Neurological Syndromes (eBook)

A Clinical Guide to Symptoms and Diagnosis
eBook Download: PDF
2013 | 2013
XIII, 279 Seiten
Springer New York (Verlag)
978-1-4614-7786-0 (ISBN)

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Neurological Syndromes - J. Gordon Millichap
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Neurological Syndromes: A Clinical Guide to Symptoms and Diagnosis offers a concise, invaluable resource for understanding how a group of neurologic symptoms or signs collectively characterize a disease or disorder. Intended as a quick reference guide to the better known and some less familiar syndromes of neurological interest and developed by a renowned pediatric neurologist with more than 40 years experience in treating children, adolescents, and young adults, this handy title provides a definition of each syndrome that includes diagnostic characteristics and abnormalities, a differential diagnosis, genetic considerations, and a short list of references. To those readers who can recall the name of a syndrome, the alphabetical presentation should facilitate a review of the major diagnostic characteristics. The original reference is provided for historical interest, and review articles are included to show recent advances in etiology and treatment. The index is arranged in alphabetical order of the named syndromes and also according to the involvement of various organs in addition to the nervous system. A unique contribution to the literature, Neurological Syndromes: A Clinical Guide to Symptoms and Diagnosis will be of great interest to the wide variety of clinicians treating patients with neurologic disease.


Neurological Syndromes: A Clinical Guide to Symptoms and Diagnosis offers a concise, invaluable resource for understanding how a group of neurologic symptoms or signs collectively characterize a disease or disorder. Intended as a quick reference guide to the better known and some less familiar syndromes of neurological interest and developed by a renowned pediatric neurologist with more than 40 years experience in treating children, adolescents, and young adults, this handy title provides a definition of each syndrome that includes diagnostic characteristics and abnormalities, a differential diagnosis, genetic considerations, and a short list of references. To those readers who can recall the name of a syndrome, the alphabetical presentation should facilitate a review of the major diagnostic characteristics. The original reference is provided for historical interest, and review articles are included to show recent advances in etiology and treatment. The index is arranged in alphabetical order of the named syndromes and also according to the involvement of various organs in addition to the nervous system. A unique contribution to the literature, Neurological Syndromes: A Clinical Guide to Symptoms and Diagnosis will be of great interest to the wide variety of clinicians treating patients with neurologic disease.

Table of Contents AAicardiAicardi-GoutieresAndermannAngelmanAntonApertAvellis BBalintBannwarthBardet-BiedlBassen-KornzweigBenediktBobble-head DollBrainstem (Table)Brown-SequardBrueghelBurning Feet CCadasilCapgrasCayler CardiofacialCentral CordCHARGECharles Bonnet  (CBS)ChiasmalChurg-StraussClaudeCockayneCoffin-LowryCohenCornelia de LangeCornelia de Lange IICostenCowden Cranial Nerve (Table)CRASH  (MASA)Crit du ChatCrouzon  DDandy WalkerDDON (Deafness-Dystonia-Optic Neuronopathy)Dejerine-RoussyDejerine (Table)De MorsierDiGeorgeDonnai-BarrowDooseDravetDuane EEdwardsElsbergEmpty Sella (ESS)Epidermal NevusEpilepsy (Electroclinical) (Table) FFazio-LondeFeingoldFerguson-CritchleyFetal Alcohol Foix-AlajouanineFoix-Chavany-MarieFoster-KennedyFovilleFragile XFragile X-Associated Tremor/AtaxiaFroehlichFroin GGanserGarcinGerstmannGoldenharGorlinGradenigoGreig CephalopolysyndactylyGuillain-Barre HHallermann-StreiffHARPHaw RiverHeerfordtHerpes Zoster OticusHopkinsHolmes-AdieHornerHHH IIsaacs JJacksonJackson-WeissJacobsenJanzJervell-Lange-NielsenJoubertJuberg-Marsidi KKabukiKallmannKearns-Sayre (KSS)KinsbourneKjellinKleefstraKlein-LevinKlinefelterKlippel-FeilKlippel-Trenaunay-WeberKluver-BucyKocher-Debre Semelaigne LLambert-EatonLance-AdamsLandau-KleffnerLeighLennox-GastautLenz Microphthalmia (LMS)Lesch-NyhanLewis-SumnerLocked-inLoeys-DietzLowe MMarcus GunnMarfanMarin AmatMarin AmatMarinesco-SjorgenMASAMcLeod NeuroacanthocytosisMeckel-GruberMECP2 DuplicationMeigeMELASMelkersson-RosenthalMERRFMicrophthalmos with Linear Skin Defects (MLS)Millard-GublerMiller-DiekerMiller-FisherMitochondrial DNA Deletion (MDDS)MobiusMohr-TranebjaergMorvanMoschcowitzMowat-WilsonMPV17-related Hepatocerebral MDDSMuenke NNeuroleptic MalignantNijmegen BreakageNoonanNothnagel OOHAHAOhtaharaOpitzOpsoclonus MyoclonusOral-Facial-Digital Type 1Osler-Weber-Rendu PPallister-HallPanayiotopoulosParaneoplastic ParinaudParry-RombergParsonage-TurnerPatau Trisomy 13PEHOPena-ShokeirPendred (DFNB4)PerryPfeiffer Type 2PHACESPhelan-McDermidPitt-HopkinsPOEMSPolandPrader-WilliProteus RRaeder’s ParatrigeminalRamsay Hunt Type IRamsay Hunt Type IIRasmussenRenpenningRettReyeRiley-DayRosenberg-ChutorianRoussy-LevyRubinstein-TaybiRussell-Silver SSaethre-ChotzenSandiferSatoyoshiSchimmelpenning-Feuerstein-MimsSchneiderSchwarts-BartterSchwartz-Jampel Type 1ASepto-Optic DysplasiaSerotoninShapiroShprintzen-GoldbergShy-DragerSimpson-Golabi-Behmel Type 1Sjogren-LarssonSmith-Lemli-OpitzSmith-MagenisSotosSticklerStiff PersonStrachenSturge-WeberSUCLA 2 DeficiencySusac TTapiaTersonThoracic Outlet (TOS)Tolosa-HuntTouretteTreacher CollinsTroyerTurner  UUsher Type 1 VVelo-Cardio-FacialVerbiestVerger-DejerineVernetViciVillaretVogt-Koyanagi-Harada WWalker-WarburgWallenbergWartenbergWeberWerdnig-HoffmannWernicke-KorsakoffWestWilliamsWolf-HirschhornWolfram X-linked Opitz G/BBB Zellweger

Erscheint lt. Verlag 4.8.2013
Zusatzinfo XIII, 279 p.
Verlagsort New York
Sprache englisch
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Allgemeinmedizin
Medizin / Pharmazie Medizinische Fachgebiete Innere Medizin
Medizin / Pharmazie Medizinische Fachgebiete Neurologie
Medizin / Pharmazie Medizinische Fachgebiete Psychiatrie / Psychotherapie
ISBN-10 1-4614-7786-7 / 1461477867
ISBN-13 978-1-4614-7786-0 / 9781461477860
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