Atypical phenylketonuria in sisters with normal offspring.
作者信息
WOOLF L I, OUNSTED C, LEE D, HUMPHREY M, CHESHIRE N M, STEED G R
出版信息
Lancet. 1961 Aug 26;2(7200):464-5. doi: 10.1016/s0140-6736(61)92434-5.
Abstract
摘要
相似文献
1
Atypical phenylketonuria in sisters with normal offspring.
Lancet. 1961 Aug 26;2(7200):464-5. doi: 10.1016/s0140-6736(61)92434-5.
2
[Phenylketonuria and precocious puberty. Internal secretory disorders in 2 phenylketonuric siblings].
Med Welt. 1961 Nov 18;46:2427-9.
3
Phenylketonuria: case history and comments.
J Am Osteopath Assoc. 1961 Nov;61:193-5.
4
Phenylketonuria: an unusual case.
J Pediatr. 1959 Feb;54(2):210-4. doi: 10.1016/s0022-3476(59)80065-2.
5
Phenylketonuria.
N Z Med J. 1960 Jul;59:343-6.
6
Phenylketonuria with borderline and normal intelligence.
N C Med J. 1961 Oct;22:528-30.
7
An unusual case of phenylketonuria.
Med J Aust. 1960 Nov 19;47(2):811-3. doi: 10.5694/j.1326-5377.1960.tb23785.x.
8
Phenylketonuria: report and discussion of three cases.
S Afr Med J. 1960 Feb 6;34:113-6.
9
[Phenylpyruvic oligophrenia in two sisters].
G Psichiatr Neuropatol. 1953;81(1):85-96.
10
Phenylpyruvic oligophrenia. Report of a case with normal intelligence.
Dis Nerv Syst. 1961 Aug;22:465-6.
引用本文的文献
1
Maternal Phenylketonuria Collaborative Study (MPKUCS)--the 'outliers'.
J Inherit Metab Dis. 2004;27(6):711-23. doi: 10.1023/B:BOLI.0000045758.86492.54.
2
Variations in intelligence in phenylktonuria.
Can Med Assoc J. 1962 Apr 21;86(16):736-43.
3
PHENYLKETONURIA PRESENTING AN INTERMITTENT PROGRESSIVE COURSE.
J Neurol Neurosurg Psychiatry. 1965 Apr;28(2):165-70. doi: 10.1136/jnnp.28.2.165.
4
CASE FINDING IN PHENYLKETONURIA. II. THE GUTHRIE TEST.
Can Med Assoc J. 1964 Jul 18;91(3):105-14.
5
Recent work on phenylketonuria and maple syrup urine disease (leucinosis).
Proc R Soc Med. 1962 Oct;55(10):824-6. doi: 10.1177/003591576205501001.
6
Outcome of pregnancy in a phenylketonuric mother after low phenylalanine diet introduced from the ninth week of pregnancy.
Eur J Pediatr. 1981 Sep;137(1):45-8. doi: 10.1007/BF00441169.
7
Four cases of hyperphenylalaninaemia: studies during pregnancy and of the offspring produced.
J Inherit Metab Dis. 1982;5(1):11-5. doi: 10.1007/BF01799748.
8
Combined tetrahydrobiopterin-phenylalanine loading test in the detection of partially defective biopterin synthesis.
Eur J Pediatr. 1984 Jun;142(2):126-9. doi: 10.1007/BF00445592.
9
Termination of dietary treatment of phenylketonuria.
Arch Dis Child. 1967 Apr;42(222):198-200. doi: 10.1136/adc.42.222.198.
10
Phenylketonuria. Early detection, diagnosis and treatment.
Calif Med. 1966 Jul;105(1):1-7.
Zotero 插件