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1 |
Two-year follow-up of musculoskeletal outcomes and quality of life in patients with mucopolysaccharidosis type IV and VI Enthalten in The journal of pediatric endocrinology and metabolism Bd. 39, 2026, Nr. 8: 756-767. 12 S.
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2 |
Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 2: 138-151. 14 S.
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3 |
Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 2: 138-151. 14 S.
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4 |
Clinical and Radiological Profile of Nine Patients with Metachromatic Leukodystrophy Enthalten in Molecular syndromology Bd. 16, 2025, Nr. 2: 138-151. 14 S.
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5 |
Laboratory and Genotype Relationship of Patients with SDHA-Related Mitochondrial Disease Enthalten in Molecular syndromology Bd. 14, 2023, Nr. 6: 459-460. 2 S.
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6 |
Two Patients Diagnosed as Succinate Dehydrogenase Deficiency: Case Report Enthalten in Molecular syndromology Bd. 14, 2023, Nr. 2: 171-174. 4 S.
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7 |
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium Enthalten in Functional & integrative genomics 31.1.2022: 1-25
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8 |
Clinical and biochemical evaluation of oral irrigation in patients with peri-implant mucositis: a randomized clinical trial Enthalten in Clinical oral investigations 12.7.2021: 1-13
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9 |
Two distinct skeletal muscle microRNA signatures revealing the complex mechanism of sporadic ALS Enthalten in Acta neurologica Belgica 9.7.2021: 1-11
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10 |
Biologia Futura: the importance of 3D organoids—a new approach for research on neurological and rare diseases Enthalten in Biologia futura 10.2.2021: 1-10
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