61. Pathology Of The Skin: With Clinical Correlations, 2nd Ed Reticulate pigmented anomaly of the flexures(Dowlingdegos disease) 2.32.Pseudoxanthoma elasticum (Grijnblad-Strandberg syndrome) 2.33. http://www.hanilmed.com/division/titleimg/patholoy/63.html

Pathology of the Skin: With Clinical Correlations, 2nd Ed Author Phillip H. McKee Publisher Mosby Pub Year Page 848 pp., 3356 ills color. Cover hard cover ISBN List Price US$345. Our Price US$310. Price KR£Ü450,000 Our Price KR£Ü405,000 Home Search Order Newbook ... e-meil Preface This dualistic approach which formed the basis for the first edition has been expanded in the second edition, which includes over 3000 colour pictures that extensively illustrate each entity. The text is substantially enlarged, aiming to provide a completely comprehensive text including over 100 new entities, more dermatological rarities with relevant histology, and increased AIDS-related skin pathology. In addition to conventional histopathology and immunofluorescence, greater space has been devoted to Immunohistochemistry and, when appropriate, to the application of molecular biological techniques. The reference lists have not only been updated, they have been greatly expanded and all references are now cited in the text. It is hoped that this new approach will provide an invaluable resource for literature in dermatopathology. The second edition has taken more than three years to write. If, as hoped, it is of help to pathologists when faced with difficult or unusual conditions, then the time will have been well spent.

62. Privattandvård I Örebro, Tandläkaren Michel Deaibes, Sjukdomslista På Engels Deafblindness. Deafness. degos disease. Dementia. Dengue Fever. DepersonalizationDisorder. Kleptomania. Klinefelter Syndrome. Kohlmeier degos disease. Krabbe Disease.L. http://www26.brinkster.com/privtand/sjuk.htm

A Aarskog Syndrome Aase Syndrome Abetalipoproteinemia Ablepharon-Macrostomia Syndrome Achilles Tendonitis Achondroplasia Acoustic Neuroma Acromegaly Activated Protein C Resistance Acute Idiopathic Polyneuritis ADD and ADHD Addiction and Recovery Addison's Disease Adiposis Dolorosa Adjustment Disorders Adrenoleukodystrophy Agnosia Agoraphobia Aicardi Syndrome AIDS Alagille Syndrome Albinism Alcoholism Alexander Disease Alkaptonuria Allergies Alopecia Alpers' Disease Alpha1 Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia Altophobia Alzheimer's Amblyopia Amputee Amyloidosis Amyoplasia Congenita Amyotrophic Lateral Sclerosis Anal Fissures Anemia Anencephaly Aneurysm Angina Pectoris Anophthalmos Anorexia Anosmia Anterior Knee Pain Syndrome Antiphospholipid Syndrome Anxiety Aortic Valve Disease Apert Syndrome Aphasia Aplastic Anemia Apnea, Sleep Appendicitis Arrhythmia Arteriohepatic Dysplasia Arthritis Arthrogryposis Asbestosis Asperger's Syndrome Aspergillosis Asthma Atherosclerosis Athlete's Foot Atrial Fibrillation Attachment Disorder Attention Deficit Disorder Autism Auto Immune Disorders Aviophobia Aviatophobia B Bacillary Angiomatosis Back Disorders Bad Breath Balanitis Baldness Barth Syndrome Bassen Kornzweig Syndrome Batten Disease Beckwith-Wiedemann Syndrome Behcet's Syndrome Bell's Palsy Benign Breast Lumps Benign Prostatic Hyperplasia Berger's Disease Beriberi Beryllium Disease Besnier Boeck Disease Betalipoprotein Deficiency Disease

63. JAMA -- Page Not Found Incredibly thorough, the book also covers more extraordinary causes of stroke,such as Kohlmeierdegos disease, pseudoxanthoma elasticum, progeria, and http://jama.ama-assn.org/issues/v287n12/ffull/jbk0327-4.html

Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery MSJAMA Science News Updates Meetings Peer Review Congress The page you requested was not found. The JAMA Archives Journals Web site has been redesigned to provide you with improved layout, features, and functionality. The location of the page you requested may have changed. To find the page you requested, click here HOME CURRENT ISSUE PAST ISSUES ... HELP Error 404 - "Not Found"

64. Browsing Health Conditions And Diseases D Category Dandy Walker Syndrome De Lange Syndrome Deafblindness Deafness degos diseaseDementia Dengue Fever Depersonalization Disorder Depression Dercum Disease http://www.uksprite.com/search/search/Health/Conditions_and_Diseases/D/

/* CSS Menu highlight- By Marc Boussard (marc.boussard@syntegra.fr) Modified by DD for NS4 compatibility Visit http://www.dynamicdrive.com for this script */ var ns4class='' WebSearch Low-cost advertising at UKSprite Join Login @UK.Sprite Home Latest Headlines UK Weather World Weather ... UK Travel Guide Fun TV Guide Lotto e-Greetings Mobile Fun Communicate Email Login Get Free Email Free Text Messages Lifestyle Horoscopes Dating Recipes Health Shop DVD's Books Videos More... Deals Auctions Classified Ads Site Map Browsing: Health Conditions and Diseases D Top Health Conditions and Diseases D A B C D ... Z Categories: Dandy Walker Syndrome De Lange Syndrome Deafblindness Deafness ... Dystonia Musculorum Deformans Last update: 20:31 PT, Sunday, September 22, 2002 Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Latest UK Headlines More UK soldier killed in ambush A UK soldier has been killed during operations in southern Iraq, while in Basra a fierce battle rages. Jobs warning over National Insurance One in five firms is planning to get rid of staff to pay for the rise in National Insurance contributions, a business lobby says. Killer father found dead Steven Wilson - jailed for life for the murder of his two young sons last week - is found hanged in his cell.

65. Open Directory - Health: Conditions And Diseases: D 9); Deafness@ (116); degos disease@ (4); Dementia@ (60); Dengue Fever@(10); Depersonalization Disorder@ (9); Depression@ (269); Dercum http://www.mptdo.com/Health/Conditions_and_Diseases/D/

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66. Developmental And Genetic Diseases Lumbosacral agenesis; Maceration; Mal de Meleda; Malignant atrophicpapulosis (degos disease); MardenWalker syndrome; Marfan syndrome; http://www.gfmer.ch/Selected_images/Developmental_genetic_diseases.htm

Geneva Foundation for Medical Education and Research Home About Search Medical education ... Selected medical images Developmental and genetic diseases 5q- syndrome Aarskog syndrome Abnormal nuchal fold Acanthosis nigricans ... Print this page Edited by Aldo Campana, March 13, 2003

67. A Listing Of Disorders Darier Disease. De Barsy Syndrome. De Santis Cacchione Syndrome. degos disease.Dejerine Sottas Disease. Depression. Dercum Disease. Dermatomyositis. Devic Disease. http://medschool.umaryland.edu/BTBank/Family/Disorders_D.htm

Brain and Tissue Bank University of Maryland, Baltimore D Dandy Walker Malformation Darier Disease De Barsy Syndrome De Santis Cacchione Syndrome Degos Disease Dejerine Sottas Disease Depression Dercum Disease Dermatomyositis Devic Disease Dextrocardia with Situs Inversus Diabetes, Insulin Dependent Diaphragmatic Hernia Diastrophic Dysplasia Diencephalic Syndrome DiGeorge Syndrome Dilatation of the Pulmonary Artery, Idiopathic DOOR Syndrome Down Syndrome Dracunculosis Drash Syndrome Duane Syndrome Dubin Johnson Syndrome Dubowitz Syndrome Duhring Disease Duodenal Atresia or Stenosis Dyggve Melchior Clausen Syndrome Dysautonomia, Familial Dyschondrosteosis Dyskeratosis Congenita Dyslexia Dysphonia, Chronic Spasmodic Dysplasia, Epiphysealis Hemimelica Dysplasia, Fibrous Dysplastic Nevus Syndrome Dystonia Dystonia, Blepharospasm Dystonia, Torsion Dystrophy, Asphyxiating Thoracic Dystrophy, Myotonic

68. Clinical Case cells (Fig.1), the pericytes and the macrophages descibedfot he erythematous lupusas it also shows the cylinders mentioned in the Case 2 (degos disease). http://www.dermocosmos.com/ingles/Clinical_Cases/solen3.htm

rd CLINICAL CASE This is a progressive dermatomyositis in a child, with its clinical features; muscular pain when walking or when being palpated, difficulties in climbing stairs, in combing the hair, in eating, etc. with typical and also progressive cutaneous signs of periorbital erythemas that slightly appear in some other spots, turn to purple with reticular livedo and zones with white atrophia. The laboratory findings confirm the muscular affection and the histopathology is quiet recognizable for its leucocytic vasculitis. It is also very aggressive considering the emarkable epifdermic lesion we can observe and that let us think, at the very beginning, to a viral infection. Electronic microscopy puts into relief, once again, the intracytoplasmic tubuloreticular structures of the enothelial cells (Fig.1), the pericytes and the macrophages descibedfot he erythematous lupus as it also shows the cylinders mentioned in the Case 2 (Degos Disease). The first time those cylinders were detected was in a dermatomyositis (Fig.2). They were then found again in the Degos Disease, in the T cells leucemia and in AIDS. There is certainly an etiopathologic explanation for this phenomenon as far as the structures are themselves a degeneration of the endopasmic reticle with a strong predominance in some diseases, in certain cells, at some stage of evolution. These ultrastructural markers should not be neglected during viral investigations. Fig.1

69. Dowling-Degos´ Disease Beim Verarbeiten des URL ist ein Fehler aufgetreten. Bitte klicken Sie hier um zur Startseite zurückzukehren. http://www.dermis.net/bilddb/diagnose/englisch/i009605.htm

While processing the URL an error encountered. Please click here to return home. Beim Verarbeiten des URL ist ein Fehler aufgetreten. Bitte klicken Sie hier um zur Startseite

70. PaperChase Search Page (custom) An atypical paediatric case of malignant atrophic papulosis (Kohlmeierdegosdisease). degos'disease who died as a result of intestinal involvement. http://www.paperchase.com/docs/R1603/F205201/B16.htm

Reference 46 of 210) Flag for Printing An atypical paediatric case of malignant atrophic papulosis (Kohlmeier-Degos disease). Barabino A, Pesce F, Gatti R, Colotto P, Nobili F, Colacino R, Giampalmo A Eur J Pediatr (1990 Apr) 149(7):457-8 ISSN: 0340-6199 Arterial Occlusive Diseases Cerebral Ischemia Malabsorption Syndromes Case Report Child Fingers Human Male Raynaud's Disease Skin Ulcer Abstract A new case of malignant atrophic papulosis (Kohlmeier-Degos disease) is reported. Vascular symptoms began at 17 months of age with cerebral ischaemia and progressive involvement of fingers and toes with torpid ulcers and apical necrotic amputations. At 6 years of age he developed chronic intestinal ischaemia with malabsorption and a new cerebral attack; in spite of Top of Abstract anti-aggregant therapy the disease progressed and he died 7 months after diagnosis from a third cerebral ictus. Since the typical skin lesions of the disease were absent, the diagnosis was made on the basis of a pathological pattern of an occluded biopsied artery. The elder brother presents clinical and instrumental vascular involvement without cutaneous lesions and could be slightly affected. III Paediatric Department G Gaslini Scientific Institute Genova Italy.

71. ILDS: ICD-10 - By Code [I00 - I972] I77800 Papulosis malignant atrophic, I77800 disease degos, I77800 degosdisease, I77800 degos syndrome, I77800 Kohlmeier degos syndrome, http://www.ilds.org/icd10/bycode/I.html

Application to Dermatology of ICD-10 Alphabetized by ICD Code starting with I: Return to Alphabetical listing... ICD Code: Disorder Rheumatic fever Fever rheumatic Arteriosclerosis of arteries of extremities Atherosclerosis of arteries of extremities Atherosclerotic gangrene Gangrene atherosclerotic Disease Raynaud's Raynaud's disease Phenomenon Raynaud's Raynaud's phenomenon Raynaud's gangrene Gangrene Raynaud's Buerger's disease Disease Buerger's Thromboangiitis obliterans Acrocyanosis Nodular erythrocyanosis Erythrocyanosis with nodules Erythrocyanosis nodular Erythrocyanosis Erythermalgia Erythralgia Erythromelalgia Mitchell's syndrome Syndrome Mitchell's Livedo racemosa Livedo reticularis Livedo annularis Arteriovenous aneurysm acquired Aneurysm arteriovenous acquired Pseudo Kaposi sarcoma Stewart Blufarb syndrome Syndrome Stewart Blufarb Syndrome Degos Malignant atrophic papulosis Syndrome Kohlmeier Degos Papulosis malignant atrophic Disease Degos Degos disease Degos syndrome Kohlmeier Degos syndrome Telangiectasia hereditary hemorrhagic Hereditary hemorrhagic telangiectasia Osler Weber Rendu syndrome Rendu Osler syndrome Syndrome Osler Weber Rendu Syndrome Rendu Osler Angiomatosis Osler Weber Rendu Spider telangiectasia Spider nevus Spider arterial Spider angioma Nevus stellar Nevus spider Nevus araneus Angioma spider Telangiectasia spider Arterial spider Senile hemangioma Senile angioma Hemangioma senile Angioma senile Arborising telangiectasia Telangiectasia arborising Generalised essential telangiectasia

72. Sfhd - Quelques Aspects De La Contribution De Robert Degos à La Dermatologie Translate this page suffisants. Depuis, le nom de maladie de degos, ou degos's disease ousyndrome dans la littérature anglo-saxonne, est adopté partout. http://www.bium.univ-paris5.fr/sfhd/ecrits/degos.htm

Quelques aspects de la contribution de Robert Degos à la Dermatologie Jean CIVATTE Robert Degos est et restera une des grandes figures de la dermatologie non seulement française mais mondiale: en ce dixième anniversaire de sa mort il n'est que juste de s'en souvenir. Une façon d'évoquer sa mémoire consiste à rappeler, sinon toutes, du moins les princiales affections qu'il a décrites ou dont il a précisé les cadres nosologiques. Certaines maladies portent à juste titre son nom. La principale est la papulose atrophiante maligne. Elle est née le 12 février 1942. Cette évolution fatale est rapportée par les mêmes auteurs le 21 mai 1942 sous le titre "dermatite papulo-squameuse atrophiante (Epilogue)": cette appellation est donc, pour l'instant, conservée pour cette affection qui comporte les mêmes altérations histologiques sur la peau et l'intestin et qui fait discuter, mais pour l'éliminer, un lupus érythémateux aigu, en particulier du fait de l'absence de fièvre. En 1948, R.Degos,J.Delort et R.Tricot présentent devant la Société Médicale des Hôpitaux de Paris un travail sur ce même sujet avec, comme titre, "papulose atrophiante maligne (syndrome cutanéo-intestinal mortel)". Ils utilisent à nouveau ce nom, qui est désormains unaninement accepté, dans un article publié en 1952 dans les Annales de Dermatologie dans lequel ils rappellent leur observation, celle de Tzanck, Civatte et Sidi, et citent un cas présente en juin 1950 par F.P.Merklen et F.Cottenot qu'ils rapprochent du leur, mais sans l'y assimiler faute de renseignements suffisants. Depuis, le nom de maladie de Degos, ou Degos's disease ou syndrome dans la littérature anglo-saxonne, est adopté partout.

73. Robert Degos (1904-1987) several dermatoses, genodermatose en cocardes in 1947, clear cells acanthoma in1962 and especially malignant atrophiant papulosis (degos' disease) in 1942. http://www.bium.univ-paris5.fr/sfhd/biographies/degos_eng.htm

Robert Degos (1904-1987) Interne des Hôpitaux de Paris in 1926, Degos was appointed in 1934 as assistant at the Saint-Louis dermatological department headed by Gougerot, Professor of Dermatology whom he succeeded in 1951. For 25 years, Degos was fulfilling all the major responsabilities of French dermatology: General Secretary of the French Society of Dermatology, Professor of Dermatology, Chief Editor of the Annales de dermatology and author of a great textbook (Dermatologie) regarded as the bible of the french speaking dermatologists untill his last up-to-date edition in 1981. Degos described several dermatoses, genodermatose en cocardes in 1947, clear cells acanthoma in 1962 and especially malignant atrophiant papulosis (Degos' disease) in 1942. Back

74. Skin And Connective Tissue Diseases link/s Search PUBMED for Skin diseases All Review Therapy Diagnosis;degos' disease Malignant Atrophic Papulosis U. of Iowa; http://www.ohsu.edu/cliniweb/C17/C17.html

Skin and Connective Tissue Diseases Back to previous level Connective Tissue Diseases [22 more specific term/s, 71 more link/s] Search PUBMED for Connective Tissue Diseases: All Review Therapy Diagnosis ... Skin Diseases [40 more specific term/s, 90 more link/s] Search PUBMED for Skin Diseases: All Review Therapy Diagnosis ... Vitamin D: A New Era in Dermatology

75. Dorlands Medical Dictionary degos' disease, syndrome (De·gos' disease, syndrome) (dschwagomacrz¢) Robertdegos, French dermatologist, born 1904 malignant atrophic papulosis. http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

76. Dorlands Medical Dictionary Dam Deaver's incision debanding - decortication decrement - definitive deflection- deglycerolize degos' disease, syndrome - delivery dell - denervation http://www.mercksource.com/pp/us/cns/cns_hl_dorlands.jspzQzpgzEzzSzppdocszSzuszS

77. Sfhd - Quelques Aspects De La Contribution De Robert Degos à La Dermatologie Translate this page suffisants. Depuis, le nom de maladie de degos, ou degos's disease ou syndromedans la littérature anglo-saxonne, est adopté partout. Un http://www.chez.com/sfhd/ecrits/degos.htm

Quelques aspects de la contribution de Robert Degos à la Dermatologie Jean CIVATTE Robert Degos est et restera une des grandes figures de la dermatologie non seulement française mais mondiale: en ce dixième anniversaire de sa mort il n'est que juste de s'en souvenir. Une façon d'évoquer sa mémoire consiste à rappeler, sinon toutes, du moins les princiales affections qu'il a décrites ou dont il a précisé les cadres nosologiques. Certaines maladies portent à juste titre son nom. La principale est la papulose atrophiante maligne. Elle est née le 12 février 1942. Cette évolution fatale est rapportée par les mêmes auteurs le 21 mai 1942 sous le titre "dermatite papulo-squameuse atrophiante (Epilogue)": cette appellation est donc, pour l'instant, conservée pour cette affection qui comporte les mêmes altérations histologiques sur la peau et l'intestin et qui fait discuter, mais pour l'éliminer, un lupus érythémateux aigu, en particulier du fait de l'absence de fièvre. En 1948, R.Degos,J.Delort et R.Tricot présentent devant la Société Médicale des Hôpitaux de Paris un travail sur ce même sujet avec, comme titre, "papulose atrophiante maligne (syndrome cutanéo-intestinal mortel)". Ils utilisent à nouveau ce nom, qui est désormains unaninement accepté, dans un article publié en 1952 dans les Annales de Dermatologie dans lequel ils rappellent leur observation, celle de Tzanck, Civatte et Sidi, et citent un cas présente en juin 1950 par F.P.Merklen et F.Cottenot qu'ils rapprochent du leur, mais sans l'y assimiler faute de renseignements suffisants. Depuis, le nom de maladie de Degos, ou Degos's disease ou syndrome dans la littérature anglo-saxonne, est adopté partout.

78. »çÀü 44, /, /, Dermatofibrosarcoma portuberans, 43, /, /, Dowlingdegos¢¥ disease,42, /, /, Drug-Induced Lyell's Syndrom / Lyell Syndrome/Epidermonecrolysis/, http://admin.koreahospital.com/newdic3/list.asp?wordid=18

79. Segundo Ejemplar De La Revista Translate this page Malignant atrophic papulosis (degos' disease) involving three generationsof a family. Endoscopic and hystopatologic features of degos' disease. http://www.svcir.org/svc/revistas/5/Artic-2.html

REVISTA VALENCIANA DE CIRUGIA Crta. ORIHUELA-ALMORADI, s/n 03.314 SAN BARTOLOME Telf. 677 61 66 Ext. 215 Fax. 677 60 60 E-Mail vazquez_jos@gva.es Director J.L. Vázquez Rojas Editor Coeditores Castellon: R. García Calvo Valencia: Milagros Borrego Galán Alicante: Francisco Mauri Barberá Tesorero F. Asencio Arana Consultores J. Aguiló Lucía A. Arroyo A. Baltasar Torrejón R. Calpena Rico J. Cano Ivorra C. Carbonell Antolí F. Delgado Gomis M. Diego Estevez P. Enriquez Valens S. LLedó Matoses E. Marcote Valdivieso B. Narbona Arnau J.V. Roig Vila J. Ruiz del Castillo R. Trullenque Peris Secretaria J. Sánchez Martinez ENFERMEDAD DE DEGOS: UNA CAUSA INFRECUENTE DE PERFORACION INTESTINAL MULTIPLE "ESPONTANEA" (Orihuela). Bibliografia 1.- Degos R. Malignant atrophic papulosis. Br J Dermatol 1997; 100:21-35. 2.- Mckee PH. Vascular diseases. In: Mckee PH, ed. Pathology of the skin with clinical correlations. London: Mosby-Wolfe, 1996: 5.33-5.34 3.- Katz SK, Mudd LJ, Roenigk HH. Malignant atrophic papulosis (Degos' Disease) involving three generations of a family. J Am Acad Dermatol 1997; 37:480-484.

80. D Disseminated Superficial Actinic Porokeratosis, 757335, 11. Donohue syndrome,259803, 5. Dowlingdegos´ disease, 9605, 2. Drug Eruption, 693010, 21. http://www.medik.sk/fotoar/koza/d.html

Fotoarchív + zvukový archív / Dermatovenerológia / D D Diagnóza Kód Poèet obrázkov Darier's Disease Decubitus Ulcer Deep Thrombophlebitis Degos' acanthoma ... Dysseborrheic Dermatitis

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