Karimi-Nejad MH - Search Results

1

A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Bicknell LS, Farrington-Rock C, Shafeghati Y, Rump P, Alanay Y, Alembik Y, Al-Madani N, Firth H, Karimi-Nejad MH, Kim CA, Leask K, Maisenbacher M, Moran E, Pappas JG, Prontera P, de Ravel T, Fryns JP, Sweeney E, Fryer A, Unger S, Wilson LC, Lachman RS, Rimoin DL, Cohn DH, Krakow D, Robertson SP. Bicknell LS, et al. Among authors: karimi nejad mh. J Med Genet. 2007 Feb;44(2):89-98. doi: 10.1136/jmg.2006.043687. Epub 2006 Jun 26. J Med Genet. 2007. PMID: 16801345 Free PMC article.

2

An/micr-ophthalmia, cleft lip/palate, and short limbs: a new syndrome simulating a short rib syndrome.

Kariminejad A, Ghaderi-Sohi S, Kariminejad MH, Lachman R. Kariminejad A, et al. Fetal Pediatr Pathol. 2012 Oct;31(5):295-9. doi: 10.3109/15513815.2012.659386. Epub 2012 Mar 20. Fetal Pediatr Pathol. 2012. PMID: 22432872

3

Hereditary bilateral conductive hearing loss caused by total loss of ossicles: a report of familial expansile osteolysis.

Daneshi A, Shafeghati Y, Karimi-Nejad MH, Khosravi A, Farhang F. Daneshi A, et al. Among authors: karimi nejad mh. Otol Neurotol. 2005 Mar;26(2):237-40. doi: 10.1097/00129492-200503000-00018. Otol Neurotol. 2005. PMID: 15793411

4

Elucidating the spectrum of alpha-thalassemia mutations in Iran.

Hadavi V, Taromchi AH, Malekpour M, Gholami B, Law HY, Almadani N, Afroozan F, Sahebjam F, Pajouh P, Kariminejad R, Kariminejad MH, Azarkeivan A, Jafroodi M, Tamaddoni A, Puehringer H, Oberkanins C, Najmabadi H. Hadavi V, et al. Haematologica. 2007 Jul;92(7):992-3. doi: 10.3324/haematol.10658. Haematologica. 2007. PMID: 17606454 Free article.

5

Neu-Laxova syndrome: report of a case and comments.

Karimi-Nejad MH, Khajavi H, Gharavi MJ, Karimi-Nejad R. Karimi-Nejad MH, et al. Am J Med Genet. 1987 Sep;28(1):17-23. doi: 10.1002/ajmg.1320280104. Am J Med Genet. 1987. PMID: 3314507 Review.

6

Ullrich Congenital Muscular Dystrophy (UCMD): Clinical and Genetic Correlations.

Bozorgmehr B, Kariminejad A, Nafissi S, Jebelli B, Andoni U, Gartioux C, Ledeuil C, Allamand V, Richard P, Kariminejad MH. Bozorgmehr B, et al. Iran J Child Neurol. 2013 Summer;7(3):15-22. Iran J Child Neurol. 2013. PMID: 24665301 Free PMC article.

7

The beta-thalassemia mutation spectrum in the Iranian population.

Najmabadi H, Karimi-Nejad R, Sahebjam S, Pourfarzad F, Teimourian S, Sahebjam F, Amirizadeh N, Karimi-Nejad MH. Najmabadi H, et al. Among authors: karimi nejad mh. Hemoglobin. 2001 Aug;25(3):285-96. doi: 10.1081/hem-100105221. Hemoglobin. 2001. PMID: 11570721

8

Genetic screening of leber congenital amaurosis in a large consanguineous Iranian family.

Rezaie T, Karimi-Nejad MH, Meshkat MR, Sohbati S, Karimi-Nejad R, Najmabadi H, Sarfarazi M. Rezaie T, et al. Among authors: karimi nejad mh. Ophthalmic Genet. 2007 Dec;28(4):224-8. doi: 10.1080/13816810701663550. Ophthalmic Genet. 2007. PMID: 18161624

9

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.

Kariminejad A, Kariminejad R, Moshtagh A, Zanganeh M, Kariminejad MH, Neuenschwander S, Okoniewski M, Wey E, Schinzel A, Baumer A. Kariminejad A, et al. Eur J Hum Genet. 2011 May;19(5):555-60. doi: 10.1038/ejhg.2010.252. Epub 2011 Feb 16. Eur J Hum Genet. 2011. PMID: 21326286 Free PMC article.

10

Intragenic SNP haplotypes associated with 84dup18 mutation in TNFRSF11A in four FEO pedigrees suggest three independent origins for this mutation.

Elahi E, Shafaghati Y, Asadi S, Absalan F, Goodarzi H, Gharaii N, Karimi-Nejad MH, Shahram F, Hughes AE. Elahi E, et al. Among authors: karimi nejad mh. J Bone Miner Metab. 2007;25(3):159-64. doi: 10.1007/s00774-007-0748-x. Epub 2007 Apr 20. J Bone Miner Metab. 2007. PMID: 17447113

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