Search

Author/Creator Quarrell, Oliver

1. A survey-based study identifies common but unrecognized symptoms in a large series of juvenile Huntington's disease. (October 2017)

Authors:
Moser, Amelia D; Epping, Eric; Espe-Pfeifer, Patricia; Martin, Erin; Zhorne, Leah; Mathews, Katherine; Nance, Martha; Hudgell, Denise; Quarrell, Oliver; Nopoulos, Peg
Journal:
Neurodegenerative disease management
Issue:
Volume 7:Number 5(2017)
Page Start:
307
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis. Issue 9 (28th June 2013)

Authors:
Burkitt Wright, Emma MM; Sach, Emma; Sharif, Saba; Quarrell, Oliver; Carroll, Thomas; Whitehouse, Richard W; Upadhyaya, Meena; Huson, Susan M; Evans, D Gareth R
Journal:
Journal of medical genetics
Issue:
Volume 50:Issue 9(2013)
Page Start:
606
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Clinical and genetic characteristics of late-onset Huntington's disease. (April 2019)

Authors:
Bachoud-Lévi, Anne-Catherine; Bentivoglio, Anna-Rita; Biunno, Ida; Bonelli, Raphael M.; Bronzova, Juliana; Burgunder, Jean-Marc; Dunnett, Stephen B.; Ferreira, Joaquim J.; Frich, Jan; Giuliano, Joe; Handley, Olivia J.; Heiberg, Arvid; Illarioshkin, Sergey; Illmann, Torsten; Klempir, Jiri; Landweh...
Journal:
Parkinsonism & related disorders
Issue:
Volume 61(2019)
Page Start:
101
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. F13 Assessment of the performance of a modified motor scale as applied to juvenile onset huntington's disease. (September 2018)

Authors:
Horton, Mike C; Nopoulos, Peggy; Nance, Martha; Landwehrmeyer, G Bernhard; Barker, Roger A; Squitieri, Ferdinando; Burgunder, Jean-Marc; Quarrell, Oliver
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 89(2018)Supplement 1
Page Start:
A44
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

10. Homozygous GDF2 nonsense mutations result in a loss of circulating BMP9 and BMP10 and are associated with either PAH or an "HHT‐like" syndrome in children. Issue 12 (9th April 2021)

Authors:
Hodgson, Joshua; Ruiz‐Llorente, Lidia; McDonald, Jamie; Quarrell, Oliver; Ugonna, Kelechi; Bentham, James; Mason, Rebecca; Martin, Jennifer; Moore, David; Bergstrom, Katie; Bayrak‐Toydemir, Pinar; Wooderchak‐Donahue, Whitney; Morrell, Nicholas W.; Condliffe, Robin; Bernabeu, Carmelo; Upton, Paul D.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 9:Issue 12(2021)
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗