164 related articles for article (PubMed ID: 6783061)
1. 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]
2. 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]
3. Angiokeratoma corporis diffusum in GM1 gangliosidosis, type 1.
Beratis NG; Varvarigou-Frimas A; Beratis S; Sklower SL
Clin Genet; 1989 Jul; 36(1):59-64. PubMed ID: 2504516
[TBL] [Abstract][Full Text] [Related]
4. A case of type 2 Gm1-gangliosidosis with long survival.
Kikuchi K; Minami R; Kudoh T; Nakao T; Tsugawa S
Brain Dev; 1982; 4(2):153-6. PubMed ID: 6807121
[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. GM1-Gangliosidosis: a molecular abnormality of acid beta-galactosidase in fibroblasts.
Furuya T; Suzuki Y
J Inherit Metab Dis; 1984; 7(3):145-6. PubMed ID: 6438402
[No Abstract] [Full Text] [Related]
7. Chronic GM1 gangliosidosis presenting as dystonia: II. Biochemical studies.
Kobayashi T; Suzuki K
Ann Neurol; 1981 May; 9(5):476-83. PubMed ID: 6791575
[TBL] [Abstract][Full Text] [Related]
8. Mongolian spots associated with cleft lip.
Kurata S; Ohara Y; Itami S; Inoue Y; Ichikawa H; Takayasu S
Br J Plast Surg; 1989 Nov; 42(6):625-7. PubMed ID: 2605396
[TBL] [Abstract][Full Text] [Related]
9. GM1-gangliosidosis type 1 involving the cutaneous vascular endothelial cells in a black infant with multiple ectopic Mongolian spots.
Tang TT; Esterly NB; Lubinsky MS; Oechler HW; Harb JM; Franciosi RA
Acta Derm Venereol; 1993 Dec; 73(6):412-5. PubMed ID: 7906450
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. A case of GM1-gangliosidosis type I: glycosphingolipid profiles of urine and transformed lymphocytes and beta-D-galactosidase activities in peripheral lymphocytes, cultured skin fibroblasts and transformed lymphocytes.
Asano K; Shindo N; Nakasuji M; Inamori K; Ohta M; Matsushita T; Yamaguchi M; Oshima M
Jpn J Exp Med; 1990 Apr; 60(2):73-9. PubMed ID: 2117086
[TBL] [Abstract][Full Text] [Related]
12. Application of a GM1 ganglioside beta-galactosidase microassay method to diagnosis of GM1 gangliosidosis.
Mutoh T; Kiuchi K; Sobue I; Naoi M
Clin Chim Acta; 1984 Jul; 140(3):223-30. PubMed ID: 6432371
[TBL] [Abstract][Full Text] [Related]
13. Cherry-red spot, optic atrophy and corneal cloudings in a patient suffering from GM1 gangliosidosis type I.
Sorcinelli R; Sitzia A; Loi M
Metab Pediatr Syst Ophthalmol (1985); 1987; 10(3):62-3. PubMed ID: 3123871
[TBL] [Abstract][Full Text] [Related]
14. Detection of generalised GM1-gangliosidosis.
Wiederschain G
Lancet; 1980 Apr; 1(8173):881-2. PubMed ID: 6103241
[No Abstract] [Full Text] [Related]
15. Adult GM1 gangliosidosis: clinical and biochemical studies on two patients and comparison to other patients called variant or adult GM1 gangliosidosis.
Wenger DA; Sattler M; Mueller OT; Myers GG; Schneiman RS; Nixon GW
Clin Genet; 1980 May; 17(5):323-34. PubMed ID: 6777095
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [GM1 gangliosidosis, type I, Landing's disease. Presentation of a case and review of the literature].
Alonso Falcón F; López-Herce J
An Esp Pediatr; 1984 Feb; 20(2):139-45. PubMed ID: 6424522
[TBL] [Abstract][Full Text] [Related]
18. Infantile sialidosis: a phenocopy of type 1 GM1 gangliosidosis distinguished by genetic complementation and urinary oligosaccharides.
Gravel RA; Lowden JA; Callahan JW; Wolfe LS; Ng Yin Kin NM
Am J Hum Genet; 1979 Nov; 31(6):669-79. PubMed ID: 117700
[TBL] [Abstract][Full Text] [Related]
19. Combined sialidase (neuraminidase) and beta-galactosidase deficiency. Clinical, morphological and enzymological observations in a patient.
Loonen MC; Reuser AJ; Visser P; Arts WF
Clin Genet; 1984 Aug; 26(2):139-49. PubMed ID: 6432381
[TBL] [Abstract][Full Text] [Related]
20. A case of GM1 gangliosidosis type I.
Cabral A; Portela R; Tasso T; Eusébio F; Moreira A; dos Santos HM; Soares J; Moura-Nunes JF
Ophthalmic Paediatr Genet; 1989 Mar; 10(1):63-7. PubMed ID: 2500629
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
