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Silver-russell Syndrome:     more detail

Silver-Russell Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References by Icon Health Publications, 2004-06-09 Growth Disorders: Achondroplasia, Dwarfism, Acromegaly, Primordial Dwarfism, Psychosocial Short Stature, Midgetville, Silver-russell Syndrome Russell-Silver syndrome: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Paul Johnson, 2005

lists with details

41. SpringerLink: Archives Of Gynecology And Obstetrics - Abstract Volume 265 Issue
    157. case report silverrussell syndrome associated to Mayer-Rokitansky-Kuster-Hausersyndrome, diabetes and hirsutism. J. Bellver  
    http://link.springer-ny.com/link/service/journals/00404/bibs/1265003/12650155.ht
    
    Extractions: ISSN: 1432-0711 (electronic version) Table of Contents Abstract Volume 265 Issue 3 (2001) pp 155-157 (1) Department of Gynecologycal Endocrinology, Hospital Universitario ''La Fe'', Calle Regacho, 8-14, Mislata 46920, Valencia, Spain e-mail: jbellverp@sego.es. Tel.: 011-34-963624399, Fax: 011-34-963694735

42. Publikationen Der Abteilung Medizinische Genetik Tübingen
    Kaiser P, Ranke MB, Eggermann T(1999) Biparental Expression of IGFBP1 and IGFBP3renders their Involvement in the Etiology of silverrussell syndrome unlikely.  
    http://www.uni-tuebingen.de/Klinische_Genetik/publ_1999.html

43. Dwarfism Types And Definitions
    silverrussell syndrome Silver syndrome. See Russell-Silver syndrome.Spherophakia-brachymorphia syndrome. See Weill-Marchesani syndrome.  
    http://www.lpaonline.org/resources_dwarftypes.html

44. •¶Œ£ˆê——
    Kishino T, Tanaka T, Yamada M, Tsutsumi O, Niikawa N, KanekoIshino T, Ishino F.No evidence of PEG1/MEST gene mutations in silver-russell syndrome patients.  
    http://www.ishino.bio.titech.ac.jp/list.html

45. UK Self Help Groups: S
    8961 7795. silverrussell syndrome. contact silver-russell syndromeSupport Group c/o CaF, Tel 020 7383 3555. Single Parents. Care for  
    http://www.ukselfhelp.info/s.htm

46. Newsletter References
    Ranke MB, Lindberg A. Growth hormone treatment of short children born small forgestational age or with silverrussell syndrome results from KIGS (Kabi  
    http://www.aap.org/sections/Endocrinology/references.htm
    
    Extractions: References Botero D, Lifshitz F. Intrauterine growth retardation and long-term effects on growth. Curr Opin Pediatr 11:340-347,1999. Chatelain P, Peretti N, Lapillonne A, Nicolino M, Salle B, et al. New insights into the postnatal growth of infants born "idiopathic' small for gestational age. J Pediatr Endocrinol Metab 14:1515-1519,2001.

47. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE
    SYNDROOM van SILVERRUSSELL silver-russell syndrome RUSSELL-SILVERSYNDROME RUSSELL SYNDROME SILVER SYNDROME RSS. Russell-Silver  
    http://www.vada.nl/medisch/medsim.htm

48. Themen Für DoktorarbeitenInstitut Für Anthropologie Und Humangenetik, Abteilun
    Translate this page Wollmann HA, Kirchner T, Enders H, Preece MA, Ranke MB (1995) Growth and symptomsin silver-russell syndrome review on the basis of 386 patients.  
    http://nero.anatom.uni-tuebingen.de/gk/anlage1_6.html

49. ËÁÍà´ç¡µÍº
    RussellSilver Syndrome (RSS) silver-russell syndrome, Silver Syndrome ? Russell Syndrome.  
    http://www.doolaedek.com/Consult/Doolae_Ans.asp?Q=1679

50. Max Planck Weekly Research Report - Human Biology/Medical Research
    Human Genetics. 6(2)114120, 1998 Mar-Apr. Author Keywords Peg1/mest,silver-russell syndrome, Uniparental disomy, Imprinting.  
    http://www.reports.mpg.de/1998/24/199824_h.htm

51. Max Planck Weekly Research Report - Human Biology/Medical Research
    VM, Wollmann HA, Eggermann T. Author email Address teggermann@post.klinikum.rwth-aachen.deTitle Gene dosage analysis in silver-russell syndrome Use of  
    http://www.reports.mpg.de/2002/05/200205_h.htm

52. Full Listing
    SHINGLES AND PHN, SHPRINTZEN SYNDROME, SHWACHMAN SYNDROME, SIALIC ACID STORAGEDISEASE, SIALIDOSIS, SICKLE CELL, silverrussell syndrome, SINGLE PARENTS  
    http://www.doctor.gp/help/full_listing.htm

53. Medizinische Genetik
    Martinez MJ, Binkert F, Schinzel A, Kotzot D. No Evidence of dup(7)(p11.2p13) insilverrussell syndrome Am J Med Genet 2001 99; 335-337 Schinzel A, Niedrist D  
    http://www.medgen.unizh.ch/Pages/Pub.html
    
    Extractions: Angelman Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Chromosomenuntersuchung cystische Fibrose FISH-Schnelltest fragiles X Syndrom Klinefelter Syndrom Myotone Dystrophie Steinert Prader-Willi Syndrom Rett Syndrom Silver-Russel Syndrom (UPD7) Subtelomer-FISH Turner Syndrom Williams Syndrom - Zytogenetik - Molekulargenetik Albright Syndrom Angelman Syndrom Bardet-Biedl Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Cystische Fibrose Chorea Huntington Fragiles X Syndrom Miller-Dieker Syndrom Myotone Dystrophie Steinert Neuralrohrdefekte Neurofibromatose Prader-Willi Syndrom Rett Syndrom Spinale Muskelatrophie Smith-Magenis Syndrom Uniparentale Disomie Williams Syndrom Martinez M-J, Binkert F, Schinzel A, Kotzot D. No Evidence of dup(7)(p11.2p13) in Silver-Russell Syndrome Am J Med Genet 2001 99; 335-337

54. Medizinische Genetik
    Translate this page Ropers HH, Kalscheuer VM. Evidence against a major role of PEG1/MESTin silver-russell syndrome. Eur J hum Genet (1998) 6, 114-120.  
    http://www.medgen.unizh.ch/Pages/Pub98.html
    
    Extractions: Angelman Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Chromosomenuntersuchung cystische Fibrose FISH-Schnelltest fragiles X Syndrom Klinefelter Syndrom Myotone Dystrophie Steinert Prader-Willi Syndrom Rett Syndrom Silver-Russel Syndrom (UPD7) Subtelomer-FISH Turner Syndrom Williams Syndrom - Zytogenetik - Molekulargenetik Albright Syndrom Angelman Syndrom Bardet-Biedl Syndrom Beckwith-Wiedemann Syndrom CATCH-22 Cystische Fibrose Chorea Huntington Miller-Dieker Syndrom Myotone Dystrophie Steinert Neuralrohrdefekte Neurofibromatose Prader-Willi Syndrom Rett Syndrom Spinale Muskelatrophie Smith-Magenis Syndrom Uniparentale Disomie Williams Syndrom 22q11.2 deletions in a series of patients with non-selective congenital heart defects: incidence, type of defects and parental origin. Clin Genet 1998;53:63-69 Robinson WP, Dutly F, Nicholls RD, Bernasconi F, Penaherrera M, Michaelis RC, Abeliovich D, Schinzel AA. The mechanisms involved in formation of deletions and duplications of 15q11-q13. J Med Genet 1998; 35: 130-136 Dutly F, Balmer D, Baumer A, Binkert F, Schinzel A. Isochromosomes 12q und 9p: parental origin and possible mechanisms of formation.

55. UCL Division Of Paediatric And Adolescent Endocrinology
    10% of patients with silverrussell syndrome have maternal uniparental disomy ofchromosome 7 which implies that maternally imprinted genes are involved with  
    http://www.ucl.ac.uk/medicine/endocrinology/res.html
    
    Extractions: Synopsis of Current Research a) Developmental Endocrinology and Growth Regulation Molecular embryology of somatotroph function in the human anterior pituitary focussing on the identification of the cause of congenital panhypopituitarism. We have described the cascade of homeobox genes in the condition of septo-optic dysplasia (SOD) in man, a (relatively) common cause of congenital panhypopituitarism in our clinic Identification of the imprinted gene(s) on human chromosome 7 responsible for intrauterine growth retardation and the role of the insulin-life growth factor axis in this syndrome. 10% of patients with Silver-Russell syndrome have maternal uniparental disomy of chromosome 7 which implies that maternally imprinted genes are involved with the SRS phenotype. Four candidate genes have been identified and are now being studied in detail. There is evidence from samples taken by cordocentesis and at birth of perturbatons in the IGF axis in IUGR but the mechanisms and effects are unclear. The role of the DAX-1 gene in the development of the adrenal cortex and of gonadotrophin-releasing hormone (GnRH).

56. S
    ShyDrager Syndrome; @ Sickle Cell Disease; @ silver-russell syndrome;@ Sinusitis; @ Sitosterolemia; @ Skin Disorders; @ Sleep Apnea;  
    http://www.ad.com/Health/Conditions_and_Diseases/S/

57. Error Page
    Translate this page MALADIE silver-russell, syndrome de, CIM Q87.17, Le syndrome desilver-russell associe un retard de croissance débutant pendant  
    http://orphanet.infobiogen.fr/Site/Exp.stm?Lng=FR&Expert=813

58. VADA GEZONDHEID En ZIEKTE - HEALTH And DISEASE
    See also RHIZOMELIC CHONDRODYSPLASIA PUNCTATA See also RUSSELLSILVER syndromeSee also SYNDROOM van silver-russell SILVER- RUSSELL syndrome See also  
    http://www.vada.nl/medisch/meddvz.htm
    
    Extractions: Angst- en Paniekstoornissen Angststoornissen - Obsessief-compulsieve stoornis OCD Vriendenkring ... Obsessive-Compulsive Disorders (OCD) page Functionele Neurochirurgie: Dwarslaesie Stichting De Schakel - vereniging van en voor mensen met een dwarslaesie Dwarslaesie: Uitleg Dwarslaesie Links See also: BOTZIEKTES BONE DISEASES

59. Misa-e
    My parents were told I have a very rare type of disease called RussellSilver( or sometimes called silver-russell) syndrome. They  
    http://www1.accsnet.ne.jp/~nagakawa/misa-e.html
    
    Extractions: Russell-Silver Syndrome January 12, 2000 Hello, everybody!!! Welcome to Misa's Home Page!!! My name is Misa. And My mom and Junko are friends. Starting from today, I want to talk about myself and the disease. My mom is a nurse and very positive in learning about the syndrome I am suffering from. So, I think I may write a little and my mom is going to write a lot more eventually. I am now 5 years and 10 months old. But I am only 89cm tall. I couldn't grow right when I was in my mommy's tummy. And also after I was born, I couldn't drink or eat any food like other normal babies. I had a lot of difficulty in taking food. My parents were told I have a very rare type of disease called Russell-Silver ( or sometimes called Silver-Russell) Syndrome. They say there only 33 cases reported in Japan so far. My mom and dad seem to feel O.K. now in accepting what I am. But still they are thinking the way how I can grow a little bit better. I think it's quite all right with this height. But I sometimes feel sad when somebody calls me "Shortie!" Today I came to Aunt Junko's house. She let me play with her computer and I really liked it. I particularly liked Kabu-san's Home Page linked through Kayuchan-chi's Home Page. Kabu-san made his page like a music shop. I kept listening to the theme songs of TV animation while Mom and Junko were talking. I've learned how to use the mouse to click. I wish I had a PC of my own!

60. Ask Jeeves: Search Results For "Types Of Genetic Disorders"
    http//habitant.org/genetics.htm 5. RusselSilver syndrome Russell-Silver syndrome,(RSS) silver-russell yndrome, Silver syndrome, Russell syndrome http//www  
    http://webster.directhit.com/webster/search.aspx?qry=Types Of Genetic Disorders

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