의학서적전문 "성보의학서적"의 신간의학도서입니다.


  • Stay fully up to date in this fast-changing field with Hematology, Immunology and Genetics, 3rd Edition.
  • The most current clinical information, including new coverage of exome sequencing, properties of donor milk, necrotizing enterocolitis and nutrition, thrombocytopenia in neonates with necrotizing enterocolitis, early diagnosis of severe combined immunodeficiency, and newborn screening.
  • New content on the genetic basis for neonatal disorders, new strategies for genetic diagnosis (such as whole exome sequencing and microarrays), antenatal genetic testing, and ethical dilemmas and genetic counselling.
  • Current coverage of using new complete blood count (CBC) parameters to help guide neonatal care, neonatal neuroprotection, and differentiating hemolytic from non-hemolytic neonatal jaundice.
  • Consistent chapter organization to help you find information quickly and easily.
  • The most authoritative advice available from world-class neonatologists who share their knowledge of new trends and developments in neonatal care.
  • Expert Consult™ eBook version included with purchase. This enhanced eBook experience allows you to search all of the text, figures, and references from the book on a variety of devices.


    • -도서목차-

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    1. Stem cell therapy in neonates-the time has (almost) come
    2. Genome and Exome Sequencing: Can it impact clinical care in the NICU
    3. Transfusion thresholds in the NICU-what have recent RCTs taught us
    4. DONOR MILK COMPARED WITH MOTHER'S OWN MILK
    5. Will standardized approaches to nutrition decrease NEC
    6. What is the value of identifying genetic causes of congenital hemolytic jaundice
    7. Using the New CBC Parameters in NICU Practice
    8. How near are we to using darbepoetin or erythropoietin as neuroprotective agents for perinatal hypoxic/ischemic encephalopathy
    9. Of what value to neonates is measuring end tidal carbon monoxide concentration
    10. How do we adopt anemia-preventing strategies in our delivery rooms
    11. Thrombocytopenia in Infants with Necrotizing Enterocolitis
    12. Genetic Risk Factors for Patent Ductus Arteriosus
    13. Genetic basis of PDA.
    14. GENETIC BASIS OF BRONCHOPULMONARY DYSPLASIA
    15. Prenatal genetic testing.
    16. Early diagnosis of severe combined immunodeficiency.
    17. Newborn Screening

    기타 신간의학서적과 의학도서에 관련된 문의사항은 고객센터(02-854-2738) 또는 저희 성보의학서적 홈페이지내 도서문의 게시판에 문의바랍니다.
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