Dedna hemokromatoza (Slovenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Dedna hemokromatoza" in Slovenian language version.

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11nih.gov

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7doi.org

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2web.archive.org

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2mayoclinic.com

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2archive.org

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1amebis.si

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1psu.edu

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1cdc.gov

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amebis.si

lsm1.amebis.si

http://lsm1.amebis.si/lsmeds/novPogoj.aspx?pPogoj=hemokromatoza^{[mrtva povezava]}, Medicinski e-slovar, vpogled: 23. 2. 2012.

archive.org

Jones H; Hedley-Whyte E (1983). »Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs«. Neurology. 33 (11): 1479–1483. PMID 6685241.
Nielsen J; Jensen L; Krabbe K (1995). »Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome«. J Neurol Neurosurg Psychiatry. 59 (3): 318–321. doi:10.1136/jnnp.59.3.318. PMC 486041. PMID 7673967.

cdc.gov

Iron Overload and Hemochromatosis Centers for Disease Control and Prevention

doi.org

Vujić Spasić M; Kiss J; Herrmann T; in sod. (2008). »Hfe acts in hepatocytes to prevent hemochromatosis«. Cell Metab. 7 (2): 173–178. doi:10.1016/j.cmet.2007.11.014. PMID 18249176.
Shizukuda Y; Bolan C; Nguyen T; Botello G; Tripodi D; Yau Y; Waclawiw M; Leitman S; Rosing D (2007). »Oxidative stress in asymptomatic subjects with hereditary hemochromatosis«. Am J Hematol. 82 (3): 249–50. doi:10.1002/ajh.20743. PMID 16955456.
Pietrangelo A (2004). »Hereditary hemochromatosis—a new look at an old disease«. N. Engl. J. Med. 350 (23): 2383–2397. doi:10.1056/NEJMra031573. PMID 15175440.
Costello D; Walsh S; Harrington H; Walsh C (2004). »Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series«. J Neurol Neurosurg Psychiatry. 75 (4): 631–633. doi:10.1136/jnnp.2003.027441. PMC 1739011. PMID 15026513.
Nielsen J; Jensen L; Krabbe K (1995). »Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome«. J Neurol Neurosurg Psychiatry. 59 (3): 318–321. doi:10.1136/jnnp.59.3.318. PMC 486041. PMID 7673967.
Barton JC; Acton RT (2009). »Hemochromatosis and Vibrio vulnificus Wound Infections«. J. Clin. Gastroenterol. 43 (9): 890–893. doi:10.1097/MCG.0b013e31819069c1. PMID 19349902.
Jolivet-Gougeon A; Loréal O; Ingels A; in sod. (2008). »Serum transferrin saturation increase is associated with decrease of antibacterial activity of serum in patients with HFE-related genetic hemochromatosis«. Am. J. Gastroenterol. 103 (10): 2502–8. doi:10.1111/j.1572-0241.2008.02036.x. PMID 18684194.

mayoclinic.com

»Hemochromatosis: Symptoms«. Mayo Foundation for Medical Education and Research (MFMER).
»Hemochromatosis: Tests and diagnosis«. Mayo Foundation for Medical Education and Research (MFMER). Pridobljeno 20. aprila 2009.

nih.gov

pubmed.ncbi.nlm.nih.gov

Vujić Spasić M; Kiss J; Herrmann T; in sod. (2008). »Hfe acts in hepatocytes to prevent hemochromatosis«. Cell Metab. 7 (2): 173–178. doi:10.1016/j.cmet.2007.11.014. PMID 18249176.
Shizukuda Y; Bolan C; Nguyen T; Botello G; Tripodi D; Yau Y; Waclawiw M; Leitman S; Rosing D (2007). »Oxidative stress in asymptomatic subjects with hereditary hemochromatosis«. Am J Hematol. 82 (3): 249–50. doi:10.1002/ajh.20743. PMID 16955456.
Pietrangelo A (2004). »Hereditary hemochromatosis—a new look at an old disease«. N. Engl. J. Med. 350 (23): 2383–2397. doi:10.1056/NEJMra031573. PMID 15175440.
Jones H; Hedley-Whyte E (1983). »Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs«. Neurology. 33 (11): 1479–1483. PMID 6685241.
Costello D; Walsh S; Harrington H; Walsh C (2004). »Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series«. J Neurol Neurosurg Psychiatry. 75 (4): 631–633. doi:10.1136/jnnp.2003.027441. PMC 1739011. PMID 15026513.
Nielsen J; Jensen L; Krabbe K (1995). »Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome«. J Neurol Neurosurg Psychiatry. 59 (3): 318–321. doi:10.1136/jnnp.59.3.318. PMC 486041. PMID 7673967.
Barton JC; Acton RT (2009). »Hemochromatosis and Vibrio vulnificus Wound Infections«. J. Clin. Gastroenterol. 43 (9): 890–893. doi:10.1097/MCG.0b013e31819069c1. PMID 19349902.
Jolivet-Gougeon A; Loréal O; Ingels A; in sod. (2008). »Serum transferrin saturation increase is associated with decrease of antibacterial activity of serum in patients with HFE-related genetic hemochromatosis«. Am. J. Gastroenterol. 103 (10): 2502–8. doi:10.1111/j.1572-0241.2008.02036.x. PMID 18684194.

ncbi.nlm.nih.gov

Costello D; Walsh S; Harrington H; Walsh C (2004). »Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series«. J Neurol Neurosurg Psychiatry. 75 (4): 631–633. doi:10.1136/jnnp.2003.027441. PMC 1739011. PMID 15026513.
Nielsen J; Jensen L; Krabbe K (1995). »Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome«. J Neurol Neurosurg Psychiatry. 59 (3): 318–321. doi:10.1136/jnnp.59.3.318. PMC 486041. PMID 7673967.

digestive.niddk.nih.gov

Hemochromatosis Arhivirano 2007-03-18 na Wayback Machine. National Digestive Diseases Information Clearinghouse, National Institutes of Health, U.S. Department of Health and Human Services

psu.edu

live.psu.edu

»Celtic Curse«. Arhivirano iz prvotnega spletišča dne 31. maja 2009. Pridobljeno 23. februarja 2012.

web.archive.org

»Celtic Curse«. Arhivirano iz prvotnega spletišča dne 31. maja 2009. Pridobljeno 23. februarja 2012.
Hemochromatosis Arhivirano 2007-03-18 na Wayback Machine. National Digestive Diseases Information Clearinghouse, National Institutes of Health, U.S. Department of Health and Human Services