000825430 000__ 04983cam\a2200517Ii\4500 000825430 001__ 825430 000825430 005__ 20230306144216.0 000825430 006__ m\\\\\o\\d\\\\\\\\ 000825430 007__ cr\cn\nnnunnun 000825430 008__ 180103s2018\\\\si\\\\\\ob\\\\000\0\eng\d 000825430 019__ $$a1017900378$$a1018245193$$a1021195369$$a1026983408$$a1032268710 000825430 020__ $$a9789811053610$$q(electronic book) 000825430 020__ $$a9811053618$$q(electronic book) 000825430 020__ $$z9789811053603 000825430 020__ $$z981105360X 000825430 0247_ $$a10.1007/978-981-10-5361-0$$2doi 000825430 035__ $$aSP(OCoLC)on1017738307 000825430 035__ $$aSP(OCoLC)1017738307$$z(OCoLC)1017900378$$z(OCoLC)1018245193$$z(OCoLC)1021195369$$z(OCoLC)1026983408$$z(OCoLC)1032268710 000825430 040__ $$aN$T$$beng$$erda$$epn$$cN$T$$dN$T$$dEBLCP$$dYDX$$dGW5XE$$dUAB$$dAZU$$dUPM$$dOCLCF$$dMERER$$dCOO$$dOCLCQ$$dVT2$$dAUD$$dU3W 000825430 049__ $$aISEA 000825430 050_4 $$aRC925.5 000825430 08204 $$a616.7/44$$223 000825430 1001_ $$aKhadilkar, Satish V.,$$eauthor. 000825430 24510 $$aNeuromuscular disorders :$$ba comprehensive review with illustrative cases /$$cSatish V. Khadilkar, Rakhil S. Yadav, Bhagyadhan A. Patel. 000825430 264_1 $$aSingapore :$$bSpringer,$$c2018. 000825430 300__ $$a1 online resource 000825430 336__ $$atext$$btxt$$2rdacontent 000825430 337__ $$acomputer$$bc$$2rdamedia 000825430 338__ $$aonline resource$$bcr$$2rdacarrier 000825430 347__ $$atext file$$bPDF$$2rda 000825430 504__ $$aIncludes bibliographical references. 000825430 5050_ $$aNeuromuscular Disorders: A clinical Approach -- Part I: Asymmetric motor weakness -- Motor Neuron Diseases [ALS] -- Hirayama disease and other focal amyotrophies -- Multifocal motor neuropathy -- Acute motor axonal neuropathy -- Facioscapulohumeral muscular dystrophy -- Progressive muscular atrophy -- Post-polio syndrome -- Part II: Symmetric proximal weakness -- Duchenne and Becker muscular dystrophies -- Spinal Muscular atrophy [SMA] -- Idiopathic Inflammatory myopathies -- Limb Girdle muscular Dystrophies [LGMDs] -- Congenital Myasthenic syndromes [CMS] -- Congenital muscular dystrophies -- Congenital myopathies -- Emery Dreifuss Muscular dystrophy -- Oculopharyngeal muscular dystrophy -- Part III: Symmetric distal weakness -- Myotonic dystrophies [DM] -- Distal myopathies -- Distal hereditary motor neuropathies -- Brown Vieletto Van Laere Syndrome -- Part IV: Fluctuating weakness -- Myasthenia Gravis [MG] -- Lambert Eaton Myasthenic Syndrome -- Periodic paralysis -- Part V: Exercise intolerance, muscle stiffness, cramps and contractures -- Metabolic myopathies -- Peripheral nerve hyperexcitability syndromes -- Non dystrophic myotonias -- Part VI: Asymmetric sensory motor weakness -- Individual neuropathies -- Vasculitic neuropathy -- Multifocal acquired demyelinating sensory and motor neuropathy -- Brachial plexopathies -- Lumbosacral plexopathies -- Compressive Radiculopathies -- Leprosy -- Hereditary neuropathy with pressure palsy -- Part VII: Symmetric sensory motor weakness -- Guillain-Barré syndrome -- Charcot-Marie-Tooth disease[CMT] -- Chronic Inflammatory Demyelinating Polyradiculoneuropathy -- X-linked Charcot Marie Tooth disease -- Other Hereditary neuropathies -- 1 -- Other hereditary neuropathies -- 2 -- Neuropathies secondary to systemic diseases -- Porphyrias.-Part VIII: Predominant sensory syndromes -- Sensory ganglionopathies -- Distal Acquired Demyelinating Symmetric neuropathy -- Paraproteinemic neuropathies -- Miller Fisher Syndrome. 000825430 506__ $$aAccess limited to authorized users. 000825430 520__ $$aThis book provides a concise overview of the diagnosis and therapy of a wide variety of neuromuscular disorders, in tabulated form and with illustrative cases. Treating neuromuscular disorders calls for a sound, step-by-step clinical approach based on differential diagnosis and laboratory investigations. Yet to date, there has been no single, compact book that offers all the relevant information related to the management of these disorders. This book fills that gap, presenting the state of the art in the field and addressing practical problems together with their solutions. Each chapter covers disorder characteristics, clinical differentiating points, relevant investigations and their interpretation, available genetic testing, best management approaches and counselling. Illustrative cases provide valuable insights, while extensive tables and illustrations mean that information can be rapidly found. 000825430 588__ $$aVendor-supplied metadata. 000825430 650_0 $$aNeuromuscular diseases. 000825430 650_0 $$aAmyotrophic lateral sclerosis. 000825430 650_0 $$aDuchenne muscular dystrophy. 000825430 650_0 $$aSpinal muscular atrophy. 000825430 7001_ $$aYadav, Rakhil S.,$$eauthor. 000825430 7001_ $$aPatel, Bhagyadhan A.,$$eauthor. 000825430 77608 $$iPrint version:$$aKhadilkar, Satish V.$$tNeuromuscular Disorders : A Comprehensive Review with Illustrative Cases.$$dSingapore : Springer, ©2017$$z9789811053603 000825430 852__ $$bebk 000825430 85640 $$3SpringerLink$$uhttps://univsouthin.idm.oclc.org/login?url=http://link.springer.com/10.1007/978-981-10-5361-0$$zOnline Access$$91397441.1 000825430 909CO $$ooai:library.usi.edu:825430$$pGLOBAL_SET 000825430 980__ $$aEBOOK 000825430 980__ $$aBIB 000825430 982__ $$aEbook 000825430 983__ $$aOnline 000825430 994__ $$a92$$bISE