81. Guillain Barre Syndrome Foundation Discussion Forums Welcome to the Guillain Barre syndrome Foundation Discussion Forums. 0418-2004 0222 AM by Brandy2, Go to last post. miller fisher Variants, 460, 87, http://www.guillain-barre.com/forums/index.php

Jump To Chatroom View Chat Schedule Guillain Barre Syndrome Foundation Discussion Forums Registered Members: threads in total posts in total Welcome to our newest member, Robynrain You last visited: 06-03-2004 12:37 AM. The time now is 12:37 AM. Today's Birthdays: pastordd View Today's Active Threads Welcome to the Guillain Barre Syndrome Foundation Discussion Forums. If this is your first visit, be sure to check out the FAQ by clicking the link above. You may have to register before you can post: click the register link above to proceed. To start viewing messages, select the forum that you want to visit from the selection below. Forum Posts Threads Last Post Main News and Announcements Current news and information about the forums, the Foundation and the GBS community. 01:25 AM by Eileen GBS - Adult 12:14 AM by gi gi GBS - Child 09:06 PM by Jerimy Teen 12:11 AM by zeesuezee CIP/CIDP 11:53 PM by Jerimy CIP - Child 02:09 AM by Vaccine Reactions 02:22 AM by Miller Fisher Variants 06:12 AM by Norm Expectant Mothers Questions and issues related to pregnancy 03:44 AM by AussieJo Family, Friends and Caregivers

82. Miller-Fisher Syndrome Associated With Campylobacter Jejuni Bearing Lipopolysacc August; 64 (8) 2945 2949 millerfisher syndrome associated with Campylobacter jejuni bearing lipopolysaccharide molecules that mimic human ganglioside GD3. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=174172&rendertype=abst

83. Abstract millerfisher syndrome is a rare variant of Guillain-Barre syndrome. miller-fisher syndrome is a rare variant of Guillain-Barre syndrome. http://www.ia.pw.edu.pl/~wujek/neurol/str/s2-02-e321.html

Miller-Fisher syndrome is a rare variant of Guillain-Barre syndrome. The triad of ophtalmoplegia, ataxia and areflexia characterizes it. We report a case of 46-year old woman with Miller-Fisher syndrome and hepatitis C. First symptom occurred after week from upper respiratory track infection of viral type. First patient noted diplopia, weakness and vertigo, then appeared ophtalmoplegia, ataxia. We didn't noted prolonged latencies and slowing of conduction velocity and there were no abnormalities in CSF examination. During first days of hospitalisation symptoms progressed. In blood examination Enterovirus IgG antibody was found. There was possitive anti-HCV blood test and with coexisting increase of hepatic enzymes we diagnosed hepatitis type C. We included the treatment with gammaglobulin 21g/day during 5 days. We noted slow recovery with ataxia and areflexia firstly and then ophtalmoplegia. Miller-Fisher syndrome is a rare variant of Guillain-Barre syndrome. The triad of ophtalmoplegia, ataxia and areflexia characterizes it. We report a case of 46-year old woman with Miller-Fisher syndrome and hepatitis C. First symptom occurred after week from upper respiratory track infection of viral type. First patient noted diplopia, weakness and vertigo, then appeared ophtalmoplegia, ataxia. We didn't noted prolonged latencies and slowing of conduction velocity and there were no abnormalities in CSF examination. During first days of hospitalisation symptoms progressed. In blood examination Enterovirus IgG antibody was found. There was possitive anti-HCV blood test and with coexisting increase of hepatic enzymes we diagnosed hepatitis type C. We included the treatment with gammaglobulin 21g/day during 5 days. We noted slow recovery with ataxia and areflexia firstly and then ophtalmoplegia.

84. Guillain-Barre Syndrome millerfisher syndrome The most common subtype is miller-fisher syndrome (MFS), or acute disseminated encephalomyeloradiculopathy, which is characterized by http://www.davidson.edu/academic/psychology/ramirezsite/neuroscience/psy324/jeca

This web page was produced as an assignment for an undergraduate course at Davidson College. Guillain-Barre Syndrome Table of Contents History Of Guillain-Barre Syndrome Epidemiology Causes Pathogenesis ... Subtypes of Guillain-Barre Syndrome History In 1859, Jean B.O. Landry, a French physician, described a disorder in which the nerves of the legs, arms, neck, and breathing muscles were paralyzed. Georges Guillain, Jean Alexander Barre, and Andre Strohl discovered the characteristic abnormality of increased protein but normal cell count in the cerebrospinal fluid in 1916. Several names have been given for the syndrome including acute idiopathic polyneuritis, acute idiopathic polyradiculoneuritis, Landry’s ascending paralysis, and Guillain Barre syndrome. Back to the top Epidemiology Back to the top Causes The causes of Guillain Barre syndrome are unknown. Many researchers theorize that the autoimmune reaction in which macrophages and T-cells attack myelin in the peripheral and cranial nerves is associated with a bacteria or virus, as many cases occur a few days to a few weeks after an infection including the common cold, sore throat, and stomach and intestinal viruses with vomiting and diarrhea. The virus might induce the demyelination via a possible mimicry between the effector virus and a human ganglioside. Salloway and colleagues (1996) discovered that the lipopolysaccharide structure of some strains of Campylobacter jejuni , specifically, the terminal structures of the core oligosaccharide, resemble the human gangliosides GM1 and GD1a. A possible mimicry also exists between the influenza A NS2 protein and a sequence region of the human P2 (myelin) protein thought to be neuritogenic in animals and mitogenic for lymphocytes from patients with GBS. This finding could provide a possible link between the large number of cases of GBS associated with the 1976 USA swine flu vaccination program (Weise and Carnegie, 1988).

85. LE SYNDROME DE GUILLAIN-BARRE : Le Syndrome De Fisher syndrome de fisher ou de miller fisher. http://users.skynet.be/gbs/Apercu/Fisher.html

86. GQ1b-Ak The determination of antiGQ1b antibodies is used for determination of the miller-fisher syndrome. Method ELISA. Material needed 5 ml serum. http://www.akh-wien.ac.at/kin/Englische Version/diagnostik/Neurochemie/eGQ1b.htm

Antibodies against the GQ1b ganglioside (Anti-GQ1b Antibodies) Mailing: Only from Monday till Wednesday by EMS Contact person for medical concerns phone: (+43) 1 40400 - 5517, 5502 Contact person for technical concerns Silvia Zimmermann phone: (+43) 1 40400 - 5514 The determination of anti-GQ1b antibodies is used for determination of the Miller-Fisher syndrome. Method: ELISA Material needed: 5 ml serum Time of acceptance: Monday till Friday 8h00 - 16h00 Notice in advance: not necessary within the time listed above Back case registration sheet

87. Index gbs.org. A collection of resources and information about GuillainBarré, CIDP, miller fisher and other related syndromes. Welcome to gbs.org! http://www.gbs.org/

gbs.org A collection of resources and information about Welcome to gbs.org! ghee yan-bah ray GBS Chronic Inflammatory Demyelinating Polyradiculoneuropathy C.I.P.D. Miller Fisher The GBS.etal email list for the discussion of GBS, CIDP and other related neurological related disorders. Last Updated: March 27, 2004 Page maintained by Jeff Steinhilber Thanks to Automated Data Systems for the generous donation of resources to gbs.org

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