Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis von Cabrera-Serrano, Macarena, Caccavelli, Laure, Savarese, Marco, Vihola, Anna, Jokela, Manu, Johari, Mridul, Capiod, Thierry, Madrange, Marine, Bugiardini, Enrico, Brady, Stefen, Quinlivan, Rosaline, Merve, Ashirwad, Scalco, Renata, Hilton-Jones, David, Houlden, Henry, Ibrahim Aydin, Halil, Ceylaner, Serdar, Vockley, Jerry, Taylor, Rhonda L, Folland, Chiara, Kelly, Aasta, Goullee, Hayley, Ylikallio, Emil, Auranen, Mari, Tyynismaa, Henna, Udd, Bjarne, Forrest, Alistair R R, Davis, Mark R, Bratkovic, Drago, Manton, Nicholas, Robertson, Thomas, McCombe, Pamela, Laing, Nigel G, Phillips, Liza, de Lonlay, Pascale, Ravenscroft, Gianina

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Time-Varying Economic Consequences of Terrorism in the USA: Evidence from TVP-SVAR MODEL von HALIL IBRAHIM, AYDIN, OMER, YALCINKAYA, EMRE, BULUT

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The Relationship between Daily Fructose Consumption and Oxidized Low-Density Lipoprotein and Low-Density Lipoprotein Particle Size in Children with Obesity von Gungor, Ali, Balamtekin, Necati, Ozkececi, Coskun Firat, Aydin, Halil İbrahim

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Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation von Ayanoğlu, Müge, Korgali, Elif, Sezer, Taner, Aydin, Halil Ibrahim, Sönmez, Fatma Müjgan

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Association between coronary artery disease severity and overactive bladder in geriatric patients von Kilinc, Muhammet Fatih, Yasar, Erdogan, Aydin, Halil Ibrahim, Yildiz, Yildiray, Doluoglu, Omer Gokhan

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Cerebral creatine deficiency syndrome with a novel missense variant in SLC6A8 gene von Turan, Betül, Göktaş, Emine, Sönmez, F. Mujgan, Aydin, Halil Ibrahim, Aydogdu, Demet, Zamani, Ayse Gul, Yildirim, Mahmut Selman

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HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Renal Tubular Acidosis and Endocrine Abnormalities von Taslipinar, Abdullah, Kebapcilar, Levent, Kutlu, Mustafa, Sahin, Mustafa, Aydogdu, Aydogan, Uckaya, Gokhan, Azal, Omer, Bolu, Erol, Aydin, Halil Ibrahim

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Three-Country Snapshot of Ornithine Transcarbamylase Deficiency von Seker Yilmaz, Berna, Baruteau, Julien, Arslan, Nur, Aydin, Halil Ibrahim, Barth, Magalie, Bozaci, Ayse Ergul, Brassier, Anais, Canda, Ebru, Cano, Aline, Chronopoulou, Efstathia, Connolly, Grainne M, Damaj, Lena, Dawson, Charlotte, Dobbelaere, Dries, Douillard, Claire, Eminoglu, Fatma Tuba, Erdol, Sahin, Ersoy, Melike, Fang, Sherry, Feillet, François, Gokcay, Gulden, Goksoy, Emine, Gorce, Magali, Inci, Asli, Kadioglu, Banu, Kardas, Fatih, Kasapkara, Cigdem Seher, Kilic Yildirim, Gonca, Kor, Deniz, Kose, Melis, Marelli, Cecilia, Mundy, Helen, O'Sullivan, Siobhan, Ozturk Hismi, Burcu, Ramachandran, Radha, Roubertie, Agathe, Sanlilar, Mehtap, Schiff, Manuel, Sreekantam, Srividya, Stepien, Karolina M, Uzun Unal, Ozlem, Yildiz, Yilmaz, Zubarioglu, Tanyel, Gissen, Paul

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Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder von Aydin, Halil Ibrahim

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Genetic Studies in Autism: Correspondence von Aydin, Halil Ibrahim

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Muhtevâ ve Üslup Açısından Kur’an’da Secde Âyetleri von AYDIN, Halil İbrahim

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Preliminary study on DNA damage in non breast-fed infants von DÜndaröz, RuŞen, Aydin, Halil İBrahim, Ulucan, Hakan, Baltaci, Volkan, Denli, Metin, Gökçay, Erdal

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A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism von Aydın, Halil İbrahim, Sönmez, Fatma Müjgan

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A novel mutation in guanidinoacetate methyltransferase (GAMT) deficiency in two patients associated with epilepsy, developmental delay, hyperactivity, autistic behavior von Aydin, Halil Ibrahim, Sonmez, F. Mujgan

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THE EFFECTS OF MACROECONOMIC INSTABILITY ON ECONOMIC GROWTH: TIME SERIES ANALYSIS WITH STRUCTURAL BREAKS ON TURKEY (1983-2015) von Yalcinkaya, Omer, Aydin, Halil Ibrahim

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Tertiary Education in Europe. What is Romania’s place? von Zaharia, Marian, Gogonea, Rodica Manuela, Bălăcescu, Aniela, Păunescu, Loredana Maria, Aydin, Halil Ibrahim

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Severe isolated sulfide oxidase deficiency with a novel mutation von Ergene, Meriç, Yarar, Nuriye, Öncel, Elif Perihan, Sezer, Taner, Çavdarlı, Büşranur, Ecevit, İsmail Zafer, Aydın, Halil İbrahim

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Lack of prolidase causes a bone phenotype both in human and in mouse von Besio, Roberta, Maruelli, Silvia, Gioia, Roberta, Villa, Isabella, Grabowski, Peter, Gallagher, Orla, Bishop, Nicholas J, Foster, Sarah, De Lorenzi, Ersilia, Colombo, Raffaella, Diaz, Josè Luis Dapena, Moore-Barton, Haether, Deshpande, Charu, Aydin, Halil Ibrahim, Tokatli, Aysegul, Kwiek, Bartlomiej, Kasapkara, Cigdem Seher, Adisen, Esra Ozsoy, Gurer, Mehmet Ali, Di Rocco, Maja, Phang, James M, Gunn, Teresa M, Tenni, Ruggero, Rossi, Antonio, Forlino, Antonella

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PARA POLİTİKASI TASARIMLARINDA FİYAT VE FİNANSAL İSTİKRAR İLİŞKİSİ: EURO ALANINDAN KANITLAR (1999:01-2020:12) von YALÇINKAYA, Ömer, AYDIN, Halil İbrahim

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Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases von Dönger, Utku, Warasnhe, Khaled, Özçay, Figen, Şule Haskoloğlu, Zehra, İbrahim Aydın, Halil, Ceylaner, Serdar

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