| Increased SRF transcriptional activity in human and mouse skeletal muscle is a signature of insulin resistance MEP Wanzhu Jin,1 Allison B. Goldfine,1 Tanner Boes,1 Robert R. Henry,2 ... Journal of Clinical Investigation 121 (3), 918-929, 2011 | 117 | 2011 |
| Novel dominant-negative GH receptor mutations expands the spectrum of GHI and IGF-I deficiency K Vairamani, L Merjaneh, P Casano-Sancho, ME Sanli, A David, ... Journal of the Endocrine Society 1 (4), 345-358, 2017 | 39 | 2017 |
| Comparison of piperacillin tazobactam and cefoperazone sulbactam monotherapy in treatment of febrile neutropenia RKMD Serap Karaman MD, Sema Vural MD, Yildiz Yildirmak MD, Merve Emecen MD ... Pediatric Blood & Cancer 58 (4), 579-583, 2012 | 34 | 2012 |
| Evaluation of risk factors for development of severe hyperbilirubinemia in term and near term infants in Turkey A Bulbul, N Cayonu, ME Sanli, S Uslu Pakistan journal of medical sciences 30 (5), 1113, 2014 | 28 | 2014 |
| Evaluation of tissue transglutaminase IgA antibody in diagnosis and following up of celiac disease in children SG Güleç, N Urgancı, F Gül, M Emecen, E Erdem Ş. EEAH Tıp Bülteni 45, 119-23, 2011 | 7* | 2011 |
| Familial hyperphosphatemic tumoral calcinosis in an unusual and usual sites and dramatic improvement with the treatment of acetazolamide, sevelamer and topical sodium thiosulfate ME Sanli, A Kilic, E Aktasoglu, A Inci, I Okur, F Ezgu, L Tumer Journal of Pediatric Endocrinology and Metabolism 34 (6), 813-816, 2021 | 5 | 2021 |
| Fructose 1,6 bisphosphatase deficiency: outcomes of patients in a single center in Turkey and identification of novel splice site and indel mutations in FBP1 M Emecen Sanli, B Cengiz, A Kilic, E Ozsaydi, A Inci, I Okur, L Tumer, ... Journal of Pediatric Endocrinology and Metabolism 35 (4), 497-503, 2022 | 4 | 2022 |
| First successful concomitant therapy of immune tolerance induction therapy and desensitization in a CRIM-negative infantile Pompe patient M Emecen Sanli, HI Ertoy Karagol, A Kilic, E Aktasoglu, A Inci, I Okur, ... Journal of Pediatric Endocrinology and Metabolism 35 (2), 273-277, 2022 | 4 | 2022 |
| Use of Thalamus L-Sign to Differentiate Periventricular Leukomalacia From Neurometabolic Disorders S Yuzkan, M Emecen Sanli, M Balci, P Cennetoglu, I Kafadar, B Kocak Journal of Child Neurology 38 (6-7), 446-453, 2023 | 3 | 2023 |
| Folate deficiency in patients with classical galactosemia: A novel finding that needs to be considered for dietary treatments FTE Muhittin Çelik 1 ,Nezir Özgün 2 ,Osman Akdeniz 3 ,Mücahit Fidan 4 ... The Turkish Journal of Pediatrics 60 (5), 540-546, 2018 | 2 | 2018 |
| GM1 gangliosidosis: patients with different phenotypic features and novel mutations M Emecen Sanli, M Dogan Journal of Pediatric Endocrinology and Metabolism 36 (6), 602-607, 2023 | 1 | 2023 |
| Fucosidosis: clinical and molecular findings of Turkish patients ME Şanlı, S Uysal The Turkish Journal of Pediatrics 64 (4), 795-803, 2022 | 1 | 2022 |
| New perspectives for the treatment and follow-up of glycogen storage disease type V: DL-3-hydroxybutyric acid with modified Atkins diet and quadriceps femoris shear wave … LT Ekin Özsaydı Aktaşoğlu 1, Ayşe Kılıç 1, Merve Emecen Şanlı 1, Aslı İnci 1 ... Journal of Pediatric Endocrinology and Metabolism, 2024 | | 2024 |
| New perspectives for the treatment and follow-up of glycogen storage disease type V: DL3-hydroxybutyric acid with modified Atkins diet and quadriceps femoris shear wave … FSELT Ekin Özsaydı Aktaşoğlu*, Ayşe Kılıç, Merve Emecen Şanlı, Aslı İnci ... J Pediatr Endocrinol Metab, 2024 | | 2024 |
| Endocrinological and metabolic profile of Gaucher disease patients treated with enzyme replacement therapy A Kilic, M Emecen Sanli, E Ozsaydı Aktasoglu, S Gokalp, G Biberoğlu, ... Journal of Pediatric Endocrinology and Metabolism 37 (5), 413-418, 2024 | | 2024 |
| Dietary Fiber Supplementation in Type I Glycogen Storage Disease; Could it Contribute to a Better Metabolic Control? ME Şanlı, E Aktaş, A İnci, İ Okur, F Ezgü, L Tümer Güncel Pediatri Dergisi, 2023 | | 2023 |
| Endocrinological, immunological and metabolic features of patients with Fabry disease under therapy M Emecen Sanli, A Kilic, A Inci, I Okur, F Ezgu, L Tumer Journal of Pediatric Endocrinology and Metabolism 36 (7), 650-658, 2023 | | 2023 |
| Causes of hereditary metabolic diseases in patients presenting with developmental delay ME Sanli | | 2023 |
| B12 Yüksekliği İle Yönlendirilen Hastalarda Kalıtsal Metabolik Hastalık Taraması KAH EMECEN ŞANLI MERVE 11. Çocuk Dostları Kongresi, 2023 | | 2023 |
| NEW PERSPECTIVES FOR THE TREATMENT and FOLLOW UP OF GYCOGEN STORAGE DISEASE TYPE V: DL-3-HYDROXYBUTYRIC ACID WITH MODIFIED ATKINS DIET and QUADRICEPS FEMORIS SHEAR WAVE … E Aktaşoğlu, A Kiliç, M Şanlı, A İnci, E Aktas, İ Akdulum, N Yayli, İ Okur, ... SSIEM Annual Symposium 2022, Freiburg, 2022 | | 2022 |
