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Journal of the American Academy of Dermatology
|
June 21, 2021
Genodermatoses with hearing impairment
Lamiaa Hamie, Edward Eid, Samar Khalil, et al.
Journal of Dermatological Science
|
March 13, 2018
A heterozygous mutation in the SAM domain of p63 underlies a mild form of ectodermal dysplasia
Toru Kawai, Ryota Hayashi, Hiroyuki Nakai, et al.
American Journal of Medical Genetics. Part A
|
February 3, 2018
CHILD syndrome: A modified pathogenesis-targeted therapeutic approach
Christina Bergqvist, Bilal Abdallah, Divina-Justina Hasbani, et al.
European Journal of Dermatology : EJD
|
November 23, 2017
FOXI2: a possible gene contributing to ectodermal dysplasia
Mazen Kurban, Savo Bou Zeineddine, Lamiaa Hamie, et al.
Postgraduate Medical Journal
|
September 5, 2018
SuPAR, an emerging biomarker in kidney and inflammatory diseases
Lamiaa Hamie, Georges Daoud, Georges Nemer, et al.
Clinical Genetics
|
May 1, 2020
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans
Georges Nemer, Nehme El-Hachem, Edward Eid, et al.
European Journal of Dermatology : EJD
|
July 26, 2017
Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous form
Tara Bardawil, Abdallah Rebeiz, Myriam Chaabouni, et al.
International Journal of Dermatology
|
December 13, 2017
SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene
Christina Bergqvist, Humam Kadara, Lamiaa Hamie, et al.
Clinical and Experimental Pharmacology & Physiology
|
June 20, 2020
SuPAR, a potential inflammatory mediator in psoriasis pathogenesis
Lamiaa Hamie, Edward Eid, Ossama Abbas, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Journal of the American Academy of Dermatology
|
June 21, 2021
Genodermatoses with hearing impairment
Lamiaa Hamie, Edward Eid, Samar Khalil, et al.
Journal of Dermatological Science
|
March 13, 2018
A heterozygous mutation in the SAM domain of p63 underlies a mild form of ectodermal dysplasia
Toru Kawai, Ryota Hayashi, Hiroyuki Nakai, et al.
American Journal of Medical Genetics. Part A
|
February 3, 2018
CHILD syndrome: A modified pathogenesis-targeted therapeutic approach
Christina Bergqvist, Bilal Abdallah, Divina-Justina Hasbani, et al.
European Journal of Dermatology : EJD
|
November 23, 2017
FOXI2: a possible gene contributing to ectodermal dysplasia
Mazen Kurban, Savo Bou Zeineddine, Lamiaa Hamie, et al.
Postgraduate Medical Journal
|
September 5, 2018
SuPAR, an emerging biomarker in kidney and inflammatory diseases
Lamiaa Hamie, Georges Daoud, Georges Nemer, et al.
Clinical Genetics
|
May 1, 2020
A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans
Georges Nemer, Nehme El-Hachem, Edward Eid, et al.
European Journal of Dermatology : EJD
|
July 26, 2017
Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous form
Tara Bardawil, Abdallah Rebeiz, Myriam Chaabouni, et al.
International Journal of Dermatology
|
December 13, 2017
SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene
Christina Bergqvist, Humam Kadara, Lamiaa Hamie, et al.
Clinical and Experimental Pharmacology & Physiology
|
June 20, 2020
SuPAR, a potential inflammatory mediator in psoriasis pathogenesis
Lamiaa Hamie, Edward Eid, Ossama Abbas, et al.
Page
of 3