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You searched for: Author/Creator Knowles, Michael R.

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1. Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia in two patients with obstructive hydrocephalus. Issue 7 (15th June 2021)

2. Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review. Issue 2 (29th September 2015)

3. Otolaryngology Manifestations of Primary Ciliary Dyskinesia: A Multicenter Study. (March 2022)

4. Randomization of Left-Right Asymmetry and Congenital Heart Defects: The Role of DNAH5 in Humans and Mice. (November 2019)

5. Recurring large deletion in DRC1 (CCDC164) identified as causing primary ciliary dyskinesia in two Asian patients. Issue 8 (4th July 2019)

6. Pseudomonas aeruginosa associated with severity of non-cystic fibrosis bronchiectasis measured by the modified bronchiectasis severity score (BSI) and the FACED: The US bronchiectasis and NTM Research Registry (BRR) study. (February 2021)

7. The expanding phenotype of OFD1‐related disorders: Hemizygous loss‐of‐function variants in three patients with primary ciliary dyskinesia. Issue 9 (1st August 2019)

8. Cytoplasmic "ciliary inclusions" in isolation are not sufficient for the diagnosis of primary ciliary dyskinesia. Issue 1 (23rd September 2019)

10. The prevalence of the defining features of primary ciliary dyskinesia within a cri du chat syndrome cohort. Issue 11 (20th September 2018)