25 results on '"Hannah, William B."'
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2. The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysis
3. Frequency of Cystic Fibrosis Transmembrane Conductance Regulator Variants in Individuals Evaluated for Primary Ciliary Dyskinesia
4. Screening data from 19 patients with late‐onset Pompe disease for a phase I clinical trial of AAV8 vector‐mediated gene therapy
5. Hemophilia A and B mice, but not VWF−/−mice, display bone defects in congenital development and remodeling after injury
6. Screening data from 19 patients with late‐onset Pompe disease for a phase I clinical trial of AAV8 vector‐mediated gene therapy.
7. Clinical insights from Wolman disease: Evaluating infantile hepatosplenomegaly
8. Very early-onset inflammatory bowel disease: Novel description in glycogen storage disease type Ia
9. Identification of auxins by a chemical genomics approach
10. A novel cause of emergent hyperammonemia: Cryptococcal fungemia and meningitis
11. “Disappearing Infarct” is Late‐onset MELAS
12. The global prevalence and ethnic heterogeneity of primary ciliary dyskinesia gene variants: a genetic database analysis
13. Genetic modifiers of liver disease in cystic fibrosis
14. Adenotonsillectomy should be avoided whenever possible in infantile-onset Pompe disease
15. Life-threatening presentations of propionic acidemia due to the Amish PCCB founder variant
16. The expanding phenotype of OFD1 ‐related disorders: Hemizygous loss‐of‐function variants in three patients with primary ciliary dyskinesia
17. Rapid Advances in Primary Ciliary Dyskinesia Research. A Brief Update for Pulmonologists
18. Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibrosis population
19. Carotid Artery Mycotic Pseudoaneurysm Associated with Campylobacter fetus Bacteremia in an Immunocompromised Host
20. Employing a Gain-of-Function Factor IX Variant R338L to Advance the Efficacy and Safety of Hemophilia B Human Gene Therapy: Preclinical Evaluation Supporting an Ongoing Adeno-Associated Virus Clinical Trial
21. Carotid Artery Mycotic Pseudoaneurysm Associated with Campylobacter fetusBacteremia in an Immunocompromised Host
22. Hemophilia A and B mice, but not VWF−/−mice, display bone defects in congenital development and remodeling after injury.
23. Employing a Gain-of-Function Factor IX Variant R338L to Advance the Efficacy and Safety of Hemophilia B Human Gene Therapy: Preclinical Evaluation Supporting an Ongoing Adeno-Associated Virus Clinical Trial
24. Rapid Advances in Primary Ciliary Dyskinesia Research. A Brief Update for Pulmonologists.
25. Using genomic databases to determine the frequency and population-based heterogeneity of autosomal recessive conditions
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