162 related articles for article (PubMed ID: 5095277)
1. Leucine equivalency system in managing branched chain ketoaciduria.
Smith BA; Waisman HA
J Am Diet Assoc; 1971 Oct; 59(4):342-6. PubMed ID: 5095277
[No Abstract] [Full Text] [Related]
2. [On the clinical picture and pathological anatomy of the maple syrup disease ("branded chain ketoaciduria"). Report on 2 cases in 1 family].
Sander C; Clotten R; Noetzel H; Wehinger H
Dtsch Med Wochenschr; 1968 May; 93(18):895-903 passim. PubMed ID: 5650843
[No Abstract] [Full Text] [Related]
3. M aple syrup urine disease. A review with a report of an additional case.
Schwartz JF; Kolendrianos ET
Dev Med Child Neurol; 1969 Aug; 11(4):460-70. PubMed ID: 5805351
[No Abstract] [Full Text] [Related]
4. Plasma amino acid analyses in two cases of maple syrup urine disease.
Surarit R; Srisomsap C; Wasant P; Svasti J; Suthatvoravut U; Chokchaichamnankit D; Liammongkolkul S
Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():138-9. PubMed ID: 11400750
[TBL] [Abstract][Full Text] [Related]
5. [Dietetics in hereditary enzyme deficiencies].
Royer P
Sem Hop; 1970 Feb; 46(10):653-9. PubMed ID: 4314674
[No Abstract] [Full Text] [Related]
6. Dietary treatment of maple sirup urine disease (branched-chain ketoaciduria).
Noel MB; Stanley PB; Girz JC; Allen RJ
J Am Diet Assoc; 1976 Jul; 69(1):62-8. PubMed ID: 932376
[No Abstract] [Full Text] [Related]
7. Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female.
Fischer MH; Gerritsen T
Pediatrics; 1971 Nov; 48(5):795-801. PubMed ID: 5125877
[No Abstract] [Full Text] [Related]
8. [Disorders of leucine, isoleucine and valine metabolism (maple syrup urine disease)].
Vulović D; Vilhar N; Hajduković R; Marjanović B; Stojanović Lj
Srp Arh Celok Lek; 1975 May; 103(5):419-36. PubMed ID: 1188483
[No Abstract] [Full Text] [Related]
9. DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).
WESTALL RG
Arch Dis Child; 1963 Oct; 38(201):485-91. PubMed ID: 14065992
[No Abstract] [Full Text] [Related]
10. A new variant of maple syrup urine disease (branched chain ketoaciduria). Clinical and biochemical evaluation.
Schulman JD; Lustberg TJ; Kennedy JL; Museles M; Seegmiller JE
Am J Med; 1970 Jul; 49(1):118-24. PubMed ID: 5431474
[No Abstract] [Full Text] [Related]
11. Multiple exchange transfusions as treatment during the acute period in maple syrup urine disease.
Schuchmann L; Witt I; Schulz P; Schumacher H; Rüdiger H
Helv Paediatr Acta; 1972 Sep; 27(4):449-56. PubMed ID: 4644280
[No Abstract] [Full Text] [Related]
12. Clinical consequences of disorders in the intermediate metabolism of branched chain amino acids (valine, leucine and isoleucine).
Mogoş T; Cheţa CP; Mincu IT
Rom J Intern Med; 1994; 32(1):57-61. PubMed ID: 8081313
[TBL] [Abstract][Full Text] [Related]
13. [Compliance of the diet restricted with leucine, isoleucine and valine in maple syrup urine disease (MSUD) children].
Kowalik A; Narojek L; Sykut-Cegielska J
Rocz Panstw Zakl Hig; 2007; 58(1):95-101. PubMed ID: 17711097
[TBL] [Abstract][Full Text] [Related]
14. [CLINICAL, BIOCHEMICAL, AND NEUROPATHOLOGIC ASPECTS OF MAPLE SYRUP URINE DISEASE. A KETOACIDURIA OF THE OPEN CHAIN AMINOACIDS LEUCINE, ISOLEUCINE AND VALINE].
SILBERMANSCHWARTZMAN J
An Fac Med Lima; 1963 Sep; 46():339-65. PubMed ID: 14122039
[No Abstract] [Full Text] [Related]
15. The therapy of maple syrup urine disease.
Snyderman SE
Am J Dis Child; 1967 Jan; 113(1):68-73. PubMed ID: 6015908
[No Abstract] [Full Text] [Related]
16. [Long-term dietetic treatment of valine-leucinuria (maple syrup urine disease)].
Schmidt GW
Z Kinderheilkd; 1967; 99(4):273-88. PubMed ID: 5586379
[No Abstract] [Full Text] [Related]
17. [MAPLE SYRUP URINE DISEASE].
TIMMERMANS J
Maandschr Kindergeneeskd; 1963 Oct; 31():337-47. PubMed ID: 14100237
[No Abstract] [Full Text] [Related]
18. [Studies on "branched chain oxoacid aciduria" (maple syrup diseases)].
Goedde HW; Blume KG; Möhlenbeck F; Rotthauwe HW; Simon HA; Lang K
Med Klin; 1966 Dec; 61(52):2063-7. PubMed ID: 4385693
[No Abstract] [Full Text] [Related]
19. [Hereditary metabolic diseases: maple syrup disease].
Berger R; Broyer M
Presse Med (1893); 1968 Jul; 76(30):1531-2. PubMed ID: 5686194
[No Abstract] [Full Text] [Related]
20. [Attempted diet therapy of a case of maple syrup disease].
Mainardi PC; Antener I
Pediatria (Napoli); 1970 Jul; 78(3):540-60. PubMed ID: 5474982
[No Abstract] [Full Text] [Related]
[Next] [New Search]
