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2. Prevention of retardation of genetic origin. Holtzman NA Pediatr Clin North Am; 1973 Feb; 20(1):151-8. PubMed ID: 4577325 [No Abstract] [Full Text] [Related]
3. [Diseases of newborn infants based on inborn anomalies of metabolism. 1. Theoretical principles]. Plöchl E Wien Med Wochenschr; 1970 Oct; 120(41):707-11. PubMed ID: 4918107 [No Abstract] [Full Text] [Related]
7. The critically ill child: acute metabolic disease in infancy and early childhood. O'Brien D; Goodman SI Pediatrics; 1970 Oct; 46(4):620-6. PubMed ID: 5503697 [No Abstract] [Full Text] [Related]
8. Laboratory diagnosis of genetic disorders. Thomas GH; Scott CI Pediatr Clin North Am; 1973 Feb; 20(1):105-19. PubMed ID: 4581982 [No Abstract] [Full Text] [Related]
9. [Severe metabolic diseases in neonates. Diagnosis and treatment (author's transl)]. Koepp P; Grüttner R Klin Padiatr; 1975 Jan; 187(1):14-9. PubMed ID: 1168276 [TBL] [Abstract][Full Text] [Related]
13. [Biochemistry of the blood and urine in members of families suspected of having hereditary metabolic defects]. Tănase-Mogoş I; Petrescu L; Jemna M; Ankăr V; Feldioreanu E Physiologie; 1980; 17(2):101-11. PubMed ID: 6770382 [No Abstract] [Full Text] [Related]
14. [Neonatal diagnosis of hereditary metabolic diseases]. Lambotte C Rev Med Liege; 1973 Dec; 28(24):837-51. PubMed ID: 4769974 [No Abstract] [Full Text] [Related]
15. Neurometabolic disorders in infancy, childhood and adolescence. Hagberg B Acta Neurol Scand; 1967; 43(S31):13-19. PubMed ID: 5583240 [No Abstract] [Full Text] [Related]