Waked N - Search Results

1

Exclusion of chromosome 15q21.1 in autosomal-recessive Weill-Marchesani syndrome in an inbred Lebanese family.

Mégarbané A, Mustapha M, Bleik J, Waked N, Delague V, Loiselet J. Mégarbané A, et al. Among authors: waked n. Clin Genet. 2000 Dec;58(6):473-8. doi: 10.1034/j.1399-0004.2000.580608.x. Clin Genet. 2000. PMID: 11149617

2

A newly recognized autosomal recessive syndrome with short stature and oculo-skeletal involvement.

Mégarbané A, Ghanem I, Waked N, Dagher F. Mégarbané A, et al. Among authors: waked n. Am J Med Genet A. 2006 Jul 15;140(14):1491-6. doi: 10.1002/ajmg.a.31316. Am J Med Genet A. 2006. PMID: 16770799

3

Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: report of a new family with additional features and review.

Mégarbané H, Zablit C, Waked N, Lefranc G, Tomb R, Mégarbané A. Mégarbané H, et al. Among authors: waked n. Am J Med Genet A. 2004 Jan 30;124A(3):323-7. doi: 10.1002/ajmg.a.20352. Am J Med Genet A. 2004. PMID: 14708109 Review.

4

Two sibs with myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders.

Mégarbané A, Khalil G, Waked N, Rötig A, Caillaud C, Loiselet J. Mégarbané A, et al. Among authors: waked n. Am J Med Genet. 1999 Dec 3;87(4):289-93. doi: 10.1002/(sici)1096-8628(19991203)87:4<289::aid-ajmg1>3.0.co;2-t. Am J Med Genet. 1999. PMID: 10588831

5

Microcephaly, cutis verticis gyrata of the scalp, retinitis pigmentosa, cataracts, sensorineural deafness, and mental retardation in two brothers.

Mégarbané A, Waked N, Chouery E, Moglabey YB, Saliba N, Mornet E, Serre JL, Slim R. Mégarbané A, et al. Among authors: waked n. Am J Med Genet. 2001 Jan 22;98(3):244-9. doi: 10.1002/1096-8628(20010122)98:3<244::aid-ajmg1084>3.0.co;2-w. Am J Med Genet. 2001. PMID: 11169562

6

Clinical and molecular findings in three Lebanese families with Bietti crystalline dystrophy: report on a novel mutation.

Haddad NM, Waked N, Bejjani R, Khoueir Z, Chouery E, Corbani S, Mégarbané A. Haddad NM, et al. Among authors: waked n. Mol Vis. 2012;18:1182-8. Epub 2012 May 5. Mol Vis. 2012. PMID: 22605929 Free PMC article.

7

Ocular findings in ichthyosis follicularis-alopecia-photophobia (IFAP) syndrome.

Traboulsi E, Waked N, Mégarbané H, Mégarbané A. Traboulsi E, et al. Among authors: waked n. Ophthalmic Genet. 2004 Jun;25(2):153-6. doi: 10.1080/13816810490514405. Ophthalmic Genet. 2004. PMID: 15370546

8

[Epidemiology of diabetic retinopathy in Lebanon].

Waked N, Nacouzi R, Haddad N, Zaini R. Waked N, et al. J Fr Ophtalmol. 2006 Mar;29(3):289-95. doi: 10.1016/s0181-5512(06)73785-8. J Fr Ophtalmol. 2006. PMID: 16557173 French.

9

Evaluation of allergic sensitization in Lebanese patients with allergic conjunctivitis.

Arej N, Irani C, Abdelmassih Y, Slim E, Antoun J, Bejjani R, Schakal A, Waked N. Arej N, et al. Among authors: waked n. Int Ophthalmol. 2018 Oct;38(5):2041-2051. doi: 10.1007/s10792-017-0696-y. Epub 2017 Aug 22. Int Ophthalmol. 2018. PMID: 28831678

10

Azithromycin 1.5% ophthalmic solution: efficacy and treatment modalities in chronic blepharitis.

Fadlallah A, Rami HE, Fahd D, Dunia I, Bejjani R, Chlela E, Waked N, Jabbour E, Fahed S. Fadlallah A, et al. Among authors: waked n. Arq Bras Oftalmol. 2012 May-Jun;75(3):178-82. doi: 10.1590/s0004-27492012000300006. Arq Bras Oftalmol. 2012. PMID: 22872200 Free article. Clinical Trial.

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