The Turkish Journal of Pediatrics
Smilar Issues: 14 Record Found
Molecular analysis of neurofibromatosis type 1 in Turkish families using polymorphic markers
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Neurological soft signs in comorbid learning and attention deficit hyperactivity disorders
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Cognitive functions in neurofibromatosis type 1 patients and unaffected siblings
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Learning Disability And Oligodendrocyte Myelin Glycoprotein (OMGP) Gene in Neurofibromatosis Type 1
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Relationship between metabolic control and neurocognitive functions in children diagnosed with type I diabetes mellitus before and after 5 years of age
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Oncologic Manifestations in Children with Neurofibromatosis Type 1 in Turkey
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Pseudoarthrosis of the Hand in Neurofibromatosis Type 1: A Case Report
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Development of a Screening Tool for Children Prior to School Entrance
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Simultaneous Presentation of Malignant Peripheral Nerve Sheath Tumor and Moyamoya Disease Associated with Neurofibromatosis Type 1 in a Child
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Are the methylenetetrahydrofolate reductase 1298 and 677 gene polymorphisms related to optic glioma and hamartoma risk in neurofibromatosis type 1 patients?
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Cognitive and behavioral impairment in mild hyperphenylalaninemia
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Systemic hypertension followed by insidious stroke in a 12-year-old boy with childhood neurofibromatosis type 1 presenting with renal and cerebral artery vasculopathy
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Neurocognitive abilities in individuals with Down syndrome-a narrative review
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Early-auditory intervention in children with hearing loss and neurodevelopmental outcomes: cognitive, motor and language development
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