Pain -- Handbooks -- diagnosis : The diagnosis and treatment of breakthrough pain / Perry G. Fine ; with contributions by Andrew N. Davies, Scott M. Fishman
Pain -- Handbooks -- therapy : The diagnosis and treatment of breakthrough pain / Perry G. Fine ; with contributions by Andrew N. Davies, Scott M. Fishman
Pain -- Imaging -- Atlases : Atlas of image-guided intervention in regional anesthesia and pain medicine / James P. Rathmell ; illustrations by Gary J. Nelson
Pain in animals -- Prevention. : Ways of minimising pain and distress in animals in research : practical information for research scientists and animal experimentation ethics committees / National Health and Medical Research Council, Animal Welfare Committee
Pain in children -- Chemotherapy. : Manual of acute pain management in children / edited by Ian M. McKenzie ... [and others] ; [foreword by Frank Shann]
1997
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Pain in children -- Great Britain -- History : Childhood, pain and emotion : a modern British medical history / Leticia Fernandez-Fontecha, University of North Carolina, Chapel Hill
Pain in infants -- Treatment : Bringing pain relief to children : treatment approaches / edited by G. Allen Finley, Patrick J. McGrath, and Christine T. Chambers
Pain in newborn infants -- Pathophysiology : Neonatal pain : suffering, pain and risk of brain damage in the fetus and newborn / edited by Giuseppe Buonocore, Carlo Valerio Bellieni
A syndrome characterized by indifference to PAIN despite the ability to distinguish noxious from non-noxious stimuli. Absent corneal reflexes and INTELLECTUAL DISABILITY may be associated. Familial forms with autosomal recessive and autosomal dominant patterns of inheritance have been described. (Adams et al., Principles of Neurology, 6th ed, p1343)
A group of inherited disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and clinically by loss of sensation and autonomic dysfunction. There are five subtypes. Type I features autosomal dominant inheritance and distal sensory involvement. Type II is characterized by autosomal inheritance and distal and proximal sensory loss. Type III is DYSAUTONOMIA, FAMILIAL. Type IV features insensitivity to pain, heat intolerance, and mental deficiency. Type V is characterized by a selective loss of pain with intact light touch and vibratory sensation. (From Joynt, Clinical Neurology, 1995, Ch51, pp142-4)
