21. Genetic Conditions List fabrys disease Facial Haemangioma. Factor V Leiden Familial adenomatous polyposis coli Familial Hiberian Fever. Familial Mediterranean Fever http://www.agsa-geneticsupport.org.au/conditions_list.html

A-Z LIST OF CONDITIONS REPRESENTED BY AGSA A B C D ... P Q R S T U ... X Y Z -A- Aarskog syndrome Achondroplasia Acid Maltase Deficiency Acoustic Neuroma Acrocallosal syndrome Adams Oliver syndrome Adrenoleukodystrophy Aicardi syndrome Alagille syndrome Albinism Alkaptonuria Alpha l Antitrypsin Deficiency Alpha Manniosidosis Alpha Thalassaemia X-Linked Mental Retardation Alport syndrome Alstroms syndrome Amyotrophic Lateral Sclerosis Androgen Insensitivity Angelman syndrome Aniridia Anticardiolipin AB Type Antiphospholipid syndrome Ankylosing Spondylitis Apert syndrome Aspergers syndrome Ataxia -hereditary [back to top] -B- Baller-Gerold syndrome Bannayan-Riley-Ruvalcaba syndrome Baret-Biedl syndrome Bartter syndrome Batten Disease Beckwith-Wiedemann syndrome Behr syndrome Berardinelli syndrome Bilateral Iris Coloboma Bloom syndrome Blount's Disease Borjeson-Forssman-Lehmann syndrome BPES Brown syndrome [back to top] -C

22. Genetic Conditions fabrys disease Facial Haemangioma Facially disfigured Familial adenomatous polyposis coli Familial Mediterranean Fever Fanconi Anaemia http://www.angelfire.com/ab/agsa/condit.html

setAdGroup('67.18.104.18'); var cm_role = "live" var cm_host = "angelfire.lycos.com" var cm_taxid = "/memberembedded" Search: Lycos Angelfire Dating Search Share This Page Report Abuse Edit your Site ... Next This list represents genetic conditions only. In addition to this list of conditions, AGSA has established a Contact Register for over 450 genetic conditions representing families and individuals seeking contact. For further information, please contact one of our information personnel on our contact details page . Genetic Conditions Supported by AGSA To find the name of the genetic condition, click on a letter below: A B C D ... P Q R S T U ... X Y Z Search Altavista for information on the Genetic Condition you are looking for (Copy and paste the name here): Select Language any language Chinese Czech Danish Dutch English Estonian Finnish French German Greek Hebrew Hungarian Icelandic Italian Japanese Korean Latvian Lithuanian Norwegian Polish Portuguese Romanian Russian Spanish Swedish Keywords or condition name here: [A] Aarskog syndrome Achondroplasia Acid Maltase Deficiency Acoustic Neuroma Acrocallosal syndrome Adams Oliver syndrome Adrenoleukodystrophy Aicardi syndrome Alagille syndrome Albinism Alkaptonuria Alpha l Antitrypsin Deficiency Alpha Thalassaemia mental retardation on the X Chromosome Alport syndrome Alstroms syndrome Amniotic Bands Amyotrophic Lateral Sclerosis Androgen Insensitivity Angelman syndrome Ankylosing Spondylitis

23. Fabrys Disease - Consulting Health Directory fabrys disease health directory. Fabry s Disease. Information sheet on this disease including treatment, prognosis and research. http://www.health-websites.info/s_Fabrys Disease.html

home sitemap suggest url LOCATION : Fabrys Disease Search Search Results Fabry's Disease Information sheet on this disease including treatment, prognosis and research. http://www.ninds.nih.gov/health_and_medical/disorders/fabrys_doc.htm HOME Conditions and Diseases Nutrition and Metabolism Disorders Cholesterol and Other Fats ... Fabry's google_ad_client = "pub-7404640694662004"; google_ad_width = 120; google_ad_height = 600; google_ad_format = "120x600_as"; google_ad_channel ='2686635208'; google_color_border = "DC0000"; google_color_bg = "FFFFFF"; google_color_link = "0000FF"; google_color_url = "008000"; google_color_text = "000000"; Consulting health search terms used on this site: a b c d ... z Partner Sites: Advice Websites Arts Websites Beauty Websites Cooking Websites ... www.health-websites.info , ALL Right Reserved. Site developed and maintained by PEC Designs Manchester Web Design

24. Consulting Health Directory - Keywords Fabry Disease Facts for Fabry Support and Infor Fabry Support and Informa fabrys disease Fabulous Family Fitness C face acupuncture http://www.health-websites.info/sw-f.html

Warning : main(/home/pecsleep/7HNWV977/htdocs/directory/inc/meta.html): failed to open stream: No such file or directory in /home/health/public_html/searchwords.php on line Warning : main(/home/pecsleep/7HNWV977/htdocs/directory/inc/meta.html): failed to open stream: No such file or directory in /home/health/public_html/searchwords.php on line Warning /home/health/public_html/searchwords.php on line home sitemap Searched keywords in Consulting Health Directory A B C D ... Familyvillage Consulting health search terms used on this site: a b c d ... z Partner Sites: Advice Websites Arts Websites Beauty Websites Cooking Websites ... www.health-websites.info , ALL Right Reserved. Site developed and maintained by PEC Designs Manchester Web Design

25. Pharmaceutical Research And Manufacturers Association fabrys disease is a rare genetic disorder affecting people who lack an enzyme that clears a fatty substance from the blood vessels of the heart, kidneys, http://www.phrma.org/publications/quickfacts/29.05.2002.412.cfm

26. Biochemistry One answer only. FarbersAlpha galactosidase; Gauchers-Beta glucosidase; Nieman pick-Beta galactosidase; fabrys disease- Sphingomyelinase http://www.aippg.com/Biochemistry Mock test.htm

Biochemistry 24 Ques. / 20 min. 1) Formation of ammonium ions to remove the excess acid in urine is produced by which of the following enzymes: One answer only. Glutaminase Glutamate pyruvate transaminase Glutamate dehydrogenase Carboxylase 2) Which of the following amino acids un-dergoes hydroxylation and is involved in the formation of collagen: One answer only. Proline Tryptophan Phenylalanine cystiene 3) The long chain fatty acids are transmitted across the inner membrane of mitochondria by : One answer only. Acyl carrier protein carnitine Glycoprotein None of the above 4) Restriction endonuclease is used in : One answer only. Recombinant DNA technology For splicing DNA For genetic engineering None of the above 5) Chromosome 5 is associated with : One answer only. Ulcerative colitis Familial adematosis polyposis Crohn's disease Down's syndrome 6) Heme synthesis true is : One answer only. ALA synthesis is catalysed by thiamine pyrophosphate Ferochelatase is inhibited by lead variegate porphylia is due to deficiency of uroporphyrin synthase Protoporphyrin oxidase is a cytosolic coenzyme 7) In respiratory cycle regarding ATP formation by oxidative phosphorylation true is A/E : One answer only.

27. Skin Disorders Information, Support And Other Resources For UK Patients fabrys disease Support, (website temporarily down) Tel 01305 774443 Fax 01305 774443 The fabrys disease Research Fund has been taken over by Society for http://www.equip.nhs.uk/topics/allergy/skin.html

var sc_project=455128; var sc_partition=2; Skin Disorders Home Information Topics Related topics: allergy cancer food intolerance infectious diseases ... Other information What are skin disorders? The following links take you straight to pages of information about skin disorders. This information has been checked by doctors to ensure it is correct and appropriate for UK patients. British Association of Dermatologists - has very detailed information about a large number of skin disorders including eczema, lichen and fungal disorders, dermatitis, psoriasis and many other less common conditions written by dermatologists Cancer BACUP - provides detailed information on all types of skin cancer, its treatment and support Patient UK Prodigy Surgery - Medicdirect has information on skin operations and surgical procedures EQUIP also has separate pages of information on Allergy in general Arthritis-related disorders Cancer Food Intolerance and Infectious diseases Back to the top of this page Links to useful websites: The following links contain information about skin disorders. The information on these websites has not been checked by our doctors, but they are rated as good quality sites.

28. Genetic Disorders Information, Support And Other Resources For UK Patients Woodthorpe, Nottinghamshire NG3 5QF Tel 0115 926 9634; fabrys disease Support, Email mps@mpssociety.co.uk also provides support on fabrys disease http://www.equip.nhs.uk/topics/genetic.html

var sc_project=455128; var sc_partition=2; Genetic disorders Home Information Topics Further information General Health Information ... Other information What are genetic disorders? The following links take you straight to pages of information about genetic disorders. This information has been checked by doctors to ensure it is correct and appropriate for UK patients. British Society for Paediatric Endocrinology and Diabetes - contains information written by a specialist doctor on: Achondroplasia, Congenital Adrenal Hyperplasia (21 hydroxylase), Congenital Adrenal Hyperplasia (11 hydroxylase), Congenital Adrenal Hyperplasia - treatment in pregnancy, Complete Androgen Insensitivity Syndrome (CAIS), Congenital Hypothyroidism, Coeliac Disease, Delayed Puberty, Diabetes Insipidus, Grave's Disease (Thyrotoxicosis), Growing Pains, Gynaecomastia, Hypopituitarism, Hypothyroidism (Acquired), Klinefelter's Syndrome, Labial Adhesions, Marfan's Syndrome, Overweight, Partial Androgen Insensitivity Syndrome (PAIS), Precocious Puberty, Steroid Replacement, Steroid Treatment, Tall Stature, Turner's Syndrome Contact a Family - information and support on many specific conditions and rare disorders written by doctors EQUIP also has separate pages of information on rheumatic disorders/arthritis congenital heart diseases food intolerance and many other

29. Fa : On Medical Dictionary Online Fabry Disease fabrys disease Face Face Bow, Orthodontic Face Bows, Orthodontic Face Flies Familial High Density Lipoprotein Deficiency Disease http://www.online-medical-dictionary.org/fa.asp?q=~Fa

30. The Health Boards Executive - Current Project Status Radiography Clinical protocols; Cardiology - Implantable Defibrillators, Biventricular Pacemakers; Drugs - fabrys disease (Costs and Medication usage) http://www.hebe.ie/ProgrammesProjects/HealthTechnologyAssessment/CurrentProjectS

About Us Health Boards News / Events Programmes/ Projects ... FAQ Search for a Topic : You are here: Home Programmes/ Projects Health Technology Assessment Current Project Status What is the Current Project Status? The sub-committees have produced discussion papers and recommendations in relation to the areas mentioned below: Scanning - Position Emmission Termography (PET) Radiography - Clinical protocols Cardiology - Implantable Defibrillators, Biventricular Pacemakers Drugs - Fabrys Disease (Costs and Medication usage) It is anticipated that the documents will be available as guidelines for practising professionals early 2005 Current Project Status Project Justification Project Vision Project Objectives Current Project Status Project Team The Health Service Executive, Block 4, Central Business Park, Clonminch, Portlaoise Road, Tullamore, Co. Offaly, Ireland info@hebe.ie www.hebe.ie

31. Means And Frequencies For Dataset Saf.patients, Patient Data MALIGNANT 80 0.0 2718B Primary oxalosis 226 0.0 2718Z OXALATE NEPHROPATHY / OXALOSIS 76 0.0 2727A fabrys disease 122 0.0 2727Z fabrys disease 22 0.0 http://www.usrds.org/resguide/appendices/appendix_g/means_frequencies/patients.t

32. CSAHS - CSLS - Handbook EWINGS SARCOMA, EXANTHEM SUBITUM, fabrys disease, FACTOR DEFICIENCY Search for all tests associated with a particular disease. http://www.cs.nsw.gov.au/csls/handbook/default.asp

Back CSAHS Home CSLS Home Contact Us Laboratories: Canterbury Concord RPAH Specialist Clinical Units ... Links CSLS Laboratory Handbook Search Page Search by TEST NAME: Starts with Exact Contains Alphabetical Test Search: A B C D ... Z Search by DISEASE: ... Choose a Disease from the list ... ABETALIPOPROTEINAEMIA ABSCESS ABSCESS BREAST ABSCESS LIVER ACARIASIS ACHONDROPLASIA ACID MALTASE DEFICIENCY ACROMEGALY ACTINOMYCOSIS ACTIVATED PROTEIN C RESISTANCE ADDISONS DISEASE ADDISONS DISEASE AUTOIMMUNE ADENOSINE DEAMINASE DEFICIENCY ADENYLATE DEAMINASE DEFICIENCY ADENYLATE KINASE DEFICIENCY ADENYLOSUCCINASE DEFICIENCY ADENYLSUCCINATE LYASE DEFICIENCY ADRENAL DISEASE AUTOIMMUNE ADRENOCORTICAL HYPERFUNCTION ADRENOCORTICAL INSUFFICIENCY ADRENOLEUCODYSTROPHY AGAMMAGLOBULINAEMIA ALCOHOL ABUSE ALLERGY ALLERGY DUST MITE ALPHA-1-ANTITRYPSIN DEFICIENCY ALVEOLAR RHABDOMYOSARCOMA ALZHEIMERS DISEASE AMINOACIDURIAS AMOEBIASIS AMYLOIDOSIS AMYLOIDOSIS RENAL FAMILIAL AMYOTROPHIC LATERAL SCLEROSIS (ALS) ANAEMIA ANAEMIA HAEMOLYTIC ANAEMIA HEREDITARY ANAEMIA HYPOCHROMIC ANAEMIA IRON DEFICIENCY ANAEMIA MEGALOBLASTIC ANAEMIA OBSCURE ANAEMIA OF CHRONIC DISEASE ANAEMIA PERNICIOUS ANAEMIA SICKLE CELL ANAEMIA SIDEROBLASTIC ANAPHYLAXIS ANGELMAN SYNDROME ANGIODYSPLASIA ANAEMIA ANGIOEDEMA ACQUIRED ANGIOEDEMA HEREDITARY ANGIOSTRONGYLIASIS ANGULAR STOMATITIS ANHYDROTIC ECTODERMAL DYSPLASIA ANKYLOSING SPONDYLITIS ANOREXIA NERVOSA ANTI CHOLINESTERASE EXPOSURE ANTI THROMBIN III DEFICIENCY ANTICARDIOLIPIN SYNDROME ANTIPHOSPHOLIPID SYNDROME AORTIC ANEURYSMS FAMILIAL APERT SYNDROME APLASIAS APLASTIC ANAEMIA APNOEA ASSOCIATED WITH ANAESTHETIC

33. Ethical Aspects In Renal Medicine 11.30, fabrys disease. Jarl Ahlmén, Göteborg, Sweden. 11.50, Interactive. 11.55, Discussion The role of the nephrologist today and in the future http://kidney.med.gu.se/sve/div/Meet.htm

Ethical Aspects in Renal Medicine 24-25 January, 2002 Wallenberg Conference Center , G teb o rg , Sweden Thursday 24 January Lunch buffet Welcome Chairman Jarl Ahlmén Future imperfect - The prospects for medicine in the new millenium James le Fanu, London UK Discussion Some remarks on priority setting and renal medicine Göran Lantz, Uppsala, Sweden Coffee + Exhibition Chairman Carl Kjellstrand Collaboration between industry, academy and health care Bengt Lindholm, Stockholm Sweden Industry -Nephrology Relationship in End-Stage Renal Disease William Bennet Oregon USA Controversies in dialysis modality selection and distribution David Mendelssohn, Toronto Canada Discussion Dinner Friday 25 January Chairman Börje Haraldsson Case presentations Stopping dialysis Carl Kjellstrand, Chicago USA Ethical aspects of kidney donation from living donors. Ingela Fehrman, Stockholm, Sweden Coffee + Exhibition Chairman William Bennet Daily hemodialysis - you must be kidding Carl Kjellstrand, Chicago, USA Interactive N ormalisation of hemoglobin in ESRD Bo G Danielson, Uppsala, Sweden

34. The News Letter ---Sir Ganga Ram Hospital Hereditary motor sensory neuropathy, Friedrichs ataxia, fabrys disease, No relevant history, Unlikely. InfectionsTabes, HIV, diphtheria, No e/o on http://www.sgrh.com/nletter/nlsgrh/jul-sep01/case.htm

C LINICO-PATHOLOGICAL CONFERENCE Treating unit: Neurology Discussant: Dr S. Prabhakar, Professor and Head of Department of Neurology, Post Graduate Institute of Medical Education and Research (PGlMER), Chandigarh. A 62-year-old lady with right frozen shoulder, left-sided sciatica and peripheral neuropathy Presentation A 62-year-old housewife from New Delhi presented with pain in the right shoulder for the past 2 years and low back pain for 2 months prior to admission. She had a past history of hypertension for 5 years treated with atenolol 50 mg o.d. Initially, she had pain in the right shoulder only on exertion, associated with stiffness and difficulty in movement. The pain was maximal after activity and at the end of the day and was relieved with rest. There was no radiation of the pain, or increase in intensity on coughing, sneezing or straining. She was treated with analgesics and anti-inflammatory gels which afforded minimal improvement. For the past 2 months, she reported progressively increasing pain and marked limitation of movement of the right shoulder. Minimal movement caused severe lancinating pain. She was examined by various physicians and an orthopaedician and was thought to have a frozen shoulder. Other than osteoporosis, X-ray of the right shoulder did not reveal any abnormality. She was treated with analgesics, calcium supplements and advised physiotherapy. Despite this, her symptoms progressively worsened. For the past 2 months she also complained of low backache, which at times radiated to her left buttock and the back of the left thigh. The pain was catching in type but did not increase with coughing, sneezing or straining. There was no history of trauma, stiffness or heaviness of the lower limbs, difficulty in walking, or of bowel or bladder involvement.

35. WOMENS-HEALTH Messages For March, 2001: Re: Endoscopy And Possible Pregnancy signature Content-Disposition Inline Content-Type Text/HTML;......how does fabrys disease affect obgyn patients. WebTVMail-11755-130 Content- http://forums.obgyn.net/womens-health/WHF.0103/1789.html

-VISIT OUR OTHER FORUMS- Breast Health Forum Endo@OBGYN.net Mujer (en español) PCOS Forum PCOS Diet Forums PCOS Medication Forum Vrouw en Gezondheid (nederland) Women's Health Forum Young Women's Health Forum s earch this forum: Re: Endoscopy and possible pregnancy From: crystal anonymous@obgyn.net Wed, 14 Mar 2001 13:37:22 -0500 (EST) Messages sorted by: [ date ] [ thread ] [ subject ] [ author ] Next message: anonymous@obgyn.net: "no subject received Wed, 14 Mar 2001 12:40:08 -0600" Previous message: Lynn D. Montgomery, MD: "Re: Endoscopy and possible pregnancy" Maybe in reply to: Erika: "Endoscopy and possible pregnancy" WebTV-Mail-11755-130 Content-Type: Text/Plain; Charset=US-ASCII Content-Transfer-Encoding: 7Bit how does fabrys disease affect obgyn patients. WebTV-Mail-11755-130 Content-Description: signature Content-Disposition: Inline Content-Type: Text/HTML; Charset=US-ASCII Content-Transfer-Encoding: 7Bit Image by FlamingText.com Next message: anonymous@obgyn.net: "no subject received Wed, 14 Mar 2001 12:40:08 -0600" Previous message: Lynn D. Montgomery, MD: "Re: Endoscopy and possible pregnancy"

36. MORE BORED ASSHOLE COPS Now, Greg suffers from fabrys disease, a debilitating genetic disorder which Due to the medical progression of his inherited genetic disease (Fabrys, http://mediafilter.org/guest/Pages/January.23.1999.13.31.05

MORE BORED ASSHOLE COPS http://Mediafilter.org/guest/Pages/January.23.1999.13.31.05 Register your Page. This Event Happened in SARASOTA FL. Your FeedBack is appreciated Display Comments on this Page Send Comments to WebProvider only Refer to this page My favorite Link: MediaFilter Sponsored by MediaFilter FeedBack mcarroll.vip.best.com. Tuesday, February 2, 1999 19:48:49 There isn't anything you can do about it. Police agencies, like this one, will generaly go after easy targets. They will not go after REAL criminals for fear of makking their job dangorous. And they know that they are accountable to nobody. Maybe it's time for the citizens to take back their cities. FeedBack p105.sas2.dialup.tyr1.flash.net. Thursday, February 4, 1999 01:55:26 If you do not like the way the police are doing their job, or do not like the laws that they enforce, call your congressman. If you think that you could do the job any better go to your local police department and get a job application. FeedBack p105.sas2.dialup.tyr1.flash.net. Thursday, February 4, 1999 01:55:35 If you do not like the way the police are doing their job, or do not like the laws that they enforce, call your congressman. If you think that you could do the job any better go to your local police department and get a job application.

37. City Of Westminster Eye Care, fabrys disease, Facial Disfigurement, Familial Dysautonomia, Familial Spastic Paraplegia, Families, Fanconis Anaemia, Fetal Alcohol Syndrome http://www3.westminster.gov.uk/weldis/subjectsearch.cfm

@import url(/style/screen.css); @import url(/style/default_theme.css); About Us Press Office Contact Us Help ... Site Map Fast Find A-Z of Services Forms Maps Find My Nearest... I want to.. Pay a parking ticket Apply for a business licence Report a street problem View planning applications Search the library catalogue Find a job vacancy Park in Westminster Dispose of commercial waste Search by Keyword Home Topics WELDIS WELDIS Subject Search Page Group Search Select Subject Here Abortion Services Access Accidents Accommodation Acne Adams-Oliver Syndrome Adaptations Addisons Disease Adoption Adrenoleukodystrophy Adult Education Advice Advice Centres Advocacy African Agenesis of the Corpus Callosum Agoraphobia Aicardi Syndrome Air Quality Air Travel Alarms Albinism Alcohol Allergies Alternating Hemiplegia Alzheimers Disease Amnesia Amputees Anaphylaxis Androgen Insensitivity Syndrome Anencephaly Angelman Syndrome Ankylosing Spondylitis Anophthalmia Anorchidism Anorexia Antidepressants Antipsychotics Anxiety Aphasia Aplastic Anaemiae Arthrogryposis Arabic Armenian Arthritis Artificial Limbs Arts Asian Assessment Centres Assistance Dogs Assistive Technology Asthma Asylum Seekers Ataxia Ataxia-Telangiectasia ATR-X Syndrome Attention Deficit Disorder Autism Autoimmune Disorders Back Pain Bangladeshi Batten Disease Beckwith-Wiedemann Befriending Behcets Syndrome Benefits Benefits Agency Offices Bengali Bereavement Birth Defects Black Bladder Bladder Exstrophy/Epispadias Blephaviphimosis Blind Bone Marrow Transplants Books Bowel Problems Bowls Braille Braille Maps Brain Injury Brain Related Disorders

38. TOB: APPROVED CE 03/03/2005, 03/03/2005, 0, 1, TYLER, TX, 5354, OCULAR MANIFESTATIONS OF fabrys disease, GENZYME,MAGGIE POWELL,4654 BEVERLY DR,,DALLAS,TX,75209,(214) 521 http://www.tob.state.tx.us/approvedce2002.htm

Licensing Doctors of Optometry and Regulating the Practice of Optometry Approved 2005 Continuing Education The following continuing education courses are the courses approved by the Texas Optometry Board for credit for 2006 renewal. If you do not see a course listed, please call the Board at 512-305-8500, to inquire about the status of that course. Please note that grand rounds, correspondence and on-line (Internet) courses may have a start date of January 1, 2005. Please verify with the provider that you will be able to receive a certificate of completion in time to submit the certificate to the Board's office. This list is provided for the convenience of license holders. The course provider has provided information concerning dates and contact procedures. Please confirm any information with the provider. The Board cannot be responsible for the accuracy of this information. See also the legal notice at the bottom of this page. Start Date End Date Gen Hours D/T Hrs Location Course No Course Title DALLAS/FORT WORTH, TX

39. London New Drugs Group: Documents - Briefings Enzyme replacement for fabrys disease. March 2002 Esomeprazole (Nexium) update 2. March 2003 Dovobet Ointment. October 2002 http://www.londonpharmacy.nhs.uk/LNDG/LNDG_Documents/Briefing.asp

home about search feedback Sections LNDG Database Prescribing Decisions Database Meetings Discussion Group ... Contacts Quick Search This site Druginfozone advance search Links Link search Link Categories A - Z Link Listing Portal ... LNDG Documents LNDG Briefing Documents B riefing documents contain points for consideration. Both will review and summarise the clinical trial evidence. Expected costs will be calculated, where possible. Regional Specialist Services Commissioning Group If you have already logged on to this site you will still require to use www.druginfozone.nhs.uk web site login details to access documents stored on that site. More info.. Fish oils for children with attention deficit hyperactivity disorder and other behavioural disturbances - updated June 2005 Rasagiline (July 05) Bivalirudin for percutaneous coronary intervention (June 05) ... Long acting methylphenidate for attention deficit hyperactivity disorder. May 2002 Regional Specialist Services Commissioning Group There are no documents available in this section Any access to a secured document on www.druginfozone.nhs.uk will require your user authentication (login details) for the site. The www.druginfozone.nhs.uk authentication system is seperate from this web site's authentication.

40. Matching Tests fabrys disease DNA. Alpha-Galactosidase. Factor 10. Clotting Factors. Coagulation Factors. Factor X. Factor 11. Clotting Factors. Coagulation Factors http://www.palmslab.com.au/labinfo/test.php?Testname=F&Orgcode=&SearchType=1

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