Publications by authors named "Davut Gul"

34Publications

Exploiting spatial heterogeneity and response characterization in non-uniform architected materials inspired by slime mould growth.

Bioinspir Biomim 2019 09 2;14(6):064001. Epub 2019 Sep 2.

Department of Civil, Environmental and Geodetic Engineering, The Ohio State University, Columbus, OH, United States of America. Equal contribution to this work.

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http://dx.doi.org/10.1088/1748-3190/ab3b12DOI Listing
September 2019

Collapsing Glomerulopathy in a Child with Galloway-Mowat Syndrome.

Case Rep Nephrol 2016 14;2016:4386291. Epub 2016 Jun 14.

Department of Pediatric Nephrology, Gulhane Military Medical Academy, Etlik, Kecioren, 06100 Ankara, Turkey.

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http://dx.doi.org/10.1155/2016/4386291DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4923528PMC
July 2016

Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group.

J Clin Res Pediatr Endocrinol 2015 Sep;7(3):183-91

Gülhane Military Medicine Academy, Department of Pediatric Endocrinology, Ankara, Turkey Phone: +90 312 304 18 98 E-mail:

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http://dx.doi.org/10.4274/jcrpe.2023DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677552PMC
September 2015

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

Bombay Blood Group in a Turkish Family: Serological and Molecular Analysis.

Indian J Hematol Blood Transfus 2015 Sep 6;31(3):396-7. Epub 2014 Aug 6.

Department of Infectious Disease and Clinical Microbiology, Gulhane Military Medical Academy, Ankara, Turkey.

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http://dx.doi.org/10.1007/s12288-014-0440-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465519PMC
September 2015

Turner syndrome and associated problems in Turkish children: a multicenter study.

J Clin Res Pediatr Endocrinol 2015 Mar;7(1):27-36

Gülhane Military Medicine Academy, Department of Pediatric Endocrinology, Ankara, Turkey. E-mail:

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http://dx.doi.org/10.4274/jcrpe.1771DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4439889PMC
March 2015

A new mutation in blau syndrome.

Case Rep Rheumatol 2015 27;2015:463959. Epub 2015 Jan 27.

Pediatric Rheumatology and Nephrology Department, Gulhane Military Medical Academy, Etlik, Kecioren, 06010 Ankara, Turkey.

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http://dx.doi.org/10.1155/2015/463959DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4322824PMC
February 2015

[Is there a relationship between gouty arthritis and Mediterranean fever gene mutations?].

Rev Bras Reumatol 2015 Jul-Aug;55(4):325-9. Epub 2014 Nov 26.

Departamento de Reumatologia, Gulhane Military Medical Academy, Ankara, Turquia.

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http://dx.doi.org/10.1016/j.rbr.2014.10.008DOI Listing
July 2017

Heterotopic brain tissue on the face and neck in a neonate: a rare case report and literature review.

J Matern Fetal Neonatal Med 2013 Apr 9;26(6):619-21. Epub 2012 Nov 9.

Karabuk Maternity Hospital, Karabuk, Turkey.

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http://dx.doi.org/10.3109/14767058.2012.743525DOI Listing
April 2013

Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene.

BMC Med Genet 2008 Oct 23;9:92. Epub 2008 Oct 23.

Genetic Disease Research Branch, National Human Genome Research Institute, NIH, Bethesda, MD, USA.

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http://bmcmedgenet.biomedcentral.com/articles/10.1186/1471-2
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http://dx.doi.org/10.1186/1471-2350-9-92DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2584628PMC
October 2008

Electronic microarray screening of podocin mutations: a single-center study.

Int Urol Nephrol 2008 6;40(4):1045-51. Epub 2008 Aug 6.

Pediatric Nephrology Unit, Gulhane Military Academy of Medicine, 06018, Etlik, Ankara, Turkey.

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http://dx.doi.org/10.1007/s11255-008-9426-8DOI Listing
March 2009

Goldenhar syndrome with duodenal atresia: a new finding.

Clin Dysmorphol 2008 Apr;17(2):141-2

Department of Pediatrics, Gülhane Military Medical Academy and Medical Faculty, Ankara, Turkey.

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http://dx.doi.org/10.1097/MCD.0b013e3282eff39fDOI Listing
April 2008

Evaluation of the relationship between C677T variants of methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in children receiving antiepileptic drug therapy.

Prog Neuropsychopharmacol Biol Psychiatry 2008 Apr 29;32(3):844-8. Epub 2008 Jan 29.

Department of Pediatric Neurology, Gulhane Military Medical Academy, School of Medicine, Turkey.

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http://dx.doi.org/10.1016/j.pnpbp.2007.12.018DOI Listing
April 2008

A very frequent mutation and remarkable association of R761H with M694V mutations in Turkish familial Mediterranean fever patients.

Clin Rheumatol 2008 Jun 14;27(6):729-32. Epub 2007 Nov 14.

Department of Pediatrics, Gülhane Military Medical Academy, Etlik, Ankara, Turkey.

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http://link.springer.com/10.1007/s10067-007-0780-1
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http://dx.doi.org/10.1007/s10067-007-0780-1DOI Listing
June 2008

The rate of pyrin mutations in critically ill patients with systemic inflammatory response syndrome and sepsis: a pilot study.

J Rheumatol 2007 Oct 1;34(10):2070-5. Epub 2007 Aug 1.

Department of Internal Medicine, Gülhane Military Medical Academy, Ankara, Turkey.

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October 2007

The phenotype-genotype correlations of FMF patients: a single center study.

Rheumatol Int 2006 May 25;26(7):638-40. Epub 2005 Sep 25.

Pediatric Nephrology and Rheumatology Unit, Gulhane Military Medicine Academy, 06018 Etlik, Ankara, Turkey.

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http://dx.doi.org/10.1007/s00296-005-0045-8DOI Listing
May 2006

Caudothalamic groove cysts in Zellweger syndrome.

Clin Dysmorphol 2005 Jul;14(3):165-7

Department of Pediatrics , Gülhane Military Medical Academy, Ankara, Turkey.

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http://dx.doi.org/10.1097/00019605-200507000-00014DOI Listing
July 2005

The correction of auricular and mandibular deformities in auriculo-condylar syndrome.

J Craniofac Surg 2005 May;16(3):489-92

Department of Plastic and Reconstructive Surgery, Gulhane Military Medical Academy, Ankara, Turkey.

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http://dx.doi.org/10.1097/01.scs.0000147655.94656.0dDOI Listing
May 2005

Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.

Ann Genet 2004 Oct-Dec;47(4):393-8

Department of Medical Biology and Genetics, School of Medicine, Pamukkale University, Kinikli/Denizli 20020, Turkey.

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http://dx.doi.org/10.1016/j.anngen.2004.03.009DOI Listing
May 2005

Acrocallosal syndrome: report of five Turkish patients.

Clin Dysmorphol 2004 Oct;13(4):241-6

Department of Medical Genetics, GATA Medical School, Ankara, Turkey.

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http://dx.doi.org/10.1097/00019605-200410000-00008DOI Listing
October 2004

Situs inversus totalis with accompanying craniodiaphysial dysplasia: a new syndrome?

J Craniofac Surg 2004 Sep;15(5):865-9

Department of Plastic and Reconstructive Surgery, Gulhane Military Medical Academy, Ankara, Turkey.

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http://dx.doi.org/10.1097/00001665-200409000-00032DOI Listing
September 2004

Neuroblastoma in a patient with 47, XXX karyotype.

Cancer Genet Cytogenet 2003 Oct;146(1):84-5

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http://dx.doi.org/10.1016/s0165-4608(03)00100-6DOI Listing
October 2003

Saethre-Chotzen syndrome presenting with incomplete renal Fanconi syndrome.

Nephron 2002 Oct;92(2):463-5

Department of Internal Medicine, Gülhane Military Medical Academy and Faculty, TR-06018 Etlik, Ankara, Turkey.

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http://dx.doi.org/10.1159/000063292DOI Listing
October 2002

Study of autoimmunity in Klinefelter's syndrome and idiopathic hypogonadotropic hypogonadism.

J Clin Immunol 2002 May;22(3):137-43

Department of Internal Medicine, Gülhane Military Medical Academy and Faculty, Ankara, Turkey.

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http://dx.doi.org/10.1023/a:1015467912592DOI Listing
May 2002

Evidence for autosomal recessive inheritance of split hand/split foot malformation: a report of nine cases.

Clin Dysmorphol 2002 Jul;11(3):183-6

Department of Medical Genetics, Gülhane Military Medical Academy and Medical Faculty, Etlik, Ankara, Turkey.

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http://dx.doi.org/10.1097/00019605-200207000-00006DOI Listing
July 2002