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Publications by Alan Balfe
Aberrant Subcellular Localization of Peroxisomal 3-Ketoacyl-CoA Thiolase in the Zellweger Syndrome and Rhizomelic Chondrodysplasia Punctata
Pediatric Research
Child Health
Pediatrics
Perinatology
Related publications
118: Multiple Peroxisomal Enzyme Deficiencies in Rhizomelic Chondrodysplasia Punctata
Pediatric Research
Child Health
Pediatrics
Perinatology
Rhizomelic Chondrodysplasia Punctata
The Neurology of Rhizomelic Chondrodysplasia Punctata
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Rhizomelic Chondrodysplasia Punctata: A Classic 'Spot' Diagnosis
BMJ Case Reports
Medicine
The 22-kD Peroxisomal Integral Membrane Protein in Zellweger Syndrome—Presence, Abundance, and Association With a Peroxisomal Thiolase Precursor Protein
Pediatric Research
Child Health
Pediatrics
Perinatology
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
Medical Journal Armed Forces India
Medicine
Chondrodysplasia Punctata
Lipidomics Analysis of Peroxisomal Disorders: Discovery of Deficits in Phosphatidyglycerol Levels in Rhizomelic Chondrodysplasia Type 1
Journal of Data Mining in Genomics & Proteomics
