Lisina (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "Lisina" in Catalan language version.

refsWebsite

Global rank Catalan rank

21doi.org

2^nd place

6^th place

12worldcat.org

5^th place

9nih.gov

4^th place

7^th place

2nature.com

234^th place

127^th place

2fao.org

318^th place

169^th place

2wiley.com

222^nd place

128^th place

1enciclopedia.cat

1,148^th place

3^rd place

1jci.org

low place

1google.cat

1,849^th place

2^nd place

1archive.org

6^th place

29^th place

1ingentaconnect.com

3,306^th place

1,682^nd place

1allaboutfeed.net

low place

1science.org

1,160^th place

1,210^th place

allaboutfeed.net (Global: low place; Catalan: low place)

«Norwegian granted for improving lysine production process» (en anglès americà). All About Feed, 26-01-2010. [Consulta: 26 juny 2022].

archive.org (Global: 6^th place; Catalan: 29^th place)

Walter, John; John Fernandes; Jean-Marie Saudubray; Georges van den Berghe (eds). Inborn metabolic diseases : diagnosis and treatment. Berlin ; New York : Springer, 2000, p. 296. ISBN 978-3-540-65626-5.

doi.org (Global: 2^nd place; Catalan: 6^th place)

dx.doi.org

Hegyi, Juraj; Schwartz, Robert A.; Hegyi, Vladimir «Pellagra: Dermatitis, dementia, and diarrhea» (en anglès). International Journal of Dermatology, 43, 1, 1-2004, pàg. 1–5. DOI: 10.1111/j.1365-4632.2004.01959.x. ISSN: 0011-9059.
Pinnell, Sheldon R.; Krane, Stephen M.; Kenzora, John E.; Glimcher, Melvin J. «A Heritable Disorder of Connective Tissue». New England Journal of Medicine, 286, 19, 11-05-1972, pàg. 1013–1020. DOI: 10.1056/NEJM197205112861901. ISSN: 0028-4793. PMID: 5016372.
Flanagan, Judith L.; Simmons, Peter A.; Vehige, Joseph; Willcox, Mark DP; Garrett, Qian «Role of carnitine in disease». Nutrition & Metabolism, 7, 1, 16-04-2010, pàg. 30. DOI: 10.1186/1743-7075-7-30. ISSN: 1743-7075. PMC: PMC2861661. PMID: 20398344.
Rudman, Daniel; Sewell, Charles W.; Ansley, Joseph D. «Deficiency of Carnitine in Cachectic Cirrhotic Patients» (en anglès). The Journal of Clinical Investigation, 60, 3, 01-09-1977, pàg. 716–723. DOI: 10.1172/JCI108824. ISSN: 0021-9738. PMC: PMC372417. PMID: 893675.
Rushton, D. H. «Nutritional factors and hair loss: Nutritional factors and hair loss» (en anglès). Clinical and Experimental Dermatology, 27, 5, 7-2002, pàg. 396–404. DOI: 10.1046/j.1365-2230.2002.01076.x.
Emery, P. W. «Metabolic changes in malnutrition» (en anglès). Eye, 19, 10, 10-2005, pàg. 1029–1034. DOI: 10.1038/sj.eye.6701959. ISSN: 1476-5454.
Ghosh, Shibani; Smriga, Miro; Vuvor, Frederick; Suri, Devika; Mohammed, Husein «Effect of lysine supplementation on health and morbidity in subjects belonging to poor peri-urban households in Accra, Ghana». The American Journal of Clinical Nutrition, 92, 4, 01-10-2010, pàg. 928–939. DOI: 10.3945/ajcn.2009.28834. ISSN: 0002-9165.
Houten, Sander M.; te Brinke, Heleen; Denis, Simone; Ruiter, Jos PN; Knegt, Alida C. «Genetic basis of hyperlysinemia». Orphanet Journal of Rare Diseases, 8, 1, 09-04-2013, pàg. 57. DOI: 10.1186/1750-1172-8-57. ISSN: 1750-1172. PMC: PMC3626681. PMID: 23570448.
Hoffmann, Georg F.; Kölker, Stefan. Cerebral Organic Acid Disorders and Other Disorders of Lysine Catabolism (en anglès). Berlin, Heidelberg: Springer, 2016, p. 333–348. DOI 10.1007/978-3-662-49771-5_22. ISBN 978-3-662-49771-5.
Danhauser, Katharina; Sauer, Sven W.; Haack, Tobias B.; Wieland, Thomas; Staufner, Christian «DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria». The American Journal of Human Genetics, 91, 6, 12-2012, pàg. 1082–1087. DOI: 10.1016/j.ajhg.2012.10.006. ISSN: 0002-9297. PMC: PMC3516599. PMID: 23141293.
Mills, Philippa B.; Struys, Eduard; Jakobs, Cornelis; Plecko, Barbara; Baxter, Peter «Mutations in antiquitin in individuals with pyridoxine-dependent seizures» (en anglès). Nature Medicine, 12, 3, 3-2006, pàg. 307–309. DOI: 10.1038/nm1366. ISSN: 1546-170X.
Mills, Philippa B.; Footitt, Emma J.; Mills, Kevin A.; Tuschl, Karin; Aylett, Sarah «Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)». Brain, 133, 7, 01-07-2010, pàg. 2148–2159. DOI: 10.1093/brain/awq143. ISSN: 0006-8950. PMC: PMC2892945. PMID: 20554659.
Anastassiadis, Savas «L-Lysine Fermentation». Recent Patents on Biotechnology, 1, 1, 01-02-2007, pàg. 11–24. DOI: 10.2174/187220807779813947.
Abelson, Philip H. «A Potential Phosphate Crisis» (en anglès). Science, 283, 5410, 26-03-1999, pàg. 2015–2015. DOI: 10.1126/science.283.5410.2015. ISSN: 0036-8075.

doi.org

Pinnell, Sheldon R.; Krane, Stephen M.; Kenzora, John E.; Glimcher, Melvin J. «A Heritable Disorder of Connective Tissue». New England Journal of Medicine, 286, 19, 11-05-1972, pàg. 1013–1020. DOI: 10.1056/NEJM197205112861901. ISSN: 0028-4793. PMID: 5016372.
Flanagan, Judith L.; Simmons, Peter A.; Vehige, Joseph; Willcox, Mark DP; Garrett, Qian «Role of carnitine in disease». Nutrition & Metabolism, 7, 1, 16-04-2010, pàg. 30. DOI: 10.1186/1743-7075-7-30. ISSN: 1743-7075. PMC: PMC2861661. PMID: 20398344.
Ghosh, Shibani; Smriga, Miro; Vuvor, Frederick; Suri, Devika; Mohammed, Husein «Effect of lysine supplementation on health and morbidity in subjects belonging to poor peri-urban households in Accra, Ghana». The American Journal of Clinical Nutrition, 92, 4, 01-10-2010, pàg. 928–939. DOI: 10.3945/ajcn.2009.28834. ISSN: 0002-9165.
Houten, Sander M.; te Brinke, Heleen; Denis, Simone; Ruiter, Jos PN; Knegt, Alida C. «Genetic basis of hyperlysinemia». Orphanet Journal of Rare Diseases, 8, 1, 09-04-2013, pàg. 57. DOI: 10.1186/1750-1172-8-57. ISSN: 1750-1172. PMC: PMC3626681. PMID: 23570448.
Hoffmann, Georg F.; Kölker, Stefan. Cerebral Organic Acid Disorders and Other Disorders of Lysine Catabolism (en anglès). Berlin, Heidelberg: Springer, 2016, p. 333–348. DOI 10.1007/978-3-662-49771-5_22. ISBN 978-3-662-49771-5.
Danhauser, Katharina; Sauer, Sven W.; Haack, Tobias B.; Wieland, Thomas; Staufner, Christian «DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria». The American Journal of Human Genetics, 91, 6, 12-2012, pàg. 1082–1087. DOI: 10.1016/j.ajhg.2012.10.006. ISSN: 0002-9297. PMC: PMC3516599. PMID: 23141293.
Mills, Philippa B.; Footitt, Emma J.; Mills, Kevin A.; Tuschl, Karin; Aylett, Sarah «Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)». Brain, 133, 7, 01-07-2010, pàg. 2148–2159. DOI: 10.1093/brain/awq143. ISSN: 0006-8950. PMC: PMC2892945. PMID: 20554659.

enciclopedia.cat (Global: 1,148^th place; Catalan: 3^rd place)

«lisina». Gran Enciclopèdia Catalana. [Consulta: 26 juny 2022].

fao.org (Global: 318^th place; Catalan: 169^th place)

Vasal, S.K.. «The role of high lysine cereals in animal and human nutrition in Asia». A: Portein sources for the animal feed industry. FAO, 2004. ISBN 92-5-105012-0.
Toride, Yasuhiko. «Lysine and other amino acids for feed: production and contribution to protein utilization in animal feeding». A: Portein sources for the animal feed industry. FAO, 2004. ISBN 92-5-105012-0.

google.cat (Global: 1,849^th place; Catalan: 2^nd place)

books.google.cat

Juo, Pei-Show. Concise Dictionary of Biomedicine and Molecular Biology (en anglès). CRC Press, 2001-12-21, p. 571. ISBN 978-1-4200-4130-9.

ingentaconnect.com (Global: 3,306^th place; Catalan: 1,682^nd place)

Anastassiadis, Savas «L-Lysine Fermentation». Recent Patents on Biotechnology, 1, 1, 01-02-2007, pàg. 11–24. DOI: 10.2174/187220807779813947.

jci.org (Global: low place; Catalan: low place)

Rudman, Daniel; Sewell, Charles W.; Ansley, Joseph D. «Deficiency of Carnitine in Cachectic Cirrhotic Patients» (en anglès). The Journal of Clinical Investigation, 60, 3, 01-09-1977, pàg. 716–723. DOI: 10.1172/JCI108824. ISSN: 0021-9738. PMC: PMC372417. PMID: 893675.

nature.com (Global: 234^th place; Catalan: 127^th place)

Emery, P. W. «Metabolic changes in malnutrition» (en anglès). Eye, 19, 10, 10-2005, pàg. 1029–1034. DOI: 10.1038/sj.eye.6701959. ISSN: 1476-5454.
Mills, Philippa B.; Struys, Eduard; Jakobs, Cornelis; Plecko, Barbara; Baxter, Peter «Mutations in antiquitin in individuals with pyridoxine-dependent seizures» (en anglès). Nature Medicine, 12, 3, 3-2006, pàg. 307–309. DOI: 10.1038/nm1366. ISSN: 1546-170X.

nih.gov (Global: 4^th place; Catalan: 7^th place)

ncbi.nlm.nih.gov

Pinnell, Sheldon R.; Krane, Stephen M.; Kenzora, John E.; Glimcher, Melvin J. «A Heritable Disorder of Connective Tissue». New England Journal of Medicine, 286, 19, 11-05-1972, pàg. 1013–1020. DOI: 10.1056/NEJM197205112861901. ISSN: 0028-4793. PMID: 5016372.
Flanagan, Judith L.; Simmons, Peter A.; Vehige, Joseph; Willcox, Mark DP; Garrett, Qian «Role of carnitine in disease». Nutrition & Metabolism, 7, 1, 16-04-2010, pàg. 30. DOI: 10.1186/1743-7075-7-30. ISSN: 1743-7075. PMC: PMC2861661. PMID: 20398344.
Rudman, Daniel; Sewell, Charles W.; Ansley, Joseph D. «Deficiency of Carnitine in Cachectic Cirrhotic Patients» (en anglès). The Journal of Clinical Investigation, 60, 3, 01-09-1977, pàg. 716–723. DOI: 10.1172/JCI108824. ISSN: 0021-9738. PMC: PMC372417. PMID: 893675.
Houten, Sander M.; te Brinke, Heleen; Denis, Simone; Ruiter, Jos PN; Knegt, Alida C. «Genetic basis of hyperlysinemia». Orphanet Journal of Rare Diseases, 8, 1, 09-04-2013, pàg. 57. DOI: 10.1186/1750-1172-8-57. ISSN: 1750-1172. PMC: PMC3626681. PMID: 23570448.
Dancis, J.; Hutzler, J.; Ampola, M. G.; Shih, V. E.; van Gelderen, H. H. «The prognosis of hyperlysinemia: an interim report». American Journal of Human Genetics, 35, 3, 5-1983, pàg. 438–442. ISSN: 0002-9297. PMC: 1685659. PMID: 6407303.
Danhauser, Katharina; Sauer, Sven W.; Haack, Tobias B.; Wieland, Thomas; Staufner, Christian «DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria». The American Journal of Human Genetics, 91, 6, 12-2012, pàg. 1082–1087. DOI: 10.1016/j.ajhg.2012.10.006. ISSN: 0002-9297. PMC: PMC3516599. PMID: 23141293.
Mills, Philippa B.; Footitt, Emma J.; Mills, Kevin A.; Tuschl, Karin; Aylett, Sarah «Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)». Brain, 133, 7, 01-07-2010, pàg. 2148–2159. DOI: 10.1093/brain/awq143. ISSN: 0006-8950. PMC: PMC2892945. PMID: 20554659.

pubchem.ncbi.nlm.nih.gov

«Lysine» (en anglès). pubchem.ncbi.nlm.nih.gov. [Consulta: 26 juny 2022].

pubmed.ncbi.nlm.nih.gov

Dancis, J.; Hutzler, J.; Ampola, M. G.; Shih, V. E.; van Gelderen, H. H. «The prognosis of hyperlysinemia: an interim report». American Journal of Human Genetics, 35, 3, 5-1983, pàg. 438–442. ISSN: 0002-9297. PMC: 1685659. PMID: 6407303.

science.org (Global: 1,160^th place; Catalan: 1,210^th place)

Abelson, Philip H. «A Potential Phosphate Crisis» (en anglès). Science, 283, 5410, 26-03-1999, pàg. 2015–2015. DOI: 10.1126/science.283.5410.2015. ISSN: 0036-8075.

wiley.com (Global: 222^nd place; Catalan: 128^th place)

onlinelibrary.wiley.com

Hegyi, Juraj; Schwartz, Robert A.; Hegyi, Vladimir «Pellagra: Dermatitis, dementia, and diarrhea» (en anglès). International Journal of Dermatology, 43, 1, 1-2004, pàg. 1–5. DOI: 10.1111/j.1365-4632.2004.01959.x. ISSN: 0011-9059.

doi.wiley.com

Rushton, D. H. «Nutritional factors and hair loss: Nutritional factors and hair loss» (en anglès). Clinical and Experimental Dermatology, 27, 5, 7-2002, pàg. 396–404. DOI: 10.1046/j.1365-2230.2002.01076.x.

worldcat.org (Global: 5^th place; Catalan: 5^th place)

Hegyi, Juraj; Schwartz, Robert A.; Hegyi, Vladimir «Pellagra: Dermatitis, dementia, and diarrhea» (en anglès). International Journal of Dermatology, 43, 1, 1-2004, pàg. 1–5. DOI: 10.1111/j.1365-4632.2004.01959.x. ISSN: 0011-9059.
Pinnell, Sheldon R.; Krane, Stephen M.; Kenzora, John E.; Glimcher, Melvin J. «A Heritable Disorder of Connective Tissue». New England Journal of Medicine, 286, 19, 11-05-1972, pàg. 1013–1020. DOI: 10.1056/NEJM197205112861901. ISSN: 0028-4793. PMID: 5016372.
Flanagan, Judith L.; Simmons, Peter A.; Vehige, Joseph; Willcox, Mark DP; Garrett, Qian «Role of carnitine in disease». Nutrition & Metabolism, 7, 1, 16-04-2010, pàg. 30. DOI: 10.1186/1743-7075-7-30. ISSN: 1743-7075. PMC: PMC2861661. PMID: 20398344.
Rudman, Daniel; Sewell, Charles W.; Ansley, Joseph D. «Deficiency of Carnitine in Cachectic Cirrhotic Patients» (en anglès). The Journal of Clinical Investigation, 60, 3, 01-09-1977, pàg. 716–723. DOI: 10.1172/JCI108824. ISSN: 0021-9738. PMC: PMC372417. PMID: 893675.
Emery, P. W. «Metabolic changes in malnutrition» (en anglès). Eye, 19, 10, 10-2005, pàg. 1029–1034. DOI: 10.1038/sj.eye.6701959. ISSN: 1476-5454.
Ghosh, Shibani; Smriga, Miro; Vuvor, Frederick; Suri, Devika; Mohammed, Husein «Effect of lysine supplementation on health and morbidity in subjects belonging to poor peri-urban households in Accra, Ghana». The American Journal of Clinical Nutrition, 92, 4, 01-10-2010, pàg. 928–939. DOI: 10.3945/ajcn.2009.28834. ISSN: 0002-9165.
Houten, Sander M.; te Brinke, Heleen; Denis, Simone; Ruiter, Jos PN; Knegt, Alida C. «Genetic basis of hyperlysinemia». Orphanet Journal of Rare Diseases, 8, 1, 09-04-2013, pàg. 57. DOI: 10.1186/1750-1172-8-57. ISSN: 1750-1172. PMC: PMC3626681. PMID: 23570448.
Dancis, J.; Hutzler, J.; Ampola, M. G.; Shih, V. E.; van Gelderen, H. H. «The prognosis of hyperlysinemia: an interim report». American Journal of Human Genetics, 35, 3, 5-1983, pàg. 438–442. ISSN: 0002-9297. PMC: 1685659. PMID: 6407303.
Danhauser, Katharina; Sauer, Sven W.; Haack, Tobias B.; Wieland, Thomas; Staufner, Christian «DHTKD1 Mutations Cause 2-Aminoadipic and 2-Oxoadipic Aciduria». The American Journal of Human Genetics, 91, 6, 12-2012, pàg. 1082–1087. DOI: 10.1016/j.ajhg.2012.10.006. ISSN: 0002-9297. PMC: PMC3516599. PMID: 23141293.
Mills, Philippa B.; Struys, Eduard; Jakobs, Cornelis; Plecko, Barbara; Baxter, Peter «Mutations in antiquitin in individuals with pyridoxine-dependent seizures» (en anglès). Nature Medicine, 12, 3, 3-2006, pàg. 307–309. DOI: 10.1038/nm1366. ISSN: 1546-170X.
Mills, Philippa B.; Footitt, Emma J.; Mills, Kevin A.; Tuschl, Karin; Aylett, Sarah «Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)». Brain, 133, 7, 01-07-2010, pàg. 2148–2159. DOI: 10.1093/brain/awq143. ISSN: 0006-8950. PMC: PMC2892945. PMID: 20554659.
Abelson, Philip H. «A Potential Phosphate Crisis» (en anglès). Science, 283, 5410, 26-03-1999, pàg. 2015–2015. DOI: 10.1126/science.283.5410.2015. ISSN: 0036-8075.

Lisina (Catalan Wikipedia)

allaboutfeed.net (Global: low place; Catalan: low place)

archive.org (Global: 6th place; Catalan: 29th place)

doi.org (Global: 2nd place; Catalan: 6th place)

dx.doi.org

doi.org

enciclopedia.cat (Global: 1,148th place; Catalan: 3rd place)

fao.org (Global: 318th place; Catalan: 169th place)

google.cat (Global: 1,849th place; Catalan: 2nd place)