21. AtCancer: Cancer/Oncology Search Engine Endocrine Neoplasia Type 1 Multiple Endocrine Neoplasia Type 2a - Multiple EndocrineNeoplasia Type 2b - multiple hamartoma syndrome - Multiple Hereditary http://atcancer.com/cancer/index2M.php3

Global Search Add Url Free Medline Contact Us ... Conferences Bookmark this page for your Future Medline/Internet Searches Try the Medline Search Designed for Cancer With FAST results Cancer Internet Search Medline Search Designed for Cancer Enter Keyword to search help Or And Match entire phrase Enter Keyword to search help Common Terminology Index [M] General Cancer (MESH 1998 © NLM) Male Breast Neoplasms Male Genital Neoplasms Malignant Carcinoid Syndrome ... Mixed-Cell Leukemia General Cancer (MESH 1998 © NLM) Mixed-Cell Lymphoma Mouth Neoplasms Mucinous Adenocarcinoma ... Myxosarcoma Index [A] [B-C] [D-G] [H-L] ... Cancer

22. NYU SoM - Dept. Of Dermatology Diagnosis multiple hamartoma syndrome (Cowden's disease). Commentmultiple hamartoma syndrome is an autosomal dominant condition. http://www.med.nyu.edu/Derm/conf/022001-3.html

23. ORPHANET® : Cowden Syndrome Translate this page ORPHANET. ORPHANET database access. Cowden syndrome. Direct accessto details Alias multiple hamartoma syndrome. Home Page. http://www.orpha.net/static/GB/cowden.html

ORPHANET database access Cowden syndrome Direct access to details Alias : Home Page

24. T Cowden's syndrome (multiple hamartoma syndrome) is an autosomal dominant diseasecharacterized by multiple cutaneous hamartoma (trichilemmoma, fibroma http://www.geocities.com/sampyroy2000/T.html

TRICHILEMMOMA Dr. Sampurna Roy M.D. HOME Trichilemmoma arises from the outer sheath of the hair follicle (mainly of the bulb region). Clinically the tumour presents as solitary or multiple papules in adults . These are dome shaped, flesh coloured lesions usually less than 5mm in diameter. Common sites are face, nose, eyelids, lips and oral cavity. Cowden's syndrome (multiple hamartoma syndrome) is an autosomal dominant disease characterized by multiple cutaneous hamartoma (trichilemmoma, fibroma, verrucous lesions),visceral hamartoma (hyperplastic gastric polyp) or visceral carcinoma (breast carcinoma). Histologically trichilemmoma is a symmetrical tumour with well circumscribed margin resting on PAS positive thickened basement membrane.The tumour is composed of glycogenated clear epithelial cells with peripheral palisading in deeper parts. These cells are PAS diastase positive. Some lesions contain eosinophilic "intermediate cells" (some times known as follicular poroma).The architectural patterns ranges from follicle like,vertically orientated , bulbous, lobular, verrucous or acrospiroma like. In many cases there is broad connection with overlying surface epithelium .Some trichilemmomas display connection with individual hair follicle. DESMOPLASTIC TRICHILEMMOMA: This is a variant of trichilemmoma characterized by extensive stromal component together with complex strands of clear epithelial cell in the periphery. Stroma is also present in the centre of epithelial nodules. Eosinophilic, amorphous alcian blue and PAS diastase positive material may be present (basement membrane material). CD34 positive cells are identified in trichilemmoma. The stroma contains vimentin positive cells.

25. CUTANEOUS MARKERS OF INTERNAL MALIGNANCY Syndrome. Inheritance. Manifestations. Associated malignancy. 9Cowden's syndrome (multiple hamartoma syndrome). Autosomal dominant. http://www.geocities.com/stantonios/mc/maligmrk.html

Cutaneous Markers of Internal Malignancy http://www.medicad.com I. Direct tumour spread: The skin is a relatively uncommon site for metastatic deposits compared to organs such as liver, lung and bone. The most common sources of cutaneous metastases are lung, breast and colon. Renal and thyroid skin deposits may be vascular and are occasionally misdiagnosed as benign haemangiomas. Direct invasion of the skin: The most frequent cause is carcinoma of the breast either as skin ulceration, Paget's disease, carcinoma erysipeloides, or carcinoma en cuirasse. Squamous-cell carcinoma of the oral cavity also may ulcerate onto the face. Paget's disease of the breast is an epidermal manifestation of an underlying ductal adenocarcinoma. Extramammary Paget's, e.g. in anogenital area may be a marker of underlying neoplasia such as adenocarcinoma of the rectum. Specific cutaneous infiltrations may occur with lymphoma and leukaemia II. The genetic group:

26. 1Up Health > Health Links Directory > Conditions And Diseases: M Cancer (28) Moyamoya Disease (5) MPS III (4) MRKH (10) Mucopolysaccharidosis 3 (4)Multiple Chemical Sensitivity (27) multiple hamartoma syndrome (3) Multiple http://www.1uphealth.com/links/conditions-and-diseases-m.html

Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health Health Directory Addictions Alternative Animal ... Weight Loss By Demography Child Health Teen Health Men's Health Women's Health ... Conditions and Diseases : M Description Browse by Alphabets A B C D ... Z 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 Open Directory Project Become an Editor Parts of the directory made available on 1UpHealth have been modified. External Web site links provided on this site are meant for convenience and for informational purposes only; they do not constitute an endorsement. Search: The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only they do not constitute endorsements of those other sites. Home Contact Us Privacy Links Directory

27. Cowden Syndrome A CHORUS notecard document about this syndrome.Category Health Conditions and Diseases Cowden Syndrome......Cowden syndrome. multiple hamartoma syndrome GItract hamartomas (incl.stomach and colon). breast Ca; thyroid Ca. circumoral papillomatosis; http://chorus.rad.mcw.edu/doc/00100.html

CHORUS Collaborative Hypertext of Radiology Colon Feedback Search Cowden syndrome "multiple hamartoma syndrome" GI-tract hamartomas (incl. stomach and colon) breast Ca thyroid Ca circumoral papillomatosis nodular gingival hyperplasia See also: polyposis syndromes Charles E. Kahn, Jr., MD - 2 February 1995 Last updated 14 March 2001 Medical College of Wisconsin

28. M Multiple Chemical Sensitivity; @ multiple hamartoma syndrome; @ MultipleMyeloma; @ Multiple Personality Disorder; @ Multiple Sclerosis; http://www.ad.com/Health/Conditions_and_Diseases/M/

search Top Categories: MAC @ MPS III @ MRKH @ Machado-Joseph Disease ... @ Myotonic Dystrophy AD.COM Web Directory is based on ODP - Open Directory Project data. No proprietary software was used in the development of this web site. Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor

29. ȸº¸ Multiple Myeloma(? ?) multiple hamartoma syndrome(? ? ?) see Hamartoma http://www.kams.or.kr/news/newsletter46-4.htm

Korea Index MedicusÀÇ ¼Ò°³ Korean Index Medicus´Â 1982³âºÎÅÍ ÇöÀç±îÁöÀÇ ±¹³» ÀÇÇÐ ÀâÁö¿¡ °ÔÀçµÈ ¿øÀú ³í¹®°ú Áõ·Ê º¸°í¸¦ MeSH(Medical Subject Heading)¿¡ ÀÇÇØ ºÐ·ùÇÑ ÁÖÁ¦»öÀΰú ÀúÀÚ»öÀÎÀÇ µÎ ºÎºÐÀ¸·Î ±¸¼ºµÈ ¿µ¹®ÆÇ Çѱ¹ÀÇÇÐ ¹®Çå»öÀÎÁö·Î¼­ ±¹¹® ÁÖÁ¦¸íÀ¸·Îµµ °Ë»öÇÒ ¼ö ÀÖ´Ù. ´ëÇÑÀÇÇÐȸ´Â ȸ¿øÀÇ ÀÌÇظ¦ µ½°í ½ÇÁ¦ °Ë»öÀ» ÇÒ ¼ö ÀÖ´Â ¹æ¹ýÀ» ¾Ë¸®°íÀÚ Çѱ¹ÀÇÇеµ»ç°üÇùÀÇȸÀÇ ÇùÁ¶¸¦ ¾ò¾î Korean Index Medicus¿¡¼­ Áö±Ý±îÁö ¼Ò°³µÈ ³»¿ª°ú °Ë»ö¹æ¹ý µîÀ» ¼Ò°³ÇÏ°íÀÚ ÇÑ´Ù. ´ëÇÑÀÇÇÐȸ´Â ȸ¿øÀÇ ¹ßÇ¥³í¹® ÀÛ¼º½ ±¹³»ÀÇ ³í¹®À» ¸¹ÀÌ ÀοëÇϽ±æ ±ÇÀåÇÕ´Ï´Ù. Korean Index Medicus´Â Çѱ¹ÀÇÇеµ¼­°üÇùÀÇȸ¿¡¼­ ±¹³»ÀÚ·áÀÇ °Ë»öÀ» À§ÇÑ 2Â÷ ÀÚ·áÀÇ Çʿ伺À» ÇØ°áÇϱâ À§ÇÏ¿© ¢°£ÇÑ ¿µ¹®ÆÇ Çѱ¹ÀÇÇÐ ¹®Çå»öÀÎÁöÀÌ´Ù. Çмú¿ø¿¡¼­ ¹ßÇàÇÑ ÇмúѶ÷(ÀÇÇÐÆí)¿¡ ÀÌÀº ±¹³» ÀÇÇй®Çå¿¡ ´ëÇÑ Æ÷°ýÀûÀÎ »öÀÎÁö·Î¼­, 1982³âºÎÅÍ ÇöÀç±îÁö ±¹³» ÀÇÇÐÀâÁö¿¡ °ÔÀçµÈ ¿øÀú³í¹®(Original Article)°ú Áõ·Êº¸°í(Case Report)¸¦ MeSH(Medical Subject Heading)¿¡ ÀÇÇØ ºÐ·ùÇÑ ÁÖÁ¦»öÀΰú ÀúÀÚ»öÀÎÀÇ µÎ ºÎºÐÀ¸·Î ±¸¼ºµÇ¾î ÀÖ´Ù. ÁÖÁ¦»öÀÎÀº MeSH¿¡ ÀÇÇÑ ÁÖÁ¦¸íÀÌ ¾ËÆĺª¼øÀ¸·Î ¹è¿­µÇ¾î ÀÖ°í ±× ¹Ø¿¡ ÁÖÁ¦¿Í °ü·µÈ ³í¹®ÀÇ ¼­Áö»çÇ×ÀÌ ±âÀçµÇ¾î ÀÖ´Ù. ¼­Áö»çÇ×Àº ÀúÀÚ, ³í¹®Á¦¸ñ, ÀâÁö¸í, ¹ßÇ¥³âµµ, ±Ç, È£, ÆäÀÌÁö ¼øÀ¸·Î ±â¼úµÇ¾î ÀÖ´Ù. ±Ç¸»¿¡´Â ÀúÀÚ»öÀÎÀÌ ÀÖÀ¸¸ç, ÀúÀÚ àõÀÇ ¾ËÆĺª¼øÀ¸·Î ¹è¿­µÇ¾î ÀÖ´Ù. Á¦1ÀúÀÚ¿¡ ´ëÇؼ­ ¼­Áö»çÇ×ÀÌ ±â¼úµÇ¾î ÀÖ°í Á¦2ÀúÀÚ ¹× ±âŸ °øÀúÀÚ¿¡ ´ëÇؼ­´Â Á¦1ÀúÀÚ¸¦ ÂüÁ¶Çϵµ·Ï ÇÏ¿´´Ù.

30. Birth Disorder Information Directory - M Multiple Epiphyseal Dysplasia See Beighton Goldberg Hoff Syndrome.multiple hamartoma syndrome See Cowden Syndrome. Multiple Hereditary http://www.bdid.com/defectm.htm

HOME M Machado Joseph Disease (Autosomic Dominant Spinocerebellar Ataxia, Autosomic Dominant Cerebellar Ataxia, Cerebelloolivary Atrophy, Olivopontocerebellar Atrophy, Pierre Marie Cerebellar Ataxia) List of Sites Macrencephaly List of Sites Macrocephaly List of Sites Macrodactyly/Megalodactyly Macrodactly of the Right Foot Macrodactyly of Both Hands and Foot Associated with Cutaneous Hemangiomata MEGALODACTYLY Macroglossia Macroglossia (Includes Ultrasounds and Photos) Also see Beckwith Wiedemann Syndrome Blomstrand Syndrome Congenital Hypothyroidism Mucopolysaccharidosis and Simpson Golabi Behmel Syndrome Macrogyria MACROGYRIA Asperger's Syndrome Macular Dystrophy Vitelliform See Best Disease/Macular Dystrophy Atypical MACULAR DYSTROPHY, ATYPICAL VITELLIFORM; VMD1 Macules Hereditary Congenital Hypopigmented and Hyperpigmented See Westerhof Beemer Cormane Syndrome Madelung's Deformity See Leri Weill Syndrome Majewski Syndrome See Short Rib-Polydactyly Syndrome, Type IV Mal de Meleda See Meleda Disease Male Pseudohermaphroditism Due to 5-Alpha-Reductase Deficiency See Pseudovaginal Perineoscrotal Hypospadias Due to Androgen Insensitivity See Androgen Insensitivity Syndrome Male Turner Syndrome See Noonan Syndrome Malignant Hyperthermia See Hyperthermia, Malignant

31. Birth Disorder Information Directory - CO-CZ Syndrome (Cystic Hygroma Lethal Cleft Palate) Cowchock wapner kurtzsyndrome. Cowden('s) Disease/Syndrome (multiple hamartoma syndrome) http://www.bdid.com/defectco.htm

HOME Co-Cy COACH Syndrome See Cerebellar Vermis Hypo/Aplasia, Oligophrenia, Congenital Ataxia, Ocular Coloboma, and Hepatic Fibrosis (COACH) Syndrome Coarctation of (the) Aorta (CoA) List of Sites Coats' Disease (Congenital Retinal Telangiectasia, Exudative Retinitis, Leber Miliary Aneurysm) Coats disease Cobb Syndrome Syndromes associated with AVMs Cocaine Antenatal Infection See Fetal Cocaine Syndrome Related Books Cochin Jewish Disorder (Haim Munk Syndrome, Keratosis Palmoplantaris Periodontopathia) Keratosis palmoplantaris periodontopathia KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA AND ONYCHOGRYPOSIS Cockayne Syndrome List of Sites COD-MD Syndrome See Walker Warburg Syndrome CODAS Syndrome (Cerebrooculodentoauriculoskeletal Syndrome) Cerebro oculo dento auriculo skeletal syndrome CODAS SYNDROME Coffin Syndrome (Arthritis Short Stature Deafness) Coffin syndrome Coffin-Lowry Syndrome List of Sites Coffin Siris Syndrome (Fifth Digit Syndrome) Coffin siris syndrome FIFTH DIGIT SYNDROME COFS Syndrome See Cerebrooculofacioskeletal (COFS) Syndrome Cohen Hayden Syndrome (Proteus-Like Syndrome with Mental Retardation and Eye Defects) Cohen hayden syndrome Cohen Lockood Wyborney Syndrome (Blepharophimosis Ptosis Syndactyly Mental Retardation) blepharophimosis ptosis syndactyly mental retardation Cohen Syndrome List of Sites Colavita Kozlowski Syndrome (Short Limb Dwarf, Lethal Colavita Kozlowski Type)

32. Directory :: Look.com Disease (4) Mouth Cancer (28) Moyamoya Disease (5) Mucopolysaccharidosis 3 (4)Multiple Chemical Sensitivity (26) multiple hamartoma syndrome (3) Multiple http://www.look.com/searchroute/directorysearch.asp?p=43355

33. Searchalot Directory For M Chemical Sensitivity (26); multiple hamartoma syndrome (3); MultipleMyeloma (17); Multiple Personality Disorder (107); Multiple Sclerosis http://www.searchalot.com/Top/Health/ConditionsandDiseases/M/

Home Search News Email Greetings Weather ... Global All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News Yahooligans Zeal Sponsored Links Top Health Conditions and Diseases : M MAC MPS III MRKH Machado-Joseph Disease ... Myotonic Dystrophy All the Internet About AltaVista AOL Search Ask Jeeves BBC Search BBC News Business Dictionary Discovery Health Dogpile CheckDomain CNN Corbis eBay Education World Employment Encyclopedia Encarta Excite Fast Search FindLaw FirstGov Google Google Groups Infomine iWon Librarians Index Looksmart Lycos Metacrawler Microsoft Northern Light Open Directory SearchEdu SearchGov Shareware Teoma Thesaurus Thunderstone WayBackMachine Webshots WiseNut Yahoo! Yahoo! Auctions Yahoo! News

34. GeneCard For PTEN THE PREDOMINANT PHENOTYPE FOR CS IS multiple hamartoma syndrome, IN MANY ORGAN SYSTEMSINCLUDING THE BREAST (70% OF CS PATIENTS), THYROID (4060%), SKIN, CNS http://www.rzpd.de/cgi-bin/cards/carddisp?PTEN

35. USCAP - 91st Annual Meeting The histologic appearance of colorectal polyps from patients with Cowden's disease(multiple hamartoma syndrome) appears identical to mucosal prolapse syndrome http://www.uscap.org/91st/case4.htm

A PRACTICAL APPROACH TO GASTROINTESTINAL PATHOLOGY COLORECTAL MUCOSAL PROLAPSE SYNDROMES Robert E. Petras, M.D. Introduction Slide 8 Slide 9 The solitary rectal ulcer syndrome, localized colitis cystica profunda, and inflammatory cloacogenic polyp are closely allied conditions that have been linked to bowel prolapse. Affected patients often demonstrate abnormal function of the anal and pelvic floor musculature during defecation that leads to rectal mucosal prolapse or even intussusception. The resulting trauma is thought to cause the clinical symptoms and the pathologic changes. The term solitary rectal ulcer syndrome is quite a misnomer because the ulcers are often multiple, there is preulcer polypoid phase, and similar lesions occur in the anal canal and sigmoid colon. Additionally, colitis cystica profunda and inflammatory cloacogenic polyp are also misnomers. Since all three conditions share a common histologic appearance, clinical presentation, clinical course, and pathogenesis, I prefer to consider them together under the heading mucosal prolapse syndromes. Clinical Presentation Patients with mucosal prolapse syndrome range in age form 10-83 years with the majority presenting in the third and fourth decade of life. The condition occurs more commonly in women.

36. 1st Diagnosis Cowden’s syndrome, also known as the multiple hamartoma syndrome, consists ofmultiple tricholemmomas on the face and oral mucosa associated with breast http://erl.pathology.iupui.edu/cases/dermcases/diag1.cfm?case=17

37. Nature Genetics Cowden disease (CD) (MIM 158350), or multiple hamartoma syndrome, is a rare autosomaldominant familial cancer syndrome with a high risk of breast cancer. http://www.nature.com/ng/wilma/v13n1.867941190.html

articles RETURN TO May 1996 TABLE OF CONTENTS volume 13 number 1 page 114 M.R. Nelen , G.W. Padberg , E.A.J. Peeters , A.Y. Lin , B. van den Helm , R.R. Frants , V. Coulon , A.M. Goldstein , M.M.M van Reen , D.F. Easton , R.A. Eeles , S. Hodgson , J.J. Mulvihill , V.A. Murday , M.A. Tucker , E.C.M. Mariman , T.M. Starink , B.A.J. Ponder , H.H. Ropers , H. Kremer , M. Longy Cowden disease (CD) (MIM 158350), or multiple hamartoma syndrome, is a rare autosomal dominant familial cancer syndrome with a high risk of breast cancer. Its clinical features include a wide array of abnormalities but the main characteristics are hamartomas of the skin, breast, thyroid, oral mucosa and intestinal epithelium. The pathognomonic hamartomatous features of CD include multiple smooth facial papules, acral keratosis and multiple oral papillomas . The pathological hallmark of the facial papules are multiple trichilemmomas . Expression of the disease is variable and penetrance of the dermatological lesions is assumed to be virtually complete by the age of twenty . Central nervous system manifestations of CD were emphasized only recently and include megalencephaly, epilepsy and dysplastic gangliocytomas of the cerebellum (Lhermitte-Duclos disease, LDD)

38. Browsing Health Conditions And Diseases M Category Morvan Disease Mouth Cancer Moyamoya Disease, MPS III MRKH Mucopolysaccharidosis3 Multiple Chemical Sensitivity multiple hamartoma syndrome Multiple Myeloma http://www.uksprite.com/search/search/Health/Conditions_and_Diseases/M/

/* 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 M Top Health Conditions and Diseases M A B C D ... Z Categories: MAC Machado-Joseph Disease Macular Degeneration Mad Cow Disease ... Myotonic Dystrophy Last update: 14:13 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 Iraq ambush kills UK marine A UK marine is killed in southern Iraq, while troops follow up gains made in fierce fighting outside Basra. Push to stamp out gun crime The owners of illegal firearms are urged to hand them in without fear of prosecution as part of a nationwide amnesty. 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.

39. [P&S Journal:Wi:97] Cowden's Syndrome: Masked Menace Instead, she suffers from a littleknown disease called Cowden's syndrome (CS;also known as multiple hamartoma syndrome)an autosomal dominant disorder http://cpmcnet.columbia.edu/news/journal/archives/jour_v17n1_0011.html

Cowden's Syndrome: Masked Menace By Devera Pine Illustration by Susan Gilbert W hen Mary Smith (not her real name) was 16 years old, she found a lump in her breast. "My mother was terrifiedshe thought it was cancer," says Ms. Smith, now 53. "But in those days, no one talked about cancer. So even though I was scared that I had to have surgery, I didn't know the overwhelming possibilities." Since then, she has had a seemingly endless series of cancer scares and actual bouts with cancer: four biopsies for suspicious breast lumps, a lumpectomy followed by a mastectomy, a hysterectomy, partial nephrectomy for what turned out to be a benign mass, and, in 1996, another mastectomy. Mary Smith does not have the BRCA1 or BRCA2 breast cancer genes. Instead, she suffers from a little-known disease called Cowden's syndrome (CS; also known as multiple hamartoma syndrome)an autosomal dominant disorder characterized by skin lesions and a high risk of both breast and thyroid cancer. The medical literature describes CS as a rare disease associated with marked disfigurement. But according to Dr. Monica Peacocke, associate professor of medicine and of dermatology, CS is fairly common, not generally disfiguring, easily missed by many doctors, and an under-recognized cause of many cases of familial breast cancer. "The genetic basis of many types of familial breast cancer is not yet known," says Dr. Peacocke, who is collecting the genetic pedigrees of people like Mary Smith. "CS is masquerading as sporadic breast cancer."

40. Cowden Disease Or Multiple Hamartoma Syndrome - Cutaneous Clue Tointernal Malign Schilddrüsentumoren. Cowden disease or multiple hamartoma syndrome cutaneous cluetointernal malignancy Review. Autor/-en Fistarol SK, Anliker MD, Itin PH. http://www.schilddruese.net/oeffentlich/wissenschaft/news/news863.php

Wissenschaft Topnews News Praxisseminar Klinische Studien ... zurück März 2003 Schilddrüsentumoren Cowden disease or multiple hamartoma syndrome - cutaneous clue tointernal malignancy [Review] Autor/-en: Fistarol SK, Anliker MD, Itin PH Quelle: European Journal of Dermatology 2002 Sep-Oct;12(5):411-421 Home Mail Sitemap Drucken Suche Zur Suche im Fachkreis-Bereich loggen Sie sich bitte ein. Login für Fachkreise Hier können Sie einen Zugang erhalten Benutzer von DocCheck Benutzername: Passwort: Passwort vergessen ? Zugangsdaten ändern Impressum und Nutzungsbedingungen ... Gesellschaften / Verbände

A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V  W  X  Y  Z

Page 2     21-40 of 94    Back | 1  | 2  | 3  | 4  | 5  | Next 20