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43. [Amino-aciduria and amino-acidemia as a clinical and diagnostic problem in child neuropsychiatry]. Milovanović D; Radojcić B Srp Arh Celok Lek; 1976 Jun; 104(6):457-62. PubMed ID: 1025761 [No Abstract] [Full Text] [Related]
44. [Combined cystinuria-lysinuria in 2 brothers with mental retardation and morphologic and neurologic anomalies]. Thiriar MJ; Szliwowski HB; Vis HL Acta Neurol Psychiatr Belg; 1968 Mar; 68(3):216-27. PubMed ID: 4972603 [No Abstract] [Full Text] [Related]
45. [Study of aminoaciduria and aminoacidemia by chromato-ion-ophoresis. Technic and application to the dynamic study of various amino acid metabolic disorders]. Vovan L; Perrimond H; Pierron H; Orsini A Pediatrie; 1967 Sep; 22(6):732-3. PubMed ID: 5621096 [No Abstract] [Full Text] [Related]
46. [Screening on aminoacid opathies in newborn infants]. Stoppoloni G; Santinelli R Pediatria (Napoli); 1976 Dec; 84(4):604-16. PubMed ID: 1035798 [No Abstract] [Full Text] [Related]
48. [The spectrum of amino acids in mental retardation and epilepsy in childhood]. Wiechert P; Cammann R; Gierow W Padiatr Grenzgeb; 1977; 16(6):355-61. PubMed ID: 611435 [No Abstract] [Full Text] [Related]
49. [Indications of renal and intestinal amino acid malabsorption in Lowe's syndrome]. Colombo JP Schweiz Med Wochenschr; 1971 Jul; 101(26):968-72. PubMed ID: 5143472 [No Abstract] [Full Text] [Related]
50. [Comparison of free amino acids in capillary and venous blood serum of children and adolescents with phenylketonuria and leucinosis]. Liappis N; Schlebusch H; Mallmann R Klin Padiatr; 1992; 204(2):107-10. PubMed ID: 1583848 [TBL] [Abstract][Full Text] [Related]
51. [Results of screening for inborn errors of aminoacid metabolism in adult and infant patients from psychiatric institutions (author's transl)]. Hyánek J; Turek S; Kríz J; Trísková J; Homolka J; Kopejtková H Cas Lek Cesk; 1975 Mar; 114(10-11):307-8. PubMed ID: 1139573 [No Abstract] [Full Text] [Related]
52. Routine investigation of amino acid patterns in blood serum and urine by thin-layer electrophoresis. Fahie-Wilson MN J Med Lab Technol; 1969 Oct; 26(4):363-70. PubMed ID: 5355354 [No Abstract] [Full Text] [Related]
53. [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]
55. Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation. Shih VE; Efron ML; Moser HW Am J Dis Child; 1969 Jan; 117(1):83-92. PubMed ID: 5782534 [No Abstract] [Full Text] [Related]
56. The pathogenesis of mental retardation in phenylketonuria and other inborn errors of amino acid metabolism. Menkes JH Pediatrics; 1967 Feb; 39(2):297-308. PubMed ID: 5335144 [No Abstract] [Full Text] [Related]
57. [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]
58. [Type I hyperprolinemia. Study of a familial case]. Fontaine G; Farriaux JP; Dautrevaux M Helv Paediatr Acta; 1970 Apr; 25(2):165-75. PubMed ID: 5419477 [No Abstract] [Full Text] [Related]
59. A simple screening test for histidinuria. Gerber MG; Gerber DA Pediatrics; 1969 Jan; 43(1):40-3. PubMed ID: 5764066 [No Abstract] [Full Text] [Related]
60. [Combined use of tandem mass spectrometry with urine gas chromatography/mass spectrometry is useful for diagnosis of inborn errors of metabolism in children]. Xie LJ; Zhu JX; Zhu XD; Li HJ; Han LS; Gu XF Zhongguo Dang Dai Er Ke Za Zhi; 2008 Feb; 10(1):31-4. PubMed ID: 18289467 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]