41. Climb - Providing Information And Support For Those Affected By A Metabolic Dise Maple Syrup disease (Mild Intermittent). Maple Syrup disease Unspecified.Marfan Syndrome. Mastocytosis. mcardles. McCune Albright. http://www.climb.org.uk/Dislist.htm

C hildren L iving with I nherited M eta b olic Diseases List of Currently Supported Diseases This list is currently being updated to include access to additional information on each Metabolic Disease. Where the symbol appears next to a disease this indicates that additional information is available. All additional information is correct at time of publishing and whilst this information has been fully research and checked Climb accepts no responsibility for any errors or omissions. 2 Methyl Acetoacetyl CoA Thiolase Deficiency 3 Hydroxybutyrate 3 Hydroxyl-Methyl Glutaryl CoAlyase Def 3 Methylglutaconic Aciduria 3 Methylglutaconic Aciduria type IV 4-Hydroxybutyric Aciduria 4-Hydroxybutyric Aciduria X Ref Succinic Semi Aldehyde Dehydrogenase 5 Alpha Reductase Def 5 Oxoprolinuria 5 Oxoprolinuria Unspecified Abetalipoprotinaemia Abetalipoprotinaemia and Autism Achondroplasia Achondroplasia - Pseudo Acrodermatitis Enteropathica ACTH Deficient Addison's Addison's - Unspecified ALD Adenosyl Cobalamin Receptor Defect ADHD - (Attention Deficit Hyperactive Disorder) Adrenal Hyperplasia Adrenal Hyperplasia - 11 Beta Hydro Adrenal Hyperplasia - 17 hydroxylas Adrenal Hyperplasia - 17 Ketosteroid Reductase Def Adrenal Hyperplasia - 17 Ketosteroid Reductase Def Unspecified Adrenal Hyperplasia - 20/22 Desmola Adrenal Hyperplasia - 21 Hydroxylase Def Adrenal Hyperplasia - Adreno Genital Syndrome Adrenal Hyperplasia - Congenital Adrenal Hyperplasia - late onset

42. .doc Mususcular Dystrophy, Disseminated Sclerosis, Huntington's disease, mcardles Syndrome,Motor Neuron disease, Multiple Sclerosis, Muscular Dystrophy, Myopathy http://home.vicnet.net.au/~pdcv/transport.html

The Physical Disability Council Victoria Inc. The Voice Of People With A Physical Disability Index About PDCV Newsletter Discussion Papers ... Contact Us TRANSPORT ON TRACK FOR ACCESSIBLE PUBLIC TRANSPORT September 2002 It is important for people with disabilities, their families and carers to have the capacity to fully participate in and enjoy community life. The Howard Government recognises that accessible public transport plays a big part in helping this to happen. In August this year, I tabled in the Federal Parliament the Disability Standards for Accessible Public Transport and accompanying Guidelines, under the Disability Discrimination Act 1992. The Transport Standards will come into effect on 15 October 2002 - exactly ten years after the Disability Discrimination Act passed through Parliament. For the first time, these standards set out formal requirements for accessibility to public transport in Australia. They will help to promote greater independence and a correspondingly better quality of life for people with a disability, the elderly and parents with young children. The standards take into account the range of disabilities covered by the Act and apply to a range of public transport conveyances, premises and infrastructure, with some limited exceptions. They provide greater certainty about rights and obligations under the Disability Discrimination Act.

43. Muscle Diseases Phosphorylase Deficiency, mcardles’ disease or Glycogenosis type 5, Isometricexercise causes muscle damage, experience common symptoms very quickly. http://www.bae.ncsu.edu/bae/research/blanchard/www/465/textbook/otherprojects/20

Muscle Diseases Previous to this information and technology age, not much was known about the body. As time went by, the body’s anatomy was better understood, but the abnormalities in human bodies were still a mystery to be solved. As time progressed, more and more information was provided about the knowledge of diseases. Today, research is still going on to find deeper knowledge about diseases and the prevention and/or treatment methods that will alleviate the pains of those who have these diseases. Muscle diseases are one of many categories of disease. Below are some common and some not-so-common muscle diseases that have been researched and tested. Some of these diseases are genetic, while others come from deficiencies of substances or too much of specific substances in the body. Myasthenia Gravis Metabolic Diseases of Muscle Myopathy Muscular Dystrophy ... General Information about Muscular Disorders Myasthenia Gravis Myasthenia gravis (also known as MG) is an autoimmune disorder that initially affects the skeletal muscles. It is a disease in which the acetylcholine (AcCh) receptors at the skeletal muscle motor end plate are destroyed by anti-acetylcholine receptor antibodies that block the binding sites to the AcCh receptor. This anti-AcCh receptor antibody destroys the receptors faster than the receptors would be destroyed in normal skeletal muscle. Acetylcholine is the neurotransmitter that is responsible for the initiation of a muscle contraction. When AcCh receptors are blocked, acetylcholine cannot cross the membrane of the motor end plate to initiate opening of the sodium channels and cause depolarization.

44. Encyclopedia M-Mm (Search FastHealth.com) Encyclopedia M-Mm blood loss Maternal deprivation syndrome Mathematics disorder Maxilla Maxillofacialinjury mcardles syndrome glycogen storage disease type V McBurneys point http://www.jacksonfasthealth.com/encyclopedia/encyclopedia_M-Mm.php

Email This! A-Am An-Az B-Bm ... Z M-Mm Macroamylasemia Macrobid Macrobiotics Macrocephaly ... Dead Links

45. Listings Of The World Health Conditions And Diseases Genetic McArdle's disease Resources Post Review Information, resources, and contacts forthose affected by this disease or any of the glycogen storage diseases. http://listingsworld.com/Health/Conditions_and_Diseases/Genetic_Disorders/McArdl

46. Listings Of The World Health Conditions And Diseases Nutrition 18) Cholesterol and Other Fats (61) Madelung's disease (12), Malnutrition (9 Mannosidosis(3) Health/Conditions_and_diseases/Genetic_Disorders/mcardles (3) Health http://listingsworld.com/Health/Conditions_and_Diseases/Nutrition_and_Metabolism

47. Diplomate In Neurology, Module 1--Dallas, Amsterdam De Stefano, N.; Argov, Z.; Matthews, PM; Karpati, G.; Arnold, DL Impairment of musclemitochondrial oxidative metabolism in mcardles's disease. MuscleNerve. http://www.dendrites.com/module1.html

Diplomate in Neurology, Module 1 Required ReadingDallas, Amsterdam Frederick R Carrick , DC, PhD, DACAN, DABCN, DACNB, DAAPM, FACCN Professor of Neurology Module one of the Diplomate in Neurology Program will be an interactive study of neuron theory as it applies to chiropractic practice. This module is a clinical module where the breadth of information common to all health care professionals will be used as a basis from which application based knowledge will be developed. The following pages in Kandel , Schwartz and Jessell: IIIrd Edition : Principles of Neural Science are required reading in preparation for module 1. Part I An Overall View pp 2-16 Part II Cell and Molecular Biology of the Neuron pp 34-120 Part III Elementary Interactions Between Neurons: Synaptic Transmission pp 120-135 pp 153-225 pp 258-270 Neuron Theory - Module 1 Essay I have used the following studies in my preparation of the depth of information in my lecture for module 1. I will explore the concepts of immediate early gene responses to a variety of frequencies of integration. Specifically I will develop the concept of neuronal membrane and action potentiation in concert with fuel delivery. The disease forms of aberrations of these systems will be emphasized so that the participant will be able to associate application with the breadth and depth of the module. We will discuss synaptogenesis and the embryologic relationships of human kind to clinical applications. A comparative anatomical review will allow the participant to understand behaviour in their patients that is more basic to lower life forms. A basic review of biochemistry may be helpful in this module. Participants must bring diagnostic equipment to each module as this round of the program is a hands on application based learning module.

48. BCcomm: Health & Fitness/Conditions & Diseases/Genetic Disorders 1 . McArdle's disease Information Source. URL http//home.att.net/~sam-dave/mcardles/mcdisclaimer.htmlReport As Bad - Recommend it - Review It - Rate It! http://www.bccomm.net/dir/Health___Fitness/Conditions___Diseases/Genetic_Disorde

HOME REGISTER USER LINKS ... LOGIN entire directory this category ADVANCED SEARCH Home Genetic Disorders SPONSORS Advertise Here Sponsor This Category (Genetic Disorders) CATEGORIES: Alkaptonuria Cystic Fibrosis Down Syndrome Fragile X Syndrome ... Xeroderma Pigmentosum LINKS: My Links Reviews Details ... McArdle's Disease Information Source Contains information on symptoms and treatment of this illness. Report As Bad Recommend it Review It Rate It! ... Floating Harbor Syndrome Support Group Provides a list of symptoms and offers support for parents whose children have Floating Harbor Syndrome. URL: - http://hometown.aol.com/jdswanson Report As Bad Recommend it Review It Rate It! ... Porphyria: The Unknown Disease URL: - http://members.tripod.com/~PorphBook/ Report As Bad Recommend it Review It Rate It! ... Nail Patella Syndrome Patient-written site about a genetic syndrome that affects the joints, eyes and kidneys with links to other resources. URL: - http://www.reck-bates.demon.co.uk/nps/ Report As Bad Recommend it Review It Rate It! ... Medical Genetics has a homepage The medical genetics resource guide: from tests to counseling to therapies to the latest in genetic discoveries URL: - http://www.dnamd.com

49. MDAchat | Muscular Dystrophy Association here or there, stan Yes, fatigue is one of the worst parts of this disease. welcomeloneone} bklynmom so having mono and being tired from mcardles is not http://database.azstarnet.com/html/mda/transcripts/20030112McArdles-Chat-Group.h

Enter Chat FAQ Calendar User Policy ... Email Comments MDAchat Chat Transcripts 03:45 PM - 05:15 PM EST GSDchat / McArdles-Chat-Group texas-lady debyh debyh Hi lady-d lady-d hi debyh and texas lady debyh hi lady-d stan will be on today and i think there should be more people today then we had last time! odie debyh great, is there a specific topic odie Hi debyh hi odie texas-lady hi y'all paco paco hello lady-d i think we were going to talk about pain and pain management or anything that we would like to discuss tim_gulick Hola :-) first time in my life to talk (via chat or otherwise) to others who have experienced McArdles debyh like pain meds used? lady-d welcome paco and tim and odie tim_gulick thanks paco first time here too lady-d what does any one take for pain mads? stan lady-d excuse my typing i have a hard time hitting the keys! lady-d welcome stan debyh hi stan stan Hi, folks and welcome to GSD Type V worldwide forum, tim_gulick I'm 38 and don't have pain except when I get a cramp - which hopefully is only once or thrice a year. Are you all talking about what to do until the painful cramp goes away? royal texas-lady haven.t had much luck with pain meds.better with rest and plenty of liquids.

50. MDAchat | Muscular Dystrophy Association without connection with McAr. disease. stan Welcome denise5. timothy and gray hair! stan Yes, conny not every ailment is mcardles. http://database.azstarnet.com/html/mda/transcripts/20021110McArdles-Chat-Group.h

Enter Chat FAQ Calendar User Policy ... Email Comments MDAchat Chat Transcripts 03:45 PM - 05:15 PM EST GSDchat / McArdles-Chat-Group lexismom lexismom stan stan Welcome to the world's first LIVE forum on McArdle's Syndrom GSD Type V MPD conny sandee stan Welcome, Conny to our live forum on GSD Type V. stan Welcome robert31 and sandee. lu-lu robert31 Hi everyone Robert stan Does anyone who is presently loged on have GSD Type V known as McArdles Syndrome? sandee I do. lexismom robert31 and me stan To help everyone out I have GSD type V. conny Hello to everybody. For me in Switzerland it's rather late (10 in the evening!) I look forward to this hour. I have Type 5 but not proven by biopsy. stan welcome denise5. stan Thank you for staying up and joining us conny. denise5 I have GSD type 5, is that the current subject? royal stan I expect some people to join us from Australia and possibly Japan. stan Japan has a very high rate of reported McArdle's. lu-lu Hello everyone, Linda here from Sunny Florida with Type V royal Hi, I am here, went to the wrong chat at first. They were speaking Spanish. Figured I better recheck!

51. Newry Democrat - 2002/06/25: Infant Continues To Battle Potentially Fatal Liver The foundation get very poor government funding and so the mcardles are trying tohelp Nicole and help the family raise awareness of this devastating disease. http://archives.tcm.ie/newrydemocrat/2002/06/25/story800.asp

TCM Archives Newry Democrat Tuesday, June 25, 2002 : FRONT NEWS SPORT LOCAL NEWS Infant continues to battle potentially fatal liver disease Looking at the smiling face of beautiful little Nicole McArdle, it is hard to believe that she has been battling a potentially fatal liver disease since birth. Nicole, daughter of Helen and Aidan McArdle, Warrenpoint, was born with biliary atresia, a congenital absence or closure of the ducts that drain bile from the liver. If left untreated, damage to the liver can be so extensive that few children survive beyond the age of two. Her parents took her to hospital when she was only 11 days old thinking she had a form of jaundice. After blood tests were carried out, they found out the real extent of the problem and little Nicole had to undergo major surgery when she was only two week’s old. It became clear that she needed a liver transplant and has been on the register for 11 weeks. “We were told that we should hear something back within 12 weeks. “If her condition deteriorates we will each give part of our liver to try and save Nicole,” said her mother Helen. Helen and Aidan are trying to raise awareness of the Children’s Liver Disease Foundation, which was set up in 1980.

52. Musculoskeletal als/. McArdle's disease http//www.mdausa.org/disease/mpd.html http//home.att.net/~samdave/mcardles/mcframe.html.Myasthenia Gravis http://www.lexington1.net/lv/wkms/hp.nsf/Files/wkmwebquest/$FILE/musculoskeletal

The Skeletal and Muscular Systems: An Internet Introduction Introduction Essential Question Task Part One ... Standards Introduction: What does our skeleton do for us? How about our muscles? Every movement and gesture we take with our body - even the look you cut someone in the hall is the product of the fine tuned work of the skeletal and muscular systems. How do our muscles and bones work together so well During this activity you will find out what the parts of these systems help us to move every day, and what makes these systems so important to our human bodies. Essential Question: What are the parts and functions of the skeletal and muscular systems? What types of diseases and disorders cause a break down of these systems? Task: Read the directions for each section carefully! Complete each of the sections in this activity that your teacher has instructed you to work on in this class period. Use your worksheet to record the information that you find and the answers to the questions that you are asked. Part One: Introduction to the Skeletal System Click on the links provided and use the information on the webpage you visit to answer the questions that follow each link to find out more about the skeletal system.

53. BS397 Neuromuscular Disorders V (mcardles pp), VII (Taruis pfk). . Lipid Storage, CPT, Carnitine. NEUROGENIC, CENTRAL(Neuronal), . Spinal Muscular Atrophy (SMA), Motor Neuron disease (MND/ALS). http://www.biomed2.man.ac.uk/ns/mm/bs397l20.html

EXIT MENU BS397 LECTURES 20-24 Neuromuscular Disorders The following topics are covered to give a feel for how the application of new methods has advanced our knowledge and understanding of muscle diseases, and to correlate pathological information with clinical data at the individual patient level. History Classification of Muscle Diseases Pathology of Specific Muscle Disorders The Duchenne Dystrophy Story ... Animal Models HISTORY Our understanding of neuromuscular disorders usually begins with clinical descriptions and attempts to classify the disease and then on to a description and understanding of its pathology (often helped by animal and experimental studies involving physiology, biochemistry and pharmacology). New breakthroughs in molecular genetics have now allowed us to accurately classify and describe the inheritance, aetiology and pathological mechanisms involved in many of these disorders and are bringing us to the verge of possible new treatments. Clinical descriptions of neuromuscular disorders in sporadic and familial groups exhibiting proximal or distal wasting and weakness and variable progression. Some attempts at relating pathology of nerve or muscle to the disease. Bell, Partridge, Little

54. 1Up Health > Health Links Directory > Conditions And Diseases: Genetic Disorders Sites. McArdle's disease Resources Information, resources, and contacts forthose affected by this disease or any of the glycogen storage diseases. http://www.1uphealth.com/links/genetic-disorders-mcardles.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 ... Genetic Disorders : McArdle's Description See Related Categories Health: Conditions and Diseases: Nutrition and Metabolism Disorders Sites McArdle's Disease Resources Information, resources, and contacts for those affected by this disease or any of the glycogen storage diseases. University of Texas Southwestern Medical Center at Dallas An article about the psychological and physical symptoms of those with McArdle's disease. 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.

55. In Loving Memory Of My Dad - Henry Otto Although it was something he carried with him for some time, we only discoveredthe disease 4 weeks toasting in living room, wiht mom in suit, with mcardles. http://www.henryotto.com/home.htm

In Loving Memory of My Dad - Henry Otto July 23, 1930 - October 24, 2002 On October 24th, 2002, my dad lost his battle with Lung Cancer. Although it was something he carried with him for some time, we only discovered the disease 4 weeks prior to his passing. I will miss my father eternally and hope that you take a moment to enjoy some of these pictures and smile for just a moment. My Father was a great man and both my Mother and myself will one day be with him again. 3 musketeers.jpg Black and white at german parade.jpg Dad and me in front of tree.jpg Dad classic sitting.jpg ... with Mcardles.jpg

56. New Page 1 Mucosal Coeliac disease. mcardles Myoglobinuria Cramping after exercise Accumulatedglycogen Recessive inheritance Deficiency of muscle phosphorylase Lactate http://www.chills.co.uk/mz.htm

a b c d ... z Associations of Mitral Valve Prolapse Marfans Osteogenesis imperfecta Polycystic kidney disease PDA Pseudoxanthoma elasticum Myocarditis SLE Muscular dystrophy Median nerve L ateral 2 lunbricals O pponens pollicis A bducter pollicis brevis F lexor pollicis longus Treatment of Malignant Hyperthermia Some Hot Dude Better Give Iced Fluids Fast!!! S: Stop all triggering agents, give 100% O2 H: Hyperventilate D: Dantrolene 2.5mg/kg B: Bicarbonate G: Glucose and Insulin I: IV Fluids, Cooling Blanket F: Fluid Output; Furosemide F: Tachycardia, be prepared to treat V Tach Skin Manifestations of Malignancy Acanthosis Nigricans Acquired icthyosis Pruritis Migratory thrombophlebitis Erythroderma Tylosis Erythema gyratum repens Necrolytic Migratory erythema Malabsorption (Causes) Mucosal Coeliac Disease Tropical Sprue Crohns Amyloid Whipples Intraluminal Gastrectomy Giardiasis Diphyllobothriasis Strongyloides Obstructive jaundice Pancreatic Chronic Pancreatits Cystic Fibrosis McArdle's syndrome MCARDLES M yoglobinuria C ramping after exercise A ccumulated glycogen R ecessive inheritance D eficiency of muscle phosphorylase L actate levels fail to rise E levated creatine kinase S keletal muscle only

57. DCL Lecture Notes Glycogen may accumulate in the storage diseases such as mcardles syndrome or in Mostcommon are sphingolipidoses, such as Tay Sachs disease where gangliosides http://www.med.uiuc.edu/m2/Pathology/DCL.htm

Diseases at the Cellular Level Lecture Handout Jill Conway, 8/00 Adaptation = reversible altered steady state of cells in response to stimuli Forms of: physiologic = hormones, aging, decreased workload in muscle pathologic = bad nutrition, loss of innervation, diminished blood supply Hypertrophy: increase in cell or organ size typically in response to increased workload. Probably triggered by mechanical stretch receptors and growth factors or cytokines. Hyperplasia increase in cell number, occurs only in dividing tissue, usually induced via hormones (breast, uterus) or compensation for lost tissue. Probably induced by growth factors, interleukins (IL-6). Atrophy: decrease in cell size through loss of cell substance. Physiologicnormal for certain structures to regressthyroglossal duct regresses. Pathologic = decreased workload, denervation, diminished blood supply. Metaplasia: reversible replacement of one adult cell type by another, probably through changes in differentiation of stem cells brought about via cytokines. Non-adaptive change: Dysplasia: loss of orientation, hyperchromasia, odd mitotic figures, changes in nuclear size and shape

58. Australian Neuromuscular Research Institute Blechyndenm L, Witon SD, Laing NG. Defining, Establishing and Exploitingan ovine model of mcardles's disease. Muscle Nerve 1998;788. http://www.anri.uwa.edu.au/pubs1999.htm

2000 Publications Garlepp MJ, Mastaglia FL. Autoantibodies in Inflammatory Myopathies. Am Journ of Med Sci 2000(In Press) Jong Y-J, Kobayashi K, Toda T, Kondo-lida E, Huang S-C, Shem Y-Z, Nonaka I, Fukyama Y. Genetic heterogeneity in three Chinese children with Fukuyama congenital muscular dystrophy. Neuromuscular Disorders2000;10:108-112 Lu QL, Morris GE, Wilton SD, Ly T, Artem'yeva OV, Strong P, Partridge TA. Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion. Jour Cell Biol12000;148(5):985-995 Nowak KJ, Walsh P, Jacob RL, Johnson RD, Peverall J, McNally EM, Wilton SD, Kakulas BA, Laing NG. Severe g-sarcoglycanopathy caused by a novel missense mutation and a large deletion. Neuromuscular Disorders2000;10:100-107 Pearce AJ, Thickbroom GW, Byrnes ML, Mastaglia FL. The corticomotor representation of an intrinsic hand muscle in skilled racquet players. Ex Brain Research2000;130(2):238-243 Panegyres PK, Zafiris-Toufexis K, Kakulas BA. Amyloid precursor protein gene isoforms in Alzheimer's disease and other neurodegenerative disorders. Neurological Sciences2000;173:81-92

59. Untitled Document mcardles sygdom kan definitivt diagnosticeres ved cykelergometri, fordi det kun erved denne sygdom, at man Summary John Vissing Diagnosis of muscle disease. http://www.dadlnet.dk/ufl/ufl2015/v_p/30900.htm

Diagnostik af muskelsygdomme OVERSIGTSARTIKEL John Vissing Baggrund Tabel 1 se UFL 162/15, p. 2174, 15. april 2000 Diagnostik Kardiologisk udredning Billeddiagnostik Arbejdstest Dr. McArdle Fig. 1 se UFL 162/15, p. 2175, 10. april 2000 ]). En modificeret udgave af underarmstesten kan bruges til diagnosticering af patienter med mitokondriemyopati (14). second wind- Fig. 2 se UFL 162/15, p. 2175, 10. april 2000 Phosphor-MR-spektroskopi ( P-MRS ses som en ekstra top i spektret ( Fig. 3 se UFL 162/15, p. 2176, 10. april 2000 P-MRS af en muskel ved mitokondriesygdomme viser typisk 1) en nedsat fosfocreatin/inorganisk fosfatratio som udtryk for lavt fosforyleringspotentiale i hvile (22), 2) en forsinket gendannelse af fosfokreatin efter muskelarbejde (22) og 3) accentuering af muskelacidose under muskelarbejde pga. laktatophobning (19). Muskelbiopsi Fig. 4 se UFL 162/15, p. 2176, 15. april 2000 limb-girdle -muskeldystrofi genetisk mhp. korrekt diagnostisk indplacering af patienterne i de nu 12 veldefinerede undergrupper af

60. Kap4 Maple syrup urine disease (MSUD) E71.0 Andra rubbningar i omsättningen av E76.3)Glykogeninlagringssjukdom E74.0 von Gierkes sjukdom mcardles sjukdom Pompes http://www.svls.se/sektioner/blf/blfbad/Kap4.htm

Ctrl+Home - till början av sidan Ctrl+End - till slutet av sidan Pg Up/Pg Dn - flytta en bildruta upp eller ned BAD 97 Förord/anvisningar till BAD 97 Sök ord/diagnoser i respektive kapitel med Redigera/Edit och Sök/Find Åter till BLF's hemsida Åter till innehållsförteckningen Kapitel IV - Endokrina sjukdomar, nutritionsrubbningar och ämnesomsättningssjukdomar (E00-E90) Sjukdomar i sköldkörteln (E00-E07) Jodbristsyndrom, medfött UNS #E00.9 Kretinism, medfödd, endemisk, UNS #E00.9 Struma, jodbristrelaterad, ospecificerad #E01.2 Jodbristhypotyreos, subklinisk #E02 Hypotyreos, medfödd, med struma #E03.0 Hypotyreos, medfödd, utan struma #E03.1 Postinfektiös hypotyreos #E03.3 Hypotyreos, ospecificerad #E03.9 Myxödem UNS #E03.9 Atoxisk diffus struma #E04.0 Atoxisk multinodulär struma #E04.2 Atoxisk struma UNS #E04.9 Hypotyreos, postoperativ #E89.0 Tyreotoxikos (Basedow, Grave's disease): med diffus struma #E05.0

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