81. Lapsuusiän Vuorotteleva Hemiplegia Kehitysvammahuollon tietopankki. Lapsuusiän vuorotteleva hemiplegia. Lapsuusiänvuorotteleva hemiplegia on harvinainen epsisodimaisen hemiplegian muoto. http://www.saunalahti.fi/kup/syndroma/althemip.htm

Kehitysvammahuollon tietopankki Lapsuusiän vuorotteleva hemiplegia Lapsuusiän vuorotteleva hemiplegia on harvinainen epsisodimaisen hemiplegian muoto. Tiheät kohtaussarjat kestävät muutamista minuuteista useisiin päiviin. Useimmissa tapauksissa esiintyy toispuoleista lihasjänteyden vaihtelua, tahattomia pakkoliikkeitä, autonomisen hermoston toiminnan häiriöitä, silmävärvettä , muita silmälihasten häiriöitä ja etenevää psyykkistä kehitysvammaisuutta Sairauden on arvioitu olevan autosomaalisesti vallitsevasti periytyvä Sairastuneet eivät ole hyötyneet epilepsia lääkityksestä eikä poikkeavaa aivosähkötoimintaa ole onnistuttu rekisteröimään EEG-tutkimuksissa. Tietokonetomografisista (CT-kuvaus - menetelmä, jolla saadaan tarkkaa tietoa aivojen epämuodostumista) kuvauksistakaan ei ole ollut hyötyä. Tauti todetaan kliinisen kuvan perusteella yleensä ensimmäisen elinvuoden aikana. Lisätietoja: CP-vammat Omim Database, Alternating hemiplegia of childhood Laadittu 19.12.1997 Kehitysvammaisten Uudenmaan tukipiiri ry. Kehitysvammahuollon tietopankki

82. Title Page B. Leonard Holman. Puneet K. Chandak. Basem M. Garada. NEXT CASE. Familial AlternatingHemiplegia. HMPAO SPECT + MRI superimposed. HMPAO SPECT. MRI. HMPAO SPECT. http://brighamrad.harvard.edu/education/online/BrainSPECT/FAH/FAH.html

PREV CASE Atlas of Brain Perfusion SPECT B. Leonard Holman Puneet K. Chandak Basem M. Garada NEXT ... CASE Familial Alternating Hemiplegia HISTORY IMAGES FINDINGS TUTORIAL SLIDE SHOW RANDOM CASE FEEDBACK CONTENTS Comments and errors to Radweb@dsg.harvard.edu Additional information through chandak@dsg.harvard.edu Last updated: Aug 23, 1995 Redesigned June 1998

83. Andermann.html TI Evidence for mitochondrial dysfunction in patients with alternatinghemiplegia of childhood. AU ArnoldDL; Silver-K; Andermann-F. http://www.indiana.edu/~pietsch/andermann.html

go to Shufflebrain main menu To Andermann menu ANDERMANN'S SYNDROME THE 1996 LITERATURE web contact: pietsch@indiana.edu A literature search at Indiana University, Bloomington, Indiana The following MEDLINE items were compiled by SilverPlatter and are presented with their generous cooperation and permission. ( See SilverPlatter's Worldwide Library for bibliographic search information For a non-technical summary of Andermann's syndrome, try here! MEDLINE EXPRESS (R) 1/96-11/96 1 of 14 TI: The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q [see comments] CM: Comment in: Am J Hum Genet 1996 Jan;58(1):7-16 AU: Casaubon-LK; Melanson-M; Lopes-Cendes-I; Marineau-C; Andermann-E; Andermann-F; Weissenbach-J; Prevost-C; Bouchard-JP; Mathieu-J; Rouleau-GA AD: Centre for Research in Neuroscience, Montreal General Hospital Research Institute, Quebec, Canada. SO: Am-J-Hum-Genet. 1996 Jan; 58(1): 28-34 ISSN: 0002-9297 PY: 1996 LA: ENGLISH CP: UNITED-STATES AB: Peripheral neuropathy with or without agenesis of the corpus callosum (ACCPN) is a devastating neurodegenerative disorder that is transmitted as an autosomal recessive trait. Genealogical studies in a large number of affected French Canadian individuals suggest that ACCPN results from a single founder mutation. A genomewide search using 120 microsatellite DNA markers in 14 French Canadian families allowed the mapping of the ACCPN gene to a 5-cM region on chromosome 15q13-q15 that is flanked by markers D15S1040 and D15S118. A maximum two-point LOD score of 11.1 was obtained with the marker D15S971 at a recombination fraction of 0. Haplotype analysis and linkage disequilibrium support a founder effect. These findings are the first step in the identification of the gene responsible for ACCPN, which may shed some light on the numerous conditions associated with the progressive peripheral neuropathy or agenesis of the corpus callosum.

84. ÇغÎÇб³½Ç The summary for this Korean page contains characters that cannot be correctly displayed in this language/character set. http://anatomy.yonsei.ac.kr/scripts/home/book_view.idc?name=CH6-PT2-TB1-TT2-ST5

85. AASH--Headache Journal, Abstracts, 9/97 Focal brain dysfunction in a 41year old man with familial alternatinghemiplegia. Eur Arch Psychiat Clin Neuros 1997;247(1)35-41. http://www.ahsnet.org/journal/archive/sep97moore.php

Abstracts and Citations Kenneth L. Moore, MD - Abstracts Editor Migraine Cluster Headache Migraine Silberstein SD. Migraine and pregnancy Neurol Clin Abstract: This article discusses migraine and other headache disorders that occur during pregnancy and stresses the necessity and safety of diagnostic testing. A review of migraine prevalence during pregnancy is followed by a summary of the adverse effects of drugs on the fetus and by recommendations for migraine treatment based on a review of the literature and personal experience. TfeltHansen P. Prophylactic pharmacotherapy of migraine: Some practical guidelines. Neurol Clin Abstract: Despite the recent advantages in abortive treatment of migraine, a significant group of patients still needs prophylactic treatment. A general checklist for prophylactic pharmacotherapy of migraine is provided. The use of the diagnostic headache diary is emphasized. Some practical guidelines of the prophylactic treatment of migraine are listed, taking the benefit-risk ratio into account. Mathew NT.

86. SearchUK Home Top Health Conditions_and_Diseases Neurological_Disorders AlternatingHemiplegia. ADULT (18+), SHOPPING, FINANCE, GAMBLING, JOBS, TRAVEL, http://www.searchuk.co.uk/Top/Health/Conditions_and_Diseases/Neurological_Disord

SearchUK http://searchuk.co.uk/

87. Últimas Novedades Por Revista Translate this page Traducción. 18, Caesarean section under general anaesthetic in a woman with alternatinghemiplegia of childhood International Journal of Obstetric Anesthesia. http://www.lasalud.com/busquedas/buscar_por_revista.htm?revi=International Journ

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