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Similar articles for PubMed (Select 7906450)

1.

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.

PMID:
7906450
2.

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.

PMID:
6783061
4.

Beta-galactosidase-deficient mouse as an animal model for GM1-gangliosidosis.

Matsuda J, Suzuki O, Oshima A, Ogura A, Noguchi Y, Yamamoto Y, Asano T, Takimoto K, Sukegawa K, Suzuki Y, Naiki M.

Glycoconj J. 1997 Sep;14(6):729-36.

PMID:
9337086
5.

Intrauterine growth retardation and placental vacuolization as presenting features in a case of GM1 gangliosidosis.

Brunetti-Pierri N, Mian A, Luetchke R, Graham BH.

J Inherit Metab Dis. 2007 Oct;30(5):823. Epub 2007 Aug 22.

PMID:
17712606
6.

Diagnosis of feline GM1 gangliosidosis by enzyme assay of cultured conjunctival cells.

Nowakowski RW, Thompson JN, Baker HJ.

Invest Ophthalmol Vis Sci. 1988 Mar;29(3):487-90.

PMID:
3125124
7.

Extensive and unusual Mongolian blue spots in a child with GM1 gangliosidosis type one.

Beattie RM, Harvey D.

J R Soc Med. 1992 Sep;85(9):574-5. No abstract available.

8.

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 31;140(3):223-30.

PMID:
6432371
9.

Extensive Mongolian spots: a clinical sign merits special attention.

Ashrafi MR, Shabanian R, Mohammadi M, Kavusi S.

Pediatr Neurol. 2006 Feb;34(2):143-5.

PMID:
16458829
10.

[The role of ophthalmological examination in the diagnosis of gangliosidosis GM1].

Krzywińska-Zdeb E, Gizewska M, Modrzejewska M, Romanowska H, Stecewicz I, Pawłowska A, Tuziak M, Walczak M.

Klin Oczna. 2011;113(7-9):266-9. Polish.

PMID:
22256571
11.

Neuroimaging findings in infantile GM1 gangliosidosis.

Erol I, Alehan F, Pourbagher MA, Canan O, Vefa Yildirim S.

Eur J Paediatr Neurol. 2006 Sep-Nov;10(5-6):245-8. Epub 2006 Oct 17.

PMID:
17052929
12.
13.

Molecular form and subcellular distribution of acid beta-galactosidase in fibroblasts from patients with GM1 gangliosidosis, Morquio B disease and galactosialidosis.

Takiyama N, Itoh K, Shimmoto M, Nishimoto J, Inui K, Sakuraba H, Suzuki Y.

Brain Dev. 1997 Mar;19(2):126-30.

PMID:
9105659
14.

Mongolian spots and GM1 gangliosidosis type one.

Leung AK, Robson WL.

J R Soc Med. 1993 Feb;86(2):120-1. No abstract available.

15.
16.

The potential action of galactose as a "chemical chaperone": increase of beta galactosidase activity in fibroblasts from an adult GM1-gangliosidosis patient.

Caciotti A, Donati MA, d'Azzo A, Salvioli R, Guerrini R, Zammarchi E, Morrone A.

Eur J Paediatr Neurol. 2009 Mar;13(2):160-4. doi: 10.1016/j.ejpn.2008.03.004. Epub 2008 Jun 20.

PMID:
18571950
17.

Transient high-level expression of beta-galactosidase after transfection of fibroblasts from GM1 gangliosidosis patients with plasmid DNA.

Balestrin RC, Baldo G, Vieira MB, Sano R, Coelho JC, Giugliani R, Matte U.

Braz J Med Biol Res. 2008 Apr;41(4):283-8.

18.

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.

PMID:
6777095
19.

Myelination arrest demonstrated using magnetic resonance imaging in a child with type I GM1 gangliosidosis.

Shen WC, Tsai FJ, Tsai CH.

J Formos Med Assoc. 1998 Apr;97(4):296-9.

PMID:
9585685
20.

Identification of a novel pseudodeficiency allele in the GLB1 gene in a carrier of GM1 gangliosidosis.

Gort L, Santamaria R, Grinberg D, Vilageliu L, Chabás A.

Clin Genet. 2007 Aug;72(2):109-11.

PMID:
17661814
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