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26. [Intestinal malabsorption is a genetic defect]. Faustino Porto JA; Mello Sda S; Junqueira A Arq Bras Endocrinol Metabol; 1969 Apr; 18(1):5-23. PubMed ID: 5385773 [No Abstract] [Full Text] [Related]
27. Survey of 336 deaf students for retinitis pigmentosa. Isaeff WB; Niswonger J Ann Ophthalmol; 1981 Oct; 13(10):1131-2. PubMed ID: 7316337 [TBL] [Abstract][Full Text] [Related]
28. [Rare causes of hypoglycemia in adults--disorders of gluconeogenesis and fatty acid oxidation disorders]. Fronczyk A; Romanowska H; Majkowska L Pol Merkur Lekarski; 2011 Feb; 30(176):147-9. PubMed ID: 21544987 [TBL] [Abstract][Full Text] [Related]
29. Ultrastructure and cytochemistry of lymphocytes in the genetic mucopolysaccharidoses. Belcher RW Arch Pathol; 1972 Jan; 93(1):1-7. PubMed ID: 4108493 [No Abstract] [Full Text] [Related]
30. The night-blinding disorders. Carr RE Int Ophthalmol Clin; 1969; 9(4):971-1003. PubMed ID: 4101337 [No Abstract] [Full Text] [Related]
31. [Contribution to the "Refsum's syndrome" retinopathia pigmentosa in hereditary enzymopathy of lipid metabolism]. Bider E Ophthalmologica; 1966; 152(5):356-63. PubMed ID: 4164013 [No Abstract] [Full Text] [Related]
32. [Biochemical aspects of mucopolysaccharidoses and theories concerning their pathogenesis]. Brovelli A; Balduini C; Castellani AA Recenti Prog Med; 1970 Jan; 48(1):19-33. PubMed ID: 4245669 [No Abstract] [Full Text] [Related]
33. [Additional remarks to the work: ocular diencephalo-hypophysary syndrome. (Further clinical findings; pathogenetic deductions. Relations of the syndrome to glaucoma and retinitis pigmentosa, and inferences of a pathogenetic nature)]. Spadavecchia V Boll Ocul; 1966 Jun; 45(6):361-88. PubMed ID: 5964256 [No Abstract] [Full Text] [Related]
36. The long-term evolution of a case of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency associated with deafness and retinitis pigmentosa. Jones KJ; Wilcken B; Kilham H J Inherit Metab Dis; 1997 Nov; 20(6):833-4. PubMed ID: 9427155 [No Abstract] [Full Text] [Related]