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         Porphyrias:     more books (87)
  1. Porphyrias: An entry from Thomson Gale's <i>Gale Encyclopedia of Nursing and Allied Health</i> by Barbara Wexler, 2002
  2. Porphyria Cutanea Tarda Medical Guide by Qontro Medical Guides, 2008-07-09
  3. Poetry by Robert Browning: Andrea Del Sarto, Porphyria's Lover, Red Cotton Night-Cap Country, Childe Roland to the Dark Tower Came
  4. Watch for the skin signs of hepatitis C infection. (Porphyria Cutanea Tarda).: An article from: Skin & Allergy News by Doug Brunk, 2002-11-01
  5. Test all PCT patients for hereditary hemochromatosis. (Porphyria Cutanea Tarda).: An article from: Skin & Allergy News
  6. Diseases: Porphyrias To Spasm (Volume 7) by Bryan Bunch, 2003-01
  7. Volutomitridae: Microvoluta, Volutomitra, Peculator, Microvoluta Marginata, Peculator Porphyria, Peculator Obconicus, Peculator Hedleyi
  8. DISTURBANCES IN HEME SYNTHESIS Special Considerations of the Sideroachresti c Anemias and Erythropoietic Porphyrias
  9. No fun in the sun: a case of idiopathic porphyria cutanea tarda in a patient with systemic scleroderma.(Section on Rheumatology): An article from: Southern Medical Journal by Amir Kaki, 2004-10-01
  10. Skin Conditions Resulting From Errors in Metabolism: Phenylketonuria, Adrenoleukodystrophy, Gout, Porphyria, Lafora Disease, Alkaptonuria
  11. Gale Encyclopedia of Nursing and Allied Health: Porphyrias by Barbara Wexler, 2002-01-01
  12. South African Journal of Laboratory and Clinical Medicine. Volume 9 Number 4 December 1963. Special Issue. Proceedings of the International Conference on the Porphyrias. Cape Town 18-24 September 1963. by A [Ed] Landau, 1963
  13. Works by Robert Browning (Study Guide): Plays by Robert Browning, Poetry by Robert Browning, Andrea Del Sarto, Porphyria's Lover
  14. Porphyria's Lover: Shmoop Poetry Guide by Shmoop, 2009-11-03

41. Nutrition And Metabolism Disorders: Porphyrias
Nutrition and Metabolism Disorders porphyrias. Diagnosing the porphyrias.An article by Thomas G. DeLoughery, Associate Professor of Medicine. EPP.
http://www.puredirectory.com/Health/Conditions-and-Diseases/Nutrition-and-Metabo
Nutrition and Metabolism Disorders: Porphyrias
Home Health Conditions and Diseases Nutrition and Metabolism Disorders : Porphyrias google_ad_client = 'pub-3272565765518472';google_ad_width = 336;google_ad_height = 280;google_ad_format = '336x280_as';google_color_border = 'FFFFFF';google_color_bg = 'FFFFFF';google_ad_channel ='7485447737';google_alternate_color = 'FFFFFF';google_color_link = '0000FF';google_color_url = '008000';google_color_text = '000000';
Standard Listings
Acute Intermittent Porphyria Forum
Information and links about Porph. Includes registration form for an email list.
Canadian Porphyria Foundation
Mission statement, objectives of the organization, newsletters and safe and unsafe drugs. Also: A Guide to Porphyria - a complete booklet of inf...
Diagnosing the Porphyrias
An article by Thomas G. DeLoughery, Associate Professor of Medicine.
EPP
Short for Erythropoetic ProtoPorhyria, which is a rare metabolic disease. A personal site about this disorder, one of the family of porphyrias.
King George II and Porphyria
Talks about the symptoms of porphyria affecting King George III who ruled England during the American revolution.

42. Hepatic Porphyrias,Congenital Erythropoietic Porphyria,CEP,Congenital Porphyria,
Hepatic porphyrias,Congenital Erythropoietic Porphyria,CEP,Congenital Porphyria,GuentherPorphyria,Gunther Disease,Congenital Erythropoietic Porphyria,CEP
http://www.icomm.ca/geneinfo/cep.htm
Hepatic Porphyrias,Congenital Erythropoietic Porphyria,CEP,Congenital Porphyria,Guenther Porphyria,Gunther Disease,Congenital Erythropoietic Porphyria,CEP,Congenital Porphyria,Guenther Porphyria,Gunther Disease
For Information on Workshops and Seminars for Special Needs Children click here The GAPS INDEX
to Information on the Internet about Genetic Disorders and Birth Defects

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HOME
DISORDERS GLOSSARY Porphyria, Congenital Erythropoietic
also known as:
CEP
Congenital Porphyria
Guenther Porphyria
Gunther Disease
Disorder Subdivisions Erythropoietic Porphyrias Hepatic Porphyrias (as defined by the National Organization for Rare Disorders
Congenital Erythropoietic Porphyria (CEP) is extremely rare and is inherited through an autosomal recessive trait. It is also known as Guenther Porphyria. The deficient enzyme is uroporphyrinogen III cosynthase. As is characteristic of the erythropoietic porphyrias, symptoms usually begin during infancy. CEP is manifested by markedly increased levels of porphyrins in bone marrow, red blood cells, plasma, urine and feces. Porphyrins are also deposited in the teeth and bones. The Porphyrias are a group of at least seven disorders. The common feature in all porphyrias is the excess accumulation in the body of "porphyrins" or "porphyrin precursors." These are natural chemicals that normally do not accumulate in the body. Precisely which one of these porphyrin chemicals builds up depends upon the type of porphyria that a patient has.

43. British National Formulary: 9.8.2 Acute Porphyrias
9.8.2 Acute porphyrias. or, (0113) 283 7010. St Thomas Hospital, London, (020)7928 9292. Subsections. HAEM ARGINATE. Drugs unsafe for use in acute porphyrias.
http://www.bnf.org/bnf/bnf/current/doc/5181.htm
Printed from: Joint Formulary Committee. British National Formulary . 47 ed. London: British Medical Association and Royal Pharmaceutical Society of Great Britain; 2004. BNF Skip navigation Previous Next Sub-sections ... 9.8 Metabolic disorders
9.8.2 Acute porphyrias
The acute porphyrias (acute intermittent porphyria, variegate porphyria, hereditary coproporphyria and 5-aminolaevulinic acid dehydratase deficiency porphyria) are hereditary disorders of haem biosynthesis; they have a prevalence of about 1 in 10 000 of the population. Great care must be taken when prescribing for patients with acute porphyria since many drugs can induce acute porphyric crises. Since acute porphyrias are hereditary, relatives of affected individuals should be screened and advised about the potential danger of certain drugs. Treatment of serious or life-threatening conditions should not be withheld from patients with acute porphyria. Where there is no safe alternative, urinary porphobilinogen excretion should be measured regularly; if it increases or symptoms occur, the drug can be withdrawn and the acute attack treated. Haem arginate is administered by short intravenous infusion as haem replacement in moderate, severe or unremitting acute porphyria crises.

44. British National Formulary: Drugs Unsafe For Use In Acute Porphyrias
Drugs unsafe for use in acute porphyrias. The following list containsdrugs on the UK market that have been classified as ‘unsafe
http://www.bnf.org/bnf/bnf/current/doc/34979.htm
Printed from: Joint Formulary Committee. British National Formulary . 47 ed. London: British Medical Association and Royal Pharmaceutical Society of Great Britain; 2004. BNF Skip navigation Previous Next Sub-sections ... 9.8.2 Acute porphyrias
Drugs unsafe for use in acute porphyrias
The following list contains drugs on the UK market that have been classified as ‘unsafe' in porphyria because they have been shown to be porphyrinogenic in animals or in vitro , or have been associated with acute attacks in patients. Further information may be obtained from: Welsh Medicines Information Centre University Hospital of Wales Cardiff Tel: (029) 2074 2979 Note Quite modest changes in chemical structure can lead to changes in porphyrinogenicity but where possible general statements have been made about groups of drugs; these should be checked first Sub-sections Drug groups (check first Individual Drugs (check groups above first ... Accessibility

45. Pediatric Oncall- Porphyria
porphyrias. UserName. Password. New Register, Dr Ira Shah MD, DCH(Gold Medalist),FCPS, DNB. Q How do porphyrias occur? A porphyrias are a rare disorder.
http://www.pediatriconcall.com/fordoctor/DiseasesandCondition/porphyrias.asp
DOCTOR CORNER Search GO Home Back Ask Doctor Post Query Education Teaching Files Question of the day Specialist Answers Latest Updates Conference Journal Search Pharma Updates Search For Pediatricians Hospitals Special Schools Drug Index ... Sign Out
PORPHYRIAS UserName Password New Register Dr Ira Shah
M.D, DCH(Gold Medalist), FCPS, DNB
Q: What is porphyria?
A:
Porphyrias are a heterogeneous group of either inherited or acquired disorders of heme biosynthesis which cause either skin problems or a condition known as acute attack. Q: How do porphyrias occur?
A:
Porphyrias are a rare disorder. They occur due to specific abnormality of various enzymes in the biosynthetic pathway of heme production. As a result, excess amounts of porphyrias and their precursors accumulate in the body causing generalized clinical abnormalities. Q: What are the various types of porphyrias ?

46. Health - Conditions And Diseases - Nutrition And Metabolism
Top Health Conditions and Diseases Nutrition and Metabolism Disorders porphyrias Apersonal site about this disorder, one of the family of porphyrias.
http://www.sedirectory.net/Health/Conditions_and_Diseases/Nutrition_and_Metaboli
Web Hosting Dir Web Design Dir Search Engine Dir Hardware Info ... Resources Search: Top Health Conditions and Diseases Nutrition and Metabolism Disorders ... Porphyrias See also:

47. Conditions And Diseases - Porphyrias Top Links
porphyrias Web Site Links. Fact sheets and links to related resources. porphyrias A brief look at the two major types, the symptoms and an example is given.
http://www.disease-resources.com/Top_Health_Conditions_and_Diseases_Nutrition_an
Sub Categories
Related Healthcare Subjects Disabilities Environmental Health Fitness Health Insurance ... Men's Health
Porphyrias Web Site Links Porphyria Page A patient guide for all people with this disorder. Compiled by Professor Michael Moore.
The American Porphyria Foundation
Non-profit organization advancing awareness, research, and treatment of Porphyria. Fact sheets and links to related resources.
Porphyrias
A brief look at the two major types, the symptoms and an example is given.
HealthCentral - Porphyria
General overview of this rare disease.
Porphyrias: Diagnosis and Treatment
Clinical manifestations, diagnosis, etiology and treatment of six types of porphyrias are discussed.
Porphyria: The Woman Who Has The Vampire Disease
Review by the FindArticles.com on this book on porphyria written by Lenore B. Weinstein.
King George II and Porphyria
Talks about the symptoms of porphyria affecting King George III who ruled England during the American revolution.
Canadian Porphyria Foundation
Mission statement, objectives of the organization, newsletters and safe and unsafe drugs. Also: A Guide to Porphyria - a complete booklet of information.
Porphyria Hub
Links to overviews, full text articles, diagnosis and treatment and research projects.

48. Porphyrins, QN, 24-HR Ur
Use. Evaluate porphyrias, including those involving deficiencies of enzymes whichare needed for heme synthesis and chemical porphyrias. porphyrias Overview.
http://www.labcorp.com/datasets/labcorp/html/chapter/mono/sc029300.htm
Porphyrins, QN, 24-HR Ur Number CPT Synonyms Coproporphyrin; Uroporphyrin Related Information Test Includes Coproporphyrins; uroporphyrins; heptacarboxylporphyrins; hexacarboxylporphyrins; and pentacarboxylporphyrins Special Instructions Request form must state 24-hour collection volume. Specimen Urine (24-hour), protected from light Volume 25 mL aliquot Minimum Volume 5 mL aliquot Container Plastic urine container with 5 g sodium carbonate (Na CO ) as the preferred preservative. No preservative is also acceptable. Do not use acid preservative. Use amber plastic transfer tube and amber stopper (order #5660190801). (If amber tubes are unavailable, cover plastic container completely, top and bottom, with aluminum foil. Identify specimen with patient name directly on the container and on the outside of the aluminum foil. Secure with tape.) Collection Instruct patient to void at 8 AM (or 8 PM) and discard the specimen. Then collect all the urine including the final specimen voided at the end of the 24-hour collection period (ie, 8 AM (or 8 PM) the following day). Specimen must be kept refrigerated during collection. Label container with patient's name, and date and time collection started and finished. Measure and record total urine volume. Mix well; send aliquot to laboratory. Storage Instructions Do not expose to light. Refrigerate.

49. :: Ez2Find :: Porphyrias
Guide porphyrias, Global Metasearch Any Language Guides, porphyrias. ez2FindHome Directory Health Conditions
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50. Gale Encyclopedia Of Medicine Porphyrias
porphyrias. Gale Encyclopedia of Medicine by Julia Barrett. Definition. The porphyriasare a group of rare disorders that affect heme biosynthesis.
http://www.findarticles.com/cf_dls/g2601/0010/2601001094/p1/article.jhtml
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Porphyrias
by Julia Barrett
Definition
The porphyrias are a group of rare disorders that affect heme biosynthesis. Heme is an essential component of hemoglobin as well as many enzymes throughout the body.
Description
Biosynthesis of heme is a multistep process that starts with simple molecules and ends with a large, complex heme molecule. Each step of the biosynthesis pathway is directed by its own task-specific protein, called an enzyme. As a heme precursor molecule moves through each step, an enzyme modifies it in some way. If the precursor is not modified, it cannot proceed to the next step. This situation is the main characteristic of the porphyrias. Owing to a defect in one of the enzymes of the heme biosynthesis pathway, protoporphyrins or porphyrin (heme precursors) are prevented from proceeding further along the pathway. Instead, precursors accumulate at the stage of the enzyme defect and cause an array of physical symptoms in the affected person. Specific symptoms depend on the point at which heme biosynthesis is blocked and which precursors accumulate. In general, the porphyrias primarily affect the skin and the nervous system. Symptoms can be debilitating or life threatening in some cases. Porphyria is an inherited condition, but it may be acquired after exposure to poisonous substances.

51. Startplane /Health/Conditions_and_Diseases/Nutrition_and_Metabolism_Disorders/Po
porphyrias. See also Top/Health/Conditions and Diseases/P. Diagnosing the porphyrias An article by Thomas G. DeLoughery, Associate Professor of Medicine.
http://www.startplane.com/Health/Conditions_and_Diseases/Nutrition_and_Metabolis
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See also: Links
  • Acute Intermittent Porphyria Forum - Information and links about Porph. Includes registration form for an email list. Canadian Porphyria Foundation - Mission statement, objectives of the organization, newsletters and safe and unsafe drugs. Also: A Guide to Porphyria - a complete booklet of information. Diagnosing the Porphyrias - An article by Thomas G. DeLoughery, Associate Professor of Medicine. EPP - Short for Erythropoetic ProtoPorhyria, which is a rare metabolic disease. A personal site about this disorder, one of the family of porphyrias. King George II and Porphyria - Talks about the symptoms of porphyria affecting King George III who ruled England during the American revolution. Me and AIP - Acute Intermittent Porphyria. A personal experience with this disease touching on nutrition, diet, doctors and a healthier safer chemically free environment. Porphgroup - An e-mail group at Yahoo dealing with the metabolic disease porphyria.

52. Porphyrias
The New Health Directory, Directory, Home Health Conditions and DiseasesNutrition and Metabolism Disorders porphyrias (17) See Also
http://www.thenewhealthfind.com/Health/ConditionsandDiseases/NutritionandMetabol
Directory Home Health Conditions and Diseases Nutrition and Metabolism Disorders : Porphyrias (17)
See Also:

53. Conditions And Diseases: Nutrition And Metabolism Disorders: Porphyrias
Health and Home. porphyrias. Fact sheets and links to related resources.http//www.enterprise.net/apf/. porphyrias. Last Update Mon May 10 2004.
http://www.health-home.net/Conditions_and_Diseases/Nutrition_and_Metabolism_Diso
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Porphyrias
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Looking for something in particular? the entire directory only this category Home Conditions and Diseases Nutrition and Metabolism Disorders : Porphyrias LINKS:
  • Acute Intermittent Porphyria Forum
    Information and links about Porph. Includes registration form for an email list.
    http://members.tripod.com/~theaipforum/
  • Canadian Porphyria Foundation
    Mission statement, objectives of the organization, newsletters and safe and unsafe drugs. Also: A Guide to Porphyria - a complete booklet of information.
    http://www.cpf-inc.ca/
  • Diagnosing the Porphyrias
    An article by Thomas G. DeLoughery, Associate Professor of Medicine.
    http://www.ohsu.edu/som-hemonc/handouts/deloughery/por.shtml
  • EPP Short for Erythropoetic ProtoPorhyria, which is a rare metabolic disease. A personal site about this disorder, one of the family of porphyrias. http://members.tripod.com/~Alzuko/epp.htm
  • King George II and Porphyria Talks about the symptoms of porphyria affecting King George III who ruled England during the American revolution. http://www.mhhe.com/biosci/ap/seeleyap/cardio/reading20.mhtml

54. Porphyria - Encyclopedia Article About Porphyria. Free Access, No Registration N
The porphyrias are inherited or acquired disorders of specific enyzmes in theheme A heme is a metalcontaining cofactor that consists of an iron atom
http://encyclopedia.thefreedictionary.com/porphyria
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Porphyria
Word: Word Starts with Ends with Definition The porphyrias are inherited or acquired disorders of specific enyzmes in the heme A heme is a metal-containing cofactor that consists of an iron atom contained in the center of a large heterocyclic organic ring called a porphyrin . And although porphyrins do not necessarily contain iron, a substantial fraction of porphyrin-containing metalloproteins do in fact have heme as their prosthetic subunit. There are three biologically important kinds of heme. The most common type of heme is called heme b . Hemoglobin and myoglobin are examples of proteins that contain heme b. Heme b is not covalently bound to the apoprotein it is found in. The structure of heme b is given here:
Click the link for more information. biosynthetic pathway. They are broadly classified as hepatic porphyrias or erythropoetic porphyrias , based on the site of the overproduction and accumulation of the porphyrins A porphyrin is a heterocyclic macrocycle made from 4 pyrrole subunits linked on opposite sides through 4 methine bridges. The macrocycle, therefore, is completely aromatic, unlike the related corrins or chlorins. Porphyrins combine readily with metals, coordinating with them in the central cavity. Iron, zinc, copper, nickel, and cobalt containing porphyrins are known, and many other metals can be inserted. A porphyrin in which no metal is inserted in its cavity is called "free base".

55. Porphyrias - New Treatments, March 2, 2004
Click here to view next page of this article. THE porphyrias. porphyrias area group of diseases that result from defective enzymes of heme biosynthesis.
http://www.medical-library.org/journals3a/porphyrias.htm
Click here to view next page of this article
THE PORPHYRIAS
Porphyrias are a group of diseases that result from defective enzymes of heme biosynthesis. The seven different porphyrias correspond to an abnormality of a specific enzyme of the heme biosynthesis pathway. The genes coding for the enzymes are known in all porphyrias, and several mutations have been identified in porphyric patients Two major types of clinical manifestations occur in porphyrias. Acute porphyric attack, which is characterized by abdominal pain and neurologic manifestations, is a feature in acute intermittent porphyria, variegate porphyria, and hereditary coproporphyria. In all three conditions the porphyrin precursors porphobilinogen and 5-aminolevulinic acid are accumulated during attacks. In other porphyrias cutaneous symptoms In symptomatic patients the specific porphyria can easily be diagnosed by specific laboratory tests. Most porphyrias are inherited in autosomal dominant fashion, but the penetrance of the disease varies greatly. In many porphyrias, the majority of patients remain asymptomatic throughout their lives. Biochemical tests are often inaccurate in the diagnosis of latent cases of porphyria. When the underlying mutation in an affected family is known, the DNA diagnosis is accurate, but the genetic heterogeneity of individual porphyrias restricts usefulness of this method.
ACUTE PORPHYRIAS
The acute porphyriasacute intermittent porphyria, porphyria variegata, and hereditary coproporphyria are characterized by episodic acute attacks. During an acute attack, symptoms include severe abdominal pain, vomiting, constipation, often pain in the extremities and in the back, and psychologic symptoms that range from anxiety to delirium. Urine may be dark or red in color because of increased amounts of porphobilin and porphyrins. Sometimes the disease progresses to peripheral motor neuropathy

56. Browning Lover Porphyrias Robert
browning lover porphyrias robert. A documentation more some browning lover porphyriasrobert throws an unintelligent undergrowth with a lack of excitement.
http://www.rouydad.com/more/sports/b/browning-lover-porphyrias-robert.asp

57. Genesis Health System - Detailed Disease Info - Porphyrias
porphyrias. Definition. porphyrias. Under normal circumstances, when heme concentrationsare at an appropriate level, precursor production decreases.
http://www.genesishealth.com/micromedex/detaileddisease/00061410.aspx
Facility Information DeWitt Comm Hosp Genesis Medical Ctr Illini Hospital Genesis Health Grp VNA
Porphyrias
Definition
The porphyrias are a group of rare disorders that affect heme biosynthesis. Heme is an essential component of hemoglobin as well as many enzymes throughout the body.
Description
Biosynthesis of heme is a multistep process that starts with simple molecules and ends with a large, complex heme molecule. Each step of the biosynthesis pathway is directed by its own task-specific protein, called an enzyme. As a heme precursor molecule moves through each step, an enzyme modifies it in some way. If the precursor is not modified, it cannot proceed to the next step. This situation is the main characteristic of the porphyrias. Owing to a defect in one of the enzymes of the heme biosynthesis pathway, protoporphyrins or porphyrin (heme precursors) are prevented from proceeding further along the pathway. Instead, precursors accumulate at the stage of the enzyme defect and cause an array of physical symptoms in the affected person. Specific symptoms depend on the point at which heme biosynthesis is blocked and which precursors accumulate. In general, the porphyrias primarily affect the skin and the nervous system. Symptoms can be debilitating or life threatening in some cases. Porphyria is an inherited condition, but it may be acquired after exposure to poisonous substances.
Heme
Heme is produced in several tissues in the body, but its primary biosynthesis sites are the liver and the bone marrow. Heme synthesis for immature red blood cells, namely the erythroblasts and the reticulocytes, occurs in the bone marrow.

58. SearchBug Directory: Health: Conditions_and_Diseases: Nutrition_and_Metabolism_D
Open Directory. Search porphyrias, disease. A personal site about thisdisorder, one of the family of porphyrias. Acute
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Web Pages - ranked by popularity The American Porphyria Foundation http://www.enterprise.net/apf/ Non-profit organization advancing awareness, research, and treatment of Porphyria. Fact sheets and links to related resources. Canadian Porphyria Foundation http://www.cpf-inc.ca/ Mission statement, objectives of the organization, newsletters and safe and unsafe drugs. Also: A Guide to Porphyria - a complete booklet of information. Porphyria Page http://www.uq.edu.au/porphyria/ A patient guide for all people with this disorder. Compiled by Professor Michael Moore. Porphyrias: Diagnosis and Treatment http://www.medstudents.com.br/metdis/metdis3.htm Clinical manifestations, diagnosis, etiology and treatment of six types of porphyrias are discussed. King George II and Porphyria http://www.mhhe.com/biosci/ap/seeleyap/cardio/reading20.mhtml

59. DiseaseSeek.com Porphyrias
Diagnosing the porphyrias profile http//www.ohsu.edu/som-hemonc/handouts/deloughery/por.shtmlAn article by Thomas G. DeLoughery, Associate Professor of
http://www.diseaseseek.com/categories/Health__Conditions_and_Diseases__Nutrition
@import url(http://www.animationseek.com/style.css); Search Directory Forum Conditions and Diseases Nutrition and Metabolism Disorders Porphyrias - Found 16 sites about Porphyrias
  • Canadian Porphyria Foundation profile http://www.cpf-inc.ca/
    Mission statement, objectives of the organization, newsletters and safe and unsafe drugs. Also: A Guide to Porphyria - a complete booklet of information.
  • Diagnosing the Porphyrias profile http://www.ohsu.edu/som-hemonc/handouts/deloughery/por.shtml
    An article by Thomas G. DeLoughery, Associate Professor of Medicine.
  • EPP profile http://members.tripod.com/~Alzuko/epp.htm
    Short for Erythropoetic ProtoPorhyria, which is a rare metabolic disease. A personal site about this disorder, one of the family of porphyrias.
  • King George II and Porphyria profile http://www.mhhe.com/biosci/ap/seeleyap/cardio/reading20.mhtml
    Talks about the symptoms of porphyria affecting King George III who ruled England during the American revolution.
  • Me and AIP profile http://hometown.aol.com/heyjude957/aip.html
    Acute Intermittent Porphyria. A personal experience with this disease touching on nutrition, diet, doctors and a healthier safer chemically free environment.

60. PORPHYRIAS
porphyrias. Tests performed by the Chemical Pathology laboratory. For results,use ward collection details). ERYTHROPOIETIC porphyrias. Only in
http://www.adhb.govt.nz/LabPlusHandbook/handbook/ManualPORPHYRIAS.htm
PORPHYRIAS Tests performed by the Chemical Pathology laboratory. For results, use ward computer or phone Lablink : 5995 or (09) 307-8995 or 0800 522 758. The samples should be collected whilst the patient has symptoms. If the patient does not have symptoms at the time of specimen collection, then it may not always be possible to eliminate porphyria as a cause for the patient's previous symptoms. ACUTE PORPHYRIA Both Acute Intermittent Porphyria and Porphyria Variegata can present with acute abdominal and/or neurological symptoms. SPECIMENS: If acute porphyria is suspected, a casual urine should be collected first and urine porphobilinogen (PBG) and porphyrins requested. PBG concentrations subside rapidly after the onset of an acute attack, and so early collection of the urine sample is important to make the diagnosis. Urine: 10 mL casual urine ( not a 24 hour collect). The sample must be protected from light by wrapping it in foil, and it should be delivered to the laboratory as quickly as possible . Request PBG and porphyrins. It is also important to collect a faecal specimen during the acute phase.

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