188 related articles for article (PubMed ID: 5557172)
1. Ocular manifestations of familial hyperlysinemia.
Smith TH; Holland MG; Woody NC
Trans Am Acad Ophthalmol Otolaryngol; 1971; 75(2):355-60. PubMed ID: 5557172
[No Abstract] [Full Text] [Related]
2. Ocular manifestations in aminoacidopathies.
François J
Adv Ophthalmol; 1972; 25():28-103. PubMed ID: 4560371
[No Abstract] [Full Text] [Related]
3. Excretion of hypusine by children and by patients with familial hyperlysinemia.
Woody NC; Pupene MB
Pediatr Res; 1973 Dec; 7(12):994-5. PubMed ID: 4753051
[No Abstract] [Full Text] [Related]
4. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease].
Raven EJ
Ned Tijdschr Geneeskd; 1969 Oct; 113(42):1850-3. PubMed ID: 5344645
[No Abstract] [Full Text] [Related]
5. [Hereditary persistant hyperlysinemia].
Petrović Lj; Milosević P
Srp Arh Celok Lek; 1977 Jun; 105(6):539-42. PubMed ID: 607472
[No Abstract] [Full Text] [Related]
6. [Familial hyperlysinemia with mental retardation, convulsion & muscular hypertonia (author's transl)].
Kobayashi T; Ueno E; Fujita T; Yanagisawa N; Tsukagoshi H
Rinsho Shinkeigaku; 1977 Sep; 17(9):600-8. PubMed ID: 923176
[No Abstract] [Full Text] [Related]
7. Hyperlysinemia associated with retardation.
Ghadimi H; Binnington VI; Pecora P
N Engl J Med; 1965 Sep; 273(14):723-9. PubMed ID: 5825685
[No Abstract] [Full Text] [Related]
8. A case of hyperlysinemia: biochemical and clinical observations.
Armstrong MD; Robinow M
Pediatrics; 1967 Apr; 39(4):546-54. PubMed ID: 6022933
[No Abstract] [Full Text] [Related]
9. Chemical pathology of amino acid diseases.
Carson NA
Acta Neurol Psychiatr Belg; 1968 Apr; 68(4):231-44. PubMed ID: 4972604
[No Abstract] [Full Text] [Related]
10. Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
Martin VA; Carson NA
Trans Ophthalmol Soc U K (1962); 1967; 87():847-70. PubMed ID: 5255262
[No Abstract] [Full Text] [Related]
11. [A patient with persistent hyperlysinemia].
Sengers RC; Trijbels JM; Corstiaensen JB
Tijdschr Kindergeneeskd; 1983 Feb; 51(1):24-6. PubMed ID: 6407142
[TBL] [Abstract][Full Text] [Related]
12. [Familial essential hyperprolinemia].
Hainaut H; Hariga J; Willems C; Heusden A; Chapelle P
Presse Med (1893); 1971 Apr; 79(21):945-8. PubMed ID: 5580522
[No Abstract] [Full Text] [Related]
13. [Ocular complications of congenital metabolism errors].
Goux JP; Kallay O
Bull Soc Belge Ophtalmol; 1971; 157(1):9-322. PubMed ID: 5565533
[No Abstract] [Full Text] [Related]
14. [Feeble mindedness caused by genetic disorders of amino acid metabolism].
Menne F
Hippokrates; 1968 May; 39(10):357-67. PubMed ID: 4886426
[No Abstract] [Full Text] [Related]
15. [Phaenotypic aspects of hereditary aminoacidopathies (author's transl)].
Becker K
Monatsschr Kinderheilkd; 1981 Oct; 129(10):556-63. PubMed ID: 6801479
[TBL] [Abstract][Full Text] [Related]
16. Multiple enzyme defects in familial hyperlysinemia.
Dancis J; Hutzler J; Woody NC; Cox RP
Pediatr Res; 1976 Jul; 10(7):686-91. PubMed ID: 934735
[TBL] [Abstract][Full Text] [Related]
17. [Familial hyperprolinemia with nephropathy].
Ortuño Mirete J; Guardiola Vicente JM; Botella García J
Rev Clin Esp; 1970 Jul; 118(2):141-50. PubMed ID: 5486371
[No Abstract] [Full Text] [Related]
18. [Disorders of amino acids].
Aoki K
Nihon Rinsho; 1993 Jan; 51 Suppl():332-9. PubMed ID: 8459561
[No Abstract] [Full Text] [Related]
19. [Maple syrup urine disease].
Rokkones T
Tidsskr Nor Laegeforen; 1970 Jan; 90(2):239-42. PubMed ID: 5430195
[No Abstract] [Full Text] [Related]
20. Ocular pathology in homocystinuria.
Henkind P; Ashton N
Trans Ophthalmol Soc U K (1962); 1965; 85():21-38. PubMed ID: 5227183
[No Abstract] [Full Text] [Related]
[Next] [New Search]
