These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. [Are there various forms of gyrate atrophy of the choroid and retina? (choroidal and retinal gyrate atrophy with and without ornithinemia)]. Jaeger W; von Kettler J; Hilsdorf C; Lutz P Ber Zusammenkunft Dtsch Ophthalmol Ges; 1978; (75):655-63. PubMed ID: 743182 [No Abstract] [Full Text] [Related]
6. [Relation between metabolic amino acid defect and familial occurring epilepsy]. Bárdosová G; Králik M; Lazorová A; Mäsiar P; Adam J Psychiatr Neurol Med Psychol Beih; 1970; 13-14():182-90. PubMed ID: 5006283 [TBL] [Abstract][Full Text] [Related]
7. [Hypersarcosinemia with sarcosinuria. Study of a new case]. Willems C; Heusden A; Hainaut A; Chapelle P J Genet Hum; 1971 Mar; 19(1):101-18. PubMed ID: 5158355 [No Abstract] [Full Text] [Related]
8. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972 [No Abstract] [Full Text] [Related]
9. [Results of screening for aminoacidopathies in pregnant women]. Hyánek J; Trnka V; Homolka J; Vácha V; Srácek J; Cervenka J; Dolezal A; Seemanová E; Kapras J; Malá M; Wünschová N; Holub J; Hoza J; Losan F; Nevsímalová S; Kubík M; Viletová H; Ronová R; Kunová V; Matousová M Cesk Pediatr; 1977 Aug; 32(8):460-3. PubMed ID: 597929 [No Abstract] [Full Text] [Related]
14. High performance liquid chromatography (HPLC) method for confirming thin layer chromatography (TLC) findings in inborn errors of metabolism children in Malaysia. Yahya NA; Ismail Z; Embong KH; Mohamad SA Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():130-3. PubMed ID: 8629091 [TBL] [Abstract][Full Text] [Related]
15. [Personal experience with chromatographic methods of demonstrating aminated substances (amino acids and amines)]. Berio A Minerva Pediatr; 1968 Mar; 20(10):536-45. PubMed ID: 5739013 [No Abstract] [Full Text] [Related]
16. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family. Mollica F; Pavone L; Antener I Pediatrics; 1971 Aug; 48(2):225-31. PubMed ID: 5560617 [No Abstract] [Full Text] [Related]
17. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase]. Cathelineau L; Navarro J; Aymard P; Baudon JJ; Mondet Y; Polonovski C; Laplane R Arch Fr Pediatr; 1972; 29(7):713-36. PubMed ID: 4644461 [No Abstract] [Full Text] [Related]
19. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders]. Khiari D; Tebib N; Kaabachi N; Ben Dridi MF; Mebazaa A Tunis Med; 1995 May; 73(5):159-67. PubMed ID: 9507277 [No Abstract] [Full Text] [Related]
20. [Personal results in screening amino acid diseases by means of the method of Scriver et al]. Di Stefano A; Berio A; Viglione M; Liotta A; Piovano B; Bellati R Minerva Pediatr; 1970 Mar; 22(10):461-70. PubMed ID: 5444384 [No Abstract] [Full Text] [Related] [Next] [New Search]