Hosny LA - Search Results

1

3-M syndrome: a report of three Egyptian cases with review of the literature.

Temtamy SA, Aglan MS, Ashour AM, Ramzy MI, Hosny LA, Mostafa MI. Temtamy SA, et al. Among authors: hosny la. Clin Dysmorphol. 2006 Apr;15(2):55-64. doi: 10.1097/01.mcd.0000198926.01706.33. Clin Dysmorphol. 2006. PMID: 16531729 Review.

2

A report of three patients with MMP2 associated hereditary osteolysis.

Temtamy SA, Ismail S, Aglan MS, Ashour AM, Hosny LA, El-Badry TH, Aboul-Ezz EH, Amr K, Fateen E, Maguire T, Ungerer K, Zankl A. Temtamy SA, et al. Among authors: hosny la. Genet Couns. 2012;23(2):175-84. Genet Couns. 2012. PMID: 22876575

3

Anthropometric measurements in Egyptian patients with osteogenesis imperfecta.

Aglan MS, Zaki ME, Hosny L, El-Houssini R, Oteify G, Temtamy SA. Aglan MS, et al. Am J Med Genet A. 2012 Nov;158A(11):2714-8. doi: 10.1002/ajmg.a.35529. Epub 2012 Aug 7. Am J Med Genet A. 2012. PMID: 22887991

4

The most encountered groups of genetic disorders in Giza Governorate, Egypt.

Afifi HH, El-Ruby MO, El-Bassyouni HT, Ismail SI, Aglan MS, El-Harouni AA, Mazen IM, Zaki MS, Bassiouni RI, Hosny LA, El-Kamah GY, El-Kotoury AI, Ashour AM, Abdel-Salam GM, El-Gammal MA, Hamed K, Kamal RM, El-Nekhely I, Temtamy SA. Afifi HH, et al. Among authors: hosny la. Bratisl Lek Listy. 2010;111(2):62-9. Bratisl Lek Listy. 2010. PMID: 20429316

5

Assessment of pubertal development in Egyptian girls.

Hosny LA, El-Ruby MO, Zaki ME, Aglan MS, Zaki MS, El Gammal MA, Mazen IM. Hosny LA, et al. J Pediatr Endocrinol Metab. 2005 Jun;18(6):577-84. doi: 10.1515/jpem.2005.18.6.577. J Pediatr Endocrinol Metab. 2005. PMID: 16042325

6

A scoring system for the assessment of clinical severity in osteogenesis imperfecta.

Aglan MS, Hosny L, El-Houssini R, Abdelhadi S, Salem F, Elbanna RA, Awad SA, Zaki ME, Temtamy SA. Aglan MS, et al. J Child Orthop. 2012 Mar;6(1):29-35. doi: 10.1007/s11832-012-0385-3. Epub 2012 Feb 8. J Child Orthop. 2012. PMID: 23449141 Free PMC article.

7

ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.

Ismail S, Essawi M, Sedky N, Hassan H, Fayez A, Helmy N, Shehab M, Farouk D, Elruby M, Otaify G, Eldarsh A, Hosny L, Gaber K, Aboul-Ezz EHA, Ramzy MI, Mehrez MI, Hassib NF, Elhadidi SMA, Aglan MS, Temtamy SA. Ismail S, et al. Genet Couns. 2016;27(3):305-323. Genet Couns. 2016. PMID: 30204960

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

7 results

Search Page