These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
70 related articles for article (PubMed ID: 17978300)
41. Protean appearances of immunodeficiencies: syndromes and inborn errors involving other systems which express associated primary immunodeficiency. Hitzig WH Birth Defects Orig Artic Ser; 1983; 19(3):307-12. PubMed ID: 6360243 [TBL] [Abstract][Full Text] [Related]
42. Mevalonate kinase deficiency nomenclature. Stoffels M; van der Meer JW; Simon A Rheumatol Int; 2014 Feb; 34(2):295-6. PubMed ID: 23921621 [No Abstract] [Full Text] [Related]
43. Mevalonate kinase deficiency in a dizygotic twin with mild mevalonic aciduria. Gibson KM; Hoffmann GF; Sweetman L; Buckingham B J Inherit Metab Dis; 1997 Jul; 20(3):391-4. PubMed ID: 9266363 [No Abstract] [Full Text] [Related]
44. Segregation of the N301T mutation in the family of the index patient with mevalonate kinase deficiency. Goebel-Schreiner B; Schreiner R; Hoffmann GF; Gibson KM J Inherit Metab Dis; 1995; 18(2):197-200. PubMed ID: 7564245 [No Abstract] [Full Text] [Related]
45. Ethanolaminuria; an obscure metabolic defect associated with a case of primary hepatoma. DENT CE; FOWLER DI; WALSHE JM Biochem J; 1951 Jan; 48(1):xiii-iv. PubMed ID: 14820809 [No Abstract] [Full Text] [Related]
46. Primary carcinoma of the liver: description of a case with ethanolaminuria, a new and obscure metabolic defect. DENT CE; WALSHE JM Br J Cancer; 1953 Jun; 7(2):166-80. PubMed ID: 13081898 [No Abstract] [Full Text] [Related]
51. [Identification of the gene for hyper-IgD syndrome: a model of modern genetics]. Drenth JP; Waterham HR; Kuis W; Houten SM; Frenkel J; Wanders RJ; Poll-The BT; van der Meer JW Ned Tijdschr Geneeskd; 2000 Apr; 144(17):782-5. PubMed ID: 10800545 [TBL] [Abstract][Full Text] [Related]