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Lamiaa Hamie

Showing results (21-30 of 29) with videos related to

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Journal of the American Academy of Dermatology|June 21, 2021
Genodermatoses with hearing impairmentLamiaa 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 dysplasiaToru Kawai, Ryota Hayashi, Hiroyuki Nakai, et al.
American Journal of Medical Genetics. Part A|February 3, 2018
CHILD syndrome: A modified pathogenesis-targeted therapeutic approachChristina Bergqvist, Bilal Abdallah, Divina-Justina Hasbani, et al.
European Journal of Dermatology : EJD|November 23, 2017
FOXI2: a possible gene contributing to ectodermal dysplasiaMazen Kurban, Savo Bou Zeineddine, Lamiaa Hamie, et al.
Postgraduate Medical Journal|September 5, 2018
SuPAR, an emerging biomarker in kidney and inflammatory diseasesLamiaa 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 decalvansGeorges 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 formTara 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 geneChristina Bergqvist, Humam Kadara, Lamiaa Hamie, et al.
Clinical and Experimental Pharmacology & Physiology|June 20, 2020
SuPAR, a potential inflammatory mediator in psoriasis pathogenesisLamiaa Hamie, Edward Eid, Ossama Abbas, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 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 impairmentLamiaa 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 dysplasiaToru Kawai, Ryota Hayashi, Hiroyuki Nakai, et al.
American Journal of Medical Genetics. Part A|February 3, 2018
CHILD syndrome: A modified pathogenesis-targeted therapeutic approachChristina Bergqvist, Bilal Abdallah, Divina-Justina Hasbani, et al.
European Journal of Dermatology : EJD|November 23, 2017
FOXI2: a possible gene contributing to ectodermal dysplasiaMazen Kurban, Savo Bou Zeineddine, Lamiaa Hamie, et al.
Postgraduate Medical Journal|September 5, 2018
SuPAR, an emerging biomarker in kidney and inflammatory diseasesLamiaa 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 decalvansGeorges 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 formTara 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 geneChristina Bergqvist, Humam Kadara, Lamiaa Hamie, et al.
Clinical and Experimental Pharmacology & Physiology|June 20, 2020
SuPAR, a potential inflammatory mediator in psoriasis pathogenesisLamiaa Hamie, Edward Eid, Ossama Abbas, et al.
Pageof 3