Hemoglobinopathy screening: approaches to diagnosis, education and counseling.
作者信息
Schmidt R M
出版信息
Am J Public Health. 1974 Aug;64(8):799-804. doi: 10.2105/ajph.64.8.799.
Abstract
摘要
相似文献
1
Hemoglobinopathy screening: approaches to diagnosis, education and counseling.血红蛋白病筛查：诊断、教育与咨询方法
Am J Public Health. 1974 Aug;64(8):799-804. doi: 10.2105/ajph.64.8.799.
2
Guidelines for haemoglobinopathy screening. The British Society for Haematology.血红蛋白病筛查指南。英国血液学学会。
Clin Lab Haematol. 1988;10(1):87-94.
3
Abnormal hemoglobins detected in screening of Puerto Rican population.
Bol Asoc Med P R. 1981 Jun;73(6):274-8.
4
[Pregnancy complications in women with a (double) heterozygote hemoglobinopathy].（双重）杂合子血红蛋白病女性的妊娠并发症
Ned Tijdschr Geneeskd. 1985 Mar 30;129(13):598-601.
5
A rare case of a compound heterozygote hemoglobin S/hemoglobin Fannin-Lubbock-I individual. Is it a sickling disorder?一例罕见的血红蛋白S/血红蛋白范宁-拉伯克-Ⅰ型复合杂合子个体。这是一种镰状细胞病吗？
Lab Hematol. 2010 Jun;16(2):26-7. doi: 10.1532/LH96.10004.
6
Screening for sickle cell hemoglobinopathy and thalassemia.镰状细胞血红蛋白病和地中海贫血的筛查。
Isr J Med Sci. 1973 Sep-Oct;9(9):1341-9.
7
Chemical heterogeneity of fetal hemoglobin in subjects with sickle cell anemia, homozygous Hb-C disease, SC disease, and various combinations of hemoglobin variants.镰状细胞贫血、纯合子血红蛋白C病、血红蛋白SC病以及各种血红蛋白变异体组合的患者中胎儿血红蛋白的化学异质性。
Clin Chim Acta. 1972 Apr;38(1):5-16. doi: 10.1016/0009-8981(72)90201-x.
8
The molecular basis of hemoglobin disease.血红蛋白疾病的分子基础。
Annu Rev Genet. 1972;6:47-70. doi: 10.1146/annurev.ge.06.120172.000403.
9
[Hemoglobinopathies and thalassemias].[血红蛋白病和地中海贫血]
Ned Tijdschr Geneeskd. 1982 Jul 3;126(27):1234-7.
10
Student screening for inherited blood disorders in Bahrain.巴林学生遗传性血液疾病筛查。
East Mediterr Health J. 2003 May;9(3):344-52.
引用本文的文献
1
Newborn Screening for SCD in the USA and Canada.美国和加拿大对镰状细胞病的新生儿筛查。
Int J Neonatal Screen. 2018 Nov 26;4(4):36. doi: 10.3390/ijns4040036. eCollection 2018 Dec.
2
Sickle Cell Trait from a Metabolic, Renal, and Vascular Perspective: Linking History, Knowledge, and Health.从代谢、肾脏和血管角度看镰状细胞特征：关联历史、知识和健康。
J Racial Ethn Health Disparities. 2015 Sep;2(3):330-5. doi: 10.1007/s40615-014-0077-4.
3
Prevention of homozygous beta-thalassemia by carrier screening and prenatal diagnosis in Sardinia.通过在撒丁岛进行携带者筛查和产前诊断预防纯合子β地中海贫血。
Am J Hum Genet. 1981 Jul;33(4):592-605.
本文引用的文献
1
Electrophoresis of hemoglobin on agar gels; frequency of hemoglobin D in a Negro population.血红蛋白在琼脂凝胶上的电泳；黑人种群中血红蛋白D的频率。
Bull Johns Hopkins Hosp. 1959 Aug;105(2):77-88.
2
Complexities of parental understanding of phenylketonuria.父母对苯丙酮尿症理解的复杂性。
Pediatrics. 1971 Aug;48(2):216-24.
3
Adult hemoglobin synthesis by reticulocytes from the human fetus at midtrimester.孕中期人胎儿网织红细胞合成成人血红蛋白。
Science. 1971 Nov 12;174(4010):698-702. doi: 10.1126/science.174.4010.698.
4
Progress in early diagnosis of sickle cell disease.镰状细胞病早期诊断的进展
Children. 1971 Nov-Dec;18(6):222-6.
5
Further studies on the antenatal detection of sickle cell anemia and other hemoglobinopathies.
Adv Exp Med Biol. 1972;28:337-46. doi: 10.1007/978-1-4684-3222-0_27.
6
Detection of the sickle gene in the human fetus. Potential for intrauterine diagnosis of sickle-cell anemia.人类胎儿镰状基因的检测。镰状细胞贫血宫内诊断的可能性。
N Engl J Med. 1972 Jul 6;287(1):1-5. doi: 10.1056/NEJM197207062870101.
7
Routine screening of umbilical cord blood for sickle cell diseases.对脐带血进行镰状细胞病的常规筛查。
JAMA. 1974 Jan 28;227(4):420-1.
8
Laboratory diagnosis of hemoglobinopathies.血红蛋白病的实验室诊断
JAMA. 1973 May 28;224(9):1276-80.
9
New horizons in medical ethics. Research investigations and the fetus.医学伦理学的新视野。研究调查与胎儿
Br Med J. 1973 May 26;2(5864):464-8. doi: 10.1136/bmj.2.5864.464.
10
Sickle-cell anemia and other hemoglobinopathies. Procedures and strategy for screening employing spots of blood on filter paper as specimens.镰状细胞贫血及其他血红蛋白病。以滤纸上的血斑为标本进行筛查的程序和策略。
N Engl J Med. 1973 Jun 14;288(24):1265-8. doi: 10.1056/NEJM197306142882403.
Zotero 插件