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Three-Country Snapshot of Ornithine Transcarbamylase Deficiency. Seker Yilmaz B, Baruteau J, Arslan N, Aydin HI, Barth M, Bozaci AE, Brassier A, Canda E, Cano A, Chronopoulou E, Connolly GM, Damaj L, Dawson C, Dobbelaere D, Douillard C, Eminoglu FT, Erdol S, Ersoy M, Fang S, Feillet F, Gokcay G, Goksoy E, Gorce M, Inci A, Kadioglu B, Kardas F, Kasapkara CS, Kilic Yildirim G, Kor D, Kose M, Marelli C, Mundy H, O'Sullivan S, Ozturk Hismi B, Ramachandran R, Roubertie A, Sanlilar M, Schiff M, Sreekantam S, Stepien KM, Uzun Unal O, Yildiz Y, Zubarioglu T, Gissen P.Life (Basel). 2022 Oct 27;12(11):1721. doi: 10.3390/life12111721.
A novel mutation in TRMT5 associated with idiopathic non-cirrhotic portal hypertension and hepatopulmonary syndrome: Case report of two siblings. Warasnhe K, Özçay F, Aydin Hİ, Özgün G, Ceylaner S.Clin Res Hepatol Gastroenterol. 2022 Oct;46(8):101928. doi: 10.1016/j.clinre.2022.101928.
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis. Cabrera-Serrano M, Caccavelli L, Savarese M, Vihola A, Jokela M, Johari M, Capiod T, Madrange M, Bugiardini E, Brady S, Quinlivan R, Merve A, Scalco R, Hilton-Jones D, Houlden H, Aydin HI, Ceylaner S, Drewes S, Vockley J, Taylor RL, Folland C, Kelly A, Goullee H, Ylikallio E, Auranen M, Tyynismaa H, Udd B, Forrest ARR, Davis MR, Bratkovic D, Manton N, Robertson T, O'Gorman C, McCombe P, Laing NG, Phillips L, de Lonlay P, Ravenscroft G.Brain. 2022 Nov 21;145(11):3985-3998. doi: 10.1093/brain/awab484.
The Relationship between Daily Fructose Consumption and Oxidized Low-Density Lipoprotein and Low-Density Lipoprotein Particle Size in Children with Obesity. Gungor A, Balamtekin N, Ozkececi CF, Aydin Hİ.Pediatr Gastroenterol Hepatol Nutr. 2021 Sep;24(5):483-491. doi: .5223/pghn.2021.24.5.483.
Severe isolated sulfide oxidase deficiency with a novel mutation. Ergene M, Yarar N, Öncel EP, Sezer T, Çavdarlı B, Ecevit İZ, Aydın Hİ.Turk J Pediatr. 2021;63(4):716-720. doi: 10.24953/turkjped.2021.04.021.
Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: a single center experience. Olgac A, Kasapkara ÇS, Derinkuyu B, Yüksel D, Çetinkaya S, Aksoy A, Ceylaner S, Güleray N, Yeşilipek A, Aydın Hİ, Orgun LT, Kılıç M.J Pediatr Endocrinol Metab. 2021 Jun 24;34(9):1169-1179. doi: 10.1515/jpem-2021-0032.
Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation. Ayanoğlu M, Korgali E, Sezer T, Aydin HI, Sönmez FM.Brain Dev. 2020 May;42(5):418-420. doi: 10.1016/j.braindev.2020.02.001.
A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism. Aydın Hİ, Sönmez FM.Turk J Pediatr. 2019;61(1):92-96. doi: 10.24953/turkjped.2019.01.014.
Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder. Aydin HI.Indian Pediatr. 2018 Jan 15;55(1):67-68.
Association between coronary artery disease severity and overactive bladder in geriatric patients. Kilinc MF, Yasar E, Aydin HI, Yildiz Y, Doluoglu OG.World J Urol. 2018 Jan;36(1):35-40. doi: 10.1007/s00345-017-2098-1.
A coronary proatherosclerotic marker: Pregnancy-associated plasma protein A and its association with coronary calcium score and carotid intima-media thickness. Guven A, Demircelik B, Gurel OM, Er O, Aydin HI, Bozkurt A.Adv Clin Exp Med. 2017 May-Jun;26(3):467-473. doi: 10.17219/acem/62225.
Galectin-3: A biochemical marker to detect paroxysmal atrial fibrillation? Selcoki Y, Aydin Hİ, Celik TH, Isleyen A, Erayman A, Demircelik MB, Demirin H, Kosus A, Eryonucu B.Clin Invest Med. 2016 Dec 1;39(6):27528.
Genetic Studies in Autism: Correspondence. Aydin HI.Indian J Pediatr. 2017 Feb;84(2):170-171. doi: 10.1007/s12098-016-2201-4.
Adipokine, adropin and endothelin-1 levels in intrauterine growth restricted neonates and their mothers. Aydin HI, Eser A, Kaygusuz I, Yildirim S, Celik T, Gunduz S, Kalman S.J Perinat Med. 2016 Aug 1;44(6):669-76. doi: 10.1515/jpm-2014-0353.
Lack of prolidase causes a bone phenotype both in human and in mouse. 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.Bone. 2015 Mar;72:53-64. doi: 10.1016/j.bone.2014.11.009.
Assessing leptin and soluble leptin receptor levels in full-term asymmetric small for gestational age and healthy neonates. Aydın Hİ, Demirkaya E, Karadeniz RS, Olgun A, Alpay F.Turk J Pediatr. 2014 May-Jun;56(3):250-8.
NMR-Based Screening for Inborn Errors of Metabolism: Initial Results from a Study on Turkish Neonates. Aygen S, Dürr U, Hegele P, Kunig J, Spraul M, Schäfer H, Krings D, Cannet C, Fang F, Schütz B, Bülbül SF, Aydin HI, Sarıcı SU, Yalaz M, Ors R, Atalan R, Tuncer O.JIMD Rep. 2014;16:101-11. doi: 10.1007/8904_2014_326.
Serum dipeptidyl peptidase-IV: a better screening test for early detection of mucopolysaccharidosis? Kurt I, Sertoglu E, Okur I, Tapan S, Uyanık M, Kayadıbı H, Ezgu FS, Aydın HI, Hasanoglu A.Clin Chim Acta. 2014 Apr 20;431:250-4. doi: 10.1016/j.cca.2014.02.012.
Is there a relationship between serum paraoxonase level and epicardial fat tissue thickness? Ertem AG, Erayman A, Efe TH, Duran Karaduman B, Aydın HI, Bilge M.Anadolu Kardiyol Derg. 2014 Mar;14(2):115-20. doi: 10.5152/akd.2014.4742.
Hand and heart, hand in hand: is radiological hand osteoarthritis associated with atherosclerosis? Cemeroglu O, Aydın HI, Yasar ZS, Bozduman F, Saglam M, Selcoki Y, Eryonucu B, Cakirbay H.Int J Rheum Dis. 2014 Mar;17(3):299-303. doi: 10.1111/1756-185X.12251.
Thrombin activatable fibrinolysis inhibitor : its role in slow coronary flow. Yildirim MN, Selcoki Y, Uysal S, Nacar AB, Demircelik B, Aydin HI, Eryonucu B.Herz. 2014 Dec;39(8):993-1000. doi: 10.1007/s00059-013-3942-8.
Tako-tsubo-like cardiomyopathy induced by pheochromocytoma crisis. Demirçelik MB, Aydın Hİ.Anadolu Kardiyol Derg. 2013 Sep 25;13(6):E35-6. doi: 10.5152/akd.2013.221.
Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance. Güzel-Ozantürk A, Ozgül RK, Unal O, Hişmi B, Aydın Hİ, Sivri S, Tokatlı A, Coşkun T, Aksöz E, Dursun A.Gene. 2013 Jun 1;521(2):293-5. doi: 10.1016/j.gene.2013.03.033.
Two novel deletions in hypotonia-cystinuria syndrome. 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.Mol Genet Metab. 2012 Nov;107(3):614-6. doi: 10.1016/j.ymgme.2012.06.011.
Four novel mutations in the ?-galactosidase gene identified in infantile type of GM1 gangliosidosis. Celtikçi B, Aydın Hİ, Sivri S, Sönmez M, Topçu M, Ozkara HA.Clin Biochem. 2012 May;45(7-8):571-4. doi: 10.1016/j.clinbiochem.2011.12.019.
3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures. Coşkun T, Aydin HI, Kiliç M, Dursun A, Haliloğlu G, Topaloğlu H, Karli-Oğuz K, de Koning TJ.Turk J Pediatr. 2009 Nov-Dec;51(6):587-92.
Cytomegalovirus infection with gastric ulcers in Ménétrier's disease and hypergammaglobulinemia. Gökçe S, Taşçilar ME, Dabak O, Devrim I, Aydin HI, Unay B.Turk J Pediatr. 2009 Sep-Oct;51(5):524.
Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters. Hörster F, Garbade SF, Zwickler T, Aydin HI, Bodamer OA, Burlina AB, Das AM, De Klerk JBC, Dionisi-Vici C, Geb S, Gökcay G, Guffon N, Maier EM, Morava E, Walter JH, Schwahn B, Wijburg FA, Lindner M, Grünewald S, Baumgartner MR, Kölker S.J Inherit Metab Dis. 2009 Oct;32(5):630. doi: 10.1007/s10545-009-1189-6.
Diagnostic work-up and management of patients with isolated methylmalonic acidurias in European metabolic centres. Zwickler T, Lindner M, Aydin HI, Baumgartner MR, Bodamer OA, Burlina AB, Das AM, DeKlerk JB, Gökcay G, Grünewald S, Guffon N, Maier EM, Morava E, Geb S, Schwahn B, Walter JH, Wendel U, Wijburg FA, Müller E, Kölker S, Hörster F.J Inherit Metab Dis. 2008 Jun;31(3):361-7. doi: 10.1007/s10545-008-0804-2.
Correlation between vascular endothelial growth factor and leptin in children with cyanotic congenital heart disease. Aydin HI, Yozgat Y, Demirkaya E, Olgun A, Okutan V, Lenk MK, Ozcan O.Turk J Pediatr. 2007 Oct-Dec;49(4):360-4.
Hearing loss in biotinidase deficiency: genotype-phenotype correlation. Sivri HS, Genç GA, Tokatli A, Dursun A, Coşkun T, Aydin HI, Sennaroğlu L, Belgin E, Jensen K, Wolf B.J Pediatr. 2007 Apr;150(4):439-42. doi: 10.1016/j.jpeds.2007.01.036.PMID: 17382128
Audiologic findings in children with biotinidase deficiency in Turkey. Genc GA, Sivri-Kalkanoğlu HS, Dursun A, Aydin HI, Tokatli A, Sennaroglu L, Belgin E, Wolf B, Coşkun T.Int J Pediatr Otorhinolaryngol. 2007 Feb;71(2):333-9. doi: 10.1016/j.ijporl.2006.11.001.
A Turkish case with molybdenum cofactor deficiency. Ichida K, Aydin HI, Hosoyamada M, Kalkanoglu HS, Dursun A, Ohno I, Coskun T, Tokatli A, Shibasaki T, Hosoya T.Nucleosides Nucleotides Nucleic Acids. 2006;25(9-11):1087-91. doi: 10.1080/15257770600894022.
Death possibly associated with interferon use in a patient with chronic hepatitis. Kendirli T, Kismet E, Demirkaya E, Aydin HI, Kesik V, Köseoğlu V.Acta Paediatr. 2005 Jul;94(7):984-5. doi: 10.1111/j.1651-2227.2005.tb02028.x.
Familial high factor VIII level in a child with necrotizing fasciitis complicating primary varicella infection. Kurekci AE, Aydin HI, Atay AA, Akar N, Cetan T, Ozcan O, Gokcay E.Pediatr Hematol Oncol. 2005 Apr-May;22(3):219-22. doi: 10.1080/08880010590921540.
A novel mutation of Na+/glucose cotransporter in a Turkish newborn with congenital glucose-galactose malabsorption. Gok F, Aydin HI, Kurt I, Gokcay E, Maeda M, Kasahara M.J Pediatr Gastroenterol Nutr. 2005 Apr;40(4):508-11. doi: 10.1097/01.mpg.0000153097.73083.a3.
Morbidity and mortality characteristics of infants hospitalized in the Pediatrics Department of the largest Turkish military hospital in 2001. Kiliç S, Tezcan S, Taşçilar E, Cakir B, Aydin HI, Hasde M, Gökçay E.Mil Med. 2005 Jan;170(1):48-51. doi: 10.7205/milmed.170.1.48.
Two cases of Ralstonia pickettii bacteremias in a pediatric oncology unit requiring removal of the Port-A-Caths. Kismet E, Atay AA, Demirkaya E, Aydin HI, Aydogan H, Koseoglu V, Gokcay E.J Pediatr Hematol Oncol. 2005 Jan;27(1):37-8. doi: 10.1097/01.mph.0000149960.89192.b0.
Bone mineral density in children with nocturnal enuresis. Sarici SU, Kismet E, Türkbay T, Kocaoğlu M, Aydin HI, Dündaröz MR, Balcioğlu I.Int Urol Nephrol. 2003;35(3):381-5. doi: 10.1023/b:urol.0000022936.78678.26.
Meningitis with multidrug-resistant Acinetobacter baumannii treated with ampicillin/sulbactam. Kendirli T, Aydín HI, Hacíhamdioğlu D, Gülgün M, Unay B, Akín R, Lenk MK, Gökçay E.J Hosp Infect. 2004 Apr;56(4):328. doi: 10.1016/j.jhin.2003.12.006.
Antiannexin V autoantibody in thrombophilic Behçet's disease. Aslan H, Pay S, Gok F, Baykal Y, Yilmaz MI, Sengul A, Aydin HI.Rheumatol Int. 2004 Mar;24(2):77-9. doi: 10.1007/s00296-002-0274-z.
Analysis of DNA damage using the comet assay in infants fed cow's milk. Dündaröz R, Ulucan H, Aydin HI, Güngör T, Baltaci V, Denli M, Sanisoğlu Y.Biol Neonate. 2003;84(2):135-41. doi: 10.1159/000071947.
Evaluation of bone mineral density in chronic glue sniffers. Dündaröz MR, Sarici SU, Türkbay T, Baykal B, Kocaoğlu M, Aydin HI, Gökçay E.Turk J Pediatr. 2002 Oct-Dec;44(4):326-9.
Preliminary study on DNA damage in non breast-fed infants. Dündaröz R, Aydin HI, Ulucan H, Baltaci V, Denli M, Gökçay E.Pediatr Int. 2002 Apr;44(2):127-30. doi: 10.1046/j.1328-8067.2001.01525.x.
Analysis of heart rate variability in children with primary nocturnal enuresis. Dundaröz MR, Denli M, Uzun M, Aydin HI, Sarici SU, Yokuşoğlu M, Ulgen S.Int Urol Nephrol. 2001;32(3):393-7. doi: 10.1023/a:1017539317009.
Bone age in children with nocturnal enuresis. Dündaröz MR, Sarici SU, Denli M, Aydin HI, Kocaoğlu M, Ozişik T.Int Urol Nephrol. 2001;32(3):389-91.
Evaluation of DNA damage using the comet assay in children on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever. Dündaröz R, Ulucan H, Denli M, Karapinar K, Aydin HI, Baltaci V.Pediatr Int. 2001 Jun;43(3):276-80. doi: 10.1046/j.1442-200x.2001.01397.x.
Sister-chromatid exchange analysis on long-term benzathine penicillin for secondary prophylaxis of rheumatic fever. Dündaröz R, Ozisik T, Baltaci V, Karapinar K, Aydin HI, Denli M.Indian J Pediatr. 2001 Feb;68(2):121-2. doi: 10.1007/BF02722027.
Thoracic ectopic kidney in a child: a case report. Aydin HI, Sarici SU, Alpay F, Gökçay E.Turk J Pediatr. 2000 Jul-Sep;42(3):253-5.
Çocukluk Çağında Kalp Üfürümlerinin Değerlendirilmesinde Muayene, EKG, Telekardiyografi ve Ekokardiyografinin rolü. GÜLHANE TIP DERGİSİ, 1999; 41(1):391-394., Yazarlar: V OKUTAN, R AKIN, MK LENK, Hİ AYDIN, E GÖKÇAY.
Çocuklarda semptomatik idrar yolu enfeksiyonlarının hızlı tanısında çeşitli tarama testlerinin etkinliklerinin araştırılması. Klinik Bilimler & Doktor, 1999; 5(5):645-650., Yazarlar: V OKUTAN, AC BAŞUSTAOĞLU, Hİ AYDIN, Ö ÖZYURT, B ÜNAY, E GÖKÇAY.
Serebral Palsili Çocuklarda Epilepsi Görülme Sıklığı ve Antiepileptik Tedavi Etkinliğin Değerlendirilmesi. EPİLEPSİ, 2001; 7(3):89-94., Yazarlar: B ÜNAY, T TUNÇ, Hİ AYDIN, R AKIN, E GÖKÇAY.
Çocukluk Çağı Zehirlenmeleri: Olgularımızın Değerlendirilmesi. GÜLHANE TIP DERGİSİ, 2001; 44(1):49-52., Yazarlar: B ÜNAY, Hİ AYDIN, R AKIN, E GÖKÇAY.
Engelli bireye sahip ailelerin beklentilerinin ve psiko-sosyal durumlarının incelenmesi. GÜLHANE TIP DERGİSİ, 2002; 44:188-194., Yazarlar: F ÖZŞENOL, B ÜNAY, Hİ AYDIN, R AKIN, E GÖKÇAY.
Krup Tedavisinde Nebulize Budesonid ve İntramuskular Deksametazonun Karşılaştırılması. T Klin Pediatri, 2002; 11:10-14., Yazarlar: B ÜNAY, ME TAŞÇILAR, Hİ AYDIN, O ÖZCAN.
Henoch-Schölein Purpuralı Çocuklarda Renal Tutulum. C. Ü. Tıp Dergisi, 2003; 25(3):123-128., Yazarlar: S KALMAN, Hİ AYDIN, SÜ SARICI, AA ATAY.
Gata çocuk sağlığı ve hastalıkları anabilim Dalı yataklı servislerinde 2001 yılında tedavi gören hastaların tanı ve tedavi özellikleri. GÜLHANE TIP DERGİSİ, 2003; 45(2):169-174., Yazarlar: S KILIÇ, S TEZCAN, ME TAŞÇILAR, B ÇAKIR, Hİ AYDIN, M HASDE, E GÖKÇAY.
Engelli çocuğa sahip ailelerin aile İşlevlerinin değerlendirilmesi. GÜLHANE TIP DERGİSİ, 2003; 45(2):156-164., Yazarlar: F ÖZŞENOL, V IŞIKHAN, B ÜNAY, Hİ AYDIN.
Doksorubisin tedavisi uygulanan solid Tümörlü çocuklarda serum BNP düzeyi. GÜLHANE TIP DERGİSİ, 2004; 46(1):38-42., Yazarlar: E KISMET, E DEMİRKAYA, N YUTTURAN, S BERBEROĞLU, S KARADEMİR, Hİ AYDIN.
GATA Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı Yataklı Servislerde 2001 Yılında Tedavi Gören Hastaların Bazı Sosdemografik Özellikleri ve Aşılanma Düzeyleri. SAĞLIK VE TOPLUM, 2004; 14(2):40-46., Yazarlar: Selim Kılıç, Sabahat Tezcan, M. Emre Taşçılar, Banu Çakır, Halil İbrahim Aydın, Metin Hasde, Erdal Gökçay.
Fimozis tedavisinde topikal kortikosteroidli kremlerin etkinliği. ERCİYES TIP DERGİSİ, 2006; 28(3):120-124., Yazarlar: N BALAMTEKİN, N ULUOCAK, AA ATAY, Hİ AYDIN.
Ada çayı yağının yanlış kullanımına bağlı Neonatal konvülziyon: olgu sunumu. GÜLHANE TIP DERGİSİ, 2004; 46(2):161-162., Yazarlar: Sü SARICI, M KUL, G CANDEMİR, Hİ AYDIN, F ALPAY, E GÖKÇAY.
Su çiçeği sonrası ortaya çıkan henoch-Schönlein Purpurası: olgu sunumu. GÜLHANE TIP DERGİSİ, 2005; 5:231- 231., Yazarlar: S Kalman, Hi AYDIN, M ALİÖMEROĞLU, B ÜNAY, E GÖKÇAY.
Yenidoğanın Doğumsal Metabolik Hastalıklarına Acil Yaklaşım. Türkiye Klinikleri Cerrahi Tıp Bilimleri Dergisi, 2007; 3(33):82-102., Yazarlar: Hİ AYDIN, T COŞKUN.
Primer karnitin eksikliğine bağlı dilate kardiyomiyopatili iki kardeş. GÜLHANE MEDİCAL JOURNAL, 2008; 50(3):209-212., Yazarlar: V OKUTAN, Y YOZGAT, Hİ AYDIN, ST YAVUZ, Mk LENK.
Hipokalemik Periyodik Paralizili Bir Türk Hastada Voltaj Bağınlı Kalsiyum Kanal Mutasyonu, R1239H: Olgu Sunumu. BAKIRKÖY TIP DERGİSİ, 2009; 5:120-122., Yazarlar: O SAKALLIOĞLU, F GÖK, Hİ AYDIN, S KALMAN, S VURUCU.
Yineleyen karın ağrısının ender bir nedeni: Porfiri. Göztepe Tıp Dergisi, 2014; 29(3):196-200., Yazarlar: M KARABEL, Hİ AYDIN, İ KURT, Y TOKGÖZ, G BAYSOY.
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