131 related articles for article (PubMed ID: 8779622)
1. [Lists of food exchanges for use in phenylketonuria and maple-syrup urine disease].
Jiménez Soto Z
Arch Latinoam Nutr; 1993 Sep; 43(3):211-6. PubMed ID: 8779622
[TBL] [Abstract][Full Text] [Related]
2. [Methodology of care for children with phenylketonuria and maple-syrup urine disease].
Jiménez Soto Z
Arch Latinoam Nutr; 1993 Sep; 43(3):204-10. PubMed ID: 8779621
[TBL] [Abstract][Full Text] [Related]
3. Nutrient intakes of adolescents with phenylketonuria and infants and children with maple syrup urine disease on semisynthetic diets.
Gropper SS; Naglak MC; Nardella M; Plyler A; Rarback S; Yannicelli S
J Am Coll Nutr; 1993 Apr; 12(2):108-14. PubMed ID: 8463509
[TBL] [Abstract][Full Text] [Related]
4. Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience.
Karam PE; Habbal MZ; Mikati MA; Zaatari GE; Cortas NK; Daher RT
Clin Biochem; 2013 Dec; 46(18):1787-92. PubMed ID: 23994778
[TBL] [Abstract][Full Text] [Related]
5. Serum-selenium concentrations in patients with maple-syrup-urine disease and phenylketonuria under dieto-therapy.
Lombeck I; Kasperek K; Feinendegen LE; Bremer HJ
Clin Chim Acta; 1975 Oct; 64(1):57-61. PubMed ID: 1183026
[TBL] [Abstract][Full Text] [Related]
6. Dietary restriction in inborn errors of amino acid metabolism.
Bickel H
Curr Concepts Nutr; 1979; 8():35-53. PubMed ID: 527358
[No Abstract] [Full Text] [Related]
7. Intermittent neurological symptoms in a girl with a maple syrup urine disease (MSUD) variant.
Holmgren G; Brundin A; Gustavson KH; Sjögren S; Kleijer WJ; Niermeijer MF
Neuropediatrics; 1980 Nov; 11(4):377-83. PubMed ID: 7207707
[TBL] [Abstract][Full Text] [Related]
8. Maple syrup urine disease in Thai infants.
Pangkanon S; Charoensiriwatana W; Sangtawesin V
J Med Assoc Thai; 2008 Oct; 91 Suppl 3():S41-4. PubMed ID: 19255991
[TBL] [Abstract][Full Text] [Related]
9. [Maple Syrup Urine Disease in a newborn infant].
Mazur A; Sykut-Cegielska J; Ciebiera M; Trzeciak J; Taybert J; Kowalik A; Ołtarzewski M
Med Wieku Rozwoj; 2007; 11(1):65-8. PubMed ID: 17965467
[TBL] [Abstract][Full Text] [Related]
10. The selenium state of children. II. Selenium content of serum, whole blood, hair and the activity of erythrocyte glutathione peroxidase in dietetically treated patients with phenylketonuria and maple-syrup-urine disease.
Lombeck I; Kasperek K; Harbisch HD; Becker K; Schumann E; Schröter W; Feinendegen LE; Bremer HJ
Eur J Pediatr; 1978 Jul; 128(4):213-23. PubMed ID: 668729
[TBL] [Abstract][Full Text] [Related]
11. A rapid ultra performance liquid chromatography tandem mass spectrometric method for measuring amino acids associated with maple syrup urine disease, tyrosinaemia and phenylketonuria.
Freeto S; Mason D; Chen J; Scott RH; Narayan SB; Bennett MJ
Ann Clin Biochem; 2007 Sep; 44(Pt 5):474-81. PubMed ID: 17761035
[TBL] [Abstract][Full Text] [Related]
12. [Diet therapy of some inborn errors of metabolism].
Perrone L
Pediatria (Napoli); 1974 Sep; 82(2):260-97. PubMed ID: 4473102
[No Abstract] [Full Text] [Related]
13. Management of maple syrup urine disease in Canada. Committee for improvement of Hereditary Disease Management.
Can Med Assoc J; 1976 Nov; 115(10):1005-13. PubMed ID: 1032577
[TBL] [Abstract][Full Text] [Related]
14. [Isolated isoleucine deficiency in diet therapy of a case of maple syrup urine disease].
Sanjurjo P; Centeno C; Vallo A; Ojembarrena E; Rodríguez Soriano J
An Esp Pediatr; 1983 Nov; 19(5):389-92. PubMed ID: 6660656
[TBL] [Abstract][Full Text] [Related]
15. Decreased essential amino acid requirements without catabolism in phenylketonuria and maple syrup urine disease.
Ruch T; Kerr D
Am J Clin Nutr; 1982 Feb; 35(2):217-28. PubMed ID: 7064884
[TBL] [Abstract][Full Text] [Related]
16. [Early diagnosis of phenylketonuria, homocystinuria and maple syrup urine disease in the GDR with the aid of Gatri's microbiological inhibitor test].
Makhill G; Knapp A
Pediatriia; 1974 Dec; (12):27-30. PubMed ID: 4614217
[No Abstract] [Full Text] [Related]
17. ["Atypical" metabolic forms of phenylketonuria (PKU) and leucinosis detected in newborn infants].
Tănase I; Ciortoloman H; Popescu M; Grigorescu G; Ankăr V
Physiologie; 1977; 14(4):257-61. PubMed ID: 413127
[No Abstract] [Full Text] [Related]
18. Trace element disturbances in dietetically treated patients with phenylketonuria and maple syrup urine disease.
Lombeck I; Kasperek K; Feinendegen LE; Bremer HJ
Monogr Hum Genet; 1978; 9():114-7. PubMed ID: 732826
[No Abstract] [Full Text] [Related]
19. [Dietary treatment of maple syrup urine diseases].
Guibaud P; de Parscau L; Guffon N; Laval MC
Pediatrie; 1993; 48(10):681-6. PubMed ID: 8015866
[TBL] [Abstract][Full Text] [Related]
20. Ophthalmic findings in maple syrup urine disease.
Burke JP; O'Keefe M; Bowell R; Naughten ER
Metab Pediatr Syst Ophthalmol (1985); 1991; 14(1):12-5. PubMed ID: 1921719
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
