81. All Showcase - Health Disease And Health Conditions cerebrocostomandibular syndrome (2). Cerebrohepatorenal Syndrome (4). CerebrotendinousXanthomatosis (1). Cervical Cancer (21). Cervical Dysplasia (8) http://www.allshowcase.com/Health_and_Fitness/Conditions_and_Diseases/C/

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82. Conditions And Diseases/Rare Disorders cerebrocostomandibular syndrome (2) Kindler Syndrome An article and casestudy of this rare disease. Includes links. http://www.healthboard.com/websites/Conditions_and_Diseases/Rare_Disorders/

Health Board Conditions and Diseases/Rare Disorders Search Health Board Directories the entire directory only this category More search options Home Conditions and Diseases : Rare Disorders CATEGORIES: Agnosia Aicardi Syndrome Alstrom Syndrome Barth Syndrome ... Wegener's Granulomatosis LINKS: Cherubs A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. http://www.cherubs-cdh.org Contact a Family Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. http://www.cafamily.org.uk Fibrosing Mediastinitis The least common, but most severe, late complication of histoplasmosis. Educational and research information. Includes interviews, patient stories, and a community forum. http://www.fibrosingmediastinitis.com Fibrous Dysplasia Support Online For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. http://members.cox.net/fdsupport/index.html

83. Genetic Disorders BeckwithWiedemann Syndrome Canavan Celiac cerebrocostomandibular syndrome Charcot-Marie-Tooth Disease Cleidocranial Dysplasia Cockayne Syndrome http://www.ebroadcast.com.au/dir/Health/Conditions_and_Diseases/Genetic_Disorder

SEARCH GUIDE NEWS AUSTRALIAN TV GUIDE DVD RENTALS ... Conditions and Diseases : Genetic Disorders An amazing one-stop shop for information on many common diseases and conditions. Gene Therapy Genetic Testing and Counseling Genetics Education Human Genetics ... Gene Clinics Medical genetics knowledge base. NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. Explains a gene defect which causes several diseases including Maternally Inherited Diabetes with Deafness. Features a newsletter, forum and definitions. Blepharophimosis Ptosis Epicanthus Inversus Syndrome The BPEI (BPES) Family Network encourages people to get in touch with each other, share information and ask questions. Explanation of this rare eye disorder. The Center For Jewish Genetics Disorders A critical effort to provide public and professional education for many of the identified Jewish genetic disorders. Find info on screening and counseling, advocacy, events and community resources. Dr. Greene's HouseCalls

84. Plastic And Reconstructive Surgery - UserLogin Two patients, one with cerebrocostomandibular syndrome (CCMS) and the other withan unspecified syndrome, were operated on a second time. http://www.plasreconsurg.com/pt/re/prs/fulltext.00006534-199710000-00007.htm

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85. Zon Webgids cerebrocostomandibular syndrome (2). CharcotMarie-Tooth Disease@ (6). CleidocranialDysplasia (3). Cockayne Syndrome@ (2). Coffin Lowry Syndrome@ (4) http://zoek.versatel.nl/odp/index.cgi?/Health/Conditions_and_Diseases/Rare_Disor

86. Conditions And Diseases/Rare Disorders - The Medword List Barth Syndrome (1). cerebrocostomandibular syndrome (1). Cleidocranial Dysplasia (1).Cystinosis (3). Degos (1). Erythromelalgia (1). Jacobsen Syndrome (2) http://www.medwordlist.com/Conditions_and_Diseases/Rare_Disorders/

HOME ADD SITE MODIFY SITE NEW ... Conditions and Diseases : Rare Disorders Categories: Agnosia Aicardi Syndrome Alstrom Syndrome Barth Syndrome ... Wegener's Granulomatosis Links: Cherubs A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. http://www.cherubs-cdh.org (Added: Mon Jan 01 2001 Hits: 29 Rating: 0.00 Votes: 0) Rate It Review It Contact a Family Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. http://www.cafamily.org.uk (Added: Mon Jan 01 2001 Hits: 32 Rating: 0.00 Votes: 0) Rate It Review It Human Growth Foundation Information about growth-related disorders through education, research, and advocacy. Member driven organization. http://www.hgfound.org/ (Added: Mon Jan 01 2001 Hits: 32 Rating: 0.00 Votes: 0) Rate It Review It Authentic WAVpedal Foot Pedal WAVpedal allows PC playback of all popular digital voice recorder formats. Better than other similar systems. ALWAYS STOCKED READY TO SHIP Safe Disk is an easy-to-use security software providing transparent "on-the-fly" encryption for Windows PCs and/or PDAs.

87. ÓÑÇéÁ´½Ó-GRE¿¼ÊÔ cerebrocostomandibular syndrome CharcotMarie-Tooth Disease CleidocranialDysplasia Cockayne Syndrome Coffin Lowry Syndrome Cornelia De Lange http://www.microedu.com/gre/resource/13.htm

Web Microedu.com TOEFL GRE GMAT LSAT ... Zollinger-Ellison Syndrome See also: Genetic Disorders Musculoskeletal Disorders Neurological Disorders Nutrition and Metabolism Disorders ... GREâ·Ñ×ÊÁÏ

88. Cerebrocostomandibular (CCM) Syndrome (CCMS) A list of synonyms, summary and major features. http://www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome098.html

Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes View the Full Record Syndrome cerebrocostomandibular (CCM) syndrome (CCMS) Synonyms Smith-Theiler-Schachenmann syndrome rib-gap syndrome rib gap defect-micrognathia syndrome Summary Mental retardation associated mainly with costovertebral malformations and orofacial defects. Mental defect may not be inherent but rather a consequence of neonatal respiratory distress. Major Features Head and neck: Microcephaly and micrognathia. Mouth and oral structures: Palatal defects include short hard palate, absent soft palate, cleft palate, and absent uvula in association with glossoptosis. Neck: Pterygium colli. Thorax: Bilateral rib gaps between the costovertebral junction area and he lateral arc, most frequently occurring between the third and seventh thoracic segments occur in most cases. Flail chest is the usual consequence. Hypoplasia of the sternum and clavicles may be associated. Extremities: Elbow hypoplasia and other limb abnormalities may occur. Spine: Fusion of the vertebrae to each other, scoliosis, and hemivertebrae may be associated.

89. Health/Conditions And Diseases/Rare Disorders/Cerebrocostomandibular Syndrome -- National Library of Medicine cerebrocostomandibular (CCM) syndrome (CCMS) A listof synonyms, summary and major features. http://www.thedoctorslounge.net/dir/Health/Conditions_and_Diseases/Rare_Disorder

Advertisement Powered by Careerbuilder Search for: Home Humor Advertising Contact ... Links Specialties Cardiology Chest diseases Dermatology Endocrinology ... Urology Other Sections Membership Research Tools Medical Tutorials Medical Software ... Specialized Centers Headlines: The Medical Website Directory Popular Categories Popular Links Web Sites National Library of Medicine: cerebrocostomandibular (CCM) syndrome (CCMS) A list of synonyms, summary and major features. url: www.nlm.nih.gov/mesh/jablonski/syndromes/syndrome0... NORD - Cerebrocostomandibular Syndrome Sample report, plus links to organisations. [Fee required for full report] url: www.rarediseases.org/search/rdbdetail_abstract.htm... mozilla.org url: mozilla.org/ More Search All the Web AltaVista Gigablast Google USENET ... Yahoo In association with ODP Help build the largest human-edited directory on the web. Submit a Site Open Directory Project Become an Editor Are you a physician or a nurse? Would you like to join us and help patients online by volunteering even a few minutes of your time? Get started here by becoming a member of The Doctors Lounge We subscribe to the HONcode principles.

90. Opera Directory National Library of Medicine cerebrocostomandibular (CCM) syndrome (CCMS).A list of synonyms, summary and major features. http://portal.opera.com/directory/?cat=523623

91. Syndrome DB - Table Of Contents cerebroosteo-nephrosis syndrome cerebrocostomandibular (CCM) syndrome (CCMS) cerebrocutaneous angiomatosis cerebrofacio-articular (CFA) syndrome http://www.nlm.nih.gov/mesh/jablonski/syndrome_toc/toc_c.html

Multiple Congenital Anomaly/Mental Retardation Syndromes Table of Contents Return to Entry Page A B C ... Z C C syndrome Caffey pseudo-Hurler syndrome Caffey syndrome Calabro syndrome ... U.S. National Library of Medicine , 8600 Rockville Pike, Bethesda, MD 20894 National Institutes of Health Privacy Accessibility Last updated: 20 November 2001

92. DARS Early Childhood Intervention Services 756.9, cerebrocostomandibular (SmithTheiler-Schachenmann) syndrome. 759.89,Cerebrohepatorenal syndrome. 759.89, CHARGE syndrome (CHARGE Association)* http://www.dars.state.tx.us/ecis/resources/diagnoses.asp?letter=c

93. Warman Lab Site - Department Of Genetics CamptodactylyArthropathy-Coxa Vara-Pericarditis syndrome; Cerebrocostomandibularsyndrome Infantile Systemic Hyalinosis Juvenile Hyaline Fibromatosis http://genetics.case.edu/warmanlab/research.php

Center for Study of Genetic Bone and Joint Disorders Current research Acromesomelic Dysplasia , Maroteaux type Brachydactyly Camptodactyly-Arthropathy-Coxa Vara-Pericarditis syndrome Cerebrocostomandibular Syndrome Infantile Systemic Hyalinosis Juvenile Hyaline Fibromatosis Multiple Synostosis Syndromes ... Osteoarthritis (Genetics of Osteoarthritis Study) Osteoporosis (The Twins Bone Health Study) Osteoporosis-Pseudoglioma Syndrome (OPPG) Progressive Pseudorheumatoid Dysplasia (PPD) Proximal Symphalangism Spondylocarpotarsal Syndrome Welcome Faculty Research Facilities ... Frequently Asked Questions Design by

94. Website Directory - Rare Disorders Aicardi syndrome Alstr¶m syndrome Barth syndrome Cerebrocostomandibularsyndrome Mascot McCune Allbright syndrome Communication Online Town http://www.shapeupamerica.com/search/directory/Conditions_and_Diseases/Rare_Diso

Shape up Blog Shape Up Directory Add Your Site Health Directory Addictions Aging Alternative Animal ... Conditions and Diseases > Rare Disorders Sub-categories: Agnosia Aicardi Syndrome Alstr¶m Syndrome Barth Syndrome ... Cherubs A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia. Contact a Family Information about this organization as well as the CaF directory of specific conditions and rare disorders. Also details about the Rare Disorders Alliance - UK. Fibrosing Mediastinitis The least common, but most severe, late complication of histoplasmosis. Educational and research information. Includes interviews, patient stories, and a community forum. Fibrous Dysplasia Support Online For those seeking support and information concerning the rare bone diseases: fibrous dysplasia, McCune Albright Syndrome and Cherubism. Human Growth Foundation Information about growth-related disorders through education, research, and advocacy. Member driven organization. Information Centre for Rare Diseases and Orphan Drugs Offers an Internet portal. Includes news, forums, rare disease and orphan drug info and registration forms

95. OMIM UVEAL, WITH CLEFT LIP AND PALATE AND MENTAL RETARDATION; 117650 CEREBROCOSTOMANDIBULARSYNDROME (searching for spina bifida heart defect cleft palate ) http://republika.pl/jmejnart/wcn_omim.htm

Ponisze odno¶niki pozwalaj± na wykorzystanie zasobów OMIM On-line Mendalian Inheritance in Man w NCBI. Strona g³ówna OMIMu Przeszukiwanie OMIMu Formularz wyszukiwania OMIMu Wpisz jedno lub wiêcej s³ów kluczowych: Aby przeszukaæ wszystkie pola, nie zaznaczaj poni¿szych kratek. Aby za¶ zawêziæ zakres szukania do poszczególnych pól, zaznacz kratki obok odpowiadaj±cej nazwy pola. Zobacz Pomoc w zadawaniu zapytañ (Query help) , aby dowiedzieæ siê jak zadawaæ zapytania w inny spoób (³±cze prowadzi do serwera OMIMu w USA). Tytu³: Numer OMIM: Odmiany alleliczne: Tekst: Bibliografia: Objawy kliniczne: Mapa genów chorób: Wpisuj±cy: Wy¶wietlaj tylko rekordy zmienione w ci±gu ostatnich 7 dni 15 dni 30 dni 60 days 90 days 180 days 365 days Bez ograniczeñ Wy¶wietla tylko 50 pozycji 100 pozycji 200 entries No Limit Wyniki przeszukiwania wg has³a "Wady cewy nerwowej" (Neural tube defect/s) w OMIMie Autosomalne dominuj±ce Autosomalne recesywne SPINA BIFIDA NEURAL TUBE DEFECT, FOLATE-RESISTANT NEURAL TUBE DEFECT, FOLATE-SENSITIVE APOLIPOPROTEIN B; APOB

96. Login http://www.dimed.com/specialista/secure/database/docsmanager/dbidparam/1464.aspx

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