Hamie L - Search Results

1

FOXI2: a possible gene contributing to ectodermal dysplasia.

Kurban M, Zeineddine SB, Hamie L, Safi R, Abbas O, Kibbi AG, Bitar F, Nemer G. Kurban M, et al. Among authors: hamie l. Eur J Dermatol. 2017 Dec 1;27(6):641-645. doi: 10.1684/ejd.2017.3130. Eur J Dermatol. 2017. PMID: 29165300

2

A novel heterozygous mutation in desmoplakin gene in a Lebanese patient with Carvajal syndrome and tooth agenesis.

Bitar F, Najjar T, Hayashi R, Nemer G, Shigehara Y, Hamie L, Abbas O, Kibbi AG, Shimomura Y, Kurban M. Bitar F, et al. Among authors: hamie l. J Eur Acad Dermatol Venereol. 2016 Dec;30(12):e217-e219. doi: 10.1111/jdv.13549. Epub 2016 Feb 1. J Eur Acad Dermatol Venereol. 2016. PMID: 26833927 No abstract available.

3

Clinical clues early in the lives of individuals with lipoid proteinosis can determine the course of the disease.

Hamie L, Knio Z, Abbas O, Akel R, Bardawil T, Kibbi AG, Kurban M. Hamie L, et al. Clin Exp Dermatol. 2017 Jun;42(4):428-430. doi: 10.1111/ced.13075. Epub 2017 Feb 28. Clin Exp Dermatol. 2017. PMID: 28244239 No abstract available.

4

Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous form.

Bardawil T, Rebeiz A, Chaabouni M, El Halabi J, Kambris Z, Abbas O, Abou Hassan O, Hamie L, Bitar F, Ghani Kibbi A, Nemer G, Kurban M. Bardawil T, et al. Among authors: hamie l. Eur J Dermatol. 2017 Oct 1;27(5):519-523. doi: 10.1684/ejd.2017.3087. Eur J Dermatol. 2017. PMID: 28739549

5

SLURP-1 is mutated in Mal de Meleda, a potential molecular signature for melanoma and a putative squamous lineage tumor suppressor gene.

Bergqvist C, Kadara H, Hamie L, Nemer G, Safi R, Karouni M, Marrouche N, Abbas O, Hasbani DJ, Kibbi AG, Nassar D, Shimomura Y, Kurban M. Bergqvist C, et al. Among authors: hamie l. Int J Dermatol. 2018 Feb;57(2):162-170. doi: 10.1111/ijd.13850. Epub 2017 Dec 12. Int J Dermatol. 2018. PMID: 29231248

6

CHILD syndrome: A modified pathogenesis-targeted therapeutic approach.

Bergqvist C, Abdallah B, Hasbani DJ, Abbas O, Kibbi AG, Hamie L, Kurban M, Rubeiz N. Bergqvist C, et al. Among authors: hamie l. Am J Med Genet A. 2018 Mar;176(3):733-738. doi: 10.1002/ajmg.a.38619. Epub 2018 Feb 2. Am J Med Genet A. 2018. PMID: 29392821

7

A heterozygous mutation in the SAM domain of p63 underlies a mild form of ectodermal dysplasia.

Kawai T, Hayashi R, Nakai H, Shimomura Y, Kurban M, Hamie L, Fujikawa H, Fujimoto A, Abe R. Kawai T, et al. Among authors: hamie l. J Dermatol Sci. 2018 Jun;90(3):360-363. doi: 10.1016/j.jdermsci.2018.02.006. Epub 2018 Feb 21. J Dermatol Sci. 2018. PMID: 29526522 No abstract available.

8

SuPAR, an emerging biomarker in kidney and inflammatory diseases.

Hamie L, Daoud G, Nemer G, Nammour T, El Chediak A, Uthman IW, Kibbi AG, Eid A, Kurban M. Hamie L, et al. Postgrad Med J. 2018 Sep;94(1115):517-524. doi: 10.1136/postgradmedj-2018-135839. Epub 2018 Sep 3. Postgrad Med J. 2018. PMID: 30177549 Review.

9

A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans.

Nemer G, El-Hachem N, Eid E, Hamie L, Bardawil T, Khalil S, El-Rassy I, Safi R, Khalil A, Abbas O, Shimomura Y, Kurban M. Nemer G, et al. Among authors: hamie l. Clin Genet. 2020 Aug;98(2):116-125. doi: 10.1111/cge.13767. Epub 2020 Jun 29. Clin Genet. 2020. PMID: 32350852

10

Malar rash in a young child with neurodevelopmental delay: a quiz.

Hamie L, Nemer G, Kurban M. Hamie L, et al. Arch Dis Child Educ Pract Ed. 2022 Feb;107(1):28-30. doi: 10.1136/archdischild-2019-318334. Epub 2020 May 23. Arch Dis Child Educ Pract Ed. 2022. PMID: 32447277

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