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Search Results to Scott D Sagel

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Sagel, Scott

One or more keywords matched the following items that are connected to Sagel, Scott

Item Type	Name
Academic Article	Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure.
Academic Article	Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms.
Concept	Cilia
Academic Article	ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.
Academic Article	Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia.
Academic Article	Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.
Academic Article	Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.
Academic Article	Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.
Academic Article	Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experience.
Academic Article	Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.
Academic Article	Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents.
Academic Article	Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline.
Academic Article	Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype.
Academic Article	Cytoplasmic "ciliary inclusions" in isolation are not sufficient for the diagnosis of primary ciliary dyskinesia.
Academic Article	Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype.
Academic Article	Airway Disease in Children with Primary Ciliary Dyskinesia: Impact of Ciliary Ultrastructure Defect and Genotype.
Academic Article	Decoding negative genetic panels in primary ciliary dyskinesia.

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Cilia