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2. Inborn errors of lipid metabolism. Familial hyperlipoproteinaemia type 3. Detection of heterozygotes. Sobra J; Heyrovský A Rev Czech Med; 1972; 18(1):34-9. PubMed ID: 5022312 [No Abstract] [Full Text] [Related]
3. [Asymptomatic familial hypolipoproteinemia involving mainly beta-lipoproteins revealed during the study of an isolated proteinuria]. Richet G; Durepaire H; Hartmann L; Ollier MP; Polonovski J; Maitrot B Presse Med (1893); 1969 Dec; 77(54):2045-8. PubMed ID: 5378461 [No Abstract] [Full Text] [Related]
4. [Inborn errors of lipid metabolism. XIX. Basic principles of complex therapy of hyperlipoproteinemias]. Sobra J Cas Lek Cesk; 1970 May; 109(21):457-63. PubMed ID: 4987971 [No Abstract] [Full Text] [Related]
5. Diagnosis of glycosphingolipidoses by urinary-sediment analysis. Desnick RJ; Dawson G; Desnick SJ; Sweeley CC; Krivit W N Engl J Med; 1971 Apr; 284(14):739-44. PubMed ID: 5548035 [No Abstract] [Full Text] [Related]
6. "The case of the yellow palms" and other syndromes in need of detection. Fredrickson DS Med Ann Dist Columbia; 1967 Apr; 36(4):207-11. PubMed ID: 5232847 [No Abstract] [Full Text] [Related]
7. [Inborn errors and lipid metabolism. XXV. Familial hyperlipoproteinemia of the type 3--detection of heterozygotes]. Sobra J; Heyrovský A Cas Lek Cesk; 1972; 111(8):192-5. PubMed ID: 5010330 [No Abstract] [Full Text] [Related]
8. [Hereditary disorders of lipid metabolism. Screening of lipids]. Adriaenssens K Maandschr Kindergeneeskd; 1969 Jun; 37(1):17-27. PubMed ID: 4307104 [No Abstract] [Full Text] [Related]
10. [Studies on primary hyperlipoproteinemia. II. Diagnosis and classification]. Ciświcka-Sznajderman M Pol Arch Med Wewn; 1971 May; 46(5):571-6. PubMed ID: 5566929 [No Abstract] [Full Text] [Related]
11. Leukocyte beta-galactosidase activity in the diagnosis of generalized GM 1 gangliosidosis. Singer HS; Nankervis GA; Schafer IA Pediatrics; 1972 Mar; 49(3):352-61. PubMed ID: 4258708 [No Abstract] [Full Text] [Related]
12. Typing of hyperlipoproteinaemias. Rifkind B Atherosclerosis; 1970; 11(3):545-6. PubMed ID: 5433092 [No Abstract] [Full Text] [Related]
13. Gene loci for the skin and their chromosomal positions. Renwick JH J Invest Dermatol; 1973 Jun; 60(6):403-6. PubMed ID: 4200220 [No Abstract] [Full Text] [Related]
14. [Physiopathology and clinical aspects of lipid metabolism disorders. Clinical aspects and therapy of primary hyperlipoproteinemias]. Haller H; Hanefeld M; Leonhardt W Dtsch Gesundheitsw; 1971 Sep; 26(37):1721-6. PubMed ID: 5122707 [No Abstract] [Full Text] [Related]
15. Evaluation of lipid disorders by lipoprotein electrophoresis. Wilson WB J Miss State Med Assoc; 1971 Jun; 12(6):287-96. PubMed ID: 5132294 [No Abstract] [Full Text] [Related]
16. Fabry's disease with hypogammaglobulinemia and without angiokeratomas. Urbain G; Philippart M; Peremans J Arch Intern Med; 1969 Jul; 124(1):72-6. PubMed ID: 5791489 [No Abstract] [Full Text] [Related]
17. Classification and features of the lipidoses affecting the nervous system. Fredrickson DS Pathol Eur; 1968; 3(2):121-42. PubMed ID: 4235064 [No Abstract] [Full Text] [Related]