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Novel human pathological mutations. Gene symbol: CPOX. Disease: Coproporphyria.
Ausenda S, Di Pierro E, Brancaleoni V, Tavazzi D, Cappellini MD.
Hum Genet. 2009 Aug;126(2):342. No abstract available. PMID: 19694028 [PubMed - indexed for MEDLINE]Related articles
Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittent.
Di Pierro E, Brancaleoni V, Stanzial F, Benedicenti F, Castellan C, Cappellini MD.
Hum Genet. 2009 Aug;126(2):339. No abstract available. PMID: 19694018 [PubMed - indexed for MEDLINE]Related articles
Alpha-melanocyte stimulating hormone analogues: the perils and the promise.
Mazza JM, Zippin JH.
J Drugs Dermatol. 2009 Aug;8(8):772-6. Review. No abstract available. PMID: 19663117 [PubMed - indexed for MEDLINE]Related articles
Relation of porphyria to atrial fibrillation.
Dhoble A, Patel MB, Abdelmoneim SS, Puttarajappa C, Abela GS, Bhatt DL, Thakur RK.
Am J Cardiol. 2009 Aug 1;104(3):373-6. Epub 2009 Jun 6.PMID: 19616670 [PubMed - indexed for MEDLINE]Related articles
Blistering skin conditions.
Welsh B.
Aust Fam Physician. 2009 Jul;38(7):484-90.PMID: 19575066 [PubMed - indexed for MEDLINE]Related articlesFree article
Role of two nutritional hepatic markers (insulin-like growth factor 1 and transthyretin) in the clinical assessment and follow-up of acute intermittent porphyria patients.
Delaby C, To-Figueras J, Deybach JC, Casamitjana R, Puy H, Herrero C.
J Intern Med. 2009 Sep;266(3):277-85. Epub 2009 Apr 23.PMID: 19570056 [PubMed - indexed for MEDLINE]Related articles
66-year-old woman with painless vesicular lesions.
Bardia A, Swanson EA, Thomas KG.
Mayo Clin Proc. 2009 Jul;84(7):639-42. No abstract available. PMID: 19567718 [PubMed - indexed for MEDLINE]Related articles
The acute porphyrias: a diagnostic and therapeutic challenge in internal and emergency medicine.
Ventura P, Cappellini MD, Rocchi E.
Intern Emerg Med. 2009 Aug;4(4):297-308. Epub 2009 May 29.PMID: 19479318 [PubMed - indexed for MEDLINE]Related articles
GoGene: gene annotation in the fast lane.
Plake C, Royer L, Winnenburg R, Hakenberg J, Schroeder M.
Nucleic Acids Res. 2009 Jul 1;37(Web Server issue):W300-4. Epub 2009 May 22.PMID: 19465383 [PubMed - indexed for MEDLINE]Related articlesFree article
Diagnostic strategies for autosomal dominant acute porphyrias: retrospective analysis of 467 unrelated patients referred for mutational analysis of the HMBS, CPOX, or PPOX gene.
Whatley SD, Mason NG, Woolf JR, Newcombe RG, Elder GH, Badminton MN.
Clin Chem. 2009 Jul;55(7):1406-14. Epub 2009 May 21.PMID: 19460837 [PubMed - indexed for MEDLINE]Related articles
Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives.
Badenas C, To-Figueras J, Phillips JD, Warby CA, Muñoz C, Herrero C.
Clin Genet. 2009 Apr;75(4):346-53.PMID: 19419417 [PubMed - indexed for MEDLINE]Related articles
Clinical aspects of acute intermittent porphyria in northern Sweden: a population-based study.
Bylesjö I, Wikberg A, Andersson C.
Scand J Clin Lab Invest. 2009;69(5):612-8.PMID: 19401933 [PubMed - indexed for MEDLINE]Related articles
Enzyme antioxidant defences and oxidative damage in red blood cells of variegate porphyria patients.
Ferrer MD, Tauler P, Sureda A, Romaguera D, Llompart I, Palacin C, Orfila J, Tur JA, Pons A.
Redox Rep. 2009;14(2):69-74.PMID: 19389274 [PubMed - indexed for MEDLINE]Related articles
Red urine and photosensitive skin rash.
Ghosh SK, Bandyopadhyay D, Haldar S.
J Fam Pract. 2009 Apr;58(4):200-2. No abstract available. PMID: 19358798 [PubMed - indexed for MEDLINE]Related articles
Porphyria in Switzerland, 15 years experience.
Schneider-Yin X, Harms J, Minder EI.
Swiss Med Wkly. 2009 Apr 4;139(13-14):198-206.PMID: 19350426 [PubMed - indexed for MEDLINE]Related articlesFree article
Plasma porphobilinogen as a sensitive biomarker to monitor the clinical and therapeutic course of acute intermittent porphyria attacks.
Sardh E, Harper P, Andersson DE, Floderus Y.
Eur J Intern Med. 2009 Mar;20(2):201-7. Epub 2008 Aug 8.PMID: 19327613 [PubMed - indexed for MEDLINE]Related articles
Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Di Pierro E, Besana V, Brancaleoni V, Fasulo MR, Cesaretti C, Cappellini MD.
Hum Genet. 2009 Apr;125(3):347. No abstract available. PMID: 19320027 [PubMed - indexed for MEDLINE]Related articles
Besana V, Di Pierro E, Brancaleoni V, Sabrina A, Fiocchi M, Cappellini MD.
Hum Genet. 2009 Apr;125(3):344. No abstract available. PMID: 19320020 [PubMed - indexed for MEDLINE]Related articles
Novel human pathological mutations. Gene symbol: PPOX. Disease: porphyria, variegate.
Ausenda S, Moriondo V, Marchini S, Besana V, Di Pierro E, Brancaleoni V, Ventura P, Rocchi E, Cappellini MD.
Hum Genet. 2009 Apr;125(3):344. No abstract available. PMID: 19320019 [PubMed - indexed for MEDLINE]Related articles
A homozygous mutation in the ferrochelatase gene underlies erythropoietic protoporphyria associated with palmar keratoderma.
Méndez M, Poblete-Gutiérrez P, Morán-Jiménez MJ, Rodriguez ME, Garrido-Astray MC, Fontanellas A, Frank J, de Salamanca RE.
Br J Dermatol. 2009 Jun;160(6):1330-4. Epub 2009 Mar 9. No abstract available. PMID: 19298273 [PubMed - indexed for MEDLINE]Related articles
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Nucleic Acids Res. 2009 Jul 1; 37(Web Server issue):W300-4.
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