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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

110 related articles for article (PubMed ID: 7526095)

  • 21. Galactosaemia workshop. Report of a workshop held at Alder Hey Children's Hospital, Liverpool, on 30 April, 1982.
    Clothier CM; Davidson DC
    Hum Nutr Appl Nutr; 1983 Dec; 37(6):483-90. PubMed ID: 6662737
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Ovarian failure in a young woman with galactosaemia.
    Morrow RJ; Atkinson AB; Carson DJ; Carson NA; Sloan JM; Traub AI
    Ulster Med J; 1985 Oct; 54(2):218-20. PubMed ID: 4095816
    [No Abstract]   [Full Text] [Related]  

  • 23. Galactosaemia with fatal cerebral oedema.
    Perelmuter B; Goodman SI; McCabe ER
    J Inherit Metab Dis; 1989; 12(4):489-90. PubMed ID: 2516182
    [No Abstract]   [Full Text] [Related]  

  • 24. Generalised uridine diphosphate galactose-4-epimerase deficiency.
    Walter JH; Roberts RE; Besley GT; Wraith JE; Cleary MA; Holton JB; MacFaul R
    Arch Dis Child; 1999 Apr; 80(4):374-6. PubMed ID: 10086948
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 26. Diagnosis of classical galactosaemia.
    Monk AM; Mitchell AJ; Milligan DW; Holton JB
    Arch Dis Child; 1977 Dec; 52(12):943-6. PubMed ID: 606167
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Increased fertility in a woman with classic galactosaemia.
    Kimonis V
    J Inherit Metab Dis; 2001 Oct; 24(5):607-8. PubMed ID: 11757592
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The lens, cataracts, and galactosemia.
    Cogan DG
    N Engl J Med; 1973 Jun; 288(23):1239-40. PubMed ID: 4700558
    [No Abstract]   [Full Text] [Related]  

  • 29. Galactosaemia with cataract and persistent hyaloid artery. A clinicopathological case report.
    Vangsted P
    Acta Ophthalmol (Copenh); 1980 Oct; 58(5):812-8. PubMed ID: 7211269
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Galactokinase deficiency].
    Colin J; Voyer M; Thomas D; Charlas J
    Ann Pediatr (Paris); 1976 May; 23(5):371-7. PubMed ID: 16104211
    [No Abstract]   [Full Text] [Related]  

  • 31. Neonatal classical galactosaemia presenting as citrin deficiency.
    McKiernan PJ; Baumann U
    J Hepatol; 2008 Sep; 49(3):463; author reply 464. PubMed ID: 18640739
    [No Abstract]   [Full Text] [Related]  

  • 32. Classical Galactosaemia in Ireland: incidence, complications and outcomes of treatment.
    Coss KP; Doran PP; Owoeye C; Codd MB; Hamid N; Mayne PD; Crushell E; Knerr I; Monavari AA; Treacy EP
    J Inherit Metab Dis; 2013 Jan; 36(1):21-7. PubMed ID: 22870861
    [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]  

  • 34. Clouds over galactosaemia.
    Lancet; 1982 Dec; 2(8312):1379-80. PubMed ID: 6129470
    [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]  

  • 40. [Neurologic characteristics of galactosemia in children].
    Iampol'skaia EI; Bel'mishchev IuE; Ermakova LI; Baryshnikova SS
    Pediatriia; 1978 Nov; (11):37-42. PubMed ID: 740436
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.