Hematology, immunology, and genetics / [edited by] Robin K. Ohls, MD, Akhil Maheshwari, MD, Robert D. Christensen, MD.
Contributor(s): Ohls, Robin K [editor.] | Maheshwari, Akhil [editor.] | Christensen, Robert D. (Pediatrician) [editor.].
Series: Neonatology questions and controversies: Publisher: Philadelphia, PA : Elsevier, ©2019Edition: Third edition.Description: xii, 213 pages : illustration; 26.5 cm.Content type: text Media type: unmediated Carrier type: volumeISBN: 9780323544009 (hardcover : alk. paper).Uniform titles: Hematology, immunology, and infectious disease. Subject(s): Neonatology -- methods | Infant, Newborn | Communicable Diseases | Hematologic Diseases | Immune System DiseasesGenre/Form: Print books.| Current location | Call number | Status | Date due | Barcode | Item holds |
|---|---|---|---|---|---|
| On Shelf | RJ269.5 .H45 2019 (Browse shelf) | Available | AU00000000013138 |
Preceded by Hematology, immunology, and infectious disease / [edited by] Robin K. Ohls, Akhil Maheshwari. 2nd ed. c2012.
Includes bibliographical references and index.
1. Stem cell therapy in neonates : the time has (almost) come --
2. Genome and exome sequencing : can it impact clinical care in the neonatal intensive care unit? --
3. Transfusion thresholds in the neonatal intensive care unit : what have recent randomized controlled trials taught us? --
4. Donor milk compared with mother's own milk --
5. Will standardized approaches to nutrition decrease necrotizing enterocolitis? --
6. Nonimmune neonatal hemolytic anemia : recent advances in diagnosis and treatment --
7. Using the new complete blood count parameters in neonatal intensive care unit practice --
8. How near are we to using darbepoetin or erythropoietin as neuroprotective agents for perinatal hypoxic/ischemic encephalopathy? --
9. How do we adopt anemia-preventing strategies in our delivery rooms? --
10. Thrombocytopenia in infants with necrotizing enterocolitis --
11. Genetic basis of necrotizing enterocolitis --
12. Genetic basis of patent ductus arteriosus --
13. Genetic basis of bronchopulmonary dysplaxia --
14. Prenatal genetic testing --
15. Early diagnosis of severe combined immunodeficiency --
16. Newborn screening.