81. NORD - National Organization For Rare Disorders, Inc. BlochSiemens Incontinentia Pigmenti Melanoblastosis Cutis Linearis; Bloch-Siemens-SulzbergerSyndrome; bloch-sulzberger syndrome; IP; Pigmented Dermatosis, http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Incontinentia

82. Science's STKE -- Sign In NEMO mutants that impair NFkB signaling are linked to several human diseases,including IP (bloch-sulzberger syndrome), ectodermal dysplasia (ED), http://stke.sciencemag.org/cgi/cm/stkecm;CMC_7133?view=print

83. Part 29. Disorders Of The Eye - KMLE: ¼Ò¾Æ°ú ³Ú½¼(Nelson) Á¤¸®Áý Translate this page medulloepithelioma, massive retinal gliosis, retinal pseudotumor of Norrie disease,pseudoglioma of the bloch-sulzberger syndrome, retinal dysplasia, http://www.kmle.co.kr/nelsonview.php?view=Part 29. Disorders of The Eye.htm

84. JMG Online -- Table Of Contents (30 [1]) Incontinentia pigmenti (blochsulzberger syndrome) SJ Landy and D Donnai J MedGenet 1993; 30 53-59. The rapid analysis of dystrophin gene deletions shows http://jmg.bmjjournals.com/content/vol30/issue1/

HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH TABLE OF CONTENTS Author Keyword(s) Vol Page [Advanced] Only Abstracts available for this issue Other Issues: January 1993 (Volume 30, Number 1). [Index by author] Find articles in this issue containing these words: [Search ALL Issues] To see an article , click its [Full Text] link. To review many abstracts , check the boxes to the left of the titles you want, and click the 'Get All Checked Abstract(s)' button. To see one abstract at a time , click its [Abstract] link. Articles The morbid anatomy of the human genome: chromosomal location of mutations causing disease VA McKusick and JS Amberger J Med Genet 1993; 30: 1-26. [Abstract] The clinical features of spondyloepiphyseal dysplasia congenita resulting from the substitution of glycine 997 by serine in the alpha 1(II) chain of type II collagen WG Cole, RK Hall, and JG Rogers J Med Genet 1993; 30: 27-35.

85. AJNR -- Sign In Page Incontinentia pigmenti (blochsulzberger syndrome) with cerebral malformation.Dev Med Child Neurol 1968;10168–174Medline. Aradhya S, Nelson DL. http://www.ajnr.org/cgi/content/full/26/6/1580

HOME HELP FEEDBACK SUBSCRIPTIONS ... SEARCH QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription to American Journal of Neuroradiology Online. Full Text Diffuse Cortical Necrosis in a Neonate with Incontinentia Pigmenti and an Encephalitis-Like... Wolf et al. AJNR Am J Neuroradiol. This Article Abstract Figures Only Full Text (PDF) ... Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager PubMed PubMed Citation Articles by Wolf, N. I. Articles by Rating, D. To view this item, select one of the options below: Sign In User Name Sign in without cookies. Can't get past this page? Help with Cookies. Need to Activate? Password Forgot your user name or password? Purchase Short-Term Access Pay per Article - You may access this article (from the computer you are currently using) for 7 days for US$10.00 Pay for Admission - You may access all content in American Journal of Neuroradiology Online (from the computer you are currently using) for 7 days for US$25.00.

86. Syndrome DB - Table Of Contents BlochSiemens syndrome bloch-sulzberger melanoblastoma bloch-sulzbergersyndrome Bohring syndrome Bourneville disease Bourneville syndrome http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_b.html

Multiple Congenital Anomaly/Mental Retardation Syndromes Table of Contents Return to Entry Page A B C ... Z B Baller-Gerold syndrome (BGS) Bannayan syndrome Bannayan-Riley-Ruvalcaba syndrome (BRRS) Bannayan-Zonana syndrome (BZS) ... U.S. National Library of Medicine , 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health Privacy Accessibility Last updated: 20 November 2001

87. Syndrome, Bloch-Sulzberger Definition - Medical Dictionary Definitions Of Popula Online Medical Dictionary and glossary with medical definitions. http://www.medterms.com/script/main/art.asp?articlekey=5619

88. AllRefer Health - Incontinentia Pigmenti Syndrome (Bloch-Sulzberger's Disease) I Incontinentia Pigmenti syndrome (blochsulzberger s Disease) information centercovers definition, alternative names, Overview, Causes, Risk Factors, http://health.allrefer.com/health/incontinentia-pigmenti-syndrome.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health Incontinentia Pigmenti Syndrome Alternate Names : Bloch-Sulzberger's Disease Definition Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Incontinentia Pigmenti on the Leg Incontinentia Pigmenti on the Leg Jump to a section Definition Prevention Treatment Expectations or Prognosis ... Calling Your Health Care Provider Topics that might be of interest to you Cataract Mental Retardation Strabismus Other Topics Central Nervous System Genetic Counseling and Prenatal Diagnosis Genetics Hair Loss ... Walking/Gait Abnormalities From Our Sponsors: A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's

89. AllRefer Health - Incontinentia Pigmenti Syndrome (Bloch-Sulzberger's Disease) Incontinentia Pigmenti syndrome (blochsulzberger s Disease) information centercovers causes, prevention, symptoms, diagnosis, treatment, incidence, http://health.allrefer.com/health/incontinentia-pigmenti-syndrome-info.html

AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Web health.allrefer.com You are here : AllRefer.com Health Incontinentia Pigmenti Syndrome Incontinentia Pigmenti Syndrome Definition Prevention Treatment Expectations or Prognosis ... Go To Main Page Alternate Names : Bloch-Sulzberger's Disease Definition Incontinentia pigmenti syndrome is an inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Incontinentia Pigmenti on the Leg Incontinentia Pigmenti on the Leg Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation. Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough or verrucous papules. Eventually, these papules clear but leave damaged hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear.

90. ► Incontinentia Pigmenti Syndrome Alternative Names. blochsulzberger s disease. Causes, incidence, and risk factors.Incontinentia pigmenti syndrome (IPS) is inherited as a dominant http://www.umm.edu/ency/article/001583.htm

var MenuLinkedBy='AllWebMenus [2]', awmBN='530'; awmAltUrl=''; Disease Nutrition Surgery Symptoms Injury ... Encyclopedia (English) Toggle English Spanish Incontinentia pigmenti syndrome Overview Symptoms Treatment Prevention Definition: An inherited disorder that causes unusual blistering of the skin followed by increased pigmentation. Alternative Names: Bloch-Sulzberger's disease Causes, incidence, and risk factors: Incontinentia pigmenti syndrome (IPS) is inherited as a dominant X-linked trait . Almost all cases are among females and the condition may be lethal in males. IPS may also arise as a spontaneous mutation. Infants with IPS are born with blistery (vesicular) lesions which appear as streaks. These lesions heal as rough or verrucous papules. Eventually, these papules clear but leave damaged hyperpigmented (too much pigment) skin behind. After several years, the skin returns to normal. In some adults, whorls and streaks of faint hypopigmentation (less pigment than normal) may appear. Most people with IPS also have other problems including abnormal teeth

91. Veröffentlichungen Von Universitätsangehörigen Translate this page ua Incontinentia pigmenti (bloch-sulzberger-syndrome) Case Report and DifferentialDiagnosis to Related Dermato-Ocular syndromes. http://www.uni-saarland.de/z-einr/ub/uni-veroeff/B99/f4_2.htm

Jahresbibliographie 1999 FR 4.2 - Augenheilkunde (29.05.00) Bohlender, Tanja - u.a.: Patientendarstellung: Malignes Melanom der Karunkel. - In: Klin. Mbl. Augenheilkd, 215 (1999), Suppl. 9, 9 Gantenbein, Claude - u.a.: An oculocutaneous presentation of essential progressive telangiectasia. - In: British Journal of Dermatology, 140 (1999), S. 969-970 Hille, Konrad Jurin-Bunte, Bernadette - u.a.: Incontinentia pigmenti (Bloch-Sulzberger-Syndrome): Case Report and Differential Diagnosis to Related Dermato-Ocular Syndromes. - In: Ophthalmologica, 213 (1999), S. 63-69 Krause, Mathias - u.a.: Ablation of Vitreous Tissue with Erbium: YAG-Laser. - In: Invest. Ophthalmol. Vis. Sci, 40 (1999), S. 1025-1032 - u.a.: Sharp or blunt tipped needles for retrobulbar anaesthesia. - In: Anaesthesia, 54 (1999), S. 86 Palmowski, Anja Pfau, Britta - u.a.: Ocular Changes in Mucopolysaccharidosis IV A (Morquio A Syndrome) and Long-Term Results of Perforating Keratoplasty. - In: Ophthalmologica, 213 (1999), S. 200-215 Ruprecht, Klaus Wilhelm Scherer, Volker

92. Siemens' Syndrome I (www.whonamedit.com) Siemens syndrome I A familial form of keratosis involving the face, neck, this syndrome resembles incontinentia pigmenti (Bloch Sulzberger syndrome). http://www.whonamedit.com/synd.cfm/1057.html

Home List categories Eponyms A-Z Biographies by country ... Contact Whonamedit.com does not give medical advice. This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A recommendation: Hypography is an open community about science and all things related Siemens' syndrome I Also known as: Touraine’s polykeratosis Synonyms: Congenital ectodermal defect syndrome, congenital polykeratosis, follicularis syndrome, ichtyosis congenita, Keratosis follicularis acneiformis Typ Siemens (German), keratosis follicularis spinulosa decalvans, keratosis follicularis spinulosa decalvans cum ophiasis, keratosis multiformis, keratosis multiformis idiopathica Siemens, melanosis corii degeneration, melanosis corii degenerativa (Siemens). Associated persons: Hermann Werner Siemens Albert Touraine Description: A familial form of keratosis present from birth. It involves the face, neck, forearms, ears, palms and soles, and backs of the hands, and is associated with loss of the eyebrows, eyelashes, and beard, thickening of the eyelids, blepharitis, ectropion, and corneal abnormalities (punctate lesions). Photophobia and lacrimation are the early symptoms. Only males show the complete picture, the heterozygotous carriers, partial expression. Inheritance is X-linked, but autosomal dominant transmission has also been reported.

93. Birth Disorder Information Directory - I Incontinentia Pigmenti (IP, Bloch Sulzberger syndrome). List of Sites. Indifferenceto Pain (Congenital Analgesia). INDIFFERENCE TO PAIN CONGENITAL http://www.bdid.com/defecti.htm

HOME I I-Cell Disease (Mucolipidosis, Type II) List of Sites ICE Syndrome (Ichthyosis-Cheek-Eyebrow Syndrome, Sidransky Feinstein Goodman Syndrome) ICHTHYOSISCHEEKEYEBROW SYNDROME ICF Syndrome See Centromeric Instability Immunodeficiency Syndrome Ichthyosiform/Ichthyosis List of Sites -Alopecia-Eclabion-Ectropion-Mental Retardation Syndrome ICHTHYOSIS WITH ALOPECIA, ECLABION, ECTROPION, AND MENTAL RETARDATION -Camptodactyly Syndrome See Camptodactyly-Ichthyosis Syndrome -Cheek-Eyebrow Syndrome See ICE Syndrome -Hepatosplenomegaly-Cerebellar Degeneration Syndrome ICHTHYOSIS, HEPATOSPLENOMEGALY, AND CEREBELLAR DEGENERATION -Spastic Neurologic Disorder-Oligophrenia Syndrome See Sjogren-Larsson Syndrome with Large Keratohyalin Granules in the Skin ICHTHYOSIS-MENTAL RETARDATION SYNDROME WITH LARGE KERATOHYALIN GRANULES IN THE SKIN Erythroderma -Corneal Involvement-Deafness Syndrome See KID Syndrome Congenital (Brocq) Also see Netherton Syndrome Bullous Form (Epidermolytic Hyperkeratosis) Bullous ichtyosiform erythroderma congenita BULLOUS ERYTHRODERMA ICHTHYOSIFORMIS CONGENITA OF BROCQ Nonbullous Form Type 1 (Nonbullous Congenital Ichthyosiform Erythroderma, Type I)

94. Incontinentia Pigmenti : Sites Et Documents Francophones Naevus chromatophore héréditaire ; syndrome de Bloch Sulzberger . http://www.chu-rouen.fr/ssf/pathol/incontinentiapigmentia.html

Incontinentia pigmenti Synonyme(s) CISMeF incontinentia pigmenti type 1 ; incontinentia pigmenti type 2 . Synonyme(s) MeSH Bloch Sulzberger, syndrome ; Dermatose pigmentaire éclaboussures ; Naevus chromatophore héréditaire ; Syndrome de Bloch Sulzberger Ne pas confondre avec troubles de la pigmentation Arborescence(s) incontinentia pigmenti incontinentia pigmenti maladies de la peau et du tissu conjonctif maladies et malformations congénitales, héréditaires et néonatales Position du mot-clé dans l' (les) arborescence(s) : Vous pouvez consulter toutes les ressources ou seulement les principales ou utiliser l' outil de recherche les recommandations les documents concernant l' enseignement les documents destinés aux patients Ou consulter ci-dessous une sélection des principales ressources : patient Incontinentia pigmenti [Par Dr Blanchet-Bardon C. Site éditeur Orphanet base de données sur les maladies rares et les médicaments orphelins. Direction Générale de la Santé / INSERM ; signes de la maladie, sites internet, dysmorphologie, conseil génétique, génodermatoses, laboratoires de diagnostic, projets de recherche en cours, associations de patients ; pays : France ; langue : français ; format : html ; accès : gratuit ; non parrainé ; daté de : 2002 ; visité le : 17/09/2003]. mots clés : conseil génétique *incontinentia pigmenti incontinentia pigmenti /diagnostic maladies rares ... signes et symptômes type : *association patients *structure recherche *texte IPF - association Incontinentia Pigmenti France [Site éditeur

95. Pakistan Pediatric Association - Jornal Section - Full DUBIN JOHNSON syndrome Abstract Detail. INCONTINENTIA PIGMENTI (BlochSulzbergersyndrome) A case report Abstract Detail. Students Corner. http://www.ppa.org.pk/journal/main/backissueindex.asp?article_volume=21&article_

96. Blackwell Synergy - Cookie Absent Particularities of clinic expression in a case of Bloch Sulzberger syndrome.L Solovastru* +, T Taranu +, C Amalinei , T Taranu§ http://www.blackwell-synergy.com/doi/abs/10.1111/j.1468-3083.2005.01269.x

Home An Error Occurred Setting Your User Cookie A cookie is a small amount of information that a web site copies onto your hard drive. Synergy uses cookies to improve performance by remembering that you are logged in when you go from page to page. If the cookie cannot be set correctly, then Synergy cannot determine whether you are logged in and a new session will be created for each page you visit. This slows the system down. Therefore, you must accept the Synergy cookie to use the system. What Gets Stored in a Cookie? Synergy only stores a session ID in the cookie, no other information is captured. In general, only the information that you provide, or the choices you make while visiting a web site, can be stored in a cookie. For example, the site cannot determine your email name unless you choose to type it. Allowing a web site to create a cookie does not give that or any other site access to the rest of your computer, and only the site that created the cookie can read it. Please read our for more information about data collected on this site.

97. Contents Of  VOLUME 5; NUMBER 2 (OCTOBER) 1998 (Bloch Sulzberger syndrome) (Bloch Siemen s syndrome). Mohammed Mohy EI-DinSelim ,Tayseer AI-Saad, Mohammed Abu Laban ,Fadila AI-Rawi A, 52-55 http://www.geocities.com/HotSprings/Spa/8355/vol_6_2.html

Contents of   VOLUME 6; NUMBER 2 (OCTOBER) 1999 Contents Page UVA PHOTOTHERAPY OF ATOPIC DERMATITIS: An experience in Qatar and review of literature. Ahmad Hazem Takiddin, Mohammed Mohy El-Din selim, Hala Mohammed Ezzat Al Homsy, Adel M Kamal An overlap of infantile systemic hyalinosis and Juvenile hyaline fibromatosis: A report of two sisters affected (and review of the literature). Ghalia Al- Thani, Mohammed Mohy El-Din Selim, Hazem Abdulrahman THE PATHOGENESIS OF HYPOPIGMENTED PSORIASIS: Ultrastructural Study of Melanocytes in Psoriatic Lesions . Adel M. Kamal NON VENEREAL TREPONEMATOSES YAWS, BEJEL AND PINTA. Clinical Review and Management . SalimAbdul RahmanAl-Harmozi, Hamda lbrahim Al- Ansari THE TREATMENT OF PERSISTENT AND RECURRENT URETHRITIS IN MALES . M. N. Kamel. EVALUATION OF DIFFERENT METHODS FOR THE TREATMENT OF COMMON WARTS. Abd El Aziz El-Taweel, Ahmed Abd El-Wahab, Adel Kamal, Adel Ali Ali  CAN OPIUM CAUSE CHRONIC ARSENIC POISONING? Simin S. Meymandi, Shahriar Dabiri, Bahram Azadeh

98. DEUTSCH-SPRACHIGE OPHTHALMOPATHOLOGEN (DOP): Originalbeiträge 1999 incontinentia pigmenti (Bloch - Sulzberger syndrome). http://dog-patho.dog.org/abstract99/dop_24.html

DOP Originalbeiträge XXVII. Jahrestagung der Deutschsprachigen Ophthalmopathologen (DOP) am 21. und 22. September 1999, Universitäts Krankenhaus Eppendorf Incontinentia pigmenti U. Schaudig Universitäts Krankenhaus Eppendorf Augenklinik und Poliklinik Martinistrasse 52 20246 Hamburg Hist. Nr.: 19150 Klinische Vorgeschichte: Augenärztliche Erstuntersuchung des Kindes im Alter von 17 Monaten bei eitriger Konjunktivitis. Unkomplizierte Schwangerschaft und Geburt im Gestationsalter von 38 Wochen. Pigmentflecken am Stamm. Pädiatrischerseits sonst keine Besonderheiten. Incontinentia pigmenti bei der älteren Schwester bekannt. Im Alter von zwei Jahren und zehn Monaten dann klinisch auffällige Visusminderung einseitig rechts ohne Schielstellung. Auffällige Weißfärbung der Pupille. Kein Funduseinblick. Differentialdiagnostische Überlegungen (Auflistung nach Unterlagen der beteiligten Augenärzte): congenitale Amotio retinae, zentrales Aderhautkolobom, Papillenanomalie, Retinoblastom, Morbus Coats. Echographisch: Totale Ablatio retinae mit zentraler Trichterbildung.

99. ³¢ÓT§Ó “A pregnancy following preimplantation genetic diagnosis (PGD) for Xlinkedautosomal dominant Incontinentia Pigmenti (Bloch Sulzberger syndrome” Hum. http://www.sinica.edu.tw/zool/chinese/hckou.htm

Hung-Chih Kuo ³¢ÓT§Ó Assistant Research Scientist ¬ã¨s§U§Þ®v 2001, Ph.D. University of London, England 2003-¡¦04 Staff Scientist, Oregon National Primate Research Center; 2000-¡¦03 Postdoctoral Fellow, Oregon National Primate Research Center. As the first step of exploring the potential application of primate ES cells for cellular therapy, drug discovery and biomedical research, we have established strategy for isolating, enriching and characterizing neural, cardiac and pancreatic cells from monkey and human ES cells. We have also derived new ES cell lines from non-human primates to investigate the fundamental cellular and molecular mechanisms governing pluripotency and differentiation of ES cells. The current main objectives of our lab are to (1) Characterize the cellular and molecular events underlying totipotency and pluripotency during preimplantatio development and their implication for pluripotent cell isolation. (2) Use ES cells as an in vitro model for organogenesis, with emphasis on in vitro formation of embryonic hear structure, pancreatic islets and craniofacial tissues. (3) Derivation of germ cells from primate embryonic stem cells. §Ú­Ì¥ç±N§Q¥Î­F­L·F²Ó­M¥h±´°Q¦bÅé¥~¾¹©x¦p¤ßŦ¡A¯Ø®q¡AÀY­±²Õ´¤Îºë²Ó­M§Î¦¨¤§¾÷Âà¡C Therapeutic Cloning and Embryonic Stem Cell Biology Kuo, H.-C., Nauert, B.J., Wolf, D.P., Lester, L.B. ¡§Non-Human Primate ES cells Directed to produce insulin¡¨

100. Http://www.sande.co.jp syndrome ?blue rubber bleb nevus syndrome, http://www.nakayamashoten.co.jp/cgi-bin/menu.cgi?ISBN=4-521-66211-0

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