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Publications by Bogna Brockhuis
A Patient With Posterior Cortical Atrophy Possesses a Novel Mutation in the Presenilin 1 Gene
PLoS ONE
Multidisciplinary
Agraphia in Patients With Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17 With P301LMAPTmutation: Dysexecutive, Aphasic, Apraxic or Spatial Phenomenon?
Neurocase
Arts
Neurology
Humanities
Related publications
Posterior Cortical Atrophy
A Novel POLG Gene Mutation in a Patient With SANDO
Journal of Experimental and Integrative Medicine
Alternative Medicine
Complementary
A Novel Mutation of the Ceruloplasmin Gene in a Patient With Heteroallelic Ceruloplasmin Gene Mutation (HypoCPGM)
Tohoku Journal of Experimental Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
A Novel Missense OPA1 Mutation in a Patient With Dominant Optic Atrophy and Cervical Dystonia
Movement Disorders Clinical Practice
Neurology
A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1
Annals of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Facilitating Text Reading in Posterior Cortical Atrophy
Neurology
Neurology
Upside-Down Drawing in Posterior Cortical Atrophy
Canadian Journal of Neurological Sciences
Medicine
Neurology
A Novel Mutation in the NCF2 Gene in a CGD Patient With Chronic Recurrent Pneumopathy
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
A Novel Nonsense Mutation of the PEPD Gene in a Japanese Patient With Prolidase Deficiency
Journal of Human Genetics
Genetics
