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         Malignant Atrophic Papulosis:     more detail

41. California Neurology Specialists-Lorne S. Label, MD, MBA, FAAN
426430; Label, Lorne S., Tandan, R., Albers, James, Polyradiculopathy andHypoglycorrhacia in malignant atrophic papulosis (Kohlmeir-Degos Disease).
http://www.cns-neurology.com/info/books.htm

Education Overview
Board Certifications
Medical Licensures SocietyMembership
Hospital Appointments ... Editing
Lorne S. Label, MD
Lorne Sheldon Label, M.D., M.B.A., F.A.A.N BOOKS/CHAPTERS/PUBLICATIONS BOOKS Lorne S. Label, M.D. Editor in Chief - "Injuries and Disorders of the Head and Brain". Mosby - Year Book Inc. 1997 Chapters
  • Label, Lorne S., Traumatic and Non-Traumatic Epilepsy, Attorneys’ Texbook of Medicine, Matthew Bender, September 2000 Label, Lorne S., Multiple Sclerosis, Attorneys Textbook of Medicine, Matthew Bender, 1995 Label, Lorne S., Peripheral Nerve Abnormalities of the Lower Extremity. Attorney’s Textbook of Medicine, Matthew Bender, 1994
PUBLICATIONS
  • Label, Lorne S., Localization of a Subthalamic Locomotor Center, AMSA-UTMB, National Student Research Forum, University of Texas Medical Branch, 1976, p.37. Presented May 1976 Label, Lorne S., Batts, Donald H., Transverse Myelitis Due to Duck Embryo Vaccine, Report of a Case of Review of the Literature. [Archives of Neurology, July 1982, pp. 426-430] Label, Lorne S., Tandan, R., Albers, James, Polyradiculopathy and Hypoglycorrhacia in Malignant Atrophic Papulosis (Kohlmeir-Degos Disease). Neurology V32, No. 3 A152, 1983

42. Diagnoses Alphabetically
Mafucci Syndrome. Malformations of Extremities. malignant atrophic papulosis. MalignantChondroid Syringoma. Malignant Fibrous Histiocytoma. Malignant Histiocytosis.
http://www.health-portal.de/content/e10/e11/index_eng.html?alpha=M%

43. ScienceDaily -- Browse Topics: Health/Conditions_and_Diseases/M
Male Turner Syndrome@ (9); malignant atrophic papulosis@ (4); Malnutrition@(8); Mannosidosis@ (2); Marburg@ (4); Marfan Syndrome@ (38
http://www.sciencedaily.com/directory/Health/Conditions_and_Diseases/M
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44. Vasculitis
Degos Disease is a rare disease, also known as malignant atrophic papulosis, initiallypresenting as a skin condition characterised by red papules with white
http://omni.ac.uk/browse/mesh/C0042384L0042384.html
low graphics
Vasculitis
broader: Vascular Diseases other: Angioneurotic Edema Arteriovenous Malformations Cerebrovascular Disorders Hemorrhoids ... Varicose Veins narrower: Behcet's Syndrome Mucocutaneous Lymph Node Syndrome Thromboangiitis Obliterans Vasculitis This interactive tutorial on vasculitis, a group of diseases that causes blood vessels to become inflamed, has been produced by the Patient Education Institute, and made available on the Web by the National Library of Medicine MEDLINEplus service. The tutorial provides background information on vasculitis and covers causes, clinical signs and symptoms, diagnosis, and treatment. Viewing this tutorial requires Flash plug-in. Vasculitis Teaching Materials Patient Education Degos disease This is the Web site of the Degos Patients Support Network. Degos Disease is a rare disease, also known as malignant atrophic papulosis, initially presenting as a skin condition characterised by red papules with white centres, and telangiectasia. Serious (possibly fatal) gastrointestinal and neurologic symptoms usually follow. This Web site brings together what little is know about the condition, providing information for patients and clinicians on symptoms, diagnosis treatment and prognosis. Vasculitis Thromboangiitis Obliterans
Last modified: 27 May 2004

45. Ulcererende Dermatosen
waarbij vaak voorkomt (vasculitis, panniculitis, periarteritis nodosa, erythema induratum(Bazin) 2, malignant atrophic papulosis 3, calciphylaxis 4), en
http://www.huidziekten.nl/woundcare/ddulcera/dermatosen.htm
Ulcererende huidziekten Er bestaan een aantal huidziekten die gepaard gaan met ulceratie als eerste of enige symptoom Daarnaast bestaan er een aantal huidziekten waarbij vaak voorkomt (vasculitis, panniculitis, periarteritis nodosa, erythema induratum (Bazin) [2], malignant atrophic papulosis [3], calciphylaxis [4]), en huidziekten waarbij ulceratie soms kan optreden (sclerodermie, lichen planus, necrobiosis lipoidica, persistant insect bites, lymfoedeem, lipoedeem, erythromelalgia [5], perniosis (chilblains), hemangioma, Stewart Bluefarb syndrome) [6]. Indeling: - pyoderma gangrenosum - parapemphigus e.a. bulleuze dermatosen, - ziekte van Degos (papulosis atrophicans maligna) - erythema exsudativum multiforme - erythema induratum (Bazin), erythema elevatum diutinum - m. Behçet, morbus Paget - heftige contactallergie - ulceratieve lichen planus, sarcoidose, SLE en CDLE, keratosis actinica - insectenbeten - panniculitis, vetnecrose / pancreatic fat necrosis

46. Index - A To Z Âå¾Ç¹Ï®ÑÀ] - °ê»Ú«p¥Í°·±d¶é°Ï - 24Drs.com
and Injuries symptomtopic Male Turner Syndrome nord MaleBC shc Malignant AppendicalTumor nord malignant atrophic papulosis nord Malignant Carcinoid
http://www.24drs.com/Health_Guide/health.asp?who=4115.21640

47. Postgraduate Medicine: Return Of The Painful Leg Ulcers
cyanotic macules, painful nodules resembling vasculitic lesions, subungual splinterhemorrhages, blue toe syndrome, malignant atrophic papulosis, and porcelain
http://www.postgradmed.com/issues/2002/04_02/puzzles_answer.htm
Return of the painful leg ulcers
Ysabel M. Bello, MD; Tania J. Phillips, MD VOL 111 / NO 4 / APRIL 2002 / POSTGRADUATE MEDICINE Return to question
The answer
Antiphospholipid-antibody syndrome
A ntiphospholipid-antibody syndrome (APS) is a multisystem disorder characterized by arterial or venous thrombosis, thrombocytopenia, recurrent fetal loss, and persistently elevated levels of antiphospholipid antibodies (1). Antiphospholipid antibodies are a heterogeneous group of circulating autoantibodies that includes anticardiolipin and anti-beta -glycoprotein I antibodies, which react with phospholipid-protein complexes, and lupus anticoagulants, which interfere with phospholipid-dependent coagulation reactions (2). APS may occur as either a primary disorder or a secondary disorder associated with (1) an underlying systemic disorder, including immunologic disease (most commonly systemic lupus erythematosus [SLE]), cancer, hematologic disease, infection, and neurologic disease, or (2) use of specific drugs (eg, procainamide hydrochloride, chlorpromazine hydrochloride and other phenothiazine derivatives, phenytoin, quinidine, streptomycin sulfate, clozapine) (1,2). Studies of patients with lupus anticoagulants have found that 50% of patients had SLE, while the remainder had various aforementioned disorders (1). Anticardiolipin antibodies are elevated in the presence of a diverse group of infectious agents, including HIV, whereas lupus anticoagulant in patients with HIV infection occurs more commonly with opportunistic infections and tends to disappear when the infection is treated (1).

48. AusMedSites - The Doctors' Reference Site -
D Degos disease malignant atrophic papulosis Dementia Care Resources DentalPractice Management Software Dept Health Aged Care Dept of Health
http://www.drsref.com.au/ausmedsite.html
Australian Medical Sites www.drsref.com.au
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49. Publications 2001-2002
Chave TA, Varma S, Patel GK, Knight AG .malignant atrophic papulosis (Degos disease) clinicopathological correlations. JEADV 2001; 15 4345.
http://www.ukdermatology.co.uk/asp/pubs0102.asp
2 users logged in
Select: General Info DPD DDSc MSc Select: Quality of Life Lab Research Clinical Trials Publications 3 current users search
Department of Dermatology Publications 2001-2002 Listed Alphabetically
Research Papers
Anstey AV. Photomedicine: Lessons from the Smith-Lemli-Opitz syndrome. J Photochemistry Photobiology 2001; 62: 123-7 Azurdia RM, Anstey AV, Rhodes LE. High cholesterol diet improves the photosensitivity in Smith-Lemli-Opitz syndrome. Br J Dermatol 2001; 144: 143-5 Chave T A, Varma S, Patel G K, Knight A G .Malignant atrophic papulosis (Degos' disease): clinicopathological correlations. JEADV 2001; 15: 43-45. Chowdhury M M U, Chakrabarti A, Prais L, Foulds I S. Occupational allergic contact dermatitis caused by 5,7-dichloro-4(4-fluorophenoxy) quinolone (quinoxyfen). Contact Dermatitis 2001; 45: 119-20. Chowdhury M M U, Motley R J. Treatment of acrodermatitis continua of Hallopeau with oral propylthiouracil and methotrexate. Clin Exp Dermatol 2001; 26: 657-60. Chowdhury M M U, Statham B N. Allergic contact dermatitis from dibutyl phthalate and benzalkonium chloride in Timodine®. Contact Dermatitis 2002; 46: 57.

50. Publications 2000-2001
malignant atrophic papulosis (Degos disease) clinicopathological correlations.J Eur Acad Dermatol Venereol 2001; 15 4345. CHOWDHURY MMU.
http://www.ukdermatology.co.uk/asp/pubs0001.asp
2 users logged in
Select: General Info DPD DDSc MSc Select: Quality of Life Lab Research Clinical Trials Publications 4 current users search
Department of Dermatology Publications 2000-2001 Listed Alphabetically
Research Papers
ANSTEY AV. Drug reactions and the skin. Medicine 2000; 28: 12: 63-64. CHAVE TA, CHOWDHURY MMU, HOLT PJA. Recalcitrant necrobiotic xanthogranuloma responsive to pulsed oral dexamethasone and maintenance prednisolone. Br J Dermatol 2001; 144: 158-61. CHAVE TA, FINLAY AY, KNIGHT AG - On behalf of the All Wales Dermatology Audit Committee. Thalidomide usage in Wales: the need to follow guidelines. Br J Dermatol 2001; 144: 310-315. CHAVE T, VARMA S, LOGAN R, HOLT PJA. A papillary lesion on the foreskin. Arch Dermatol 2001; 137: 815-20 (off-centre). CHAVE TA, VARMA S, PATEL GK, KNIGHT AG. Malignant atrophic papulosis (Degos' disease): clinicopathological correlations. J Eur Acad Dermatol Venereol 2001; 15: 43-45. CHOWDHURY MMU. The management of psoriasis in primary care. Prescriber 2000; 11(18): 99-107.

51. Full List Of Skin Conditions
BCell 1; Lymphoma - Cutaneous B-Cell 2; Lymphoma - Cutaneous B-Cell3; malignant atrophic papulosis; Malignant Melanoma 1; Malignant
http://www.herbaltherapy.net/list_of_skin_conditions.htm
"We are living in the NU trition- AGE " Home Full List of Skin Conditions Click on links below to find more information about each condition More Useful Links Dermatology pictures Internet Dermatology Society's Global Lectures Dermatology E-Mail List Services World Wide Dermatology Bulletin Board Helpful Newsgroups: alt.support.skin-diseases alt.support.skin-diseases.psoriasis alt.support.psoriasis Not too pretty.org This site goes into the many products on the market that can be very harmful to you and your children giving us even more reasons to go with all natural ingredients (remember just because a product states "all-natural" doesn't mean it is, always look at the ingredient listing). Click here About Us Testimonies Awards ... Contact Us

52. Meckel's
4 A rare cause of perforation of two regions of the gastrointestinal tract isDegos’ disease (malignant atrophic papulosis), a rare form of arteritis.
http://www.rcsed.ac.uk/journal/vol46_5/4650014.html
J.R. SAUNDERS, M.P. GRIFFITHS and S.S. KADIRKAMANATHAN
Homerton Hospital, Homerton, London, UK Introduction Case report Discussion References J.R.Coll.Surg.Edinb., 46, October 2001, 311-312 Figure 1: Erect chest radiograph demonstrating free intraperitoneal gas INTRODUCTION CASE REPORT DISCUSSION It is a true diverticulum (consisting of all intestinal layers) and is due to the persistence of the vitellointestinal duct. It is present in approximately two percent of the population with a male: female ratio of 2:1 and approximately 20% may contain ectopic gastric mucosa. However, we believe that we are the first to report such a combination of conditions causing perforation in the proximal and distal end of the small bowel. Figure 2: REFERENCES 1. Meckel JF. Arch Physiol
Surg Gynecol Obstet
Br J Surg

4. Mechat F, Zerouali ON. Non-traumatic perforation of the small intestine. Journal de Chirugie
Nippon Geka Gakkai Zasshi
j.r.saunders@mds.qmw.ac.uk

53. Contents Of  VOLUME 4; NUMBER 2 (OCTOBER) 1997
Sathish Pai B, MD, DVD, CR Srinivas, MD. malignant atrophic papulosis(Degos’ disease) Report of a rapidly fatal ease. Mostafa
http://www.geocities.com/HotSprings/Spa/8355/vol_4_2.html
Contents of   VOLUME 4; NUMBER 2 (OCTOBER) 1997 Contents Page Histopathology of Cutaneous Leishmaniasis Darius R. Mehregan, MD, David A. Mehregan, MD, Amir H. Mehregan, MD Dyslipidemia Marwan Ramadan, FACRyP, Mohamed Osman Abdel-Rahman, MB FRC Path., Mahmoud A l Zyoud, MD,Amna Mohamed Mohamed Sharif, MRCP, DDS A spectrum of Skin diseases in Dammam Central Hospital (DCH) Eastern Province (EP) Kingdom of Saudi Arabia (K.S.A.). Part one. Dr. Mohammed Mohy El-Din Selim, Dr. Sami Mohammed A 1 Soghair, Dr. Nafeesa Kamel, Dr. Sameeha Arafat House dust allergy in atopic dermatitis patients in Jeddah, Saudi Arabia Obaid Bin-Obaid, MD A cytological study of macrophages in cutaneous leishmaniasis Shahriar Dabiri, MD, Simin Shamsi-Meymandi*, MD, Mohsen Bashiri, MS, Faramarz Soleimani, MSc. Inflammatory linear verrucose epidermal nevus A promising treatment “case report” Salim Abdul Rahman Al-Harmozi, MBBCh, MSc Mohammed Mohy El-Dine Selim, MD Dermabrasion and cryotherapy in the treatment of verrucous Nevus - a case report Sathish Pai B, MD, DVD, C.R. Srinivas, MD

54. 5th Disease
malignant atrophic papulosis KöhlmeierDegos disease INCIDENCE Rare DISEASE ASSOCIATIONS Degos disease...... htm
http://health-megasite.com/articles/1/5th-disease.html
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Title: Disease Information
http://www.naspgn.org/sub/celiac_disease.asp

55. Connective Tissue Disease
Diseases 22 more Diseases All Review Therapy Diagnosis Degos Disease malignant atrophic papulosis U. of Title Abstract
http://health-megasite.com/articles/14/connective-tissue-disease.html
Click here to find out everything that you could ever want to know about connective tissue disease , there is more information here than you ever dreamed of
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connective tissue disease Here are some more sites that may be of interest: Title: Skin and Connective Tissue Diseases
http://www.mic.ki.se/Diseases/c17.html
Description: ... Lupus Erythematosus, Systemic - Marfan Syndrome - Mastocytosis - Melanosis - Mixed Connective Tissue Disease - Nail Diseases - Nails, Ingrown - Panniculitis - Panniculitis - Parapsoriasis ...
Title: Mixed Connective Tissue Disease (MCTD)
http://www.cibliga.com/mctd.html
Description: Mixed Connective Tissue Disease (MCTD): Een artikel over diagnose, behandeling, erfelijkheid, klachten, symptomen ... Connective Tissue Disease (UCTD) Wat is Mixed Connective Tissue Disease (MCTD)? Sinds ...
Title: Mixed Connective Tissue Disease (MCTD)
http://www.cibliga.com/en/mctd.html

56. Indian Journal Of Dermatology, Venereology And Leprology (IJDVL): Table Of Conte
ABSTRACT Full Text not available malignant atrophic papulosis, p. 93. MittalRaniRadha, Bansal Naresh, Gupta Seema, ABSTRACT Full Text not available
http://www.ijdvl.com/showbackissue.asp?issn=0378-6323;year=1998;volume=64;issue=

57. Atlasy Zo Sveta
1 13K Lymphoma Cutaneous B-Cell - 1 20K Lymphoma - Cutaneous B-Cell - 2 25K Lymphoma- Cutaneous B-Cell - 3 35K malignant atrophic papulosis 23K Malignant
http://www.medik.sk/fotoar/koza/koza2.html

58. Arch Dermatol -- Abstracts: Muller And Landry 112 (3): 357
malignant atrophic papulosis (Degros disease). SA Muller and M. Landry. Twowomen had malignant atrophic papulosis that affected the skin only.
http://archderm.ama-assn.org/cgi/content/abstract/112/3/357
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA For The Media Classified Ads Meetings Peer Review Congress
Vol. 112 No. 3, March 1976 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Muller SA Landry M Contact me when this article is cited
Malignant atrophic papulosis (Degros disease). A report of two cases with clinical and histological studies
S. A. Muller and M. Landry
Two women had malignant atrophic papulosis that affected the skin only. Immunologic studies showed normal amounts of serum immunoglobulins and complement and normal delayed hypersensitivity skin test results. Fibrinolysis autografts showed complete loss of fibrinolysis within the lesions but normal fibrinolysis in uninvolved skin. Histopathologic studies showed moderate inflammatory infiltration consisting of lymphocytes in addition to the typical cone-shaped regions of necrobiosis. Large amounts

59. Arch Dermatol -- Abstracts: Howsden Et Al. 112 (11): 1582
, Contact me when this article is cited. malignant atrophic papulosis ofDegos. Report of a patient who failed to respond to fibrinolytic therapy.
http://archderm.ama-assn.org/cgi/content/abstract/112/11/1582
Select Journal or Resource JAMA Archives of Dermatology Facial Plastic Surgery Family Medicine (1992-2000) General Psychiatry Internal Medicine Neurology Ophthalmology Surgery Student JAMA For The Media Classified Ads Meetings Peer Review Congress
Vol. 112 No. 11, November 1976 Featured Link E-mail Alerts ARTICLE Article Options Send to a Friend Readers Reply Submit a reply Similar articles in this journal Literature Track Add to File Drawer Download to Citation Manager PubMed citation Articles in PubMed by Howsden SM Freeman RG Contact me when this article is cited
Malignant atrophic papulosis of Degos. Report of a patient who failed to respond to fibrinolytic therapy
S. M. Howsden, S. J. Hodge, J. H. Herndon and R. G. Freeman
A 21-year-old woman with eventually fatal malignant atrophic papulosis (Degos disease) was treated primarily with the fibrinolytic agents phenformin hydrochloride and ethylestrenol. In spite of therapy, primarily central nervous system manifestations led to the patient's death.
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60. GASNet Anesthesiology: Contents M - R
Papulosis. Köhlmeier Degos Disease (malignant atrophic papulosis). ParamyotoniaCongenita. Paramyotonia Congenita (Eulenberg Syndrome). Paralysis.
http://www.gasnet.org/pediatric-syndromes/m2r_br.php
Contents M - R - pediatric syndromes - Mandibular Dysostosis Treacher - Collins Syndrome (Mandibulofacial Dysostosis) Maple Syrup Maple Syrup Urine Disease (Branched Chain Ketonuria) Marble Bone Disease Albers - Schönberg Disease (Osteopetrosis, Marble Bone Disease) Marfan Marfan's Syndrome Marie Charcot - Marie - Tooth Disease Maroteaux Maroteaux - Lamy Disease McArdle McArdle Disease (Type V Glycogen Storage Disease) McCune McCune - Albright Syndrome Meckel Meckel's Syndrome MEN - Type II Sipple's Syndrome (MEN - type II) Menkes Menkes' Syndrome Merritt Kasabach - Merritt Syndrome Mikity Wilson - Mikity Syndrome Miller Miller's Syndrome Möbius Möbius Syndrome Moon Lawrence - Moon - Biedl Syndrome Morquio Morquio Syndrome (Mucopolysaccharidosis Type IV) Moschkowitz Moschkowitz Disease (Thrombotic Thrombocytopenic Purpura) Moss Gorlin - Chaudhry - Moss Syndrome Mucopolysaccharidosis Type I Hurler Syndrome (Mucopolysaccharidosis Type I) Mucopolysaccharidosis Type II Hunter's Syndrome (Mucopolysaccharidosis Type II) Mucopolysaccharidosis Type III Sanfilippo Syndrome (Mucopolysaccharidosis Type III) Mucopolysaccharidosis Type IV Morquio Syndrome (Mucopolysaccharidosis Type IV) Mucopolysaccharidosis Type V Scheie Disease (Mucopolysaccharidosis Type V) Myasthenia Gravis Myasthenia Gravis Myositis Myositis Ossificans (Fybrodysplasia Ossificans) Myotonia Myotonic Dystrophy (Steinert's Disease) Necrolysis Lyell Disease (Toxic Epidermal Necrolysis) Neonatal Ectopia Cordis Neonatal Ectopia Cordis Neurofibromatosis Neurofibromatosis (von Recklinghausen Syndrome) Nielsen

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