Cerliponase alfa (English Wikipedia)

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

refsWebsite

Global rank English rank

17nih.gov

4^th place

9doi.org

2^nd place

4web.archive.org

1^st place

3fda.gov

447^th place

338^th place

2semanticscholar.org

11^th place

8^th place

1hres.ca

low place

1canada.ca

1,712^th place

1,063^rd place

1thelancet.com

2,393^rd place

3,174^th place

1biomarin.com

low place

1nice.org.uk

3,258^th place

2,666^th place

1pharmatimes.com

low place

1chemdiv.com

low place

biomarin.com

investors.biomarin.com

"European Commission Approves Brineura (cerliponase alfa), the First Treatment for CLN2 Disease, a Form of Batten Disease and Ultra-Rare Brain Disorder in Children". BioMarin. 1 June 2017. Archived from the original on 10 August 2017. Retrieved 23 July 2017.

canada.ca

"Drug and medical device highlights 2018: Helping you maintain and improve your health". Health Canada. 14 October 2020. Retrieved 17 April 2024.

chemdiv.com

"FDA Approves BioMarin's Batten Disease Drug. Cost Per Year is $702,000". ChemDiv. 1 May 2017. Retrieved 2 December 2019.

doi.org

Markham A (July 2017). "Cerliponase Alfa: First Global Approval". Drugs. 77 (11): 1247–1249. doi:10.1007/s40265-017-0771-8. PMID 28589525. S2CID 25845031.
Mole SE, Cotman SL (October 2015). "Genetics of the neuronal ceroid lipofuscinoses (Batten disease)". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. Current Research on the Neuronal Ceroid Lipofuscinoses (Batten Disease). 1852 (10 Pt B): 2237–41. doi:10.1016/j.bbadis.2015.05.011. PMC 4567481. PMID 26026925.
Sleat DE, Donnelly RJ, Lackland H, Liu CG, Sohar I, Pullarkat RK, et al. (September 1997). "Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis". Science. 277 (5333): 1802–5. doi:10.1126/science.277.5333.1802. PMID 9295267.
Gardner E, Bailey M, Schulz A, Aristorena M, Miller N, Mole SE (November 2019). "Mutation update: Review of TPP1 gene variants associated with neuronal ceroid lipofuscinosis CLN2 disease". Human Mutation. 40 (11): 1924–1938. doi:10.1002/humu.23860. PMC 6851559. PMID 31283065.
Mole SE, Anderson G, Band HA, Berkovic SF, Cooper JD, Kleine Holthaus SM, et al. (January 2019). "Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis". The Lancet. Neurology. 18 (1): 107–116. doi:10.1016/S1474-4422(18)30368-5. PMID 30470609. S2CID 53711337.
Johnson TB, Cain JT, White KA, Ramirez-Montealegre D, Pearce DA, Weimer JM (March 2019). "Therapeutic landscape for Batten disease: current treatments and future prospects". Nature Reviews. Neurology. 15 (3): 161–178. doi:10.1038/s41582-019-0138-8. PMC 6681450. PMID 30783219.
Mukherjee AB, Appu AP, Sadhukhan T, Casey S, Mondal A, Zhang Z, et al. (January 2019). "Emerging new roles of the lysosome and neuronal ceroid lipofuscinoses". Molecular Neurodegeneration. 14 (1): 4. doi:10.1186/s13024-018-0300-6. PMC 6335712. PMID 30651094.
Kohlschütter A, Schulz A, Bartsch U, Storch S (April 2019). "Current and Emerging Treatment Strategies for Neuronal Ceroid Lipofuscinoses". CNS Drugs. 33 (4): 315–325. doi:10.1007/s40263-019-00620-8. PMC 6440934. PMID 30877620.
Guhaniyogi J, Sohar I, Das K, Stock AM, Lobel P (February 2009). "Crystal structure and autoactivation pathway of the precursor form of human tripeptidyl-peptidase 1, the enzyme deficient in late infantile ceroid lipofuscinosis". The Journal of Biological Chemistry. 284 (6): 3985–97. doi:10.1074/jbc.M806943200. PMC 2635056. PMID 19038967.

fda.gov

"FDA approves first treatment for a form of Batten disease". U.S. Food and Drug Administration (FDA) (Press release). 27 April 2017. Archived from the original on 10 December 2019. Retrieved 9 December 2019. This article incorporates text from this source, which is in the public domain.
New Drug Therapy Approvals 2017 (PDF). U.S. Food and Drug Administration (FDA) (Report). January 2018. Retrieved 16 September 2020.
"Drug Trials Snapshot: Brineura". U.S. Food and Drug Administration (FDA). 25 May 2017. Archived from the original on 10 December 2019. Retrieved 9 December 2019. This article incorporates text from this source, which is in the public domain.

hres.ca

hpr-rps.hres.ca

"Summary Basis of Decision (SBD) for Brineura". Health Canada. 23 October 2014. Retrieved 29 May 2022.

nice.org.uk

"Evaluation consultation document: Cerliponase alfa for treating neuronal ceroid lipofuscinosis type 2". NICE. Retrieved 9 August 2018.

nih.gov

pubmed.ncbi.nlm.nih.gov

Markham A (July 2017). "Cerliponase Alfa: First Global Approval". Drugs. 77 (11): 1247–1249. doi:10.1007/s40265-017-0771-8. PMID 28589525. S2CID 25845031.
Mole SE, Cotman SL (October 2015). "Genetics of the neuronal ceroid lipofuscinoses (Batten disease)". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. Current Research on the Neuronal Ceroid Lipofuscinoses (Batten Disease). 1852 (10 Pt B): 2237–41. doi:10.1016/j.bbadis.2015.05.011. PMC 4567481. PMID 26026925.
Sleat DE, Donnelly RJ, Lackland H, Liu CG, Sohar I, Pullarkat RK, et al. (September 1997). "Association of mutations in a lysosomal protein with classical late-infantile neuronal ceroid lipofuscinosis". Science. 277 (5333): 1802–5. doi:10.1126/science.277.5333.1802. PMID 9295267.
Gardner E, Bailey M, Schulz A, Aristorena M, Miller N, Mole SE (November 2019). "Mutation update: Review of TPP1 gene variants associated with neuronal ceroid lipofuscinosis CLN2 disease". Human Mutation. 40 (11): 1924–1938. doi:10.1002/humu.23860. PMC 6851559. PMID 31283065.
Mole SE, Anderson G, Band HA, Berkovic SF, Cooper JD, Kleine Holthaus SM, et al. (January 2019). "Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis". The Lancet. Neurology. 18 (1): 107–116. doi:10.1016/S1474-4422(18)30368-5. PMID 30470609. S2CID 53711337.
Johnson TB, Cain JT, White KA, Ramirez-Montealegre D, Pearce DA, Weimer JM (March 2019). "Therapeutic landscape for Batten disease: current treatments and future prospects". Nature Reviews. Neurology. 15 (3): 161–178. doi:10.1038/s41582-019-0138-8. PMC 6681450. PMID 30783219.
Mukherjee AB, Appu AP, Sadhukhan T, Casey S, Mondal A, Zhang Z, et al. (January 2019). "Emerging new roles of the lysosome and neuronal ceroid lipofuscinoses". Molecular Neurodegeneration. 14 (1): 4. doi:10.1186/s13024-018-0300-6. PMC 6335712. PMID 30651094.
Kohlschütter A, Schulz A, Bartsch U, Storch S (April 2019). "Current and Emerging Treatment Strategies for Neuronal Ceroid Lipofuscinoses". CNS Drugs. 33 (4): 315–325. doi:10.1007/s40263-019-00620-8. PMC 6440934. PMID 30877620.
Guhaniyogi J, Sohar I, Das K, Stock AM, Lobel P (February 2009). "Crystal structure and autoactivation pathway of the precursor form of human tripeptidyl-peptidase 1, the enzyme deficient in late infantile ceroid lipofuscinosis". The Journal of Biological Chemistry. 284 (6): 3985–97. doi:10.1074/jbc.M806943200. PMC 2635056. PMID 19038967.

ncbi.nlm.nih.gov

Mole SE, Cotman SL (October 2015). "Genetics of the neuronal ceroid lipofuscinoses (Batten disease)". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. Current Research on the Neuronal Ceroid Lipofuscinoses (Batten Disease). 1852 (10 Pt B): 2237–41. doi:10.1016/j.bbadis.2015.05.011. PMC 4567481. PMID 26026925.
Gardner E, Bailey M, Schulz A, Aristorena M, Miller N, Mole SE (November 2019). "Mutation update: Review of TPP1 gene variants associated with neuronal ceroid lipofuscinosis CLN2 disease". Human Mutation. 40 (11): 1924–1938. doi:10.1002/humu.23860. PMC 6851559. PMID 31283065.
Johnson TB, Cain JT, White KA, Ramirez-Montealegre D, Pearce DA, Weimer JM (March 2019). "Therapeutic landscape for Batten disease: current treatments and future prospects". Nature Reviews. Neurology. 15 (3): 161–178. doi:10.1038/s41582-019-0138-8. PMC 6681450. PMID 30783219.
Mukherjee AB, Appu AP, Sadhukhan T, Casey S, Mondal A, Zhang Z, et al. (January 2019). "Emerging new roles of the lysosome and neuronal ceroid lipofuscinoses". Molecular Neurodegeneration. 14 (1): 4. doi:10.1186/s13024-018-0300-6. PMC 6335712. PMID 30651094.
Kohlschütter A, Schulz A, Bartsch U, Storch S (April 2019). "Current and Emerging Treatment Strategies for Neuronal Ceroid Lipofuscinoses". CNS Drugs. 33 (4): 315–325. doi:10.1007/s40263-019-00620-8. PMC 6440934. PMID 30877620.
Guhaniyogi J, Sohar I, Das K, Stock AM, Lobel P (February 2009). "Crystal structure and autoactivation pathway of the precursor form of human tripeptidyl-peptidase 1, the enzyme deficient in late infantile ceroid lipofuscinosis". The Journal of Biological Chemistry. 284 (6): 3985–97. doi:10.1074/jbc.M806943200. PMC 2635056. PMID 19038967.

ninds.nih.gov

"Cerliponase alfa (Brineura) – Ceroid lipofuscinosis 2 (CLN2 disease)". National Institute of Neurological Disorders and Stroke. Archived from the original on 13 July 2021. Retrieved 2 December 2019.

dailymed.nlm.nih.gov

"Brineura- cerliponase alfa kit". DailyMed. 18 December 2018. Retrieved 9 December 2019.

pharmatimes.com

McKee S (13 February 2018). "NICE deems Batten disease therapy too costly for NHS use". Pharma Times. Retrieved 9 August 2018.

semanticscholar.org

api.semanticscholar.org

Markham A (July 2017). "Cerliponase Alfa: First Global Approval". Drugs. 77 (11): 1247–1249. doi:10.1007/s40265-017-0771-8. PMID 28589525. S2CID 25845031.
Mole SE, Anderson G, Band HA, Berkovic SF, Cooper JD, Kleine Holthaus SM, et al. (January 2019). "Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis". The Lancet. Neurology. 18 (1): 107–116. doi:10.1016/S1474-4422(18)30368-5. PMID 30470609. S2CID 53711337.

thelancet.com

Mole SE, Anderson G, Band HA, Berkovic SF, Cooper JD, Kleine Holthaus SM, et al. (January 2019). "Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis". The Lancet. Neurology. 18 (1): 107–116. doi:10.1016/S1474-4422(18)30368-5. PMID 30470609. S2CID 53711337.

web.archive.org

"FDA approves first treatment for a form of Batten disease". U.S. Food and Drug Administration (FDA) (Press release). 27 April 2017. Archived from the original on 10 December 2019. Retrieved 9 December 2019. This article incorporates text from this source, which is in the public domain.
"Cerliponase alfa (Brineura) – Ceroid lipofuscinosis 2 (CLN2 disease)". National Institute of Neurological Disorders and Stroke. Archived from the original on 13 July 2021. Retrieved 2 December 2019.
"European Commission Approves Brineura (cerliponase alfa), the First Treatment for CLN2 Disease, a Form of Batten Disease and Ultra-Rare Brain Disorder in Children". BioMarin. 1 June 2017. Archived from the original on 10 August 2017. Retrieved 23 July 2017.
"Drug Trials Snapshot: Brineura". U.S. Food and Drug Administration (FDA). 25 May 2017. Archived from the original on 10 December 2019. Retrieved 9 December 2019. This article incorporates text from this source, which is in the public domain.