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Items: 1 to 20 of 25

1.

Protein measurement with the Folin phenol reagent.

LOWRY OH, ROSEBROUGH NJ, FARR AL, RANDALL RJ.

J Biol Chem. 1951 Nov;193(1):265-75. No abstract available.

2.

Tay-Sachs' disease with visceral involvement and its relationship to Niemann-Pick's disease.

NORMAN RM, URICH H, TINGEY AH, GOODBODY RA.

J Pathol Bacteriol. 1959 Oct;78:409-21. No abstract available.

PMID:
14427628
3.

GENERALIZED GANGLIOSIDOSIS: ANOTHER INBORN ERROR OF GANGLIOSIDE METABOLISM?

O'BRIEN JS, STERN MB, LANDING BH, O'BRIEN JK, DONNELL GN.

Am J Dis Child. 1965 Apr;109:338-46. No abstract available.

PMID:
14261015
4.
5.

The assay of arylsulphatases A and B in human urine.

BAUM H, DODGSON KS, SPENCER B.

Clin Chim Acta. 1959 May;4(3):453-5. No abstract available.

PMID:
13663253
6.
7.

Generalized gangliosidosis: beta-galactosidase deficiency.

Okada S, O'Brien JS.

Science. 1968 May 31;160(3831):1002-4.

PMID:
5647842
8.

Two types of ribosome in mouse-hamster hybrid cells.

Stanners CP, Eliceiri GL, Green H.

Nat New Biol. 1971 Mar 10;230(10):52-4. No abstract available.

PMID:
5279808
9.

Automated assay of hexosaminidases in serum.

Lowden JA, Skomorowski MA, Henderson F, Kaback M.

Clin Chem. 1973 Dec;19(12):1345-9. No abstract available.

10.

Juvenile GM1 gangliosidosis. Occurrence with absence of two beta-galactosidase components.

Lowden JA, Callahan JW, Norman MG, Thain M, Prichard JS.

Arch Neurol. 1974 Sep;31(3):200-3. No abstract available.

PMID:
4368854
11.

The structures of oligosaccharides accumulating in the liver of G-M1-gangliosidosis, type I.

Wolfe LS, Senior RG, Ng-Ying-Kin NM.

J Biol Chem. 1974 Mar 25;249(6):1828-38. No abstract available.

12.

Localized beta-galactosidase deficiency. Occurrence in cerebellar ataxia with myoclonus epilepsy and macular cherry-red spot--a new variant of GM1-gangliosidosis?

Yamamoto A, Adachi S, Kawamura S, Takahashi M, Kitani T.

Arch Intern Med. 1974 Oct;134(4):627-34. No abstract available.

PMID:
4278184
14.

Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.

Derry DM, Fawcett JS, Andermann F, Wolfe LS.

Neurology. 1968 Apr;18(4):340-8. No abstract available.

PMID:
4173446
15.

Structure of nine sialyl-oligosaccharides accumulated in urine of eleven patients with three different types of sialidosis. Mucolipidosis II and two new types of mucolipidosis.

Strecker G, Peers MC, Michalski JC, Hondi-Assah T, Fournet B, Spik G, Montreuil J, Farriaux JP, Maroteaux P, Durand P.

Eur J Biochem. 1977 May 16;75(2):391-403. No abstract available.

16.

Characterization of oligosaccharides and glycopeptides excreted in the urine of GMl-gangliosidosis patients.

Ng-Ying-Kin NM, Wolfe LS.

Biochem Biophys Res Commun. 1975 Sep 2;66(1):123-30. No abstract available.

PMID:
809040
18.

Hypersialyloligosacchariduria in mucolipidoses: a method for diagnosis.

Okada S, Kato T, Miura S, Yabuuchi H, Nishigaki M, Kobata A, Chiyo H, Furuyama JI.

Clin Chim Acta. 1978 Jun;86(2):159-67.

PMID:
657539
19.

Sialidosis (mucolipidosis I).

Durand P, Gatti R, Cavalieri S, Borrone C, Tondeur M, Michalski JC, Strecker G.

Helv Paediatr Acta. 1977 Nov;32(4-5):391-400.

PMID:
617984
20.

Isolated acid neuraminidase deficiency: a distinct lysosomal storage disease.

Kelly TE, Graetz G.

Am J Med Genet. 1977;1(1):31-46.

PMID:
610425

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