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3. Screening for aminoacid disorders in mental retardation. Jyothy A; Reddy PP Indian Pediatr; 1984 May; 21(5):381-8. PubMed ID: 6480090 [No Abstract] [Full Text] [Related]
4. Metabolic diseases and the skin. Lee EB Pediatr Clin North Am; 1983 Aug; 30(4):597-608. PubMed ID: 6136951 [No Abstract] [Full Text] [Related]
5. Ocular manifestations in aminoacidopathies. François J Monogr Hum Genet; 1972; 6():99-113. PubMed ID: 4541412 [No Abstract] [Full Text] [Related]
6. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease]. Raven EJ Ned Tijdschr Geneeskd; 1969 Oct; 113(42):1850-3. PubMed ID: 5344645 [No Abstract] [Full Text] [Related]
9. Ochronotic arthropathy: the black hip. Case report and review of the literature. Dom K; Pittevils T Acta Orthop Belg; 1997 Jun; 63(2):122-5. PubMed ID: 9265798 [TBL] [Abstract][Full Text] [Related]
10. [Skin lesions in the congenital metabolism disorders]. Kozlowski J; Wierzbicki T Przegl Dermatol; 1969; 56(3):355-61. PubMed ID: 4898937 [No Abstract] [Full Text] [Related]
11. [Neonatal and infant jaundice associated with congenital metabolic disorders]. Tazawa Y Nihon Rinsho; 1985 Aug; 43(8):1684-91. PubMed ID: 4057620 [No Abstract] [Full Text] [Related]
12. [Congenital tyrosine metabolism disorders in children with hemoblastoses]. Raushenbakh MO; Ivanova VD; Shevchenko VE; Makhonova LA; Sergeev AV Vestn Akad Med Nauk SSSR; 1981; (7):19-24. PubMed ID: 6974929 [No Abstract] [Full Text] [Related]
13. [Alkaptonuria]. Berger R; Broyer M Presse Med (1893); 1968 May; 76(24):1182-3. PubMed ID: 5673387 [No Abstract] [Full Text] [Related]
14. [Inborn errors of amino acid metabolism and convulsions]. Endo F Ryoikibetsu Shokogun Shirizu; 2002; (37 Pt 6):157-61. PubMed ID: 12483852 [No Abstract] [Full Text] [Related]
16. Anterior megalophthalmos associated with lamellar cataract on alkaptonuria. Rao VA Indian J Ophthalmol; 1982 Mar; 30(2):109-10. PubMed ID: 7141594 [No Abstract] [Full Text] [Related]
17. Neonatal severe primary hyperparathyroidism and alkaptonuria in a boy born to related parents with familial hypocalciuric hypercalcemia. Steinmann B; Gnehm HE; Rao VH; Kind HP; Prader A Helv Paediatr Acta; 1984 May; 39(2):171-86. PubMed ID: 6543841 [TBL] [Abstract][Full Text] [Related]
18. [Metabolic disorders of amino acids associated with respiratory distress]. Sano H; Inagaki H; Wada Y Ryoikibetsu Shokogun Shirizu; 1994; (4):608-11. PubMed ID: 8007253 [No Abstract] [Full Text] [Related]