Síndrome de Lowe (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "Síndrome de Lowe" in Catalan language version.

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1medlineplus.gov

1,581^st place

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low place

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doi.org

dx.doi.org

Loi M Orphanet Journal of Rare Diseases, 1, 2006, pàg. 16. DOI: 10.1186/1750-1172-1-16. PMC: 1526415. PMID: 16722554.
Hagemann, Nina; Hou, Xiaomin; Goody, Roger S.; Itzen, Aymelt; Erdmann, Kai S. Small GTPases, 3, 2, 01-06-2017, pàg. 107–110. DOI: 10.4161/sgtp.19380. ISSN: 2154-1256. PMID: 22790198.
American Journal of Diseases of Children, 83, 2, 1952, pàg. 164–84. DOI: 10.1001/archpedi.1952.02040060030004. PMID: 14884753.

google.cat

books.google.cat

Kelly, Evelyn B. Encyclopedia of human genetics and disease (en anglès). Santa Barbara, Calif.: Greenwood, 2013. ISBN 9780313387142.
Loring, David W. INS Dictionary of Neuropsychology and Clinical Neurosciences (en anglès). Oxford University Press, Incorporated, 2015. ISBN 9780195366457.

medlineplus.gov

«Fanconi syndrome: MedlinePlus Medical Encyclopedia». medlineplus.gov. [Consulta: 21 desembre 2016].

medscape.com

emedicine.medscape.com

«Oculocerebrorenal Syndrome: Background, Pathophysiology, Epidemiology». , 01-06-2016.
«Oculocerebrorenal Syndrome: Background, Pathophysiology, Epidemiology». , 01-06-2016.

nih.gov

ncbi.nlm.nih.gov

Lewis, Richard Alan. «Lowe Syndrome». A: Pagon. GeneReviews. Seattle (WA): University of Washington, Seattle, 1993. update 2012
Loi M Orphanet Journal of Rare Diseases, 1, 2006, pàg. 16. DOI: 10.1186/1750-1172-1-16. PMC: 1526415. PMID: 16722554.
Hagemann, Nina; Hou, Xiaomin; Goody, Roger S.; Itzen, Aymelt; Erdmann, Kai S. Small GTPases, 3, 2, 01-06-2017, pàg. 107–110. DOI: 10.4161/sgtp.19380. ISSN: 2154-1256. PMID: 22790198.
«Lowe syndrome - Conditions - GTR - NCBI». www.ncbi.nlm.nih.gov. [Consulta: 21 desembre 2016].
American Journal of Diseases of Children, 83, 2, 1952, pàg. 164–84. DOI: 10.1001/archpedi.1952.02040060030004. PMID: 14884753.

ghr.nlm.nih.gov

Reference, Genetics Home. «Lowe syndrome». Genetics Home Reference. [Consulta: 21 desembre 2016].
Reference, Genetics Home. «OCRL gene». Genetics Home Reference. [Consulta: 21 desembre 2016].

omim.org

«OMIM Entry - # 309000 - LOWE OCULOCEREBRORENAL SYNDROME; OCRL». omim.org. [Consulta: 21 desembre 2016].

orpha.net

RESERVED, INSERM US14 -- ALL RIGHTS. «Orphanet: Oculocerebrorenal syndrome of Lowe». www.orpha.net. [Consulta: 21 desembre 2016].

patient.info

«Lowe's (Oculo-Cerebro-Renal) Syndrome | Doctor | Patient». Patient. [Consulta: 21 desembre 2016].

worldcat.org

Hagemann, Nina; Hou, Xiaomin; Goody, Roger S.; Itzen, Aymelt; Erdmann, Kai S. Small GTPases, 3, 2, 01-06-2017, pàg. 107–110. DOI: 10.4161/sgtp.19380. ISSN: 2154-1256. PMID: 22790198.