WordNet

relating to or affecting the infant during the first month after birth; "neonatal care"; "the neonatal period"
relating to or involving or causing hemolysis; "hemolytic anemia" (同)haemolytic
a deficiency of red blood cells (同)anaemia
a lack of vitality (同)anaemia
genus of terrestrial or lithophytic ferns having pinnatifid fronds; chiefly of tropical America (同)genus Anemia

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1. 胎児および新生児における溶血性疾患の出生後診断およびマネージメント postnatal diagnosis and management of hemolytic disease of the fetus and newborn
2. 小児における溶血性貧血の概要 overview of hemolytic anemias in children
3. 妊娠中の非Rh（D）RBC同種抗体のマネージメント management of non rh d red blood cell alloantibodies during pregnancy
4. グルコース-6-リン酸脱水素酵素欠損症の遺伝学および病態生理 genetics and pathophysiology of glucose 6 phosphate dehydrogenase deficiency
5. 遺伝性球状赤血球症：臨床的特徴、診断および治療 hereditary spherocytosis clinical features diagnosis and treatment

Giordano PC.SourceHuman and Clinical Genetics Department, Leiden University Medical Center, Leiden, The Netherlands. p.c.giordano@lumc.nl
Methods in molecular biology (Clifton, N.J.).Methods Mol Biol.2013;919:131-45. doi: 10.1007/978-1-62703-029-8_13.
This chapter reports the essential elements needed to understand basic laboratory diagnostics consisting of separation and measurement of the hemoglobin fractions. Although well established, basic diagnostics require some background and some degree of experience for application and interpretation. L
PMID 22976097

Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab.

Besbas N, Gulhan B, Karpman D, Topaloglu R, Duzova A, Korkmaz E, Ozaltin F.SourceDepartment of Pediatric Nephrology, Hacettepe University Faculty of Medicine, 06100 Sihhiye, Ankara, Turkey.
Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2013 Jan;28(1):155-8. doi: 10.1007/s00467-012-2296-4. Epub 2012 Sep 6.
BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is characterized by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and renal impairment. Neonatal cases are extremely uncommon. Plasma therapy is the first choice therapy in patients with aHUS based on the belief of an underlyi
PMID 22956028

Anti-Ge3 causes late-onset hemolytic disease of the newborn: the fourth case in three Hispanic families.

Pate LL, Myers JC, Palma JP, Viele M, Galel SA, Ferrer Z, Gonzalez CL, Benitz WE, Garratty G, Fontaine MJ.SourceDepartment of Pathology, Stanford University Medical Center, and the Division of Neonatal and Developmental Medicine, Lucile Packard Children's Hospital, Stanford University, Stanford, California; American Red Cross Blood Services (Southern California Region), Pomona, California.
Transfusion.Transfusion.2012 Dec 12. doi: 10.1111/trf.12027. [Epub ahead of print]
BACKGROUND: The Gerbich (Ge) blood group system consists of 11 antigens carried on red blood cell (RBC) membrane glycophorins C and D; of these, Ge:3 antigen is of high prevalence, and the anti-Ge3 is found to be clinically significant.CASE REPORT: A 34-week neonate born to a Hispanic mother with an
PMID 23241141