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Myopathies: more books (96)

Acute steroid myopathies rising over past 5 years: suspect rheumatologic drugs. (Clinical Rounds).: An article from: Internal Medicine News by Sherry Boschert, 2003-04-01
Histoire des myopathies by Patrice Pinell Franï¿½ois Delaporte, 1998-10-19
Myotubular myopathy: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Chitra, MBBS, MD Venkatasubramanian, 2005
Experimental Myopathies and Muscular Dystrophy: Studies in the Formal Pathogenesis of the Myopathy of 2,4-Dichlorophenoxyacetate (Schriftenreihe Neurologie Neurology Series) by R. Heene, 1975-11-10
Myositis & Myopathies: Raynauld's Phenomenon by Lawrence J. Kagen, 1994-11
Physiology of capture myopathy: Quinquennial report : a study of capture myopathy (overstraining syndrome) in wild ungulates in southern Africa by Antonie Marinus Harthoorn, 1976
Inflammatory Myopathies (Bailliere's Clinical Neurology) by Frank L. Mastaglia, 1993-11
Evaluation and Treatment of Myopathies
On Myopathy and a Distal Form. by William R. GOWERS, 1902
Atlas of Neuromuscular Diseases: A Practical Guideline by Eva L. Feldman, Wolfgang Grisold, et all 2004-12-15
A Simple Scale of Gorski's Warning Signs for Relapse(*).(Statistical Data Included): An article from: Journal of Studies on Alcohol by William R. Miller, Richard J. Harris, 2000-09-01
Mitochondrial Disorders by Claude Desnuelle, 2002-12-05
Carnitine palmitoyltransferase deficiency: An entry from Thomson Gale's <i>Gale Encyclopedia of Genetic Disorders, 2nd ed.</i> by Scott, MS, CGC Polzin, 2005
Alcohol-Induced Hallucinations: Prompt Care IS Key.: An article from: Clinical Psychiatry News by Carl Sherman, 2001-10-01

lists with details

Congenital Myopathies
Penn State Hershey Medical Center provides world class care and services to patients.
http://www.hmc.psu.edu/healthinfo/c/congenitalmyopathies.htm
CONGENITAL MYOPATHIES AND ANESTHESIA Pediatric Oncall
CONGENITAL myopathies AND ANESTHESIA Pediatric Oncall.
http://www.pediatriconcall.com/fordoctor/diseasesandcondition/conmyoAnesthesia.a

Extractions: BJ Wadia Childrens hospital MYOPATHIES: Myopathies are primary diseases of striated muscles in which biochemical, morphological or neurophysiological changes occur singly or in combination. They are characterized by the description of the histologic lesion and the clinical and genetic picture. Congenital myopathies are mainly of 3 types: Central core disease: It is a rare disorder. It is so named because of the metabolically inactive cores present in the muscle fibres. Patients have decreased fetal movements and breech presentation. They have hypotonia and delay in motor milestones with increased proximal weakness. In childhood, they have difficulty in climbing stairs and getting up from the floor. Legs are more affected than arms. Investigations reveal increased CPK levels. EMG shows myopathic pattern and muscle biopsy shows fibres with single or multiple central or eccentric discrete zones devoid of oxidative enzymes.
Myopathies
myopathies. Progressive Proximal Weakness. Click here to return.
http://daffodil.uthscsa.edu/faculty/dumitru/emgs/myopathies/Default.htm
UpToDate Metabolic Myopathies: Disorders Of Lipid Metabolism
INTRODUCTION Patients with metabolic myopathies have underlying deficiencies The clinical manifestations of the myopathies resulting from nonlysosomal
http://patients.uptodate.com/topic.asp?file=pedirheu/7518
UpToDate Drug-induced Myopathies
Druginduced myopathies. Marc L Miller, MD. UpToDate performs a continuous review of over 330 journals and other resources. Updates are added as important
http://patients.uptodate.com/topic.asp?file=muscle/6981
FIRSTConsult - Sdfdsf
FIRSTConsult, Muscular dystrophies and related myopathies (Medical Condition File). Published for medical students and primary healthcare providers by
http://www.firstconsult.com/?action=view_article&id=1014471&type=101&bref=1
Core Curriculum - POSNA
Congenital myopathies. pdf Objectives 1. Describe clinical features which accompany congenital myopathies 2. Discuss pertinent anesthetic risk factors when
http://www.posna.org/index?service=page/coreCurriculum&article=congenitalMyopath
Summary Folders
Hereditary myopathies Acquired myopathies Developmental disorders of muscle Complications of myopathies Other related disorders.
http://www.medlink.com/PublicCIP.asp?UID=0112&MODE=8&access=public&code=
IngentaConnect Drug-induced Myopathies
Apart from isolated myalgias, druginduced myopathies can be divided into five In some cases (eg, statin-induced myopathies), risk factors have been
http://www.ingentaconnect.com/content/apl/eds/2002/00000001/00000001/art00008

Extractions: For Researchers For Librarians Author: Bannwarth B. Source: Expert Opinion on Drug Safety , Volume 1, Number 1, 1 May 2002, pp. 65-70(6) Publisher: Ashley Publications View Table of Contents full text options Abstract: Keywords: adverse effects corticosteroids drugs myopathies ... statins Document Type: Review article Affiliations: Department of Rheumatology, Groupe Hospitalier Pellegrin, 33076 Bordeaux Cedex, France, Tel: +33 556 795 556, Fax: +33 556 930 407, Email: bernard.bannwarth@u-bordeaux2.fr The full text is free. View now: View Table of Contents Back to top Terms and Conditions Page Help Quick Search
Gene Expression In Inflammatory Myopathies
The goals of Gene Expression in Inflammatory myopathies are (1) to formulate and validate hypotheses relevant to the pathogenesis of the inflammatory
http://www.chip.org/chip/research/projects_geneexpression.html

Extractions: (3) to explore possible gene function for genes, cDNAs, and expressed sequence tags (ESTs) of unknown function through computational techniques applied to these expression profiles. High-density oligonucleotide microarrays are used to assay gene expression in muscle biopsy specimens from patients with inflammatory myopathies. Data analysis of differential gene expression provides leads relevant to pathogenesis that will then be validated biologically. Gene expression profiles are linked with clinical data to refine disease classification. This work may provide further understanding of the pathogenesis of inflammatory myopathies with a consequent generation of hypotheses for treatment and may contribute to clinical classification of this group of diseases. Staff
Project: Nemaline Myopathies In Human And Mouse, Unique Diseases Of Sarcomere Pr
Project Nemaline myopathies in human and mouse, unique diseases of sarcomere proteins and contractile unit; clinical, physiological, histological and
http://www.onderzoekinformatie.nl/en/oi/nod/onderzoek/OND1295744/toon

Extractions: Login English KNAW Research Information NOD - Dutch Research Database ... Research entire www.onderzoekinformatie.nl site fuzzy match Print View Titel Nemaline myopathie«n bij mens en muis, unieke ziekten van sarcomeer eiwitten en de contractiele unit; klinische, fysiologische, histologische en genetische kenmerken Abstract The main complaint of a patient with muscular disease is weakness. Muscle slowness is a problem in the field of neuromuscular diseases which has not yet been described before. In some nemaline muscular disease patients there seems to occur of form of muscle slowness (in addition to muscle weakness), due to which they are e.g. not able to intercept a fall. It will be studied if this also occurs in the rest of the nemaline muscular disease patients known to us and if this phenomenon is related to a genetic cause of nemaline muscular disease. In addition nemaline mice will be used in order to characterize muscle slowness even more precisely and to correlate it with microscopic muscle study. Also the mice will enable us to study in detail if muscle weakness and possibly also slowness may be influenced by drugs. Period Status completed Related organisations
HighWire -- Browse Journals - Mitochondrial Myopathies
Browse Journals publishing on Mitochondrial myopathies, (return to Topic List Journals focusing on Mitochondrial myopathies (in order by highest focus)
http://highwire.stanford.edu/lists/topic_dir/608683/608684/610114/610136/610158/

Extractions: Chronic Progressive External Ophthalmoplegia Mitochondrial Encephalomyopathies Sort by: Alphabet Frequency of articles in Mitochondrial Myopathies Focus of journal on Mitochondrial Myopathies What's this? Journals focusing on Mitochondrial Myopathies (in order by highest focus) Journal of Histochemistry and Cytochemistry info free ISSUES Journal of Medical Genetics ... Muscular Diseases Mitochondrial Myopathies Home Adv. Search For Institutions For Publishers ... partners/suppliers
HighWire -- Browse Journals - Congenital Structural Myopathies
Browse Journals publishing on Congenital Structural myopathies, (return to Topic List page) Central Core Myopathy, Nemaline myopathies
http://highwire.stanford.edu/lists/topic_dir/608683/618131/626183/626251/626291/

Extractions: Central Core Myopathy Nemaline Myopathies Sort by: Alphabet Frequency of articles in Congenital Structural Myopathies Focus of journal on Congenital Structural Myopathies What's this? Journals focusing on Congenital Structural Myopathies (in order by highest focus) Human Molecular Genetics info free ISSUES Journal of Biological Chemistry ... Muscular Diseases Congenital Structural Myopathies Home Adv. Search For Institutions For Publishers ... partners/suppliers
Lipid Storage Myopathies (from Muscle Disease) -- Encyclopædia Britannica
Lipid storage myopathies (from muscle disease) Lipid storage myopathy is a potentially confusing term because the more severe forms of muscle disease ( e eg
http://www.britannica.com/eb/article-58898

Extractions: Home Browse Newsletters Store ... Subscribe Already a member? Log in Content Related to this Topic This Article's Table of Contents Expand all Collapse all Introduction Indications of muscle disease Muscle weakness Signs and symptoms Assessment Classification of muscle weakness Upper motor neuron disease ... Inflammatory myopathies Endocrine and metabolic myopathies Hormones Vitamin D deficiency Mitochondrial myopathies Glycogenoses changeTocNode('toc58893','img58893'); Lipid storage myopathies Myotonic diseases The periodic paralyses Fatigue ... Print this Table of Contents Shopping Price: USD $1495 Revised, updated, and still unrivaled. The Official Scrabble Players Dictionary (Hardcover) Price: USD $15.95 The Scrabble player's bible on sale! Save 30%. Merriam-Webster's Collegiate Dictionary Price: USD $19.95 Save big on America's best-selling dictionary. Discounted 38%! More Britannica products muscle disease
Mitochondrial Myopathies (from Muscle Disease) -- Encyclopædia Britannica
Mitochondrial myopathies (from muscle disease) The mitochondria are the cellular structures in which biochemical processes produce energy (in the form of
http://www.britannica.com/eb/article-58896

Extractions: Home Browse Newsletters Store ... Subscribe Already a member? Log in Content Related to this Topic This Article's Table of Contents Expand all Collapse all Introduction Indications of muscle disease Muscle weakness Signs and symptoms Assessment Classification of muscle weakness Upper motor neuron disease ... Inflammatory myopathies Endocrine and metabolic myopathies Hormones Vitamin D deficiency changeTocNode('toc58893','img58893'); Mitochondrial myopathies Glycogenoses Lipid storage myopathies Myotonic diseases ... Print this Table of Contents Shopping Price: USD $1495 Revised, updated, and still unrivaled. The Official Scrabble Players Dictionary (Hardcover) Price: USD $15.95 The Scrabble player's bible on sale! Save 30%. Merriam-Webster's Collegiate Dictionary Price: USD $19.95 Save big on America's best-selling dictionary. Discounted 38%! More Britannica products muscle disease
Northwestern University Medical School Neuromuscular Disorder Program
Muscular Dystrophies Motor Neuron Diseases Inflammatory myopathies Diseases of the neuromuscular Junction myopathies due to Endocrine Abnormalities
http://www.neurogenetics.northwestern.edu/index.jsp?ca=patienthome&mp=patient|my
Northwestern University Medical School Neuromuscular Disorder Program
myopathies due to Endocrine Abnormalities Diseases of Peripheral Nerve Other myopathies Inflammatory myopathies. Dermatomyositis. Polymyositis
http://www.neurogenetics.northwestern.edu/index.jsp?ca=patienthome&mp=patient|de
Classification Of Metabolic Myopathies
Metabolic myopathies are a group of hereditary muscle disorders and the result According to the biochemical classification, the metabolic myopathies are
http://www.charite.de/ch/medgen/eumedis/neurogenetics05/class-metabolic-myopathi

Extractions: Home Up Up topic About Clinical and genetic aspect of autosomal dominant cerebellar ataxia type II (ADCA II) Autosomal dominant cerebellar ataxias Physiopathological aspects of spinocerebellar ataxias ... Clinical and genetic aspects of Congenital Muscular Dystrophy Classification of metabolic myopathies Pathological aspects of metabolic myopathy disorders Glycogen Storage Myopathies: from clinical features to treatment Font size: Table of Contents These diseases are grouped into abnormalities affecting glycogen, lipids, purines, or mitochondrial pathways metabolism. According to the biochemical classification, the metabolic myopathies are divided into 4 categories, as follows: Glycogen is the main immediate source of energy in the muscle. It is a form of carbohydrate storage: muscle cells transport glucose from the circulating blood, synthesize and store glycogen. When energy is required for muscle contraction, glycogen is degraded to glucose and provides the energy required for muscle work. Any disturbance in either the synthesis or the degradation of glycogen could result in glycogen storage diseases commonly named glycogenoses. To date, 11 different diseases caused by an underlying defect in glycogen synthesis, glycogenolysis (and glycolysis) have been identified. The glycogen is accumulated in muscle as a consequence of the defect. GSDs are named according to their specific defective enzyme function, an eponym, or by Roman numerals that correlate to the time of their discovery.
Glycogen Storage Myopathies From Clinical Features To Treatment
Glycogen storage myopathies are a group of inborn errors of metabolism Recently, three major clinical sindromes of glycogen storage myopathies have been
http://www.charite.de/ch/medgen/eumedis/neurogenetics05/gly-stor-myopathies.html

Extractions: Home Up Up topic About Clinical and genetic aspect of autosomal dominant cerebellar ataxia type II (ADCA II) Autosomal dominant cerebellar ataxias Physiopathological aspects of spinocerebellar ataxias ... Pathological aspects of metabolic myopathy disorders Glycogen Storage Myopathies: from clinical features to treatment Font size: Table of Contents Glycogen storage myopathies are a group of inborn errors of metabolism characterized by glycogen accumulation in muscular tissues carrying enzyme defects of the glycogenolytic or glycolytic pathways. In skeletal muscle, glycogen content is about 1g/100g fresh muscle and it is utilized as a major source of energy production for the contraction-relaxation mechanism. Anaerobic glycolysis is primarily involved during conditions of high intensity isometric muscular activity and an enzyme deficiency in glycogen or glucose pathways could induce a bioenergetic crisis in muscle. Recently, three major clinical sindromes of glycogen storage myopathies have been recognized: the first is fixed with slowly progressive weakness,often accompanied by involvement of other organs (i.e. peripheral nerve, heart, brain etc.), the second form presents with exercise intolerance, recurrent, acute and reversible muscle dysfunction, rhabdomyolisis and myoglobinuria whereas the third one may show a mixed pattern (2).
United Mitochondrial Disease Foundation - Medical Article List By Subject
Dalakas ; MC ; 696 ; Retroviruses and inflammatory myopathies in humans and Lindal ; S ; 786 ; Mitochondrial diseases and myopathies a series of muscle
http://biochemgen.ucsd.edu/umdf/mito-myopa.htm

Extractions: The UMDF Medical Article List Subject: Mitochondrial Myopathies Back to the Subject List United Mitochondrial Disease Foundation We welcome any suggested additions to our list. Last updated: 26-Jun-98 REFERENCE FORMAT: Author Lastname; Firstname; Article Number; Article Title; Journal or Book; Year; Volume; Page Numbers Aasly ; J ; 2711 ; Early mitochondrial changes in chronic progressive ocular myopathy. ; Eur Neurol ; 1990 ; 30(6) ; 314-8 Abe ; K ; 5672 ; Measurement of tissue oxygen consumption in patients with mitochondrial myopathy by noninvasive tissue oximetry. ; Neurology ; 1997 ; 49(3) ; 837-41 Abe ; K ; 1027 ; Marked reduction in CSF lactate and pyruvate levels after CoQ therapy in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). ; Acta Neurologica Scandinavica ; 1991 ; 83(6) ; 356-9 Abramowicz ; MJ ; 3109 ; Pernicious anaemia and hypoparathyroidism in a patient with Kearns- Sayre syndrome with mitochondrial DNA duplication. ; J Inherit Metab Dis ; 1996 ; 19(2) ; 109-111

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