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Motor activity in early life. 3. Premature babies with neonatal tyrosinaemia; a pilot study.

作者信息

Partington M W, Campbell D, Kuyek J, Mehlomakulu M

出版信息

Biol Neonate. 1971;18(1):121-8. doi: 10.1159/000240353.

DOI:10.1159/000240353
PMID:5123899
Abstract
摘要

相似文献

1
Motor activity in early life. 3. Premature babies with neonatal tyrosinaemia; a pilot study.生命早期的运动活动。3. 患有新生儿酪氨酸血症的早产儿;一项试点研究。
Biol Neonate. 1971;18(1):121-8. doi: 10.1159/000240353.
2
Neonatal tyrosinaemia: a follow-up study.新生儿酪氨酸血症:一项随访研究。
Arch Dis Child. 1968 Apr;43(228):195-9. doi: 10.1136/adc.43.228.195.
3
Motor activity in early life. II. Daily motor activity output in the neonatal period.生命早期的运动活动。II. 新生儿期的每日运动活动输出量
Biol Neonate. 1971;18(1):108-20. doi: 10.1159/000240352.
4
[The fate of very early premature babies. Mortality, morbidity and 2-year follow-up in a population of 96 very early premature babies].
Rev Fr Gynecol Obstet. 1992 Nov;87(11):533-9.
5
Neonatal tyrosinaemaia.新生儿酪氨酸血症
Biol Neonat. 1968;12(5):316-30.
6
Neonatal smiling in REM states, IV. Premature study.快速眼动睡眠状态下的新生儿微笑,IV. 早产研究。
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7
Predictive value of Apgar scores for developmental outcome in premature infants.阿氏评分对早产儿发育结局的预测价值
Am J Perinatol. 1989 Jan;6(1):18-21. doi: 10.1055/s-2007-999536.
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[Neonatal viability and resuscitation in preterm newborns with an extremely low birth weight].
An Esp Pediatr. 1999 Jun;50(6):594-602.
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An evaluation of various parameters of maturity at birth as predictors of development at one year of life.对出生时成熟度的各种参数作为一岁时发育预测指标的评估。
Percept Mot Skills. 1974 Aug;39(1 Pt 2):631-52. doi: 10.2466/pms.1974.39.1.631.
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[Blood tyrosine in the newborn. IV. Behavior of phenylalanine in relation to birth weight, to blood tyrosine and protein supply].
Minerva Pediatr. 1978 May 15;30(9):681-5.

引用本文的文献

1
Neonatal hair profiling reveals a metabolic phenotype of monochorionic twins with selective intrauterine growth restriction and abnormal umbilical artery flow.新生儿毛发分析揭示了具有选择性宫内生长受限和异常脐动脉血流的单绒毛膜双胞胎的代谢表型。
Mol Med. 2020 May 1;26(1):37. doi: 10.1186/s10020-020-00160-8.
2
Screening for inborn errors of metabolism among newborns with metabolic disturbance and/or neurological manifestations without determined cause.对有代谢紊乱和/或无明确病因的神经学表现的新生儿进行先天性代谢缺陷筛查。
Sao Paulo Med J. 2001 Sep 6;119(5):160-4. doi: 10.1590/s1516-31802001000500002.
3
Transient neonatal tyrosinaemia.
短暂性新生儿酪氨酸血症
J Inherit Metab Dis. 1989;12(1):13-22. doi: 10.1007/BF01805526.
4
Hereditary tyrosinaemia type II in a consanguineous Ashkenazi Jewish family: intrafamilial variation in phenotype; absence of parental phenotype effects on the fetus.
J Inherit Metab Dis. 1992;15(2):198-203. doi: 10.1007/BF01799631.
5
Neonatal hypertyrosinemia and evidence for deficiency of ascorbic acid in Arctic and subarctic peoples.北极和亚北极地区人群中的新生儿高酪氨酸血症及维生素C缺乏证据。
Can Med Assoc J. 1975 Oct 4;113(7):624-6.
6
Tyrosine and its metabolites in urine and serum of premature and mature newborns: increased values during formula versus breast feeding.
Eur J Pediatr. 1979 Nov;132(3):179-87. doi: 10.1007/BF00442434.