Morovvati S - Search Results

1

Isolated congenital anosmia locus maps to 18p11.23-q12.2.

Ghadami M, Morovvati S, Majidzadeh-A K, Damavandi E, Nishimura G, Kinoshita A, Pasalar P, Komatsu K, Najafi MT, Niikawa N, Yoshiura K. Ghadami M, et al. Among authors: morovvati s. J Med Genet. 2004 Apr;41(4):299-303. doi: 10.1136/jmg.2003.015313. J Med Genet. 2004. PMID: 15060109 Free PMC article. No abstract available.

2

Isolated congenital anosmia with morphologically normal olfactory bulb in two Iranian families: a new clinical entity?

Ghadami M, Majidzadeh-A K, Morovvati S, Damavandi E, Nishimura G, Komatsu K, Kinoshita A, Najafi MT, Niikawa N, Yoshiura K. Ghadami M, et al. Among authors: morovvati s. Am J Med Genet A. 2004 Jun 15;127A(3):307-9. doi: 10.1002/ajmg.a.30025. Am J Med Genet A. 2004. PMID: 15150785

3

Osteopetrosis; a report of two Iranian patients with autosomal recessive inheritance pattern.

Morovvati S, Amirpour Amraii S, Zahed Shekar Abi H, Shahbazi N, Ranjbar R. Morovvati S, et al. Int J Mol Cell Med. 2012 Summer;1(3):173-7. Int J Mol Cell Med. 2012. PMID: 24551774 Free PMC article.

4

Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family.

Morovvati Z, Morovvati S, Alishiri G, Moosavi SH, Ranjbar R, Bolouki Moghaddam Y. Morovvati Z, et al. Among authors: morovvati s. Cell J. 2014 Feb 3;16(1):91-4. Epub 2014 Feb 3. Cell J. 2014. PMID: 24518978 Free PMC article.

5

Investigating the Association Between miR-608 rs4919510 and miR-149 rs2292832 with Colorectal Cancer in Iranian Population.

Ranjbar R, Chaleshi V, Aghdaei HA, Morovvati S. Ranjbar R, et al. Among authors: morovvati s. Microrna. 2018;7(2):100-106. doi: 10.2174/2211536607666180206145540. Microrna. 2018. PMID: 29412127

6

Detection of the GJB2 Mutation in Iranian Children with Hearing Loss Treated with Cochlear Implantation.

Peyvandi A, Morovvati S, Rabiee H, Ranjbar R, Ajalloueyan M, Hassanalifard M. Peyvandi A, et al. Among authors: morovvati s. Balkan J Med Genet. 2011 Jun;14(1):19-24. doi: 10.2478/v10034-011-0013-4. Balkan J Med Genet. 2011. PMID: 24052698 Free PMC article.

7

Isolation of clinical strains of Pseudomonas aeruginosa harboring different plasmids.

Ranjbar R, Owlia P, Saderi H, Bameri Z, Izadi M, Jonaidi N, Morovvati S. Ranjbar R, et al. Among authors: morovvati s. Pak J Biol Sci. 2007 Sep 1;10(17):3020-2. doi: 10.3923/pjbs.2007.3020.3022. Pak J Biol Sci. 2007. PMID: 19090223

8

An outbreak of gastroenteritis of unknown origin in Tehran, July 2003.

Ranjbar R, Salimkhani E, Sadeghifard N, Yazdi JZ, Morovvati S, Jonaidi N, Izadi M. Ranjbar R, et al. Among authors: morovvati s. Pak J Biol Sci. 2007 Apr 1;10(7):1138-40. doi: 10.3923/pjbs.2007.1138.1140. Pak J Biol Sci. 2007. PMID: 19070067

9

Molecular analysis of patients with severe congenital factor X deficiency: First report from north and northwest of Iran.

Morovvati S, Ranjbar R, Younesi M. Morovvati S, et al. Hematology. 2015 May 18. doi: 10.1179/1607845415Y.0000000019. Online ahead of print. Hematology. 2015. PMID: 25984924 Free article.

10

Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss.

Zardadi S, Razmara E, Asgaritarghi G, Jafarinia E, Bitarafan F, Rayat S, Almadani N, Morovvati S, Garshasbi M. Zardadi S, et al. Among authors: morovvati s. Mol Genet Genomic Med. 2020 Dec;8(12):e1550. doi: 10.1002/mgg3.1550. Epub 2020 Nov 18. Mol Genet Genomic Med. 2020. PMID: 33205915 Free PMC article.

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