81. Aniridia apparently not been reported previously, although cerebellar ataxia mental deficiencyand congenital cataracts are known in the Marinesco Sjogren syndrome. http://ibis-birthdefects.org/start/aniridia.htm

Tips for printing Aniridia Syndrome About I.B.I.S. Home Search Topics Search all contents ... "In the News" Messages... Questions/comments Report Dead Links S.O.S. - Exchange Join I.B.I.S. ... Etchings Please Explore: 11p Chromosome Eye / Ocular WAGR S. Wilms Tumor ... Key Information Sources Topics include Title and An2 Paired Box Homeotic Gene; PAX6 Gillespie S. Special Resources Aniridia A Selection of Internet Sites [*] Outstanding [P] For Professionals [S] Support Group ANIRIDIA; AN1 from OMIM ... A form of aniridia is not linked to markers on 2p as previously thought, ... There probably is no form of autosomal dominant aniridia other than that which maps to 11p13 and was designated AN2 ... Shaw et al. (1960) ascertained 176 cases of aniridia in the lower Michigan peninsula ... mutation rate about 4 x 10(-6) per gamete per generation. Affected persons may be visually handicapped because of nystagmus, cataract or glaucoma ... Undoubtedly more than one "cause" of aniridia exists ... Gove et al. (1961) identified 77 cases of aniridia descended from an affected woman born in 1824 ... Delleman and Winkelman (1973) emphasized that atypical colobomata and slitlike defects of the iris stroma may be partial expressions of aniridia ... a fourth type associated with Wilms tumor, genital abnormalities, and deletion of 11p13 ( WAGR syndrome ) ... PAIRED BOX GENE 6; PAX6

82. Malattie Rare E Genetiche Lettera "M" Translate this page Sindrome di Garland-Moorhause/Sindrome di Marinesco-Garland/Sindrome di Sjogren/Sindromecataratta-oligofrenia•Marinesco Sjogren syndrome/Marinesco-Sjögren http://utenti.lycos.it/fmfpc/M.htm

HOME FORUM Site Map / Mappa del sito FMFPC's International Guest/Book ... E-mail Dal 22 Marzo 2003 il server Lycos, che ospita le pagine FMFPC, subirà un *fermo tecnico*. Le pagine resteranno accessibili ma non verranno aggiornate per circa una settimana. - Tutti i servizi di FMFPC continueranno a funzionare. - È ora possibile accedere al sito anche attraverso l'indirizzo alternativo di FMFPC (sito mirror) all'URL http://digilander.libero.it/fmfpc/portale.htm ultimi aggiornamenti Elenco malattie rare e genetiche"lettera M" © FMFPC è un sito ideato, realizzato ed aggiornato da un malato di FMF (Febbre Mediterranea Familiare) © FMFPC is a site conceived, realized and updated by a patient of FMF (Familial Mediterranean Fever) aggiornato 5 marzo, 2003 Cerca nel menu aree FMFPC AREE FMFPC Malattie Rare Febbre Mediterranea Familiare Laboratori Diagnosi Genetica Associazioni Malati Disabilità/Handicap Categorie Medicina (Directory) Ricerche WEB (Medicina) FMFPC è partner AidWeb.org Cerca nel sito / Search in this site I contatti fino ad oggi possibili con FMFPC: Cerca in questa pagina / Search in this page con i tasti / with the keys Ctrl+F A B C D ... L - M - N O P Q ... legenda M Maaswinkel Mooij Stokvis Brantsma Sindrome di Maaswinkel mooij stokvis brantsma syndrome de MacDermot Patton Williams Sindrome di Mac dermot patton williams syndrome de[Hypertrichose cubitale petite taille] ... Machado-Joseph, maladie de[Ataxie spinocérébelleuse autosomique dominante/ Ataxie cérébelleuse autosomique dominante]

83. Untitled HUMMOLGEN DIAGnostics/Clinical Research. 9/10/96 marinesco-sjogrensyndrome/PT request. dear sir. our daughter of 3,5 has a form of http://www.hum-molgen.de/clinical/91096-1.html

HUM-MOLGEN DIAGnostics/Clinical Research marinesco-sjogren syndrome/PT request dear sir our daughter of 3,5 has a form of mss we want to know more about this syndrome because in Holland its very rare can you please give us somre more information in advance , many thanks Apparent patient location: Holland PLEASE REPLY DIRECTLY TO HUMAN MOLECULAR GENETICS NETWORK ( gambacorti@icil64.cilea.it

84. Marinesco-Sjögrenin Oireyhtymä Kehitysvammahuollon tietopankki. MarinescoGarlandin oireyhtymä Harmaakaihi-oligofrenia-oireyhtymäTorsten Sjögrenin oireyhtymä. http://www.saunalahti.fi/kup/syndroma/mss.htm

Kehitysvammahuollon tietopankki Marinesco-Garlandin oireyhtymä Harmaakaihi-oligofrenia-oireyhtymä Torsten Sjögrenin oireyhtymä Marinesco-Sjögrenin oireyhtymä Oireyhtymän pääpiirteet ovat pikkuaivo-ataksia ja synnynnäiset harmaakaihit, jotka aiheuttavat sokeutta ja psykomotorisen kehityksen jälkeenjääneisyyttä. Lihaksisto on usein heikko ja vajaakehittynyt. Selkäranka saattaa olla skolioottinen ja kyttyräinen. Sukurauhaset voivat olla kehittymättömät. Toisinaan esiintyy myös lattajalkaisuutta ja rintakehän kuperuutta. Oireisto periytyy peittyvästi autosomin (ei sukukromosomi) välityksellä. Lisätietoja: Marinesco-Sjögren syndrome (MSS), U.S. National Library of Medicine MARINESCO-SJOGREN SYNDROME; MSS, OMIM Database Marinesco-Sjögrenin tapainen oireyhtymä Kari Viitapohja 15.3.2002 Kehitysvammaisten Uudenmaan tukipiiri ry. Kehitysvammahuollon tietopankki

85. Marinesco-Sjögrenin Tapainen Oireyhtymä Kehitysvammahuollon tietopankki. Juveniilikatarakti-pikkuaivosurkastuma-lihassairaus-kehitysvammaoireyhtymä.Marinesco-Sjögrenin tapainen oireyhtymä. http://www.saunalahti.fi/kup/syndroma/msls.htm

Kehitysvammahuollon tietopankki Juveniili-katarakti-pikkuaivosurkastuma-lihassairaus-kehitysvammaoireyhtymä Marinesco-Sjögrenin tapainen oireyhtymä Oireyhtymä muistuttaa Marinesco-Sjögrenin oireyhtymää . Varhaislapsuuden aikainen velttous, näkyvin oire, kestää esikouluikään. Sen lisäksi esiintyy ataksiaa , harmaakaihia ja kehitysvammaisuutta . Lisäksi oireistoon liittyy pikkuaivojen surkastumista ja lihassairautta, kuten verisuonten rappeutumista, rasvakudoksen liikakasvua ja omaa kudosta syöviä solurakkuloita. Myös karsastus ja laajentunut pikkuaivo-selkäydinsammio kuuluvat oireisiin. Kasvu ja puheen oppiminen on hidasta, Puberteetti tulee myöhään. Lihassairaus näkyy kasvoista. Oireisto periytyy peittyvästi Lisätietoja: Marinesco-Sjögren-like syndrome (MSLS), U.S. National Library of Medicine MARINESCO-SJOGREN-LIKE SYNDROME; MSLS, OMIM Database Kari Viitapohja 15.3.2002 Kehitysvammaisten Uudenmaan tukipiiri ry. Kehitysvammahuollon tietopankki

86. Medical Genetics: Faculty: Wertelecki Superneau, DW, Wertelecki, W., Zellweger, H. Letter to the Editor The MarinescoSjogrenSyndrome Described a Quarter of a Century Before Marinesco. Am. http://www.southalabama.edu/genetics/wwer.htm

W. Wertelecki, M.D., F.A.C.M.G., F. A. A. P. CURRICULUM VITAE (Alternative spelling Werteleckyj) Professor and Chairman Department of Medical Genetics University of South Alabama Room 214, Cancer Center/Clinical Building Mobile, AL 36688-0002 MEDICAL EDUCATION: University of Buenos Aires School of Medicine - 1955-61; Assistant in Human Anatomy 1957-58; Assistant in Physiology, 1958-60; Internship, Muniz Hospital, Buenos Aires, 1961; Rotating Internship, Deaconess Hospital, St. Louis, Mo., 1962-63; Residency in Pediatrics, St. Louis Children's Hospital, Washington University Medical School, St. Louis 1963-65 POST-GRADUATE TRAINING: Research Fellow (Clinical Genetics), Harvard Medical School/Children's Hospital Medical Center, Boston, 1965-67 ACADEMIC AND OTHER APPOINTMENTS: Instructor of Pediatrics, Harvard Medical School/Children's Hospital Medical Center, Boston, MA 1967-68; Senior Surgeon (Commander), U.S. Public Health Commissioned Corps., National Cancer Institute, Epidemiology Branch, Bethesda, MD, 1968-70; National Institute of Health Consultant to the Bethesda Naval Medical Center; Assistant Professor, Dept. of Pediatrics, Medical University of South Carolina, Charleston, SC 1970-72; Chief, Division of Medical Genetics, Medical University of South Carolina, Charleston, SC 1970-74; Associate Professor, Departments of Pediatrics and Pathology, Medical University of South Carolina, 1972-74; Professor and Chairman, Department of Medical Genetics, University of South Alabama, Mobile, AL, 1974 - present.

87. Genes, Locations And Genetic Disorders On Chromosome Unknown_or_Multiple_Locatio DISPROPORTION. MS, GDB229116, SCLEROSIS; MS. MSS, GDB118743, MARINESCOSJOGRENSYNDROME; MSS. MTATP6, GDB118897, ATP SYNTHASE 6; MTATP6. MTCO1, http://wehih.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

88. University Of South Alabama Biomedical Library - Faculty Publications 82(1)10311, 1996 Feb. Brogdon BG. Snow RD. Williams JP. Skeletal findings in Marinesco-Sjogrensyndrome. Skeletal Radiology. 25461-5, 1996. Broughton WA. http://southmed.usouthal.edu/library/bf/fac33.htm

FACULTY PUBLICATIONS Listed below are journal publications by USA Faculty indexed in Index Medicus for August-September 1996. This list is generated from the address of the first listed author in MEDLINE and from Current Currents. Department chairs are also asked to submit citations of recent publications for their department members. If we missed your latest contribution to the literature, please let us know so we can include it in a future listing. New faculty are encouraged to submit their latest publications to the Editor. Ardell MD. Aragon I. Oliveira L. Porche GE. Burke E. Pittler SJ. The beta subunit of human rod photoreceptor cgmp-gated cation channel is generated from a complex transcription unit. FEBS Letters. 389(2):213-218, 1996 Jul 1. Bao LM. Zimmer WE. Balczon R. Autoepitope mapping of the centrosome autoantigen pcm-1 using scleroderma sera with anticentrosome autoantibodies. Autoimmunity. 22(4):219-228, 1995. Boerth SR. Artman M. Thyroid hormone regulates na+-ca2+ exchanger expression during postnatal maturation and in adult rabbit ventricular myocardium. Cardiovascular Research. 31(Special Issue SI):E 145-E 152, 1996 Feb. Bozner P. The heat shock response and major heat shock proteins of Tritrichomonas mobilensis and Tritrichomonas augusta. Journal of Parasitology. 82(1):103-11, 1996 Feb.

89. University Of South Alabama Biomedical Library - Faculty Publications Snow RD. Brogdon BG. Wertelecki W. Neuroradiologic findings in MarinescoSjogrensyndrome. AJNR American Journal of Neuroradiology. 19(2)281-3, 1998 Feb. http://southmed.usouthal.edu/library/bf/fac40.htm

FACULTY PUBLICATIONS Listed below are journal publications by USA Faculty indexed in MEDLINE and CINAHL for Feburary1998-July1998. This list is generated from the address of the first listed author in MEDLINE and from Current Currents. Department chairs are also asked to submit citations of recent publications for their department members. If we missed your latest contribution to the literature, please notify the Editor so it can be included in a future listing. New faculty are encouraged to submit their latest publications to the Editor. Almeida OD. Valgallas JM. Rizk B . Appendectomy under local anaesthesia following conscious pain mapping with microlaparoscopy. Human Reproduction . 13(3):588-590, 1998 Mar. Anglade D. Corboz M. Menaouar A. Parker JC. Sanou S. Bayat S. Benchetrit G. Grimbert FA. Blood flow vs. venous pressure effects on filtration coefficient in oleic acid-injured lung. Journal of Applied Physiology. 84(3):1011-1023, 1998 Mar. Armour JA. Collier K. Kember G. Ardell JL. Differential selectivity of cardiac neurons in separate intrathoracic autonomic ganglia.

90. ‘—§—×{ŠÒŠƒ•a‰@_Œo“à‰È‹ÆÑW The summary for this Japanese page contains characters that cannot be correctly displayed in this language/character set. http://www.saigata-nh.go.jp/saigata/sinnai/paper/paper6.htm

_Œo“à‰È‹ÆÑW _Œo“à‰ÈAƒŠƒnƒrƒŠ‰È‚ª“¯ˆêŽž‘ã‚̐_Œo“à‰È‚É‚¨‚¯‚é 1997”N •ŸŒ´M‹`A’†“‡FF_Œo“ï•a‚̏î•ñƒlƒbƒgƒ[ƒNB_ŒoŽ¡—A14: 113-118,1997. Ikeuchi, T., Asaga,T., Saito,M., Tanaka,H., Higuchi,S., Tanaka,K., Saida,K., Uyama,E., Mizusawa,H., Fukuhara,N., Nonaka,I., Takamori,M., Tsuji,S.: The gene for autosomal recessive diatal myopathy with rimmed vacuoles maps to chromosome 9. Ann.Neurol.,41: 432-437, 1997. Œˆä‰p‰îAâKŒ°ˆêA•ŸŒ´M‹`FMarchiafava-Bignami•a‚Æ’s•ðBDementia JapanA11: 249-254, 1997. •ŸŒ´M‹`F¡”N‚ÌŠw‰ï‚̈óÛBã‰zˆãŽt‰ï•ñA53†F19-20, 1997. Œˆä‰p‰îA–k‘ºG–¾AŠªŸº—²•vA•ŸŒ´M‹`F’W‘“‹ ƒ‹ƒC‘ÌŒn‚̃OƒŠƒI[ƒVƒX‚ªŒy“x‚ÈŽ•óŠjÔŠj’W‘“‹ ƒ‹ƒC‘̈ޏkÇ(DRPLA)‚Ì1–UŒŸ—áBMBˆãŠwŽA45: 457-458, 1997. Œˆä‰p‰îA–k‘ºG–¾AŠªŸº—²•vA’†“‡FA•ŸŒ´M‹`F•a•Ï•”‚É”äŠr“Iˆê’v‚µ‚ăIƒŠƒSƒfƒ“ƒhƒƒOƒŠƒA“àšn‹â«••“ü‘̂̏oŒ»‚ð”F‚ß‚½ƒIƒŠ[ƒu‹´¬”]ˆÞkÇ‚Ì1–UŒŸ—áBMBˆãŠwŽA45: 461-462, 1997. Miki A, Nakajima T, Hasebe H, Abe H. :Related Articles Functional magnetic resonance imaging of visual function in postpapilledema optic atrophy.J. Neuroophthalmol., 17(4):223-5.1997. •ŸŒ´M‹`FLeigh”]ÇBKey Words 1998-'99•Ï«Ž¾Š³i –ì”ü–MA–ö‘òM•vA’†–썡Ž¡•ÒjAP.198-199, 1997.

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