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Items: 1 to 20 of 40

1.

Hyperphenylalanemia without phenylketonuria.

O'Flynn ME, Tillman P, Hsia DY.

Am J Dis Child. 1967 Jan;113(1):22-30. No abstract available.

PMID:
6015901
2.

Hyperphenylalanemia.

Hsia DY, O'Flynn ME.

Metabolism. 1967 Feb;16(2):99-101. Review. No abstract available.

PMID:
5335265
3.

[Diagnosis and therapy of 6 inherited, metabolic diseases, leading to mental deficiency. 1].

Menne F, Enzenauer J, Matz D.

Med Klin. 1976 Apr 23;71(17):724-8. Review. German. No abstract available.

PMID:
775276
4.

[Problems around phenylketonuria].

Svatý J.

Cesk Pediatr. 1969 Aug;24(8):740-3. Review. Czech. No abstract available.

PMID:
4896732
5.

Hyperphenylalaninemia: diagnosis and classification of the various types of phenylalanine hydroxylase deficiency in childhood.

Güttler F.

Acta Paediatr Scand Suppl. 1980;280:1-80. Review. No abstract available.

PMID:
7006308
6.

Malnutrition with early treatment of phenylketonuria.

[No authors listed]

Nutr Rev. 1971 Jan;29(1):11-3. Review. No abstract available.

PMID:
4950196
7.
8.

[Congenital disorders of phenylalanine metabolism].

Rampini S.

Schweiz Med Wochenschr. 1973 Apr 14;103(15):537-46. Review. German. No abstract available.

PMID:
4572324
9.

Phenylketonuria and other phenylalaninaemias.

Blaskovics ME.

Clin Endocrinol Metab. 1974 Mar;3(1):87-105. Review. No abstract available.

PMID:
4609651
10.

Phenylketonuria and other disorders of amino acid metabolism.

Ampola MG.

Pediatr Clin North Am. 1973 May;20(2):507-36. Review. No abstract available.

PMID:
4573597
11.

Biochemical factors in mental retardation.

Hsia DY.

Proc Annu Meet Am Psychopathol Assoc. 1967;56:28-44. Review. No abstract available.

PMID:
4966303
12.

[Diet therapy successes in treating hereditary metabolic diseases in children].

Ladodo KS, Barashneva SM.

Vestn Akad Med Nauk SSSR. 1978;(3):55-60. Review. Russian. No abstract available.

PMID:
347823
13.

[Importance of the diagnoses and treatment of phenylketonuria].

Mira NV, Marquez UM.

Rev Saude Publica. 2000 Feb;34(1):86-96. Review. Portuguese.

14.

[Clinico-chemical symptom: hyperphenylalaninemia].

Nothjunge J.

Hippokrates. 1974 May;45(2):203-9. Review. German. No abstract available.

PMID:
4602712
15.

Phenylketonuria: a review.

Yu JS.

Postgrad Med J. 1970 Jul;46(537):430-6. Review. No abstract available.

16.

Hyperphenylalaninemia syndromes: current status of diagnosis and management.

Matsuo N.

Keio J Med. 1988 Mar;37(1):1-9. Review. No abstract available.

17.

Results of dietary treatment in phenylketonuria.

[No authors listed]

Nutr Rev. 1971 Sep;29(9):203-5. Review. No abstract available.

PMID:
4938376
18.

The pathogenesis of mental retardation in phenylketonuria and other inborn errors of amino acid metabolism.

Menkes JH.

Pediatrics. 1967 Feb;39(2):297-308. Review. No abstract available.

PMID:
5335144
19.

Phenylketonuria: an update.

Cederbaum S.

Curr Opin Pediatr. 2002 Dec;14(6):702-6. Review.

PMID:
12436039
20.

Phenylketonuria and its variants.

Hsia DY.

Prog Med Genet. 1970;7:29-68. Review. No abstract available.

PMID:
4915811

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