŒóŒQj –쑺@–FŽq ƒWƒXƒgƒjƒAÇŒóŒQ aD ‹ÇŠ«C•ªß«ƒWƒXƒgƒjƒA 1j èò•”ƒWƒXƒgƒjƒAiáz«ŽÎèòj –쌳@³O 2j MeigeÇŒóŒQ œA£@˜a•F 3j ‘@@áz bD ‘Sg«ƒWƒXƒgƒjƒA 1j ”P“]ƒWƒXƒgƒjƒA –ڍè@‚L 2j ‘Šú”­Ç”P“]ƒWƒXƒgƒj[ –쑺@–FŽq 3j ’˜–¾‚È“ú“à•Ï“®‚ð’æ‚·‚éˆâ“`«is«ƒWƒXƒgƒj[i£ì•aj 4j LubagÇŒóŒQiXq13„Ÿlinked dystonia„Ÿparkinsonismj ƒ~ƒIƒNƒ[ƒkƒXÇŒóŒQ aD is«ƒ~ƒIƒNƒ[ƒkƒX‚Ä‚ñ‚©‚ñ 1j Lafora•a 2j Unverricht„ŸLundborg•a “à“¡@–¾•F 3j Ž•óŠjÔŠjE’W‘“‹…ƒ‹ƒC‘̈ޏkÇiDRPLAƒ~ƒIƒNƒ[ƒkƒX‚Ä‚ñ‚©‚ñ‚Ì^nŠÓ•Êf’f‚Æ‚µ‚āj “à“¡@–¾•F 4j Cherry„Ÿred spot myoclonusÇŒóŒQ ƒVƒAƒŠƒh[ƒVƒX1Œ^ —é–؁@‹`”V ƒVƒAƒŠƒh[ƒVƒX2Œ^ —é–؁@‹`”V 5j ˆäã@—Y‹g 6j GM2ƒKƒ“ƒOƒŠƒIƒVƒh[ƒVƒX

    60. PHCentral - Medical Issues: Scientific Literature Archive: 02/15/01
    T; Kawabata M; Osame M; Kitajima I Title VEGF is causative for pulmonary hypertensionin a patient with crowfukase (POEMS) syndrome Journal INTERNAL MEDICINE
    http://www.phcentral.org/medical/sci-lit/021501.html
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    Current Scientific Literature: Archive 02/15/01 ARCHIVE PAGES Before 7/17/99 Author/s: Schenk P; Petkov V; Madl C; Kramer L; Kneussl M; Ziesche R; Lang I
    Title: Aerosolized Iloprost Therapy Could Not Replace Long-term IV Epoprostenol (Prostacyclin) Administration in Severe Pulmonary Hypertension
    Journal: CHEST, Volume 119, Issue 1, pages 296-300 (2001)
    Abstract
    Author/s: Cockrill BA; Kacmarek RM; Fifer MA; Bigatello LM; Ginns LC; Zapol WH, Semigran JM
    Title: Comparison of the Effects of Nitric Oxide, Nitroprusside, and Nifedipine on Hemodynamics and Right Ventricular Contractility in Patients With Chronic Pulmonary Hypertension
    Journal: CHEST, Volume 119, Issue 1, pages 128-136 (2001)
    Abstract
    Author/s: Lee S-D; Kim D-S; Shim T-S; Lim C-M, Koh Y; Kim W-S; Kim W-D
    Title: Nitric Oxide and Molsidomine in the Management of Pulmonary Hypertension in Takayasu's Arteritis
    Journal: CHEST, Volume 119, Issue 1, pages 302-307 (2001)

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