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         Acute Idiopathic Polyneuritis:     more detail
  1. GBS, Guillain-Barre syndrome (acute idiopathic polyneuritis): An overview for the layperson by Joel S Steinberg, 1983
  2. GBS, Guillain-Barré syndrome: Acute idiopathic polyneuritis and chronic inflammatory polyneuropathy : an overview for the layperson by Joel S Steinberg, 1995

81. Upchaar - Health, Medical,India Doctors, Medical Education, All About Jaipur Hea
Acute HIV infection. acute idiopathic polyneuritis. Acute inflammatory polyneuropathy.Acute intermittent porphyria. Acute interstitial (allergic) nephritis
http://www.upchaar.com/disease a.htm
"You can change any thing in this country" Emergency Zone : Blood Bank Eye Bank Ambulance 24 Hours Clinic ... Disease Info : A A B C D ... Z A-fib Aarskog syndrome Aase syndrome Aase-Smith syndrome AAT deficiency Abacterial cystitis Abdominal aortic aneurysm Abdominal pregnancy Abducens palsy Abetalipoproteinemia Ablatio placentae Abnormal breast mass Abnormal heart rhythms Abnormality of the urea cycle - hereditary ABO incompatibility Abortion - complete Abortion - elective or therapeutic Abortion - incomplete Abortion - inevitable Abortion - infected Abortion - spontaneous Abortion - threatened ABPA Abruptio placentae Abscess Abscess - amebic liver Abscess - anorectal Abscess - areolar gland Abscess - Bartholin's Abscess - brain Abscess - epidural Abscess - intra-abdominal Abscess - peritonsillar Abscess - skin Abscess - spinal cord Abscess - tooth Absence seizure Absent menses Absent periods Acanthamoeba keratitis Acanthocytosis Acanthosis nigricans Accelerated hypertension Accelerated silicosis Accelerating angina Accidental hemorrhage Achalasia Achilles tendinitis Achondrogenesis Achondroplasia Acidosis Acidosis - metabolic Acidosis - respiratory Acne Acne rosacea Acne vulgaris Acoustic neuroma Acoustic trauma Acquired aplastic anemia Acquired bronchiectasis Acquired disorders of platelet function Acquired hyperlipoproteinemia Acquired nephrogenic diabetes insipidus Acquired platelet function defect Acquired qualitative platelet disorders Acrocephalosyndactyly Acrochordons Acrodermatitis Acrodermatitis - infantile lichenoid Acrodermatitis - papular infantile

82. The Use Of Steroids In The Treatment Of Idiopathic Polyneuritis -- Swick And McQ
The use of steroids in the treatment of idiopathic polyneuritis in thetreatment of acute idiopathic polyneuritis (GuillainBarre syndrome) continues to
http://www.neurology.org/cgi/content/abstract/26/3/205
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The use of steroids in the treatment of idiopathic polyneuritis
HM Swick and MP McQuillen
The efficacy of steroids in the treatment of acute idiopathic polyneuritis (Guillain-Barre syndrome) continues to be uncertain. Since 1965, 38 patients with idiopathic polyneuritis have been at the University of Kentucky Medical Center, and 16 of them were entered in a prospective double blind study designed to assess the effectiveness of steroid therapy. Seriously ill patients were excluded from the study and most of them received steroids. In both the double-blind group and the entire group of

83. Neurology -- Table Of Contents (August 1 1976, 26, [8])
Neurology 1976 26 800801. S Stolzberg Letter acute idiopathic polyneuritisno residua after steroid treatment? Neurology 1976 26 801-802.
http://www.neurology.org/content/vol26/issue8/
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Receive this page by email each issue: [Sign up for eTOCs] Contents: August 1 1976, Volume 26, Issue 8 [Index by Author] Other Issues: ARTICLES Find articles in this issue containing these words:
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Autosomal dominant striatonigral degeneration. A clinical, pathologic, and biochemical study of a new genetic disorder
Neurology 1976 26: 703-714. [Abstract]
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Phenytoin kinetics in children
Neurology 1976 26: 715-720. [Abstract]
CP Panayiotopoulos and S Scarpalezos
Muscular dystrophies and motoneuron diseases. A comparative electrophysiologic study
Neurology 1976 26: 721-725. [Abstract]
RP Moser, JA Robinson, and ER Prostko

84. Drug Information: Mercaptopurine (Print Version)
rheumatoid arthritis, acute idiopathic polyneuritis, acute idiopathic nephroticsyndrome, psoriatic arthritis, erythroid aplasia, or myelofibrosis;
http://www.nlm.nih.gov/medlineplus/print/druginfo/medmaster/a682653.html
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Drug Information: Mercaptopurine
URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a682653.html (mer kap toe pyoor' een)
About your treatment
Your doctor has ordered the drug mercaptopurine to help treat your illness. The drug is taken by mouth in tablet form. This medication is used to treat:
  • leukemia
This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information. Mercaptopurine belongs to a group of drugs known as antimetabolites. It resembles a normal cell nutrient needed by cancer cells to grow. The cancer cells take up mercaptopurine which then interferes with their growth.
Other uses for this medicine
Mercaptopurine is also used to treat many types of autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis, acute idiopathic polyneuritis, acute idiopathic nephrotic syndrome, psoriatic arthritis, erythroid aplasia, or myelofibrosis; idiopathic hemolytic anemia; macroglobulinemia; idiopathic thrombocytopenia purpura; idiopathic pulmonary hemosiderosis; multiple sclerosis; myasthenia gravis; uveitis; and ulcerative colitis. Talk to your doctor about the possible risks of using this drug for your condition.
Precautions
Before taking mercaptopurine

85. MedlinePlus Medical Encyclopedia: Topics Beginning With A-Ag
acute idiopathic polyneuritis see GuillainBarre syndrome; Acute inflammatorypolyneuropathy see Guillain-Barre syndrome; Acute intermittent porphyria see
http://www.nlm.nih.gov/medlineplus/ency/encyclopedia_A-Ag.htm
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86. Medical Terminology - Medword Transcription
Acute HIV infection acute idiopathic polyneuritis Acute illness Acute leukemiaAcute lymphoblastic leukemia Acute lymphocytic leukemia
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Medword Reference: Medical Terms A Find on this page:
These medical terms are in an alphabetized list including some medical phrases. This not a complete listing of course-just a sampling. Some examples of medical abbreviations, terms, diseases, syndromes, etc., are also sprinkled throughout the list. Medword provides this medical terms list in part so that those who are thinking of becoming a medical transcriptionist may see firsthand some of the terminology and phraseology used by MTs in their daily work. For those already performing medical transcription, the list is a good reference source. We have also complimented the medical terminology list with a text version for copying and adding to your medical spell-checking feature in your word processor if you wish. A B C D ... Z a.c. (on prescription)
AAA (abdominal aortic aneurysm)
AAAS (Amer. Assn. for the Advancement of Science)
AAD (American Association of Dermatology)
AAFP (American Academy of Family Physicians)
AAMC
AAO (ambiguity)
AAOS (American Academy of Orthopaedic Surgeons)
AAP (American Academy of Pediatrics)
Aarskog-Scott syndrome Aase-Smith syndrome II Ab ovo Ab- (prefix) Abdomen Abdomen, acute

87. Disease - Guillain-Barre Syndrome - Detroit, Michigan
LandryGuillain-Barre syndrome; acute idiopathic polyneuritis; Infectiouspolyneuritis; Acute inflammatory polyneuropathy. Causes And Risk
http://www.henryfordhealth.org/15207.cfm
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Disease - Guillain-Barre syndrome
Superficial anterior muscles Definition: Guillain-Barre syndrome is a disorder caused by nerve inflammation involving progressive muscle weakness or paralysis , which often follows an infectious illness. Alternative Names: Landry-Guillain-Barre syndrome; Acute idiopathic polyneuritis; Infectious polyneuritis; Acute inflammatory polyneuropathy Causes And Risk: Guillain-Barre syndrome is an acute type of nerve inflammation. The inflammation damages portions of the nerve cell, resulting in muscle weakness or paralysis and sensory loss. The damage usually includes loss of the myelin sheath of the nerve (demyelination ), which slows the conduction of impulses through the nerve. The damage can also cause denervation (kill the axon part of the nerve cell), which stops nerve function entirely. Without the axon, messages cannot be transferred from one nerve cell to another.
The exact cause of this disorder is unknown. It may occur at any age but is most common in people of both sexes between the ages 30 and 50. It often follows a minor infection, usually a

88. Assessment And Management Of Cancer Risks From Radiological And
GuillianBarré Syndrome, A type of acute idiopathic polyneuritis. reactivearthritides, Acute joint inflamation which is triggered by an infection
http://www.hc-sc.gc.ca/hecs-sesc/ccrpb/publication/98ehd216/chapter8.htm

89. Graft Versus Host Disease
GuillainBarre Landry-Guillain-Barre syndrome; acute idiopathic polyneuritis;infectious polyneuritis; acute inflammatory polyneuropathy A disorder
http://www.doctorpage.com/findit/Diseases_and_Conditions/Guillain_Barre_Syndrome

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Diseases and Conditions Guillain Barre Syndrome Displaying listings 1-3
  • Guillain-Barre Landry-Guillain-Barre syndrome; acute idiopathic polyneuritis; infectious polyneuritis; acute inflammatory polyneuropathy A disorder involving progressive or , usually following an infectious illness. ... http://www.healthanswers.com/database/ami/converted/000684.html Guillain-Barre Syndrome Fact Sheet What is Guillain-Barre syndrome? Guillain-Barre syndrome is a disorder in which the body's immune system attacks part of the nervous system. The first symptoms of this disorder include varying .. http://www.mediconsult.com/pregnancy/shareware/barre/ Guillain-Barre syndrome (MAYO CLINIC) - Guillain-Barre syndrome can occur without warning and result in serious paralysis. Learn about the signs and symptoms and why quick diagnosis and treatment are important. http://www.mayohealth.org/mayo/9708/htm/guillain.htm
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90. CNS Case 7
Compare and contrast the clinical, pathologic, and pathophysiologic features ofacute idiopathic polyneuritis (GuillainBarré syndrome) with diabetic distal
http://pathcuric1.swmed.edu/PathDemo/cns7/learnobj.htm
Learning Objectives
1. Describe the functional and supportive elements of the peripheral nervous system. 2. List the five etiologic categories into which peripheral neuropathies can be classified. 3. Identify the pathologic features of both axonal degeneration and segmental demyelination. 5. Explain the similarities and the differences between the pathologies of schwannomas and neurofibromas. 6. Describe the major clinical features of both neurofibromatosis types (1 and 2). Associate the known chromosomal abnormality with each type.
Resources
1. (Robbins 5th Ed., p. 1273-1285, 1351-1354) or (Robbins 6th Ed., p. 1269-1280, 1352-1355) 2. Images 1 and 2 are related to this case; 3-8 are for the study of other learning objectives.
Scenario
Normal Reference Range Table
This 59-year-old diabetic man complained to his doctor that he was " losing feeling in his feet . He said that his feet often felt like they had "pins and needles " in them. "Oh, and another strange thing, is that my feet seem worse at night ." He said that these unusual sensations had begun a few years before , but that they had not bothered him very much until now.

91. NEJM -- Sign In
Fisher M. An unusual variant of acute idiopathic polyneuritis (syndrome ofophthalmoplegia, ataxia and areflexia). N Engl J Med 1956;2555765. Ropper AH.
http://content.nejm.org/cgi/content/full/341/26/1996

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92. JW Neurology -- Sign In
Patients with acute idiopathic polyneuritis, or GuillainBarre syndrome (GBS),typically have significant weakness in all limbs at the time of maximal motor
http://neurology.jwatch.org/cgi/content/full/2000/906/3

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93. GUILLAIN-BARRE SYNDROME
, GuillainBarre syndrome is an inflammatory disorder of the peripheral......Infectious polyneuropathy, acute idiopathic polyneuritis). Common Name.
http://www.rxmed.com/b.main/b1.illness/b1.1.illnesses/GUILLAIN-BARRE SYNDROME.ht
General Illness Information
Medical Term:

GUILLAIN-BARRE SYNDROME ( Infectious polyneuropathy, Acute Idiopathic polyneuritis). Common Name: Description: Guillain-Barre syndrome is an inflammatory disorder of the peripheral nervous system that produces rapidly worsening muscle weakness, sometimes leading to paralysis. Causes generalized and symmetrical weakness involving muscles at the extremities and on the trunk, as well as sensory symptoms. Weakness appears either rapidly or over 1-2 weeks, and can produce failure of breathing muscles over several days. It is a rare illness. Incidence 1 per million per month. Most common between age of 30-50. Both sexes equally affected. Causes: Exact cause unknown, but all available evidence point to an auto-immune disorder. The body's immune system attacks the myelin sheath (layers of insulation around the nerve fibers). Myelin sheath permits electrical impulses to be conducted along the nerve fibers with speed and accuracy. When myelin is damaged, nerves do not conduct impulses properly. In about 80% of the people, symptoms begin about 5 days to 3 weeks after a mild infection, surgery or immunization.

94. Multifocal Motor Neuropathy
Busby M, Donaghy M. Predominant arm weakness in acute idiopathic polyneuritisa distinct regional variant. J Neurol 2000; 247 343345.
http://www.neuro.jhmi.edu/MMN/references.html
  • Abbruzzese M. Multifocal motor neuropathy with conduction block after Campylobacter jejuni enteritis. Neurology 1997 Feb 48: 544-MID.
  • Adams RD, Asbury AK, Michelsen JJ. Multifocal pseudohypertrophic neuropathy. Trans Am Neurol Assoc 1965; 90: 30-32.
  • Al Lozi M, Pestronk A. Organ-specific autoantibodies with muscle weakness. Curr Opin Rheumatol 1999; 11: 483-488.
  • Alaedini A, Latov N. Detection of anti-GM1 ganglioside antibodies in patients with neuropathy by a novel latex agglutination assay. J Immunoassay 2000; 21: 377-386.
  • Alaedini A, Latov N. A surface plasmon resonance biosensor assay for measurement of anti- GM(1) antibodies in neuropathy. Neurology 2001; 56: 855-860.
  • Alaedini A, Wirguin I, Latov N. Ganglioside agglutination immunoassay for rapid detection of autoantibodies in immune-mediated neuropathy. J Clin Lab Anal 2001; 15: 96-99.
  • Arasaki K, Kusunoki S, Kudo N, Kanazawa I. Acute conduction block in vitro following exposure to antiganglioside sera. Muscle Nerve 1993; 16: 587-593.
  • Ariga T, Miyatake T, Yu RK. Recent studies on the roles of antiglycosphingolipids in the pathogenesis of neurological disorders. J Neurosci Res 2001; 65: 363-370.
  • 95. Polyneuritis, Acute Idiopathic Definition - Medical Dictionary Definitions Of Po
    Online Medical Dictionary and glossary with medical definitions.
    http://www.medterms.com/script/main/art.asp?articlekey=8012

    96. Polyneuritis, Acute Idiopathic - Talk Medical
    Humanfriendly medical definition of polyneuritis, acute idiopathic.
    http://www.talkmedical.com/medical-dictionary/11363/Polyneuritis-Acute-Idiopathi

    97. Journal Of Intensive Care Medicine -- Sign In Page
    The inflammatory lesion in idiopathic polyneuritis its role in pathogenesis . Circulating demyelinating factors in acute idiopathic polyneuropatby.
    http://jic.sagepub.com/cgi/content/refs/20/4/212

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    Therapeutic Apheresis in Neurology Critical Care
    Natarajan and Weinstein J Intensive Care Med.
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    98. Glossary.13. Poliomyelitis, Pott's Fracture And Proprioceptive
    p., acute idiopathic. Landry s paralysis. p., Jamaica ginger. polyneuritis, esp.of the nerves of the extremities following ingestion of Jamaica ginger
    http://www.kneelsit.com/glossary/glossary13.html
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      the kneelsit GLOSSARY Pg.13
      medical and general terms relating to posture, sitting, musculoskeletal and back problems
      ABBREVIATIONS:- Gr.= Greek; L.= Latin; Fr.= French; Ger = German; NA = Nomina Anatomica
      P.(cont.)
      pachymeningitis to Parkinson passive to point - - polio to pyramid polio. poliomyelitis, acute anterior.
      polio- [Gr. polios, gray]. Combining form indicating relationship to the gray matter of the nervous system.
      polioclastic (pol"e-o-klas'tik) [" + klastos, breaking]. Destructive to gray matter of the nervous system.
      polioencephalitis (pol"e-o-en-sef'a-li'tis) [" + enkephalos, brain, + itis, inflammation]. Condition characterized by inflammatory lesions of the gray matter of the brain.
      p., anterior superior. A disease involving necrotic changes in gray matter about the 3rd ventricle, anterior portion of the 4th ventricle, and aqueduct of Sylvius. Characterized by ocular abnormalities, mental disturbances, and ataxia. Of nutritional origin. probably thiamine (vitamin B,) deficiency. SYN: Wernicke's syndrome.
      p. hemorrhagica.

    99. GBS Domande E Risposte
    Translate this page acute infective polyneuritis (Bradford e colleghi 1918) Landry-Guillain-Barrésyndrome CIDP (chronic GBS, oppure chronic idiopathic polyneuritis)
    http://www.dsa.unipr.it/giavelli/GBS/faq_gbs.html
    omande e
    isposte GBS FAQ
    Ovvero: alcune delle domande che aveste desiderato rivolgere ai vostri medici, ma avevate paura di non capire o di restare spaventati dalle loro risposte Avete da proporre arricchimenti, integrazioni, o suggerimenti per nuove domande e risposte? Siete i benvenuti, scrivetemi Cosa significano i termini GBS e CIDP ?
    GBS CIDP
    Chronic Inflammatory Demyelinating Polyradiculoneuropathy (poliradicolonevrite infiammatoria demielinizzante cronica).
    Fu nel 1856 che il medico francese Jean Landry descrisse per primo una malattia, in seguito denominata "paralisi ascendente di Landry", ma fu solo negli anni 1914-1918 che tre giovani medici francesi, specializzandi in neurologia (Georges Charles Guillain, Jean-Alexandre Barré e André Strohl), ebbero modo di esaminare due soldati paralizzati e di condurre accertamenti sulle caratteristiche del liquido presente attorno al cervello e all'interno della spina dorsale, cercando di trovare cause e rimedi per quella strana, inusuale e apparentemente inspiegabile patologia [www.gbs.org.uk/whowere.html

    100. GUILLIAN-BARRƒ SYNDROME
    Other names which are used include idiopathic polyneuritis, acute inflammatorypolyneuritis, Landry’s (ascending) paralysis, LandryGuillain-Barré Syndrome
    http://www.podiatry.curtin.edu.au/encyclopedia/guillain/guillain_barre_syndrome.
    Student: Rachele Ferrari Subject: Podiatric Medicine 357
    Lecturer: Dr Paul Tinley
    Due Date: 22 nd May 2000
    Contents
    Introduction
    Landryâs Paralysis
    Guillain, Barre and Stroh
    Treatment Advances
    Etiology
    Motor Abnormalities
    Sensory Abnormalities
    Cerebrospinal Fluid Abnormalities Autonomic Abnormalities Pathology Neurophysiological Features References Back to Encyclopedia Index Introduction
    • Relatively symmetrical muscle weakness Distal paraesthesia ascending proximally and, Widespread loss of reflexes Spontaneous gradual recovery over several weeks to months Elevated cerebrospinal fluid protein concentration, with few cells
    (Cull and Will, 1995, p. 1106; Ropper, Wijdicks and Truax, 1991, p. xix). Munsat and Barnes, in Ropper, Wijdicks and Truax, 1991, stated "·the Guillain-Barré Syndrome is easy to diagnose but impossible to define." Most recently, Asbury and Cornblath, cited in Hughes, 1995, have redefined the diagnostic boundaries for Guillain-Barré Syndrome, but again note the disease defies strict definition. Back to top Table 1.

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