I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Onoufriadis, A.
170
results:
Search for persons
X
Format
Online (170)
Mediatypes
Articles (Online) (55)
OpenAccess-fulltext (115)
Sorted by: Relevance
Sorted by: Year
?
1
A decade of next‐generation sequencing in genodermatoses: t..:
Chiu, F.P.‐C.
;
Doolan, B.J.
;
McGrath, J.A.
.
British Journal of Dermatology. 184 (2021) 4 - p. 606-616 , 2021
Link:
https://doi.org/10.1111/..
?
2
A germline mutation in the platelet‐derived growth factor r..:
Onoufriadis, A.
;
Boulouadnine, B.
;
Dachy, G.
...
British Journal of Dermatology. 184 (2021) 5 - p. 967-970 , 2021
Link:
https://doi.org/10.1111/..
?
3
WNT10A, dermatology and dentistry:
Doolan, B. J.
;
Onoufriadis, A.
;
Kantaputra, P.
.
British Journal of Dermatology. 185 (2021) 6 - p. 1105-1111 , 2021
Link:
https://doi.org/10.1111/..
?
4
Genetic analysis in three Egyptian patients with Griscelli ..:
Abd Elmaksoud, M. S.
;
Gomaa, N. S.
;
Azouz, H. G.
...
Clinical and Experimental Dermatology. 45 (2020) 6 - p. 789-792 , 2020
Link:
https://doi.org/10.1111/..
?
5
A study of gene mutations and how they relate to the differ..:
Simpson, J.K.
;
Martinez‐Queipo, M.
;
Onoufriadis, A.
...
British Journal of Dermatology. 182 (2020) 3 - p. , 2020
Link:
https://doi.org/10.1111/..
?
6
一项关于基因突变及其与不同鱼鳞病类型相关性的研究:
Simpson, J.K.
;
Martinez‐Queipo, M.
;
Onoufriadis, A.
...
British Journal of Dermatology. 182 (2020) 3 - p. , 2020
Link:
https://doi.org/10.1111/..
?
7
Autosomal recessive hypotrichosis with loose anagen hairs a..:
Onoufriadis, A.
;
Cabezas, A.
;
Ng, J.C.F.
...
British Journal of Dermatology. 184 (2020) 5 - p. 935-943 , 2020
Link:
https://doi.org/10.1111/..
?
8
Molecular basis and inheritance patterns of amyloidosis cut..:
Chiu, F. P. C.
;
Wessagowit, V.
;
Cakmak, M. F.
...
Clinical and Experimental Dermatology. 45 (2020) 5 - p. 650-653 , 2020
Link:
https://doi.org/10.1111/..
?
9
Prevalence, pathophysiology and management of itch in epide..:
Papanikolaou, M.
;
Onoufriadis, A.
;
Mellerio, J.E.
...
British Journal of Dermatology. 184 (2020) 5 - p. 816-825 , 2020
Link:
https://doi.org/10.1111/..
?
10
Autosomal recessive mutations in plakoglobin and risk of ca..:
Oktem, A.
;
Doolan, B. J.
;
Akay, B. N.
...
Clinical and Experimental Dermatology. 45 (2020) 5 - p. 654-657 , 2020
Link:
https://doi.org/10.1111/..
?
11
Genotype–phenotype correlation in a large English cohort of..:
Simpson, J.K.
;
Martinez‐Queipo, M.
;
Onoufriadis, A.
...
British Journal of Dermatology. 182 (2019) 3 - p. 729-737 , 2019
Link:
https://doi.org/10.1111/..
?
12
Nonsyndromic erythrodermic ichthyosis resulting from a homo..:
Onoufriadis, A.
;
Simpson, J. K.
;
McDonald, C.
...
Clinical and Experimental Dermatology. 45 (2019) 3 - p. 391-394 , 2019
Link:
https://doi.org/10.1111/..
?
13
Genetic analysis in Egyptian patients with Chediak–Higashi ..:
Gomaa, N. S.
;
Lee, J. Y. W.
;
El Sharkawy, A.
...
Clinical and Experimental Dermatology. 44 (2019) 7 - p. 814-817 , 2019
Link:
https://doi.org/10.1111/..
?
14
Primary Ciliary Dyskinesia Due to Microtubular Defects is A..:
Irving, S.
;
Dixon, M.
;
Fassad, M. R.
...
Lung. 196 (2018) 2 - p. 231-238 , 2018
Link:
https://doi.org/10.1007/..
?
15
Gene discovery for motile cilia disorders: mutation spectru..:
Onoufriadis, A
;
Hjeij, R
;
Watson, CM
...
Cilia. 4 (2015) S1 - p. , 2015
Link:
https://doi.org/10.1186/..
1-15