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3. Hereditary pancreatitis: report of an affected Canadian kindred and review of the disease. Girard RM; Dubé S; Archambault AP Can Med Assoc J; 1981 Sep; 125(6):576-80. PubMed ID: 7026015 [TBL] [Abstract][Full Text] [Related]
4. Rare association of hyperglycinuria and lenticonus in two members of the same family. Reccia R; Magli A; Pignalosa B; Sannolo N; Strisciuglio P Ophthalmologica; 1979; 178(3):131-6. PubMed ID: 471431 [TBL] [Abstract][Full Text] [Related]
5. Familial neuromuscular disease with nonketotic hyperglycinemia. Bank WJ; Morrow G Trans Am Neurol Assoc; 1971; 96():21-3. PubMed ID: 5159084 [No Abstract] [Full Text] [Related]
6. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants. Turner B; Brown DA Med J Aust; 1972 Jan; 1(2):62-5. PubMed ID: 5025157 [No Abstract] [Full Text] [Related]
7. [Results of a period of research (1967-1974) in the field of disorders of transport amino acid and metabolism using chromatographic, electrophoretic and dosimetric methods]. Berio A; Allegranza A; Scapaticci E; Cadoni M; Camozzi C; Cavallo V; Di Stefano A; Santos JG Minerva Pediatr; 1975 Sep; 27(30):1609-23. PubMed ID: 1177852 [No Abstract] [Full Text] [Related]
11. Hereditary pancreatitis: three new kindreds and a critical review of the literature. Kattwinkel J; Lapey A; Di Sant'Agnese PA; Edwards WA Pediatrics; 1973 Jan; 51(1):55-69. PubMed ID: 4567584 [No Abstract] [Full Text] [Related]
12. Genetic disorders of gamma-aminobutyric acid, glycine, and serine as causes of epilepsy. Jaeken J J Child Neurol; 2002 Dec; 17 Suppl 3():3S84-7; discussion 3S88. PubMed ID: 12597057 [TBL] [Abstract][Full Text] [Related]