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5. [Mitochondrial encephalomyopathies and West's syndrome: a frequently underdiagnosed association]. Blanco-Barca O; Pintos-Martínez E; Alonso-Martín A; Escribano-Rey MD; Campos-González Y; Arenas-Barbero J; Eirís-Puñal J; Castro-Gago M Rev Neurol; 2004 Oct 1-15; 39(7):618-23. PubMed ID: 15490346 [TBL] [Abstract][Full Text] [Related]
6. Detection of the carrier state of Hurler's syndrome by assay of alpha-L-iduronidase in leukocytes. Dulaney JT; Milunsky A; Moser HW Clin Chim Acta; 1976 Jun; 69(2):305-10. PubMed ID: 819189 [TBL] [Abstract][Full Text] [Related]
8. [West's syndrome associated with inversion duplication of chromosome 15]. Cabrera JC; Martí M; Toledo L; Giné R; Vázquez C Rev Neurol; 1998 Jan; 26(149):77-9. PubMed ID: 9533212 [TBL] [Abstract][Full Text] [Related]
9. [Case of early hydrocephalus in mucopolysaccharidosis type 1]. Roussey M; Le Marec B; Faivre J; Gandon Y; Le Gall JY; Senecal J Pediatrie; 1983 Jun; 38(4):243-8. PubMed ID: 6413948 [TBL] [Abstract][Full Text] [Related]
11. Cord-blood transplants from unrelated donors in patients with Hurler's syndrome. Staba SL; Escolar ML; Poe M; Kim Y; Martin PL; Szabolcs P; Allison-Thacker J; Wood S; Wenger DA; Rubinstein P; Hopwood JJ; Krivit W; Kurtzberg J N Engl J Med; 2004 May; 350(19):1960-9. PubMed ID: 15128896 [TBL] [Abstract][Full Text] [Related]
12. Enzyme measurements of hair follicles in the study of some inborn erros of metabolism, with particular reference to Hurler's disease. Gibbs DA Ann Clin Biochem; 1977 May; 14(3):157-60. PubMed ID: 405918 [No Abstract] [Full Text] [Related]
17. Computerized tomography in the study of West's syndrome. Gastaut H; Gastaut JL; Régis H; Bernard R; Pinsard N; Saint-Jean M; Roger J; Dravet C Dev Med Child Neurol; 1978 Feb; 20(1):21-7. PubMed ID: 640253 [TBL] [Abstract][Full Text] [Related]
18. A familial occurrence of a mucopolysaccharidosis: Hurler's or Hunter's syndrome? Bhambhani R; Singh SM; Kuspira J; Muntjewerff N Hum Hered; 1974; 24(2):219-24. PubMed ID: 4213627 [No Abstract] [Full Text] [Related]
19. [Hurler syndrome. Early diagnosis and successful enzyme replacement therapy: a new therapeutic approach. Case report]. Dupont C; El Hachem C; Harchaoui S; Ribault V; Amiour M; Guillot M; Maire I; Froissart R; Guffon-Fouilhoux N Arch Pediatr; 2008 Jan; 15(1):45-9. PubMed ID: 18162380 [TBL] [Abstract][Full Text] [Related]
20. Benign myoclonus of early infancy: an imitator of West's syndrome. Maydell BV; Berenson F; Rothner AD; Wyllie E; Kotagal P J Child Neurol; 2001 Feb; 16(2):109-12. PubMed ID: 11292215 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]