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Halil Aydin, PhD

TitlePostdoctoral Scholar
InstitutionUniversity of California San Francisco
DepartmentCellular Molecular Pharmacology
Address600-16th St., San Francisco
Phone415-514-4825
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Aydin H. Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder. Indian Pediatr. 2018 01 15; 55(1):67-68. PMID: 29396939.
      View in: PubMed
    2. Kilinc MF, Yasar E, Aydin H, Yildiz Y, Doluoglu OG. Association between coronary artery disease severity and overactive bladder in geriatric patients. World J Urol. 2018 Jan; 36(1):35-40. PMID: 29032450.
      View in: PubMed
    3. Guven A, Demircelik B, Gurel OM, Er O, Aydin H, Bozkurt A. A coronary proatherosclerotic marker: Pregnancy-associated plasma protein A and its association with coronary calcium score and carotid intima-media thickness. Adv Clin Exp Med. 2017 May-Jun; 26(3):467-473. PMID: 28791822.
      View in: PubMed
    4. Aydin H. Genetic Studies in Autism: Correspondence. Indian J Pediatr. 2017 02; 84(2):170-171. PMID: 27506425.
      View in: PubMed
    5. Aydin H, Eser A, Kaygusuz I, Yildirim S, Celik T, Gunduz S, Kalman S. Adipokine, adropin and endothelin-1 levels in intrauterine growth restricted neonates and their mothers. J Perinat Med. 2016 Aug 01; 44(6):669-76. PMID: 26352058.
      View in: PubMed
    6. Besio R, Maruelli S, Gioia R, Villa I, Grabowski P, Gallagher O, Bishop NJ, Foster S, De Lorenzi E, Colombo R, Diaz JL, Moore-Barton H, Deshpande C, Aydin H, Tokatli A, Kwiek B, Kasapkara CS, Adisen EO, Gurer MA, Di Rocco M, Phang JM, Gunn TM, Tenni R, Rossi A, Forlino A. Lack of prolidase causes a bone phenotype both in human and in mouse. Bone. 2015 Mar; 72:53-64. PMID: 25460580.
      View in: PubMed
    7. Aydin H, Demirkaya E, Karadeniz RS, Olgun A, Alpay F. Assessing leptin and soluble leptin receptor levels in full-term asymmetric small for gestational age and healthy neonates. Turk J Pediatr. 2014 May-Jun; 56(3):250-8. PMID: 25341596.
      View in: PubMed
    8. Kurt I, Sertoglu E, Okur I, Tapan S, Uyanik M, Kayadibi H, Ezgu FS, Aydin H, Hasanoglu A. Serum dipeptidyl peptidase-IV: a better screening test for early detection of mucopolysaccharidosis? Clin Chim Acta. 2014 Apr 20; 431:250-4. PMID: 24582858.
      View in: PubMed
    9. Ertem AG, Erayman A, Efe TH, Duran Karaduman B, Aydin H, Bilge M. Is there a relationship between serum paraoxonase level and epicardial fat tissue thickness? Anadolu Kardiyol Derg. 2014 Mar; 14(2):115-20. PMID: 24449622.
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    10. Cemeroglu O, Aydin H, Yasar ZS, Bozduman F, Saglam M, Selcoki Y, Eryonucu B, Cakirbay H. Hand and heart, hand in hand: is radiological hand osteoarthritis associated with atherosclerosis? Int J Rheum Dis. 2014 Mar; 17(3):299-303. PMID: 24330251.
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    11. Demirçelik MB, Aydin H. Tako-tsubo-like cardiomyopathy induced by pheochromocytoma crisis. Anadolu Kardiyol Derg. 2013 Sep 25; 13(6):E35-6. PMID: 24064103.
      View in: PubMed
    12. Güzel-Ozantürk A, Ozgül RK, Unal O, Hismi B, Aydin H, Sivri S, Tokatli A, Coskun T, Aksöz E, Dursun A. Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance. Gene. 2013 Jun 01; 521(2):293-5. PMID: 23542076.
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    13. Régal L, Aydin H, Dieltjens AM, Van Esch H, Francois I, Okur I, Zeybek C, Meulemans S, Van Mol C, Van Bruwaene L, Then SH, Jaeken J, Creemers J. Two novel deletions in hypotonia-cystinuria syndrome. Mol Genet Metab. 2012 Nov; 107(3):614-6. PMID: 22796000.
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    14. Celtikçi B, Aydin H, Sivri S, Sönmez M, Topçu M, Ozkara HA. Four novel mutations in the ß-galactosidase gene identified in infantile type of GM1 gangliosidosis. Clin Biochem. 2012 May; 45(7-8):571-4. PMID: 22234367.
      View in: PubMed
    15. Coskun T, Aydin H, Kiliç M, Dursun A, Haliloglu G, Topaloglu H, Karli-Oguz K, de Koning TJ. 3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures. Turk J Pediatr. 2009 Nov-Dec; 51(6):587-92. PMID: 20196394.
      View in: PubMed
    16. Gökçe S, Tasçilar ME, Dabak O, Devrim I, Aydin H, Unay B. Cytomegalovirus infection with gastric ulcers in Ménétrier's disease and hypergammaglobulinemia. Turk J Pediatr. 2009 Sep-Oct; 51(5):524. PMID: 20112615.
      View in: PubMed
    17. Kuskonmaz B, Unal S, Cördükcü E, Aydin H, Coskun T, Gurgey A, Gumruk F. Lymphocytic vacuolization in sialic acid storage disease. Am J Hematol. 2008 Oct; 83(10):821. PMID: 18050357.
      View in: PubMed
    18. Aydin H, Yozgat Y, Demirkaya E, Olgun A, Okutan V, Lenk MK, Ozcan O. Correlation between vascular endothelial growth factor and leptin in children with cyanotic congenital heart disease. Turk J Pediatr. 2007 Oct-Dec; 49(4):360-4. PMID: 18246735.
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    19. Sivri HS, Genç GA, Tokatli A, Tokatlý A, Dursun A, Coskun T, Aydin H, Aydýn HY, Sennaroglu L, Belgin E, Jensen K, Wolf B. Hearing loss in biotinidase deficiency: genotype-phenotype correlation. J Pediatr. 2007 Apr; 150(4):439-42. PMID: 17382128.
      View in: PubMed
    20. Kendirli T, Kismet E, Demirkaya E, Aydin H, Kesik V, Köseoglu V. Death possibly associated with interferon use in a patient with chronic hepatitis. Acta Paediatr. 2005 Jul; 94(7):984-5. PMID: 16188832.
      View in: PubMed
    21. Gok F, Aydin H, Kurt I, Gokcay E, Maeda M, Kasahara M. A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption. J Pediatr Gastroenterol Nutr. 2005 Apr; 40(4):508-11. PMID: 15795603.
      View in: PubMed
    22. Kismet E, Atay AA, Demirkaya E, Aydin H, Aydogan H, Koseoglu V, Gokcay E. Two cases of Ralstonia pickettii bacteremias in a pediatric oncology unit requiring removal of the Port-A-Caths. J Pediatr Hematol Oncol. 2005 Jan; 27(1):37-8. PMID: 15654276.
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    23. Kiliç S, Tezcan S, Tasçilar E, Cakir B, Aydin H, Hasde M, Gökçay E. Morbidity and mortality characteristics of infants hospitalized in the Pediatrics Department of the largest Turkish military hospital in 2001. Mil Med. 2005 Jan; 170(1):48-51. PMID: 15724854.
      View in: PubMed
    24. Dündaröz R, Ulucan H, Aydin H, Güngör T, Baltaci V, Denli M, Sanisoglu Y. Analysis of DNA damage using the comet assay in infants fed cow's milk. Biol Neonate. 2003; 84(2):135-41. PMID: 12907847.
      View in: PubMed
    25. Dündaröz R, Aydin H, Ulucan H, Baltaci V, Denli M, Gökçay E. Preliminary study on DNA damage in non breast-fed infants. Pediatr Int. 2002 Apr; 44(2):127-30. PMID: 11896867.
      View in: PubMed
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