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Child Neurology
  • Language: en
  • Pages: 1210

Child Neurology

Revised to incorporate the latest advances in the neurosciences and clinical neurology, the Seventh Edition of this classic text provides practical, cost-effective problem-solving approaches to all diseases affecting the developing nervous system. In clinically relevant terms, the book explains how recent developments in molecular biology, genetics, neurochemistry, neurophysiology, neuropathology, and neuroimaging impact on diagnosis and treatment. Chapters focus on specific disorders or groups of disorders and emphasize differential diagnosis, disease course, treatment, and prognosis. This edition has a new chapter on mitochondrial cytopathies.

The Angry Puppet Syndrome
  • Language: en

The Angry Puppet Syndrome

From the moment Dr. Dan Lerner discovers a bizarre behavior pattern, he is plunged into a maelstrom. Patient after patient is experiencing violent outbursts for no apparent reason. And they all feel manipulated by a sinister force. As he tries to diagnose and treat The Angry Puppet Syndrome, in this thrilling medical mystery, he is drawn along a terrifying path. He confronts not only a hit-and-run killing and anonymous threatening phone calls, but also murder and suicide. How do his patients figure in a web of deceit and lies involving a major pharmaceutical company? How could they tip the scales of justice in a legal case that is being conducted by Dan's lover, Maureen? It is not until Dan unearths a long-hidden secret about his own past and Maureen is kidnapped that he learns the truth about a so-called genius on the staff of the university hospital and a deadly conspiracy. This debut novel mixes insider's medical knowledge with the frightening human potential for greed that affects even the most noble of professions. Its insights provide a mesmerizing tale told at the pace of a great thriller.

Uncommon Causes of Stroke
  • Language: en
  • Pages: 418

Uncommon Causes of Stroke

An essential resource for diagnosis and treatment of stroke patients outside the usual clinical categories.

The Molecular and Genetic Basis of Neurological Disease
  • Language: en

The Molecular and Genetic Basis of Neurological Disease

This volume, which is at the cutting edge of the interface between clinical and basic neuroscience, will be of value to clinicians caring for patients with hereditary neurological disorders and for investigators concerned with the scientific issues that these disorders propose. Five editors and 108 contributing authors are responsible for the 66 chapters arranged in 22 parts: general topics, chromosomes, carbohydrate disorders, amino acids, purines, lipoprotein disorders, porphyrins, metal metabolism, peroxisomes, lysosomal disorders, vitamins, prions, muscle disorders, mitochondrial disorders, degenerative disorders, the phakomatoses--disorders of skin and brain, neuro-oncology, membrane excitibility disorders, neuronopathies and neuropathies, epilepsy, schizophrenia, and gene therapy and human genome. Annotation copyright by Book News, Inc., Portland, OR.

Connective Tissue and Its Heritable Disorders
  • Language: de
  • Pages: 1201

Connective Tissue and Its Heritable Disorders

The Second Edition of Connective Tissue and Its Heritable Disorders: Molecular, Genetic, and Medical Aspects is the definitive reference text in its field, with over 40% more pages on the nature, diagnosis, and treatment of disease than its predecessor. Collecting new research on disorders detailed in the first edition as well as on those previously excluded, editors Peter Royce and Beat Steinmann provide the most up-to-date clinical and scientific information for medical specialists treating affected individuals. Features of this revised and updated volume include detailed reviews of the clinical diagnosis, mode of inheritance, risk of recurrence, and prenatal diagnosis of each inherited connective tissue disorder; a thorough description of the morphology of connective tissues; a completely updated and revised section on the biology of the extracellular matrix; and the addition of syndromes such as craniosyntosis, and disorders of sulfate metabolism.

Encyclopedia of the Neurological Sciences
  • Language: en
  • Pages: 4744

Encyclopedia of the Neurological Sciences

The Encyclopedia of the Neurological Sciences, Second Edition, Four Volume Set develops from the first edition, covering all areas of neurological sciences through over 1000 entries focused on a wide variety of topics in neurology, neurosurgery, psychiatry and other related areas of neuroscience. The contributing authors represent all aspects of neurology from many viewpoints and disciplines to provide a complete overview of the field. Entries are designed to be understandable without detailed background knowledge in the subject matter, and cross-referencing and suggested further reading lead the reader from a basic knowledge of the subject to more advanced understanding. The easy-to-use 'en...

The Molecular and Genetic Basis of Neurologic and Psychiatric Disease
  • Language: en
  • Pages: 930

The Molecular and Genetic Basis of Neurologic and Psychiatric Disease

Completely updated for its Fourth Edition, this book is the most comprehensive, current review of the molecular and genetic basis of neurologic and psychiatric diseases. More than 120 leading experts provide a fresh, new assessment of recent molecular, genetic, and genomic advances, offer new insights into disease pathogenesis, describe the newest available therapies, and explore promising areas of therapeutic development. This edition features an updated section on psychiatric disease and expanded, updated chapters on human genomics, gene therapy, and ethical issues. Six new chapters cover congenital myasthenic syndromes, hereditary spastic paraplegia, ion channel disorders, the phakomatoses, beta-galactosidase deficiency, and prion diseases. A Neurologic Gene Map describes the chromosome locus of all the genetic diseases and their gene product where known. The fully searchable online text will be available on a companion Website. (www.rosenbergneuroandpsychdisease.com)

The Causes of Epilepsy
  • Language: en
  • Pages: 1013

The Causes of Epilepsy

Expanded and revised, this unique book provides concise descriptions of the many causes of epilepsy, for use in clinical practice.

Genetics of Movement Disorders
  • Language: en
  • Pages: 585

Genetics of Movement Disorders

  • Type: Book
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  • Published: 2002-10-25
  • -
  • Publisher: Elsevier

Hereditary or genetic diseases featuring involuntary movements constitute a major aspect of the practice of neurology, functional neurosurgery, genetics, and many areas of basic and applied neuroscience research. Describing the current knowledge on these disorders, Genetics of Movement Disorders brings together information essential for clinicians, geneticists, and neuroscientists in one source. Utilizing a convenient and accessible format, the book is designed to allow easy identification of relevant information, with the overall organization of topics following established phenotypic classifications of movement disorders such as Parkinsonian syndromes, chorea, ataxia, and major categories ...

Melancholia: A Disorder of Movement and Mood
  • Language: en
  • Pages: 356

Melancholia: A Disorder of Movement and Mood

It has long been accepted that depressive disorders comprise a biologically-based type, the so-called 'endogenous' or 'melancholic' depression, and a residual set of depressive conditions resulting from social factors. The difficulty has been in distinguishing the melancholic type of depression on the basis of clinical features. This book describes the development of a behavioral sign-based approach, the CORE system, and demonstrates its superiority to previous symptom-based diagnostic systems for depression. The authors suggest that the psychomotor signs elicited may indicate the likely pathogenesis of melancholic depression, involving the basal ganglia and connections to the frontal cortex. This is therefore a challenging new account of the classification and neurobiology of depression, that is certain to interest all clinicians involved in the evaluation or treatment of such patients. The CORE measure itself is incorporated as an appendix.