25 related articles for article (PubMed ID: 19320027)
1. Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Besana V; Di Pierro E; Brancaleoni V; Sabrina A; Fiocchi M; Cappellini MD
Hum Genet; 2009 Apr; 125(3):344. PubMed ID: 19320020
[No Abstract] [Full Text] [Related]
2. Novel human pathological mutations. Gene symbol: HMBS. Disease: porphyria, acute intermittent.
Di Pierro E; Besana V; Brancaleoni V; Ausenda S; Lonati P; Cappellini MD
Hum Genet; 2007 Nov; 122(3-4):417. PubMed ID: 18350657
[No Abstract] [Full Text] [Related]
3. A novel 19-bp deletion of exon 15 in the HMBS gene causing acute intermittent porphyria associating with rhabdomyolysis during an acute attack.
Yrjönen A; Pischik E; Mehtälä S; Kauppinen R
Clin Genet; 2008 Oct; 74(4):396-8. PubMed ID: 18647325
[No Abstract] [Full Text] [Related]
4. 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. PubMed ID: 19694018
[No Abstract] [Full Text] [Related]
5. Gene symbol: HMBS. Disease: Acute intermittent porphyria.
Solis CS; Lopez-Echaniz I; Sefarty-Graneda D; Astrin KH; Desnick RJ
Hum Genet; 2004 Mar; 114(4):402. PubMed ID: 15046057
[No Abstract] [Full Text] [Related]
6. 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. PubMed ID: 19320027
[No Abstract] [Full Text] [Related]
7. The three-dimensional structures of mutants of porphobilinogen deaminase: toward an understanding of the structural basis of acute intermittent porphyria.
Brownlie PD; Lambert R; Louie GV; Jordan PM; Blundell TL; Warren MJ; Cooper JB; Wood SP
Protein Sci; 1994 Oct; 3(10):1644-50. PubMed ID: 7849582
[TBL] [Abstract][Full Text] [Related]
8. Acute intermittent porphyria: laboratory diagnosis by molecular methods.
Schreiber WE
Clin Lab Med; 1995 Dec; 15(4):943-56. PubMed ID: 8838232
[TBL] [Abstract][Full Text] [Related]
9. Homozygous acute intermittent porphyria in a 7-year-old boy with massive excretions of porphyrins and porphyrin precursors.
Hessels J; Voortman G; van der Wagen A; van der Elzen C; Scheffer H; Zuijderhoudt FM
J Inherit Metab Dis; 2004; 27(1):19-27. PubMed ID: 14970743
[TBL] [Abstract][Full Text] [Related]
10. Molecular basis of acute intermittent porphyria.
Wood S; Lambert R; Jordan PM
Mol Med Today; 1995 Aug; 1(5):232-9. PubMed ID: 17607885
[TBL] [Abstract][Full Text] [Related]
11. Neurological manifestations of acute intermittent porphyria.
Pischik E; Kauppinen R
Cell Mol Biol (Noisy-le-grand); 2009 Feb; 55(1):72-83. PubMed ID: 19268005
[TBL] [Abstract][Full Text] [Related]
12. Nitric oxide and the clinical manifestations of acute porphyria.
Thachil J
Intern Med J; 2008 Sep; 38(9):732-5. PubMed ID: 19143888
[TBL] [Abstract][Full Text] [Related]
13.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
