82 related articles for article (PubMed ID: 2993742)
1. Lectin-histochemistry: glycogenosis in cattle.
Zlotowski P; Gimeno EJ; Diaz A; Barros R; Barros SS; Cruz CE; Driemeier D
Vet Res Commun; 2006 May; 30(4):369-77. PubMed ID: 16502105
[TBL] [Abstract][Full Text] [Related]
2. [Protein-carbohydrate recognition. Foundation and medical application with illustrations of tumor lectin studies].
Gabius HJ; Kayser K; Gabius S
Naturwissenschaften; 1995 Dec; 82(12):533-43. PubMed ID: 8569848
[TBL] [Abstract][Full Text] [Related]
3. New sites of ocular involvement in late-infantile metachromatic leukodystrophy revealed by histopathologic studies.
Scott IU; Green WR; Goyal AK; de la Cruz Z; Naidu S; Moser H
Graefes Arch Clin Exp Ophthalmol; 1993 Mar; 231(3):187-91. PubMed ID: 8462893
[No Abstract] [Full Text] [Related]
4. Arylsulfatase B-deficient mucopolysaccharidosis in rats.
Yoshida M; Noguchi J; Ikadai H; Takahashi M; Nagase S
J Clin Invest; 1993 Mar; 91(3):1099-104. PubMed ID: 8450039
[TBL] [Abstract][Full Text] [Related]
5. Estimation of genotype distributions and posterior genotype probabilities for beta-mannosidosis in Salers cattle.
Taylor JF; Abbitt B; Walter JP; Davis SK; Jaques JT; Ochoa RF
Genetics; 1993 Nov; 135(3):855-68. PubMed ID: 8293984
[TBL] [Abstract][Full Text] [Related]
6. A new form of ovine GM1-gangliosidosis.
Skelly BJ; Jeffrey M; Franklin RJ; Winchester BG
Acta Neuropathol; 1995; 89(4):374-9. PubMed ID: 7610770
[TBL] [Abstract][Full Text] [Related]
7. The lesions of an ovine lysosomal storage disease. Initial characterization.
Murnane RD; Prieur DJ; Ahern-Rindell AJ; Parish SM; Collier LL
Am J Pathol; 1989 Feb; 134(2):263-70. PubMed ID: 2916646
[TBL] [Abstract][Full Text] [Related]
8. Lectin histochemistry of an ovine lysosomal storage disease with deficiencies of beta-galactosidase and alpha-neuraminidase.
Murnane RD; Ahern-Rindell AJ; Prieur DJ
Am J Pathol; 1989 Oct; 135(4):623-30. PubMed ID: 2508478
[TBL] [Abstract][Full Text] [Related]
9. [Phenotypes in heteroglycanoses and sphingolipidoses (author's transl)].
Gehler J
Monatsschr Kinderheilkd; 1981 Nov; 129(11):610-20. PubMed ID: 6798422
[TBL] [Abstract][Full Text] [Related]
10. Lysosomal storage diseases.
Glew RH; Basu A; Prence EM; Remaley AT
Lab Invest; 1985 Sep; 53(3):250-69. PubMed ID: 2993742
[No Abstract] [Full Text] [Related]
11. [Recent advances in sphingolipidosis research].
Tamai Y; Kojima H
Tanpakushitsu Kakusan Koso; 1990 May; 35(7 Suppl):1291-303. PubMed ID: 1972585
[No Abstract] [Full Text] [Related]
12. Inherited neuropathies related to disorders of lipid metabolism.
Thomas PK
Adv Neurol; 1988; 48():133-44. PubMed ID: 2446477
[No Abstract] [Full Text] [Related]
13. The biochemistry of sphingolipid storage diseases.
Sandhoff K
Angew Chem Int Ed Engl; 1977 May; 16(5):273-85. PubMed ID: 406814
[No Abstract] [Full Text] [Related]
14. Enzymatic diagnosis of sphingolipidoses.
Suzuki K
Methods Enzymol; 1987; 138():727-62. PubMed ID: 2885713
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
