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| 001 - NÚMERO DE CONTROL |
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84462 |
| 003 - IDENTIFICADOR DEL NÚMERO DE CONTROL |
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ES-MaUEC |
| 005 - FECHA Y HORA DE LA ÚLTIMA TRANSACCIÓN |
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160628s2016 xxu| s |||| 0|eng d |
| 020 ## - NÚMERO INTERNACIONAL ESTÁNDAR DEL LIBRO |
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| Número Internacional Estándar del Libro |
9781493933846 |
| 040 ## - FUENTE DE LA CATALOGACIÓN |
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| Centro catalogador/agencia de origen |
ES-MaUEC |
| 050 #4 - SIGNATURA TOPOGRÁFICA DE LA BIBLIOTECA DEL CONGRESO |
|---|
| Número de clasificación |
RE48.2.C5 |
| Número de documento/Ítem |
2016 EB |
| 100 1# - ENTRADA PRINCIPAL--NOMBRE DE PERSONA |
|---|
| Nombre de persona |
Brodsky, Michael C. |
| 9 (RLIN) |
96656 |
| Número de control del registro de autoridad o número normalizado |
Local |
| 245 10 - MENCIÓN DE TÍTULO |
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| Título |
Pediatric Neuro-Ophthalmology |
| Mención de responsabilidad, etc. |
by Michael C Brodsky |
| 250 ## - MENCIÓN DE EDICIÓN |
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| Mención de edición |
3rd ed. |
| 260 ## - PUBLICACIÓN, DISTRIBUCIÓN, ETC. |
|---|
| Lugar de publicación, distribución, etc. |
New York, NY |
| Nombre del editor, distribuidor, etc. |
Springer New York |
| Fecha de publicación, distribución, etc. |
2016 |
| 300 ## - DESCRIPCIÓN FÍSICA |
|---|
| Extensión |
1 recurso en línea (XXI, 823 páginas) |
| Otras características físicas |
294 ilustraciones, 146 ilustraciones en color |
| 336 ## - TIPO DE CONTENIDO |
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| Término de tipo de contenido |
Texto |
| Código de tipo de contenido |
txt |
| Fuente |
rdacontent |
| 337 ## - TIPO DE MEDIO |
|---|
| Nombre/término del tipo de medio |
electrónico |
| Código del tipo de medio |
c |
| Fuente |
rdamedia |
| 338 ## - TIPO DE SOPORTE |
|---|
| Nombre/término del tipo de soporte |
recurso electrónico |
| Código del tipo de soporte |
cr |
| Fuente |
rdacarrier |
| 505 0# - NOTA DE CONTENIDO CON FORMATO |
|---|
| Nota de contenido con formato |
1. The Apparently Blind Infant -- Introduction -- Hereditary Retinal Disorders -- Leber Congenital Amaurosis -- Joubert Syndrome -- Congenital Stationary Night Blindness -- Achromatopsia -- Congenital Optic Nerve Disorders -- Cortical Visual Insufficiency -- Causes of Cortical Visual Loss -- Neurologic and Systemic Disorders -- Characteristics of Visual Function -- Neuro-Ophthalmologic Findings -- Diagnostic and Prognostic Considerations -- Role of Visual Attention -- Subcortical Visual Loss (or Periventricular Leukomalacia) -- Neuroimaging Abnormalities and their Implications -- Neuro-Ophthalmologic Findings -- Perceptual Difficulties -- Dorsal and Ventral Stream Dysfunction -- Pathophysiology -- Intraventricular Hemorrhage -- Periventricular and Intraventricular Hemorrhage -- Hemianopic Visual Field Defects in Children -- Delayed Visual Maturation -- Blindsight -- The Effect of Total Blindness on Circadian Regulation -- Horizons -- 2. Congenital Optic Disc Anomalies -- Introduction -- Optic Nerve Hypoplasia -- Excavated Optic Disc Anomalies -- Morning Glory Disc Anomaly -- Optic Disc Coloboma -- Peripapillary Staphyloma -- Megalopapilla -- Optic Pit -- Papillorenal Syndrome (The Vacant Optic Disc) -- Congenital Tilted Disc Syndrome -- Optic Disc Dysplasia -- Congenital Optic Disc Pigmentation -- Aicardi Syndrome -- Doubling of the Optic Disc -- Optic Nerve Aplasia -- Myelinated (Medullated) Nerve Fibers -- The Albinotic Optic Disc -- 3. The Swollen Optic Disc -- Papilledema -- Idiopathic Intracranial Hypertension (IIH) in Children -- Optic Disc Swelling Secondary to Neurological Disease -- Optic Disc Swelling Secondary to Systemic Disease -- Uveitis -- Posttraumatic Optic Disc Swelling -- Intrinsic Optic Disc Tumors -- Optic Disc Hemangioma -- Tuberous Sclerosis -- Optic Disc Glioma -- Combined Hamartoma of the Retina and RPE -- Retrobulbar Tumors -- Optic Neuritis in Children -- History and Physical Examination -- Postinfectious Optic Neuritis -- Disseminated Encephalomyelitis -- MS and Pediatric Optic Neuritis -- Devic Disease (Neuromyelitis Optica) -- Prognosis and Treatment -- Course of Visual Loss and Visual Recovery -- Systemic Prognosis -- Systemic Evaluation of Pediatric Optic Neuritis -- Treatment -- Leber Idiopathic Stellate Neuroretinitis -- Ischemic Optic Neuropathy -- Autoimmune Optic Neuropathy -- Pseudopapilledema -- Optic Disc Drusen -- Ocular Disorders Associated with Pseudopapilledema -- Systemic Disorders Associated with Pseudopapilledema -- 4. Optic Atrophy -- Introduction -- Optic Atrophy Associated with Retinal Disease -- Optic Atrophy Vs. Hypoplasia -- Causes of Optic Atrophy in Children -- Compressive/Infiltrative Intracranial Lesions -- Noncompressive Causes of Optic Atrophy in Children with Brain Tumors -- Hereditary Optic Atrophy -- Dominant Optic Atrophy (Kjer Type) -- Leber Hereditary Optic Neuropathy -- Recessive Optic Atrophhy -- Behr Syndrome -- Wolfram Syndrome (DIDMOAD) -- Toxic/Nutritional Optic Neuropathy -- Neurodegenerative Disorders with Optic Atrophy -- Organic Acidurias -- Optic Atrophy due to Hypoxia-Ischemia -- Traumatic Optic Atrophy -- Miscellaneous Causes -- Summary of the General Approach to the Child with Optic Atrophy -- 5. Transient, Unexplained, and Psychogenic Visual Loss -- Introduction -- Transient Visual Loss -- Migraine -- Epilepsy -- Posttraumatic Transient Cerebral Blindness -- Cardiogenic Embolism -- Nonmigrainous Cerebrovascular Disease -- Miscellaneous Transient Visual Disturbances in Children -- Toxic and Nontoxic Drug Effects -- Summary of Clinical Approach to the Child with Transient Visual Disturbances -- Laboratory Evaluation of Transient Visual Disturbances in Children -- Unexplained Visual Loss in Children -- Causes of Unexplained Visual Loss in Childhood -- Psychogenic Visual Loss in Children -- Clinical Profile -- Neuro-Ophthalmologic Findings -- Categories of Psychogenic Visual Loss in Children -- Management of Psychogenic Visual Loss in Children -- Horizons -- 6. Ocular Motor Nerve Palsies -- Introduction -- Oculomotor Nerve Palsy -- Clinical Anatomy -- Clinical Features -- Partial Forms of Oculomotor Palsy -- Oculomotor Synkinesis -- Etiology -- Vascular Third Nerve Palsy in Children -- Differential Diagnosis -- Management -- Trochlear Nerve Palsy -- Clinical Anatomy -- Clinical Features -- Bilateral Trochlear Nerve Palsy -- Etiology -- Differential Diagnosis -- Treatment -- Abducens Nerve Palsy -- Anatomy -- Clinical Features -- Causes of Sixth Nerve Palsy -- Differential Diagnosis -- Duane Retraction Syndrome -- Management of Sixth Nerve Pals -- Multiple Cranial Nerve Palsies in Children -- Horizons -- 7. Complex Ocular Motor Disorders -- Introduction -- Strabismus in Children with Neurological Dysfunction -- Visuovestibular Disorders -- Neurologic Esotropia -- Neurologic Exotropia -- Skew Deviation -- Gaze Palsies, Gaze Deviations, and Ophthalmoplegia -- Horizontal Gaze Palsy in Children -- Congenital Ocular Motor Apraxia -- Vertical Gaze Palsies in Children -- Diffuse Ophthalmoplegia in Children -- Chronic Progressive External Ophthalmoplegia -- Myasthenia Gravis -- Olivopontocerebellar Atrophy -- Botulism -- Fisher Syndrome: A Variant of Guillain Barré Syndrome -- Bickerstaff Brainstem Encephalitis -- Tick Paralysis -- Wernicke Encephalopathy -- Miscellaneous Causes of Ophthalmoplegia -- Transient Ocular Motor Disturbances of Infancy -- Transient Neonatal Strabismus -- Transient Idiopathic Nystagmus -- Tonic Downgaze -- Tonic Upgaze -- Neonatal Opsoclonus -- Transient Vertical Strabismus in Infancy -- Congenital Cranial Dysinnervation Syndromes -- Congenital Ptosis -- Marcus Gunn Jaw Winking (Trigemino-Oculomotor Synkinesis) -- Congenital Fibrosis Syndrome -- Congenital Horizontal Gaze Palsy with Scoliosis -- Möbius Sequence -- Monocular Elevation Deficiency, or zDouble Elevator Palsyy -- Brown Syndrome -- Other Pathologic Synkineses -- Internuclear Ophthalmoplegia -- Cyclic, Periodic, or Aperiodic Disorders Affecting Ocular Structures -- Ocular Neuromyotonia -- Ocular Motor Adaptations and Disorders in Patients with Hemispheric Abnormalities -- Movement Tics -- Eyelid Abnormalities in Children -- Congenital Ptosis -- Excessive Blinking in Children -- Hemifacial Spasm -- Eyelid Retraction -- Apraxia of Eyelid Opening -- Pupillary Abnormalities -- Congenital Bilateral Mydriasis -- Accommodative Paresis -- Adie Syndrome -- Horner Syndrome -- 8. |
| 505 0# - NOTA DE CONTENIDO CON FORMATO |
|---|
| Nota de contenido con formato |
Nystagmus -- Introduction -- Infantile Nystagmus -- Clinical Features -- Onset of Infantile Nystagmus -- Terminology -- History and Physical Examination -- ERG -- Hemispheric Visual Evoked Potentials -- Overlap of Infantile Nystagmus and Strabismus -- Eye Movement Recordings in Infantile Nystagmus -- Contrast Sensitivity and Pattern Detection Thresholds in Infantile Nystagmus -- Theories of Causation -- Visual Disorders Precipitating Infantile Nystagmus -- When to Obtain Neuroimaging Studies in Children with Nystagmus -- Treatment -- Spasmus Nutans -- Russell Diencephalic Syndrome of Infancy -- Monocular Nystagmus -- Nystagmus Associated with Infantile Esotropia -- Torsional Nystagmus -- Horizontal Nystagmus -- Nystagmus -- Nystagmus Blockage Syndrome -- Treatment of Nystagmus Blockage Syndrome -- Vertical Nystagmus -- Upbeating Nystagmus in Infancy -- Congenital Downbeat Nystagmus -- Hereditary Vertical Nystagmus -- Periodic Alternating Nystagmus -- Seesaw Nystagmus -- Congenital versus Acquired Seesaw Nystagmus -- Saccadic Oscillations that Simulate Nystagmus -- Retraction Nystagmus -- Opsoclonus and Ocular Flutter -- Voluntary Nystagmus -- Ocular Bobbing -- Neurological Nystagmus -- Leigh Subacute Necrotizing Encephalomyelopathy -- Pelizaeus-Merzbacher Disease -- Joubert Syndrome -- Santavuori-Haltia Disease -- Infantile Neuroaxonal Dystrophy -- Deficient Glycoprotein Syndromes -- Down Syndrome -- Hypothyroidism -- Maple Syrup Urine Disease -- Nutritional Nystagmus -- Epileptic Nystagmus -- Cobalamin C Methylmalonic Aciduria and Homocystinuria -- Familial Vestibulocerebellar Disorder -- Summary -- 9. Torticollis and Head Oscillations -- Introduction -- Torticollis -- Ocular Torticollis -- Head Tilts -- Head Turns -- Vertical Head Positions -- Refractive Causes of Torticollis -- Neuromuscular Causes of Torticollis -- Systemic Causes of Torticollis -- Head Oscillations -- Head Nodding with Nystagmus -- Head Nodding without Nystagmus -- Visual Disorders -- Otological Abnormalities -- Systemic Disorders -- 10. Neuro-Ophthalmologic Manifestations of Neurodegenerative Disorders -- Introduction -- Neuronal Disease -- Neuronal Ceroid Lipofuscinosis -- Lysosomal Diseases -- Gangliosidoses -- Mucopolysaccharidoses -- Subacute Sclerosing Panencephalitis -- White Matter Disorders -- Metachromatic Leukodystrophy -- Canavan Disease (Spongy Degeneration of Cerebral White Matter) -- Krabbe Disease -- Pelizaeus Merzbacher Disease -- Cockayne Syndrome -- Alexander Disease -- Sjögren Larsson Syndrome -- Cerebrotendinous Xanthomatosis -- Peroxisomal Disorders -- Zellweger Syndrome -- Adrenoleukodystrophy -- Basal Ganglia Disease -- Pantothenate Kinase-Associated Neurodegeneration -- Wilson Disease -- Aminoacidopathies and Other Biochemical Defectsl -- Maple Syrup Urine Disease -- Homocystinuria -- Abetalipoproteinemia -- Mitochondrial Encephalomyelopathies -- Chronic Progressive External Ophthalmoplegia (CPEO) -- Leigh Subacute Necrotizing Encephalomyelopathy -- Mitochondrial Encephalomyelopathy and Stroke-Like Episodes (MELAS) -- Myoclonic Epilepsy and Ragged Red Fibers (MERRF) -- Mitochondrial Depletion Syndrome -- Congenital Disorders of Glycosylation -- Horizons -- 11. Neuro-Ophthalmologic Manifestations of Systemic and Intracranial Disease -- Introduction -- The Phakomatoses -- Neurofibromatosis (NF1) -- Neurofibromatosis 2 (NF2) -- Tuberous Sclerosis -- Sturge Weber Syndrome -- von Hippel Lindau Disease -- Ataxia Telangiectasia -- Linear Nevus Sebaceous Syndrome -- Klippel. |
| 520 3# - SUMARIO, ETC. |
|---|
| Sumario, etc. |
Pediatric Neuro-Ophthalmology, 3rd edition provides the single authoritative resource on the pathophysiology, diagnostic evaluation, and treatment of neuro-ophthalmologic disorders in children. This book is encyclopedic in scope, incorporating extensive references for each condition, numerous diagrams and pictures, and a detailed analysis of the clinical disorders included in the differential diagnosis of each condition. The third edition builds upon this format to incorporate new discoveries about mechanisms of disease, new diagnostic modalities, advances in treatment in the field of pediatric neuro-ophthalmology, and updated neuroimaging figures. |
| 650 #7 - PUNTO DE ACCESO ADICIONAL DE MATERIA--TÉRMINO DE MATERIA |
|---|
| Término de materia o nombre geográfico como elemento de entrada |
Medicina |
| Número de control del registro de autoridad o número normalizado |
comprobar BNE19900959047 |
| Fuente del encabezamiento o término |
embne |
| 9 (RLIN) |
405021 |
| 650 #7 - PUNTO DE ACCESO ADICIONAL DE MATERIA--TÉRMINO DE MATERIA |
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| Término de materia o nombre geográfico como elemento de entrada |
Neurología |
| Número de control del registro de autoridad o número normalizado |
comprobar BNE19900967585 |
| Fuente del encabezamiento o término |
embne |
| 9 (RLIN) |
139040 |
| 650 #7 - PUNTO DE ACCESO ADICIONAL DE MATERIA--TÉRMINO DE MATERIA |
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| Término de materia o nombre geográfico como elemento de entrada |
Oftalmología |
| Número de control del registro de autoridad o número normalizado |
comprobar BNE19900969318 |
| Fuente del encabezamiento o término |
embne |
| 9 (RLIN) |
139186 |
| 710 2# - PUNTO DE ACCESO ADICIONAL--NOMBRE DE ENTIDAD CORPORATIVA |
|---|
| Nombre de entidad corporativa o nombre de jurisdicción como elemento de entrada |
SpringerLink (Online service) |
| Número de control del registro de autoridad o número normalizado |
Local |
| 9 (RLIN) |
106996 |
| 856 40 - LOCALIZACIÓN Y ACCESO ELECTRÓNICOS |
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| Identificador Uniforme del Recurso |
https://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-1-4939-3384-6 |
| Nota pública |
Acceso a este recurso digital (usuarios Universidad Europea de Madrid) |
| 942 ## - ELEMENTOS DE PUNTO DE ACCESO ADICIONAL (KOHA) |
|---|
| Fuente del sistema de clasificación o colocación |
Library of Congress Classification |
| Tipo de ítem Koha |
LIBRO-E NO PRÉSTAMO |
| 901 ## - ID MILLENIUM |
|---|
| Id Millenium |
i9781493933846 |
| 907 ## - TRANSACCIONES MILLENIUM |
|---|
| id bib interno millenium |
.b1293740x |
| fecha actualizac reg bib |
10-10-17 |
| fecha creacion reg bib |
21-11-16 |
| 988 ## - NOTA LOCAL 598 |
|---|
| Nota local 598 |
Springer_Medicine_2016 |
| 998 ## - FONDO MILLENIUM |
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m |
| -- |
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| Fecha creación |
- - |
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m |
| Tipo de materia |
E-book |
| e |
- |
| Idioma |
eng |
| País |
xxu |
| h |
0 |
| 945 ## - ITEM MILLENIUM |
|---|
| Signatura |
RE48.2.C5 B763 2016 EB |
| Número de copia |
1 |
| Código de barras |
eBOOK |
| Agencia |
0 |
| Localización del ejemplar (ubicación) |
mae |
| Código 2 (categoría) |
- |
| Precio |
EUR0.00 |
| Mensaje (popup en cliente staff) |
- |
| Mensaje (visible en OPAC) |
- |
| Estado |
b |
| Tipo de ejemplar |
15 |
| Total de préstamos |
0 |
| Total de renovaciones |
0 |
| Préstamos del año en curso |
0 |
| Préstamos del año anterior |
0 |
| Identificador de la copia de ejemplar en Millennium |
.i11582236 |
| Fecha de creación del ejemplar |
06-04-17 |
| 999 ## - NÚMEROS DE CONTROL DE SISTEMA (KOHA) |
|---|
| -- |
1 |