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Respiratory tract paralysis
(phenotype)
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Genetic Markers
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No genes found
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OMIM - Congenital disorder
OMIM - Multisystem Complex Disorders
OMIM - Congenital laryngeal adductor palsy
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INTRAVENTRICULAR CONDUCTION DEFECT AND RESPIRATORY TRACT PARALYSIS IN DIABETIC KETOACIDOSIS.
PCR diagnosis of primary herpesvirus type I in poliomyelitis-like paralysis and respiratory tract di…
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Transformation of Paralysis to Stepping
Prospective Cohort Study of Molecular Mechanism of Lower Respiratory Tract Microbes in Patients With…
Chronic Respiratory Disease Burden in Bangladesh
Trial of ECMO to De-Sedate, Extubate Early and Mobilise in Hypoxic Respiratory Failure
The REDEEM Pilot Study: A Feasibility RCT of Early ECMO in Severe Acute Respiratory Infection, Inclu…
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