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         Alpers Disease:     more books (21)
  1. The Official Parent's Sourcebook on Alpers' Disease: Updated Directory for the Internet Age by Icon Health Publications, 2003-12
  2. Alpers' disease: An entry from Thomson Gale's <i>Gale Encyclopedia of Neurological Disorders</i> by Bryan, PhD Cobb, 2005
  3. Slow, Latent, and Temperate Virus Infections (National Institute of Neurological Diseases and Blindness)
  4. Spontaneous coronary artery dissection / Spontan koroner arter disseksiyonu.(Case Reports / Olgu Sunumlari)(Disease/Disorder overview): An article from: ... of Cardiology (Anadolu Kardiyoloji Dergisi) by Ozlem Ozcan, Nermin Bayar, et all 2007-09-01
  5. The Official Parent's Sourcebook on Alpers' Disease Updated Directory for the Internet Age by Icon Health Publications, 1980
  6. Salmonella Agona outbreak from contaminated aniseed, Germany.(DISPATCHES): An article from: Emerging Infectious Diseases by Judith Koch, Annette Schrauder, et all 2005-07-01
  7. Leptospirosis in Germany, 1962-2003.(RESEARCH): An article from: Emerging Infectious Diseases by Andreas Jansen, Irene Schoneberg, et all 2005-07-01
  8. Changing epidemiology of human brucellosis, Germany, 1962-2005.(RESEARCH): An article from: Emerging Infectious Diseases by Sascha Al Dahouk, Heinrich Neubauer, et all 2007-12-01
  9. Atlas of Gastroenterology: Self-Assessment Guide
  10. Genetic Disorders of the Skin
  11. Textbook of Gastroenterology: Self-Assessment Review by David H. Alpers, Loren, M.D. Laine, et all 2000-10
  12. Handbook of Gastroenterology by Tadataka Yamada, 1998-04-27
  13. Principles of Clinical Gastroenterology
  14. Clinical neurology by Bernard Jacob Alpers, 1949

41. Rare Diseases List - Office Of Rare Diseases
Alopecia, epilepsy, pyorrhea, mental subnormality. alpers disease.Alpha 1antitrypsin deficiency. Alpha-2 deficient collagen disease.
http://ord.aspensys.com/diseases.asp
Office of Rare Diseases
Rare Diseases List
An orphan or rare disease is generally considered to have a prevalence of less than 200,000 affected individuals in the USA. Certain diseases with more than 200,000 affected individuals are included but subpopulations of these conditions may be less than the prevalence standard for rare disease. This list includes rare diseases and conditions for which information requests have been made to the Office of Rare Diseases. It is updated on a regular basis. We welcome suggestions for additions to the list and your recommendations may be sent via email to: ord@od.nih.gov
Please Note: The names of the conditions (listed in alphabetical order) may not necessarily be the most frequently used ones. Clicking on one of the names below will take you to a page that contains information specific for that disease. The links on that page will take you to several sources of information, including:
  • ClinicalTrials.gov, an NIH site that lists ongoing clinical trials;
  • Online Mendelian Inheritance in Man (OMIM), an NIH site authored and edited by Johns Hopkins University, with information on specific genetic diseases; and

42. Medicalseek - Search Engine For The Healthcare Industry
li= NORD alpers disease A brief description along with alternatename, followed by a list of resources for further information.
http://www.medicalseek.net/Conditions_and_Diseases_Neurological_Disorders_Neurod
CATEGORIES ADD A LINK ADVERTISE CONTACT US ... Neurodegenerative Diseases Alpers'
Conditions and Diseases:Neurological Disorders:Neurodegenerative Diseases:Alpers'

  • About com
    Symptoms, diagnosis, and treatment of Alpers' disease. Information on research, community outreach and support.
    genetics.about.com/science/genetics/library...
    Alpers' Disease

    Information sheet compiled by NINDS.
    ninds.nih.gov/health_and_medical/disord...
    Alpers' Progressive Infantile Poliodystophy

    Features listed for this disorder.
    hgmp.mrc.ac.uk/dhmhd-bin/hum-look-up?63... Institute of Neurology A brief description of Alpers' disease, links to further resources and support groups. ion.ucl.ac.uk/library/patient/alper.htm... James Madison University An article about Alpers' disease, including the alternate names, symptoms and statistics. cs.jmu.edu/common/projects/mtDNA/alpers... MedicineNet.com An Alpers' disease article with some general information. medicinenet.com/Script/Main/Art.asp?li=... NORD - Alpers Disease A brief description along with alternate name, followed by a list of resources for further information. stepstn.com/cgi-win/nord.exe?proc=GetDo...

43. Human And Animal Prion Diseases
GerstmannStraussler-Scheinker disease. Fatal familial insomnia. alpers disease?Animal prion diseases. Some prion diseases which occur in other species Scrapie.
http://www.mds.qmw.ac.uk/statgen/dcurtis/lectures/bsecjd1.html
Human prion diseases
The following prion diseases are recognised in humans:
  • Creutzfeld Jacob disease
  • Kuru
  • Gerstmann-Straussler-Scheinker disease
  • Fatal familial insomnia
  • Alpers disease?
Animal prion diseases
Some prion diseases which occur in other species:
  • Scrapie
  • Bovine spongiform encephalopathy
  • Transmissible mink encephalopathy
  • Chronic wasting disease (mule deer, elk)
  • Feline spongiform encephalopathy
  • Zoological spongiform encephalopathy (eland, nyala, oryx, kudu, gemsbok, cheetah, puma, ocelot, ostrich)

44. Health Library
Allylamines for ringworm of the skin. Alopecia Areata. alpers disease. Alpha1-AntitrypsinDeficiency. Alpha-adrenergic agonists for urinary incontinence.
http://healthinfo.carolinas.org/library/healthguide/IllnessConditions/_SearchRes

45. A Listing Of Disorders
Albinism. Alexander's Disease. Alkaptonuria. Allan Herndon Syndrome. alpers disease.AlpersHuttenlocher Syndrome. Alpha-1-Antitrypsin Deficiency. Alport Syndrome.
http://medschool.umaryland.edu/BTBank/Family/Disorders_A.htm
Brain and Tissue Bank
University of Maryland, Baltimore A Aarskog Syndrome Aase Syndrome Ablepharon Macrostomia Syndrome Acanthocheilonemiasis Acanthocytosis Acanthosis Nigricans Achard Thiers Syndrome Achondrogenesis Achondroplasia Acidemia, Isovaleric Acidemia, Methylmalonic Acidemia, Propionic Acrocallosal Syndrome, Schinzel Type Acrodermatitis Enteropathica Acrodysostosis Acromegaly Acromesomelic Dysplasia Acromicric Dysplasia ACTH Deficiency Acute Endocarditis Adams Oliver Syndrome Adie Syndrome Adrenal Hyperplasia, Congenital (General) Adrenoleukodystrophy Adrenomyeloneuropathy Afibrinogenemia, Congenital Agammaglobulinemias, Primary Agenesis of Corpus Callosum Agnosia, Primary Visual Agranulocytosis, Acquired Ahumada Del Castillo Syndrome Aicardi Syndrome Alagille Syndrome Albinism Alexander's Disease Alkaptonuria Allan Herndon Syndrome Alpers Disease Alpers-Huttenlocher Syndrome Alpha-1-Antitrypsin Deficiency Alport Syndrome Alstrom Syndrome Alternating Hemiplegia of Childhood Alveolitis, Extrinsic Allergic Alveolitis, Fibrosing Ameloblastoma Amelogenesis Imperfecta Amniotic Band Syndrome Amyloidosis Amyotrophic Lateral Sclerosis Andersen Disease Anemia, Aplastic

46. Metabolic Diseaese Children Self Help And Support Groups
Adrenal Hypoplasia Adrenomyeloneuropathy (AMN) Adrenoleukodystrophy (Leukodystrophy)Albrights Alcaptonuria Alexander (Leukodystrophy) alpers disease Alpha One
http://www.webhealth.co.uk/Self_Help_and_Support_Groups_R/Metabolic_Diseaese_Chi
METABOLIC DISEASES IN CHILDREN Climb
About Climb
We are a national umbrella organisation working on behalf of children, young people and families affected by metabolic disease. Our aim is
"To ensure the best possible quality of life for children and families affected by metabolic disease and alleviate their suffering with the ultimate aim of prevention and cure." We do this by
funding research and facilitating medical treatment
providing information, counselling and advice for families and professionals
supporting families through grants to help meet equipment and other costs
educating professionals and others about this group of diseases In doing this we:
affirm the right of families to access services of a consistently high quality;
affirm families' right to information which is accurate, up to date and which they will understand, about their child's condition;
complement the other services that exist;

47. A
Alopecia; alpers disease ( Cerebral Sclerosis, Diffuse); Alpha1 AntitrypsinDeficiency; Alport's Syndrome ( Nephritis, Hereditary);
http://www.fortunecity.co.uk/southbank/hornton/11/notes/topics.htm
web hosting domain names email addresses related sites A B C

48. Tusdata.com
Allergy ( Hypersensitivity); Alopecia; alpers disease ( DiffuseCerebral Sclerosis of Schilder); Alphavirus Infections; Alpha
http://www.tusdata.com/saglika/hast_a.htm
GÜNÜN "EN"LERÝ ONLÝNE DENEME GÜNÜN KONUSU GÜNÜN ÝPUCU KUTUSU ... KÜLTÜR SANAT HALK SAÐLIÐI Saðlýk Ansiklopedisi
Ýlkyardým

Aile Planlamasý

Kadýn Saðlýðý
...
Hastalýk - Beslenme
ECZANELER Nöbetçi eczaneler ve adresleri
ADLÝ TIP
Adli týpla ilgili bilmeniz gerekenler: Haklarýnýz ve Sorumluluklarýnýz B inlerce hastalýk hakkýnda ingilizce bilgi A B C D ...
  • Albinism (Skin Diseases ..)
  • Albinism, Ocular
  • Alcoholism
  • Alexanders Disease
  • Alkalosis ...
  • Arthritis, Rheumatoid (Musculoskeletal Diseases)
  • Arthritis
  • Arthrogryposis
  • Arthropathy, Neurogenic
  • Arthropod Diseases ... Z Yukarýdaki kaynaklara ek olarak ADAM Medical Encyclopedia ' dan 4,000 den fazla konuda açýklama istediðiniz her türlü bulgu, belirti ve testler hastalýðýn seyri hakkýnda bilgi.. yapýlacak, yapýlmasý gereken testler ve bu testlerin normal deðerleri.....(Not bu konularda bilgilenmek içindir. Kesinlikle doktora danýþmadan kendine taþhis koyup tedaviye baþlamayýnýz.) A B C D ... Z PARAMEDÝKAL Haber Kaynaklarý
    Son Dakika Haber

    Eðlence

    Otomobil
    ...
    Borsa,Döviz,Para
  • 49. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : A Diseases Da
    ALP low see Alkaline phosphatase levels low (plasma or serum) ALP raised see Alkalinephosphatase levels raised (plasma or serum) alpers disease Alpha 1
    http://www.diseasesdatabase.com/sieve/disease_index_a.asp
    Diseases Database [Previous page] [Search] [Index] [Feedback]
    Diseases Database disease, symptom, sign, etc alphabetical index : A
    AA amyloidosis
    Aagenaes syndrome see Cholestasis-oedema syndrome, Norwegian type
    Aarskog Ose Pande syndrome see SHORT syndrome
    Aarskog syndrome

    Aarskog-Scott syndrome see Aarskog syndrome
    Aase syndrome

    Abacavir

    Abciximab

    Abdo distended see Abdominal distention
    Abdo mass see Abdominal mass
    Abdo pain see Abdominal pain Abdomen distended see Abdominal distention Abdominal and pelvic pain see Abdominal pain Abdominal decompression Abdominal distention Abdominal mass Abdominal obesity-metabolic syndrome see Reaven syndrome X Abdominal pain Abdominal swelling see Abdominal distention Abducens nerve lesion see 6th cranial nerve disorder Abducent nerve pathology see 6th cranial nerve disorder Abetalipoproteinaemia Abetalipoproteinemia see Abetalipoproteinaemia Abnormal heart rhythm see Cardiac arrhythmia Abnormal heart sounds Abnormal reflexes Abnormal splitting of heart sounds ... Abnormal sputum ABO incompatibility (feto-maternal) see ABO isoimmunization of fetus and newborn ABO isoimmunization of fetus and newborn Abortion, missed

    50. Diseases Database Disease, Symptom, Sign, Etc Alphabetical Index : P Diseases Da
    see Miliary aneurysms of retina Progressive familial intrahepatic cholestasis Progressiveinfantile poliodystrophy see alpers disease Progressive lipodystrophy
    http://www.diseasesdatabase.com/sieve/disease_index_p.asp
    Diseases Database [Previous page] [Search] [Index] [Feedback]
    Diseases Database disease, symptom, sign, etc alphabetical index : P
    P mitrale
    P pulmonale

    P wave amplitude increased

    P wave inversion
    ...
    P wave low amplitude

    P450 induction see Cytochrome P450 induction
    P450 inhibition see Cytochrome P450 inhibition
    P450 metabolism see Cytochrome P450 substrate
    p53 oncogene

    PABA see Para-aminobenzoic acid
    Pacemakers, artificial cardiac
    Pachydermatocele Pachydermoperiostosis ... Pachyonychia Pachyonychia congenita type 1 see Jadassohn-Lewandowsky syndrome Pachyonychia congenita type 3 see Tylosis Paclitaxel Paget's disease of bone Paget's disease of penis see Penis carcinoma Paget's disease of the breast see Paget's disease of the nipple Paget's disease of the nipple Pagon syndrome see Walker-Warburg syndrome Pahvant Valley fever see Tularaemia Pain Pain insensitivity Paine syndrome see Seemanova syndrome 1 Painful bruising syndrome see Gardner-Diamond syndrome Painful intercourse see Dyspareunia Painful micturition see Dysuria Painful swallowing see Dysphagia Painful urination see Dysuria Palindromic rheumatism Palivizumab Pallister mosaic aneuploidy see Chromosome 12p tetrasomy syndrome Pallister-Hall syndrome Palmar erythema Palmar fascial fibromatosis see Dupuytren's contracture Palmar fibromatosis see Dupuytren's contracture Palmar pits Palmidrol see Palmitoylethanolamide Palmitoyl-CoA oxidase deficiency see Peroxisomal acyl-CoA oxidase deficiency Palmitoylethanolamide Palmoplantar ectodermal dysplasia type 4 see Papillon Lefevre syndrome Palmoplantar ectodermal dysplasia type 5

    51. Bernard Jacob Alpers (www.whonamedit.com)
    Associated with alpers' disease. Associated eponyms alpers' disease A rare degenerativedisease of the brain, predominantly involving the grey matter.
    http://www.whonamedit.com/doctor.cfm/185.html

    Home

    List categories

    Eponyms A-Z

    Biographies by country
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    Bernard Jacob Alpers
    American neurosurgeon, born 1900, Salem, Massachusetts.
    Associated eponyms:
    Alpers' disease

    A rare degenerative disease of the brain, predominantly involving the grey matter. Biography: Bernard Jacob Alpers was educated at Harvard College and Harvard Medical School. a student of. After graduating in medicine from Harvard in 1923 he went to Europe for advanced training in neuropathology, working with Alfons Maria Jakob (1884-1931) in Hamburg. He subsequently began working in the Department of Neurosurgery at the University of Pennsylvania, and in 1939 became head of the Department of Nervous and Mental Disease at Jefferson Medical College, where he soon established an independent department of neurology. In his private time he enjoyed music and he had a life-long interest in religion. Bibliography:
    • Clinical Neurology. Philadelphia, Davis, 1945. xii, 797 pages. Also 1946. 2nd edition, Philadelphia, 1949. xvi, 846 pages.
    • Essentials of the neurological examination
    • Alpers and Mancall's Essentials of the Neurologic Examination.

    52. NINDS Alpers' Disease Information Page
    alpers' disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS). What is alpers' disease? alpers' disease is a rare, progressive neurodegenerative disease of the brain that occurs in
    http://accessible.ninds.nih.gov/health_and_medical/disorders/alpersdisease_doc.h
    Disorders - National Institute of Neurological Disorders and Stroke (NINDS) Skip menus
    Main sections of the NINDS web site
    Home About NINDS Disorders-you are in this section ... Find People
    Disorders section pages and search
    Image Description
    Science For the Brain
    The nation's leading supporter of biomedical research on disorders of the brain and nervous system. Select Topic Disorder Quick Links Alzheimer's Autism Cerebral Palsy Chronic Pain Epilepsy Headache Multiple Sclerosis Parkinson's Stroke Traumatic Brain Injury
    More about NINDS Alpers' Disease Information Page
  • Studies with patients Research literature Press release
  • NINDS Search (search help) Contact us My privacy NINDS is part of the National Institutes of Health Contact us
    Content for this page
    NINDS Alpers' Disease Information Page
    Synonym(s): Progressive Sclerosing Poliodystrophy Reviewed 07-01-2001 Get Web page suited for printing
    Email this to a friend or colleague

    Table of Contents (click to jump to sections)
    What is Alpers' Disease?

    Is there any treatment?

    What is the prognosis?

    What research is being done?
    ...
    Organizations

    What is Alpers' Disease?
    Alpers' disease is a rare, progressive neurodegenerative disease of the brain that occurs in infants and children. It is an autosomal recessive disorder that is sometimes seen in siblings. First signs of the disease, which include intractable seizures and failure to meet meaningful developmental milestones, usually occur in infancy. Primary symptoms of the disease are developmental delay, progressive mental retardation, hypotonia (low muscle tone), spasticity (stiffness of the limbs), and dementia. Seizures may include epilepsia partialis continua, a type of seizure that consists of repeated myoclonic (muscle) jerks. Optic atrophy may also occur, often leading to blindness. And, although physical signs of chronic liver dysfunction may not be present, many patients suffer liver impairment leading to liver failure. While some researchers believe that Alpers' disease is caused by an underlying metabolic defect, no consistent defect has been identified.

    53. NINDS - News And Events
    Health. Sorry! There are no press releases for alpers' disease. Useyour browser's Back button to return to your previous activity.
    http://www.ninds.nih.gov/health_and_medical/news.htm?url=/health_and_medical/dis

    54. Biology - Past Issues Of Weekly Features
    Symptoms, diagnosis, and treatment of alpers' disease. Information on research, community outreach and support.
    http://genetics.about.com/science/genetics/library/blalp.htm
    zfp=-1 About Homework Help Biology Search in this topic on About on the Web in Products Web Hosting
    Biology
    with Regina Bailey
    Your Guide to one of hundreds of sites Home Articles Forums ... Help zmhp('style="color:#fff"') Subjects ESSENTIALS Science Fair Projects Top Biology Programs Biology How Tos ... All articles on this topic Stay up-to-date!
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    55. 1Up Health > Alpers' Disease [Progressive Sclerosing Poliodystrophy] - Brain & N
    What is alpers' disease? alpers' disease is a rare, progressive neurodegenerative disease of the brain that occurs in
    http://www.1uphealth.com/medical/disease/brain-neurological-disease/alpers%27-di
    Home Contact Us Privacy Caring For Your Well Being Alternative Medicine Clinical Trials Health News Poisons ... Health Topics A-Z Search 1Up Health 1Up Health Alpers' Disease [Progressive Sclerosing Poliodystrophy]
    Diseases and Conditions A B C D ... Z
    Alpers' Disease [Progressive Sclerosing Poliodystrophy]
    What is Alpers' Disease?

    Is there any treatment?

    What is the prognosis?

    What research is being done?
    ...
    Organizations
    What is Alpers' Disease? Alpers' disease is a rare, progressive neurodegenerative disease of the brain that occurs in infants and children. It is an autosomal recessive disorder that is sometimes seen in siblings.
    First signs of the disease, which include intractable seizures and failure to meet meaningful developmental milestones, usually occur in infancy.
    Primary symptoms of the disease are developmental delay, progressive mental retardation, hypotonia (low muscle tone), spasticity (stiffness of the limbs), and dementia. Seizures may include epilepsia partialis continua, a type of seizure that consists of repeated myoclonic (muscle) jerks.
    Optic atrophy may also occur, often leading to blindness. And, although physical signs of chronic liver dysfunction may not be present, many patients suffer liver impairment leading to liver failure.

    56. Health And Medical Information: Diseases And Conditions, Medical Dictionary, Pro
    An alpers' disease article with some general information.
    http://www.medicinenet.com/Script/Main/Art.asp?li=MNI&d=152&ArticleKey=8

    57. Alpers' Disease (www.whonamedit.com)
    alpers' disease A rare degenerative disease of the brain, predominantlyinvolving the grey matter. Also known alpers' disease Also known
    http://www.whonamedit.com/synd.cfm/1459.html

    Home

    List categories

    Eponyms A-Z

    Biographies by country
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    Alpers' disease Also known as:
    Christensen's disease
    Christensen-Krabbe disease
    Synonyms:
    Diffuse cortical sclerosis, familial degeneration of the cerebral grey matter in childhood, poliodysplasia cerebri, poliodystrophia cerebri progressiva, poliodystrophia progressiva corticalis, poliodystrophia cerebri progressiva infantilis, progressive cerebral degeneration in infancy, progressive cerebral poliodystrophy, progressive infantile poliodystrophy, progressive poliodystrophy. Associated persons: Bernard Jacob Alpers Erna Christensen Knud Haraldsen Krabbe Description: A rare degenerative disease of the brain, predominantly involving the grey matter. It is characterised by acute onset of severe convulsions leading to rapid intellectual and bodily breakdown. Other characteristics are blindness and deafness, myoclonus, spasticity, choroathetosis, cerebellar ataxia, growth retardation, and terminal decortication. Manifests in early childhood and usually causes death within months. In its familial form, the disorder is transmitted as an autosomal recessive trait. Alpers’ disease was first recognized by Alfons Maria Jakob (1884-1931), and accounts of this were published by three of his students, Souza (Madrid), Freedom (Baltimore), and Alpers in Philadelphia. The eponymic term Alper's disease was introduced by Blackwood, et al in 1963.

    58. Rd.com:
    General information about alpers' disease including the alternate names.
    http://www.rd.com/common/nav/index.jhtml?articleId=8612597

    59. Alpers’ Disease Factsheet
    alpers’ disease. Download Factsheet. Not available. Feedback. Why is it calledalpers’ disease? The condition was first described in 1931 by Dr alpers.
    http://www.ich.ucl.ac.uk/factsheets/illnesses/alpers_disease/

    60. Directory Of Factsheets - Illnesses And Disease
    Title, Created by Abdominal Wall Defects, NICU. alpers’ disease, CNS Neurology.Anaemia (Erythropoietin), Dialysis Unit. Anaemias (Rare anaemias), Host Defence.
    http://www.ich.ucl.ac.uk/factsheets/illnesses/

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