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Publications by William R. Wilcox

Response to Saul

Genetics in Medicine
MedicineGenetics
2015English

Fabry Disease in Infancy and Early Childhood: A Systematic Literature Review

Genetics in Medicine
MedicineGenetics
2014English

FGFR3 Signaling Induces a Reversible Senescence Phenotype in Chondrocytes Similar to Oncogene-Induced Premature Senescence

Bone
EndocrinologyPhysiologyHistologyMetabolismDiabetes
2010English

Neutral Endopeptidase-Resistant C-Type Natriuretic Peptide Variant Represents a New Therapeutic Approach for Treatment of Fibroblast Growth Factor Receptor 3-Related Dwarfism

Journal of Pharmacology and Experimental Therapeutics
Molecular MedicinePharmacology
2015English

Two-Tiered Newborn Screening With Post-Analytical Tools for Pompe Disease and Mucopolysaccharidosis Type I Results in Performance Improvement and Future Direction

International Journal of Neonatal Screening
Child HealthPediatricsGynecologyPerinatologyMicrobiology ObstetricsImmunology
2020English

Sustained, Long-Term Renal Stabilization After 54 Months of Agalsidase Beta Therapy in Patients With Fabry Disease

Journal of the American Society of Nephrology : JASN
MedicineNephrology
2007English

Dynamic Cervicomedullary Cord Compression and Alterations in Cerebrospinal Fluid Dynamics in Children With Achondroplasia

Journal of Neurosurgery: Pediatrics
Child HealthPerinatologyNeurologyMedicinePediatricsSurgery
2007English

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