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Author/Creator Walker, Woolf

2. Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort. Issue 5 (25th December 2019)

Authors:
Fassad, Mahmoud R.; Patel, Mitali P.; Shoemark, Amelia; Cullup, Thomas; Hayward, Jane; Dixon, Mellisa; Rogers, Andrew V.; Ollosson, Sarah; Jackson, Claire; Goggin, Patricia; Hirst, Robert A.; Rutman, Andrew; Thompson, James; Jenkins, Lucy; Aurora, Paul; Moya, Eduardo; Chetcuti, Philip; O'Callagha...
Journal:
Journal of medical genetics
Issue:
Volume 57:Issue 5(2020)
Page Start:
322
Record Type:
Journal Article
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3. High prevalence of CCDC103 p.His154Pro mutation causing primary ciliary dyskinesia disrupts protein oligomerisation and is associated with normal diagnostic investigations. Issue 2 (8th August 2017)

Authors:
Shoemark, Amelia; Moya, Eduardo; Hirst, Robert A; Patel, Mitali P; Robson, Evelyn A; Hayward, Jane; Scully, Juliet; Fassad, Mahmoud R; Lamb, William; Schmidts, Miriam; Dixon, Mellisa; Patel-King, Ramila S; Rogers, Andrew V; Rutman, Andrew; Jackson, Claire L; Goggin, Patricia; Rubbo, Bruna; Olloss...
Journal:
Thorax
Issue:
Volume 73:Issue 2(2018)
Page Start:
157
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. An international survey on nasal nitric oxide measurement practices for the diagnosis of primary ciliary dyskinesia. Issue 2 (4th April 2022)

Authors:
Beydon, Nicole; Ferkol, Thomas; Harris, Amanda Lea; Colas, Murielle; Davis, Stephanie D.; Haarman, Eric; Hogg, Claire; Kilbride, Emma; Kouis, Panayotis; Kuehni, Claudia E.; Latzin, Philipp; Marangu, Diana; Marthin, June; Nielsen, Kim G.; Robinson, Phil; Rumman, Nisreen; Rutter, Matthew; Walker, W...
Journal:
ERJ open research
Issue:
Volume 8:Issue 2(2022)
Page Start:
Record Type:
Journal Article
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