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         Crow-fukase Syndrome:     more detail

61. 2000”N‘²‹ÆŽŽŒ±
1 1.KennedyAlter-Sung syndrome 2.Amyotrophic lateral 1.Guillain-Barr 2.crow-fukase? 3.? 4
http://www.med.nagasaki-u.ac.jp/intmed-1/sotugyosiken/2000sotu03.html
2000”N‘²‹ÆŽŽŒ±
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m‚R‚PnÇ—áF54Î —«B1”N‘O¶ãŽˆ‚Ì’E—́A‹Ø“÷‚̃sƒNƒsƒN‚·‚é‚Ì‚É‹C•t‚¢‚½B6ƒ–ŒŽ‘O‚æ‚è‰EãŽˆ‚É‚à“¯—l‚̏ǏóoŒ»B2ƒ–ŒŽ‘O‚æ‚è•àsŽž‚ɉºŽˆ‚̃cƒbƒpƒŠ‚ðŠ´‚¶‚é‚悤‚É‚È‚Á‚½B‚Ü‚½AãŽˆ––½‚̋؈ޏk‚ª–¾‚ç‚©‚Æ‚È‚Á‚Ä‚«‚½BŒ»Ý‚Ü‚ÅŠ´ŠoáŠQ‚É‚Í‹C•t‚¢‚Ä‚«‚È‚¢Bf’f‚Æ‚µ‚čłà“K“–‚È‚Ì‚Í‚Ç‚ê‚©B‚P‚‘I‚ׁB

‚PDKennedy-Alter-Sung syndrome
‚QDAmyotrophic lateral sclerosis ‚RDKugelberg-Welander disease ‚SDHTLV-I associated myelopathy ‚TDCervical myelopathy @@‚j1@@‚‚j2@@‚ƒj3@@‚„j4@@‚…j‚T m‚R‚QnGuillain-BarrŽÇŒóŒQ‚ɂ‚¢‚ÄŒë‚Á‚Ä‚¢‚é‚à‚Ì‚ð1‚‘I‚ׁB ‚PDŠ´õÇŒã‚Ì’E‘«‚Ì‘½”­ª_Œo‰Š‚Å‚ ‚éB ‚QD_Œo“`“±‘¬“x‚͐³í‚Ì‚±‚Æ‚ª‚ ‚éB ‚RD”]_ŒoáŠQ‚Æ‚µ‚Ä––½«Šç–ʐ_Œo–ƒáƒ‚ð‚«‚½‚·‚±‚Æ‚ª‚ ‚éB ‚SDŒŒ´’†‚ɍRƒKƒ“ƒOƒŠƒIƒVƒhR‘Ì‚ªŒŸo‚³‚ê‚邱‚Æ‚ª‚ ‚éB ‚TD‘‰t‚Ì’`”’‚͐³í‚ŁA×–E”‚ª‘‰Á‚·‚é(’`”’×–E‰ð—£Œ»Û )@@‚±‚Æ‚ª‚ ‚éB @@‚j1@@‚‚j2@@‚ƒj3@@‚„j4@@‚…j‚T

62. ”¼nDoctor-Trias‚È‚Ç
POEMS syndrome, crowfukase,polyneuropathy/organomegaly/endocrinopathy/Mprotein/Skin Changes.
http://www8.ocn.ne.jp/~halfboil/note/not-13.html
Trias
‚¾‚¢‚½‚¢Ad—v‚ȏ‡‚Å‚·BŠo‚¦‚é‚ׂ«‚Å‚È‚¢‚à‚Ì‚à¬‚¶‚Á‚Ä‚¢‚é‚Ì‚Å‚²’ˆÓB
Beck's trias
–¬ˆ³ã¸EŒŒˆ³’ቺES‰¹”÷Žã
’A‚µA‚R‚‘µ‚¤‚à‚̂͏­‚È‚¢B Deadly@Quartet ƒCƒ“ƒXƒŠƒ“’ïR«ÇŒóŒQB
Charcot's trias (ŠÌ’_äX)@
‰Eã• •”’ɁE”­”ME‰©át Merseburg trias Basedow•a‚̗Տ°ŠŒ©
Šá‹…“ˏoEbó‘BŽîE•p–¬B Menier'•a@trias u‚ß‚Ü‚¢vu‚Ý‚Ý‚È‚èvu“ï’®v Tetralogy of Fallot ”x“®–¬‹·óE‰EŽº”ì‘åESŽº’†ŠuŒ‡‘¹E‘å“®–¬‹Ræ Whipple triad
CRESTÇŒóŒQ
Kartagener's trias Kartagener‚̏Ǐó
“à‘Ÿ‹tˆÊE‹CŠÇŽxŠg’£ÇE–«•›•@o‰Š Korsakov psychosis Trias ƒRƒ‹ƒTƒRƒtÇŒóŒQAƒAƒ‹ƒR[ƒ‹”ÓŠú¸_•a
Ž¸Œ©“–Ž¯Aì˜bA‹L–Á—͒ቺ Wernicke”]Ç Trias ƒEƒFƒ‹ƒjƒbƒP”]Ç‚ÍVitamin B1•s‘«‚ɂ悶‚Ü‚·B ˆÓŽ¯áŠQAŽ¸’²«•àsAŠá‹Ø–ƒáƒ Hutchinson's trias æ“V”~“ł̏Ǐó ŽÀŽ¿«Šp–Œ‰ŠE“àŽ¨«“ï’®EHutchinsonŽ•‰å CCF‚ÌTrias CCFFCarotid-cavernous fistulaèò“®–¬ŠC–Ȑ–¬“´á‘ PTSD‚Ì‚R‘åÇó N“üE‰ñ”ðE‰ßŠoÁ Hemochromatosis Trias ŠÌd•Ï (Å‚à’¾’…‚µ‚â‚·‚¢) ”畆‚̐F‘f’¾’…(•K”­)ADM RCC‚Ì3’¥ RCCFrenal cell carcinoma ”½•œ«–³ÇŒóŒŒ”AAt•”áu’ɁA˜”w•”ŽîᎠSaint's triad Œ´ˆö•s–¾‚¾‚ªH“¹—ôEƒwƒ‹ƒjƒAEŒeŽºÇE’_ÎÇ‚̍‡•¹Ç Treacher collins‚Ìtrias Wilson•a‚ÌTrias ŠÌd•ÏiLCjAis«‚̐‘ÌŠO˜HÇóAƒJƒCƒU[Eƒtƒ‰ƒCƒVƒƒ[—Ö Kayser-Fleischeri—΁`‰©ŠŒF’¾’…j • ’ɁEšq“fE•Ö”éB Charcot's trias (_Œo)@ ‘½”­«d‰»Ç(PS)‚̏Ǐó Dieulafoy's trias ”畆’mŠo‰ß•qE‹Ø«–hŒäEMcBurney“_—z« Triad of Herz S‘Ÿ_ŒoÇH‚̂ЂƂF S‘Ÿ•”áu’ɁEŒÄ‹z‹‡”—ES”‘£i Triad of Luciani ¬”]Ž¾Š³F–³—͏ǁE–³‹Ù’£ÇEŽ¸—§Ç

63. AWMF Online - Leitlinie Neurologie: Neuritis: Chronische Immunvermittelte Polyne
Translate this page demyelinating sensory and motor neuropathy = MADSAM, Lewis-Sumner syndrome), fokaleCIDP M-Protein und Skin Changes), auch als crow-fukase-Syndrom bezeichnet
http://www.uni-duesseldorf.de/WWW/AWMF/ll/neur-048.htm
AWMF online
A rbeitsgemeinschaft der
W issenschaftlichen
M edizinischen
F achgesellschaften
AWMF-Leitlinien-Register Nr. 030/048 Entwicklungsstufe:
Neuritis: Chronische immunvermittelte Polyneuritis,
  • der GBS-Varianten (ca. 10%)
    • akute motorische axonale Neuropathie (AMAN),
    • akute motorische und sensible axonale Neuropathie (AMSAN),
    • Miller-Fisher Syndrom (MFS),
    • Polyneuritis cranialis,
    • akute Pandysautonomie
  • Neuritis bei Kollagenosen,
  • Facialisparese,
  • Neuritis vestibularis,
  • Neuroborreliose und
  • Neuro-AIDS
siehe entsprechende DGN-Leitlinien.
Definitionen
    Neuritis
    Immunvermittelt
    Chronische inflammatorische demyelinisierende Polyneuropathie (CIDP)
    CIDP-Varianten Ataktische Form der CIDP, multifokale CIDP (multifocal acquired demyelinating sensory and motor neuropathy = MADSAM, Lewis-Sumner syndrome), fokale CIDP (focal acquired demyelinating neuropathy), distal acquired demyelinating symmetric neuropathy (DADS), axonale Form der chronischen inflammatorischen Polyneuropathie (CIAP), rein motorische Variante der CIDP.
    Multifokale motorische Neuropathie (MMN)
    Sonderformen wie die GALOP (Gait disorder, Autoantibody, Late age Onset Polyneuropathy) sowie die Anti-Sulfatid-Neuropathie werden auch in spezialisierten Einrichtungen nur selten gesehen.

64. References Chapter 8
Matsuo,K, Arisato,T, Osame,M Overproduction of vascular endothelial growth factor/vascularpermeability factor is causative in crowfukase (POEMS) syndrome.
http://www.uchsc.edu/misc/diabetes/oxref8.html
References - Chapter 8 1. Schmidt,MB: Eine biglandulare Erkrankung (Nebennieren und Schilddruse) bei Morbus Addisonii. Verh Dtsch Ges Pathol 21:212-221, 1926
2. Nerup,J: Addison's disease - clinical studies: A report of 108 cases. Acta Endocrinol 76:127-141, 1974
3. Patel,DD: Escape from tolerance in the human X-linked autoimmunity-allergic disregulation syndrome and the Scurfy mouse. J Clin Invest 107:155-157, 2001
4. Ahonen,P, Myllarniemi,S, Sipila,I, Perheentupa,J: Clinical variation of autoimmune polyendocrinopathy - candidiasis - ectodermal dystrophy (APECED) in a series of 68 patients. N Engl J Med 322:1829-1836, 1990
5. Flier,JS, Kahn,CR, Roth,J, Bar,RS: Antibodies that impair insulin receptor binding in an unusual diabetic syndrome with severe insulin resistance. Science 190:63-65, 1975
6. Flier,JS, Bar,RS, Muggeo,M, Kahn,CR, Roth,J, Gorden,P: The evolving clinical course of patients with insulin receptor autoantibodies: Spontaneous remission or receptor proliferation with hypoglycemia. J Clin Endocrinol Metab 47:985-995, 1978
7. Souadjian,JV, Enriquez,P, Silverstein,MN, Pepin,J-M: The spectrum of diseases associated with thymoma. Arch Intern Med 134:374-379, 1974

65. Title
K, Jonosono M, Hashiguchi T, Kawabata M, Osame M, andKitajima I VEGF is causativefor pulmonaryhypertension in apatients with crowfukase (POEMS) syndrome.
http://kenkyu.toyama-mpu.ac.jp/kenkyu25.nsf/3a0c1e79a82fbb7a492565020027ace4/5ae

66. Mortality Forum Feb1999 - May1999
Others have described the clinical features involved under the terms of crowfukase'ssyndrome, PEP syndrome (pigmentation, oedema, plasma cell dyscrasia, or
http://www.pubcare.uu.se/nordwho/verksam/mortforum/mort99_2.html
1999-02-15 Q1 Code for "hypothenar hammer syndrome"
[The question is from Augusto Hasiak Santo:] The Brazilian Ministry of Health is preparing a manual on occupational diseases and a coding problem with the diagnosis hypothenar hammer syndrome occurs. This is a rather rare vascular injury that is seen in posttraumatic digital ischaemia causes by irregularity or occlusion of the digital ulnar artery at the level of the hamate bone. It characteristically occurs in the dominant hand of middle-aged men whose occupational or recreational activities require the use of the hand as a hammer. One of the proposed codes is "I77.8 - Other specified disorders of arteries and arterioles". The other possible code is "I73.8 - Other specified peripheral vascular diseases", because the hypothenar hammer syndrome also occurs with peripheral vascular affections. I would [like] to submit this coding problem to discussion. There is also a suggestion of a member of the group that is preparing the manual to include the hypothenar hammer syndrome in the next version of the Index. [Suggested coding:] Canada X50 S650
[Comments:] Canada /Patricia Wood/: Given Augusto's description of Hypothenar Hammer Syndrome, I wonder if a possible classification would be S65.0 Injury of ulnar artery at wrist and hand level? A possible external cause code could be X50, Overexertion and strenuous or repetitive movements.

67. Birth Disorder Information Directory - T
HOME T. Takatsuki('s) syndrome See Crow Fukase syndrome. Tamari Goodman syndrome(Congenital Heart Disease Radio Ulnar Synostos Mental Retardation)
http://www.bdid.com/defectt.htm

HOME
T
Takatsuki('s) Syndrome Tamari Goodman Syndrome (Congenital Heart Disease Radio Ulnar Synostos Mental Retardation) Tangier Disease Tardive Tibial Muscular Dystrophy Tarsal-Carpal Coalition Syndrome (Synostosis of Talus and Calcaneus with Short Stature) Tauri Disease (Glycogen Storage Disease, Type VII) Tay Sachs Disease Taybi Linder Syndrome (Cephaloskeletal Dysplasia) Teebi Syndrome (Brachycephalofrontonasal Dysplasia; Craniofrontonasal Syndrome, Teebi Type) Teebi Naguib Alawadi Syndrome Telfer Sugar Jaeger Syndrome (Piebald Trait with Neurologic Defects) Temporal-Central Focal Epilepsy

68. POEMS Syndrome
Links to information and resources for POEMS syndrome, a multisystem disorder. Mayo Clinic Information About POEMS syndrome. Excellent, easy to Tufts POEMS syndrome. Listing of medical journal related to POEMS syndrome, from Tufts University Neurology
http://rarediseases.about.com/cs/poemssyndrome
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POEMS Syndrome
Guide picks A plasma cell dyscrasia (bone marrow disorder) that causes multiple body system disorders, including neuropathy, organ overgrowth, glandular problems, and skin changes.
Mayo Clinic: Information About POEMS Syndrome
Excellent, easy to understand information on the disorder, from the Hematology Division, Department of Internal Medicine, Mayo Clinic Rochester (U.S.). NORD: POEMS Syndrome Medical information (technical) on the disorder. Tufts: POEMS Syndrome Listing of medical journal articles related to POEMS syndrome, from Tufts University Neurology (U.S.). Email this page! Sponsored Links Need Health Insurance?

69. Abstract
of MN. 4PO-18 IMMUNOHISTOCHEMICAL ANALYSIS OF VEGF AND Flk1 PROTEINEXPRESSION IN THE KIDNEY OF CROW FUKASE syndrome. T. Ohashi
http://www.knt-ec.com/event/icim/abstract/4-PO-3.html
ABSTRACTS 4-PO: Nephrology: nephrotic syndrome May 27 (Mon.), 2002 4-PO-14: SYNCHRONOUS TOXOPLASMOSIS AND NEPHROTIC SYNDROME F. Tavares , M. Fonseca , J. Barbas , C. Ferreira , A. Palma Carlos Dept. of Internal Medicine III, Dept. of Nephrology, Santa Maria Hospital, Lisbon, Portugal PURPOSE Although renal disease is an uncommon presenting feature of Toxoplasma gondii infection, related glomerular lesions have been reported with congenital attaint. The association toxoplasmosis / nephrotic syndrome is exceptional in adults. Only 3 cases are noticed on literature. We present another patient, who developed a nephrotic syndrome, with concurren clinical evidence of T. gondii illness.
METHOD We resume investigation proceedings, treatment and evolution of a 31 year-old, non-diabetic man, with frequent exposure to cats, transferred to our hospital with generalized oedema, proteinuria (9.6g/day), hypoalbuminemia (12g/l) and dyslipidemia (total cholesterol- 10.5mmol/l, triglyceride- 2,7mmol/l).
RESULT The histologic appearance and the fluorescence pattern of glomeruli pointed to minimal-change disease. The asymptomatic enlarged cervical and axillary lymph nodes and an anterior mediastinal mass made lymphoma and metastatic cancer possible, but extensive evaluation, including a left cervical lymphadenopathy biopsy failed to show neoplasm. HIV,
HBV, HCV, CMV, EBV, cat-scratch disease, syphilis, sarcoidosis and tuberculosis were excluded. A confirmed positive serology for toxoplasmosis was detected (IgG agglutination,IgA and IgM ELISA). Major defects in T-cell mediated immunity were absent. Although enlarged nodes have spontaneously regressed, proteinuria rose to 20g/day before starting therapy (pyrimethamine + clindamycin + folinic acid - 21 days and prednisolone 1mg/Kg/day).

70. Author
PATIENTS. Nihei, H. 4PO-18, IMMUNOHISTOCHEMICAL ANALYSIS OF VEGF ANDFlk1 PROTEIN EXPRESSION IN THE KIDNEY OF CROW FUKASE syndrome. Nihei
http://www.knt-ec.com/event/icim/author/N_O.html
AUTHORS' INDEX [N] Program No. Abstract Title Nadaraia , K. 2-PO-17 FREQUENCY OF DETECTION OF POOR PROGNOSIS PREDICTORS IN PRIMARY DIAGNOSTIC IN PATIENTS WITH DILATED CARDIOMYOPATHY Nadeau, R.A. 2-PO-65 ELECTRICAL POTENTIAL LOSSES CAN PREDICT LEFT VENTRICULAR FUNCTION IN UNSTABLE CORONARY ARTERY DISEASE Nadeau, R.A. 2-PO-60 HEMODINAMIC INFORMATION OF THE ELECTRICAL POTENTIAL LOSSES IN UNSTABLE CORONARY ARTERY DISEASE Nadeau, R.A. 2-PO-63 NEW QUANTITATIVE ELECTRICAL PARAMETERS IN THE DIAGNOSIS OF THE MYOCARDIAL INFARCTION Nagahara, D. 2-PO-39 ST-SHIFT AUGMENTATION CAN INDICATE ARRHYTHMOGENIC RIGHT VENTRICULAR SUBSTRATE IN BRUGADA SYNDROME Nagahashi, S. H.PYLORI - UNDERSTANDING PATHOGENESIS AND HOST DEFENSE Nagai, A. 7-PO-48 GENERATION AND CHARACTERIZATION OF HUMAN HYBRID NEURONS PRODUCED BETWEEN EMBRYONIC CNS NEURONS AND NEUROBLASTOMA CELLS Nagai, A. 7-PO-5 INFLUENCE OF CEREBRAL WHITE MATTER LESION ON AUTOREGULATION OF CEREBRAL BLOOD FLOW Nagai, H. 5-PO-7 A PROSPECTIVE STUDY OF LONG-TERM TREATMENT WITH CLARITHROMYCIN IN PATIENTS WITH DIFFUSE PANBRONCHIOLITIS: EFFICACY AND SAFETY Nagai, R.

71. Mioti: Medical Condition
Crohns Disease, • Cronkhite Canada Disease. • Croup, • Crouzon syndrome.• Crow Fukase, • Cryoglobulinemia. • Cryptococcosis, • Cryptosporidiosis.
http://www.mioti.com/cat/condition/results.asp?Alpha=C

72. Mioti: Medical Condition
Condition Crow Fukase. NORD POEMS syndrome. Information from the NationalOrganization for Rare Disorders. General Topics. Clinical Trials. Conferences.
http://www.mioti.com/cat/condition/condition.asp?Cat=CrowFukase

73. Immune Demyelinating PN
Clubbing of fingers. POEMS syndrome 21. Nosology Other names CrowFukasesyndrome; Takatsuki disease; PEP syndrome. General Features
http://www.neuro.wustl.edu/neuromuscular/antibody/pnimdem.html

Front
Search Index Links ... Patient Info
CHRONIC IMMUNE POLYNEUROPATHIES: DEMYELINATING
Comparative features: Demyelinating PN
Treatment strategies

CIDP
...
GALOP syndrome

GD1a antibody
Motor-Sensory neuropathy

Multifocal motor neuropathy

MAG antibody associated neuropathy

Osteosclerotic Myeloma
...
Antibody testing
Myelinated Axons: Segmental demyelination in Multifocal Motor Neuropathy (MMN) CHRONIC IMMUNE DEMYELINATING NEUROPATHIES COMPARATIVE FEATURES Neuropathy Clinical Features Electrophysiology Antibody M-Protein Treatment CIDP Weakness: Symmetric Onset: 1 to 80 yrs Chronic or Relapsing Motor + Sensory D Slow NCV Conduction Block Distal Latency: Long Slow F-waves Targets b -tubulin Heparan sulfate Class: IgM or IgG Frequency: 20% T-cell immunosuppression Prednisone Cyclosporine A Methotrexate HIG Plasma Exchange Multifocal CIDP Also see: CIDP variants Chronic Weakness: Asymmetric Onset: 15 to 75 yrs Motor + Sensory D Slow NCV Conduction Block Distal Latency: Long Slow F-waves T-cell immunosuppression Prednisone HIG MMN Motor only Asymmetric Onset: 25 to 60 yrs Slowly progressive Motor only Conduction Block Axonal Loss EMG: No paraspinous denervation Targets Co-GM1 or NP-9 Class: IgM Frequency: 80% HIG B-cell immunosuppression Plasma Exchange + Cyclophosphamide Rituxan Anti-MAG Distal; Symmetric

74. Foot Disorder
See Crow Fukase syndrome. Tamari Goodman syndrome (Congenital Heart Disease RadioUlnar Synostos Mental Retardation) Congenital heart disease radio ulnar
http://www.mykristi.org/history-on-fashion.htm

75. [Recent Advance In Neuroimmunology]
Serum vascular endothelial factor (VEGF) levels in crowfukase (POEMS) syndromewere about 15 to 30 times than those in the control subjects and other
http://www.aegis.com/pubs/aidsline/1999/dec/A99C0983.html
Important note: Information in this article was accurate in 1999. The state of the art may have changed since the publication date.
[Recent advance in neuroimmunology] Rinsho Shinkeigaku. 1998 Dec;38(12):993-6. Unique Identifier : AIDSLINE MED/99278953
Arimura K; Osame M; 3rd Department of Interna Medicine, Faculty of Medicine,; Kagoshima University. Abstract: Many important reports have been published during these several years in Japan Keywords: LECTURES REVIEW REVIEW, TUTORIAL JOURNAL ARTICLE Autoantibodies Capillary Permeability Central Nervous System/CYTOLOGY/VIROLOGY Endothelial Growth Factors English Abstract *Fasciculation/IMMUNOLOGY Human Lymphokines *Neuroimmunomodulation *Paraparesis, Tropical Spastic/IMMUNOLOGY Potassium Channels/IMMUNOLOGY *POEMS Syndrome/ETIOLOGY T-Lymphocytes, Cytotoxic/IMMUNOLOGY
National Library of Medicine
. Reproduced under license with the National Library of Medicine, Bethesda, MD. Boehringer Ingelheim iMetrikus, Inc. , the National Library of Medicine , and donations from users like you. Always watch for outdated information. This article first appeared in 1999. This material is designed to support, not replace, the relationship that exists between you and your doctor.

76. AnsMe Directory - Health > Conditions And Diseases > C
Cri du Chat syndrome. CriglerNajjar syndrome. Crohn's Disease. Crow-Fukasesyndrome. Cryptosporidiosis. Cubital Tunnel syndrome. Cushing's syndrome.
http://dir.ansme.com/health/43345.html
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77. Bibliographies Related To HAM From Our Department
15. Maruyama I, Shinmyouzu K, Ichinose A, Ijichi S, Kashio N, Osame M, Igata AImmunohematologic aspect of Crow Fukase syndrome Neuroimmunological diseases.
http://www.kufm.kagoshima-u.ac.jp/~intmed3/hambibli.htm
Bibliographies related to HAM from our department
1. Osame M, Usuku K, Izumo S, Ijichi N, Amitani H, Igata A, Matsumoto M, Tara M: HTLV-I associated myelopathy, A new clinical entity. Lancet i:1031-1032, 1986 2. Osame M, Izumo S, Igata A, Matsumoto M, Matsumoto T, Sonoda S, Tara M, Sibata Y: Blood transfusion and HTLV-I associated myelopathy. Lancet ii:104-105, 1986 4. Osame M, Matsumoto M, Ijichi, S, Rosales R, Niina K, Kashio N, Kawatsu M, Nagata K, Usuku K, Izumo S, Igata A: In vitro removal of anti-HTLV-I antibodies with a new immunoadsorbent from the sera of HTLV-I associated myelopathy patients. Acta Med Univ Kagoshima 28:105-109, 1986 5. Usuku K, Osame M, Matsumoto M, Matsumoto T, Sano Y, Matsubara H, Niina K, Tara M, Rosales R, Izumo S, Igata A: Intra-blood brain barrier syntheses of IgG in patients with HTLV-I associated myelopathy. Acta Med Univ Kagoshima 28:101-104, 1986 6. Osame M, Matsumoto M, Usuku K, Izumo S, Ijichi, N, Amitani H, Tara M, Igata A: Chronic progressive myelopathy associated with elevated antibodies to human T-lymphotropic virus type I and adult T-cell leukemialike cells. Annals of Neurology 21:117-122, 1987 7. Osame M, Igata A, Usuku K, Rosales L, Matsumoto M: Mother-to-child transmission in HTLV-I associated myelopathy. Lancet i:106, 1987

78. AMEDEO: The Medical Literature Guide
VEGF is causative for pulmonary hypertension in a patient with Crow Fukase(POEMS) syndrome. Intern Med 2000; 39 1101-4. Abstract Related articles.
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Capsaicin pre- and post-treatment on rat monocrotaline pneumotoxicity.
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79. MDinteractive--Neurology
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80. Directory :: Look.com
Look.com The Search Engine of Search Engines, Enterprise Search Look Search,
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