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Publications by A. Onoufriadis
S88 Electron Tomography Detects Ultrastructural Abnormalities in Patients With PCD Due to a Dnah11 Defect
Thorax
Pulmonary
Respiratory Medicine
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31P NMR Spectroscopy Detects Metabolic Abnormalities in Asymptomatic Patients With Hypertrophic Cardiomyopathy
Circulation
Cardiovascular Medicine
Physiology
Cardiology
Chromosomal Abnormalities in 1354 Japanese Patients With Azoospermia Due to Spermatogenic Dysfunction
International Journal of Urology
Urology
Electron Tomography With In-Situ Deformation
Materia Japan
Congenital Jaundice in Rats, Due to a Defect in Glucuronide Formation1
Journal of Clinical Investigation
Medicine
Quantitative Proton Magnetic Resonance Spectroscopy Detects Abnormalities in Dorsolateral Prefrontal Cortex and Motor Cortex of Patients With Frontotemporal Lobar Degeneration
Journal of Neurology
Neurology
Periodic Attacks of Lethargy in a Baby With Ammonia Intoxication Due to a Congenital Defect in Ureogenesis.
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Lactic Acidosis Due to a Defect in Pyruvate Metabolism in 3 Siblings
Pediatric Research
Child Health
Pediatrics
Perinatology
Actions on a Railway Track, Due to an Isolated Defect
International Journal of Control and Automation
Control
Systems Engineering
PCD - What's in a Name?
British Dental Journal
Dentistry
