Michael N Badminton
Overview
Explore the profile of Michael N Badminton including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
19
Citations
404
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Fontanellas A, Avila M, Deybach J, Badminton M
Liver Int
. 2024 Sep;
45(3):e16061.
PMID: 39248503
No abstract available.
2.
Badminton M, Anderson K, Deybach J, Harper P, Sandberg S, Elder G
Liver Int
. 2024 May;
44(9):2144-2155.
PMID: 38767598
We describe developments in understanding of the porphyrias associated with each step in the haem biosynthesis pathway and the role of individuals whose contributions led to major advances over the...
3.
Stein P, Badminton M, Rees D
Br J Haematol
. 2016 Dec;
176(4):527-538.
PMID: 27982422
Acute porphyrias are rare inherited disorders due to deficiencies of haem synthesis enzymes. To date, all UK cases have been one of the three autosomal dominant forms, although penetrance is...
4.
5.
Schulenburg-Brand D, Katugampola R, Anstey A, Badminton M
Dermatol Clin
. 2014 Jun;
32(3):369-84, ix.
PMID: 24891059
The porphyrias are a group of mainly inherited disorders of heme biosynthesis where accumulation of porphyrins and/or porphyrin precursors gives rise to 2 types of clinical presentation: cutaneous photosensitivity and/or...
6.
Whatley S, Mason N, Rhodes J, Stewart M, Reed P, Crowley V, et al.
Clin Chem
. 2013 Apr;
59(7):1123-5.
PMID: 23609978
No abstract available.
7.
8.
Sarkany R, Ibbotson S, Whatley S, Lawrence C, Gover P, Mufti G, et al.
J Invest Dermatol
. 2011 Feb;
131(5):1172-5.
PMID: 21326293
No abstract available.
9.
Whatley S, Mason N, Woolf J, Newcombe R, Elder G, Badminton M
Clin Chem
. 2009 May;
55(7):1406-14.
PMID: 19460837
Background: Clinically indistinguishable attacks of acute porphyria occur in acute intermittent porphyria (AIP), hereditary coproporphyria (HCP), and variegate porphyria (VP). There are few evidence-based diagnostic strategies for these disorders. Methods:...
10.
Holme S, Whatley S, Roberts A, Anstey A, Elder G, Ead R, et al.
J Invest Dermatol
. 2008 Sep;
129(3):599-605.
PMID: 18787536
Erythropoietic protoporphyria (EPP) is an inherited disorder that results from partial deficiency of ferrochelatase (FECH). It is characterized clinically by acute photosensitivity and, in 2% of patients, liver disease. Inheritance...