41. Penn State Faculty Research Expertise Database (FRED) Ataxia. marinescosjogren syndrome, Spinocerebellar Degeneration. Early Degeneration. Maries Cerebellar Ataxia, Marinesco Sjogren Syndrome. Primary http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D013132

42. Gillespie GS is similar to marinescosjogren syndrome, but is considered to be caused by a different mutation. Conditions observed in GS patients. http://w1.891.telia.com/~u89105266/text/gillespie2.html

Kasper and his rare condition, Gillespie syndrome! We dont know why a person gets Gillespie Syndrome and we don't know if its an autosomally recessive genetic condition. This is the typical look of the eye in someone with Gillespie. The thin irises and the large pupils. This is what the write about GS at www.aniridia.org Gillespie Syndrome is a very rare genetically inherited disorder, which is inherited Recievely. It was first identified in 1965 when F. D. Gillespie described brothers and sisters with this combination which had apparently not been reported previously. GS is similar to Marinesco-Sjogren syndrome, but is considered to be caused by a different mutation. Conditions observed in GS patients Bilateral partial aniridia cerebellar ataxia, cerebellar hypoplasia cerebral and cerebellar atrophy mental deficiency developmental delay in both mental and motor skills gross uncoordination, attention tremor, scanning speech. persistent hypotonia congenital pulmonic stenosis Aniridia is the distuniguishing feature of GS, but aniridia in GS is identifable different from dominantly inherited aniridia, one note worth observation is that GS patients not develop cataracts and cornea pannus which are common in dominantly inherited aniridia. Diagnois can be made in the first months of life on the basis of the ocular findings. From slit lamp examination, the pupil border of the iris typically shows iris strands extending onto the anterior lens surface at regular intervals.

43. The Kuwait Medical Genetics Centre entity of syndromic dextrocardia, cases of Joubert s syndrome, SmithLemli-Opitz syndrome, Sjogren-Larsen syndrome, marinesco-sjogren syndrome, Troyer- like http://www.safat.com/kgc.html

The Kuwait Medical Genetics Centre (KMGC) was established in January, 1979, with the following aims: The accurate diagnosis of rare monogenic diseases. Investigating cases of congenital malformations. Providing genetic counselling for families with genetic disorders e.g. cases of male/female primary infertility, recurrent pregnancy loss, congenital malformations, structural/numerical chromosomal abnormalities, genetic forms of mental retardation, f amilial visual disorders and pre-marital counselling. Exploring the possible means of reducing neonatal mortality and physical disability. Providing training programmes for doctors and technical staff in the area of genetic counselling. The KMGC represents an independent entity located in the Maternity Hospital, and is affiliated to the Ministry of Health. The service is provided to a population size of 1.575.983 persons, including 655.820 (41.6%) Kuwaiti citizens and 920.163 (58.4%) non -Kuwaiti residents, mostly of Arab nationalities. The service is provided in liaison with departments of different specialities in satellite Genetics clinics attached to 5 regional hospitals including: Sabah and Ameri Hospital (serving 192.800 persons)

44. OMIM - MARINESCO-SJOGREN SYNDROME; MSS http://www3.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248800

45. AtaxiasUntitled and eunuchoidism), Hereditary ataxia (with myotonia and cataracts), Hypertrophic interstitial neuritis, marinescosjogren syndrome, Pelizaeus-Merzbacher disease http://www.cmdg.org/Movement_/ataxias/ataxias.htm

The Canadian Movement Disorder Group Ataxia Ataxia is a term to describe loss of balance. The part of the brain that is involved in balance is at the back of the brain, attached to the brainstem, and is called the "Cerebellum". Damage to the cerebellum or its connections will result in unsteadiness of walking, and clumsiness of hand and foot coordination. Many conditions can cause the cerebellum to stop working normally. Cause of Ataxia include a huge number of conditions: Drug / Toxin induced cerebellar dysfunction: These include drugs; Clonazepam, Tegretol, Phenobarb, Primidone, Dilantin and toxins including; acute alcohol intoxication, alcoholism, solvent abuse , lead / mercury Trauma to the cerebellum Head Injury Endocrine Disorders (diseases of the glands that release hormones) Hypothyroidism Nutritional Deficiencies Vitamin B12 deficiency Neoplastic (Tumor) Paraneoplastic (Associated with a distant tumor) Vascular Causes (Stroke) These include; vasculitis (inflamation of blood vessels eg. Lupus), angioblastoma (a tumor of the blood vessels), embolism (a blood clot plugging a blood vessel), hemorrhage (a blood vessel rupturing and bleeding into the cerebellum), and Von-Hippel-Lindau Syndrome (a disorder of blood vessel formation)

46. Select Entries From OMIM -- Online Mendelian Inheritance In Man 123580 CRYSTALLIN, ALPHAA; CRYAA *120140 COLLAGEN, TYPE II, ALPHA-1; COL2A1 *261600 PHENYLKETONURIA *248800 marinesco-sjogren syndrome; MSS *115650 CATARACT http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/eye/congen_cataract.htm

Select Entries from OMIM Online Mendelian Inheritance in Man Back to Senses Abnormalities 109 entries found, searching for "congenital cataracts" CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKE FACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION SPINOCEREBELLAR DEGENERATION WITH MACULAR CORNEAL DYSTROPHY, CONGENITAL CATARACTS, AND MYOPIA SPLIT-HAND WITH CONGENITAL NYSTAGMUS, FUNDAL CHANGES, AND CATARACTS HYPERFERRITINEMIA-CATARACT SYNDROME CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES; CCT CATARACT, CONGENITAL OR JUVENILE OCULOFACIOCARDIODENTAL SYNDROME PAIRED-LIKE HOMEODOMAIN TRANSCRIPTION FACTOR 3; PITX3 CATARACT, CONGENITAL, CERULEAN TYPE, 2; CCA2 CATARACT, CONGENITAL, CERULEAN TYPE, 1; CCA1 LACTOSE INTOLERANCE, CONGENITAL GLUCOSE-6-PHOSPHATE DEHYDROGENASE; G6PD DYSTROPHIA MYOTONICA COCHLEOSACCULAR DEGENERATION OF THE INNER EAR WITH PROGRESSIVE CATARACTS CORNEA GUTTATA WITH ANTERIOR POLAR CATARACTS MICROPHTHALMIA-CATARACT CATARACT, TOTAL CONGENITAL; CC

47. UNSW Embryology-OMIM Muscular Dystrophy List PROXIMAL MYOTONIC MYOPATHY; PROMM *314850 KELL BLOOD GROUP PRECURSOR; XK *602415 DYSTROBREVIN, BETA; DTNB *248800 marinescosjogren syndrome; MSS *151628 LINE http://anatomy.med.unsw.edu.au/cbl/embryo/OMIMfind/skmus/OMIM-dystophy_list.htm

UNSW Embryology MUSCULOSKELETAL DEVELOPMENT Embryology Home Page Select Entries from OMIM Online Mendelian Inheritance in Man (Internet Link) This page is for computers without external internet access. Internet access computers can see the full description of the abnormality from the links below. Back to UNSW Embryology-Musculoskeletal Notes 186 entries found, searching for " muscular dystrophy MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER TYPES FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; FCMD MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2A; LGMD2A EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2C; LGMD2C EMERY-DREIFUSS MUSCULAR DYSTROPHY SARCOGLYCAN, ALPHA; SGCA

48. GeneTests: Search Results 2227 Research Tests 2227 GeneReview friedreich 30927 Resources 2227 Infantile Onset Spinocerebellar Ataxia (IOSCA) marinescosjogren syndrome Research Tests http://www.genetests.org/query?mim=551500

49. SearchBug Directory: Health: Conditions_and_Diseases: M 5) Malnutrition (8) Malta Fever (11) Mannosidosis (2) Marburg (4) Marfan Syndrome (37) MarieSainton Disease (4) marinesco-sjogren syndrome (9) Master s http://www.searchbug.com/directory.aspx/Health/Conditions_and_Diseases/M/

All Searches Auctions CompanyFinder Entertainment ... Travel Search the Web: Web Images Audio Files News Multimedia Shopping Open Directory Search: Featured Websites Business ValueXpress: Business Valuation Software - businessvaluexpress.com 1st interactive deal-making tool for buyers/sellers/advisors. No arbitrary inputs. New theory gives objective valuation for any business based on terms, financing, deal structure, etc. Unmatched features, do-it-yourself simplicity, what-if analysis. BusinessBroker.net - 8500+ Business For Sale Ads - businessbroker.net Post a business for sale ad on BusinessBroker.net for just $34.95! Search over 7,200 businesses for sale, franchise opportunities, business brokers, and other business opportunities and resources. New York Investment and Merchant Banking Firm - firstwallst.com - barnesandnoble.com M Health Conditions and Diseases Go to Directory Home Categories MAC Machado-Joseph Disease Macular Degeneration Mad Cow Disease ... Myotonic Dystrophy Help build the largest human-edited directory on the web. Submit a Site Update URL Open Directory Project Become an Editor ... Report a Problem 2004, SearchBug.com, LLC

50. Welcome To AJC! Trisomy 13; Conradi syndrome; Ectodermal dysplasia syndrome; marinescosjogren syndrome. Ency. home Disease C Congenital cataract. http://www.ajc.com/health/healthfd/shared/health/adam/ency/article/001615.html

Main Contact us Edit profile Subscribe ... Register Now It's Free! Log in E-mail preferences Site Index Search: Site Yellow Pages Customer care ajc.com Nation/World Metro ... Personals ajc services Archives Advertise online Advertise in print Obituaries ... Sitemap Print edition Today This week A1 image E-mail News  Sign up for our  FREE newsletters: News Sports Business Travel Deals ... Logged in? ajc store Gifts Photos/pages Browser tip  Make ajc.com  your homepage: ajc guides Schools Visitors Illustrated Health Encyclopedia Important notice Ency. home Disease C Congenital cataract See images Overview Symptoms Treatment ... Prevention Alternative names: Cataract - congenital Definition: A cataract is any clouding of the lens of the eye. a congenital cataract is an opacity of the lens that occurs in the fetus at some time during pregnancy and is present at birth. Causes and Risks Although there are many diseases and inherited disorders that can lead to congenital cataracts, the actual incidence of congenital cataracts is low. In most patients with congenital cataract, no specific cause can be identified. This is a partial list of possible causes of congenital cataracts: galactosemia chondrodysplasia syndrome congenital rubella syndrome Down's syndrome (trisomy 21) Pierre-Robin syndrome familial congenital cataracts Hallerman-Streiff syndrome cerebrohepatorenal syndrome (Lowe's syndrome) Trisomy 13 Conradi syndrome Ectodermal dysplasia syndrome Marinesco-Sjogren syndrome Ency. home

51. MedlinePlus Medical Encyclopedia: Congenital Cataract Trisomy 13; Conradi syndrome; Ectodermal dysplasia syndrome; marinescosjogren syndrome. Although many diseases and inherited disorders http://www.nlm.nih.gov/medlineplus/ency/article/001615.htm

@import url(http://www.nlm.nih.gov/medlineplus/images/advanced.css); Skip navigation Medical Encyclopedia Other encyclopedia topics: A-Ag Ah-Ap Aq-Az B-Bk ... Z Congenital cataract Contents of this page: Illustrations Alternative names Definition Causes, incidence, and risk factors ... Prevention Illustrations Eye Cataract - close-up of the eye Rubella Syndrome Cataract Alternative names Return to top Cataract - congenital Definition Return to top A congenital cataract involves clouding of the lens of the eye that is present at birth. Causes, incidence, and risk factors Return to top The number of people born with cataracts is low. Possible causes of congenital cataracts include the following: Galactosemia Chondrodysplasia syndrome Congenital rubella syndrome Down syndrome (trisomy 21) Pierre-Robin syndrome Familial congenital cataracts Hallerman-Streiff syndrome Lowe syndrome Trisomy 13 Conradi syndrome Ectodermal dysplasia syndrome Marinesco-Sjogren syndrome Although many diseases and inherited disorders can lead to congenital cataracts, in most patients, no specific cause can be identified. Symptoms Return to top Opacity of the lens, often evident at birth without special viewing equipment and appearing as a whitish discoloration in an otherwise normally dark pupil

52. Neurology -- Abstracts: Walker Et Al. 35 (3): 415 ARTICLES. marinescosjogren syndrome evidence for a lysosomal storage disorder. The inherited abnormality of the marinesco-sjogren syndrome is not known. http://www.neurology.org/cgi/content/abstract/35/3/415

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: Email this article to a friend Correspondence: Submit a response to this article Similar articles found in: Neurology Online PubMed PubMed Citation This Article has been cited by: other online articles Search PubMed for articles by: Walker, P. D. Shapira, E. Alert me when: new articles cite this article Download to Citation Manager ARTICLES Marinesco-Sjogren syndrome: evidence for a lysosomal storage disorder PD Walker, MG Blitzer and E Shapira The inherited abnormality of the Marinesco-Sjogren syndrome is not known. We studied four patients from two different families and ethnic groups. Electron microscopic studies revealed numerous, abnormally enlarged lysosomes that contained whorled lamellar or amorphous inclusion bodies. Enzyme studies excluded previously described lysosomal storage disorders. This article has been cited by other articles: A. Reinhold, I. Scheer, R. Lehmann, L. M. Neumann, T. Michael, R. Varon, and A. von Moers MR Imaging Features in Marinesco-Sjogren Syndrome: Severe Cerebellar Atrophy Is Not an Obligatory Finding AJNR Am. J. Neuroradiol., May 1, 2003; 24(5): 825 - 828.

53. Friedreich's Ataxia (FRDA) more prominent spasticity and cerebellar atrophy. 4. marinescosjogren syndrome. - ataxia with short stature, mental retardation, and cataracts. http://www.uwo.ca/clinns/resident/pocketbook/disorders/movement/frda.htm

Friedreich's Ataxia (FRDA) Epidemiology First described in 1863 The most common early-onset hereditary ataxia - prevalence in North America estimated at 2 per 100,000 - carrier frequency of 1:120 Genetics Autosomal recessive inheritance - high risk if consanguinous unions - risk for sibling is 25% Gene for FRDA (X25) maps to 9q - codes for highly conserved protein, frataxin - most FRDA due to homozygous alleles with GAA triplet repeat expansions in first intron of X25 - rarely may have compound heterozygotes, with one allele bearing the intronic expansion and the other allele having a truncation or missense mutation (usually atypical or milder disease) - expanded repeats are unstable in transmission, esp paternal ( anticipation FRDA is due to deficiency of frataxin protein - GAA expansion interferes with transcription of protein - larger repeats more profoundly inhibit frataxin production - lead to earlier more severe form while small pathological expansions may allow small amount of residual production - frataxin is expressed mostly in heart, liver, skeletal muscle and spinal cord - protein localized on inner mitochondrial membrane - possibly leads to iron accumulation when deficient making mitochondria more susceptible to oxidative stress ( free radical toxicity Pathology - minimal involvement of brainstem, cerebellum and cerebrum (ie. not a cerebellar disease!)

54. ASHG: 2004 Annual Meeting - Exhibitor Prospectus M, MachereyNagel, Inc. Mammalian Genotyping Service. marinesco-sjogren syndrome Support Group. Marligen Biosciences, Inc. Mayo Medical Laboratories. McGraw-Hill. http://genetics.faseb.org/genetics/ashg/2004exhibitors/attendance-05.shtml

General Information Attendance History Registrant History: 2000-2003 Geographic Distribution ... Online Service Kit A Academia Book Exhibits ACGT, Inc. ACLARA BioSciences, Inc. Actelion Pharmaceuticals US, Inc. Affymetrix, Inc. Agencourt Bioscience Agilent Technologies AGRE-Autism Genetic Resource Exchange Alpha Innotech Corporation Ambion Diagnostics Ambion, Inc. American College of Medical Genetics American Journal of Human Genetics American Peptide Company American Type Culture Collection Amersham Biosciences Corp. AMRESCO, Inc. Apogee Instruments, Inc. Apple Computer Applied Biosystems Applied Imaging Applied Precision, Inc. Applied Spectral Imaging, Inc. Appropriate Technical Resources, Inc. Arcturus Asper Biotech Athena Diagnostics AutoGen, Inc. AutoGenomics B Axon Instruments, Inc. Bangs Laboratories, Inc. Baylor College of Medicine, Medical Genetics Laboratories Beckman Coulter, Inc. Benetech Medical Systems BioCal Technology, Inc. Biochrom Ltd BioDiscovery, Inc. BioDot, Inc. BioMarin Pharmaceutical, Inc. BIOPHILE, Inc. Biosearch Technologies Inc. BioTechniques - Eaton Publishing BioView Ltd.

55. ASHG 2003 Exhibitors List marinescosjogren syndrome Support Group; Mayo Medical Laboratories; MEDGIS-PSA Computer Consultants; Mendelssohn Customs Services; MetaSystems; MJ Research, Inc. http://www.ashg.org/genetics/ashg/annmeet/2003/exhibits/exlist.shtml

ANNUAL MEETING ASHG 2003 Exhibitors Awards Information List of Exhibitors Abstract Search and Personal Itinerary Planner Preliminary Schedule ... Awards Information Millennium Biltmore Hotel Conference/Mezzanine Level Galeria Level Convention Center Level 1 Level 2 The purpose of the exhibit program is to further the education of registrants by providing an opportunity for exhibitors to present information on products or services relevant to registrants' professional interests. In keeping with that purpose, sales and order-taking (entering into a contract of sale) are discouraged on the exhibit floor and other related convention areas. Registrants are encouraged to view the exhibits in Hall C-E on Wednesday, 10:30 am - 6:30 pm; Thursday, 10:30 am - 6:30 pm; and Friday, 10:30 am - 3:30 pm. To assist in locating specific products and services of interest, a product and service index is available. This index is organized alphabetically by products/services, followed by names of exhibiting companies offering the product/service and their respective booth numbers. Booth numbers also follow the names of the exhibiting companies below. Academia Book Exhibits Actelion Pharmaceuticals US, Inc.

56. Centre National De Génotypage L., Chaigne, D., Gribaa, M., Dollfus, H., Silvestri, G., Bétard, C., Warter, JM and Koenig, M., Homozygosity mapping of marinescosjogren syndrome to 5q31. http://www.cng.fr/en/publications/pub2003.html

57. Genes, Locations And Genetic Disorders On Chromosome Unknown_or_Multiple_Locatio DISPROPORTION. MS, GDB229116, SCLEROSIS; MS. MSS, GDB118743, marinescosjogren syndrome; MSS. MTATP6, GDB118897, ATP SYNTHASE 6; MTATP6. MTCO1, http://gdb.wehi.edu.au/gdbreports/Chr.Unknown_or_Multiple_Locations.omim.html

Genes, Locations and Genetic Disorders on Chromosome Unknown_or_Multiple_Locations Last Updated: Sun Aug 13 22:00:02 EDT 2000 Gene GDB AccessionID Location OMIM Link ABAT GDB:581658 GAMMA-AMINOBUTYRATE TRANSAMINASE AEZ GDB:128360 ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE; AEZ AFA GDB:265277 FILIFORME ADNATUM AND CLEFT PALATE ASAH GDB:6837715 FARBER LIPOGRANULOMATOSIS GDB:6276019 ATRIAL SEPTAL DEFECT; ASD ASMT GDB:136259 ACETYLSEROTONIN METHYLTRANSFERASE; ASMT ACETYLSEROTONIN METHYLTRANSFERASE, Y-CHROMOSOMAL; ASMTY; HIOMTY BCH GDB:118758 CHOREA, HEREDITARY BENIGN; BCH GDB:9864171 BRACHYDACTYLY, TYPE B; BDB BSCL GDB:9957720 SEIP SYNDROME BZS GDB:265278 MACROCEPHALY, MULTIPLE LIPOMAS AND HEMANGIOMATA CCAT GDB:118738 CATARACT, CONGENITAL OR JUVENILE GDB:9957389 CORNEAL DYSTROPHY, CONGENITAL HEREDITARY ... CEROID-LIPOFUSCINOSIS, NEURONAL 4; CLN4 CPO GDB:119070 COPROPORPHYRIA GDB:118777 COLONY STIMULATING FACTOR 2 RECEPTOR, ALPHA; CSF2RA ... CARPAL TUNNEL SYNDROME; CTS; CTS1 DF GDB:132645 FACTOR D GDB:439243 DIAPHRAGMATIC DWS GDB:128371 SYNDROME; DWS GDB:118788 DYSTONIA MUSCULORUM DEFORMANS 2; DYT2 ... EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA ECT GDB:128640 CENTRALOPATHIC EPILEPSY ED# GDB:6928857 ECTODERMAL DYSPLASIA, ANHIDROTIC

58. Mental Retardation, Directory MarinescoSjögren syndrome (MSS), Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes marinesco-sjogren syndrome; MSS, OMIM Marinesco-Sjögren http://www.saunalahti.fi/kup/engl/webs_m.html

Finnish Information Center on Mental Retardation English links A B C D ... Z MacDermot-Winter Syndrome Two brothers with facial anomalies, microcephaly, hypoplastic genitalia, and a failure of psychomotor development, PubMed 247990 MACDERMOT-WINTER SYNDROME, OMIM MacDermot-Winter syndrome. Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes Macrocephaly MACROCEPHALY, OMIM MACROCEPHALY, MULTIPLE LIPOMAS, AND HEMANGIOMATA, OMIM MACROCEPHALY, BENIGN FAMILIAL, OMIM MACROCEPHALY/AUTISM SYNDROME, OMIM ... Increased head circumference, MedlinePlus Malouf Syndrome Malouf syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes 212112 CARDIOMYOPATHY, CONGESTIVE, WITH HYPERGONADOTROPIC HYPOGONADISM, OMIM Hypogonadism cardiomyopathy, Orphanet Malpuech Sybdrome MALPUECH FACIAL CLEFTING SYNDROME, OMIM, Victor A. McKusick Malpuech syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes Two sibs with Malpuech syndrome, Giangiorgio Crisponi, Andrea Raffaele Marras and Adriano Corrias, American Journal of Medical Genetics Aniridia Network Maple Syrup Urine Disease MAPLE SYRUP URINE DISEASE, OMIM, Victor A. McKusick et al.

59. PharmGKB: Spinocerebellar Degenerations Marie Cerebellar Ataxia; Marie s Cerebellar Ataxia; Maries Cerebellar Ataxia; Marinesco Sjogren Syndrome; marinescosjogren syndrome; Primary Cerebellar http://www.pharmgkb.org/do/serve?objId=PA445716&objCls=Disease

60. Arch Neurol -- Table Of Contents (Vol. 47 No. 11, November 1990) The marinescosjogren syndrome examined by computed tomography, magnetic resonance, and 18F-2-fluoro-2-deoxy-D-glucose and positron emission tomography MB http://archneur.ama-assn.org/content/vol47/issue11/index.dtl

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA For The Media Classified Ads Meetings Peer Review Congress Vol. 47 No. 11, pp. 1170-1260, November 1990 Content Access Register Subscribe One-time Access E-mail Alerts Table of Contents Jump to Section ARTICLES ARTICLES Rolling chair sign M. Cole Arch Neurol. Strokes associated with cocaine use A. J. Tuchman; M. Daras Arch Neurol. The practice of neurology M. Menken Arch Neurol. The influence of hyperglycemia and diabetes mellitus on immediate and 3-month morbidity and mortality after acute stroke J. Woo; C. W. Lam; R. Kay; A. H. Wong; R. Teoh; M. G. Nicholls Arch Neurol. ABSTRACT Circadian variation in onset of acute ischemic stroke E. E. Marsh, 3rd; J. Biller; H. P. Adams, Jr; J. R. Marler; J. R. Hulbert; B. B. Love; D. L. Gordon Arch Neurol. ABSTRACT Nontraumatic coma. Glasgow coma score and coma etiology as predictors of 2-week outcome R. L. Sacco; R. VanGool; J. P. Mohr; W. A. Hauser

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