61. JustCan.com Disability Directory cerebrocostomandibular syndrome (2); CharcotMarie-Tooth Disease@ (7) Kindler Syndrome - - An article and case study of this rare disease. http://directory.justcan.com/odpphp/odp.php?browse=/Health/Conditions_and_Diseas

62. JustCan.com Disability Directory Celiac@ (39); cerebrocostomandibular syndrome@ (2); CharcotMarie-ToothDisease@ (7) Includes nutritional links to disorders such as Down syndrome, http://directory.justcan.com/odpphp/odp.php?browse=/Health/Conditions_and_Diseas

63. Tale Of Determination - 2004-05-10 Mary was born with a condition known as cerebrocostomandibular syndrome.The condition caused her to be born with an abnormally narrow rib cage that http://www.bizjournals.com/philadelphia/stories/2004/05/10/story3.html

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64. AnyWho: Internet Directory Assistance; Yellow Pages, White Pages, Toll-Free Numb cerebrocostomandibular syndrome (2) Charcot-Marie-Tooth Disease (7) - CleidocranialDysplasia (3) - Cockayne Syndrome (2) - Coffin Lowry Syndrome (4) http://www.anywho.com/cgi-bin/webdrill?catkey=gwd/Top/Health/Conditions_and_Dise

65. HalfthePlanet Is The Authoritative Online Source Of Reliable Tools Cerebral Palsy@ (142); cerebrocostomandibular syndrome@ (2); CerebrohepatorenalSyndrome@ (4); Cerebrotendinous Xanthomatosis@ (1); Cervical Cancer@ http://www.halftheplanet.org/cgi-bin/resources/apexec.pl?etype=odp&passurl=/Heal

66. Clinical Genetics Batten (7); BeckwithWiedemann Syndrome (9); Canavan@ (4); Celiac@ (40);cerebrocostomandibular syndrome@ (2); Charcot-Marie-Tooth Disease@ (5) http://www.perinatology.com/genetics.htm

perinatology.com Genetics Directory Search Site Map Agencies and Organizations Calculators Critical Care Exposures Chemicals Drugs Infection Physical Agent ... Ultrasound See Also: Genetic Counselor's Toolbox California DHS Genetic Disease Branch GeneClinics is a medical knowledge base relating genetic testing to the diagnosis, management, and genetic counseling of individuals and families with specific inherited disorders. Angelman Syndrome GeneClinics Beckwith-Wiedemann Syndrome GeneClinics Muscular Dystrophy GeneClinics Fragile X Syndrome GeneClinics Phenylalanine Hydroxylase Deficiency (PKU) GeneClinics Prader-Willi Syndrome GeneClinics Smith-Lemli-Opitz Syndrome GeneClinics Tuberous-Sclerosis GeneClinics Genetic Analysis Software Rockefeller University The Gene Letter Genetic Education Materials (GEM) Database Searchable listing of public health genetics policy documents and clinical genetics educational materials Information For Genetic Professionals University of Kansas Medical Center International Birth Defects Information Systems Online Mendelian Inheritance in Man OTIS Organization of Teratology Information Services Pediatric Database Description of pediatric conditions.

67. Pediatrics -- Sign In Page The genetic diagnosis was cerebrocostomandibular syndrome. The patient wasdischarged 2.5 months later, in good clinical condition. http://pediatrics.aappublications.org/cgi/content/full/peds.2004-1468v1

QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This item requires a subscription. If you have an individual print subscription to Pediatrics , online access is included. Full Text Laryngeal Mask Airway for the Interhospital Transport of Neonates Trevisanuto et al. Pediatrics. This Article Abstract Full Text (PDF) P ... Alert me if a correction is posted Services E-mail this article to a friend 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 Trevisanuto, D. Articles by Zanardo, V. Related Collections Emergency Medicine To view this item, select one of the options below: Sign In: Please use your AAP ID Number or Temporary Activation Code for your User Name. 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 2 days for US$12.00

68. Health Library cerebrocostomandibular syndrome Cerebro Oculo Facio Skeletal Syndrome Cervical biopsy for abnormal cervical cell changes Cervical Cancer http://myhealth.ucsd.edu/library/healthguide/en-us/IllnessConditions/SearchResul

69. Health Library - Birth Defects and Genetic DiseasesDown Syndrome Prenatal Risk Assessment and Diagnosis Canavan@ (4); Celiac@ (40);cerebrocostomandibular syndrome@ (2); CharcotMarie-Tooth Disease@ (5) http://12.42.224.152/library/healthguide/en-us/illnessconditions/topic.asp?hwid=

70. Smith-Theiler-Schachenmannin Oireyhtymä - Kehitysvamm. Tietopankki cerebrocostomandibular (CCM) syndrome (CCMS), Multiple Congenital cerebrocostomandibular syndrome, OMIM, Victor A. McKusick, Iosif W. Lurie et al. http://www.saunalahti.fi/kup/syndroma/smith-theiler-schachenmann.htm

Kehitysvammahuollon tietopankki Rintanikamien epämuodostumat, suun ja kasvojen kehityshäiriöt Smith-Theiler-Schachenmannin oireyhtymä Kerebrokostomandibulaarinen oireyhtymä Aivo-kylkiluu-alaleuka-oireyhtymä Kylkiluun rakoilu-oireyhtymä Psyykkinen kehitysvammaisuus liittyy tässä oireyhtymässä pääasiassa rintanikamien epämuodostumiin ja suun sekä kasvojen kehityshäiriöihin. Henkisen suorituskyvyn madaltuminen saattaa johtua vastasyntyneen hengitysvaikeuksista. Oireyhtymän muita piirteitä ovat pienipäisyys ( mikrokefalia ), alaleuan pienikokoisuus, suulaen kovuus, lyhyys ja suulaen pehmeän osan puuttuminen, suulaen halkio, kitakielekkeen ja kielipoimun puuttuminen, kaulan ihon siipikalvomainen poimuttuminen, kylkiluun molemminpuoliset raot kylkinikamien liitos- ja sivukaarien alueella, mahdollisesti rintalastan ja solis- sekä kyynärluun vajaakasvuisuus, nikamien luhistuminen, selkärangan kieroutuminen ( skolioosi ) ja puolinikamaisuus sekä hermosolujen myeliinisaation (valkean aineen muodostuminen) viivästyminen. Noin kolmannes vammautuneista menehtyy ensimmäisen elinvuoden aikana.

71. Link Directory - Finnish Information Center On Mental Retardation cerebrocostomandibular syndrome, OMIM, Victor A. McKusick, Iosif W. Lurie et al . cerebrocostomandibular syndrome in four sibs, two pairs of twins, http://www.saunalahti.fi/kup/engl/webs_s.html

Finnish Information Center on Mental Retardation English links A B C D ... Z Sabinas Brittle Hair Syndrome BRITTLE HAIR AND MENTAL DEFICIT, OMIM Victor A. McKusick brittle hair-mental deficit syndrome, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes Sabinas brittle hair syndrome, Orphanet ... Trichothiodystrophy-neurotrichocutaneous syndrome of Pollitt: a report of two unrelated cases, King MD, Gummer CL, Stephenson JB, PubMrd Salla Disease Salla disease, Multiple Congenital Anomaly/Mental Retardation (MCA/MR) Syndromes SIALURIA, FINNISH TYPE, OMIM, Victor A. McKusick 6q14-q15, SLC17A5 to 6q21, APG5L, The OMIM Gene map INFANTILE SIALIC ACID STORAGE DISORDER, OMIM, Victor A. McKusick, Orest Hurko et al. ... Central and peripheral nervous system dysfunction in the clinical variation of Salla disease, T. Varho et al, Neurology 2000 Salonen-Herva-Norio Syndrome Hydrolethalus Syndrome, OMIM, Victor A. McKusick Hydrolethalus Syndrome, TheFetus.net Hydrolethalus syndrome, Orphanet, E. Robert-Gnansia Analysis of Hydrolethalus syndrome, G2D ... Hydrolethalus syndrome, Finnish Disease Database, Findis.org Sandhoff Disease SANDHOFF DISEASE, OMIM, Victor A. McKusick, Perseveranda M. Cagas, Ada Hamosh et al.

72. All Topics - Quest Diagnostics Patient Health Library Cerebro Oculo Facio Skeletal Syndrome CerebroOculorenal Dystrophy cerebrocostomandibular syndrome cerebrocostomandibular syndrome Support Group http://www.questdiagnostics.com/kbase/list/all/c.htm

All Topics Click a letter to see a list of topics beginning with that letter. A B D E ... C-Peptide [Medical Test] C-Reactive Protein (CRP) [Medical Test] C.A.I.R. (Changing Attitudes in Recovery) - Mental Health (General) [Support Group] C.A.S.A. (Cleptomaniacs And Shoplifters Anonymous) - Crime Victims / Offenders [Support Group] C1-INH CA Ca (Calcium), Blood [Medical Test] Ca (Calcium), Urine [Medical Test] CA-125 (Cancer Antigen) Test [Medical Test] Cacchi-Ricci Disease CAD (Coronary Artery Disease) CAH Caitlin Raymond International Bone Marrow Registry - Marrow Transplants Helpline [Support Group] Calcaneal Valgus Calcaneovalgus Calcipotriene for psoriasis [Medication] Calcitonin [Medication] Calcitonin for osteoporosis [Medication] Calcitonin for Paget's disease [Medication] Calcium (Ca) in Blood [Medical Test] Calcium (Ca) in Urine [Medical Test] Calcium channel blockers for atrial fibrillation [Medication] Calcium channel blockers for cluster headaches [Medication] Calcium channel blockers for coronary artery disease [Medication] Calcium channel blockers for fast heart rates [Medication] Top Calcium channel blockers for heart attack and unstable angina [Medication] Calcium channel blockers for high blood pressure [Medication] Calcium channel blockers for migraine headaches [Medication] Calcium for kidney stones [Medication] Calcium for osteoporosis Calcium Gout, Familial

73. Three-dimensional Ultrasonographic Presentation Of Micrognathia -- Lee Et Al. 21 cerebrocostomandibular syndrome, 36.4 menstrual weeks. Cerebrocostomandibularsyndrome was diagnosed on the basis of micrognathia, a posterior cleft http://www.jultrasoundmed.org/cgi/content/full/21/7/775

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract Full Text (PDF) Alert me when this article is cited ... 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 ... Cited by other online articles PubMed PubMed Citation Articles by Lee, W. Articles by Comstock, C. H. by the American Institute of Ultrasound in Medicine Image Presentation Three-dimensional Ultrasonographic Presentation of Micrognathia Wesley Lee, MD Beverley McNie Tinnakorn Chaiworapongsa, MD Giancarlo Conoscenti, MD Karim D. Kalache, MD Ivana M. Vettraino, MD Roberto Romero, MD and Christine H. Comstock, MD Division of Fetal Imaging, Department of Obstetrics and Gynecology, William Beaumont Hospital, Royal Oak, Michigan (W.L., B.M., I.M.V., C.H.C.); and Perinatology Research Branch, National Institute of Child Health and Human Development, Wayne State University, Detroit, Michigan (W.L., T.C., G.C., K.D.K., R.R.). Address correspondence and reprint requests to Wesley Lee, MD, Division of Fetal Imaging, Department of Obstetrics and Gynecology, William Beaumont Hospital, 3601 W Thirteen Mile Rd, Royal Oak, MI 48073-6769.

74. The World Diseases A 2 Z Names By Countrylinks And Dr Impex cerebrocostomandibular syndrome. Cerebrohepatorenal Syndrome. CerebrotendinousXanthomatosis. Cervical Cancer. Chicken Pox. Childhood Depression. Chlamydia http://www.countrylinks.biz/diseases.htm

Country Links Dr Impex free on-line Services Note: search with CTRL + F 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

75. Mountain States Genetics Network Homepage CardioFacio-Cutaneous Syndrome Family Network. United Cerebral Palsy Associations.cerebrocostomandibular syndrome Support Group. Charcot-Marie-Tooth (CMT) http://www.mostgene.org/support/c-d.htm

Home About the Network Our Online Publications Regional Directory of Genetic Services ... Online Genetic Support Groups Directory Topics Genetic Services Genetic Testing Education Newborn Screening ... Other Links Directory of Online Genetic Support Groups C-D The inclusion of any resource or link in MoStGeNe does not imply endorsement. They are provided for educational purposes only. Consult with your health care provider regarding how any educational information found on the Internet may apply to your own situation. = Genetic Alliance Member = NORD Member = Medical Advisory - C - Cancer National Cancer Institute American Cancer Society National Childhood Cancer Foundation Candlelighters Childhood Cancer Foundation ... Y-ME Breast Cancer Information and Support FORCE: Facing Our Risk of Cancer Empowered - for individuals with an increased risk for breast and/or ovarian cancer Carbohydrate Deficient Glycoprotien Syndrome Society Cardio-Facio-Cutaneous Syndrome F amily Network United Cerebral Palsy Associations Cerebrocostomandibular Syndrome Support Group Charcot-Marie-Tooth (CMT) CMTnet CMT International Charcot-Marie-Tooth Association Carnitine Palmitoyl Transferase Deficiency ... CHARGE Syndrome Foundation Charge Family Support Group Chromosome Abnormalities Chromosome Deletion Outreach Chromosome 4 Wolf-Hirschorn Syndrome 4p- Parent Network Homepage Chromosome 5 Cri du Chat syndrome Support Group (Culcheth, England)

76. Pediatric Ribs: A Spectrum Of Abnormalities -- Glass Et Al. 22 (1): 87 -- RadioG cerebrocostomandibular syndrome.— cerebrocostomandibular syndrome is very rare . cerebrocostomandibular syndrome in a female neonate. http://radiographics.rsnajnls.org/cgi/content/full/22/1/87

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract Figures Only Full Text (PDF) ... Citation Map Services Email this article to a friend 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 Glass, R. B. J. Articles by Kang, E. Related Collections Musculoskeletal Radiology Pediatric Radiology Radiographics. RSNA EDUCATION EXHIBIT Pediatric Ribs: A Spectrum of Abnormalities Ronald B. J. Glass, MD Karen I. Norton, MD Sandra A. Mitre, MD and Eugene Kang, MD From the Department of Radiology, Mount Sinai School of Medicine, One Gustave L. Levy Pl, New York, NY 10029. Presented as an education exhibit at the 2000 RSNA scientific assembly. Received April 4, 2001; revision requested May 22 and received June 11; accepted June 14. Address correspondence to R.B.J.G. (e-mail: ronald_glass@smtplink.mssm.edu Abstract Top Abstract LEARNING OBJECTIVES FOR TEST...

77. Pediatric Ribs: A Spectrum Of Abnormalities -- Glass Et Al. 22 (1): 87 -- RadioG cerebrocostomandibular syndrome in a female neonate. Frontal chest radiographshows lucent ossification gaps in all of the posterior ribs. http://radiographics.rsnajnls.org/cgi/content/figsonly/22/1/87

HOME HELP FEEDBACK SUBSCRIPTIONS ... TABLE OF CONTENTS QUICK SEARCH: [advanced] Author: Keyword(s): Year: Vol: Page: This Article Abstract Full Text Full Text (PDF) ... Citation Map Services Email this article to a friend 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 Glass, R. B. J. Articles by Kang, E. Related Collections Musculoskeletal Radiology Pediatric Radiology Radiographics. RSNA Pediatric Ribs: A Spectrum of Abnormalities Ronald B. J. Glass, MD Karen I. Norton, MD Sandra A. Mitre, MD and Eugene Kang, MD From the Department of Radiology, Mount Sinai School of Medicine, One Gustave L. Levy Pl, New York, NY 10029. Presented as an education exhibit at the 2000 RSNA scientific assembly. Received April 4, 2001; revision requested May 22 and received June 11; accepted June 14. Address correspondence to R.B.J.G. (e-mail: ronald_glass@smtplink.mssm.edu View larger version [in a new window] Figure 1.

78. EMedicine - Skeletal Dysplasia : Article By Harold Chen, MD, MS, FAAP, FACMG embryopathy (teratogen), and cerebrocostomandibular syndrome (hypoxia) Neutropenia is a feature of Schwachman syndrome (metaphyseal dysplasia and http://www.emedicine.com/ped/topic625.htm

(advertisement) Home Specialties Resource Centers CME ... Patient Education Articles Images CME Advanced Search Consumer Health Link to this site Back to: eMedicine Specialties Pediatrics Genetics And Metabolic Disease Skeletal Dysplasia Last Updated: April 4, 2002 Rate this Article Email to a Colleague Synonyms and related keywords: disproportional short stature, short stature, dwarfism, osteochondrodysplasias, thanatophoric dysplasia, achondroplasia, osteogenesis imperfecta, achondrogenesis, chondrodysplasia punctata, homozygous achondroplasia, chondrodysplasia punctata, camptomelic dysplasia, congenital lethal hypophosphatasia, perinatal lethal type of osteogenesis imperfecta, short-rib polydactyly syndromes, hypochondroplasia, rhizomelic type of chondrodysplasia punctata, Jansen-type metaphyseal dysplasia, spondyloepiphyseal dysplasia congenita, atelosteogenesis, diastrophic dysplasia, congenital short femur, Langer-type mesomelic dysplasia, Nievergelt-type mesomelic dysplasia, Robinow syndrome, Reinhardt syndrome, acrodysostosis, peripheral dysostosis, Kniest dysplasia, fibrochondrogenesis, Roberts syndrome, acromesomelic dysplasia, micromelia, Morquio syndrome, Kniest syndrome, metatrophic dysplasia, spondyloepimetaphyseal dysplasia AUTHOR INFORMATION Section 1 of 10 Author Information Introduction Clinical Differentials ... Bibliography Author: Harold Chen, MD, MS, FAAP, FACMG

79. Gigablast Search Results Cerebral Palsy@ (150); cerebrocostomandibular syndrome@ (2); CerebrohepatorenalSyndrome@ (4); Cerebrotendinous Xanthomatosis@ (1); Cervical Cancer@ http://dir.gigablast.com/Health/Conditions_and_Diseases/C/

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80. Gigablast Search Results cerebrocostomandibular syndrome@ (2); CharcotMarie-Tooth Disease@ (7) as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis. http://dir.gigablast.com/Health/Conditions_and_Diseases/Genetic_Disorders/

Family filter: On Off Entire Directory Entire Category Pages in Base Category Sites in Base Category Top Health Gene Therapy Genetic Testing and Counseling ... Zellweger Syndrome Related Categories: Health: Conditions and Diseases: Congenital Anomalies Health: Conditions and Diseases: Rare Disorders This category in other languages: Danish Dutch French German ... Dr. Greene's HouseCalls A discussion of medical information on trisomy, trisomy 13, genetics, and his own personal family experience with this rare disease. www.drgreene.com/html/21614.html [archived copy] [stripped] [older copies] - indexed: Apr 26 2005 Genetic and Rare Conditions Lay advocacy groups, support groups, information on genetic conditions and birth defects for professionals, educators and individuals. Disorders from A-Z. Category: Health: Support Groups: Conditions and Diseases www.kumc.edu/gec/support/ [archived copy] [stripped] [older copies] - indexed: Apr 26 2005 The UDGD Spot Resources and information for families of children with genetic disabilities or syndromes that are still awaiting a diagnosis.

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