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25. Early neurological complications in children with classical galactosemia and p.gln188arg mutation. Özgün N; Celik M; Akdeniz O; Ozbek MN; Bulbul A; Anlar B Int J Dev Neurosci; 2019 Nov; 78():92-97. PubMed ID: 31336146 [TBL] [Abstract][Full Text] [Related]
33. Early manifestation of cataract in a child heterozygous for classical galactosaemia and with diabetes mellitus type I: increased plasma mannitol concentration in cataract patients. Shin YS; Reiter K; Urban A; Lorenz B; Kiess W J Inherit Metab Dis; 1994; 17(1):151-3. PubMed ID: 8051929 [No Abstract] [Full Text] [Related]
35. Congenital ocular malformations (lens subluxation, pupillary displacement, cataract, myopia) and classic galactosaemia associated with Q188R and /or G1391A mutations. Schmidt D; Shin YS; Auw-Haedrich C; Tacke U Acta Ophthalmol; 2011 Aug; 89(5):489-94. PubMed ID: 20222886 [TBL] [Abstract][Full Text] [Related]
36. [Letter: Galactosemia in adults]. Pár A; Gógl A; Székessy V Orv Hetil; 1974 Aug; 115(34):2033. PubMed ID: 4849076 [No Abstract] [Full Text] [Related]
37. Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experience. Zekanowski C; Nowacka M; Radomyska B; Cabalska B J Med Screen; 2001; 8(3):132-6. PubMed ID: 11678552 [TBL] [Abstract][Full Text] [Related]
38. Unusual late neurological sequelae in galactosaemia. Jan JE; Wilson RA Dev Med Child Neurol; 1973 Feb; 15(1):72-4. PubMed ID: 4729415 [No Abstract] [Full Text] [Related]
39. Hereditary galactosaemia measurements of galactose-1-phosphate-uridyltransferase with reference to diagnosis and mode of inheritance. Tolstrup N Dan Med Bull; 1966 Aug; 13(4):127-30. PubMed ID: 5945006 [No Abstract] [Full Text] [Related]