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Publications by Harald Stefanits
Initial Diagnosis of the Congenital Disorder of Glycosylation PMM2-CDG (CDG1a) in a 4-Year-Old Girl After Neurosurgical Intervention for Cerebral Hemorrhage
Journal of Neurosurgery: Pediatrics
Child Health
Perinatology
Neurology
Medicine
Pediatrics
Surgery
Clinical Neuropathology Practice Guide 3-2013: Levels of Evidence and Clinical Utility of Prognostic and Predictive Candidate Brain Tumor Biomarkers
Clinical Neuropathology
Medicine
Forensic Medicine
Pathology
Neurology
Related publications
Pmm2-CDG
Anesthetic Management of a Boy With Congenital Disorder of Glycosylation (CDG) I-X
International Journal of Clinical Medicine
Further Delineation of the Phenotype of Congenital Disorder of Glycosylation DPAGT1-CDG (CDG-Ij) Identified by Homozygosity Mapping
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Nutritional Therapies in Congenital Disorders of Glycosylation (CDG)
Nutrients
Nutrition
Food Science
Dietetics
Congenital Disorder of Glycosylation Type Ia (CDG-Ia): Phenotypic Spectrum of the R141h/F119l Genotype
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Congenital Disorder of Glycosylation
Child Neurology: A Case of PMM2-CDG (CDG 1a) Presenting With Unusual Eye Movements
Neurology
Neurology
P89 Toxic Epidermal Necrolysis in a 4 Year Old Girl in the UAE
Early Initial Diagnosis of Gardner Syndrome in a 12-Year-Old Boy
Advances in Computed Tomography
