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Publications by William A. Gahl
The Immunome in Two Inherited Forms of Pulmonary Fibrosis
Frontiers in Immunology
Allergy
Immunology
Cellular and Clinical Report of New Griscelli Syndrome Type III Cases
Pigment Cell and Melanoma Research
Biochemistry
Dermatology
Oncology
Genetics
Molecular Biology
Identification, Tissue Distribution, and Molecular Modeling of Novel Human Isoforms of the Key Enzyme in Sialic Acid Synthesis, UDP-GlcNAc 2-Epimerase/ManNAc Kinase
Biochemistry
Biochemistry
Novel 47.5-Kb Deletion in RAB27A Results in Severe Griscelli Syndrome Type 2
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Clinical and Molecular Phenotyping of a Child With Hermansky-Pudlak Syndrome-7, an Uncommon Genetic Type of HPS
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Combined Alpha-Delta Platelet Storage Pool Deficiency Is Associated With Mutations in GFI1B
Molecular Genetics and Metabolism
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
Management of Bone Disease in Cystinosis: Statement From an International Conference
Journal of Inherited Metabolic Disease
Genetics
Non-Specific Accumulation of Glycosphingolipids in GNE Myopathy
Journal of Inherited Metabolic Disease
Genetics
Metabolic Acetate Therapy Improves Phenotype in the Tremor Rat Model of Canavan Disease
Journal of Inherited Metabolic Disease
Genetics
Immunophenotypic and Ultrastructural Analysis of Mast Cells in Hermansky-Pudlak Syndrome Type-1: A Possible Connection to Pulmonary Fibrosis
PLoS ONE
Multidisciplinary
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