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.
116 related articles for article (PubMed ID: 5590140)
61. UDP-glucose: alpha-D-galactose-1-phosphate uridylytransferase activity in cultured human fibroblasts. Russell JD; DeMars R Biochem Genet; 1967 Jun; 1(1):11-24. PubMed ID: 5610697 [No Abstract] [Full Text] [Related]
62. Childbearing by a galactosemic woman. Roe TF; Hallatt JG; Donnell GN; Ng WG J Pediatr; 1971 Jun; 78(6):1026-30. PubMed ID: 5577182 [No Abstract] [Full Text] [Related]
63. Reagent that restores galactose-1-phosphate uridylyltransferase activity in dry blood spots. Berry HK; Croft CC Clin Chem; 1987 Aug; 33(8):1471-2. PubMed ID: 3038378 [No Abstract] [Full Text] [Related]
64. Galactosemia caused by a point mutation that activates cryptic donor splice site in the galactose-1-phosphate uridyltransferase gene. Wadelius C; Lagerkvist A; Molin AK; Larsson A; von Döbeln U; Pettersson U Genomics; 1993 Aug; 17(2):525-6. PubMed ID: 8406510 [No Abstract] [Full Text] [Related]
65. Transient kinetics of formation and reaction of the uridylyl-enzyme form of galactose-1-P uridylyltransferase and its Q168R-variant: insight into the molecular basis of galactosemia. Geeganage S; Frey PA Biochemistry; 1998 Oct; 37(41):14500-7. PubMed ID: 9772178 [TBL] [Abstract][Full Text] [Related]
66. Outcomes of siblings with classical galactosemia. Hughes J; Ryan S; Lambert D; Geoghegan O; Clark A; Rogers Y; Hendroff U; Monavari A; Twomey E; Treacy EP J Pediatr; 2009 May; 154(5):721-6. PubMed ID: 19181333 [TBL] [Abstract][Full Text] [Related]
67. Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Mutation in brief no. 235. Online. Seyrantepe V; Ozguc M; Coskun T; Ozalp I; Reichardt JK Hum Mutat; 1999; 13(4):339. PubMed ID: 10220154 [TBL] [Abstract][Full Text] [Related]
68. Molecular characterization of galactosemia (type 1) mutations in Japanese. Ashino J; Okano Y; Suyama I; Yamazaki T; Yoshino M; Furuyama J; Lin HC; Reichardt JK; Isshiki G Hum Mutat; 1995; 6(1):36-43. PubMed ID: 7550229 [TBL] [Abstract][Full Text] [Related]
69. Galactose metabolism in the newborn infant. Donnell GN; Ng WG; Hodgman JE; Bergren WR Pediatrics; 1967 Jun; 39(6):829-37. PubMed ID: 6026549 [No Abstract] [Full Text] [Related]
70. Molecular basis for phenotypic heterogeneity in galactosaemia: prediction of clinical phenotype from genotype in Japanese patients. Hirokawa H; Okano Y; Asada M; Fujimoto A; Suyama I; Isshiki G Eur J Hum Genet; 1999; 7(7):757-64. PubMed ID: 10573007 [TBL] [Abstract][Full Text] [Related]
71. Galactose-1-phosphate uridyl transferase actiivity in hemolysates of newborn infants. Ng WG; Bergren WR; Donnell GN; Hodgman JE Pediatrics; 1967 Feb; 39(2):293-4. PubMed ID: 6017968 [No Abstract] [Full Text] [Related]
72. Functional analysis of the human galactose-1-phosphate uridyltransferase promoter in Duarte and LA variant galactosemia. Elsas LJ; Lai K; Saunders CJ; Langley SD Mol Genet Metab; 2001 Apr; 72(4):297-305. PubMed ID: 11286503 [TBL] [Abstract][Full Text] [Related]
73. [Secondary results of a Guthrie test programm. Galactose blood level in children of various ages following approximate physiologic galactose administrations]. Thalhammer O Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):419-21. PubMed ID: 5523695 [No Abstract] [Full Text] [Related]
74. Incidence of galactosemia at birth in New York State. Kelly S; Burns J; Desjardins L Am J Epidemiol; 1974 Jan; 99(1):8-13. PubMed ID: 4811177 [No Abstract] [Full Text] [Related]
75. [Enzymatic methods for the diagnosis of galactosemia and galactose deficiency]. Kruas H; Mönch E Klin Wochenschr; 1970 Apr; 48(7):437-9. PubMed ID: 4398808 [No Abstract] [Full Text] [Related]
76. Normal pregnancy and childbirth in a galactosemic woman. Tedesco TA; Morrow G; Mellman WJ J Pediatr; 1972 Dec; 81(6):1159-61. PubMed ID: 4674573 [No Abstract] [Full Text] [Related]
77. [Galactose-1-phosphate-uridyltransferase in erythrocytes of children with hepatitis epidemica]. Kaloud H; Sitzmann FC Wien Klin Wochenschr; 1970 Oct; 82(42):750-3. PubMed ID: 5470735 [No Abstract] [Full Text] [Related]
79. Diagnosis and treatment of galactosaemia. HUDSON FP; IRELAND JT; OCKENDEN BG; WHITE-JONES RH Br Med J; 1954 Jan; 1(4856):242-5. PubMed ID: 13115681 [No Abstract] [Full Text] [Related]
80. [Letter: Discussion comment on the article: Studies on polymorphism of galactose-l-phosphate-uridyl-transferase (EC:2.7.7.12) using agarose gel electrophoresis; by P. Kuehnl, L. Nowicki, and W. Spielmann; Humangenetik 24,227-230(1974)]. Ritter H Humangenetik; 1975; 27(1):75-6. PubMed ID: 1140816 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]