Clinical Neurology For Psychiatrists

Completely revised in response to the new format of the ABPN certifying exam, Kaufman’s Clinical Neurology for Psychiatrists is the ideal reference to enhance your mastery of the neurology knowledge needed for the Psychiatry Board exam. Description For more than 35 years, Kaufman’s Clinical Neurology for Psychiatrists has been the only reference to focus on the must-know aspects of neurology for psychiatrists.

Overview

For more than 35 years, PdfKaufman’s Clinical Neurology for Psychiatrists has been the only reference to focus on the must-know aspects of neurology for psychiatrists. Now in a revised 8th Edition, this classic text brings you up to date with essential knowledge in clinical neurology with Clinical Neurology For Psychiatrists

Clinical Neurology for Psychiatrists. Articles from Journal of Psychiatry & Neuroscience: JPN are provided here courtesy of Canadian Medical Association. Clinical Neurology and Psychiatry for Psychiatrists (CNPP) is the most important, intensive, dynamic five-day review course available. Offered for over 45 years, it has been revamped for the new ABPN certification format. David Kaufman's previous editions of Clinical Neurology for Psychiatrists have a curious reputation among psychiatrists as being both poorly written yet essential reading. This latest fourth edition is not likely to change that perception.

new topics, new illustrations, and new questions to help you excel on the American Board of Psychiatry and Neurology examination.
  • Explains each condition's neurologic and psychiatric features, easily performed office and bedside examinations, appropriate tests, differential diagnosis, and management options.
  • Expert Consult eBook version included with purchase. This enhanced eBook experience allows you to search all of the text, figures, images, and references from the book on a variety of devices.

Kaufman's Clinical Neurology For Psychiatrists 7th Edition Pdf

  • Discusses timely, clinically-relevant topics such as traumatic brain injury, Alzheimer and non-Alzheimer dementias, other age-related neurologic conditions, neurologic illnesses that present with symptoms of autism, neurologic effects of illicit drug use, and current treatments.
  • Correlates neurologic illnesses with the DSM-5.
  • Includes nearly 2,000 multiple-choice questions both in print and online, – all written to help you succeed on the ABPN certifying exam.
  • Features new and improved clinical illustrations throughout: life-like patient sketches, anatomy line drawings, CTs, MRIs, and EEGs that demonstrate clinical features.

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Course Director: David Myland Kaufman, MD

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Clinical Neurology For Psychiatrists Pdf

  1. 1. Question
    1 points

    A 70 year-old man, who was previously healthy, sustained a stroke in the left side of this structure. Examination reveals dysarthria, Horner’s syndrome, and ipsilateral facial hypalgesia with crossed body hypalgesia. Which other symptom will most likely be present?

    Correct

    The structure that has been sketched is the medulla, which should be identified by the paired scalloped, concave nuclei. The lateral medulla contains the cerebellar outflow tracts and several important brainstem nuclei. He has developed the “lateral medullary syndrome.” As part of that syndrome, injury of the cerebellar outflow tract will cause an ipsilateral intention tremor. More important, lesions of the brainstem generally do not cause aphasia, dementia, or epilepsy – all manifestations of cerebral injury.

    Incorrect

    The structure that has been sketched is the medulla, which should be identified by the paired scalloped, concave nuclei. The lateral medulla contains the cerebellar outflow tracts and several important brainstem nuclei. He has developed the “lateral medullary syndrome.” As part of that syndrome, injury of the cerebellar outflow tract will cause an ipsilateral intention tremor. More important, lesions of the brainstem generally do not cause aphasia, dementia, or epilepsy – all manifestations of cerebral injury.

  2. Question 2 of 5
    2. Question
    1 points

    Regarding genetic diseases that result from excessive trinucleotide repeats, which of the following statements is false?

    Correct

    Paternal rather than maternal inheritance confers a greater degree of illness. Genetic material in sperm is apparently more unstable than in eggs. Myotonic dystrophy, fragile-X syndrome, certain spinocerebellar ataxias and Huntington’s disease result from expansion of abnormal genes characterized by excessive trinucleotide repeats.

    Incorrect

    Paternal rather than maternal inheritance confers a greater degree of illness. Genetic material in sperm is apparently more unstable than in eggs. Myotonic dystrophy, fragile-X syndrome, certain spinocerebellar ataxias and Huntington’s disease result from expansion of abnormal genes characterized by excessive trinucleotide repeats.

  3. Question 3 of 5
    3. Question
    1 points

    A 4 year-old mentally retarded boy eats compulsively and voraciously. He eventually develops extreme obesity. Other than poor coordination, his neurologic examination shows no particular abnormality. Also, his routine blood tests, an MRI of the brain, and endocrine tests are normal. His father has mental impairment and obesity, but not to the same extent. At this point, which of the following illnesses is indicated?

    Correct

    While all the choices might be considered, the familial incidence, lack of neurologic abnormalities, and normal MRI and endocrine studies eliminate almost all of them. The most likely condition is the Prader-Willi syndrome, which results from abnormal genetic material that is usually inherited from the father.

    Incorrect

    While all the choices might be considered, the familial incidence, lack of neurologic abnormalities, and normal MRI and endocrine studies eliminate almost all of them. The most likely condition is the Prader-Willi syndrome, which results from abnormal genetic material that is usually inherited from the father.

  4. Question 4 of 5
    4. Question
    1 points

    A 72 year-old man developed dementia. Then he became reticent, but when he spoke his speech was aggressive and contained many sexual innuendos. He was ambulatory and had no focal physical neurologic signs. He had marked frontal release signs and tended to put inedible objects into his mouth. Visuo-spatial relationships are preserved. Which of the following is the most likely diagnosis?

    Correct

    He has uninhibited behavior, often with a sexual flavor, and other signs of frontal lobe dysfunction. Notably, he has no lateralized signs, but preserved visuo-spatial relationships. This is a case of fronto-temporal dementia, which typically has aspects of the human Kluver-Bucy syndrome. Pick’s disease is probably the commonest cause of this variety of dementia.

    Incorrect

    He has uninhibited behavior, often with a sexual flavor, and other signs of frontal lobe dysfunction. Notably, he has no lateralized signs, but preserved visuo-spatial relationships. This is a case of fronto-temporal dementia, which typically has aspects of the human Kluver-Bucy syndrome. Pick’s disease is probably the commonest cause of this variety of dementia.

  5. Question 5 of 5
    5. Question
    1 points

    Which of the following visual fields is usually found with nonfluent aphasia?

    Correct

    Nonfluent aphasia, which usually results from a left cerebral hemisphere lesion, is associated with a right homonymous hemianopsia. Remember that visual fields are portrayed from the patient’s perspective.

    Incorrect

    Nonfluent aphasia, which usually results from a left cerebral hemisphere lesion, is associated with a right homonymous hemianopsia. Remember that visual fields are portrayed from the patient’s perspective.