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The British Journal of Dermatology
|
March 8, 2014
Congenital erythropoietic porphyria: a case in which symptoms were precipitated by an unrelated anaemia
A Verma, E Rashidghamat, A Martinez, et al.
Journal of Surgical Case Reports
|
January 20, 2022
Bilateral cochlear implantation in a young patient with xeroderma pigmentosum (XP-D) and progressive sensorineural hearing loss-How to do it?
H Woodun, H Woodun, R Vetrivel Vedachalam, et al.
The British Journal of Dermatology
|
September 11, 2017
Chronic actinic dermatitis: successful treatment with psoralen-ultraviolet A photochemotherapy
S N Chee, L Novakovic, H Fassihi, et al.
The British Journal of Dermatology
|
December 16, 2020
Treatment of multiple facial basal cell carcinomas in a child with xeroderma pigmentosum complementation group C with Mohs micrographic surgery
A Greig, K Aloni, G Orchard, et al.
Clinical and Experimental Dermatology
|
February 21, 2006
Target proteins in inherited and acquired blistering skin disorders
H Fassihi, T Wong, V Wessagowit, et al.
The British Journal of Dermatology
|
February 19, 2010
Development and successful clinical application of preimplantation genetic haplotyping for Herlitz junctional epidermolysis bullosa
H Fassihi, L Liu, P J Renwick, et al.
The British Journal of Dermatology
|
June 14, 2005
Thalidomide in the management of epidermolysis bullosa pruriginosa
S Ozanic Bulic, H Fassihi, J E Mellerio, et al.
Clinical and Experimental Dermatology
|
February 24, 2005
Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in nonidentical twins
H Fassihi, G H S Ashton, J Denyer, et al.
The British Journal of Dermatology
|
February 1, 2006
Preimplantation genetic diagnosis of skin fragility-ectodermal dysplasia syndrome
H Fassihi, J Grace, A Lashwood, et al.
Clinical and Experimental Dermatology
|
April 6, 2005
An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene
G Sethuraman, H Fassihi, G H S Ashton, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
The British Journal of Dermatology
|
March 8, 2014
Congenital erythropoietic porphyria: a case in which symptoms were precipitated by an unrelated anaemia
A Verma, E Rashidghamat, A Martinez, et al.
Journal of Surgical Case Reports
|
January 20, 2022
Bilateral cochlear implantation in a young patient with xeroderma pigmentosum (XP-D) and progressive sensorineural hearing loss-How to do it?
H Woodun, H Woodun, R Vetrivel Vedachalam, et al.
The British Journal of Dermatology
|
September 11, 2017
Chronic actinic dermatitis: successful treatment with psoralen-ultraviolet A photochemotherapy
S N Chee, L Novakovic, H Fassihi, et al.
The British Journal of Dermatology
|
December 16, 2020
Treatment of multiple facial basal cell carcinomas in a child with xeroderma pigmentosum complementation group C with Mohs micrographic surgery
A Greig, K Aloni, G Orchard, et al.
Clinical and Experimental Dermatology
|
February 21, 2006
Target proteins in inherited and acquired blistering skin disorders
H Fassihi, T Wong, V Wessagowit, et al.
The British Journal of Dermatology
|
February 19, 2010
Development and successful clinical application of preimplantation genetic haplotyping for Herlitz junctional epidermolysis bullosa
H Fassihi, L Liu, P J Renwick, et al.
The British Journal of Dermatology
|
June 14, 2005
Thalidomide in the management of epidermolysis bullosa pruriginosa
S Ozanic Bulic, H Fassihi, J E Mellerio, et al.
Clinical and Experimental Dermatology
|
February 24, 2005
Prenatal diagnosis of Herlitz junctional epidermolysis bullosa in nonidentical twins
H Fassihi, G H S Ashton, J Denyer, et al.
The British Journal of Dermatology
|
February 1, 2006
Preimplantation genetic diagnosis of skin fragility-ectodermal dysplasia syndrome
H Fassihi, J Grace, A Lashwood, et al.
Clinical and Experimental Dermatology
|
April 6, 2005
An Indian child with Kindler syndrome resulting from a new homozygous nonsense mutation (C468X) in the KIND1 gene
G Sethuraman, H Fassihi, G H S Ashton, et al.
Page
of 3