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Publications by Akif Ayaz
Familial Mutation in Caffey Disease With Reduced Penetrance: A Case Report
Turkish Journal of Pediatrics
Child Health
Pediatrics
Perinatology
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Caffey Disease or Infantile Cortical Hyperostosis: A Case Report
IOSR Journal of Dental and Medical Sciences
TDP-43 Proteinopathy in Familial Motor Neurone Disease With TARDBP A315T Mutation: A Case Report
Neuropathology and Applied Neurobiology
Forensic Medicine
Pathology
Neurology
Histology
Physiology
Low-Penetrance of RB-1 Gene Mutation in Familial Retinoblastoma 135
Pediatric Research
Child Health
Pediatrics
Perinatology
Familial Hypercholesterolemia With Early Coronary Atherosclerotic Heart Disease: A Case Report
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Rare Genetic Creutzfeldt-Jakob Disease With E196A Mutation: A Case Report
Prion
Biochemistry
Molecular Neuroscience
Infectious Diseases
Cell Biology
Cellular
Cognitive Impairment and Fabry Disease: A Case Report With Mutation S126G
Neuropsychological Trends
Molecular Neuroscience
Physiological Psychology
Neuropsychology
Cellular
Case Report: Maple Syrup Urine Disease With a Novel DBT Gene Mutation
BMC Pediatrics
Child Health
Pediatrics
Perinatology
Familial Hypercalcaemic Hypocalciuria in a Woman With Graves[apos] Disease: A Case Report of Mistaken Identity
Endocrine Abstracts
A Novel Compound Heterozygous Stxbp2 Mutation in a Case With Familial Hemophagocytic Lymphohistiocytosis
Turkish Journal of Pediatric Disease