Search Results - "Vildan, Ciftci"

Genetic alterations of C9orf72, SOD1, TARDBP, FUS, and UBQLN2 genes in patients with Amyotrophic Lateral Sclerosis by Vildan, Ciftci, Sule, Darbas, Turker, Bilgen, Hilmi, Uysal, Sibel, Karauzum Berker

“…Amyotrophic lateral sclerosis is the most common motor neuron disease of the adulthood. Genetic analyses performed on cases with sporadic ALS (sALS) and…”
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Another de novo mutation in the SOD1 gene: the first Turkish patient with SOD1-His47Arg, a case report by Bayraktar, Elif, Çiftçi, Vildan, Uysal, Hilmi, Başak, A. Nazlı

“…Amyotrophic lateral sclerosis (ALS) is a fatal, progressive neurodegenerative disease of motor neurons. Most ALS cases are considered sporadic due to the…”
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First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population by Canatan, Duran, Bilgen, Türker, Çiftçi, Vildan, Yazıcı, Gülsüm, Delibaş, Serpil, Keser, İbrahim

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First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population/Türk Toplumunda Gözlenen ilk Hemoglobin G-Waimanalo ve Hemoglobin Fontainebleau Olgulari by Canatan, Duran, Bilgen, Türker, Çiftçi, Vildan, Yazici, Gülsüm, Delibas, Serpil, Keser, Ibrahim

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Another de novo mutation in the SOD1 gene: the first Turkish patient with SOD1-His47Arg, a case report by Bayraktar, Elif, Çiftçi, Vildan, Uysal, Hilmi, Başak, A Nazlı

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