274 related articles for article (PubMed ID: 5592531)
1. [Brain atrophy and disorders of the amino acid metabolism].
Bickel H
Monatsschr Kinderheilkd (1902); 1967 Apr; 115(4):254-8. PubMed ID: 5592531
[No Abstract] [Full Text] [Related]
2. [Dietetics in hereditary enzyme deficiencies].
Royer P
Sem Hop; 1970 Feb; 46(10):653-9. PubMed ID: 4314674
[No Abstract] [Full Text] [Related]
3. Recent advances in the early detection and treatment of inborn errors with brain damage.
Bickel H
Neuropadiatrie; 1969; 1(1):1-11. PubMed ID: 4942066
[No Abstract] [Full Text] [Related]
4. Central nervous system lesions in disorders of amino-acid metabolism. A neuropathological study.
Martin JJ; Schlote W
J Neurol Sci; 1972; 15(1):49-76. PubMed ID: 5008716
[No Abstract] [Full Text] [Related]
5. Ocular manifestations in aminoacidopathies.
François J
Adv Ophthalmol; 1972; 25():28-103. PubMed ID: 4560371
[No Abstract] [Full Text] [Related]
6. [Current views on therapy of some dysmetabolic oligophrenias].
Giovannini M
Minerva Pediatr; 1967 Dec; 19(51):2286-90. PubMed ID: 5607848
[No Abstract] [Full Text] [Related]
7. [Clinical problems of the genetic heterogeneity in hyperphenylalaninemias].
Grüttner R; Sternowsky HJ; Rybak C
Monatsschr Kinderheilkd (1902); 1971 Nov; 119(11):600-4. PubMed ID: 5133646
[No Abstract] [Full Text] [Related]
8. [Feeble mindedness caused by genetic disorders of amino acid metabolism].
Menne F
Hippokrates; 1968 May; 39(10):357-67. PubMed ID: 4886426
[No Abstract] [Full Text] [Related]
9. Neuropathological study of aminoacidurias.
Martin JJ; Schlote W
Monogr Hum Genet; 1972; 6():64-78. PubMed ID: 4663916
[No Abstract] [Full Text] [Related]
10. Diet therapy for inborn errors of amino acid metabolism.
Efron ML
J Am Diet Assoc; 1967 Jul; 51(1):40-5. PubMed ID: 6027632
[No Abstract] [Full Text] [Related]
11. Phenylketonuria and other disorders of amino acid metabolism.
Ampola MG
Pediatr Clin North Am; 1973 May; 20(2):507-36. PubMed ID: 4573597
[No Abstract] [Full Text] [Related]
12. [The early recognition of congenital metabolic diseases].
Steuber W
Munch Med Wochenschr; 1971 Mar; 113(13):463-7. PubMed ID: 5108281
[No Abstract] [Full Text] [Related]
13. [Hereditary amino acid metabolism disorders. Indications for early diagnosis].
Kroll S; Zebisch P; Toussaint W
Fortschr Med; 1972 Apr; 90(11):423-8. PubMed ID: 4680607
[No Abstract] [Full Text] [Related]
14. Simple biochemical methods for the study of lipidoses and aminoacidopathies.
Adriaenssens K; Karcher D
Riv Patol Nerv Ment; 1970 Oct; 91(5):274-6. PubMed ID: 5525772
[No Abstract] [Full Text] [Related]
15. A study of cerebral atrophy in phenylketonuria. Sonoencephalographic examination of 45 PKU patients.
Mostafawy A; Nagle JB; Newill A; Braatz E
Neuropadiatrie; 1970 Dec; 2(2):215-25. PubMed ID: 4941188
[No Abstract] [Full Text] [Related]
16. Dietary treatment of inborn errors of amino acid and carbohydrate metabolism.
Bickel H; Schmidt H; Schürrle L
Bibl Nutr Dieta; 1973; (18):181-201. PubMed ID: 4566397
[No Abstract] [Full Text] [Related]
17. [Screening newborn infants for phenylketonuria, histadinemia, homocystinuria and maple syrup disease. Results from north rhein-westphalia (1974-1976) (author's transl].
Menne F; Otte HJ; Krüger M; Winterhoff D
MMW Munch Med Wochenschr; 1978 May; 120(18):619-22. PubMed ID: 306535
[TBL] [Abstract][Full Text] [Related]
18. Inborn errors of metabolism (IEM) -- an Indian perspective.
Kumta NB
Indian J Pediatr; 2005 Apr; 72(4):325-32. PubMed ID: 15876762
[TBL] [Abstract][Full Text] [Related]
19. [Simultaneous thin-layer chromatography of blood and urine samples for the diagnosis of hereditary amino acid metabolism disorders].
Peters WH; Lubs H; Knapp A
Z Arztl Fortbild (Jena); 1974 Jul; 68(14):716-25. PubMed ID: 4216183
[No Abstract] [Full Text] [Related]
20. [A screening test for phenylketonuria using a paper chromatography method].
Halvorsen S; Skjelkvåle L
Lakartidningen; 1974 Mar; 71(12):1166-7. PubMed ID: 4821497
[No Abstract] [Full Text] [Related]
[Next] [New Search]
