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.
3. [Clinical, ultrastructural and biochemical study of a case of GM1 type 2 gangliosidosis]. Mammelle JC; Vanier MT; Baraton G; Gilly J; Carrier H; Guichard Y; Richard A; Gilly R Arch Fr Pediatr; 1975 Dec; 32(10):925-39. PubMed ID: 821451 [TBL] [Abstract][Full Text] [Related]
4. Type III (chronic) GM1-gangliosidosis. Histochemical and ultrastructural studies of rectal biopsy. Ushiyama M; Ikeda S; Nakayama J; Yanagisawa N; Hanyu N; Katsuyama T J Neurol Sci; 1985 Dec; 71(2-3):209-23. PubMed ID: 3936902 [TBL] [Abstract][Full Text] [Related]
5. A case of chronic GM1 gangliosidosis presenting as dystonia: clinical and biochemical studies. Inui K; Namba R; Ihara Y; Nobukuni K; Taniike M; Midorikawa M; Tsukamoto H; Okada S J Neurol; 1990 Dec; 237(8):491-3. PubMed ID: 2127425 [TBL] [Abstract][Full Text] [Related]
6. [The use of loading tests with labeled GM1-ganglioside for differential diagnosis of GM1-gangliosidosis]. Akhunov VS; Krasnopol'skaia KD; Mirenburg TV Vopr Med Khim; 1989; 35(5):119-22. PubMed ID: 2515652 [TBL] [Abstract][Full Text] [Related]
7. Infantile GM1-gangliosidosis with marked manifestation of lungs. Matsumoto T; Matsumori H; Taki T; Takagi T; Fukuda Y Acta Pathol Jpn; 1979 Mar; 29(2):269-76. PubMed ID: 121907 [TBL] [Abstract][Full Text] [Related]
8. Congenital ascites as a presenting sign of lysosomal storage disease. Gillan JE; Lowden JA; Gaskin K; Cutz E J Pediatr; 1984 Feb; 104(2):225-31. PubMed ID: 6420531 [TBL] [Abstract][Full Text] [Related]
9. Hyperpigmented macules and patches in a patient with GM1 type 1 gangliosidosis. Selsor LC; Lesher JL J Am Acad Dermatol; 1989 May; 20(5 Pt 2):878-82. PubMed ID: 2497160 [TBL] [Abstract][Full Text] [Related]
12. [A case of gangliosidosis GM1 in an infant]. Kordyasz E; Woźniewicz B Pol Tyg Lek; 1988 May 2-9; 43(18-19):608-9. PubMed ID: 3138677 [No Abstract] [Full Text] [Related]
14. Report of an infant with GM1 gangliosidosis type I and extensive and unusual mongolian spots. Weissbluth M; Esterly NB; Caro WA Br J Dermatol; 1981 Feb; 104(2):195-200. PubMed ID: 6783061 [TBL] [Abstract][Full Text] [Related]
15. Manifestation of infantile GM1 gangliosidosis in the fetal eye. An electron microscopic study. Schmitt-Gräff A Graefes Arch Clin Exp Ophthalmol; 1988; 226(1):84-8. PubMed ID: 3125087 [TBL] [Abstract][Full Text] [Related]
16. Hyperphosphatasemia in infantile GM1 gangliosidosis: possible association with microscopic bone marrow osteoblastosis. Mogilner BM; Barak Y; Amitay M; Zlotogora J J Pediatr; 1990 Nov; 117(5):758-61. PubMed ID: 2135166 [No Abstract] [Full Text] [Related]