Publications by authors named "Mehmet Seven"

32Publications

Assessment of Fetal Rhesus D and Gender with Cell-Free DNA and Exosomes from Maternal Blood.

Reprod Sci 2020 Sep 23. Epub 2020 Sep 23.

Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1007/s43032-020-00321-4DOI Listing
September 2020

The effectiveness of prolotherapy on failed rotator cuff repair surgery.

Turk J Phys Med Rehabil 2019 Jun 6;65(4):394-401. Epub 2019 Feb 6.

Department of Orthopedics and Traumatology, Gülhane Training and Research Hospital, Ankara, Turkey.

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http://dx.doi.org/10.5606/tftrd.2019.3222DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6935731PMC
June 2019

The Effect of PAI-1 Gene Variants and PAI-1 Plasma Levels on Development of Thrombophilia in Patients With Klinefelter Syndrome.

Am J Mens Health 2018 11;12(6):2152-2156

1 Department of Medical Genetics, İstanbul University-Cerrahpaşa, Cerrahpaşa School of Medicine, İstanbul, Turkey.

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http://dx.doi.org/10.1177/1557988318801158DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6199429PMC
November 2018

Three novel mutations in 20 patients with hereditary spastic paraparesis.

Neurol Sci 2018 Sep 16;39(9):1551-1557. Epub 2018 Jun 16.

Department of Medical Genetics, Cerrahpaşa Medical School, Istanbul University-Cerrahpaşa, 34098, Fatih, Istanbul, Turkey.

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http://link.springer.com/10.1007/s10072-018-3454-7
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http://dx.doi.org/10.1007/s10072-018-3454-7DOI Listing
September 2018

Neonatal fractures as a presenting feature of LMOD3-associated congenital myopathy.

Am J Med Genet A 2017 Oct 16;173(10):2789-2794. Epub 2017 Aug 16.

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.

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http://dx.doi.org/10.1002/ajmg.a.38383DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603416PMC
October 2017

A randomized-controlled trial of prolotherapy injections in the treatment of plantar fasciitis.

Turk J Phys Med Rehabil 2018 Mar 12;64(1):59-65. Epub 2017 Aug 12.

Department of Orthopedics and Traumatology, Gulhane Training and Research Hospital, Ankara, Turkey.

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http://dx.doi.org/10.5606/tftrd.2018.944DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709612PMC
March 2018

A novel case of autosomal dominant cutis laxa in a consanguineous family: report and literature review.

Clin Dysmorphol 2017 Jul;26(3):142-147

aDepartment of Medical Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey bCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.

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http://dx.doi.org/10.1097/MCD.0000000000000179DOI Listing
July 2017

Determining and Managing Fetal Radiation Dose from Diagnostic Radiology Procedures in Turkey.

Korean J Radiol 2015 Nov-Dec;16(6):1276-82. Epub 2015 Oct 26.

Department of Nuclear Medicine, Cerrahpasa Medical Faculty, Istanbul University, Istanbul 34090, Turkey.

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http://dx.doi.org/10.3348/kjr.2015.16.6.1276DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4644749PMC
July 2016

Revealing the function of a novel splice-site mutation of CHD7 in CHARGE syndrome.

Gene 2016 Feb 10;576(2 Pt 2):776-81. Epub 2015 Nov 10.

Department of Medical Genetics, Istanbul University Cerrahpasa Medical School, Istanbul, Turkey; Department of Medical Genetics, Biruni University Medical School, Istanbul, Turkey; Department of Pathology & Immunology, Baylor College of Medicine, Michael E. DeBakey VAMC, Houston, TX, United States. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2015.11.006DOI Listing
February 2016

Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease.

Neuron 2015 Nov;88(3):499-513

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA; Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08966273150083
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http://dx.doi.org/10.1016/j.neuron.2015.09.048DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4824012PMC
November 2015

Evaluation and comparison of the effect of hypothermia and ozone on ischemia-reperfusion injury of skeletal muscle in rats.

J Surg Res 2015 Jun 11;196(2):313-9. Epub 2015 Mar 11.

Department of Sport Medicine, Gulhane Military Medical Faculty, Ankara, Turkey.

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http://dx.doi.org/10.1016/j.jss.2015.01.053DOI Listing
June 2015

Whole-exome sequencing revealed two novel mutations in Usher syndrome.

Gene 2015 Jun 30;563(2):215-8. Epub 2015 Mar 30.

Department of Medical Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey; Department of Pathology & Immunology, Baylor College of Medicine, Houston, TX 77030, USA; Biruni University, Istanbul, Turkey. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2015.03.060DOI Listing
June 2015

The role of miRNAs in cancer: from pathogenesis to therapeutic implications.

Future Oncol 2014 May;10(6):1027-48

Department of Medical Genetics, Istanbul University Cerrahpasa Medical School, Istanbul, Turkey.

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http://dx.doi.org/10.2217/fon.13.259DOI Listing
May 2014

A novel frameshift mutation and infrequent clinical findings in two cases with Dyggve-Melchior-Clausen syndrome.

Clin Dysmorphol 2014 Jan;23(1):1-7

aDepartment of Medical Genetics, Cerrahpasa Medical School, Istanbul University bDepartment of Medical Genetics, Zeynep Kamil Women and Children Diseases Education and Research Hospital, Istanbul, Turkey cCentre for Human Genetics (Zentrum für Humangenetik, ZHMA), Mannheim, Germany.

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http://dx.doi.org/10.1097/MCD.0000000000000020DOI Listing
January 2014

The drug-transporter gene MDR1 C3435T and G2677T/A polymorphisms and the risk of multidrug-resistant epilepsy in Turkish children.

Mol Biol Rep 2014 Jan 10;41(1):331-6. Epub 2013 Nov 10.

Department of Medical Genetics, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1007/s11033-013-2866-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3877425PMC
January 2014

A novel EFNB1 mutation in a patient with craniofrontonasal syndrome and right hallux duplication.

Gene 2013 Sep 8;527(2):675-8. Epub 2013 Jul 8.

Istanbul University, Cerrahpasa Medical School, Department of Medical Genetics, Fatih, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.gene.2013.06.038DOI Listing
September 2013

Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism.

J Med Genet 2013 Aug 7;50(8):515-20. Epub 2013 Jun 7.

Department of Molecular Biology and Genetics, Boğaziçi University, Istanbul, Turkey.

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http://dx.doi.org/10.1136/jmedgenet-2013-101634DOI Listing
August 2013

A rare case of split hand/foot malformation with sensorineural hearing loss and Mondini dysplasia.

Clin Dysmorphol 2013 Jan;22(1):33-5

Department of Medical Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1097/MCD.0b013e32835b8e6eDOI Listing
January 2013

Deficiency of selenium and zinc as a causative factor for idiopathic intractable epilepsy.

Epilepsy Res 2013 Mar 25;104(1-2):35-9. Epub 2012 Oct 25.

Istanbul University, Cerrahpaşa Medical Faculty, Department of Medical Genetics, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.eplepsyres.2012.09.013DOI Listing
March 2013

Marked improvement in Segawa syndrome after L-dopa and selegiline treatment.

Pediatr Neurol 2010 May;42(5):348-50

Department of Medical Genetics, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.

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http://dx.doi.org/10.1016/j.pediatrneurol.2010.01.008DOI Listing
May 2010

Polymorphisms of the DNA repair genes XPD and XRCC1 and the risk of age-related macular degeneration.

Invest Ophthalmol Vis Sci 2010 Sep 7;51(9):4732-7. Epub 2010 Apr 7.

Department of Ophthalmology, Yeditepe University Medical Faculty, Istanbul, Turkey.

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http://iovs.arvojournals.org/article.aspx?doi=10.1167/iovs.0
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http://dx.doi.org/10.1167/iovs.09-4842DOI Listing
September 2010

Warburg Micro syndrome in a Turkish boy.

Clin Dysmorphol 2007 Apr;16(2):89-93

Department of Medical Genetics, Istanbul University Cerrahpasa Medical Faculty, Istanbul, Turkey.

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https://insights.ovid.com/crossref?an=00019605-200704000-000
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http://dx.doi.org/10.1097/MCD.0b013e328054c404DOI Listing
April 2007

Facial dysmorphism in Leigh syndrome with SURF-1 mutation and COX deficiency.

Pediatr Neurol 2006 Jun;34(6):486-9

Department of Medical Genetic, Division of Pediatric Neurology, Cerrahpaşa Medical Faculty, Istanbul University, Turkey.

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http://dx.doi.org/10.1016/j.pediatrneurol.2005.10.020DOI Listing
June 2006

The effects of vigabatrin on rat liver antioxidant status.

Drug Metabol Drug Interact 2005 ;21(2):109-15

Medical and Biological Sciences, Cerrahpaşa Medical Faculty, Istanbul University, Cerrahpaşa, Istanbul, Turkey.

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http://dx.doi.org/10.1515/dmdi.2005.21.2.109DOI Listing
June 2006

Is the novel SCKL3 at 14q23 the predominant Seckel locus?

Eur J Hum Genet 2003 Nov;11(11):851-7

Department of Molecular Biology and Genetics, Bogaziçi University, Istanbul, Turkey.

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http://dx.doi.org/10.1038/sj.ejhg.5201057DOI Listing
November 2003

Neuroblastoma in a dysmorphic girl with a partial duplication of 2p caused by an unbalanced translocation.

Clin Dysmorphol 2002 Jan;11(1):39-42

Genetic and Teratology Research Center (GETAM), Cerrahpaş Medical Faculty, Istanbul University, Turkey.

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http://dx.doi.org/10.1097/00019605-200201000-00008DOI Listing
January 2002