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11. Congenital ichthyosis preceding neurologic symptoms in two sibs with type 2 Gaucher disease. Fujimoto A; Tayebi N; Sidransky E Am J Med Genet; 1995 Nov; 59(3):356-8. PubMed ID: 8599361 [TBL] [Abstract][Full Text] [Related]
12. [Principles of diagnosis and the clinical course of 8 cases of Gaucher's disease (beta-glucocerebrosidase deficiency)]. Tylki-Szymańska A; Maciejko D; Rujner J; Goryluk B; Pronicka E Pediatr Pol; 1987 Jan; 62(1):9-18. PubMed ID: 3615053 [No Abstract] [Full Text] [Related]
13. New perspectives in type 2 Gaucher disease. Sidransky E Adv Pediatr; 1997; 44():73-107. PubMed ID: 9265968 [No Abstract] [Full Text] [Related]
14. [Gaucher disease in childhood]. Levrat V; Forest I; Fouilhoux A; Guffon N Rev Med Interne; 2007 Oct; 28 Suppl 2():S183-6. PubMed ID: 18228686 [TBL] [Abstract][Full Text] [Related]
15. Non-neuronopathic Gaucher disease due to saposin C deficiency. Tylki-Szymańska A; Czartoryska B; Vanier MT; Poorthuis BJ; Groener JA; Ługowska A; Millat G; Vaccaro AM; Jurkiewicz E Clin Genet; 2007 Dec; 72(6):538-42. PubMed ID: 17919309 [TBL] [Abstract][Full Text] [Related]
16. South African variants of Gaucher disease. Goldblatt J; Beighton P Prog Clin Biol Res; 1982; 95():95-106. PubMed ID: 7122645 [No Abstract] [Full Text] [Related]
17. Variant Gaucher disease characterized by dysmorphic features, absence of cardiovascular involvement, laryngospasm, and compound heterozygosity for a novel mutation (D409H/C16S). Bodamer OA; Church HJ; Cooper A; Wraith JE; Scott CR; Scaglia F Am J Med Genet; 2002 May; 109(4):328-31. PubMed ID: 11992489 [TBL] [Abstract][Full Text] [Related]