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Halil Aydin, PhD

Title(s)Postdoctoral Scholar, Biochemistry and Biophysics
SchoolSchool of Medicine
AddressLocation Required
Varies CA 00000
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. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation. Brain Dev. 2020 May; 42(5):418-420. Ayanoglu M, Korgali E, Sezer T, Aydin HI, Sönmez FM. PMID: 32173091.
      View in: PubMed   Mentions:    Fields:    
    2. A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism. Turk J Pediatr. 2019; 61(1):92-96. Aydin HI, Sönmez FM. PMID: 31559727.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    3. Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder. Indian Pediatr. 2018 01 15; 55(1):67-68. Aydin HI. PMID: 29396939.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    4. Association between coronary artery disease severity and overactive bladder in geriatric patients. World J Urol. 2018 Jan; 36(1):35-40. Kilinc MF, Yasar E, Aydin HI, Yildiz Y, Doluoglu OG. PMID: 29032450.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. 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. Guven A, Demircelik B, Gurel OM, Er O, Aydin HI, Bozkurt A. PMID: 28791822.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Genetic Studies in Autism: Correspondence. Indian J Pediatr. 2017 02; 84(2):170-171. Aydin HI. PMID: 27506425.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    7. Adipokine, adropin and endothelin-1 levels in intrauterine growth restricted neonates and their mothers. J Perinat Med. 2016 Aug 01; 44(6):669-76. Aydin HI, Eser A, Kaygusuz I, Yildirim S, Celik T, Gunduz S, Kalman S. PMID: 26352058.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    8. Lack of prolidase causes a bone phenotype both in human and in mouse. Bone. 2015 Mar; 72:53-64. 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 HI, Tokatli A, Kwiek B, Kasapkara CS, Adisen EO, Gurer MA, Di Rocco M, Phang JM, Gunn TM, Tenni R, Rossi A, Forlino A. PMID: 25460580.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    9. 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. Aydin HI, Demirkaya E, Karadeniz RS, Olgun A, Alpay F. PMID: 25341596.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    10. Serum dipeptidyl peptidase-IV: a better screening test for early detection of mucopolysaccharidosis? Clin Chim Acta. 2014 Apr 20; 431:250-4. Kurt I, Sertoglu E, Okur I, Tapan S, Uyanik M, Kayadibi H, Ezgu FS, Aydin HI, Hasanoglu A. PMID: 24582858.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    11. Is there a relationship between serum paraoxonase level and epicardial fat tissue thickness? Anadolu Kardiyol Derg. 2014 Mar; 14(2):115-20. Ertem AG, Erayman A, Efe TH, Duran Karaduman B, Aydin HI, Bilge M. PMID: 24449622.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    12. Hand and heart, hand in hand: is radiological hand osteoarthritis associated with atherosclerosis? Int J Rheum Dis. 2014 Mar; 17(3):299-303. Cemeroglu O, Aydin HI, Yasar ZS, Bozduman F, Saglam M, Selcoki Y, Eryonucu B, Cakirbay H. PMID: 24330251.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansPHPublic Health
    13. Tako-tsubo-like cardiomyopathy induced by pheochromocytoma crisis. Anadolu Kardiyol Derg. 2013 Sep 25; 13(6):E35-6. Demirçelik MB, Aydin HI. PMID: 24064103.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    14. Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance. Gene. 2013 Jun 01; 521(2):293-5. Güzel-Ozantürk A, Ozgül RK, Unal O, Hismi B, Aydin HI, Sivri S, Tokatli A, Coskun T, Aksöz E, Dursun A. PMID: 23542076.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    15. Two novel deletions in hypotonia-cystinuria syndrome. Mol Genet Metab. 2012 Nov; 107(3):614-6. Régal L, Aydin HI, 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. PMID: 22796000.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    16. Four novel mutations in the ß-galactosidase gene identified in infantile type of GM1 gangliosidosis. Clin Biochem. 2012 May; 45(7-8):571-4. Celtikçi B, Aydin HI, Sivri S, Sönmez M, Topçu M, Ozkara HA. PMID: 22234367.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    17. 3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures. Turk J Pediatr. 2009 Nov-Dec; 51(6):587-92. Coskun T, Aydin HI, Kiliç M, Dursun A, Haliloglu G, Topaloglu H, Karli-Oguz K, de Koning TJ. PMID: 20196394.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    18. Cytomegalovirus infection with gastric ulcers in Ménétrier's disease and hypergammaglobulinemia. Turk J Pediatr. 2009 Sep-Oct; 51(5):524. Gökçe S, Tasçilar ME, Dabak O, Devrim I, Aydin HI, Unay B. PMID: 20112615.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    19. Lymphocytic vacuolization in sialic acid storage disease. Am J Hematol. 2008 Oct; 83(10):821. Kuskonmaz B, Unal S, Cördükcü E, Aydin H, Coskun T, Gurgey A, Gumruk F. PMID: 18050357.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    20. 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. Aydin HI, Yozgat Y, Demirkaya E, Olgun A, Okutan V, Lenk MK, Ozcan O. PMID: 18246735.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    21. Hearing loss in biotinidase deficiency: genotype-phenotype correlation. J Pediatr. 2007 Apr; 150(4):439-42. Sivri HS, Genç GA, Tokatli A, Tokatlý A, Dursun A, Coskun T, Aydin HI, Aydýn HY, Sennaroglu L, Belgin E, Jensen K, Wolf B. PMID: 17382128.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    22. Death possibly associated with interferon use in a patient with chronic hepatitis. Acta Paediatr. 2005 Jul; 94(7):984-5. Kendirli T, Kismet E, Demirkaya E, Aydin HI, Kesik V, Köseoglu V. PMID: 16188832.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    23. 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. Gok F, Aydin HI, Kurt I, Gokcay E, Maeda M, Kasahara M. PMID: 15795603.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    24. 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. Kiliç S, Tezcan S, Tasçilar E, Cakir B, Aydin HI, Hasde M, Gökçay E. PMID: 15724854.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    25. 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. Kismet E, Atay AA, Demirkaya E, Aydin HI, Aydogan H, Koseoglu V, Gokcay E. PMID: 15654276.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCellsPHPublic Health
    26. Analysis of DNA damage using the comet assay in infants fed cow's milk. Biol Neonate. 2003; 84(2):135-41. Dündaröz R, Ulucan H, Aydin HI, Güngör T, Baltaci V, Denli M, Sanisoglu Y. PMID: 12907847.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    27. Preliminary study on DNA damage in non breast-fed infants. Pediatr Int. 2002 Apr; 44(2):127-30. Dündaröz R, Aydin HI, Ulucan H, Baltaci V, Denli M, Gökçay E. PMID: 11896867.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimals