Ghanem I - Search Results

1

A 20-year Clinical and Genetic Neuromuscular Cohort Analysis in Lebanon: An International Effort.

Megarbane A, Bizzari S, Deepthi A, Sabbagh S, Mansour H, Chouery E, Hmaimess G, Jabbour R, Mehawej C, Alame S, Hani A, Hasbini D, Ghanem I, Koussa S, Al-Ali MT, Obeid M, Talea DB, Lefranc G, Lévy N, Leturcq F, El Hayek S, Delague V, Urtizberea JA. Megarbane A, et al. Among authors: ghanem i. J Neuromuscul Dis. 2022;9(1):193-210. doi: 10.3233/JND-210652. J Neuromuscul Dis. 2022. PMID: 34602496 Free PMC article.

2

Congenital contractures, short stature, abnormal face, microcephaly, scoliosis, hip dislocation, and severe psychomotor retardation in two unrelated girls. a new MCA/MR syndrome?

Mégarbané A, Ghanem I, Romana S, Gosset P, Caillaud C. Mégarbané A, et al. Among authors: ghanem i. Genet Couns. 2002;13(2):123-31. Genet Couns. 2002. PMID: 12150211

3

Prenatal growth deficiency with narrowness of the cervical spine, subglottic stenosis, hip dislocation, and severe delayed bone ossification: a new skeletal dysplasia.

Mégarbané A, Ghanem I, Rizk T, Jabbour P. Mégarbané A, et al. Among authors: ghanem i. Am J Med Genet. 2002 Sep 15;112(1):70-4. doi: 10.1002/ajmg.10653. Am J Med Genet. 2002. PMID: 12239724

4

Tibial/femoral hypoplasia with "hook" pelvis: a potentially unique dysostosis.

Mégarbané A, Ghanem I. Mégarbané A, et al. Among authors: ghanem i. Am J Med Genet. 2002 Nov 1;112(4):394-6. doi: 10.1002/ajmg.10684. Am J Med Genet. 2002. PMID: 12376943

5

Spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type: report of a new patient and review of the literature.

Mégarbané A, Ghanem I, Le Merrer M. Mégarbané A, et al. Among authors: ghanem i. Am J Med Genet A. 2003 Oct 15;122A(3):252-6. doi: 10.1002/ajmg.a.20262. Am J Med Genet A. 2003. PMID: 12966527 Review.

6

A newly recognized chondrodysplasia with multiple dislocations.

Mégarbané A, Ghanem I. Mégarbané A, et al. Among authors: ghanem i. Am J Med Genet A. 2004 Sep 15;130A(1):107-9. doi: 10.1002/ajmg.a.30179. Am J Med Genet A. 2004. PMID: 15368507 No abstract available.

7

[Results of long-term rehabilitation in the treatment of patellofemoral syndrome: retrospective study about 63 patients].

Ghoussoub K, Ghanem I, Sabbagh S, Hassane A, Kharrat K, Dagher F. Ghoussoub K, et al. Among authors: ghanem i. J Med Liban. 2003 Oct-Dec;51(4):198-205. J Med Liban. 2003. PMID: 15623134 French.

8

Coexistence of Kallmann syndrome and complete androgen insensitivity in the same patient.

Gannagé-Yared MH, Dodé C, Ghanem I, Chouery E, Jalkh N, Hardelin JP, Mégarbané A. Gannagé-Yared MH, et al. Among authors: ghanem i. Eur J Endocrinol. 2005 Jun;152(6):813-7. doi: 10.1530/eje.1.01915. Eur J Endocrinol. 2005. PMID: 15941919

9

Molecular study of WISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: identification of two novel mutations, and description of a founder effect.

Delague V, Chouery E, Corbani S, Ghanem I, Aamar S, Fischer J, Levy-Lahad E, Urtizberea JA, Mégarbané A. Delague V, et al. Among authors: ghanem i. Am J Med Genet A. 2005 Oct 1;138A(2):118-26. doi: 10.1002/ajmg.a.30906. Am J Med Genet A. 2005. PMID: 16152649

10

Severe autosomal dominant upper-limb mesomelic dysplasia: report of a second family.

Mégarbané A, Ghanem I. Mégarbané A, et al. Among authors: ghanem i. Clin Genet. 2005 Dec;68(6):567-9. doi: 10.1111/j.1399-0004.2005.00542.x. Clin Genet. 2005. PMID: 16283892 No abstract available.

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