81. Isaacs Syndrom - Små Och Mindre Kända Handikappgrupper isaacs H. A syndrome of continuous musclefibre activity. isaacs syndromesuccessfully treated with immunoadsorption plasmapheresis. http://www.sos.se/smkh/2004-29-176/2004-29-176.HTM

Socialstyrelsen 106 30 Stockholm Socialstyrelsen klassificerar sin utgivning i olika dokumenttyper Isaacs syndrom Sjukdom/skada/diagnos Orsak till sjukdomen/skadan Symtom Diagnostik ... Dokumentinformation Dokumentdatum: 2004-03-25 HTML-version: 1.0 Socialstyrelsen Detta är ett utdrag ur Socialstyrelsens kunskapsdatabas om små och mindre kända handikappgrupper. Med små och mindre kända handikappgrupper avses ovanliga sjukdomar/skador som leder till omfattande funktionshinder och som finns hos högst 100 personer per miljon invånare. Syftet med databasen är att ge aktuell information om små och mindre kända handikappgrupper och om det stöd och den service som dessa grupper behöver. För ytterligare information om aktuell diagnos hänvisas till informationsmaterial, litteratur och databaser som anges under resp diagnos. Sjukdom/skada/diagnos Orsak till sjukdomen/skadan Symtom Diagnostik Praktiska tips Resurspersoner christopher.lindberg@vgregion.se Kurser, erfarenhetsutbyte, rekreation nhr@nhr.se , Internetadress www.nhr.se info@riks.rbu.se

82. CNI Review Medical Journal - Online Library - Colorado Neurological Institute Neuromyotonia (isaacs syndrome) appears to be due to antibodyinduced blockade Immunological associations of acquired neuromyotonia (isaacs syndrome). http://www.thecni.org/reviews/13-2-p02-england.htm

CNI Home CNI Home Contents Peripheral Neuropathies Fall 2002 Volume 13, Number 2 This Issue Contents Next Article Channelopathies John D. England, MD, FAAN Introduction. Voltage-gated ion channels are responsible for the generation and propagation of action potentials along electrically excitable membranes. Ion channels are fundamentally important for the conduction of impulses along the membranes of neurons, skeletal muscle, and cardiac muscle. All ion channels are transmembrane proteins that form selective ion-conducting pores in the cell membrane. Voltage-gated ion channels, specifically sodium, potassium, and calcium channels, are sensitive to changes in transmembrane voltage. Thus, voltage-gated ion channels activate (ie, open) or inactivate (ie, close) in response to changes in transmembrane voltage. Targeted disorders of ion channels are increasingly recognized as causes of specific neurological and muscular diseases. What follows is a review of some of the most well characterized channelopathies with specific attention to those disorders affecting nerves and muscles. Toxin-Mediated Channelopathies.

83. Entrez PubMed isaacs syndrome (autoimmune neuromyotonia) in a patient with systemic lupuserythematosus. Taylor PW. Cape Girardeau Physician Associates, Cape Girardeau, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1

84. Teeter's Page If you or someone you know has Apert syndrome like me, or if you have any questions, August 29, 2000, Maria and Forrest isaacs sevilla346@msn.com http://www.apert.org/

Hi, hola, kia ora, bonjour, hallo, ciao, aloha! I'm Elizabeth Sears, but all my friends call me Teeter! My mom and dad made this page for me. If you or someone you know has Apert Syndrome like me, or if you have any questions, we would love to hear from you! This Internet safe haven is dedicated to the strength and determination of all of the people with craniofacial differences and their families. This website was created January 1, 1996 as a single page on America Online. We grew quickly, and moved our own domain on August 10, 1997. This page was last updated August 17, 2005. You are visitor number and we are glad you are here! You can make a difference! If you are able to help financially, please visit our charity website at www.apert-international.org

85. Immunological Associations Of Acquired Neuromyotonia (Isaacs' Syndrome). Report Immunological associations of acquired neuromyotonia (isaacs syndrome). Report offive cases and literature review. J NewsomDavis and KR Mills http://brain.oxfordjournals.org/cgi/content/abstract/116/2/453

JOURNAL HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Cited by other online articles Search for citing articles in: ISI Web of Science (136) Request Permissions PubMed PubMed Citation Articles by Newsom-Davis, J. Articles by Mills, K. R. ARTICLES Immunological associations of acquired neuromyotonia (Isaacs' syndrome). Report of five cases and literature review J Newsom-Davis and KR Mills Department of Clinical Neurology, University of Oxford, Radcliffe Infirmary, UK. Neuromyotonia is a syndrome of spontaneously occurring muscle activity of peripheral nerve origin, which can be triggered by voluntary or induced muscle contraction. It is one among several causes of visible myokymia. Although neuromyotonia may sometimes accompany hereditary neuropathies

86. Potassium Current Suppression In Patients With Peripheral Nerve Hyperexcitabilit Acquired neuromyotonia (isaacs syndrome) is characterized by the Antibodies topotassium channels of PC12 in serum of isaacs syndrome western blot http://brain.oxfordjournals.org/cgi/content/full/122/11/2057

JOURNAL HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract FREE Full Text (PDF) Alert me when this article is cited ... Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed ... Cited by other online articles Search for citing articles in: ISI Web of Science (18) Request Permissions PubMed PubMed Citation Articles by Nagado, T. Articles by Osame, M. Brain, Vol. 122, No. 11, 2057-2066, November 1999 Oxford University Press Invited review Potassium current suppression in patients with peripheral nerve hyperexcitability Tatsui Nagado Kimiyoshi Arimura Yoshito Sonoda Asutsugu Kurono Yasushi Horikiri Asako Kameyama Masaki Kameyama Olaf Pongs and Mitsuhiro Osame Third Department of Internal Medicine, Department of Neuropsychiatry and Second Department of Physiology, Kagoshima University School of Medicine, Kagoshima, Japan and Correspondence to: Dr Tatsui Nagado, Third Department of Internal Medicine, Kagoshima University School of Medicine, 8-35-1 Sakuragaoka, Kagoshima 890-8520, Japan

87. Przypadek Zespo³u Isaacs'a A case of isaacs syndrome isaacs syndrome (neuromiotonia) is clinicalycharacterized by muscle stiffness, cramps, difficulty in muscle relaxation after http://www.neurologiapolska.pl/streszczenia/aaa8.htm

Przypadek zespo³u Isaacs'a Jolanta Balcewicz, Karina Kierkus Oddzia³ Neurologii WSS im. M. Kopernika w £odzi Abstract A case of Isaacs' syndrome We start treatment with phenytoin receiving improvement-cramps retired. Streszczenie Zespó³ Isaacs'a (neuromiotonia) charakteryzuje siê klinicznie sztywno¶ci± i skurczami miê¶ni, trudno¶ci± w ich rozlu¼nianiu po ruchu dowolnym oraz wzmo¿on± potliwo¶ci±. Mimowolne skurcze miê¶ni nie ustêpuj± podczas snu. Zespó³ mo¿e rozwijaæ siê spontanicznie, mieæ charakter dziedziczny lub towarzyszyæ polineuropatii. 73-letni chory przyjêty zosta³ do Oddzia³u Neurologii WSS im. M. Kopernika w £odzi z powodu bolesnych skurczów ³ydek wystêpuj±cych przez ca³± dobê, pieczenia i drêtwienia podudzi, os³abienia si³y miê¶niowej kkd podczas chodzenia. Badaniem przedmiotowym stwierdzano liczne fascykulacje w kkd i pojedyncze w kkg, zaniki mm.naramiennych, sztywno¶æ i bolesne skurcze miê¶ni kkd, brak odr. skokowych, zaburzenia czucia powierzchniowego typu ,,skarpetek'', nadmiern± potliwo¶æ. Wykonano badanie EMG,które wykaza³o w spoczynku sta³± czynno¶æ bioelektryczn± miê¶ni pod postaci± wy³adowañ PJR, fascykulacji i miokimii, co potwierdzi³o rozpoznanie zespo³u Isaacs'a. Rozpoczêto leczenie fenytoin± uzyskuj±c poprawê skurcze ³ydek ust±pi³y.

88. Journal Of Clinical Neurophysiology - UserLogin ADULT ONSET isaacs syndrome WITH CHRONIC, SEVERE DISABILITY, AND EVIDENCE isaacs syndrome characterized by generalized muscle twitching, stiffness, http://www.clinicalneurophys.com/pt/re/jclnneurophys/fulltext.00004691-200309000

LWWOnline LOGIN eALERTS REGISTER ... Archive You are attempting to access protected content. To access this content please login using an established account or create/activate an account. If you have already created/ activated an online account, please login below: User Name: Password: Note: passwords are CASE SENSITIVE If you are a new user or guest visiting an LWWonline site for the first time, please complete the new account setup process to view or purchase content. Forgot your password? Subscribe Renewal Information Subscribe to RSS feed utrdc-pt02 Release 4.0

89. Isaacs, Syndrome : Arborescences MeSH page PubMed du motclef loge musculaire, syndromes C05.651.180 + page PubMed http://www.chu-rouen.fr/navimesh/I/naviisaacssyndrome.html

Isaacs, syndrome : arborescences MeSH Menu général CISMeF Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF appareil locomoteur, maladies muscle, maladies arthrogrypose cellulalgie ... tumeur système nerveux périphérique 11 juin 2004 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

90. Syndrome D'isaacs : Arborescences MeSH isaacs arborescences MeSH syndrome d isaacs C05.651.392 page PubMed du motclef syndrome eosinophilie-myalgie C05.651.290 page http://www.chu-rouen.fr/navimesh/S/navisyndromedisaacs.html

Syndrome d'isaacs : arborescences MeSH Vous pouvez aussi consulter toutes les arborescences des mots clés utilisés dans CISMeF maladies de l'appareil locomoteur maladies musculaires arthrogrypose cellulalgie ... tumeur système nerveux périphérique 25 février 2005 courriel Menu général CISMeF Haut de page © CHU de Rouen . Toute utilisation partielle ou totale de ce document doit mentionner la source.

91. Neurologic Manifestations Fasciculation. isaacs syndrome Baylor College Med (US) About Brown-Sequardsyndrome - Wheeless Textbook of Orthopaedics. Brown-Sequard syndrome C http://www.mic.ki.se/Diseases/C10.597.html

search search staff sitemap ABOUT KAROLINSKA INSTITUTET ... print this page Diseases and Disorders Links pertaining to Neurologic Manifestations Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Agnosia Amnesia Anomia Aphasia ... Vertigo Cerebellar Ataxia Classification of Ataxias - Washington U./School of Med. (US) Hereditary Ataxia Overview - GeneTests The US National Ataxia Foundation - Minneapolis European Federation of Hereditary Ataxias Int'l Network of Ataxia Friends About Episodic Ataxia [Mark ? ] Chorea Sydenham's Chorea (St. Vitus' Dance, Rheumatic Chorea) - Adam, via MedlinePlus Sydenham Chorea - WeMove The legend about Vitus - Catholic Online Saints Tardive Dyskinesia (not on MeSH) About Tardive Dyskinesia [JR Brasic] - eMedicine Tardive Dyskinesia [B Alexander] - Virtual Hoispital Dystonia What is Dystonia? - Dystonia Support Dystonia Dialogue , and about

92. Research to elucidate pathomechanism of isaacs syndrome (acquired neuromyotonia). that autoantibody against K channels is the cause of isaacs syndrome. http://www.kufm.kagoshima-u.ac.jp/~physiol2/research_eng.html

Research Projects 1. Regulation of Ca channels in nerve and muscle cells Voltage-gated (or voltage-dependent) Ca channels are composed of at least 5 (T, L, N, P/Q, R) types as determined by electrophysiological and pharmacological properties. In neurons, N- and P/Q-type channels are located in presynaptic terminals and trigger release of neurotransmitters. In cell bodies and dendrites of neurons, almost all the types of Ca channels are found, but their composition seems to be different in different types of neurons. Although their physiological roles are not fully understood, the channels are thought to play roles in plasticity of neural circuits and regulation of enzymes and gene expression. In the last decade, several classes of genes coding different types of Ca channels have been cloned and sequenced. It is interesting to investigate how expression and subcellular localization of each type of the channel are regulated. Ca channels are playing important roles also in muscle cells. In the skeletal and cardiac muscles, a plenty number of the channels are located in the transvers tubular system and transduce electrical signal to an intracellular signal that triggers release of Ca from sarcoplasmic reticulum. In addition, the channels contribute to the generation of action potential in the pacemaker cells, that is important for the automaticity of the heart. Activity of Ca channels is regulated by transmitters and hormones. For example, L-type Ca channel is up-regulated by beta-adrenergic stimulation through cAMP-protein kinase A (PKA) system. It has been shown that PKA phophorylates alpha and/or beta subunit of the channel protein. However, an exact molecular mechanism underlying regulation of the channel function is not fully understood. We have recently found that unidentified factors in cytoplasm of cardiac myocytes significantly affect activity of the Ca channel. We are now exploring to isolate the factors to elucidate the mechanism of action of the factors.

93. KoreaMed - Basic Search A Case of isaacs syndrome. J Korean Neurol Assoc. 1993 Dec;11(4)592598. Primary Antiphospholipid syndrome Presenting Dementia and Brain Atrophy. http://www.koreamed.org/SearchBasic.php?QY=J Korean Neurol Assoc [JTI] AND 1993

94. A Listing Of Disorders Ichthyosis, Chanarin Dorfman syndrome. Ichthyosis, CHILD syndrome InterstitialCystitis. Intestinal Pseudoobstruction. isaacs syndrome. Ivemark syndrome. http://medschool.umaryland.edu/BTBank/Family/Disorders_I.htm

Brain and Tissue Bank University of Maryland, Baltimore I I Cell Disease Ichthyosis Ichthyosis Congenita Ichthyosis Hystrix, Curth Macklin Type Ichthyosis Vulgaris Ichthyosis, Chanarin Dorfman Syndrome Ichthyosis, CHILD Syndrome Ichthyosis, Erythrokeratodermia Progressiva Symmetrica Ichthyosis, Erythrokeratodermia Variabilis Ichthyosis, Erythrokeratolysis Hiemalis Ichthyosis, Harlequin Type Ichthyosis, Keratosis Follicularis Spinulosa Decalvans Ichthyosis, Lamellar Recessive Ichthyosis, Netherton Syndrome Ichthyosis, Sjogren Larsson Syndrome Ichthyosis, Tay Syndrome Ichthyosis, X Linked IgA Nephropathy Inclusion Body Myositis Incontinentia Pigmenti Interstitial Cystitis Intestinal Pseudoobstruction Isaacs' Syndrome Ivemark Syndrome

95. AAPM&R - Case No. 47, Cont Stiff Person syndrome. isaacs syndrome. Benign Fasciculations. Myopathy.Motor Neuron Disease. Alcohol Ingestion/Toxic exposure. Tremor or dystonia http://www.aapmr.org/education/archive/emg0010b.htm

Search Entire Site Member Center PASSOR Practice Issues Legislative/Business/Clinical Annual Assembly Medical Education Industry Opportunities What is a Physiatrist? Legislative, Business and Clinical Practice Issues Annual Assembly Medical Education ... EMG EMG Case No. 47, October 2000, continued History A 22-year-old woman with a 4-year history of insulin dependent diabetes mellitus and hypothyroidism presents to the electrodiagnostic laboratory with a chief complaint of involuntary muscle tightening and spasms. She has not experienced pain in association with the spasms, and she has no muscle cramps. She denies weakness. Her symptoms began 8 years ago while she was in high school, and the muscle tightening and spasms have been slowly progressive in severity and duration. The episodic tightening or twitching of her muscles involves her abdominal, hand, and lower limb muscles bilaterally. These paroxysmal episodes last for approximately 5 seconds and occur many times during the day. On occasion, she notices that objects fall from her hands. She believes that cold may induce her symptoms. Initially, she was not concerned about the abdominal spasms since they helped maintain her muscle tone. Prior to continuing, please develop a differential diagnosis and list each possible diagnosis in order of likelihood.

96. Health Topics - Quest Diagnostics Patient Health Library Irregular or Missed Periods Irregular Periods Irritable Bowel syndrome (IBS).IS. isaacs syndrome isaacsMerten syndrome Ischemic Necrosis of Bone http://www.questdiagnostics.com/kbase/list/ht/i.htm

Health Topics Click a letter to see a list of topics beginning with that letter. A B C D ... I Cell Disease IB IBIDS Syndrome IBM IBS (Irritable Bowel Syndrome) IC IC ICD ICE Syndrome, Cogan-Reese Type ICE Syndrome, Essential Iris Atrophy Type ... Ichthyosis, Congenital, with Trichothiodystrophy Top Ichthyosis, Erythrokeratodermia Progressiva Symmetrica Ichthyosis, Erythrokeratodermia Variabilis Ichthyosis, Erythrokeratolysis Hiemalis Ichthyosis, Harlequin Type ... Icterus Intermittens Juvenalis ID Identifying and avoiding migraine triggers Identifying and avoiding tension headache triggers Identifying asthma triggers IDET ... Idiopathic Arteritis of Takayasu Top Idiopathic Autoimmune Hemolytic Anemia Idiopathic Basal Ganglia Calcification (IBGC) Idiopathic Blepharospasm-Oromandibular Dystonia Syndrome Idiopathic Brachial Plexus Neuropathy ... IDPA IG IgA Nephropathy Top IH IHIS IL Ileoanal or ileorectal anastomosis for ulcerative colitis Illinois Type Amyloidosis IM Immune Defect due to Absence of Thymus Immune Globulin Immune Hemolytic Anemia Immune Hemolytic Anemia, Paroxysmal Cold ... Impotent Neutrophil Syndrome Top IN In vitro fertilization for infertility INAD Inborn Error of Urea Synthesis, Arginase Type

97. Arq. Neuro-Psiquiatr. - Vol.57 no.2A isaacs syndrome report of three cases SCOLA, ROSANA HERM?IA; COMERLATO, ENIOALBERTO; TEIVE, H?IO AFONSO GUIZZONI; GERMINIANI, FRANCISCO; WERNECK, http://www.scielo.br/scielo.php?pid=0004-282X19990002&script=sci_issuetoc

98. Myokymia And Neonatal Epilepsy Caused By A Mutation In The Voltage Sensor Of The Sera from patients with isaacs syndrome suppressed voltagegated outward potassiumcurrents Beside the autoimmune pathophysiology in isaacs syndrome, http://www.pnas.org/cgi/content/full/98/21/12272

Published online before print September 25, 2001, 10.1073/pnas.211431298 October 9, 2001 This Article Abstract Full Text (PDF) Alert me when this article is cited ... Citation Map Services Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles Search for citing articles in: ISI Web of Science (38) PubMed PubMed Citation Articles by Dedek, K. Articles by Steinlein, O. K. Neurobiology Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K channel Karin Dedek Bernhard Kunath Colette Kananura Ulrike Reuner Thomas J. Jentsch , and Ortrud K. Steinlein Communicated by Bert Sakmann, Max Planck Institute for Medical Research, Heidelberg, Germany, August 15, 2001 (received for review May 8, 2001) Abstract Top Abstract Introduction Materials and Methods Results Discussion References KCNQ2 and KCNQ3 are two homologous K channel subunits that can combine to form heterotetrameric channels with properties of neuronal M channels. Loss-of-function mutations in either subunit

99. Clinical Evaluation Of Plasma Exchange And High Dose Intravenous Immunoglobulin and high dose intravenous immunoglobulin in a patient with isaacs syndrome (IVIg) were evaluated in a 41 year old woman with isaacs syndrome. http://jnnp.bmjjournals.com/cgi/content/abstract/57/7/840

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] This Article Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Services Email this link to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal ... Cited by other online articles PubMed PubMed Citation Articles by Ishii, A. Articles by Shoji, S. Journal of Neurology, Neurosurgery, and Psychiatry, 1994, Vol 57, 840-842 PAPERS Clinical evaluation of plasma exchange and high dose intravenous immunoglobulin in a patient with Isaacs' syndrome A Ishii, A Hayashi, N Ohkoshi, E Oguni, M Maeda, Y Ueda, K Ishii, K Arasaki, H Mizusawa and S Shoji Department of Neurology, University of Tsukuba, Japan. The clinical effects of plasma exchange and high dose intravenous immunoglobulin (IVIg) were evaluated in a 41 year old woman with Isaacs' syndrome. After double filtration plasma exchange, symptoms almost

100. The Neurologist - UserLogin It can be seen in idiopathic form (isaacs syndrome), inherited neuropathies, orin acquired diseases, including peripheral neuropathy and paraneoplastic http://www.theneurologist.org/pt/re/neurologist/fulltext.00127893-200201000-0000

LWWOnline LOGIN eALERTS REGISTER ... Archive You are attempting to access protected content. To access this content please login using an established account or create/activate an account. If you have already created/ activated an online account, please login below: User Name: Password: Note: passwords are CASE SENSITIVE If you are a new user or guest visiting an LWWonline site for the first time, please complete the new account setup process to view or purchase content. Forgot your password? Subscribe Renewal Information Subscribe to RSS feed utrdc-pt01 Release 4.0

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 5     81-100 of 103    Back | 1  | 2  | 3  | 4  | 5  | 6  | Next 20