Galactosialidosis (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Galactosialidosis" in English language version.

refsWebsite

Global rank English rank

6nih.gov

4^th place

4doi.org

2^nd place

2semanticscholar.org

11^th place

8^th place

2clinicaltrials.gov

5,225^th place

4,062^nd place

1orpha.net

3,537^th place

7,177^th place

1raregenomics.org

low place

1medlineplus.gov

1,581^st place

1,299^th place

1stlouischildrens.org

low place

1ismrd.org

low place

1worldcat.org

5^th place

clinicaltrials.gov

"Characterization of the Patient Population With Galactosialidosis - Full Text View - ClinicalTrials.gov". clinicaltrials.gov. 9 October 2018. Retrieved 2020-11-11.
"Longitudinal Studies of the Glycoproteinoses". ClinicalTrials.gov. Retrieved 2023-09-26.

doi.org

Koike K, Hamaguchi T, Kitamura H, Imasawa T, Joh K (2008). "Galactosialidosis associated with IgA nephropathy: morphological study of renal biopsy". Pathol. Int. 58 (5): 295–9. doi:10.1111/j.1440-1827.2008.02226.x. PMID 18429828. S2CID 205477388.
Kleijer WJ, Geilen GC, Janse HC, et al. (1996). "Cathepsin A deficiency in galactosialidosis: studies of patients and carriers in 16 families". Pediatr. Res. 39 (6): 1067–71. doi:10.1203/00006450-199606000-00022. PMID 8725271.
Caciotti A, Catarzi S, Tonin R, Lugli L, Perez CR, Michelakakis H, Mavridou I, Donati MA, Guerrini R, D'Azzo A, Morrone A (2013). "Galactosialidosis: review and analysis of CTSA gene mutations". Orphanet J Rare Dis. 8 (1): 114. doi:10.1186/1750-1172-8-114. PMC 3737020. PMID 23915561.
Kleijer, W. J.; Hoogeveen, A.; Verheijen, F. W.; Niermeijer, M. F.; Galjaard, H.; O'Brien, J. S.; Warner, T. G. (July 1979). "Prenatal diagnosis of sialidosis with combined neuraminidase and beta-galactosidase deficiency". Clinical Genetics. 16 (1): 60–61. doi:10.1111/j.1399-0004.1979.tb00851.x. ISSN 0009-9163. PMID 477017. S2CID 41124809.

ismrd.org

"Galactosialidosis". ISMRD. Retrieved 2020-11-11.

medlineplus.gov

"Galactosialidosis: MedlinePlus Genetics". medlineplus.gov. Retrieved 2020-11-11.

nih.gov

pubmed.ncbi.nlm.nih.gov

Koike K, Hamaguchi T, Kitamura H, Imasawa T, Joh K (2008). "Galactosialidosis associated with IgA nephropathy: morphological study of renal biopsy". Pathol. Int. 58 (5): 295–9. doi:10.1111/j.1440-1827.2008.02226.x. PMID 18429828. S2CID 205477388.
Kleijer WJ, Geilen GC, Janse HC, et al. (1996). "Cathepsin A deficiency in galactosialidosis: studies of patients and carriers in 16 families". Pediatr. Res. 39 (6): 1067–71. doi:10.1203/00006450-199606000-00022. PMID 8725271.
Caciotti A, Catarzi S, Tonin R, Lugli L, Perez CR, Michelakakis H, Mavridou I, Donati MA, Guerrini R, D'Azzo A, Morrone A (2013). "Galactosialidosis: review and analysis of CTSA gene mutations". Orphanet J Rare Dis. 8 (1): 114. doi:10.1186/1750-1172-8-114. PMC 3737020. PMID 23915561.
Kleijer, W. J.; Hoogeveen, A.; Verheijen, F. W.; Niermeijer, M. F.; Galjaard, H.; O'Brien, J. S.; Warner, T. G. (July 1979). "Prenatal diagnosis of sialidosis with combined neuraminidase and beta-galactosidase deficiency". Clinical Genetics. 16 (1): 60–61. doi:10.1111/j.1399-0004.1979.tb00851.x. ISSN 0009-9163. PMID 477017. S2CID 41124809.

rarediseases.info.nih.gov

"Galactosialidosis | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2020-10-14.

ncbi.nlm.nih.gov

Caciotti A, Catarzi S, Tonin R, Lugli L, Perez CR, Michelakakis H, Mavridou I, Donati MA, Guerrini R, D'Azzo A, Morrone A (2013). "Galactosialidosis: review and analysis of CTSA gene mutations". Orphanet J Rare Dis. 8 (1): 114. doi:10.1186/1750-1172-8-114. PMC 3737020. PMID 23915561.

orpha.net

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Galactosialidosis". www.orpha.net. Retrieved 11 April 2019.{{cite web}}: CS1 maint: numeric names: authors list (link)

raregenomics.org

"Galactosialidosis". Rare Genomics Institute. Retrieved 2020-10-14.

semanticscholar.org

api.semanticscholar.org

Koike K, Hamaguchi T, Kitamura H, Imasawa T, Joh K (2008). "Galactosialidosis associated with IgA nephropathy: morphological study of renal biopsy". Pathol. Int. 58 (5): 295–9. doi:10.1111/j.1440-1827.2008.02226.x. PMID 18429828. S2CID 205477388.
Kleijer, W. J.; Hoogeveen, A.; Verheijen, F. W.; Niermeijer, M. F.; Galjaard, H.; O'Brien, J. S.; Warner, T. G. (July 1979). "Prenatal diagnosis of sialidosis with combined neuraminidase and beta-galactosidase deficiency". Clinical Genetics. 16 (1): 60–61. doi:10.1111/j.1399-0004.1979.tb00851.x. ISSN 0009-9163. PMID 477017. S2CID 41124809.

stlouischildrens.org

"Autosomal Recessive Inheritance". www.stlouischildrens.org. Retrieved 2020-11-11.

worldcat.org

search.worldcat.org

Kleijer, W. J.; Hoogeveen, A.; Verheijen, F. W.; Niermeijer, M. F.; Galjaard, H.; O'Brien, J. S.; Warner, T. G. (July 1979). "Prenatal diagnosis of sialidosis with combined neuraminidase and beta-galactosidase deficiency". Clinical Genetics. 16 (1): 60–61. doi:10.1111/j.1399-0004.1979.tb00851.x. ISSN 0009-9163. PMID 477017. S2CID 41124809.