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  • Book
    Giulio Del Popolo, Donatella Pistolesi, Vincenzo Li Marzi, editors.
    Summary: This book aims to offer a comprehensive and up-to-date overview of male stress urinary incontinence that will serve as a useful tool and reference for urologists, andrologists, physiotherapists, general practitioners, and nurses. Detailed information is provided on diagnostic workup, including clinical assessment and the role of urodynamic evaluations and other instrumental examinations, and on the full range of potential treatments, from conservative and pharmacological interventions to surgical options. In addition to careful descriptions of the surgical procedures themselves, clear advice is given on the management of iatrogenic complications of incontinence surgery. Helpful treatment algorithms and recommendations offer further practical support. Relevant background knowledge is provided in expert reviews of topics such as the functional anatomy of the male pelvis and the pathophysiology, epidemiology, and classification of male urinary incontinence.

    Contents:
    Morphological and functional anatomy of male pelvis
    Continence physiology and male stress incontinence pathophysiology.- Incontinence definition and classification
    From many type of surgical damage (open/endoscopic/laparoscopic/robot assisted surgery) to different treatments
    Diagnostic workup
    Treatment algorithm and recommendations
    Rehabilitative and pharmacological treatment
    Surgical treatment
    Surgery complications and their management.
    Digital Access Springer 2015
  • Article
    Neu RL, Dennis NR, Lanman JT, Bannerman RM.
    Ann Genet. 1979;22(3):151-4.
    A newborn infant with a 47,XY,+ der(.),t(1;9) (p36;q22)mat chromosome complement and the clinical features of the 9p trisomy is described. A review of the reproductive histories of five cases with trisomy 9pter yields 9q21 or 22 indicate that the balanced translocation mothers of these infants may have as high as a 23% chance of producing a chromosomally unbalanced offspring due to 3:1 disjunction.
    Digital Access Access Options