94 related articles for article (PubMed ID: 612752)
1. [Blue diaper syndrome].
Tada K
Nihon Rinsho; 1977; 35 Suppl 1():1116-7. PubMed ID: 612752
[No Abstract] [Full Text] [Related]
2. [Blue diaper syndrome].
Takita H
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):574-5. PubMed ID: 9645138
[No Abstract] [Full Text] [Related]
3. [Tryptophan metabolism in screening metabolic diseases of the newborn].
Chiancone FM; Mainardi L; Tenconi LT
Acta Vitaminol Enzymol; 1973; 27(5):211-5. PubMed ID: 4274937
[No Abstract] [Full Text] [Related]
4. THE BLUE DIAPER SYNDROME: FAMILIAL HYPERCALCEMIA WITH NEPHROCALCINOSIS AND INDICANURIA; A NEW FAMILIAL DISEASE, WITH DEFINITION OF THE METABOLIC ABNORMALITY.
DRUMMOND KN; MICHAEL AF; ULSTROM RA; GOOD RA
Am J Med; 1964 Dec; 37():928-48. PubMed ID: 14246093
[No Abstract] [Full Text] [Related]
5. [Disorders of tryptophan metabolism in dermatology].
Jouve I; Berbis P; Garnier JP; Privat Y
Ann Dermatol Venereol; 1987; 114(12):1571-82. PubMed ID: 3328548
[No Abstract] [Full Text] [Related]
6. [Aminoacid metabolism disorders in infancy with special reference to phenylketonuria. II. Aminoacid metabolism and general physiopathology of aminoacidopathies].
Segni G
Minerva Nipiol; 1970; 20(4):83-110. PubMed ID: 4396023
[No Abstract] [Full Text] [Related]
7. Hartnup syndrome.
WOOLF LI
Bull Schweiz Akad Med Wiss; 1962 Jan; 17():377-81. PubMed ID: 14008282
[No Abstract] [Full Text] [Related]
8. [Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer].
Boisse J; Moatti N
Ann Biol Clin (Paris); 1973; 31(4):249-55. PubMed ID: 4579284
[No Abstract] [Full Text] [Related]
9. Newer trends in the genetic and biochemical studies in the etiopathogenesis of aminoacidopathies.
Nair KR; Virmani V
Neurol India; 1973 Sep; 21(3):128-36. PubMed ID: 4784816
[No Abstract] [Full Text] [Related]
10. [THE "BLUE DIAPER" SYNDROME].
BICKEL H
Dtsch Med Wochenschr; 1965 May; 90():929-30. PubMed ID: 14278087
[No Abstract] [Full Text] [Related]
11. The ocular abnormalities of blue diaper syndrome.
Chen Y; Wu L; Xiong Q
Metab Pediatr Syst Ophthalmol (1985); 1991; 14(3-4):73-5. PubMed ID: 1818237
[TBL] [Abstract][Full Text] [Related]
12. [Metabolic disorders, their early diagnosis and therapy in newborn infants].
Tabolin VA
Vestn Akad Med Nauk SSSR; 1973; 28(6):76-86. PubMed ID: 4729650
[No Abstract] [Full Text] [Related]
13. Factors which alter the metabolism of tryptophan.
Price JM
Med J Osaka Univ; 1968 Sep; 19(1):31-3. PubMed ID: 4886324
[No Abstract] [Full Text] [Related]
14. Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited disease.
Vaca G; Hernández A; Ibarra B; Velázquez A; Olivares N; Sanchez-Corona J; Medina C; Cantú JM
Arch Invest Med (Mex); 1981; 12(3):341-8. PubMed ID: 7294941
[TBL] [Abstract][Full Text] [Related]
15. [B6-dependent xanthurenic aciduria].
Tada K; Yokoyama Y
Tanpakushitsu Kakusan Koso; 1968 Apr; 13(4):311-8. PubMed ID: 5749458
[No Abstract] [Full Text] [Related]
16. [Inborn errors of amino acid metabolism].
Owada M
Ryoikibetsu Shokogun Shirizu; 1995; (8):352-7. PubMed ID: 8581651
[No Abstract] [Full Text] [Related]
17. [Diseases caused by altered intermediate metabolism of amino acids].
Bulgarelli R; Berio A
Minerva Nipiol; 1969; 19(6):328-61 contd. PubMed ID: 4923874
[No Abstract] [Full Text] [Related]
18. American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism.
Pediatrics; 1976 May; 57(5):783-92. PubMed ID: 940719
[TBL] [Abstract][Full Text] [Related]
19. [Acute metabolic critical conditions in hereditary metabolic diseases].
von Döbeln U; Larsson A; Hagenfeldt L
Lakartidningen; 1989 Aug; 86(35):2849-50. PubMed ID: 2796465
[No Abstract] [Full Text] [Related]
20. [Abnormalities of the tryptophan metabolism in trisomy 21].
Jérôme H
Union Med Can; 1968 Jul; 97(7):929-35. PubMed ID: 5709534
[No Abstract] [Full Text] [Related]
[Next] [New Search]