Lowe-Syndrom (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Lowe-Syndrom" in German language version.

refsWebsite

Global rank German rank

7zdb-katalog.de

123^rd place

6^th place

7nih.gov

4^th place

7^th place

4doi.org

2^nd place

3^rd place

1uni-hamburg.de

3,809^th place

433^rd place

1omim.org

4,380^th place

781^st place

doi.org

M. Loi: Lowe syndrome. In: Orphanet Journal of Rare Diseases. Band 1, 2006, S. 16, ISSN 1750-1172. doi:10.1186/1750-1172-1-16. PMID 16722554. PMC 1526415 (freier Volltext). (Review).
L. R. Charnas, I. Bernardini u. a.: Clinical and laboratory findings in the oculocerebrorenal syndrome of Lowe, with special reference to growth and renal function. In: The New England journal of medicine. Band 324, Nummer 19, Mai 1991, S. 1318–1325, ISSN 0028-4793. doi:10.1056/NEJM199105093241904. PMID 2017228.
L. Kenworthy, T. Park, L. R. Charnas: Cognitive and behavioral profile of the oculocerebrorenal syndrome of Lowe. In: American journal of medical genetics. Band 46, Nummer 3, Mai 1993, S. 297–303, ISSN 0148-7299. doi:10.1002/ajmg.1320460312. PMID 8488875.
L. Charnas, J. Bernar u. a.: MRI findings and peripheral neuropathy in Lowe's syndrome. In: Neuropediatrics. Band 19, Nummer 1, Februar 1988, S. 7–9, ISSN 0174-304X. doi:10.1055/s-2008-1052393. PMID 2834662.

nih.gov

ncbi.nlm.nih.gov

M. Loi: Lowe syndrome. In: Orphanet Journal of Rare Diseases. Band 1, 2006, S. 16, ISSN 1750-1172. doi:10.1186/1750-1172-1-16. PMID 16722554. PMC 1526415 (freier Volltext). (Review).
O. T. Mueller, J. K. Hartsfield u. a.: Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint. In: American Journal of Human Genetics. Band 49, Nummer 4, Oktober 1991, S. 804–810, ISSN 0002-9297. PMID 1897526. PMC 1683175 (freier Volltext).
R. C. Tripathi, G. W. Cibis, B. J. Tripathi: Pathogenesis of cataracts in patients with Lowe's syndrome. In: Ophthalmology. Band 93, Nummer 8, August 1986, S. 1046–1051, ISSN 0161-6420. PMID 3763153.
L. R. Charnas, I. Bernardini u. a.: Clinical and laboratory findings in the oculocerebrorenal syndrome of Lowe, with special reference to growth and renal function. In: The New England journal of medicine. Band 324, Nummer 19, Mai 1991, S. 1318–1325, ISSN 0028-4793. doi:10.1056/NEJM199105093241904. PMID 2017228.
L. Kenworthy, T. Park, L. R. Charnas: Cognitive and behavioral profile of the oculocerebrorenal syndrome of Lowe. In: American journal of medical genetics. Band 46, Nummer 3, Mai 1993, S. 297–303, ISSN 0148-7299. doi:10.1002/ajmg.1320460312. PMID 8488875.
L. Charnas, J. Bernar u. a.: MRI findings and peripheral neuropathy in Lowe's syndrome. In: Neuropediatrics. Band 19, Nummer 1, Februar 1988, S. 7–9, ISSN 0174-304X. doi:10.1055/s-2008-1052393. PMID 2834662.
C. U. Lowe, M. Terrey, E. A. MacLachlan: Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity. In: American Journal of Diseases of Children. Band 83, Nummer 2, Februar 1952, S. 164–184, ISSN 0096-8994. PMID 14884753.

omim.org

Lowe-Syndrom. In: Online Mendelian Inheritance in Man. (englisch)

uni-hamburg.de

ediss.sub.uni-hamburg.de

V. A. van Rahden: Auswirkungen einer Depletion der humanen Inositol-Polyphosphat 5-Phosphatase OCRL auf Transportwege des Mannose 6-Phosphat-Rezeptors. (PDF; 5,6 MB) Dissertation, Universität Hamburg, 2011, S. 1.

zdb-katalog.de

M. Loi: Lowe syndrome. In: Orphanet Journal of Rare Diseases. Band 1, 2006, S. 16, ISSN 1750-1172. doi:10.1186/1750-1172-1-16. PMID 16722554. PMC 1526415 (freier Volltext). (Review).
O. T. Mueller, J. K. Hartsfield u. a.: Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint. In: American Journal of Human Genetics. Band 49, Nummer 4, Oktober 1991, S. 804–810, ISSN 0002-9297. PMID 1897526. PMC 1683175 (freier Volltext).
R. C. Tripathi, G. W. Cibis, B. J. Tripathi: Pathogenesis of cataracts in patients with Lowe's syndrome. In: Ophthalmology. Band 93, Nummer 8, August 1986, S. 1046–1051, ISSN 0161-6420. PMID 3763153.
L. R. Charnas, I. Bernardini u. a.: Clinical and laboratory findings in the oculocerebrorenal syndrome of Lowe, with special reference to growth and renal function. In: The New England journal of medicine. Band 324, Nummer 19, Mai 1991, S. 1318–1325, ISSN 0028-4793. doi:10.1056/NEJM199105093241904. PMID 2017228.
L. Kenworthy, T. Park, L. R. Charnas: Cognitive and behavioral profile of the oculocerebrorenal syndrome of Lowe. In: American journal of medical genetics. Band 46, Nummer 3, Mai 1993, S. 297–303, ISSN 0148-7299. doi:10.1002/ajmg.1320460312. PMID 8488875.
L. Charnas, J. Bernar u. a.: MRI findings and peripheral neuropathy in Lowe's syndrome. In: Neuropediatrics. Band 19, Nummer 1, Februar 1988, S. 7–9, ISSN 0174-304X. doi:10.1055/s-2008-1052393. PMID 2834662.
C. U. Lowe, M. Terrey, E. A. MacLachlan: Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity. In: American Journal of Diseases of Children. Band 83, Nummer 2, Februar 1952, S. 164–184, ISSN 0096-8994. PMID 14884753.