41. HEREDITARY AUDITORY, VESTIBULAR, MOTOR AND SENSORY NEUROPATHY; A CHROMOSOME 8 DI 28 members of a gypsy family, with two siblings age 31 and 30 and one, age 20 years,suffering from hereditary motor and sensory neuropathy associated with http://www.ausp.memphis.edu/ierasg/abstract99/butinar.html

HEREDITARY AUDITORY, VESTIBULAR, MOTOR AND SENSORY NEUROPATHY: A CHROMOSOME 8 DISORDER D. Butinar , B.J.B. Keats , Y.S. Sininger , and A. Starr Institute of Clinical Neurophysiology, Ljubljana, SLOVENIA Center for Molecular and Human Genetics, New Orleans, LOUISIANA House Ear Institute, Los Angeles, CALIFORNIA Department of Neurology, Irvine, CALIFORNIA

42. THE LIGHTNING HYPERTEXT OF DISEASE. motor and sensory neuropathy type iv hereditary type iv motor and sensory neuropathyhereditary sensorymotor neuropathy, type iv neuropathy, hereditary motor http://www.pathinfo.com/cgi-bin/lh.cgi?tx=heredopathia

43. Disorder Information - MDAC's Full Disorder List CharcotMarie-Tooth, X-linked (CMTX) / hereditary motor and sensory neuropathy Xlinked (HMNSX) Locus Xq13.1 Gene CX32 Gene product connexin 32 Inheritance http://www.mdac.ca/english/disorder-info/disorder-info-23_long_disorder_3.htm

DISORDERS LIST Diseases of Skeletal Muscle a) Muscular dystrophies (MD) b) Structural myopathies c) Acquired inflammatory myopathies d) Myotonic disorders (distinct from channelopathies or dystrophies) e) Channelopathies f) Metabolic diseases of Muscle Diseases of the Neuromuscular Junction 3. Diseases of the Peripheral Nerve X-Linked Autosomal Dominant Autosomal Recessive Acquired Disorders ... Hereditary Ataxias 3. Diseases of the Peripheral Nerve X-linked Charcot-Marie-Tooth, X-linked (CMTX) / Hereditary motor and sensory neuropathy X linked (HMNSX) Locus: Gene: Gene product: connexin 32 Inheritance: Locus: Gene: Gene product: Inheritance: Locus: Gene: Gene product: Inheritance: Axonal motor-sensory neuropathy with deafness and mental retardation Locus: Gene: Gene product: Inheritance: Autosomal Dominant Charcot-Marie-Tooth (CMT1A) / Hereditary motor and sensory neuropathy type I (HMSN1A) Locus: Gene: Gene product: peripheral myelin protein 22 Inheritance: CMT with deafness Locus: Gene: Gene product: peripheral myelin protein 22 Inheritance: CMT1B / HMSNI Locus: Gene: Gene product: peripheral myelin protein zero Inheritance: Locus: Gene: Gene product: Inheritance: HMSN type III/Dejerine-Sottas type A Locus: Gene: Gene product: peripheral myelin protein 22 Inheritance: Locus: Gene: Gene product: early growth response 2 Inheritance: Locus: Gene: PRX Gene product: periaxin Inheritance: HMSN type III/Dejerine-Sottas type B Locus: Gene: Gene product: peripheral myelin protein zero Inheritance: HMSN type II (CMT2A) Locus:

44. HONselect - Hereditary Motor And Sensory Neuropathies sensory Neuropathies, Dejerine-Sottas Disease - HMSN - HMSN Type III - HMSN TypeVII - hereditary, Type III, motor and sensory neuropathy - hereditary, Type http://www.hon.ch/HONselect/RareDiseases/C10.500.300.html

List of rare diseases: English Deutsch Language: MeSH term: Accepted terms: English: Hereditary Motor and Sensory Neuropathies - Dejerine-Sottas Disease - HMSN - HMSN Type III - HMSN Type VII - Hereditary, Type III, Motor and Sensory Neuropathy - Hereditary, Type VII, Motor and Sensory Neuropathy Français: NEUROPATHIES HEREDITAIRES MOTRICES ET SENSORIELLES - NEUROPATHIES HEREDITAIRES MOTRICES ET SENSITIVES Deutsch: Hereditäre motorische und sensorische Neuropathien - Déjerine-Sottas-Krankheit - Hereditäre motorische und sensorische Neuropathie, Typ VII - Hereditäre motorische und sensorsische Neuropathie, Typ III - HMSN - HMSN Typ III - HMSNTyp VII Español: NEUROPATIAS MOTORAS Y SENSORIALES HEREDITARIAS - ENFERMEDAD DE DEJERINE-SOTTAS - NEUROPATIA MOTORA Y SENSORIAL HEREDITARIA TIPO VII - NEUROPATIA MOTORA Y SENSORIAL HEREDITARIA TIPO III - HMSN - HMSN TIPO III - HMSN TIPO VII Português: NEUROPATIAS MOTORAS E SENSORIAIS HEREDITARIAS - DOENCA DE DEJERINE-SOTTAS - NEUROPATIA HEREDITARIA MOTORA E SENSORIAL TIPO VII - NEUROPATIA HEREDITARIA MOTORA E SENSORIAL TIPO III - HMSN - HMSN TIPO III - HMSN TIPO VII HONselect ressources Definition: Yes Articles: Yes Images: No News: No Conferences: No Clinical trials: Yes Web sites: English Yes Français No Deutsch No Español No Português No Home About us Site map Feedback ... HONewsletter http://www.hon.ch/HONselect/RareDiseases/C10.500.300.html

45. HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE I (HMSN1) CHARCOT-MARIE-TOOTH ASSOC hereditary motor AND sensory neuropathy TYPE I (HMSN1) CHARCOTMARIE-TOOTH ASSOCIATEDWITH A PARTIAL, UNILATERAL OCULOmotor NERVE PALSY - A CASE REPORT. http://www.dog.org/1999/e-abstract99/692.html

97th DOG Annual Meeting 1999 HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE I (HMSN1) CHARCOT-MARIE-TOOTH ASSOCIATED WITH A PARTIAL, UNILATERAL OCULOMOTOR NERVE PALSY - A CASE REPORT C. Burkhard, I. Mildenberger, U. Schiefer Introduction: In 1886 Charcot and Marie reported a case of hereditary motor and sensory neuropathy that was identical to a case simultaneously and independently described by Tooth. Inherited in an autosomal dominant pattern, HMSN1 is characterized by slowly progressive weakness and muscle wasting in distal limb muscles, initially in the legs. It progresses slowly upwards to involve the muscles of the upper extremities. During the past century, several reports have described cases of HMSN1 in which oculomotor dysfunction was found in combination with the more typical findings of the disease. On occasion, oculomotor abnormalities, such as ptosis or diplopia, have been reported as cases of HMSN1, when other problems may have been at fault, such as myasthenia gravis, CPEO, or Horner's syndrome. We describe a case in which a patient previously diagnosed as having HMSN1 was found to have a partial IIIrd cranial nerve palsy. Case: A 38 year old man was referred to our out patient department with a two year history of vertical diplopia. As an infant he had been treated for hip joint dysplasia, and he had also had childhood onset of a gait disorder and unsteadiness on his feet. At the age of 19 he acquired the diagnosis of HMSN1. During subsequent years he had only minimal and slow progression of his neurological symptoms. An ophthalmic examination found evidence of a partial, unilateral IIIrd cranial nerve paresis, but the remainder of his ophthalmic examination was unremarkable.

46. NORD - National Organization For Rare Disorders, Inc. These symptoms may involve sensory, motor, reflex, or blood vessel (vasomotor)functions. Organizations related to neuropathy, hereditary sensory, Type I http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Neuropathy, H

47. Polyneuropathy With Other Specific Features Diphtheria. Perhexilene toxicity. hereditary motor and sensory neuropathy types1 and 3. hereditary motor sensory neuropathy (CharcotMarie-Tooth disease). http://neuroland.com/nm/pn_specific.htm

Neuroland Neurology information Click on the brain to index page Search NeuroLand Neuro disease Notes ... Neuro Med Polyneuropathy with other specific features Prominent Dysautonomia Diabetes mellitus Guillain Barre Syndrome Amyloidosis - Wash Univ (familial and acquired) Vincristine induced Porphyria - Wash Univ Hereditary sensory and autonomic neuropathy HIV-related autonomic neuropathy Idiopathic pandysautonomia Paraneoplastic sensory and autonomic ganglionopathy Ataxic sensory neuropathy Paraneoplastic sensory neuronpathy - Wash Univ Nomalignant inflammatory sensory ganglionopathy Monoclonal protein-associated neuropathy cis-Platinum tocicity - Wash Univ Pyridoxine toxicity - Wash Univ Vitamin B12 deficiency Tabes dorsalis Hereditary sensory and autonomic neuropathy Friedreich's ataxia (Baylor) and other spinocerebellar ataxias Demyelinating Polyneuropathies Guillain Barre Syndrome and variants Chronic inflammatory demyelinating polyradiculoneuropathy CIDP review - Baylor Monoclonal protein-associated neuropathy ( Search for meaning in Monoclonal protein - Postgrad Med Aug 99 Osteosclerotic myeloma Diphtheria Perhexilene toxicity Hereditary motor and sensory neuropathy types 1 and 3 Hereditary neuropathy with predisposition to pressure palsies Hereditary Neuropathy Hereditary Motor Sensory Neuropathy (Charcot-Marie-Tooth disease) Hereditary neuropathy with predisposition to pressure palsies Familial brachial plexopathy Familial amyloidosis Porphyria Other rare peripheral neuropathies:

48. NeuroCAST - Diagnosing Hereditary Peripheral Neuropathy 1 Among idiopathic peripheral neuropathy cases, DNA testing ultimately identifiesabout 42% of the cases as hereditary motorsensory neuropathy (HMSN), also http://www.neurocast.com/site/content/sessions_06_2002.asp

Peripheral neuropathy encompasses a host of conditions resulting from damage to the peripheral nerves. Diagnosing peripheral neuropathies can present a challenge to neurologists because other diseases and disorders have similar symptoms - numbness, weakness, incoordination or other sensory or motor disturbance. Following a method described by Cornblath (see Figure 1), the clinician should first evaluate the central nervous system causes for disorders of the brain and spinal cord. If these diseases are excluded, the clinician should next determine if the clinical presentation is consistent with acquired or hereditary peripheral neuropathy. If both central and peripheral nervous system involvement is indicated, the clinician may need to include mitochondrial disorders in the differential evaluation. Acquired peripheral neuropathy can be caused by diabetes, toxic exposure, drug interactions, autoimmune diseases and alcoholism. If the clinician is able to exclude the common causes of peripheral neuropathy, DNA and autoimmune testing can play a critical role in making a diagnosis in cases of suspected hereditary or autoimmune peripheral neuropathies. Without the aid of DNA and autoimmune testing, about 30% of peripheral neuropathies remain idiopathic.

49. Medical Dictionary Online : V, HMSN (Hereditary Motor And Sensory Neuropathy Typ V, HMSN (hereditary motor and sensory neuropathy Type V) on the Free Online MedicalDictionary. V, HMSN (hereditary motor and sensory neuropathy Type V). http://www.online-medical-dictionary.org/medical-dictionary-v/V-HMSN-Hereditary-

Medical Dictionary Online a free online medical dictionary search engine for definitions of medical terminology, pharmaceutical drugs, healthcare equipment, health conditions, medical devices, specialty terms and medical abbreviations. A B C D ... Link to the Medical Dictionary Online V, HMSN (Hereditary Motor and Sensory Neuropathy Type V) A group of inherited diseases that share similar phenotypes but are genetically diverse. Different genetic loci for autosomal recessive, autosomal dominant, and x-linked forms of hereditary spastic paraplegia have been identified. Clinically, patients present with slowly progessive distal limb weakness and lower extremity spasticity. Peripheral sensory neurons may be affected in the later stages of the disease. (J Neurol Neurosurg Psychiatry 1998 Jan;64(1):61-6; Curr Opin Neurol 1997 Aug;10(4):313-8) Contact us with questions, suggestions or general feedback Link to the Medical Dictionary Online

50. Search By Disease 62 hereditary ironloading anemia. 63 hereditary motor and sensory neuropathy(HMSN). 69 hereditary motor sensory neuropathy 2A (HMSN2A). http://www.eddnal.com/directory/disease.php?letter=H&page=5

51. Journal Articles Written About Charcot-Marie-Tooth Disease In CMT International and Abstracts of Some of the Articles May Be Found By SearchingMedline for Charcot Marie Tooth or hereditary motor sensory neuropathy . http://www.geocities.com/dgosling_rn/journal.html

We subscribe to the HONcode principles of the Health On the Net Foundation and the Medinex Code Of Online Excellence The Full Text of the Following Articles Can Be Found At Your Local Medical Library, Some Of Them May Be Available Through Membership In CMT International and Abstracts of Some of the Articles May Be Found By Searching Medline for "Charcot Marie Tooth" or "Hereditary Motor Sensory Neuropathy" Text Only and Version To Print Pages: General Overviews of CMT Anaesthesia And The CMT Patient Autosomal Recessive CMT Bone Density and CMT ... Vocal Cords In CMT General Overviews of CMT "Charcot-marie-tooth disease and related neuropathies: molecular basis for distinction and diagnosis." Pareyson D. Muscle Nerve. 1999 Nov;22(11):1498-509. " Hereditary peripheral neuropathies: clinical forms, genetics, and molecular mechanisms", Warner LE, et al.;Annu Rev Med. 1999;50:263-75. Review. "The Roussy-Levy family: from the original description to the gene. ", Plante-Bordeneuve V, et al. Ann Neurol. 1999 Nov;46(5):770-3. "Hereditary motor and sensory neuropathy: the plot thickens. "Pleasure D. Arch Neurol. 1999 Oct;56(10):1195.

52. Hereditary Motor And Sensory Neuropathy-Lom hereditary motor and sensory neuropathy – Lom. Author Professor Luba KalaydjievaScientific Editor Professor Marianne de Visser. Creation date August 2002. http://orphanet.infobiogen.fr/data/patho/GB/uk-HMSNL.html

Hereditary Motor and Sensory Neuropathy – Lom Author: Professor Luba Kalaydjieva Scientific Editor: Professor Marianne de Visser Creation date: August 2002 Disease name and synonyms Hereditary motor and sensory neuropathy Lom, HMSNL, Charcot-Marie-Tooth disease type 4D, CMT4D. Excluded diseases Other autosomal recessive demyelinating neuropathies. Diagnostic criteria / Definition HMSNL is a severe form of demyelinating CMT disease, associated with neural deafness in the majority of affected individuals. The diagnosis is based on: Clinical signs : Severe neuropathy with onset in the first decade of life, distally accentuated muscle weakness and wasting more pronounced in the lower limbs, foot and hand deformities. Hearing loss develops almost invariably in the 2nd-3rd decade; Electrophysiological signs : Nerve conduction velocities severely reduced in younger patients and usually unobtainable after age 15 years. Brainstem auditory evoked potentials (BAEPs) are markedly abnormal, with evidence of retrocochlear involvement of the central auditory pathways. Neuropathological signs : Severe reduction in myelinated fibre density and extensive endoneurial collagen deposition, increasing in severity with age. Abnormalities in the myelin sheath include uncompacted lamellae, abnormally oblique Schmidt-Lanterman incisures, and variable myelin thickness in adjacent internodes and complete demyelinisation of scattered internodes. Small onion bulb formations in younger patients gradually disappear with age. Active myelinated fibre degeneration is occasionally present in young patients. There is no evidence of regeneration of myelinated fibres, but the density of unmyelinated fibres is increased. Occasional demyelinated axons are packed with curvilinear profiles, similar to experimental vitamin E deficiency and dystorphic axons.

53. CJNS - Autosomal Recessive Motor And Sensory Neuropathy With Excessive Myelin Ou Two siblings, a 35year-old male and a 37-year-old female, offspring of first cousins,presented with a hereditary motor and sensory neuropathy with type I http://www.canjneurolsci.org/21febtoc/autosoma.htm

Abstract Close Window Autosomal Recessive Motor and Sensory Neuropathy with Excessive Myelin Outfolding in Two Siblings F. Barbieri, R. Santangelo, G. Capparelli, A. Ciccarelli and C. Crisci Abstract: Two siblings, a 35-year-old male and a 37-year-old female, offspring of first cousins, presented with a hereditary motor and sensory neuropathy with type I clinical features which began to manifest at about age 10 years. Nerve biopsy in the proband showed it to be a type characterized by excessive myelin outfolding. Morphometric study revealed hypomyelination with focal thickenings due to outfoldings. Clinical, electrophysiological and morphological findings are virtually identical to those described by Ohnishi et al. The peculiarity of the neuropathological picture suggests a particular form of hereditary motor and senory neuropathy. Can. J. Neurol. Sci. 1994; 21: 29-33

54. The Association Of Hereditary Spastic Paraplegia And Hereditary Motor And Sensor In the third case (the mother of the siblings), the clinical diagnosis was consistentwith hereditary motor sensory neuropathy type 2, which was also confirmed http://medicine.inonu.edu.tr/dergi/Contents/Volume2/Issue2/Abstract/193-195.html

The association of hereditary spastic paraplegia and hereditary motor and sensory neuropathy in the same family Münife Müftüoðlu , M.D., Ý. Özcan Ertürk , M.D., Cemal Özcan , M.D., Hakan Ekmekçi , M.D. The association of hereditary spastic paraplegia (HSP) and sensory neuropathies have been reported in a number of cases. But it is rare to detect both entities seperately in different members of the same family. In the present study, we report clinical and electrophysiological findings of three members of a family. In two of the siblings the clinical picture was indistinguishable from "pure" hereditary spastic paraplegia, but electrophysiological studies revealed a predominantly sensory polyneuropathy. In the third case (the mother of the siblings), the clinical diagnosis was consistent with hereditary motor sensory neuropathy type 2, which was also confirmed by electrophysiological studies. We believe that, with the further genetic reevaluations, the hereditary spastic paraplegia with sensory abnormalities may take a new place in the classification of hereditary motor and sensory polyneuropathies, as a distinct entity.[Journal of Turgut Özal Medical Center 2(2):193-195,1995] Key Words : Hereditary spastic paraplegia, hereditary motor and sensory neuropathy

55. AAPM&R - Case No. 43, Cont Predominantly sensory axonal polyneuropathy with some evidence of motor involvement,axonal and hereditary sensory Autonomic neuropathy IV (HSAN IV http://www.aapmr.org/education/emgcases/emg5903e.htm

What is a Physiatrist? Legislative, Business and Clinical Practice Issues Annual Assembly Medical Education ... EMG EMG CASE No. 59, January 2003, continued Diagnostic Impression Nerve conduction studies showed absent sural sensory nerve potentials bilaterally, with borderline right ulnar sensory nerve evoked amplitude. Borderline low tibial compound motor action potential amplitude and delay in distal latencies bilaterally are also noted. Motor nerve conduction velocities were all borderline slow. Electromyography was essentially normal. The electrodiagnostic impression: Predominantly sensory axonal polyneuropathy with some evidence of motor involvement, axonal and demyelinating in nature. What other diagnostic procedures (laboratory tests, etc.), if any, are needed? What treatment would you recommend? Commentary V Bibliography Hilz MJ. Assessment and evaluation of hereditary sensory and autonomic neuropathies with autonomic and neurophysiological examinations. Clin Auton Res 2002 May;12 Suppl 1:I33-43. Nolano M, Crisci C, Santoro L et al. Absent innervation of skin and sweat glands in congenital insensitivity to pain with anhidrosis. Clin Neurophysiol 2000 Sep;111(9):1596-601.

56. AAPM&R - EMG Case No. 59, Cont abetalipoproteinemia, idiopathic sensory neuropathy, autoimmune disorders includingHIV), hereditary sensory Autonomic Neuropathies child has any motor symptoms http://www.aapmr.org/education/emgcases/emg5903b.htm

What is a Physiatrist? Legislative, Business and Clinical Practice Issues Annual Assembly Medical Education ... EMG EMG CASE No. 59, January 2003, continued History A 13-year-old African American boy was admitted to the hospital for swelling of the left knee. This started 3 months earlier after having jumped from the second story of a building. There was a significant delay in seeking medical attention. He had been in foster care for the last 11 years for reported neglect, physical and sexual abuse on several occasions. The child had a longstanding history of behavioral problems and self-mutilation. His medical history consisted of numerous injuries including electrical burns and scalds on the hands, face, torso, and lower extremities, some of which required skin grafting. Around the age of 3 years, he developed ataxia and an occipital headache. An MRI revealed Arnold-Chiari Type I malformation. He was treated with a suboccipital craniectomy and C1 laminectomy. Prior to continuing, please develop a differential diagnosis and list each possible diagnosis in order of likelihood.

57. A GUIDE TO PERIPHERAL NEUROPATHY. Includes Charcot Marie Tooth Disease, an hereditary motor and sensory neuropathy(HMSN). May be as high as 1in 2500 people affected in some form. http://www.pdn-info.co.uk/Page_7.html

PERIPHERAL NEUROPATHY. The phrase is a general term for disorders affecting the peripheral nerves. The nerves and nerve fibres of the peripheral nervous system transport information to and from the brain and spinal cord to the skin, blood vessels and muscles in other parts of the body. The motor nerves control muscle contraction and may also control some functions of the autonomic (involuntary) system. Any peripheral nerve damage via the latter could result in problems with bowels or bladder, sweat glands and blood pressure. Sensory nerves carry signals mediating sensation from receptors (such as our touch and heat receptors) to the Central Nervous System. Neuropathies may affect a single peripheral nerve (known as a mononeuropathy) or several nerves (a polyneuropathy). If sensory nerves are damaged the sufferer may experience numbness, burning, sensory loss and pain, varying from the mild to searing hand or foot pain. If motor nerves are

58. Leucodistrofie/Parametri Genetici Delle Neuropatie Sensomotorie Ereditarie (HMSN hereditary neuralgic amyotrophy (HNA) Focal signs sensory loss at unusual sitesof compression Progressive generalized sensorymotor neuropathy May occur http://www.peacelink.it/appeal/gianmarco/parametr.html

a) Parametri Genetici delle Neuropatie Sensomotorie Ereditarie (HMSN) Andermann syndrome Cowchock Dejerine-Sottas Focally folded myelin sheaths HMSN: Complex HMSN: Demyelinating Dominant: IA; IB; HNPP; III Recessive: III; 4A; 4B; ?4C X-linked HMSN: Axonal Dominant: II; IIA; IIB; IIC; IID; 5; 6 X-linked HMSN: Types Liability to pressure palsies Other: Myelin disorders; Recessive Cockayne's Congenital hypomyelinating neuropathy Krabbe Metachromatic leukodystrophy Refsum's disease Other: Childhood onset Types IA, IB, III, HNPP, and neuropathy with focally folded myelin sheaths have demyelinationas a prominent component. Type II is predominantly axonal. X-linked forms may have demyelination or predominantly axonal loss. Other hereditary motor-sensory neuropathies are often associated with complex clinical syndromes or specific metabolic abnormalities. Among them also the hereditary distal motor neuropathies. < 6 y.o. Myelin sheaths thinner than normal Homozygotes PMP-22 duplication (4 copies); Chromosome 17p11.2-p12 Clinical features Most severe weakness Earlier onset < 20 yrs): Classic form Phytanic Acid Oxidase ; Recessive Retinitis Pigmentosa Demyelinating Neuropathy Course may be Progressive or Relapsing High CSF Protein Anosmia; deafness Cardiac Failure (may cause sudden death) Less common: Ataxia, Ichthyosis Biochemistry Elevated serum phytanic acid Reduced oxidation of phytanic acid in fibroblasts Treatment with low phytanic acid diet Infantile onset ?peroxisomal disorder; Autosomal recessive Mental retardation Demyelinationg neuropathy Deafness Retinitis pigmentosa Biochemistry Hepatomegaly; steatorrhea Hypocholesterolemia Accumulation of phytanic acid, pipecolic acid, very long chain fatty acids Adult onset with increased pipecolicacidemia ; ? peroxisomal disorder; Chromosome 10p; Recessive

59. OUP USA: ToC: Diagnosis And Management Of Peripheral Nerve Disorders Diabetic Neuropathies 20. Peripheral neuropathy Associated with HIV Infection 21.hereditary motor and sensory Neuropathies and Giant Axonal neuropathy 22. http://www.oup-usa.org/toc/tc_0195133013.html

Diagnosis and Management of Peripheral Nerve Disorders Jerry R. Mendell, John T. Kissel, and David R. Cornblath CONTENTS 1. Evaluation of the Patient with Peripheral Neuropathy: The Challenges 2. Clues to Diagnosis of Peripheral Neuropathy: History and Examination of the Patient 3. Electrodiagnostic Evaluation of the Peripheral Neuropathy Patient 4. Evaluation of the Peripheral Neuropathy Patient Using Quantitative Sensory Testing 5. Evaluation of the Peripheral Neuropathy Patient Using Autonomic Reflex Tests 6. The Role of Autoantibody Testing 7. The Role of Peripheral Nerve and Skin Biopsies 8. Approach to Painful Peripheral Neuropathies 9. Guillain-Barre Syndrome 10. Chronic Inflammatory Demyelineating Polyradiculoneuropathy 11. Multifocal Motor Neuropathy 12. Vasculitic Neuropathy 13. Peripheral Neuropathies Associated with Connective Tissue Diseases 14. Sarcoid Peripheral Neuropathy 15. Neuropathies Associated with Monoclonal Gammopathies 16. Toxic Neuropathies: Drugs, Metals, and Alcohol 17. Porphyric Neuropathy

60. Neuromuscular Diseases - Internet Handbook Of Neurology Louis; hereditary motor sensory Neuropathies CharcotMarie-Tooth - Washington University,St. Louis; neuropathy of Friedreich Ataxia - eMedicine/Neurology. Nerve http://www.neuropat.dote.hu/nmd.htm

Internet Handbook of Neurology Compiled by K atalin H Department of Neurology University of Debrecen, Hungary Neuromuscular Diseases Chapters: A Collection of High Quality Online Resources for Health Professionals Pathology see Pathology of Nerve and Muscle Overview Neuromuscular Diseases - Washington University, St. Louis Neuromuscular Diseases - Muscular Dystrophy Association (MDA), AU Neuromuscular Diseases - Wake Forest University Neuromuscular Disease Info Center - Neuroland Muskelkrankheiten - Neurologische Klinik Zentralkrankenhaus Bremen Ost, DE (in German) Diagnostic Criteria for Neuromuscular Disorders - European Neuro Muscular Centre Ion Channel Diseases - Washington University, St. Louis HIV-1 Associated Myopathies - eMedicine/Neurology EMG - TeleEMG EMG - CASA Engineering (with pictures) Conventional Needle EMG - Uppsala University, SE Single Fiber EMG - eMedicine/Neurology Nerve Conduction Studies and Electromyography in the Evaluation of Peripheral Nerve Injuries - Othopaedic Journal, Spring 1999 Nerve Conduction Studies - Journal of Neurological Sciences (Turkish), April-June 2000

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