298 related articles for article (PubMed ID: 17022534)
1. [Galactosemia].
Ohtake A; Amemiya S
Nihon Rinsho; 2006 Sep; Suppl 3():215-9. PubMed ID: 17022534
[No Abstract] [Full Text] [Related]
2. Rare cases of galactose metabolic disorders: identification of more than two mutations per patient.
Schulpis KH; Thodi G; Chatzidaki M; Iakovou K; Molou E; Dotsikas Y; Loukas YL
J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1119-1120. PubMed ID: 28902631
[No Abstract] [Full Text] [Related]
3. [Tests for galactose metabolism].
Ohya N
Nihon Rinsho; 1997 Mar; 55 Suppl 1():244-7. PubMed ID: 9097598
[No Abstract] [Full Text] [Related]
4. Molecular basis of disorders of human galactose metabolism: past, present, and future.
Novelli G; Reichardt JK
Mol Genet Metab; 2000; 71(1-2):62-5. PubMed ID: 11001796
[TBL] [Abstract][Full Text] [Related]
5. [Galactose-1-phosphate uridyltransferase deficiency].
Okano Y; Isshiki G
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):15-21. PubMed ID: 9589977
[No Abstract] [Full Text] [Related]
6. Diagnosis of inherited disorders of galactose metabolism.
Cuthbert C; Klapper H; Elsas L
Curr Protoc Hum Genet; 2008 Jan; Chapter 17():Unit 17.5. PubMed ID: 18428423
[TBL] [Abstract][Full Text] [Related]
7. Galactose and cataract.
Stambolian D
Surv Ophthalmol; 1988; 32(5):333-49. PubMed ID: 3043741
[TBL] [Abstract][Full Text] [Related]
8. [Galactosemia].
Owada M
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):647-51. PubMed ID: 3270877
[No Abstract] [Full Text] [Related]
9. [Galactosemia].
Grodzka Z; Zbieg-Sendecka E
Probl Med Wieku Rozwoj; 1979; 8():70-6. PubMed ID: 263529
[TBL] [Abstract][Full Text] [Related]
10. [UDP-galactose-4-epimerase deficiency].
Okano Y; Isshiki G
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):25-6. PubMed ID: 9589979
[No Abstract] [Full Text] [Related]
11. [The diagnosis of galactosemia: screening or clinical diagnosis?].
Derksen-Lubsen G
Ned Tijdschr Geneeskd; 1980 Jul; 124(30):1250-6. PubMed ID: 7412896
[No Abstract] [Full Text] [Related]
12. On the screening for inborn errors of galactose metabolism.
Vaca G; Sànchez-Corona J; Olivares N; Medina C; Ibarra B; Cantú JM
Ann Genet; 1983; 26(3):191-2. PubMed ID: 6606384
[TBL] [Abstract][Full Text] [Related]
13. Hereditary galactosemia.
Demirbas D; Coelho AI; Rubio-Gozalbo ME; Berry GT
Metabolism; 2018 Jun; 83():188-196. PubMed ID: 29409891
[TBL] [Abstract][Full Text] [Related]
14. The molecular basis of galactosemia - Past, present and future.
Timson DJ
Gene; 2016 Sep; 589(2):133-41. PubMed ID: 26143117
[TBL] [Abstract][Full Text] [Related]
15. Galactosemia caused by generalized uridine diphosphate galactose-4-epimerase deficiency.
Garibaldi L; Superti-Furga A; Borrone C
J Pediatr; 1986 Dec; 109(6):1074-5. PubMed ID: 3783336
[No Abstract] [Full Text] [Related]
16. Perinatal galactose metabolism.
Kliegman RM; Sparks JW
J Pediatr; 1985 Dec; 107(6):831-41. PubMed ID: 3906069
[TBL] [Abstract][Full Text] [Related]
17. [Double heterozygosity (transferase-/epimerase-defect) and galactosemia cataract].
Heyne K; Shin YS; Schwinger E
Monatsschr Kinderheilkd; 1988 Dec; 136(12):828-30. PubMed ID: 2853298
[TBL] [Abstract][Full Text] [Related]
18. Galactosemia: when is it a newborn screening emergency?
Berry GT
Mol Genet Metab; 2012 May; 106(1):7-11. PubMed ID: 22483615
[TBL] [Abstract][Full Text] [Related]
19. Problems in the diagnosis of transferase and galactokinase deficient galactosemia.
Pesce MA; Bodourian SH
Ann Clin Lab Sci; 1980; 10(1):26-32. PubMed ID: 7362195
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of galactose-1-phosphate uridyltransferase (GALT)-deficient galactosemia.
Elsas LJ
Prenat Diagn; 2001 Apr; 21(4):302-3. PubMed ID: 11288121
[No Abstract] [Full Text] [Related]
[Next] [New Search]
