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Publications by Peter G Barth
The Neurology of Rhizomelic Chondrodysplasia Punctata
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Natural Course of Pontocerebellar Hypoplasia Type 2A
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
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Rhizomelic Chondrodysplasia Punctata
Rhizomelic Chondrodysplasia Punctata: A Classic 'Spot' Diagnosis
BMJ Case Reports
Medicine
118: Multiple Peroxisomal Enzyme Deficiencies in Rhizomelic Chondrodysplasia Punctata
Pediatric Research
Child Health
Pediatrics
Perinatology
Chondrodysplasia Punctata
Medical Journal Armed Forces India
Medicine
Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene
JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
Chondrodysplasia Punctata
Aberrant Subcellular Localization of Peroxisomal 3-Ketoacyl-CoA Thiolase in the Zellweger Syndrome and Rhizomelic Chondrodysplasia Punctata
Pediatric Research
Child Health
Pediatrics
Perinatology
X-Linked Dominant Chondrodysplasia Punctata
Oral Administration of a Synthetic Vinyl-Ether Plasmalogen Normalizes Open Field Activity in a Mouse Model of Rhizomelic Chondrodysplasia Punctata
DMM Disease Models and Mechanisms
Immunology
Molecular Biology
Biochemistry
Microbiology
Neuroscience
Medicine
Genetics