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Barth syndrome: Natural history in infants and young children.
Molecular Genetics and MetabolismBarth syndrome (BTHS) is a rare X-linked mitochondrial disorder caused by pathogenic variants in TAFAZZIN. It is characterized by cardiomyopathy, neutropenia, growth delay, skeletal myopathy, and developmental concerns.
Sharada Vishwanath +4 more
semanticscholar +1 more source
Clinical utility of the Negative Symptom Assessment-16 in individuals with schizophrenia.
European Neuropsychopharmacology, 2019This study examined the clinical utility of the Negative Symptom Assessment-16 (NSA-16) in schizophrenia. 274 individuals with schizophrenia were assessed on the NSA-16, Positive and Negative Syndrome Scale (PANSS), Clinical Assessment for Negative ...
G. Rekhi, L. Alphs, M. Ang, Jimmy Lee
semanticscholar +1 more source
Neuropsychology of sports-related head injury: Dementia Pugilistica to Post Concussion Syndrome.
Clinical Neuropsychologist, 1999D. Erlanger +3 more
semanticscholar +1 more source
Long-Term Follow-up of an Epidemiologically Defined Cohort of Patients With Tourette Syndrome
Journal of Child Neurology, 2001L. Burd +5 more
semanticscholar +1 more source
Fungiform Papilla Number and Olfactory Threshold Assessment in Males With and Without Barth Syndrome
Chemosensory Perception, 2017S. Reynolds +4 more
semanticscholar +1 more source
Clinical presentation and natural history of Barth Syndrome: An overview
Journal of Inherited Metabolic Disease, 2022Hilary Vernon +2 more
exaly
Psychosocial functioning in Barth syndrome: Assessment of individual and parental adjustment
, 2017Marni L. Jacob +4 more
semanticscholar +1 more source
Experimental models of Barth syndrome
Journal of Inherited Metabolic Disease, 2022William T Pu
exaly